Neudle.com: episodic ataxia

Differential
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abdominal distention

abdominal migraine

abducens nerve paralysis

abducens nerve paralysis, bilateral

acquired immunodeficiency syndrome

acromicria

acute cerebellar ataxia

acute disseminated encephalomyelitis

acyl CoA dehydrogenase deficiency

Addison's disease

adrenoleukodystrophy

advances in neurology

adverse drug reaction

alcohol, neurologic complications with

alcoholic amblyopia

alcoholic polyneuropathy

alcoholic withdrawal states, DT's, convulsions, etc.

alcoholism

Alexanders disease

Alexanders disease, adult onset

algorithm

alkalosis

alkalosis, respiratory

alkylating agents

alopecia

altered states of consciousness

alternating hemiplegia

alternating hemiplegia of childhood

alternating rapid movement

AMPA receptor antibodies

amyloid angiopathy, cerebral

amyloid angiopathy, cerebral, inflammatory type

anemia

aneurysm

aneurysm, vertebral basilar system

Angelman syndrome

angiitis

angiitis, granulomatous of CNS

angiography, cerebral, beaded vessels

angiography, cerebral

angiography, cerebral, negative

angiography, vertebral artery

angiokeratoma

angiotensin-converting enzyme

animal exposure

anorexia

anosmia

anti GQ1b IgG antibody

anti IgLON5

anti MAG antibodies

antibiotics

antibiotics, neurologic complications with

antibodies to measles

antibodies to voltage-gated calcium channels

anticonvulsants

anticonvulsants, effectiveness

anticonvulsants, selection of

anticonvulsants, untoward effects of

antiendomysial antibodies

antimetabolite

antioxidant

antithyroid antibodies

apnea, primary central

autoimmune basal ganglia encephalitis

autoimmune disease

autoimmune GFAP astrocytopathy

automobile accidents

autonomic dysfunction

bacterial infection, CNS

ballismus, bilateral

basal ganglia

basal ganglia, calcification of

basal ganglia, degeneration

basal ganglia, lesion of

basal ganglia, lesion, bilateral

basilar artery migraine

basophilic stippling of red blood cells

Bassen-Kornzweig syndrome

behavior modification

behavior, combative

behavioral disorder

Behcet's syndrome

benign positional vertigo

biotin deficiency, juvenile form

biotinidase deficiency

bitemporal visual field defect

blood dyscrasias, neurologic findings with

bone demineralization

bone marrow biopsy

bone marrow transplantation

boomerang sign

brachial plexus neuropathy

brain biopsy, negative

brain biopsy, stereotaxic

brain scan, abnormal

brainstem, atrophy

brainstem, infarction of

brainstem, lesion of

brucellosis

brucellosis, nervous system involvement with

calcification, intracranial

calcification, periventricular

calcium antagonist

calcium channel dysfunction

carbamazepine

carbamazepine, toxicity

carcinoma

carcinoma of breast

carcinoma of lung

carcinoma of pancreas

CAT scan, angiography

CAT scan, contrast enhanced, subepend.

cataplexy

cataracts

cat-scratch disease

caudate nucleus, atrophy

CD4 counts

celiac disease, adult

central core disease

central nervous system, infection of

central pontine myelinolysis

central retinal artery occlusion

cephalosporins

cerebellar ataxia, children

cerebellar ataxia, hereditary

cerebellar ataxia, primary

cerebellar atrophy, primary

cerebellar degeneration

cerebellar disease, eye movement disorder in

cerebellar hypoplasia

cerebellar lesion

cerebellar peduncle

cerebellar vermis

cerebral autosomal dominate arteriopathy with subcortical infarction and leukoencephalopathy

cerebral autosomal recessive arteriopathy with subcortical infarction and leukoencephalopathy

