Neudle.com: loss of developmental milestones

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Differential
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abortion, spontaneous

acid maltase deficiency

acid maltase deficiency, adult

acquired immunodeficiency syndrome

acquired immunodeficiency syndrome dementia complex

acquired immunodeficiency syndrome, congenital

acquired immunodeficiency syndrome, infants and children

activities of daily living scale

acute cerebellar ataxia

acute disseminated encephalomyelitis

acute necrotizing encephalitis

Addison's disease

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

alcohol, neurologic complications with

Alexanders disease

alpha glucosidase

altered states of consciousness

alternating hemiplegia

alternating hemiplegia of childhood

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, treatment of

aminoacidopathies

AMPA receptor antibodies

amphiphysin antibodies

amyloid angiopathy, cerebral

amyloid angiopathy, cerebral, inflammatory type

amyotrophic lateral sclerosis

aneurysm, asymptomatic

aneurysm, intracranial

Angelman syndrome

angiitis, granulomatous of CNS

angiitis, isolated of CNS

angiography, cerebral

angiography, cerebral, false negative

angiography, cerebral, negative

angiography, spinal

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, treatment

anticonvulsants

anticonvulsants, blood level determination of

anticonvulsants, teratogenicity of

anticonvulsants, untoward effects of

antithyroid antibodies

antiviral agents

aphasia, conduction

aphasia, progressive, non-fluent

aphasia, progressive, primary

apraxia of eye movements

aqueduct of Sylvius, stenosis

arm swing, reduced

aromatic amino acid decarboxylase deficiency

arrhythmia, cardiac

arthropathy, neuropathic

arylsulfatase A

ascending paralysis

aspartate aminotransferase

asterixis, causes of

asterixis, unilateral

ataxia, cerebellar

ataxia, congenital

ataxia, hereditary

ataxia, progressive

ataxia, truncal

attention deficit disorder with hyperactivity

audiologic test to localize site of pathology

autoimmune disease

autoimmune encephalopathy

autoimmune epilepsy

automobile accidents

autonomic dysfunction

autonomic nervous system

axonal degeneration

axonal spheroid

azidodeoxythymidine

B 12 deficiency

B 12 deficiency, infants

B cell lymphoma

bacterial infection

ballismus, bilateral

basal cell carcinoma

basal ganglia, calcification of

basal ganglia, lesion of

basal ganglia, lesion, bilateral

basilar artery migraine

behavior modification

behavior, combative

behavioral disorder

behavioral disorder, acute

Binswanger disease

biologic markers

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

brainstem, atrophy

brainstem, dysfunction

brainstem, lesion of

Brown-Vialetto-Van Laere syndrome

bulbar dysfunction

burning paresthesia

calcification, gyral

calcification, intracranial

calf hypertrophy

Canavan's disease

carbon monoxide poisoning

carbonic anhydrase II deficiency

carcinoma of lung

cardiac arrest and resuscitation

CAT scan, abnormal

CAT scan, angiography

CAT scan, angiography, false negative

CAT scan, chest

CAT scan, contrast enhanced, delayed

CAT scan, contrast enhanced, double dose

CAT scan, emission

CAT scan, emission, abnormal

CAT scan, false negative

CAT scan, venography

cataracts, congenital

caudate nucleus

caudate nucleus, atrophy

caudate nucleus, infarction

caudate nucleus, lesion of

caudate nucleus, lesion of, bilateral

celiac disease, childhood

central hypoventilation, congenital

central nervous system, infection of

cerebellar ataxia, children

cerebellar ataxia, primary

cerebellar atrophy, primary

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, territory of

cerebral cortex

cerebral cortical atrophy

cerebral edema, cytotoxic

cerebral edema, vasogenic

cerebral embolism

cerebral folate deficiency syndrome

cerebral glucose metabolism

cerebral infarction

cerebral palsy, risk factors

cerebral palsy, work up

cerebral vasculature

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, proteincytologic dissociation

