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abortion, spontaneous

acid maltase deficiency

acid maltase deficiency, adult

acquired immunodeficiency syndrome

acquired immunodeficiency syndrome dementia complex

acquired immunodeficiency syndrome dementia complex, pathogenesis

acquired immunodeficiency syndrome, congenital

acquired immunodeficiency syndrome, infants and children

activities of daily living

activities of daily living scale

acute cerebellar ataxia

acute disseminated encephalomyelitis

acute disseminated encephalomyelitis, relapsing

acute necrotizing encephalitis

addiction, heroin

addiction, heroin-neurologic complications with

Addison's disease

adenosine deaminase deficiency

adenylate kinase 5 autoantibodies

adolescent medicine

adrenal crisis, acute

adrenoleukodystrophy

adrenoleukodystrophy, adult onset

adrenoleukodystrophy, carrier

adrenomyeloneuropathy

adult polyglucosan body disease

adult-onset leukodystrophy, with neuroaxonal spheroids

advances in neurology

adverse drug reaction

affect, inappropriate

agenesis of corpus callosum

Aicardi-Goutieres syndrome

Aicardi's syndrome

alcohol, neurologic complications with

Alexanders disease

Alexanders disease, adult onset

alpha glucosidase

altered states of consciousness

alternating hemiplegia

alternating hemiplegia of childhood

alternative medicine

alveolar hypoventilation

Alzheimer's disease

Alzheimer's disease, behavioral symptoms

Alzheimer's disease, early symptoms

Alzheimer's disease, noncognitive symptoms

Alzheimer's disease, preclinical

Alzheimer's disease, risk factors in

Alzheimer's disease, treatment of

aminoacidopathies

aminopyridine, 4

AMPA receptor antibodies

amphiphysin antibodies

amyloid angiopathy, cerebral

amyloid angiopathy, cerebral, inflammatory type

amyloid beta protein

amyloid beta-related angiitis

amyloid deposition

amyotrophic lateral sclerosis

anemia, megaloblastic

anesthesia, general

aneurysm, abdominal aortic

aneurysm, asymptomatic

aneurysm, intracranial

aneurysm, intracranial, acute deterioration

aneurysm, intracranial, delayed cerebral ischemia with

aneurysm, intracranial, natural history

aneurysm, thoracic aortic

Angelman syndrome

angiitis, granulomatous of CNS

angiitis, isolated of CNS

angiitis, isolated of CNS, benign focal

angiofibroma, facial

angiography, cerebral, beaded vessels

angiography, cerebral

angiography, cerebral, false negative

angiography, cerebral, negative

angiography, cerebral, reversible abnormality

angiography, spinal

animal exposure

ankle, swelling of

anterior horn cell disease

anterior tibial muscle weakness

anti citrullinated antibody

anti MAG antibodies

anti Ro antibody

antibiotic prophylaxis

antibodies to measles

antibodies to voltage-gated calcium channels

anticholinesterase

anticoagulant, complications of

anticoagulant, contraindications

anticoagulant, treatment

anticoagulant, treatment in CVD

anticonvulsants

anticonvulsants, blood level determination of

anticonvulsants, cognitive function with

anticonvulsants, selection of

anticonvulsants, teratogenicity of

anticonvulsants, untoward effects of

antithyroid antibodies

antiviral agents

aphasia, conduction

aphasia, progressive, non-fluent

aphasia, progressive, primary

apolipoprotein E

apraxia of eye movements

apraxia, constructional

aqueduct of Sylvius, stenosis

arm swing, reduced

Arnold Chiari malformation

aromatic amino acid decarboxylase deficiency

arrhythmia, cardiac

arterial dissection

arterial dissection, carotid

arteriovenous malformation, cerebral

arthrogryposis multiplex

arthropathy, neuropathic

artificial intelligence

arylsulfatase A

ascending paralysis

aspartate aminotransferase

Asperger's syndrome

asterixis, causes of

asterixis, unilateral

ataxia, cerebellar

ataxia, congenital

ataxia, hereditary

ataxia, progressive

ataxia, truncal

atrial fibrillation

attention deficit disorder with hyperactivity

audiologic test to localize site of pathology

auditory evoked brainstem potentials

autism, screening for

autistic behavior

autoimmune disease

autoimmune encephalopathy

autoimmune epilepsy

automobile accidents

autonomic dysfunction

autonomic nervous system

axonal degeneration

axonal spheroid

azidodeoxythymidine

B 12 deficiency

B cell lymphoma

bacterial infection

ballismus, bilateral

Bannayan-Riley-Ruvalcaba syndrome

basal cell carcinoma

basal ganglia, calcification of

basal ganglia, hemorrhage

basal ganglia, infarction

basal ganglia, lesion of

basal ganglia, lesion, bilateral

basilar artery migraine

behavior modification

behavior, combative

behavioral disorder

behavioral disorder, acute

Behcet's syndrome

benign essential tremor

beta adrenergic blocker

bilateral periventricular nodular heterotopia

Binswanger disease

biologic markers

bionic reconstruction

biopterin deficiency

biotin deficiency

biotin deficiency, juvenile form

biotinidase deficiency

bladder dysfunction

blindness, sudden

blood transfusion

bone marrow biopsy

bone marrow infarction

bone marrow necrosis

bone marrow transplantation

bovine spongiform encephalopathy

brachial plexus injury

brain biopsy, false negative

brain plasticity

brainstem, atrophy

brainstem, dysfunction

brainstem, hypoplasia

brainstem, infarction of

brainstem, ischemia

brainstem, lesion of

bruit, abdominal

bruit, supraclavicular

bulbar dysfunction

burning paresthesia

calcification, gyral

calcification, intracranial

calcium antagonist

calf hypertrophy

Call-Fleming syndrome

campylobacter infection

Canavan's disease

carbon monoxide poisoning

carbonic anhydrase II deficiency

carcinoma of breast

carcinoma of lung

cardiac arrest and resuscitation

cardiac surgery, hypothermia and circulatory arrest for

cardiac surgery, neurologic complications with

cardiopulmonary bypass

cardiovascular disease

carotid artery disease

carotid artery disease, asymptomatic

carotid artery disease, medical management

carotid artery ligation

carotid artery occlusion, intracranial

carotid artery stenosis

carotid artery stenosis, bilateral

CAT scan, abnormal

CAT scan, angiography

CAT scan, angiography, false negative

CAT scan, cerebrovascular disease

CAT scan, chest

CAT scan, contrast enhanced

CAT scan, contrast enhanced, delayed

CAT scan, contrast enhanced, double dose

CAT scan, dense artery sign

CAT scan, early changes in CVA

CAT scan, emission

CAT scan, emission, abnormal

CAT scan, false negative

CAT scan, venography

cataracts, congenital

cauda equina, enhancement

cauda equina, lesion of

caudate nucleus

caudate nucleus, atrophy

caudate nucleus, infarction

caudate nucleus, lesion of

caudate nucleus, lesion of, bilateral

celiac disease, childhood

central hypoventilation

central hypoventilation, congenital

central nervous system, infection of

central pontine myelinolysis

cerebellar ataxia, children

cerebellar ataxia, primary

cerebellar atrophy, primary

cerebellar atrophy, secondary

cerebellar cognitive affective syndrome

cerebellar degeneration