cerebral cortex

cerebral cortical atrophy

cerebral edema

cerebral folate deficiency syndrome

cerebral infarction

cerebral infarction, subcortical

cerebral palsy

cerebral venous thrombosis

cerebroretinal microangiopathy with calcifications and cysts

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, culture of, viral

cerebrospinal fluid, cytology

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, gammaglobulin of

cerebrospinal fluid, lactic acid concentration

cerebrospinal fluid, oligoclonal IgG in

cerebrospinal fluid, pressure increased

cerebrospinal fluid, pressure low

cerebrospinal fluid, proteincytologic dissociation

cerebrospinal fluid, xanthochromia of

cerebrovascular accident

cerebrovascular accident, mimics

cerebrovascular accident, recurrent

cerebrovascular accident, young adult

cerebrovascular disease

channelopathy

Charcot-Marie-Tooth

chemical weapons

chemotherapy, CNS treatment and complications with

cherry red spot

cherry red spot-myoclonus syndrome

chest x-ray

chest x-ray, abnormal

children

chills

chloride channel dysfunction

chromosomal abnormality

chronic progressive external ophthalmoplegia

Chvostek sign

ciguatera poisoning

cisterna magna, enlarged

Clinical Pathologic Conference(C.P.C.)

clonus

cobalamin C deficiency

cocaine

Cockayne's syndrome

coenzyme Q10

coenzyme Q10 deficiency

collagen vascular disease

color vision, impaired

concentration, impaired

confusion

congenital infection, CNS

congenital infection, viral

congenital malformation

corpus callosum, atrophy of

corpus callosum, lesion of

cortical blindness

cough

cranial nerve palsies

cranial neuropathy

cranial neuropathy, multiple

craniopharyngioma

creatine phosphokinase(CPK)elevated

cry, abnormal

cry, weak

crying

cryopyrin-associated periodic syndrome

cultured skin fibroblasts

Cushing's syndrome

cyclic vomiting

cyclic vomiting syndrome

cyclosporine

cyst

cyst, arachnoid

cyst, arachnoid, posterior fossa

cyst, porencephalic

cytomegalovirus infection

degenerative diseases of CNS

dementia, differential diagnosis of

dementia, presenile

dementia, rapidly progressive

dementia, reversible

dementia, subcortical

dementia, treatment of

demyelinating disease

dentate nuclei

dentate nuclei, lesion of

dentatorubral-pallidoluysian atrophy

developmental milestones

developmental milestones, loss of

developmental retardation

diabetes insipidus

diabetes mellitus

diabetes mellitus, neurologic manifestations of

differential diagnosis

difficulty climbing stairs

digital subtraction angiography

dilantin

diplopia

disability, neurological

disorientation

distal muscle atrophy

down-beat nystagmus, primary position of gaze

downward gaze, paralysis of

Dravet syndrome

drooling

dropped head syndrome

drowsiness

drug induced neurologic disorders

drug induced neurologic disorders in children

dyskinesia, buccal lingual facial

dyssynergia cerebellaris myoclonica

dystonia

dystonia, psychogenic

electroencephalogram, abnormalities of

electroencephalogram, periodic complexes

encephalitis, autoimmune

encephalitis, brainstem

encephalitis, diagnosis of

encephalitis, episodic

encephalitis, etiology

encephalitis, paraneoplastic

encephalitis, viral

encephalitis, viral-causes of

encephalomyopathy

encephalopathy

encephalopathy, acute

encephalopathy, Hashimoto's

encephalopathy, progressive

epidemiology of neurology

epileptic encephalopathy

epinephrine

episodic disorders

episodic neurologic deficits

episodic unconsciousness

extinction on double simultaneous stimulation

eye movement, disorders of

Fabry's disease

face, numbness of

facial appearance, abnormal

facial expression abnormality

facial movement disorder

facial nerve palsy

facial nerve palsy, bilateral

facial nerve palsy, recurrent

facial pain

facial weakness

faciobrachial dystonic seizure

familial hemiplegic migraine

familial periodic ataxia

fine motor function, impaired

fingerprint bodies

fish

Fisher's syndrome

fistula, perilymphatic

flu-like illness

fluorescene in situ hybridization

fluorescent treponema antibody absorption(FTA-ABS)