cerebrospinal fluid, xanthochromia of

cerebrotendinous xanthomatosis

cerebrovascular accident

cerebrovascular accident, bilateral

cerebrovascular accident, complications with

cerebrovascular accident, familial occurrence

cerebrovascular accident, infancy and childhood

cerebrovascular accident, mass effect with

cerebrovascular accident, multiple

cerebrovascular accident, nonvascular territory

cerebrovascular accident, recurrent

cerebrovascular disease

ceruloplasmin, serum

cervical spine manipulation

chemotherapy, CNS treatment and complications with

cherry red spot

cherry red spot-myoclonus syndrome

chest x-ray, abnormal

chilbran skin lesions

chiropractic manipulation

choreoathetosis

chorioretinitis

chromosomal abnormality

cingulate island sign

Clinical Pathologic Conference(C.P.C.)

clubbing of fingers

cochlear implant

Cockayne's syndrome

Coffin-Siris syndrome

cognition, slowed

cognitive delay

cogwheel rigidty

coin rotation test

cold hands sign

collapsin response mediator protein 5 IgG

coma, prognosis of

compression fracture

concentration, impaired

confusional state, acute

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 myopathy

congenital myopathy, inflammatory

congestive heart failure

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

corpus callosum

corpus callosum, atrophy of

corpus callosum, hypoplastic

corpus callosum, lesion of

corpus callosum, thinning

cortical blindness

cortical blindness, transient

cost effectiveness

cranial nerve enhancement

cranial nerve enlargement

cranial nerve palsies

cranial nerve palsies, bilateral

cranial neuropathy

cranial neuropathy, multiple

craniectomy, decompressive

crawl regression

C-reactive protein, elevated

creatine phosphokinase(CPK)elevated

crying, pathologic

cryopyrin-associated periodic syndrome

cryptococcal antigen

cryptococcal meningitis

cultured skin fibroblasts

Cushing's syndrome

cyclophosphamide

cyst, odontogenic

cyst, parenchymal

cyst, porencephalic

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

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, treatment of

demyelinating disease

dentate nuclei, lesion of

depression, psychotic

developmental abnormality of brain

developmental disability

developmental evaluation

developmental milestones

developmental milestones, loss of

developmental retardation

dexterity, impaired

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

dopa responsive dystonia

DPPX, antibodies

DPPX, antibodies, encephalitis

Dravet syndrome

dropped head syndrome

dural arteriovenous malformation

dural sinus thrombosis

dysdiadochokinesia

dyskinesia, buccal lingual facial

dyskinesia, facial

dysostosis multiplex

dystonia, children

dystonia, focal

dystonic reaction, acute

ears of the Lynx MR sign

eating disorder

electroencephalogram

electroencephalogram, abnormalities of

electroencephalogram, brain mapping

electroencephalogram, periodic complexes

electron microscopy

emergencies, neurologic

emotional lability

encephalitis, autoimmune

encephalitis, brainstem

encephalitis, human immunodeficiency virus type 1

encephalitis, paraneoplastic

encephalitis, viral

encephalomyelitis, postinfectious

encephalopathy, anoxic

encephalopathy, delayed

encephalopathy, Hashimoto's

encephalopathy, metabolic

encephalopathy, neonatal

encephalopathy, post anoxic

encephalopathy, progressive

endoscopic surgery

endovascular therapy

enzyme treatment

epidemiology of neurology

epidural blood patch

epileptic encephalopathy

episodic disorders

episodic neurologic deficits

Epstein-Barr virus

esophageal varices

evoked potentials

executive dysfunction

exercise intolerance

exome sequencing

extralimbic encephalitis

eye movement, disorders of

face, numbness of

facial anomalies

facial appearance, abnormal

facial expression abnormality

facial nerve palsy

facial weakness

facial weakness, bilateral

failure to thrive

Farber's disease

FARS2 deficiency

fatty acid, elevated plasma content

feeding disorder

fetal alcohol syndrome

fetal movements, reduced

fever, recurrent

fine motor function, impaired

finger nose finger test

finger swelling

fingernails, abnormal

fingernails, hypoplastic

fingerprint bodies

fistula, arterio-venous