cerebellar disease, eye movement disorder in

cerebellar hypoplasia

cerebellar infarction

cerebellar lesion

cerebellar peduncle

cerebellar vermis

cerebellum, disease of

cerebral arteries

cerebral arteries, territory of

cerebral atherosclerosis

cerebral atherosclerosis, medical management

cerebral cortex

cerebral cortical atrophy

cerebral dominance

cerebral edema, cytotoxic

cerebral edema, origin and treatment

cerebral edema, vasogenic

cerebral embolism

cerebral embolism, cardiac origin

cerebral embolism, mechanical extraction

cerebral folate deficiency syndrome

cerebral glucose metabolism

cerebral hypoperfusion

cerebral infarction

cerebral infarction, hemorrhagic

cerebral ischemia

cerebral palsy, adults

cerebral palsy, associated problems with

cerebral palsy, etiology

cerebral palsy, risk factors

cerebral palsy, work up

cerebral venous thrombosis

cerebro hepato renal syndrome

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, amonia

cerebrospinal fluid, cytology

cerebrospinal fluid, drainage of

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, enzymes in

cerebrospinal fluid, gammaglobulin of

cerebrospinal fluid, glutamine

cerebrospinal fluid, lactic acid concentration

cerebrospinal fluid, leak

cerebrospinal fluid, oligoclonal IgG in

cerebrospinal fluid, pressure low

cerebrospinal fluid, protein of

cerebrospinal fluid, proteincytologic dissociation

cerebrospinal fluid, red cells in

cerebrospinal fluid, xanthochromia of

cerebrotendinous xanthomatosis

cerebrovascular accident

cerebrovascular accident, acute management of

cerebrovascular accident, arterial occlusion, location

cerebrovascular accident, bilateral

cerebrovascular accident, classification

cerebrovascular accident, clinical diagnosis

cerebrovascular accident, complications with

cerebrovascular accident, delay in treatment

cerebrovascular accident, etiology

cerebrovascular accident, familial occurrence

cerebrovascular accident, incidence of

cerebrovascular accident, infancy and childhood

cerebrovascular accident, mass effect with

cerebrovascular accident, misdiagnosis

cerebrovascular accident, multiple

cerebrovascular accident, neonatal

cerebrovascular accident, non atherosclerotic cause of

cerebrovascular accident, nonvascular territory

cerebrovascular accident, prehospital screening

cerebrovascular accident, prehospital treatment

cerebrovascular accident, prevention of

cerebrovascular accident, prognosis in

cerebrovascular accident, recurrent

cerebrovascular accident, rehabilitation of

cerebrovascular accident, severity

cerebrovascular accident, silent

cerebrovascular accident, surgical treatment of

cerebrovascular accident, thrombolytic agents in treatment

cerebrovascular accident, time of onset

cerebrovascular accident, time to treatment

cerebrovascular accident, volume

cerebrovascular accident, women

cerebrovascular accident, work up for

cerebrovascular accident, young adult

cerebrovascular disease

cerebrovascular disease, natural history of

cerebrovascular disease, risk factors in

ceruloplasmin, serum

cervical spine injury

cervical spine manipulation

Charcot-Marie-Tooth

chasing the dragon

chemotherapy, CNS treatment and complications with

chenodeoxycholic acid

cherry red spot

cherry red spot-myoclonus syndrome

chest x-ray, abnormal

chewing movements

chilbran skin lesions

chiropractic manipulation

choreoathetosis

chorioretinitis

chromosomal abnormality

chronic fatigue syndrome

chronic traumatic encephalopathy

cingulate island sign

cisterna magna, enlarged

claudication, extremity

Clinical Pathologic Conference(C.P.C.)

clinicoradiologic dissociation

clubbing of fingers

clubfoot as related to neurologic disease

cocaine, intrauterine exposure

cochlear implant

Cockayne's syndrome

codfish vertebrae

Coffin-Siris syndrome

cognition, slowed

cognitive delay

cogwheel rigidty

coin rotation test

cold hands sign

cold temperature

collapsin response mediator protein 5 IgG

color vision, impaired

coma, prognosis of

compression fracture

concentration, impaired

conduction block

confusional state, acute

congenital bilateral perisylvian syndrome

congenital birth defects

congenital deformities

congenital heart disease

congenital heart disease, CNS complications with

congenital infection, CNS

congenital infection, viral

congenital malformation

congenital malformation, dilantin therapy causing

congenital malformation, non CNS

congenital myasthenic syndromes

congenital myopathy

congenital myopathy, inflammatory

congenital ocular motor apraxia

congestive heart failure

conjugate gaze, forced

conjunctival biopsy

contractures, joint

controversies in neurology

conversion reaction

cooling therapy

copper deficiency

copper metabolism, abnormal

cornea, opacification in infancy-causes of

cornea, opacity of

coronary artery bypass

coronary artery disease

corpus callosum

corpus callosum, atrophy of

corpus callosum, hypoplastic

corpus callosum, lesion of

corpus callosum, thinning

cortical blindness

cortical blindness, transient

cortical demyelination

cortical dysplasia, focal

cortical vein thrombosis

cost effectiveness

cranial nerve palsies

cranial nerve palsies, bilateral

cranial neuropathy, multiple

craniectomy, decompressive

C-reactive protein, elevated

creatine phosphokinase(CPK)elevated

critical care unit

critical illness

crying, pathologic

cryopyrin-associated periodic syndrome

cryptococcal antigen

cryptococcal meningitis

cultured skin fibroblasts

Cushing's syndrome

cyclophosphamide

cyst, odontogenic

cyst, parenchymal

cyst, porencephalic

cytoarchitectonics, cerebral cortex

cytochrome c oxidase

cytochrome c oxidase, deficiency

cytomegalic inclusion disease

cytomegalovirus infection

cytomegalovirus infection, congenital

cytosine arabinoside

Dandy Walker malformation

deafness, congenital

decerebrate posture

decision analysis

deep gray nuclei

degenerative diseases of CNS

delay in diagnosis

delayed dentition

delayed muscle relaxation

delivery, complicated

dementia, age at onset

dementia, autoimmune

dementia, cerebrovascular disease causing

dementia, childhood

dementia, familial

dementia, frontal lobe type

dementia, frontotemporal

dementia, presenile

dementia, rapidly progressive

dementia, reversible

dementia, subcortical

dementia, thalamic

dementia, transmissible

dementia, treatment of

demyelinating disease

dentate nuclei, lesion of

Denver Developmental Screening test

depression, psychotic

dermatoglyphics

developmental abnormality of brain

developmental disability

developmental evaluation

developmental milestones

developmental milestones, loss of

developmental retardation

dexterity, impaired

diabetes mellitus

diagnostic criteria

dietary supplement

differential diagnosis

difficulty climbing stairs

difficulty going down stairs

digits, abnormal

diplegia, spastic cerebral

disability rating scale, neurological

disability, neurological

disconnection syndrome

disseminated intravascular coagulation(DIC)

