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abdominal distention

abdominal x-ray

adverse drug reaction

alcohol intolerance

alien hand syndrome

altered states of consciousness

alternating rapid movement

AMPA receptor antibodies

anti Ri antibody

antibiotics, neurologic complications with

antibodies to measles

anticonvulsants

anticonvulsants, effectiveness

anticonvulsants, selection of

antithyroid antibodies

arm swing, reduced

ataxia, cerebellar

ataxia, hereditary

ataxia, progressive

ataxia, truncal

ataxia, truncal, associated with ocular oscillations

autoimmune disease

autonomic dysfunction

axonal spheroid

bacterial infection

basal ganglia, calcification of

basal ganglia, degeneration

basal ganglia, lesion of

basal ganglia, lesion, bilateral

behavioral disorder

bovine spongiform encephalopathy

brainstem, atrophy

brainstem, lesion of

carbon monoxide poisoning

carcinoma of breast

carcinoma of lung

CAT scan, abnormal

CAT scan, emission

CAT scan, emission, abnormal

celiac disease, adult

central nervous system, infection of

cerebellar ataxia, children

cerebellar atrophy, primary

cerebellar degeneration

cerebellar lesion

cerebellum, disease of

cerebral cortex

cerebral cortical atrophy

cerebral glucose metabolism

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, gammaglobulin of

cerebrospinal fluid, lactic acid concentration

cerebrospinal fluid, oligoclonal IgG in

cerebrovascular accident

cerebrovascular accident, young adult

cherry red spot

cherry red spot-myoclonus syndrome

chewing movements

chorea, familial

choreoathetosis

chorioretinitis

chromosomal abnormality

chronic progressive external ophthalmoplegia

Clinical Pathologic Conference(C.P.C.)