fistula, arterio-venous, dural

fistula, arterio-venous, dural, spinal

fluorescein angiography

fluorescene in situ hybridization

folic acid deficiency

fontanel, bulging

food-borne infection

fornix, lesion of

fourth ventricle, floor

fracture, long bone

fracture, pathologic

Fragile-X associated tremor/ataxia-syndrome

fragile-X syndrome

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

gamma amino butyric acid receptor antibody

gammaglobulin therapy, intravenous

gangliosidosis GM2

gastric partitioning

gastroenteritis

gastrointestinal disease, neurologic complications

Gaucher's disease

gaze palsy, supranuclear

gaze palsy, vertical

genetic counselling

genetic diagnosis, prenatal

genetic linkage

genetic neurologic disorders

genetic screening

genetic testing

genu of corpus callosum

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

glutamic acid decarboxylase, antibody

glycine receptor antibodies

glycogen storage disease

Gorlin-Goltz syndrome

Gowers maneuver

granular osmiphilic material

granulomatosis with polyangiitis

granulomatous disease

growth hormone deficiency

growth retardation

Guillain Barre syndrome

gyrus, abnormal

Hallervorden Spatz disease

Hallervorden Spatz disease, late onset

hallucination, visual

head circumference

head injury, management of

head injury, mild

head injury, pediatric

head injury, prognosis in

headache, chronic

headache, intractable

headache, positional

headache, post traumatic

headache, recurrent

headache, severe

headache, sudden onset of

headache, vascular

health insurance

hearing loss, bilateral

heavy metal intoxication

hemangioma, facial

hemangioma, leptomeningeal

hemangioma, skin

hemiparesis, recurrent

hemiparesis, transient

hemoglobin abnormality, neurologic complications of

hemophagocytic lymphohistiocytosis, cerebromeningeal

hemophagocytosis

hemorrhage, intracranial, newborn

hemorrhage, thalamic

hemorrhagic diathesis

hemorrhagic shock encephalopathy syndrome

hemosiderosis of CNS, superficial

hepatic encephalopathy

hepatic failure

hepatolenticular degeneration(Wilson's disease)

hepatolenticular degeneration(Wilson's disease), presymptomatic

hepatolenticular degeneration, non-Wilsonian

hepatosplenomegaly

heralding manifestation

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, 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, 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

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, complications with

hydrocephalus, congenital

hydrocephalus, etiology

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

hypertensive encephalopathy, venous

hypertriglyceridemia

hypertrophic cardiomyopathy

hypertrophic intracranial pachymeningitis

hypoalbuminemia

hypofibrinogenemia

hypoglycorrhachia

hypomyelination

hypopigmentation of skin

hypotension, systemic

hypothalamus, lesion of

hypothermia, causes of

hypothyroidism, congenital

hypotonia, infants

hypoxic encephalopathy

iatrogenic neurologic disorders

ideomotor apraxia

ileus, paralytic

imbalance, postural

immunocompetent

immunofluorescent exam of CSF cells

immunohistochemistry

immunologic disease

immunomodulation

immunosuppression

immunosuppressive agents

inappropriate antidiuretic(A.D.H.)hormone

inappropriate behavior

inborn errors of metabolism

inclusion bodies

inclusion bodies, eosinophilic cytoplasmic

inclusion bodies, eosinophilic intranuclear

inclusion bodies, intracytopasmic

inclusion bodies, intranuclear

incontinence, fecal

incontinentia pigmenti

infant, evaluation of

infantile hemiplegia

infantile spasm

infantile tremor syndrome

infection, recurrent

infectious mononucleosis

infectious mononucleosis, neurologic findings with

inflexibility, mental

initiative, lack of

intellectual deficit

intellectual deterioration

intelligence quotient

interferon alpha

interferon inducer

internal capsule

intracerebral hemorrhage

intracerebral hemorrhage, recurrent

intracranial hemorrhage

intracranial pressure, increased

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

jaw contractures

joint hypermobility

Kayser-Fleischer ring

keratoconjunctivitis

Kleine-Levin syndrome

Krabbe's disease

kyphoscoliosis, neurologic causes of

lactic acidemia

lactic dehydrogenase(LDH)