distal muscle weakness

door to needle time

dopamine agonist

DPPX, antibodies

DPPX, antibodies, encephalitis

Dravet syndrome

driving restrictions

dropped head syndrome

drug abuse, inhalation

drug abuse, neurologic complications of

drug induced neurologic disorders

dural arteriovenous malformation

dural sinus thrombosis

dysdiadochokinesia

dyskinesia, buccal lingual facial

dyskinesia, facial

dysostosis multiplex

dystonia, cervical

dystonia, children

dystonia, focal

dystonic reaction, acute

ears of the Lynx MR sign

eating disorder

educational status

electrocardiogram, abnormal

electrocardiogram, LVH

electroencephalogram

electroencephalogram, abnormalities of

electroencephalogram, brain mapping

electroencephalogram, interictal

electroencephalogram, periodic complexes

electroencephalogram, video monitoring with

electron microscopy

electroretinograph

embolism, vertebral-basilar artery

emergencies, neurologic

emotional lability

encephalitis, autoimmune

encephalitis, brainstem

encephalitis, clinical picture and treatment of

encephalitis, diagnosis of

encephalitis, focal

encephalitis, human immunodeficiency virus type 1

encephalitis, La Crosse

encephalitis, paraneoplastic

encephalitis, Powassan

encephalitis, Rasmussen's

encephalitis, viral

encephalitis, viral-causes of

encephalomalacia

encephalomyelitis

encephalomyelitis, postinfectious

encephalopathy, anoxic

encephalopathy, delayed

encephalopathy, Hashimoto's

encephalopathy, metabolic

encephalopathy, neonatal

encephalopathy, post anoxic

encephalopathy, post traumatic

encephalopathy, progressive

endovascular photoacoustic recanalization

endovascular therapy

endovascular therapy, time window

enterovirus infection of CNS

entrapment neuropathy

enzyme treatment

enzyme, muscle disease

eosinophilia-myalgia syndrome

epicanthal folds

epidemiology of neurology

epidural blood patch

epileptic encephalopathy

episodic disorders

episodic neurologic deficits

Epstein-Barr virus

esophageal varices

ethics in neurology

ethylmalonic aciduria

ethylmalonic encephalopathy

evidence-based research

evoked potentials

executive dysfunction

exercise intolerance

exome sequencing

extension-flexion injury of cervical spine

extracorporeal membrane oxygenation

extralimbic encephalitis

eye movement, disorders of

face, numbness of

facial anomalies

facial appearance, abnormal

facial expression abnormality

facial hypoplasia

facial nerve palsy

facial weakness

facial weakness, bilateral

failed back syndrome

failure to thrive

Farber's disease

FARS2 deficiency

fatty acid, elevated plasma content

feeding disorder

fetal alcohol syndrome

fetal movements, reduced

fetal valproate syndrome

fever, recurrent

fibrinolytic agents

fibrinolytic agents, intra-venous local infusion

fibrinolytic therapy, timing of administration

fibroma, ungual

fine motor function, impaired

finger nose finger test

finger swelling

fingernails, abnormal

fingernails, hypoplastic

fingerprint bodies

Fisher's syndrome

fistula, arterio-venous

fistula, arterio-venous, dural

fistula, arterio-venous, dural, spinal

flaccid paralysis

flu-like illness

fluorescein angiography

fluorescene in situ hybridization

folic acid deficiency

food-borne infection

fornix, lesion of

fourth ventricle, enlargement of

fourth ventricle, floor

fracture, long bone

fracture, pathologic

Fragile-X associated tremor/ataxia-syndrome

fragile-X syndrome

fragile-X syndrome, carrier

Friedreich's ataxia

frontal bossing

frontal lobe, atrophy

frontal lobe, behavior with disease of

frontal lobe, pathologic signs of

frontotemporal dementia, behavioral variant

fundus, abnormality of

fungal infection

fungal infection, CNS

gag reflex, depressed

gamma amino butyric acid receptor antibody

gammaglobulin therapy, intravenous

gangliosidosis GM2

gastric partitioning

gastroenteritis

gastrointestinal disease, neurologic complications

Gaucher's disease

gaze palsy, horizontal

gaze palsy, supranuclear

gaze palsy, vertical

general movements

genetic counselling

genetic diagnosis, prenatal

genetic linkage

genetic neurologic disorders

genetic screening

genetic testing

genital ulcerations

genu of corpus callosum

geographic location

Gerstmann syndrome

Gilles de la Tourette syndrome

Gilles de la Tourette syndrome, natural history

Gillespie syndrome

Glasgow coma score

glioblastoma multiforme(astrocytoma Gr.III)

glioma, low-grade

globus pallidus

globus pallidus, lesion of

globus pallidus, lesion of, bilateral

glucocerebrosidase

GLUT1 deficiency syndrome

glutamic acid decarboxylase, antibody

glycine receptor antibodies

glycogen storage disease

Gorlin-Goltz syndrome

Gowers maneuver

gram negative rod

granular osmiphilic material

granulomatosis with polyangiitis

granulomatous disease

growth hormone deficiency

growth retardation

Guillain Barre syndrome

Guillain Barre syndrome, axonal form

Guillain Barre syndrome, complications

Guillain Barre syndrome, differential diagnosis of

Guillain Barre syndrome, etiology of

Guillain Barre syndrome, prognosis of

gyrus, abnormal

Hallervorden Spatz disease

Hallervorden Spatz disease, late onset

hallucination, visual

hand-foot-mouth disease

head circumference

head injury, driving and

head injury, management of

head injury, mild

head injury, pediatric

head injury, prognosis in

head injury, repetitive

headache, children

headache, chronic

headache, intermittent

headache, intractable

headache, positional

headache, post traumatic

headache, recurrent

headache, severe

headache, sudden onset of

headache, throbbing

headache, thunderclap

headache, unilateral

headache, vascular

health insurance

hearing loss, bilateral

heavy metal intoxication

hemangioma, facial

hemangioma, leptomeningeal

hemangioma, skin

hematoma, epidural-cranial

hemifacial spasm

hemiparesis, recurrent

hemiparesis, transient

hemoglobin abnormality, neurologic complications of

hemophagocytic lymphohistiocytosis, cerebromeningeal

hemophagocytosis

hemorrhage, intracranial, newborn

hemorrhage, periventricular

hemorrhage, putamenal

hemorrhage, thalamic

hemorrhagic diathesis

hemorrhagic shock encephalopathy syndrome

hemosiderosis of CNS, superficial

heparin, low-molecular-weight

hepatic encephalopathy

hepatic failure

hepatolenticular degeneration(Wilson's disease)

hepatolenticular degeneration(Wilson's disease), presymptomatic

hepatolenticular degeneration, non-Wilsonian

hepatosplenomegaly

heralding manifestation

herniated disc, lumbar

herniated disc, lumbar-conservative vs.surgical treat.of

herniated disc, lumbar-laminectomy

herniated disc, thoracic

herniation syndromes, intracranial

herpes labialis

herpes simplex encephalitis

herpes simplex encephalitis, atypical

herpes simplex encephalitis, diagnosis of

herpes simplex encephalitis, differential diagnosis of

herpes simplex encephalitis, infancy and childhood

herpes simplex encephalitis, prognosis of

herpes simplex encephalitis, recurrent

herpes simplex encephalitis, treatment of

herpes simplex myelitis

herpes simplex virus

herpes simplex virus infection, immunosuppressed patient

herpes simplex virus infection, newborn

herpes simplex virus, human nervous system and

herpes simplex virus, localization of

herpes simplex virus, malignancy with

herpes simplex virus, pathogenesis of

herpes simplex virus, pathology of

herpes simplex, neurocutaneous lesions in

herpes virus infection

herpes, genital

hexosaminidase-A

hexosaminidase-A and B

high arched feet

high arched palate

highly active antiretroviral therapy

hippocampal atrophy

hippocampus, hyperintense

Hirschprung's disease

histochemistry of muscle

HIV CSF viral escape syndrome

Hodgkin's disease

Hodgkin's disease, neurologic involvement with

Hoehn-Yahr scale

holoprosencephaly

hospital length of stay

human herpesvirus 6

human immunodeficiency virus type 1

human immunodeficiency virus type 1, asymptomatic

human immunodeficiency virus type 1, infants and children

human immunodeficiency virus type 1, pathogenesis

human T-lymphotropic virus type I(HTLV-I)