coenzyme Q10 deficiency

cogwheel rigidty

cold intolerance

color vision, impaired

congenital infection, CNS

congenital paresis

conjugate gaze, forced

contactin associated protein like 2 antibodies

cortical-basal ganglionic degeneration

cranial nerve palsies

Creutzfeldt-Jakob disease, genetic

deep gray nuclei

degenerative diseases of CNS

delay in diagnosis

dementia, differential diagnosis of

dementia, rapidly progressive

dementia, reversible

dementia, transmissible

dementia, treatment of

demyelinating disease

dentate nuclei, lesion of

dentatorubral-pallidoluysian atrophy

developmental milestones

developmental milestones, loss of

developmental retardation

diabetes insipidus

diabetes mellitus

dialysis dementia

differential diagnosis

disability, neurological

doll's head maneuver

downward gaze, paralysis of

Dravet syndrome

drug induced neurologic disorders

dysdiadochokinesia

dyssynergia cerebellaris myoclonica

dystonia, focal

Ekbom's Syndrome

electroencephalogram

electroencephalogram, abnormalities of

electroencephalogram, periodic complexes

electroencephalogram, triphasic delta waves

encephalitis, autoimmune

encephalitis, brainstem

encephalitis, diagnosis of

encephalitis, etiology

encephalitis, paraneoplastic

encephalitis, viral

encephalitis, viral-causes of

encephalomyelitis

encephalomyelitis, postinfectious

encephalopathy, delayed

encephalopathy, Hashimoto's

encephalopathy, parainfectious

enterovirus infection of CNS

epidemiology of neurology

episodic disorders

episodic neurologic deficits

episodic unconsciousness

eye movement, disorders of

facial movement disorder

faciobrachial dystonic seizure

fatal familial insomnia

fine motor function, impaired

finger nose finger test

fingerprint bodies

flaccid paralysis

gamma amino butyric acid receptor antibody

gammaglobulin therapy, intravenous

gaze palsy, supranuclear

gaze palsy, vertical

genetic counselling

genetic neurologic disorders

genetic testing

gliadin antibodies

globus pallidus, lesion of

glutamic acid decarboxylase, antibody

gram positive rod

granular osmiphilic material

gyrus, abnormal

Hallervorden Spatz disease

hand-foot-mouth disease

heavy metal intoxication

heel-knee-shin test

hemimyoclonic jerks

hepatosplenomegaly

heralding manifestation

human immunodeficiency virus type 1

hyperpigmentation of skin

hyperthyroidism

hypothalamus, disturbance of

hypotonia, infants

iatrogenic neurologic disorders

imbalance, postural

immune reconstitution inflammatory syndrome

immunohistochemistry

immunosuppressive agents

inborn errors of metabolism

inclusion bodies

inclusion bodies, eosinophilic cytoplasmic

inclusion bodies, eosinophilic intranuclear

incontinence, fecal

intellectual deficit

intellectual deterioration

intestinal biopsy

intestinal pseudoobstruction

intrauterine infection

intrauterine infection, viral of CNS

Jakob-Creutzfeldt disease

Jakob-Creutzfeldt disease, cerebellar variant

Jakob-Creutzfeldt disease, variant

Jakob-Creutzfeldt disease, young adult

juvenile paresis

Kearns-Sayre syndrome

lactic acidemia

Lafora's disease

Leber's hereditary optic neuropathy

Leigh's disease

Leigh's disease, adult variety

leucine rich glioma inactivated 1 antibodies

leukocyte enzyme abnormality

leukoencephalopathy

leukoencephalopathy, differential diagnosis

leukoencephalopathy, hereditary diffuse

level of consciousness, decreased

limbic encephalitis

lipid storage disorder of CNS

liver function enzymes

lymphadenopathy

macular degeneration

malabsorption syndrome

memory, defect of recent

memory, impairment of

meningitis, aseptic

meningoencephalitis

mental retardation

mental status, abnormal

mitochondrial disease

mitochondrial encephalomyopathy

molecular genetics

motor neuron disease

motor neuron disease, misdiagnosis

movement disorder

movement disorder, drug induced

movement disorder, extrapyramidal

MRI, diffusion weighted

MRI, false negative

MRI, high signal intensity of basal ganglia

MRI, spinal cord

MRI, susceptibility weighted

myelitis, longitudinal

myelitis, transverse

myoclonic ataxia

myoclonic jerks

myoclonus, cortical

myoclonus, epilepsy

myoclonus, orthostatic

myoclonus, segmental

myoclonus, stimulus sensitive

myoclonus, treatment of

myopathy, mitochondrial

N-acetylcysteine

nausea and vomiting

neuraminidase deficiency

neuroaxonal dystrophy

neuroaxonal dystrophy, infantile

neuroaxonal dystrophy, juvenile

neuroaxonal leukodystrophy

neurologic complications of, systemic cancer

neurologic complications of, systemic disease

neurologic disease

neurologic disease, diagnoses of

neurologic disease, diagnoses of, clinical bedside

neurologic signs

neurologic symptoms

neuronal ceroid-lipofuscinosis

neuroophthalmology

neuropathology, brain

neuropathy, ataxia, retinitis pigmentosa

next-generation sequencing

nystagmus, rotary

nystagmus, vertical

ocular motility, disorders of

oculomasticatory myorhythmia

old age, neurology of

olivary degeneration, hypertrophic

ophthalmoplegia

ophthalmoplegia, progressive external

opsoclonus, differential diagnosis of

opsoclonus-myoclonus syndrome

optic atrophy, hereditary

optic neuropathy

oral ulcerations

organ transplantation

orthostatic hypotension

pain, abdominal

palatal myoclonus

paralysis, acute

paralysis, acute areflexic

paraparesis, spastic

Parkinson disease

Parkinsonism syndrome

paroxysmal neurologic deficits

PAS positive material in the brain

pathologic reflex

personality change

pigmentary retinopathy

pleocytosis of cerebrospinal fluid