lacunar infarction

language disorder in adults

language disorders in children

laughing, pathologic

learning disability

learning disability, in children

leg weakness, bilateral

leg weakness, unilateral

Leigh's disease

lens, dislocation of

lenticular nucleus, lesion of, bilateral

leucine rich glioma inactivated 1 antibodies

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's sign

life expectancy

limbic encephalitis

lipid storage disorder of CNS

listeria monocytogenes

listeriosis, CNS

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, axillary

lymphadenopathy, hilar

lymphadenopathy, paraaortic

lymphoma involving CNS

lymphoma, primary of CNS

lysosomal storage disease

lysosomes, abnoral

malaria, cerebral

malformation, CNS, congenital

marche a petits pas

meconium staining

mediastinum, mass of

medical-legal aspects of neurology

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, 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

menses, seizure with

mental retardation

mental status, abnormal

mesial temporal lobe

metabolic acidosis

metabolic disorder, primary

metabolic disorder, primary-screening tests

metachromatic leukodystrophy

metachromatic leukodystrophy, adult onset

metachromatic leukodystrophy, late-infantile

methylene tetrahydrofolate reductase

methylenetetrahydrofolate reductase deficiency

methylglutaconic aciduria

mGlu R5 antibodies

microaneurysm, retinal

microangiopathy, brain

microhemorrhage, intracerebral

midbrain, atrophy

midbrain, lesion of

middle cerebellar peduncle, lesion

middle cerebellar peduncle, lesion, bilateral

middle cerebral artery territory infarction

middle cerebral artery territory infarction, malignant

migraine, cost of

migraine, hemiplegic

migraine, seizures in

migraine, treatment of

mild cognitive impairment

mitochondrial disease

mitochondrial encephalomyopathy

molecular genetics

molybdenum cofactor deficiency

monoamines, brain

monoclonal antibodies

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, contrast enhanced

MRI, cortical enhancement

MRI, demyelinating disease

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, flow void, blood

MRI, functional

MRI, gray matter enhancement

MRI, hypointense signal foci on

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, venography

mucopolysaccharidoses

mucopolysacchariduria

multinucleated giant cell

multiple sclerosis

multiple sclerosis, benign form of

multiple sclerosis, clinical patterns

multiple sclerosis, cognitive presenttion

multiple sclerosis, disability status scale

multiple sclerosis, misdiagnosis

multiple sclerosis, monosymptomatic

multiple sclerosis, presenting manifestations

multiple sclerosis, prognosis

multiple sclerosis, relapsing

muscle atrophy, progressive

muscle stiffness

muscle wasting, diffuse

muscle weakness

muscle weakness, proximal

muscular dystrophy

muscular dystrophy, central nervous system abnormality

muscular dystrophy, congenital

muscular dystrophy, congenital, Fukuyama type

muscular dystrophy, Duchenne

muscular dystrophy, LAMA2

myasthenia gravis

myasthenia gravis, infantile and juvenile

myelination of nervous system

myelitis, longitudinal

myelitis, transverse

myeloneuropathy

myelopathy, ascending

myelopathy, chronic progressive

myelopathy, vacuolar

myocardial infarction

myoclonic jerks

myoclonus, epilepsy

myopathy, mitochondrial

myositis ossificans, progressive

myxedema, neurologic manifestations of

nasal bridge, wide

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-treatment of

nerve conduction studies

neuroaxonal degeneration

neuroaxonal dystrophy

neuroaxonal leukodystrophy

neurocutaneous disease

neuroendocrinology

neurofibrillary degeneration

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, diagnoses of

neurologic disease, multifocal

neurologic disease, tempo

neurologic evaluation

neurologic examination

neurologic examination, focal

neurologic signs

neurologic symptoms

neurologic symptoms, unexplained

neurologic testing

neurological intensive care

neurology clinic

neuromyelitis optica (Devic's disease)