Hunter's syndrome

Huntington's chorea

Huntington's disease, children

hydrocephalus, acute

hydrocephalus, classification of

hydrocephalus, communicating

hydrocephalus, congenital

hydrocephalus, exvacuo

hydrocephalus, fetal

hydrocephalus, non-communicating(obstructive)

hydrocephalus, normal pressure

hydrocephalus, normal pressure, etiology

hydrocephalus, treatment of

hydroxyglutaric aciduria

hyperbilirubinemia

hyperglycinemia

hyperglycinemia, nonketotic

hyperhomocysteinemia

hyperpigmentation of skin

hyperpyrexia, CNS disorder causing

hypersegmented polys

hypertension, cerebrovascular disease with

hypertensive encephalopathy, venous

hypertriglyceridemia

hypertrophic cardiomyopathy

hypertrophic intracranial pachymeningitis

hypoalbuminemia

hypochondriasis

hypofibrinogenemia

hypoglycemia, newborn and infant

hypoglycorrhachia

hypoglycorrhachia, causes of

hypomelanosis of Ito

hypomyelination

hypopigmentation of skin

hypoplastic left heart syndrome

hypotension, systemic

hypothalamus, lesion of

hypothermia, causes of

hypothyroidism, congenital

hypothyroxinemia

hypotonia, infants

hypoxia, newborn

hypoxic encephalopathy

hypoxic-ischemic leukoencephalopathy

iatrogenic neurologic disorders

ideomotor apraxia

ileus, paralytic

imbalance, postural

immune reconstitution inflammatory syndrome

immunization, neurologic complications with

immunocompetent

immunodeficiency

immunofluorescent exam of CSF cells

immunohistochemistry

immunologic disease

immunology and the nervous system

immunomodulation

immunosuppression

immunosuppressive agents

inappropriate antidiuretic(A.D.H.)hormone

inappropriate behavior

inborn errors of metabolism

inborn errors of metabolism, screening

inclusion bodies

inclusion bodies, eosinophilic cytoplasmic

inclusion bodies, eosinophilic intranuclear

inclusion bodies, intracytopasmic

inclusion bodies, intranuclear

incontinence, fecal

incontinentia pigmenti

industrial neurologic disorders

infant, evaluation of

infantile hemiplegia

infantile spasm

infantile tremor syndrome

infection, recurrent

infectious mononucleosis

infectious mononucleosis, neurologic findings with

inflexibility, mental

influenza A virus

influenza immunization

infraspinatus muscle

initiative, lack of

insulin resistance

intellectual deficit

intellectual deficit, treatable causes of

intellectual deterioration

intelligence quotient

intelligence testing in children

interferon alpha

interferon antibodies

interferon beta 1-a

interferon beta 1-b

interferon inducer

internal capsule

internal carotid artery

internuclear ophthalmoplegia

interobserver agreement

intracerebral hemorrhage

intracerebral hemorrhage, clot evacuation

intracerebral hemorrhage, lobar

intracerebral hemorrhage, location of

intracerebral hemorrhage, recurrent

intracerebral hemorrhage, treatment of

intracranial hemorrhage

intracranial hypotension

intracranial infection

intracranial pressure, increased

intrathecal chemotherapy

intrauterine infection

intrauterine infection, viral

intrauterine infection, viral of CNS

intraventricular hemorrhage

intrinsic hand muscles, wasting of

iodine deficiency

iododeoxyuridine

iron, serum, elevated

Jakob-Creutzfeldt disease

Jakob-Creutzfeldt disease, cerebellar variant

Jakob-Creutzfeldt disease, unilateral

Jakob-Creutzfeldt disease, variant

jaw contractures

joint hypermobility

Joubert syndrome

Karnofsky performance scale

Kayser-Fleischer ring

keratoconjunctivitis

Kleine-Levin syndrome

klippel feil syndrome

Krabbe's disease

kyphoscoliosis, neurologic causes of

lactic acidemia

lactic dehydrogenase(LDH)