polymerase chain reaction

pons, lesion of

pontocerebellar atrophy

potassium channel antibodies

pregnancy, neurologic complications in

prevention of neurologic disorders

progressive infantile poliodystrophy

progressive myoclonic epilepsy

progressive neurologic disorder

progressive pallidum atrophy

protein 14-3-3, cerebrospinal fluid

protein 14-3-3, cerebrospinal fluid, false negative

pseudobulbar palsy

psychiatric disorder

psychiatric problems in neurologic disorders

psychomotor retardation

psychosis, acute

pulmonary edema

Purkinje cell surface antibody

pursuit eye movements, abnormal

pyramidal tract dysfunction

pyruvate metabolism, abnormality of

ragged-red fibers

Ramsay Hunt syndrome

rapidly progressing neurologic illness

real-time quaking-induced conversion

release phenomena

REM sleep behavior disorder

remote effect of cancer on the nervous system

respiratory failure

respiratory tract infection

retinal degeneration

Rett's syndrome

rubella encephalitis

rubella encephalitis, progressive

rubella syndrome

saccadic eye movements, abnormal

salivation, excessive

sedimentation rate, elevated

seizure, children

seizure, familial

seizure, febrile

seizure, intractable

seizure, neonatal

seizure, paradoxical

seizure, photosensitive

seizure, tonic-clonic

seizure, treatment of

sensorineural hearing loss

sensory loss, cortical

serologic testing

serologic testing of cerebrospinal fluid

sleep apnea, obstructive

sleep pathology and physiology

slow virus infection of CNS

sodium channel dysfunction

sodium valproate

speech disorder

speech, loss of

spinal cord, lesion of

spinocerebellar ataxia

spinocerebellar ataxia type 1

spinocerebellar ataxia type 16

spinocerebellar ataxia type 7

splenium of corpus callosum

spongy degeneration of brain

square wave jerks

standing difficulty

startle myoclonus

startle reaction

status epilepticus

stem cell transplantation

steroid therapy, CNS treatment and complications with

stiff man syndrome

storage disease of CNS

striatonigral degeneration

striatonigral degeneration, infantile

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

symmetric brain lesions

syphilis, diagnosis and treatment

syphilis, neurologic complications with

systemic illness

tandem gait, ataxic

temporal lobe, lesion, bilateral

teratoma, ovarian

thalamus, lesion of

thalamus, lesion of-bilateral

toxins, nervous system

transplacental virus infections

treatment of neurologic disorder

tremor, intention

tremor, postural

triangle of Guillain and Mollaret

trinucleotide repeats

ultrasonography

unconsciousness

unconsciousness, episodic

unconsciousness, transient

Unverricht-Lundborg disease

upgaze, paralysis of

urinary incontinence

viral infection

viral infection, CNS

viral isolation

vision, blurred

visual acuity, decreased

visual impairment

visuospatial disturbance

vitreous opacities

walking, difficulty with

weakness, acute

weakness, focal

Whipple's disease

white matter disease

wide based gait

Wolfram syndrome

Showing articles 950 to 1000 of 1450 << Previous Next >>

Capsular Hypesthetic Ataxic Hemiparesis
Stroke 21:24-33, Helgason,C.M.&Wilbur,A.C., 1990

Relative Increase of T Cells Expressing Gamma/Delta Rather than Alpha/Beta Receptor in Ataxia-Telangietasia
NEJM 322:73-76, 1241990., Carbonari,M.,et al, 1990

Epileptic Seizures and Syndromes
Lancet 336:161-163, Gram,L., 1990

Neuronal Intranuclear Inclusion Disease in a Child:Diagnosis by Rectal Biopsy
Ann Neurol 27:103-106, Goutieres,F.,et al, 1990

Olivopontocerebellar Atrophy:MR Diagnosis and Relationahip to Multisystem Atrophy
Radiology 174:693-696, Savoiardo,M.,et al, 1990

Idiopathic Cerebellar Ataxia of Late Onset:Natural History and MRI Morphology
JNNP 53:297-305, Klockgether,T.,et al, 1990

Neurologic Manifestations of Giant Cell Arteritis
Am J Med 89:67-72, Reich,K.A.,et al, 1990

Neuropsychological Changes in Olivopontocerebellar Atrophy
Arch Neurol 47:997-1001, Berent,S.,et al, 1990

Cortical-Basal Ganglionic Degeneration
Neurol 40:1203-1212, Riley,D.E.,et al, 1990

Geriatrics:Gait Disorders in the Elderly
NEJM 322:1441-1446, Sudarsky,L., 1990

'Rubral'Gait Ataxia
Neurol 40:1004-1005, Felice,K.J.,et al, 1990

Acceleration-Induced Loss of Consciousness, A Review of 500 Episodes
Arch Neurol 47:764-776, Whinnery,J.E.&Whinnery,A.M., 1990

Migraine Assoc with Focal Cerebral Edema, CSF Pleocytosis, & Prog Cerebellar Ataxia:MRI Documentation
Neurol 40:1284-1287, Goldstein,J.M.,et al, 1990

Progressive Rubella Panencephalitis
In Handbk of Clin Neurol, Vinken & Bruyn, Ed, N Holland Publ Co, 56:405-416, Wolinsky,J.S., 1990

Miller Fisher Syndrome Associated with Q Fever
JNNP 53:615-616, Diaz Ortuno,A.,et al, 1990

Neurological Deterioration in Young Adults with Phenylketonuria
Lancet 336:602-605, Thompson,A.J.,et al, 1990

Acute Triphenyltin Intoxication:A Case Report
JNNP 53:356-357, Wu,RM.,et al, 1990

Cerebral Cortex and Brainstem Involvement in Marinesco-Sjogren Syndrome
Ann Neurol 27:448-449, Katafuchi,Y.,et al, 1990

A Quantitative Evaluation of Pontine Volume by Computed Tomography in Patients with Cerebral Degeneration
Neurol 40:1241-1245, Chida,K.,et al, 1990

Antemortem Diagnosis of Diffuse Lewy Body Disease
Neurol 40:1523-1528, Crystal,H.A.,et al, 1990

The Marinesco-Sjogren Syndrome Examined by CT, MR, and 18F-2-Fluoro-2-Deoxy-D-Glucose & PET
Arch Neurol 47:1239-1242, Bromberg,M.B.,et al, 1990

Chronic Acetazolamide Monotherapy in the Treatment of Juvenile Myoclonic Epilepsy
Neurol 40:1677-1681, Resor,S.R.&Resor,L.D., 1990