neuromyelitis optica spectrum disorder

neuromyelitis optica, IgG

neuronal ceroid-lipofuscinosis

neuronal migration disorder

neuroophthalmology

neuropathology, brain

neuropathy, demyelinating

neuropathy, peripheral

neuropathy, sensory

neuropathy, vasculitic, systemic

neurotoxicity, acute

newborn, evaluation of

Niemann-Pick disease

NMDA antagonists

Noonan Syndrome

nutritional deficiency

nystagmus, monocular

nystagmus, rotary

obsessive-compulsive disorder

obstetric neurologic injuries

occipital lobe, lesion of

ocular motility, disorders of

oculogyric crisis

old age, neurology of

ophelia syndrome

ophthalmoplegia

opportunistic infection

opportunistic infection, CNS

optic atrophy, bilateral

optic atrophy, infants

optic chiasm, enlarged

optic chiasm, lesion of

optic nerve, enlarged

optic nerve, hypoplasia of

optic neuritis, bilateral

optic neuritis, recurrent

optic neuropathy

optic neuropathy, nutritional

oral contraceptives

orthostatic hypotension

otitis, neurologic complications with

outcome research

pachymeningitis, cranial

pain, increased response

palmomental response

paradichlorobenzene

paraparesis, familial spastic

paraparesis, spastic

parietal lobe, atrophy

Parkinson disease

Parkinson disease, axial symptoms

Parkinson disease, dystonia with

Parkinson disease, treatment of

Parkinson disease, tremor, absence of

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

perceptual-motor dysfunction

periaqueductal lesion

perineum, numbness of

periventricular leukomalacia

pernicious anemia

peroxisomal disease

Persistent postural-perceptual dizziness

persistent vegetative state

personality change

phenylketonuria, variant form of

photosensitivity, skin

physical therapy

picking at skin

pigmentary retinopathy

pleocytosis of cerebrospinal fluid

pleocytosis of cerebrospinal fluid, neutrophilic

pneumoencephalogram(PEG)

poison, mercury

poison, neurologic problems with

polycystic kidneys

polyglucosan body

polyglucosan body disease

polyinosinic cytidic acid(poly IC)

polymerase chain reaction

polymerase chain reaction, false negative

polyradiculoneuropathy

Pompe's disease of glycogen storage

pons, lesion of

pontine tegmental cap dysplasia

port wine nevus

post concussive syndrome

post infectious cerebellar ataxia

posterior column disease

posterior cortical atrophy

postural abnormality

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 supranuclear palsy

prolactin, elevated

proprioception, abnormal

pseudobulbar palsy

psychiatric disorder

psychiatric problems in neurologic disorders

psychological testing

psychological testing, children

psychomotor retardation

ptosis, unilateral

pulmonary infiltrates

pulmonary nodules

pulmonary stenosis

pupil, abnormality in neurologic disorders

pupil, dilated and fixed, bilateral

putamen, lesion of

putamen, lesion of, bilateral

pyramidal tract

pyramidal tract dysfunction

pyruvate dehydrogenase deficiency

pyruvate metabolism, abnormality of

quality of life

radiation necrosis

radiation therapy, CNS treatment and complications with

radiation, ionizing

radiation, ionizing, intrauterine

ragged-red fibers

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

retina, abnormal

retinal artery occlusion

retinal branch artery occlusion

retinal degeneration

retinal dysplasia

retinal hemorrhages

retinal microvascular disease

retinitis pigmentosa

Rett's syndrome

reversible neurologic disorder

rheumatoid arthritis

rheumatoid arthritis factor(R.A.factor)