lacunar infarction

Lafora's disease

language disorder in adults

language disorders in children

laughing, pathologic

lead and the nervous system

learning disability

learning disability, in children

left handedness

leg weakness, bilateral

leg weakness, unilateral

Legius syndrome

Leigh's disease

lens, dislocation of

lenticular nucleus, lesion of

lenticular nucleus, lesion of, bilateral

leucine rich glioma inactivated 1 antibodies

leukemia, neurologic findings assoc.with

leukocyte enzyme abnormality

leukodystrophy, 4H

leukoencephalopathy

leukoencephalopathy, adult onset, sporadic

leukoencephalopathy, differential diagnosis

leukoencephalopathy, hereditary diffuse

leukoencephalopathy, toxic

level of consciousness, decreased

Lewy body disease, diffuse

Lhermitte-Duclos disease

Lhermitte's sign

life expectancy

limbic encephalitis

lipid storage disorder of CNS

listeria monocytogenes

listeriosis, CNS

livedo reticularis

liver function enzymes

liver transplantation

locked-in syndrome

loss of sympathy

low birth weight

lumbar puncture

lumbar puncture, complications of

lumbar puncture, indications for

lumbar spine manipulation

lymphadenopathy

lymphadenopathy, hilar

lymphoma involving CNS

lymphoma, primary of CNS

lysosomal storage disease

lysosomes, abnoral

magnetoencephalography

malaria, cerebral

malformation, CNS, congenital

malformation, vascular

malformation, vascular, cerebral

maple syrup urine disease

marche a petits pas

marfanoid skeletal abnormalities

McDonald criteria for MS

meconium staining

mediastinum, mass of

medical-legal aspects of neurology

megalencephaly, idiopathic

melanomatosis, primary malignant

memory, defect of recent

memory, impairment of

meningeal biopsy

meningeal enhancement

meningeal enhancement, nodular

meningitis, adults

meningitis, aseptic

meningitis, bacterial

meningitis, bacteriologic etiology of

meningitis, basilar

meningitis, carcinomatous

meningitis, children

meningitis, chronic

meningitis, clinical features of

meningitis, CSF cell count-normal

meningitis, CSF findings in

meningitis, factors influencing mortality in

meningitis, fungal

meningitis, granulomatous

meningitis, late neurologic sequelae in

meningitis, meningococcal

meningitis, neurologic aspects and complications of

meningitis, neutrophilic

meningitis, neutrophilic, persistent

meningitis, noninfectious

meningitis, pneumococcal

meningitis, prophylaxis against

meningitis, rheumatoid

meningitis, seizures with

meningitis, spinal fluid smear and culture of

meningitis, treatment of

meningitis, treatment of, empirical

meningoencephalitis

meningoencephalomyelitis

menses, seizure with

mental retardation

mental status, abnormal

mental status, evaluation of

mesial temporal lobe

metabolic acidosis

metabolic disorder, primary

metabolic disorder, primary-screening tests

metachromatic leukodystrophy

metachromatic leukodystrophy, adult onset

metachromatic leukodystrophy, juvenile

methylene tetrahydrofolate reductase

methylenetetrahydrofolate reductase deficiency

methylglutaconic aciduria

methylmalonic acidemia

mGlu R5 antibodies

microaneurysm, retinal

microangiopathy, brain

microhemorrhage, intracerebral

microhemorrhage, intracerebral, anatomic rating scale

microspherophakia

midbrain, atrophy

midbrain, lesion of

middle cerebellar peduncle

middle cerebellar peduncle, lesion

middle cerebellar peduncle, lesion, bilateral

middle cerebral artery

middle cerebral artery territory infarction

middle cerebral artery territory infarction, malignant

middle cerebral artery, emboli to

middle cerebral artery, occlusion of

migraine, cost of

migraine, hemiplegic

migraine, pathogenesis

migraine, prophylaxis

migraine, seizures in

migraine, treatment of

mild cognitive impairment

Mini Mental Status Examination

mitochondrial disease

mitochondrial encephalomyopathy

mobile interventional stroke teams

molecular genetics

molybdenum cofactor deficiency

monoamines, brain

monoclonal antibodies

monoclonal gammopathy

mononeuritis multiplex

mononeuropathy multiplex

Montreal cognitive assessment

motion perception

motor development

motor dysfunction

motor neuron disease

movement disorder

movement disorder, extrapyramidal

movement disorder, hyperkinetic

movement disorder, psychogenic

MRI, angiography

MRI, angiography, false negative

MRI, black holes on

MRI, CAT scan compared to

MRI, cerebrovascular disease

MRI, contrast enhanced

MRI, cortical enhancement

MRI, demyelinating disease

MRI, diffusion tensor

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, early changes in CVA

MRI, eye of tiger sign

MRI, false negative

MRI, flow void, blood

MRI, functional

MRI, gradient-echo

MRI, gray matter enhancement

MRI, high signal foci on

MRI, hypointense signal foci on

MRI, indications for

MRI, lesion burden

MRI, magnetization transfer sequence

MRI, nodular enhancement

MRI, paramagnetic effect

MRI, spinal cord

MRI, spinal cord, increased intramedullary cord signal

MRI, starfield pattern

MRI, sulcal hyperintensity

MRI, susceptibility weighted

MRI, venography

MRI, vessel wall enhancement

MRI, voxel-based morphometry

mucopolysaccharidoses

mucopolysacchariduria

multimodal neuroimaging

multinucleated giant cell

multiple sclerosis

multiple sclerosis, acute

multiple sclerosis, aggressive

multiple sclerosis, benign form of

multiple sclerosis, children

multiple sclerosis, chronic progressive

multiple sclerosis, clinical patterns

multiple sclerosis, cognitive presenttion

multiple sclerosis, conversion to clinically definite

multiple sclerosis, diagnosis of

multiple sclerosis, diagnostic criteria

multiple sclerosis, differential diagnosis of

multiple sclerosis, disability status scale

multiple sclerosis, disease activity

multiple sclerosis, misdiagnosis

multiple sclerosis, monosymptomatic

multiple sclerosis, plaque

multiple sclerosis, presenting manifestations

multiple sclerosis, prognosis

multiple sclerosis, relapsing

multiple sclerosis, secondary progressive

multiple sclerosis, spinal form

multiple sclerosis, treatment of

multiple sclerosis, treatment of, first attack

multiple sclerosis, worsening

multiple system atrophy

muscle atrophy, progressive

muscle spasm, face

muscle stiffness

muscle transfer

muscle wasting, diffuse

muscle weakness

muscle weakness, proximal

muscular dystrophy

muscular dystrophy, Becker, carrier

muscular dystrophy, cardiovascular changes with

muscular dystrophy, central nervous system abnormality

muscular dystrophy, congenital

muscular dystrophy, congenital, Fukuyama type

muscular dystrophy, Duchenne

muscular dystrophy, Duchenne, carrier

muscular dystrophy, LAMA2

myasthenia gravis

myasthenia gravis, congenital

myasthenia gravis, familial incidence of

myelin basic protein

myelinolysis, extrapontine

myelitis, autoimmune

myelitis, longitudinal

myelitis, transverse

myelitis, transverse, idiopathic

myelitis, transverse, prognosis

myelomeningocele

myeloneuropathy

myelopathy, ascending

myelopathy, chronic progressive

myelopathy, paraneoplastic

myelopathy, vacuolar

myocardial infarction

myoclonic jerks

myoclonus, epilepsy

myofascial pain syndrome

myopathy, critically ill

myopathy, mitochondrial

myopathy, proximal

myositis ossificans, progressive

myxedema, neurologic manifestations of

nasal bridge, wide

natalizumab, discontinuation

nausea and vomiting

necrotizing granuloma

neisseria meningitis

neonatal infection, viral

neonatal screening, genetic neurologic disorders

neoplasm, primary intracerebral

neoplasm, primary of CNS

neoplasm, primary of CNS-children

neoplasm, primary of CNS-treatment of

neoplastic angioendotheliosis

nerve conduction studies

nerve root enhancement

nerve root, lumbar, lesion of

neural tube defect

neuroaxonal degeneration

neuroaxonal dystrophy

neuroaxonal dystrophy, infantile

neuroaxonal dystrophy, juvenile

neuroaxonal leukodystrophy

neurocutaneous disease

neurodegeneration with brain iron accumulation

neuroendocrinology

neurofibrillary degeneration

neurofibromatosis 1

neurogenic bladder

neuroleptic sensitivity

neuroleptic, atypical

neurolipidosis IV

neurologic complications

neurologic complications of, surgery

neurologic complications of, systemic disease

neurologic consultation

neurologic disease

neurologic disease, burden

neurologic disease, diagnoses of

neurologic disease, multifocal

neurologic disease, tempo

neurologic education

neurologic evaluation

neurologic examination

neurologic examination, focal

neurologic history

neurologic recovery

neurologic signs

neurologic symptoms

neurologic symptoms, unexplained

neurologic testing

neurological intensive care

neurology clinic

neuromuscular disease, electrodiagnosis of

neuromuscular junction

neuromyelitis optica (Devic's disease)