fluorouracil

flush syndrome

folic acid

folic acid deficiency

fundus, abnormality of

gamma amino butyric acid receptor antibody

gammaglobulin therapy, intravenous

ganciclovir

gargoylism

gastric partitioning

gastrointestinal disease, neurologic complications

gaze palsy

gaze palsy, supranuclear

gaze palsy, vertical

gene

gene mutation

general paresis of the insane

genetic counselling

genetic diagnosis, prenatal

genetic neurologic disorders

globus pallidus, lesion of

globus pallidus, lesion of, bilateral

glutamic acid

glutamic acid decarboxylase, antibody

granular osmiphilic material

granulomatous disease

gray hair

growth hormone deficiency

growth retardation

grunting

Guillain Barre syndrome

gynecomastia

Hallervorden Spatz disease

Hallgren's syndrome

hallucination

hallucination, auditory

hallucination, visual

hand clapping

hand flapping

hand wringing

Hand-Schuller-Christian disease

head turning, neurologic complications with

headache, progressive

heavy metal intoxication

hemianopia

hemianopia, homonymous

hemimyoclonic jerks

hemiparesis

hemiplegia

hemophagocytic lymphohistiocytosis, cerebromeningeal

hemophagocytosis

hemosiderosis of CNS, superficial

heralding manifestation

herpes simplex encephalitis, differential diagnosis of

herpes virus

herpes zoster

herpes zoster, disseminated

HLA

hoarseness

Hodgkin's disease

Hodgkin's disease, neurologic involvement with

homocystinuria

human immunodeficiency virus type 1

hung reflex

Huntington's chorea

Huntington's disease, children

Hurler's syndrome

hydrocephalus

hydrocephalus, normal pressure

hydrocephalus, treatment of

hydroxyglutaric aciduria

hypertrophic intracranial pachymeningitis

hyperventilation

hypocalcemia

hypocalcemia, causes of

hypokalemic periodic paralysis

hypopigmentation of skin

hyporeflexia

hyposmia

hypothalamus

hypothalamus, disturbance of

iatrogenic neurologic disorders

immunosuppressive agents

immunotherapy

impotence

impulsivity

inappropriate antidiuretic(A.D.H.)hormone

inappropriate antidiuretic(A.D.H.)hormone, CNS involvement with

inappropriate behavior

inattention

inborn errors of metabolism

incidence

inclusion bodies

inclusion bodies, eosinophilic cytoplasmic

inclusion bodies, eosinophilic intranuclear

inclusion bodies, intranuclear

incoordination

industrial neurologic disorders

infection

infectious mononucleosis

infectious mononucleosis, neurologic findings with

influenza

intellectual deficit

intellectual deterioration

intestinal biopsy

intestinal pseudoobstruction

intracerebral hemorrhage

intracerebral hemorrhage, recurrent

intracerebral hemorrhage, young adult

intracranial infection

intracranial pressure, increased

intrathecal chemotherapy

intrathecal medication

intrauterine

intrauterine infection, viral

intrauterine infection, viral of CNS

intrinsic hand muscles, wasting of

Jakob-Creutzfeldt disease

Jakob-Creutzfeldt disease, cerebellar variant

Kearns-Sayre syndrome

keratoconjunctivitis

keratoconus

Korsakoff's psychosis

language disorders in children

laryngismus stridulus

lateropulsion

laughing, pathologic

Laurence-Moon-Bardet-Biedl syndrome

L-dopa

lead and the nervous system

lead line, gingival

lead poisoning

learning disability, in children

Leber's hereditary optic neuropathy

leg numbness

leg weakness, bilateral

Legionnaires'disease

Leigh's disease

Leigh's disease, adult variety

lenticular nucleus, lesion of, bilateral

leptospirosis

lethargy

leucine rich glioma inactivated 1 antibodies

leukemia

leukemia, neurologic findings assoc.with

leukoencephalopathy, differential diagnosis

leukopenia

level of consciousness, decreased

lightheaded

limbic encephalitis

limbic system

lipid storage disorder of CNS

liver disease

liver function enzymes

long bone lesion