rheumatoid arthritis, neurologic complications of

rheumatoid vasculitis

riboflavin transporter deficiency

rickettsial organism

rigidity, axial

Rosenthal fibers

rubella encephalitis, progressive

rubella syndrome

saccadic eye movements, abnormal

sagging of the brain

Sandhoff's disease

Schilder's disease

scoliosis, neurologic association with

sea-blue histiocytes

sedimentation rate, elevated

seizure, adult onset

seizure, children

seizure, drug resistance

seizure, familial

seizure, febrile

seizure, injury following

seizure, intractable

seizure, intractable, treatment of

seizure, neonatal

seizure, pregnancy

seizure, psychomotor-temporal lobe

seizure, tonic-clonic

seizure, treatment of

seizure, treatment of, polytherapy

seizure, unknown origin

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

serotonin norepinephrine reuptake inhibitors

serum alanine aminotransferase

sexual behavior, disorder of

sexual dysfunction in neurologic disease

shock, hypovolemic

shunt procedure, lumboperitoneal

shunt procedure, ventricular

shunt procedure, ventricular-complications of

sickle cell crisis

sickle cell disease

sickle cell trait

single photon emission computed tomography

Sjogren's syndrome

Sjogren's syndrome, neurologic manifestations 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 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

spastic diplegia

spastic paraplegia, type 11

speech disorder

speech disorder, childhood

speech disorder, non aphasic

speech, delayed development of

speech, loss of

spinal cord, cervical

spinal cord, lesion of

spinal cord, vascular malformation of

spinal muscular atrophy

spinal muscular atrophy, classification

spongy degeneration of brain

sprain, cervical

sprain, cervical-treatment of

startle reaction

status epilepticus

stem cell transplantation

stereotyped behavior

steroid responsive encephalopathy

steroid therapy, CNS treatment and complications with

stimulant drugs

stooped posture

striatonigral degeneration

striatonigral degeneration, infantile

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

subdural hematoma

subdural hematoma, neonates and infants

suboccipital decompression

substantia nigra

subtemporal decompression

sulfite oxidase deficiency

superior sagittal sinus thrombosis

Susac's syndrome

sweating, abnormality of

symmetric brain lesions

sympathetic block

synucleinopathy

syphilis, congenital

syphilis, diagnosis and treatment

syphilis, neurologic complications with

systemic illness

systemic juvenile idiopathic arthritis

systemic lupus erythematosus

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

tension headache

tentorium cerebelli

teratogenic drugs

thalamic amnesia

thalamus, infarction of

thalamus, lesion of

thalamus, lesion of-bilateral

third nerve palsy

third nerve palsy, bilateral

thrombocytopenia

tinnitus, causes of

tinnitus, pulsatile

tone, muscle, increased

tongue, enlarged

tongue, fasciculations of

tongue, impaired movements of

tongue, protrusion of

toxins, nervous system

toxoplasmosis, acquired

toxoplasmosis, CNS

transient ischemic attack

transient ischemic attack, venous

transient neurologic deficit

transplacental virus infections

treatment of neurologic disorder

treatment, empirical

treatment, non-pharmacologic

tremor, intention

tremor, writing

trichopoliodystrophy

trientine dihydrochloride

trigeminal neuralgia

trinucleotide repeats

tuberous sclerosis

tumor necrosis factor

tyrosine hydroxylase deficiency

ultrasonography

ultrasonography, head

ultrasonography, head, fetus-neonate

unconsciousness

upgaze, paralysis of

urinary incontinence

urinary retention

urinary sulfatidase excretion

urinary tract infection

urine test for metabolic disorders

urine test in toxic screen

varicella zoster virus

venous hypertension

venous ischemia

ventricular enlargement

ventriculostomy

ventriculostomy, endoscopic

very long chain fatty acids

vibratory sensation, abnormal

viral infection

viral infection, CNS

vision, blurred

vision, failure of in childhood

visual acuity, decreased

visual evoked response

visual fields, constricted

visual impairment

visual loss, progressive

visual loss, slow

visual loss, sudden

visual symptoms

visual tracking

visuospatial disturbance

vitamin deficiency

vitamin supplementation

vomiting, episodic

vomiting, recurrent

Walker-Warburg syndrome

walking, delayed

walking, difficulty with

water channel antibodies

weakness, congenital

weakness, generalized

weakness, progressive

weakness, proximal

Werdnig-Hoffman disease

white matter disease

white matter disease, periventricular

white matter disease, subcortical

wide based gait

word-finding difficulty

work performance

workers' compensation

x-linked hydrocephalus

Showing articles 250 to 300 of 5757 << Previous Next >>

Hemorrhagic Shock and Encephalopathy:Clinical, Pathologic, and Biochemical Features
J Pediatr 114:194-203, Levin,M.,et al, 1989