neuromyelitis optica spectrum disorder

neuromyelitis optica, IgG

neuron specific enolase

neuronal ceroid-lipofuscinosis

neuronal intranuclear inclusion disease

neuronal migration disorder

neuroophthalmology

neuropathology, brain

neuropathy, demyelinating

neuropathy, diabetic

neuropathy, painful

neuropathy, peripheral

neuropathy, peripheral, treatment

neuropathy, sensory

neuropathy, vasculitic, systemic

neuroprotective agents

neuroradiology, interventional

neurotoxicity, acute

new onset refractory status epilepticus

newborn, evaluation of

Niemann-Pick disease

NIH stroke scale

NMDA antagonists

nonsteroidal anti-inflammatory drug

Noonan Syndrome

nutritional deficiency

nystagmus, monocular

obsessive-compulsive disorder

obstetric neurologic injuries

occipital lobe, infarction

occipital lobe, lesion of

occupational neurologic disorders

ocular motility, disorders of

oculodentodigital dysplasia

oculogyric crisis

old age, neurology of

operculum syndrome

operculum syndrome, bilateral

ophelia syndrome

ophthalmoplegia

opportunistic infection

opportunistic infection, CNS

opsoclonus-myoclonus syndrome

optic atrophy, bilateral

optic atrophy, infants

optic chiasm, enlarged

optic chiasm, lesion of

optic nerve, enlarged

optic nerve, hypoplasia of

optic nerve, lesion of

optic neuritis, bilateral

optic neuritis, recurrent

optic neuropathy

optic neuropathy, nutritional

optokinetic nystagmus, abnormal

oral contraceptives

oral ulcerations

orthostatic hypotension

osmotic demyelination syndrome

otitis, neurologic complications with

outcome research

out-of-hospital emergency care

owl's eye sign of spinal cord

pachymeningitis, cranial

pain, increased response

pain, neuropathic

palatal myoclonus

palmomental response

paradichlorobenzene

paralysis, acute

paralysis, acute areflexic

paramyotonia congenita

paraparesis, familial spastic

paraparesis, spastic

paraspinal muscle

parenteral alimentation

parietal lobe, atrophy

parietal lobe, lesion of

Parkinson disease

Parkinson disease, axial symptoms

Parkinson disease, driving with

Parkinson disease, dystonia with

Parkinson disease, fluctuations in

Parkinson disease, incidence

Parkinson disease, late onset

Parkinson disease, nonmotor problems of

Parkinson disease, on-off phenomena in

Parkinson disease, self-assessment

Parkinson disease, surgical treatment of

Parkinson disease, treatment of

Parkinson disease, tremor, absence of

Parkinson disease, young onset

Parkinsonism syndrome

paroxysmal hemiplegia

paroxysmal neurologic deficits

partial thromboplastin time, prolonged

PAS positive material in the brain

patent ductus arteriosus

pathologic reflex

patient information and support

pectus excavatum

pediatric neurology

Pelizaeus Merzbacher

penguin silhouette sign

penis, pigmented macules

perceptual-motor dysfunction

percussion induced muscle contraction

periaqueductal lesion

perineum, numbness of

peripheral pulse, absent

periventricular leukomalacia

pernicious anemia

peroxisomal disease

Persistent postural-perceptual dizziness

persistent vegetative state

personality change

personality disorder

pertussis immunization

phenylketonuria

phenylketonuria, variant form of

photosensitivity, skin

physical therapy

physician as patient

physician assisted suicide

picking at skin

pigmentary retinopathy

pigmented macules

pituitary hyperemia

pituitary, hormones of

platelet inhibiting drugs

platelet inhibiting drugs, combined

pleocytosis of cerebrospinal fluid

pleocytosis of cerebrospinal fluid, neutrophilic

pneumoencephalogram(PEG)

poison, mercury

poison, neurologic problems with

poliomyelitis-like illness

polychlorinated biphenyls

polycystic kidneys

polyglucosan body

polyglucosan body disease

polyinosinic cytidic acid(poly IC)

polymerase chain reaction

polymerase chain reaction, false negative

polyneuropathy, critically ill

polyps, gastrointestinal tract

polyradiculoneuropathy

Pompe's disease of glycogen storage

pons, infarction of

pons, lesion of

pontine tegmental cap dysplasia

port wine nevus

post concussive syndrome

post hemorrhagic hydrocephalus

post infectious cerebellar ataxia

post infectious polyneuropathy

post polio syndrome

posterior column disease

posterior cortical atrophy

posterior fossa, lesion of

posterior leukoencephalopathy syndrome

postoperative neurologic complications

postural abnormality

postviral fatigue syndrome

potassium channel antibodies

practice guidelines

Prader-Labhart-Willi syndrome

precipitating factors

precocious puberty

pregnancy, anticonvulsants during

pregnancy, neurologic complications in

premature infant

premature infant, problems in

prenatal diagnosis by amniocentesis

prevention of neurologic disorders

primary intracranial hypotension

primary lateral sclerosis

progressive infantile poliodystrophy

progressive multifocal leucoencephalopathy

progressive myoclonic epilepsy

progressive neurologic disorder

progressive spinal muscular atrophy

progressive supranuclear palsy

proprioception, abnormal

protein 14-3-3, cerebrospinal fluid

proximal muscle atrophy

pseudobulbar palsy

psychiatric disorder

psychiatric problems in neurologic disorders

psychological testing

psychological testing, children

psychological testing, neurologic problems

psychomotor retardation

psychosocial aspects

PTEN hamartoma tumor syndrome

ptosis, bilateral

ptosis, unilateral

pulmonary edema

pulmonary embolism

pulmonary infiltrates

pulmonary nodules

pulmonary stenosis

pupil, abnormality in neurologic disorders

pupil, dilated and fixed, bilateral

pure motor stroke

putamen, lesion of

putamen, lesion of, bilateral

pyramidal tract

pyramidal tract dysfunction

pyruvate dehydrogenase deficiency

pyruvate metabolism, abnormality of

quality of life

radiation encephalopathy, delayed

radiation necrosis

radiation therapy, CNS treatment and complications with

radiation, ionizing

radiation, ionizing, intrauterine

ragged-red fibers

range-of-motion, neck

rapid onset dystonia parkinsonism

rapidly progressing neurologic illness

reading disorder, acquired

reflex sympathetic dystrophy

reflex sympathetic dystrophy, children

reflex, brainstem

Refsum's disease

rehabilitation for neurologic disorders

release phenomena

REM sleep behavior disorder

remote effect of cancer on the nervous system

renal tubular acidosis

repetitive questioning

respirations in CNS disease

respiratory arrest

respiratory failure

respiratory tract infection

retina, abnormal

retinal artery occlusion

retinal branch artery occlusion

retinal degeneration

retinal dysplasia

retinal hamartoma

retinal hemorrhages

retinal microvascular disease

retinitis pigmentosa

Retriever Device

Rett's syndrome

REVASCAT trials

reversible cerebral vasoconstrictive syndromes

reversible neurologic disorder

rheumatoid arthritis

rheumatoid arthritis factor(R.A.factor)