lorazepam

lymphadenopathy

lymphocytic choriomeningitis

lymphoma

lymphoma involving CNS

lymphoma, primary of CNS

lymphomatoid granulomatosis

lysosomal storage disease

malabsorption syndrome

malaise

malaria

malaria, cerebral

malformation, CNS, congenital

malignancy screen

malignant hyperpyrexia

mania

maple syrup urine disease

marche a petits pas

Marchiafava-Bignami disease

mastoiditis

medulla oblongata, lesion of

melanoma, malignant

MELAS syndrome

Melkersson's syndrome

memory, defect of recent

memory, impairment of

Meniere's disease

meningeal biopsy

meningeal enhancement

meningitis, bacterial

meningitis, carcinomatous

meningitis, chronic

meningitis, CSF cell count-normal

meningitis, elderly

meningitis, fungal

meningitis, lymphomatous

meningitis, Mollaret's

meningitis, recurrent

meningitis, syphilitic

meningitis, TB

meningoencephalitis

meningoencephalomyelitis

meningoencephalopathy

mental retardation

mental status, abnormal

meralgia paresthetica

MERRF syndrome

metabolic acidosis

metabolic disorder, primary

metabolic disorder, primary-screening tests

metachromatic leukodystrophy

metachromatic leukodystrophy, juvenile

methotrexate

methylhydrazine derivatives

methylmalonic acidemia

metronidazole

Mexican

microangiopathy, brain

microcephaly

microdontia

microglial nodules

microhemorrhage, intracerebral

midbrain, atrophy

middle cerebellar peduncle

middle cerebellar peduncle, lesion

middle cerebellar peduncle, lesion, bilateral

migraine

migraine, children

migraine, equivalents

migraine, hemiplegic

migraine, visual symptoms in

mitochondrial disease

mitochondrial disease, pathogenesis

mitochondrial encephalomyopathy

molecular genetics

monoamine oxidase inhibitors

monoclonal antibodies

mononeuritis multiplex

mononeuropathy

mononeuropathy multiplex

motor neuron disease, misdiagnosis

movement disorder

movement disorder, drug induced

movement disorder, extrapyramidal

movement disorder, hyperkinetic

movement disorder, psychogenic

MRI, CAT scan compared to

MRI, contrast enhanced

MRI, contrast enhanced, subependymal

MRI, curvilinear peppering enhancement

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, FLAIR

MRI, muscle

MRI, negative

MRI, nodular enhancement

MRI, serial

mucopolysaccharidoses

multimodal neuroimaging

multiple sclerosis

multiple sclerosis, children

multiple sclerosis, differential diagnosis of

multiple sclerosis, misdiagnosis

multiple sclerosis, pain in

multiple sclerosis, paroxysmal symptoms in

multiple sclerosis, presenting manifestations

multiple sclerosis, prognosis

multiple system atrophy

muscle weakness, causes of

muscle weakness, proximal

mycoplasma pneumoniae

myelitis

myelogram

myelopathy

myelopathy, chronic progressive

myopathy, mitochondrial

myxedema, neurologic manifestations of

N-acetylcysteine

nasal septum, perforation of

nausea and vomiting

neck pain

negative

neoplasm, metastatic to CNS

neoplasm, pituitary

neoplasm, primary of CNS

nephrotic syndrome

nerve agents

nerve biopsy

neuraminidase deficiency

neuritis

neuroendocrinology

neurologic complications

neurologic complications of, surgery

neurologic complications of, systemic cancer

neurologic complications of, systemic disease

neurologic disease

neurologic disease, diagnoses of

neurologic evaluation

neurologic examination, focal

neurologic signs

neurologic symptoms

neurologic symptoms, unexplained

neurologic testing

neuromuscular disease, electrodiagnosis of

neuromyotonia

neuronal cell surface antigen

neuronal ceroid-lipofuscinosis

neuronal intranuclear inclusion disease

neuroophthalmology

neuropathology

neuropathology, brain

neuropathy

neuropathy, hereditary peripheral

neuropathy, painful

neuropathy, peripheral

neuropathy, recurrent

neuropathy, sensory