Sulfite Oxidase Deficiency:Clinical, Neuroradiologic, and Biochemical Features in Two New Patients
Neurol 39:252-257, Brown,G.K.,et al, 1989

Maternal Alcohol Use During Breast-Feeding and Infant Mental and Motor Development at One Year
NEJM 321:425-430, Little,R.E.,et al, 1989

The Acquired Immunodeficiency Syndrome (AIDS) Dementia Complex
Ann Int Med 111:400-410, Ho,D.D.,et al, 1989

Elevated Serum Levels of Tumor Necrosis Factor are Associated with Prog Encephalopathy in Children with AIDS
Am J Dis Child 143:771-774, Mintz,M.,et al, 1989

MR Imaging of a Group I Case of Hallervorden-Spatz Disease
J Comput Assist Tomogr 12:851-853, Mutoh,K.,et al, 1988

Brain Metabolism in Mitochondrial Encephalomyopathy:A PET Study
J Comput Assist Tomogr 12:854-857, DeVolder,A.,et al, 1988

The Peroxisome:Nervous System Role of a Previously Underrated Organelle, The 1987 Robert Wartenberg Lecture
Neurol 38:1617-1627, Moser,H.W., 1988

Predictive Value of Glasgow Coma Score for Awakening After Out-of-Hospital Cardiac Arrest
Lancet 1:137-140, Mullie,A.,et al, 1988

Unclear Speech:Recognition & Significance of Unintelligible Speech in Preschool Children
Pediatrics 82:447-452, Coplan,J.&Gleason,J.R., 1988

Rett Syndrome:Natural History and Management
Pediatrics 82:1-10, Moeschler,J.B.,et al, 1988

Hallervorden-Spatz Syndrome:Clinical and Magnetic Resonance Imaging Correlations
Ann Neurol 24:692-694, Sethi,K.D.,et al, 1988

Neurologic Manifestations of AIDS
Medicine 66:407-437, McArthur,J.C., 1987

Cytochrome c Oxidase Deficiency in Leigh Syndrome
Ann Neurol 22:498-506, DiMauro,S.,et al, 1987

Neurological Manifestations in Three German Children with AIDS
Neuropediatrics 18:99-106, Biggemann,B.,et al, 1987

Incontinentia Pigmenti:Association with Anterior Horn Cell Degeneration
Neurol 37:446-450, Larsen,R.,et al, 1987

The AIDS Dementia Complex:I. Clinical Features
Ann Neurol 19:517-524, Navia,B.A.,et al, 1986

Neurological Complications in Infants & Children with Acquired Immune Deficiency Syndrome
Ann Neurol 18:560-566, Belman,A.L.,et al, 1985

Biotinidase Deficiency:Initial Clinical Features & Rapid Diagnosis
Ann Neurol 18:614-617, Wolf,B.,et al, 1985

Clinical Findings in Four Children with Biotinidase Deficiency Detected Through a Statewide Neonatal Screening Program
NEJM 313:16-19, 43-441985., Wolf,B.,et al, 1985

Coffin-Siris Syndrome, Neuropathologic Findings
Arch Neurol 42:350-353, DeBassio,W.A.,et al, 1985

Carbonic Anhydrase II Deficiency in 12 Families with Osteopetrosis with Renal Tubular Acidosis & Cerebral Calcification
NEJM 313:139-181, Sly,W.S.,et al, 1985

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

Showing articles 250 to 300 of 5757 << Previous Next >>