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Differential
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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 atrophy, secondary

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

exome sequencing

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

gluten sensitivity

gluten-free diet

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

hypometric saccades

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

lysosomal storage disease

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

myoclonus-ataxia syndrome

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

Niemann-Pick disease

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

psychological testing

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, laughing as manifestation

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

whole genome sequencing

wide based gait

Wolfram syndrome

Showing articles 650 to 700 of 1474 << Previous Next >>

Stiripentol in Severe Myoclinic Epilepsy in Infancy: A Randomised Placebo-Controlled Syndrome-Dedicated Trial
Lancet 356:1638-1642,1623, Chiron,C.,et al, 2000

The Clinical Spectrum of Anti-GAD Antibody-Positive Patients with Stiff-Person Syndrome
Neurol 55:1531-1535, Dalakas,M.C.,et al, 2000

Increased Levels of Plasma Malondialdehyde in Friedreich Ataxia
Neurol 55:1752-1753,1600, Emond,M.,et al, 2000

Vertigo and Gait Ataxia Without Usual Signs of Lateral Medullary Infarction: A Clinical Variant Related to Rostral-dorsolateral Lesions
Cerebrovasc Dis 10:471-474, Kim,J.S., 2000

Niemann-Pick Disease Type C: Two Cases and an Update
Movement Disorders 15:1199-1203, Uc,E.Y.,et al, 2000

Paraneoplastic Cerebellar Ataxia Due to Autoantibodies Against a Glutamate Receptor
NEJM 342:21-27, Smitt,P.S.,et al, 2000

Very Late-Onset Friedreich Ataxia Despite Large GAA Triplet Repeat Expansions
Arch Neurol 57:246-251, Bidichandani,S.I.,et al, 2000

A Six-Year-Old Girl with Tick paralysis
NEJM 342:90-94, Felz,M.W.,et al, 2000

Nitrous Oxide Anesthesia-Associated Myelopathy
ArchNeurol 57:380-382, Marie,R.,et al, 2000

Intravenous Valproic Acid for Myoclonic Status Epilepticus
Neurol 54:1201, Sheth,R.D. & Gidal,B.E., 2000

Rotational Vertebral Artery Occlusion Syndrome with Vertigo Due to "Labyrinthine Excitation"
Neurol 54:1376-1379, Strupp,M.,et al, 2000

Clinicopath Conf,Cerebral Amyloid Angiogpathy and Giant-Cell Inflammatory Reaction to Beta 4-Amyloid and Vasculitis, Case 10-2000
NEJM 342:957-965, , 2000

Progression of Parkinsonian Signs in Alzheimer's Disease
Neurol 54:1284-1289, Wilson,R.S.,et al, 2000

Cardiac Dysfunction in Neuromuscular Diseases
The Neurologist 6:67-82, Pourmand,R., 2000

A Man with Progressive Weakness in His Legs
Lancet 354:830, van der Meulen,M.F.G.,et al, 1999

Clinical and MRI Findings in Spinocerebellar Ataxia Type 5
Neurol 53:1355-1357, Stevanin,G.,et al, 1999

Cerebellar Ataxia Associated with Subclinical Celiac Disease Responding to Gluten-Free Diet
Neurol 53:1606-1608, Pellecchia,M.T.,et al, 1999

Localization of a Gene for Myoclonus-Dystonia to Chromosome 7q21-q31
Ann Neurol 46:794-798, Nygaard,T.G.,et al, 1999

Genetic Localization of the Familial Adult Myoclonic Epilepsy (FAME) Gene to Chromosome 8q24
Neurol 53:1180-1183, Plaster,N.M.,et al, 1999

Distal Myopathies:Clinical and Molecular Diagnosis and Classification
JNNP 67:703-709, Mastaglia,F.J.&Laing,N.G., 1999

Superficial Siderosis of the Central Nervous System,A Late Complication of Cerebellar Tumors
Neurol 52:163-169, Anderson,N.E.,et al, 1999

Rapidly Progressive Dementia
Lancet 353:1150, Bornke,C.,et al, 1999

Paraneoplastic Syndromes
Arch Neurol 56:405-408, Dalmau,J.O.&Posner,J.B., 1999

Infantile Neuroaxonal Dystrophy,Clinical Spectrum and Diagnostic Criteria
Neurol 52:1472-1478, Nardocci,N.,et al, 1999