neuropathy, toxic

neuropathy, vasculitic, systemic

next-generation sequencing

nutritional deficiency

nystagmus

nystagmus, gaze-paretic

nystagmus, hereditary

nystagmus, intermittent

nystagmus, monocular

nystagmus, periodic

nystagmus, rotary

nystagmus, spontaneous

nystagmus, vertical

obesity

ocular motility, disorders of

ocular myopathy

oculodentodigital dysplasia

oculomasticatory myorhythmia

old age, neurology of

ophelia syndrome

ophthalmoplegia

ophthalmoplegia, progressive external

ophthalmoplegia, recurrent

ophthalmoplegia, total

opisthotonus

opportunistic infection

opportunistic infection, CNS

optic ataxia

optic atrophy

optic atrophy, bilateral

optic atrophy, hereditary

optic disc edema

optic nerve

optic neuritis

optic neuritis, children

optic neuropathy

optic neuropathy, ischemic

optokinetic nystagmus, abnormal

organ transplantation

orthostatic hypotension

oscillopsia

otitis, neurologic complications with

paralysis, acute areflexic

paramyotonia congenita

paranoia

paraparesis

paraparesis, familial spastic

Parkinson disease, arteriosclerotic

Parkinson disease, dystonia with

Parkinsonism syndrome

paroxysmal hemiplegia

paroxysmal neurologic deficits

paroxysmal tonic upgaze

PAS positive

PAS positive material in the brain

pathologic reflex

pathology

patient information and support

pediatric autoimmune neuropsychiatric disorders associated with streptococcal infection

periodic paralysis, thyrotoxic

peripheral blood smear

perivascular enhancement

perivascular inflammation

peroxisomal disease

Persistent postural-perceptual dizziness

pigmentary retinopathy

pleocytosis of cerebrospinal fluid

pleurisy

pneumoencephalogram(PEG)

pneumonia

poison, mercury

poison, neurologic problems with

poison, organophosphate

POLG1 gene

poliosis

polydactyly

polymerase chain reaction

polymyositis

polyneuritis

polyneuropathy

polyneuropathy, chronic relapsing

polyuria

pons, atrophy

pons, lesion of

pontocerebellar atrophy

post transplant lymphoproliferative disease

posterior leukoencephalopathy syndrome

postural abnormality

potassium

potassium channel antibodies

potassium channel dysfunction

practice guidelines

Prader-Labhart-Willi syndrome

precipitating factors

pregnancy, neurologic complications in

prenatal diagnosis by amniocentesis

pretectal syndrome

prevention of neurologic disorders

primary aldosteronism

primary episodic ataxia

procarbazine

prognathism

prognosis

progressive infantile poliodystrophy

progressive multifocal leucoencephalopathy

progressive myoclonic epilepsy

progressive neurologic disorder

progressive pallidum atrophy

progressive supranuclear palsy

pseudoretinitis pigmentosa

pseudoxanthoma elasticum

psychiatric disorder

psychiatric problems in neurologic disorders

psychomotor retardation

pulmonary infiltrates

pupil, abnormality in neurologic disorders

pupil, tonic

Purkinje cell

putamen, lesion of

putamen, lesion of, bilateral

pyramidal tract

pyramidal tract dysfunction

pyruvate dehydrogenase deficiency

pyruvate metabolism, abnormality of

quadriparesis

quadriplegia

quadriplegia, transient

radiation therapy, CNS treatment and complications with

rapid onset dystonia parkinsonism

rapidly progressing neurologic illness

rash

reading disorder, acquired

relapsing polychondritis

release phenomena

REM sleep behavior disorder

remote effect of cancer on the nervous system

renal cell carcinoma

renal failure

renal transplantation

respirations in CNS disease

respiratory depression

respiratory failure

respiratory tract infection

reticulum cell sarcoma

retina, abnormal

retinal artery occlusion

reversible cerebral vasoconstrictive syndromes

reversible neurologic disorder

review article

rheumatoid arthritis

rheumatoid arthritis factor(R.A.factor)