rheumatoid arthritis, neurologic complications of

rheumatoid vasculitis

rickettsial organism

rigidity, axial

risk factors, modification

robotic therapy

root lesion, nerve

Rosenthal fibers

rubella encephalitis, progressive

rubella syndrome

saccadic eye movements, abnormal

sagging of the brain

salivation, excessive

Sandhoff's disease

Sanfilippo syndrome

Schilder's disease

scoliosis, neurologic association with

sea-blue histiocytes

sedimentation rate

sedimentation rate, elevated

seizure, adult onset

seizure, age of onset

seizure, children

seizure, complications following

seizure, diagnosis of

seizure, drug resistance

seizure, etiology of

seizure, familial

seizure, febrile

seizure, immunization causing

seizure, incidence of

seizure, injury following

seizure, intractable

seizure, intractable, treatment of

seizure, neonatal

seizure, new onset

seizure, pregnancy

seizure, prognosis in childhood

seizure, psychomotor-temporal lobe

seizure, surgical treatment of

seizure, teenager

seizure, tonic-clonic

seizure, treatment of

seizure, treatment of, polytherapy

seizure, unknown origin

seizure, workup of

selective serotonin reuptake inhibitors

self-mutilation

semantic dementia

semialdehyde dehydrogenase deficiency

sensorineural hearing loss

sensory loss, cutaneous

sequencing difficulty

serologic testing

serologic testing of cerebrospinal fluid

serologic testing, false negative

serotonin agonist

serotonin norepinephrine reuptake inhibitors

serum alanine aminotransferase

sexual behavior, disorder of

sexual dysfunction in neurologic disease

shock, hypovolemic

shoulder, pain in

shunt procedure, lumboperitoneal

shunt procedure, ventricular

shunt procedure, ventricular-complications of

sickle cell crisis

sickle cell disease

sickle cell trait

simultanagnosia

single photon emission computed tomography

single photon emission computed tomography, false positive

Sjogren's syndrome

Sjogren's syndrome, neurologic manifestations of

skin, darkening of

skin, discoloration

skin, lesions in neurologic disorders

skin, temperature difference

skull bone, thickening

skull x-ray, abnormal

skull x-ray, bony defect on

sleep apnea, obstructive

sleep pathology and physiology

slit lamp examination

slow virus infection of CNS

small for dates infant, problems in

small vessel disease

small vessel vasculitis

sodium channel dysfunction

sodium valproate

sodium valproate, toxicity

solitaire device

spastic diplegia

spastic paraplegia, type 11

spatial neglect

speech disorder

speech disorder, childhood

speech disorder, non aphasic

speech, delayed development of

speech, loss of

spinal cord, cervical

spinal cord, infarction of

spinal cord, injury of

spinal cord, injury, complications with

spinal cord, injury, functional capacity of patient with

spinal cord, injury, prognosis in

spinal cord, injury, sexual dysfunction in

spinal cord, ischemic lesion of

spinal cord, lesion of

spinal cord, vascular malformation of

spinal manipulation

spinal muscular atrophy

spinal muscular atrophy, classification

spongy degeneration of brain

sports medicine, neurology of

sprain, cervical

sprain, cervical-treatment of

SPRED1 mutation

startle reaction

status epilepticus

status epilepticus, nonconvulsive

stem cell rescue

stem cell transplantation

stent, carotid artery

stereotaxic surgery

stereotyped behavior

stereotyped behavior, drug induced

steroid responsive encephalopathy

steroid therapy, CNS treatment and complications with

stiff man syndrome

stimulant drugs

stimulation, deep brain

stooped posture

striopallidodentate calcifications, familial idiopathic

stroke disability scale

stroke unit, mobile

stroke, progression of

strokelike episodes

Sturge-Weber syndrome

subacute myelo-opticoneuropathy(S.M.O.N.)complex

subacute sclerosing panencephalitis(S.S.P.E.)Dawson's disease

subacute sclerosing panencephalitis, adult onset

subarachnoid hemorrhage

subarachnoid hemorrhage, cerebral convexity

subarachnoid hemorrhage, prognosis

subdural hematoma

subdural hematoma, neonates and infants

subependymal nodules

suboccipital decompression

substantia nigra

subtemporal decompression

sulfite oxidase deficiency

superior sagittal sinus thrombosis

suprascapular nerve

suprascapular neuropathy

supraspinatus muscle

Susac's syndrome

sweating, abnormality of

SWIFT PRIME Trials

symmetric brain lesions

sympathetic block

synucleinopathy

syphilis, congenital

syphilis, diagnosis and treatment

syphilis, neurologic complications with

systemic illness

systemic lupus erythematosus

T lesion of MCA-ICA

Takayasu's arteritis

tandem gait, ataxic

Tay-Sachs disease

teeth, abnormal

teeth, number of in infants

teeth, wide-spaced

temper tantrums

temporal lobe, atrophy

temporal lobe, lesion

temporal lobe, lesion, bilateral

temporal lobe, status

temporal lobectomy

tension headache

tentorium cerebelli

teratogenic drugs

testicular enlargement

thalamic amnesia

thalamus, infarction of

thalamus, lesion of

thalamus, lesion of-bilateral

third nerve palsy

third nerve palsy, bilateral

thoracic outlet syndromes

thrombocytopenia

thrombolysis, mechanical

thyroid peroxidase antibodies

tick-borne encephalitis

tinnitus, causes of

tinnitus, pulsatile

tissue plasminogen activator, intravenous

tone, muscle, increased

tongue, enlarged

tongue, fasciculations of

tongue, impaired movements of

tongue, protrusion of

toxins, nervous system

toxoplasmosis, acquired

toxoplasmosis, CNS

tranexamic acid

transient ischemic attack

transient ischemic attack, venous

transient neurologic deficit

transluminal angioplasty, intracranial

transplacental virus infections

treatment of neurologic disorder

treatment, empirical

treatment, non-pharmacologic

tremor, intention

tremor, surgical treatment of

tremor, thalamic stimulation for suppression of

tremor, treatment of

tremor, writing

trichopoliodystrophy

trientine dihydrochloride

trigeminal neuralgia

trigeminovascular system

trinucleotide repeats

tuberous sclerosis

tumefactive lesion

ultrasonography

ultrasonography, head

ultrasonography, head, fetus-neonate

unconsciousness

Unified Parkinson Rating Scale

upgaze, paralysis of

urinary incontinence

urinary retention

urinary sulfatidase excretion

urinary tract infection

urine test for metabolic disorders

urine test in toxic screen

vaccination, neurologic complications with

varicella zoster virus

vascular malformation, children, intracranial

vasoconstrictive drugs

vasospasm, cerebral

venous hypertension

venous ischemia

ventricular enlargement

ventriculostomy

vertebral anomalies

vertebral artery stenosis

very long chain fatty acids

vibratory sensation, abnormal

viral infection

viral infection, CNS

Virchow-Robin spaces, dilated

vision, blurred

vision, failure of in childhood

visual acuity, decreased

visual evoked response

visual field defect

visual fields, constricted

visual impairment

visual loss, progressive

visual loss, slow

visual loss, sudden

visual symptoms

visual tracking

visuospatial disturbance

vitamin deficiency

vitamin supplementation

vocal cord paralysis

vomiting, recurrent

Walker-Warburg syndrome

walking, delayed

walking, difficulty with

Wallerian degeneration

water channel antibodies

weakness, congenital

weakness, fatiguable

weakness, generalized

weakness, progressive

weakness, proximal

Werdnig-Hoffman disease

white matter disease

white matter disease, periventricular

white matter disease, subcortical

white matter, dirty-appearing

wide based gait

word-finding difficulty

work performance

workers' compensation

x-linked mental retardation

Showing articles 650 to 700 of 2808 << Previous Next >>

Alexander's Disease, A Disease of Astrocytes
Brain 108:367-385, Borrett,D.&Becker,L.E., 1985

Clinicopathological Conference Metachromatic Leukodystrophy (juvenile type)
Case 7-1984, NEJM 310:445-4551984., , 1984