Topiramate in Clinical Practice:First Year's Postlicensing Experience in a Specialist Epilepsy Clinic
JNNP 66:759-763, Kellett,M.W.,et al, 1999

Molecular Basis of the Neurodegenerative Disorders
NEJM 340:1970-1980, Martin,J.B., 1999

Multiple Sclerosis in Children Under 6 Years of Age
Neurol 53:478-484, Ruggieri,M.,et al, 1999

Clinicopath Conf,Multifocal Inflammatory Leukoencephalopathy Related to Combination Chemo with Fluorouracil/levamisole
NEJM 341:512-519, Case 24-1999, 1999

Isolated,Chronic,Epilepsia Partialis Continua in an HIV-Infected Patient
Arch Neurol 56:111-114, Bartolomei,F.,et al, 1999

Opsoclonus as a Dominant Sign in Primary Sjogrens Syndrome
Neuro-Opthlhal 22:135-138, Lubec,D.,et al, 1999

Leukoencephalopathy and Raised Brain Lactate from Heroin Vapor Inhalation ("Chasing the Dragon")
Neurol 53:589-1048, Kriegstein,A.R., et al, 1999

Delayed Movement Disorders After Carbon Monoxide Poisoning
Eur Neurol 42:141-144, Choi,I.S. &Cheon,H.Y., 1999

Clinical Correlates of Vascular Parkinsonism
Arch Neurol 56:98-102, Winikates,J.&Jancovic,J., 1999

Pseudochoreoathetosis in Four Patients with Hypesthetic Ataxic Hemiparesis in a Thalamic Lesion
J Neurol 246:1075-1079, Kim, J.W., et al, 1999

Usefulness of CT and MR Imaging in the Diagnosis of Acute Wernickes Encephalopathy
AJR 171:1131-1137, Antunez, E.,et al, 1998

Subcotical Arteriosclerotic Encephalopathy (Binswangers Disease)
, Ghika,J. &Bogousslavsky, J., 1998

Hypophosphatemia-Induced Neuropathy: Clinical and Electrophysiologic Findings
Muscle Nerve 21:650-652, Siddiqui,M.F. &Bertorini,T.E., 1998

Creutzfeldt-Jakob Disease and Related Transmissible Spongiform Encephalopathies
NEJM 339:1994-2004, Johnson,R.T. & Gibbs,Jr.,C.J., 1998

Clinicopath Conf,Sarcoidosis,with Involvement of Spinal Cord,Brain,Mediastinal Lymph Nodes and ? Lung,Case 35-1998
NEJM 339:1534-1541, , 1998

Adult Brainstem Gliomas
Neurol 51:1136-1139, Landolfi,J.C.,et al, 1998

Clinical,Radiological,Neurophysiological,and Neuropathological Characteristics of Gluten Ataxia
Lancet 352:1582-1585, Hadjivassiliou,M.,et al, 1998

Lateral Medullary Infarction
Stroke, Pathophysiology, Diagnosis and management, Churchhill Livingstone, NY 3rd Ed, Ch 22, p. 534, Amarenco,P.,et al, 1998

Cerebellar Degeneration Associated With Human Immunodeficiency Virus Infection
Neurol 50:244-251, Tagliati,M.,et al, 1998

Ion Channels and Neurological Disease:DNA Based Diagnosis is Now Possible,and Ion Channels May be Important in Common Paroxysmal Disorders
JNNP 65:427-431, Hanna,M.G.,et al, 1998

Disequilibrium in Patients with Atherosclerosis; Relevance of Pontine Ischemic Rarefaction
Neurol 51:570-573, Kwa,V.I.H.,et al, 1998

Consequences of the Delayed Diagnosis of Ataxia-Telangiectasia
Pediatrics 102:98-100, Cabana,M.D.,et al, 1998

Clinicopath Conf
Dementia with Lewy Bodies, Anaplastic Astrocytoma of Right Insular Region, Case 7-1998, NEJM 338:603, 61098., 1998

Neuroradiologic Findings in Marinesco-Sjogren Syndrome
AJNR 19:281-283, Georgy,B.A.,et al, 1998

Slater Revisited:6 Year Follow Up Study of Pts with Medically Unexplained Motor Symptoms
BMJ 316:582-586, 5641998., Crimlisk,H.L.,et al, 1998

Cortical Myoclonus
Neurol 50:933-942, Mima,T.T.,et al, 1998

Showing articles 650 to 700 of 1474 << Previous Next >>