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Differential
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acquired immunodeficiency syndrome

acute ataxia of childhood

acute cerebellar ataxia

adverse drug reaction

alcohol, neurologic complications with

alien hand syndrome

alternating rapid movement

amyotrophic lateral sclerosis, differential diagnosis

amyotrophic lateral sclerosis, misdiagnosis

amyotrophic lateral sclerosis-like syndrome

ankle reflex, absent

anterior horn cell disease

anterior tibial muscle weakness

anti citrullinated antibody

anti Yo antibody

anticholinergic drugs

anticonvulsants

anticonvulsants, blood level determination of

anticonvulsants, mechanism of action of

anticonvulsants, teratogenicity of

anticonvulsants, untoward effects of

antiviral agents

arylsulfatase A

ataxia telangiectasia

ataxia, acute onset

ataxia, cerebellar

ataxia, hereditary

ataxia, progressive

ataxia, truncal

attention deficit disorder with hyperactivity

autonomic dysfunction

autosomal rcessive spastic ataxia of Charlevoix-Saguenay

axonal spheroid

basal ganglia, calcification of

basal ganglia, lesion of

behavioral disorder

benign essential tremor

benign essential tremor, refractory

beta adrenergic blocker

biologic markers

calcification, intracranial

carcinoma of lung

CAT scan, abnormal

central nervous system, infection of

cerebellar ataxia, autosomal recessive

cerebellar ataxia, hereditary

cerebellar atrophy, primary

cerebellar degeneration

cerebellar disease, eye movement disorder in

cerebellar hemorrhage

cerebellar hypoplasia

cerebellar lesion

cerebellum, disease of

cerebral cortical atrophy

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, cytology

cerebrospinal fluid, enzymes in

cerebrospinal fluid, gammaglobulin of

cerebrospinal fluid, gold sol.curve of

cerebrospinal fluid, lactic acid concentration

cerebrospinal fluid, oligoclonal IgG in

cerebrospinal fluid, red cells in

cerebrovascular accident

chest x-ray, abnormal

chylomicron retention disease

Clinical Pathologic Conference(C.P.C.)

cogwheel rigidty

conduction block

conversion reaction

corpus callosum, lesion of

corpus callosum, thinning

cortical-basal ganglionic degeneration

cranial neuropathy, multiple

creatine phosphokinase(CPK)elevated

cyclophosphamide

decerebrate posture

degenerative diseases of CNS

developmental disability

developmental milestones

developmental milestones, loss of

developmental retardation

diabetes mellitus

differential diagnosis

difficulty going down stairs

dilantin, factors influencing metabolism of

distal muscle weakness

drug induced neurologic disorders

dysdiadochokinesia

dystonia, focal

dystonia, post traumatic

electroencephalogram

electroencephalogram, abnormalities of

electroencephalogram, focal delta activity

entrapment neuropathy

erythema nodosum

exome sequencing

eye movement, disorders of

facial weakness

facial weakness, bilateral

failed medical management

false positive VDRL

fine motor function, impaired

finger nose finger test

fingerprint bodies

Fragile-X associated tremor/ataxia-syndrome

fragile-X syndrome

fragile-X syndrome, carrier

Friedreich's ataxia

gamma amino butyric acid

gammaglobulin therapy, intravenous

gastrointestinal perforation

genetic counselling

genetic neurologic disorders

genetic screening

genetic testing

glucose tolerance test, abnormal

granular osmiphilic material

head injury, delayed deterioration following

heavy metal intoxication

hemochromatosis

hemochromatosis, primary

hepatic encephalopathy

hepatolenticular degeneration(Wilson's disease)