Myoclonic Status Epilepticus:A Clinical and Electroencephalographic Study
Neurol 40:1199-1202, Jumao-as,A.&Brenner,R.P., 1990

Movement Disorders in Alcoholism:A Review
Neurol 40:741-746, Neiman,J.,et al, 1990

Ataxic Sensory Neuropathy and Dorsal Root Ganglionitis Associated with Sjogren's Syndrome
Ann Neurol 27:304-315, Griffin,J.W.,et al, 1990

Clinicopath Conf
Familial Visceral Myopathy (Oculogastrointestinal Muscular Dystrophy) , Case 12-1990, NEJM 322:829-8, 1, 19, 1990

Clinicopath Conf
Sarcoidosis of CNS and Mediastinal Lymph Nodes, Case Record 6-1990, NEJM 322:388-397990., , 1990

Bismuth Absorption and Myoclonic Encephalopathy During Bismuth Subsalicylate Therapy
Ann Int Med 112:140-141, Mendelowitz,P.C.,et al, 1990

MRI Demonstration of Cortical Laminar Necrosis and Delyaed White Matter Injury in Anoxic Encephalopathy
Neuroradiology 32:319-321, Sawada,H.,et al, 1990

Hypoxic-Ischemic Damage of the Basal Ganglia
Mov Disord 5:219-224, Hawker, K. & Lang, A.E., 1990

Paroxysmal Cerebellar Ataxia
Aust NZ J Med 19:113-117, Feeney,G.F.&Boyle,R.S., 1989

Neuromuscular Involvement in Mild, Asymptomatic Primary Hyperparathyroidism
Am J Med 87:553-557, Turken,S.A., 1989

Opsoclonus-Myoclonus Syndrome:Correlation of Radiographic and Pathological Observations
Neuroradiology 31:250-252, Turchman,R.F.,et al, 1989

Cerebral Palsy Diplegia:Improvements for Walking
BMJ 299:1115-1116, Patrick,J., 1989

Variables Predicting Surgical Outcome in Symptomatic Hydrocephalus in the Elderly
Neurol 39:1601-1604, Graff-Radford,R.N.,et al, 1989

Symptomatic Congenital Hydrocephalus in the Elderly Simulating Normal Pressure Hydrocephalus
Neurol 39:1596-1600, Graff-Radford,N.R.&Godersky,J.C., 1989

Isolated Midbrain Lesion Resulting From Closed Head Injury:A Unique Presentation of Ataxia Hemiparesis
Neurol 39:452-453, Hershkowitz,N.,et al, 1989

Agenesis of the Corpus Callosum and Gyral Malformations are Frequent Manifestations of Nonketotic Hyperglycinemia
Neurol 39:817-820, Dobyns,W.B., 1989

Primary Progressive Cerebellar Ataxia
Neuroradiology 31:16-18, Bradac,G.B.,et al, 1989

Hypesthetic Ataxic Hemiparesis in a Thalamic Lacune
Stroke 20:819-821, Lee,N.,et al, 1989

Clinicopath Conf
Subacute Cerebellar Degeneration, Cystadenocarcinoma of Ovary, (with Paraneoplastic Syndrome) , Case, 34-1EJM 321:524-535,1989., 1989

Adrenoleukodystrophy
JAMA 262:1504-1506, Ladenson,P.W., 1989

Clinicopath Conf
Chronic Osteomyelitis of Spine, with Intervertebral Diskitis (T3-T4) & Epidural Abscess (Staph Aureu, ) , Cas9,NEJM 320:1610-1618,1989., 1989

Central Nervous System Manifestations of Lyme Disease
Arch Neurol 46:790-795, Pachner,A.R.,et al, 1989

Late Onset of Distinct Neurologic Syndromes in Galactosemic Siblings
Neurol 39:741-742, Friedman,J.H.,et al, 1989

Dopa Responsive Dystonia:A Treatable Condition Misdiagnosed as Cerebral Palsy
BMJ 298:1019-1020, Boyd,K.&Patterson,V., 1989

Hysterical Gait Disorders:60 Cases
Neurol 39:586-589, Keane,J.R., 1989

Neonatal Seizures:Current Concepts and Revised Classification
Pediatrics 84:422-428, Volpe,J.J., 1989

Juvenile Myoclonic Epilepsy:An Autosomal Recessive Disease
Ann Neurol 25:440-443, Panayiotopoulos,C.P.&Obeid,T., 1989

Syndrome of Cerebellar Ataxia and Hypogonadotrophic Hypogonadism:Evidence for Pituitary Gonadotrophin Deficiency
JNNP 52:407-409, Fox,A.C.K.,et al, 1989

Showing articles 950 to 1000 of 1450 << Previous Next >>