rubella encephalitis, progressive

rubella syndrome

rubella virus

rubeola virus

saccadic eye movements, abnormal

sedimentation rate, elevated

seizure

seizure, children

seizure, differential diagnosis of

seizure, drug-induced

seizure, laughing as manifestation

seizure, neonatal

seizure, paradoxical

seizure, photosensitive

seizure, psychomotor-temporal lobe

seizure, tonic-clonic

seizure, treatment of

seizure, withdrawal

selective serotonin reuptake inhibitors

self-mutilation

semialdehyde dehydrogenase deficiency

sensorineural hearing loss

sensory loss

serologic testing

serologic testing of cerebrospinal fluid

serologic testing, false negative

seronegative

serotonin norepinephrine reuptake inhibitors

short stature

shunt procedure, ventricular

shunt procedure, ventricular-complications of

simultanagnosia

sinusitis

Sjogren's syndrome

Sjogren's syndrome, neurologic manifestations of

skin, biopsy

skin, lesions in neurologic disorders

skin, pale

skull bone, thickening

skull x-ray

skull x-ray, abnormal

sleep apnea

sleep pathology and physiology

slow virus infection of CNS

slurred speech

small vessel disease

small vessel disease, cerebral

smiling

sneeze

sodium channel dysfunction

speech disorder, childhood

speech, delayed development of

speech, loss of

Spielmeyer Vogt syndrome

spinal cord

spinal cord, lesion of

spinocerebellar ataxia

spinocerebellar ataxia type 1

spinocerebellar ataxia type 10

spinocerebellar ataxia type 6

spinocerebellar degeneration

spirochete infection

splenium of corpus callosum

splenomegaly

spongy degeneration of brain

steroid responsive encephalopathy

steroid therapy, CNS treatment and complications with

stiff man syndrome

storage disease of CNS

strabismus

stress, emotional

striatal encephalitis

striatonigral degeneration

striatonigral degeneration, infantile

strokelike episodes

stuporous

stuttering

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

subarachnoid hemorrhage

subarachnoid hemorrhage, cerebral convexity

superior cerebellar artery infarction

superior cerebellar peduncle

supratentorial lymphocytic inflam parenchy perivasc enhanc responsive to steroids

swimming

symmetric brain lesions

syncope

syndactyly

syphilis, diagnosis and treatment

syphilis, meningomyelitis

syphilis, neurologic complications with

temporal lobe, lesion

temporal lobe, lesion, bilateral

tetany, normocalcemic

tongue, protrusion of

tonic spasms

topiramate

toxic encephalopathy

toxins, nervous system

transient ischemic attack

transient ischemic attack, recurrent

transient neurologic deficit

trauma

treatment of neurologic disorder

trigeminal neuropathy

trigeminal neuropathy, sensory

trimethyltin

trinucleotide repeats

triphenyltin intoxication

tuberculosis, miliary

tubulopathy

ulcerative colitis

unconsciousness

unconsciousness, episodic

unconsciousness, transient

undiagnosed

Unverricht-Lundborg disease

upgaze

upgaze, paralysis of

upgaze, sustained

urea-cycle enzymopathies

uremia

urinary incontinence

urine test for metabolic disorders

urine test in toxic screen

Usher's syndrome

uveitis

vaccination, neurologic complications with

valium

valsalva maneuver

varicella zoster virus

varicella zoster virus, encephalitis

Venereal Disease Research Laboratory test

venous thrombosis, non-cerebral

ventriculitis

vertebral artery

vertebral artery disease

vertebral artery occlusion

vertebral artery stenosis

vertebral-basilar insufficiency

vertigo

vertigo, episodic

vertigo, treatment of

vibratory sensation, abnormal

vinblastine

vincristine neurotoxicity

Virchow-Robin spaces, dilated

virus, slow

vision, blurred

vision, failure of in childhood

visual acuity, decreased

visual evoked response

visual field defect

visual fields, constricted

visual impairment

visual loss

visual loss, progressive

visual loss, slow

visual loss, sudden-unilateral

visual loss, transient

visuospatial disturbance

Vogt-Koyanagi-Harada syndrome

von Bonsdorff's sign

walking, difficulty with

weakness, generalized

weakness, progressive

weakness, proximal

web sites

weight loss

Wernicke's encephalopathy

white matter disease, subcortical

Showing articles 2150 to 2200 of 4493 << Previous Next >>

Epileptic Seizures After a First Stroke:The Oxfordshire Community Stroke Project
BMJ 315:1582-1587, Burn,J.,et al, 1997