hepatosplenomegaly

high arched feet

Huntington's chorea

hyperosmolality

hyperthyroidism

hypoparathyroidism

hypotonia, infants

immunosuppressive agents

inborn errors of metabolism

inclusion bodies

inclusion bodies, eosinophilic cytoplasmic

inclusion bodies, eosinophilic intranuclear

inclusion bodies, intranuclear

infantile spasm

intellectual deficit

intellectual deterioration

Jakob-Creutzfeldt disease

Jakob-Creutzfeldt disease, cerebellar variant

Krabbe's disease

lactic acidemia

lactic dehydrogenase(LDH)

laminectomy, lumbar

laughing, pathologic

leg weakness, bilateral

Leigh's disease

leukoencephalopathy

leukoencephalopathy, hereditary diffuse

liver function enzymes

lysosomal storage disease

memory, impairment of

meningeal enhancement

meningitis, carcinomatous

meningoencephalitis

mental retardation

metachromatic leukodystrophy

metachromatic leukodystrophy, juvenile

middle cerebellar peduncle

middle cerebellar peduncle, lesion

middle cerebellar peduncle, lesion, bilateral

molecular genetics

motor neuron disease

movement disorder

movement disorder, delayed onset

movement disorder, drug induced

movement disorder, extrapyramidal

movement disorder, psychogenic

MRI, diffusion weighted

multiple sclerosis

multiple sclerosis, treatment of

multiple system atrophy

muscle stiffness

muscle weakness, proximal

myelinolysis, extrapontine

myoclonic jerks

myoclonus, epilepsy

nausea and vomiting

nerve conduction studies

nerve conduction studies, motor

neuroaxonal leukodystrophy

neuroendocrinology

neurologic disease, diagnoses of

neuromuscular disease, electrodiagnosis of

neuronal ceroid-lipofuscinosis

neuronal intranuclear inclusion disease

neuropathology, brain

neuropathy, demyelinating

neuropathy, motor

neuropathy, motor, multifocal

neuropathy, peripheral

nutritional deficiency

nystagmus, rotary

nystagmus, vertical

occupational neuropathies

oculogyric crisis

ophthalmoplegia

optic neuropathy

optic neuropathy, bilateral

orthostatic hypotension

osmotic demyelination syndrome

Parkinson disease

Parkinson disease, benign tremulous

Parkinson disease, L-dopa nonresponsive

Parkinsonism multiple-system atrophy

Parkinsonism syndrome

PAS positive material in the brain

pleocytosis of cerebrospinal fluid

pneumoencephalogram(PEG)