Human Cytomegalovirus Infection & Disorders of the Nervous System
Jr. , Arch Neurol 41:310-320984., Bale,J.F., 1984

Pure Psychic Akinesia with Bilateral Lesions of Basal Ganglia
JNNP 47:377-385, Laplane,D.,et al, 1984

The Cerebrohepatorenal (Zellweger) Syndrome
NEJM 310:1141-1146, Moser,A.E.,et al, 1984

A Progressive Neurologic Disorder with Supranuclear Vertical Gaze Paresis & Distinctive Bone Marrow Cells
Mayo Clin Proc 59:404-410, Yan-go,F.L.,et al, 1984

Schizencephaly:A Clinical & CT Study
Neurol 34:997-1001, Miller,G.M.,et al, 1984

Cerebro-ocular Dysgenesis (Walker-Warberg Syndrome) :Neuropathologic & Etiologic Analysis
Neurol 34:1531-1541, Williams,R.S.,et al, 1984

A Progressive Syndrome of Autism, Dementia, Ataxia, & Loss of Purposeful Hand Use in Girls:Rett's Syndrome
Ann Neurol 14:471-491, Hagberg,B., 1983

Recognising & Preventing Duchenne Muscular Dystrophy
BMJ 287:1083-1084, Firth,M.A.,et al, 1983

Neurodegenerative Disease of Infancy & Childhood
Ann Neurol 13:351-364, Dyken,P.,et al, 1983

Familial Porencephaly
Arch Neurol 40:567-569, Berg,R.A.,et al, 1983

Diagnostic Delay in Duchenne's Muscular Dystrophy
JAMA 247:478-480, Crisp,D.E.,et al, 1982

Santavuori Disease:Diagnosis by Leukocyte Ultrastructure
Neurol 32:1277-1281, Baumann,R.J.,et al, 1982

Fibrodysplasia Ossificans Progressiva, The Clinical Features & Natural Hx of 34 Pts
J Bone Joint Surg 64B:76-83, Connor,J.M.&Evans,D.A.P., 1982

Progressive Infantile Poliodystrophy, Assoc. With Disturbed Pyruvate Oxidation in Muscle & Liver
Arch Neurol 38:767-772, Prick,M.J.J.,et al, 1981

Ataxia with Aniridia of Gillespie:A Case Report
Neurol 31:95-97, Lechtenberg,R.,et al, 1981

Biotin-Responsive Carboxylase Deficiency Associated With Subnormal Plasma & Urinary Biotin
NEJM 304:817-820, Thoene,J.,et al, 1981

Diagnosis of Infatile Neuroaxonal Dystrophy by Skin Biopsy
Ann Neurol 7:377-379, Wisniewski,K.,et al, 1980

Maternal & Fetal Sequelae of Anticoagulation During Pregnancy
Am J Med 68:122-140, Hall,J.G.,et al, 1980

Hazards of Oral Anticoagulants During Pregnancy
JAMA 243:1549-1551, Stevenson,R.E.,et al, 1980

Fetal Methylmercury Poisoning:Clinical & Toxicological Data on 29 Cases
Ann Neurol 7:348-353, Marsh,D.O.,et al, 1980

Amelioration Of Neurologic Abnormalities After"Enzyme Replacement"In Adenosine Deaminase Deficiency
NEJM 303:377-380, Hirschhorn,R.,et al, 1980

Human Cerebellar Hypoplasia, A Syndrome of Diverse Causes
Arch Neurol 37:300-305, Sarnatt,H.B.,et al, 1980

Alternating Hemiplegia in Infants:Report of Five Cases
Dev Med Child Neurol 22:784-791, Krageloh,I.&Aicardi,J., 1980

CT Scans in Menkes Disease
Neurol 29:304-312, Seay,A.R.,et al, 1979

Cockayne Syndrome:Unusual Neuropathological Findings & Review of the Literature
Ann Neurol 6:340-348, 1979, Soffer,D.,et al, 1979

Congenital Ocular Motor Apraxia
Arch Neurol 36:29-31, Orrison,W.W.,et al, 1979

The Aicardi Syndrome:Report of 4 Cases & Review of the Literature
Ann Neurol 5:475-482, Bertoni,J.M.,et al, 1979

Growth & Development in Children with Sickle-Cell Trait
NEJM 299:686-689, Kramer,M.S.,et al, 1978

Hyperphenylalaninemia Due To A Deficiency of Biopterin
NEJM 299:673-679, Stanley,S.K.,et al, 1978

Chronic Hexosaminidase A & B Deficiency
et al. , Ann Neurol 2:156977., Goldie,W.D., 1977

Neuropathology of Sanfilippo Syndrome
Ann Neurol 2:161, Ghatak,N.R.,et al, 1977

Adverse Effects on Offspring of Maternal Alcohol Abuse During Pregnancy
NEJM 297:528, Ouellette,E.M.,et al, 1977

Globoid cells, Glial nodules, & Peculiar Fibrillary Changes in the cerebro-hepato-renal Syndrome of Zellweger
Ann Neurol 2:473, deLeon,G.A.,et al, 1977

Neurological Complications of Infantile Osteopetrosis
Ann Neurol 2:378, Lehman,R.A.W.,et al, 1977

The Thyroid Gland:Its Relationship to Neurology
In Handbook of Clin Neurol, Vinken & Bruyn (Ed) , North Holland Publ Co, Amsterdam 27:255, Greene,R., 1976

A Comparison of the Physical & Intellectual Development of Black Children with & without Sickle-Cell Trait
Pediatrics 56:1021, McCormack,M.K.,et al, 1975

Prader-Willi-Syndrome, In Endocrine & Genetic Diseases of Childhood & Adolescence
(Ed) , 1975. W. B. Saunders Co, p, Gardner,L.I., 1975

Herpes Simplex & the Human Nervous System
Milit Med 140:765, Finelli,P.F., 1975

Progressive Rubella Panencephalitis
NEJM 292:990-993,1023, Townsend,J.,et al, 1975

Chronic Progressive Panencephalitis due to Rubella Virus Simulating Subacute Sclerosing Panencephalitis
NEJM 292:994-998,1023, Weil, M.L.,et al, 1975

Hepatic Encephalopathy:Current Status
Gastroenter 66:121:1974., Schenker,S.,et al, 1974

Diphenylhydantoin & Selected Congenital Malformations
NEJM 289:1049, 1973; 289:1089973., Monson,R.,et al, 1973

Perceptual-Motor Dysfunction in Children w/Sickle Cell Trait
Perceptual & Motor Skills 36:234973., Flick,G.L.,et al, 1973

Congenital Anomalies & Herpesvirus Infection
Am J Dis Child 126:364, Montogomery,J.R.,et al, 1973

Encephalomyelopathy of Leigh
Editorial BMJ 238, 1971, May., , 1971

Fetal & Newborn Virus Infections
J Pediatr 77:315, Overall,J.,et al, 1970

Rubella, Clinical Manifestations & Management
Am J Dis Child 118:18-29, Cooper,L.Z.,et al, 1969

Triethylene Melamine in the Treatment of Neoplastic Disease
Arch Int Med 87:477-516, Karnofsky,D.A.,et al, 1951

Showing articles 650 to 700 of 2808 << Previous Next >>