Basilar Artery Embolism, Clin Synd & Neuroradiologic Patterns in Pts Without Perm Occl of Basilar Artery
Neurol 49:1346-1352, Schwarz,S.,et al, 1997

Giant Cell Arteritis With Unusual Flow-Related Neuroophthalmologic Manifestations
Neurol 49:1463-1465, Galetta,S.L.,et al, 1997

Diffusion-Weighted MRI in Transient Global Amnesia Precipitated by Cerebral Angiography
Stroke 28:2311-2314, Woolfenden,A.R.,et al, 1997

The Expansion of the CAG Repeat in Ataxin-2 is a Frequent Cause of Autosomal Dominant Spinocerebellar Ataxia
Neurol 49:1009-1013, Lorenzetti,D.,et al, 1997

Spinocerebellar Ataxia Type 6, Molecular & Clin Features of 35 Japanese Pts (1 Homozygous for CAG Repeat Expan)
Neurol 49:1238-1243, 11961997., Matsumura,R.,et al, 1997

Clinical and Molecular Features of Spinocerebellar Ataxia Type 6
Neurol 49:1243-1246, 11961997., Stevanin,G.,et al, 1997

Gabapentin Monotherapy:An 8-Day, Study in Hosp Pts with Refractory Complex Partial or Secondarily Gen Seizures
Neurol 49:739-745, Bergey,G.K.,et al, 1997

Assessment of Vagus Nerve Stimulation for Epilepsy
Neurol 49:293-297, Fisher,R.S.,et al, 1997

Focal Cortical Dysplasia:Appearance on MR Images
Radiology 203:553-559, Yagishita,A.,et al, 1997

Head Injuries Due to Falls Caused by Seizures:A Group at High Risk for Traumatic Intracranial Hematomas
J Neurosurg 86:433-437, Zwinpfer,T.J.,et al, 1997

New Variant Creutzfeldt-Jakob Disease:Neurological Features and Diagnostic Tests
Lancet 350:903-907, Zeidler,M.,et al, 1997

Ocular Findings in Ramsay Hunt Syndrome
J Neuro-Ophthalmol 17:199-201, Mansour,A.M.&Bailey,B.J., 1997

Cerebral & Cerebellar Atrophy on Serial MRI in an Initially Symptom Free Subject at Risk of Familial Prion Disease
BMJ 315:856-857, Fox,N.C.,et al, 1997

Cerebral Manifestation of Erdheim-Chester Disease:Clinical and Radiologic Findings
Neurol 49:1702-1705, Bohlega,S.,et al, 1997

An Acute Neurologic Syndrome Temporally Associated with Postexposure Trtm of Rabies
Pediatrics 100:720-721, Mortiere,M.D.&Falcone,A.L., 1997

Patients Who Should Not be Driving
CT State Med Soc 12:2, , 1997

Friedreich's Ataxia GAA Repeat Expansion in Pts with Recessive or sporadic Ataxia
Neurol 49:1004-1009, Geschwind,D.H.,et al, 1997

Broadened Friedreich's Ataxia Phenotype after Gene Cloning, Minimal GAA Expan Causes Late Spastic Ataxia
Neurol 49:1617-1620, Ragno,M.,et al, 1997

Atrophy of Cerebellum & Brainstem in Dentatorubral Pallidoluysian Atrophy, CAG Repeat Size on MRI Findings
Neurol 49:1605-1612, Koide,R.,et al, 1997

Coma From Long-Term Overingestion of Isoniazid
Arch Int Med 157:2518-2520, Salkind,A.R.&Hewitt,C.C., 1997

Lamotrigine for Generalized Seizures Associated with the Lennox-Gestaut Syndrome
NEJM 337:1807-1812, Motte,J.,et al, 1997

Cerebral Tuberculosis in Pts with AIDS, Report of 6 Cases & Review
Medicine 76:423-431, Lesprit,P.,et al, 1997

Bilat Periventricular Nodular Heterotopia with Mental Retard & Syndactyly in Boys:New X-Linked MR Synd
Neurol 49:1042-1047, Dobyns,W.B.,et al, 1997