poison, neurologic problems with

polymerase chain reaction, false negative

pons, lesion of

postoperative neurologic complications

prevention of neurologic disorders

progressive neurologic disorder

prothrombin time, prolonged

pyramidal tract dysfunction

pyruvate metabolism, abnormality of

Raynaud's phenomenon

reflex sympathetic dystrophy

remote effect of cancer on the nervous system

respiratory myoclonus

respiratory tract infection

rheumatoid arthritis

rheumatoid arthritis, neurologic complications of

Sabin-Feldman dye test

saccadic eye movements, abnormal

sedimentation rate, elevated

seizure, children

seizure, minor motor

seizure, petit mal

seizure, tonic-clonic

seizure, treatment of

serum glutamic oxaloacetic transaminase

skin, darkening of

sodium valproate

sodium valproate, toxicity

speech disorder

speech disorder, childhood

speech, delayed development of

speech, loss of

spinocerebellar ataxia

spinocerebellar ataxia type 12

spinocerebellar ataxia type 3/Machado Joseph disease

startle myoclonus

startle reaction

status epilepticus

stimulation, deep brain

storage disease of CNS

striatonigral degeneration

striatonigral degeneration, infantile

systemic lupus erythematosus

systemic lupus erythematosus, neurologic complications with

systemic lupus erythematosus, skin changes in

tandem gait, ataxic

thalamus, focused ultrasound ablation

thrombocytopenia

thrombotic thrombocytopenia purpura

tongue, fasciculations of

tonic foot response

torticollis, post traumatic

toxoplasma complement fixation test

toxoplasmosis, acquired

toxoplasmosis, CNS

treatment of neurologic disorder

tremor, cerebellar

tremor, classification

tremor, differential diagnosis of

tremor, intention

tremor, orthostatic

tremor, physiologic

tremor, post traumatic

tremor, postural

tremor, psychogenic

tremor, resting

tremor, surgical treatment of

tremor, thalamic stimulation for suppression of

tremor, treatment of

tremor, writing

trimethoprim-sulfamethoxazole

trinucleotide repeats

ulnar nerve, compression of

ulnar neuropathy

vagus nerve stimulation

Venereal Disease Research Laboratory test

viral infection

viral infection, CNS

vitamin E deficiency

walking, delayed

walking, difficulty with

West Nile fever

white matter disease

wide based gait

X-linked bulbospinal neuronopathy

Showing articles 0 to 50 of 1257 Next >>

Complex Ataxia
Neurol 95:136-141, Abkur, T.,et al, 2020

Pes Cavus and Neuropathy
Neurol 93:e823-e826, Alderson,J.,& Ghosh,P.S., 2019

Essential Tremor
NEJM 378:1802-1810, Haubenberger, D.,et al, 2018

Action Tremor, Impaired Balance, and Executive Dysfunction in Midlife
JAMA Neurol 74:603-604, Birch, R.C. & Trollor, J.N., 2017

A 27-year-old man with Acute-Onset Ataxia
Neurol 88:e207-e211, Risco, J. & Weiss, M., 2017

Orthostatic Tremor
Neurol 86:458-464, Hassan, A.,et al, 2016

A 57-year-old Man with Subacute Gait Difficulty and Hand Tremor
Neurol 87:e110-e113, Paliwal, V.K.,et al, 2016

Clinical Reasoning: A Woman with Rapidly Progressive Apraxia
Neurol 80:e162-e165, Pressman, P.,et al, 2013

The Autosomal Recessive Cerebellar Ataxias
NEJM 366:636-646, Anheim,M.,et al, 2012

Clinicopathologic Conference, Kufs Disease (Autosomal Dominant) Parry Type Neuronal Ceroid Lypofuscinosis
NEJM 364:1062-1074, Case 8-2011, 2011

A 75-Year-Old Woman with Progressive Right-Hand Tremor and Inability to Use Her Right Side
Neurol 73:1399-1405, Kertesz,A.,et al, 2009

Fragile X-Associated Tremor/Ataxia Syndrome: An Aging Face of the Fragile X Gene
Arch Neurol 65:19-25, Amiri,K.,et al, 2008

Clinicopath Conf., Multifocal Motor Neuropathy With Conduction Block
NEJM 357: 2707-2715, Case 40-2007, 2007

Benign Tremulous Parkinsonism
Arch Neurol 63:354-357,321, Josephs,K.A.,et al, 2006

Vagal Nerve Stimulation Effect on Cerebellar Tremor in Multiple Sclerosis
Neurol 65:499, Marrosu,F.,et al, 2005

Penetrance of the Fragile X-Associated Tremor/Ataxia Syndrome in a Premutation Carrier Population
JAMA 291:460-469, Jacquemont,S.,et al, 2004

Clinicopath Conf., West Nile Virus Meningoencephalitis
NEJM 348:2239-2247, Case17-2003, 2003

SCA-12: Tremor with Cerebellar and Cortical Atrophy is Associated with a CAG Repeat Expansion
Neruol 56:299-303,287, O'Hearn,E.,et al, 2001

Essential Tremor
NEJM 345:887-891, Louis,E.D., 2001

Electrophysiological Aids in Distinguishing Organic from Psychogenic Tremor
neurol 50:1882-1884, McAuley,J.H.,et al, 1998

Wobbly Handwriting
Lancet 351:336, Rosario,M.A.F.,et al, 1998

Tremor Caused by Trimethoprim-Sulfamethoxazole in a Patient with AIDS
Neurol 48:537-538, VanGerpen,J.A., 1997

Paraneoplastic Cerebellar Degeneration
Arch Int Med 157:1258-1262, Bolla,L.&Palmer,R.M., 1997

Delayed-Onset Cerebellar Syndrome
Arch Neurol 53:450-454, Louis,E.D.,et al, 1996

Terfenadine-Induced Tremor
Ann Neurol 33:226, Soto,J.,et al, 1993

Stimulus-Specific pathological Laughter:A Case Report with Discrete Unilateral Localization
Neurol 43:229-230, Doorenbos,D.I.,et al, 1993

Thalamic Stimulation & Prox Tremor, A Specific Target in Nucleus Ventrointermedius Thalamik
Arch Neurol 50:498-500, Nguyen,J-P.&Degos,J-D., 1993

Risk Factors for Nursing Home Placement in Advanced Parkinson's Disease
Neurol 43:2227-2229, Goetz,C.G.&Stebbins,G.T., 1993

The Motor Disorder of Multiple System Atrophy
JNNP 56:1239-1242, Quinn,N.P.&Marsden,C.D., 1993

High-Frequency Diaphragmatic Flutter:Symptoms and Treatment by Carbamazepine
Lancet 339:265-267, Vantrappen,G.,et al, 1992

Clinicopath Conf
Infantile Striatonigral Regeneration, with Cerebellar Degeneration, Familial, Case 30-1992, NEJM 327, 261-1992., 1992

Classification and Treatment of Tremor
JAMA 266:1115-1117, Hallett,M., 1991

Glutethimide Treatment of Disabling Action Tremor in Patients with MS and Traumatic Brain Injury
Arch Neurol 48:513-515, Aisen,M.L.,et al, 1991

Clinical and Electrodignostic Features of X-Linked Recessive Bulbospinal Neuronopathy
Neurol 41:823-828, Olney,R.K.,et al, 1991

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

Distal Ulnar Neuropathy as a Cause of Finger Tremor:A Case Report
Neurol 40:153-154, Streib,E.W., 1990

Treatment of Cerebellar Tremors with Carbamazepine:A Controlled Trial with Long-Term Follow-Up
Neurol 39:1113-1115, Sechi,G.P.,et al, 1989

Clinicopath Conf
Adenocarcinoma of Lung, with Metastasis to Meninges of Brain, Spinal Cord & Optic Nerves, Case Recor, 14-1EJM 318:903-915,1988., 1988

Dystonia and Tremor Induced by Peripheral Trauma:Predisposing Factors
JNNP 51:1512-1519, Jankovic,J.&VanDer Linden,C., 1988

Primary Writing Tremor & Myoclonic Writer's Cramp
Neurol 35:1387-1391, Ravits,J.,et al, 1985

Action Tremor as a Manifestation of Chylomicron Retention Disease
Ann Neurol 14:591, Gauther,S.,et al, 1983

Clin. Path. Conference
Creutzfeldt-Jakob Disease, Ataxic Type, with Kuru Plaques, Case Record 45-1980, NEJM 303:1162-11710., , 1980

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

Juvenile Metachromatic Leukodystrophy
Arch Neurol 37:42-46, Haltia,T.,et al, 1980

Valproic Acid
NEJM 302:661-666, Brown,T.R., 1980

Diagnosis & Treatment, Physiologic & Pathologic Tremors
Ann Int Med 93:460-465, Jankovic,J.,et al, 1980

Valproic Acid, Review of a New Antiepileptic Drug
Arch Neurol 36:393-398, Bruni,J.,et al, 1979

Azorean Disease of the Nervous System
NEJM 296:1505, Romanul,F.C.A.,et al, 1977

Reversible Cerebellocerebral Disorder in Primary Hemochromatosis
Arch Neurol 34:123, Singh,N.,et al, 1977

Showing articles 0 to 50 of 1257 Next >>