Painful Generalised Clonic and Tonic-Clonic Seizures with Retained Consciousness
JNNP 63:792-795, Bell,W.L.,et al, 1997

Reversible MRI Lesions After Seizures
Seizure 6:237-239, Aykut-Bingol,C.,et al, 1997

Autoantibodies to Glutamic Acid Decarboxylase in Three Patients With Cerebellar Ataxia, Late-Onset Insulin-Dependent Diabetes Mellitus, and Polyendocrine Autoimmunity
Neurol 49:1026-1030, Saiz,A.,et al, 1997

Vagus Nerve Stimulation for the Treatment of Medically Intractable Seizures
Arch Neurol 53:1176-1180, Salinsky,M.C.,et al, 1996

Clinical Correlates of White Matter Findings on Cranial Magnetic Resonance Imaging of 3301 Elderly People
Stroke 27:1274-1282, 12691996., Longstreth,W.T.,et al, 1996

Subcortical Heterotopia:A Distinct Clinicoradiologic Entity
AJNR 17:1315-1322, Barkovich,A.J., 1996

X-Linked Malformation of Neuronal Migration
Neurol 47:331-339, Dobyns,W.B.,et al, 1996

Neuroimaging in the Emergency Patient Presenting with Seizure
Neurol 47:26-32, 2881996., Greenberg,M.K.,et al, 1996

Leigh Syndrome:Clinical Features and Biochemical DNA Abnormalities
Ann Neurol 39:343-351, Rahman,S.,et al, 1996

Niemann-Pick Disease Type C from Bench to Bedside
JAMA 276:561-564, Schiffmann,R., 1996

Falls and Urinary Incontinence in a 66-Year Old Woman
Lancet 347:1738, Yusuf,S.W.,et al, 1996

Opsoclonus
Semin Neurol 16:21-26, Averbuch-Heller,L.&Remler,B., 1996

Yelling Attacks and Wasted Hands
Lancet 348:238, Bosboom,W.M.J.,et al, 1996

Transient Encephalopathy after Paclitaxel (Taxol) Infusion
Neurol 46:1596-1599, Perry,J.R.&Warner,E., 1996

Hereditary Spastic Paraplegia:Advances in Genetic Research
Neurol 46:1507-1514, Fink,J.K.,et al, 1996

Discontinuation of Anticonvulsant Therapy in Children Free of Seizures for 1 Year:A Prospective Study
Neurol 46:969-974, Dooley,J.,et al, 1996

Practice Parameter:A Guideline for Discontinuing Antiepileptic Drugs in Seizure-Free Patients-Summary Statement
Neurol 47:600-602, Rosenberg,J.H., 1996

Temporal Lobectomy for Refractory Epilepsy
JAMA 276:470-475, Sperling,M.R.,et al, 1996

Practice Parameter:The Neurodiagnostic Evaluation of the Child with First Simple Febrile Seizure
Pediatrics 97:769-772, Bergman,D.A.,et al, 1996

Iron Deficiency Anaemia and Febrile Convulsions:Case-Control Study in Children Under 2 Years
BMJ 313:343, Pisacane,A.,et al, 1996

Simple Partial Status Epilepticus:Causes, Treatment and Outcome in 47 Patients
JNNP 61:90-92, Scholtes,F.B.,et al, 1996

The Outcome of Absence Epilepsy:A Meta-Analysis
Neurol 47:802-808, Bouma,P.A.D.,et al, 1996

Non-Convulsive Status Epilepticus:Causes, Treatment, and Outcome in 65 Patients
JNNP 61:93-95, Scholtes,F.B.,et al, 1996

Random Comp Monother Trial of Phenobarb, Phenytoin, Carbamazepine, or Sod Valp for Newly Dx Child Epilep
Lancet 347:709-713, deSilva,M.,et al, 1996

Obesity and Endocrine Disorders in Women Taking Valproate for Epilepsy
Ann Neurol 39:579-584, 5591996., Isojarvi,J.I.T.,et al, 1996

Psychogenic Seizures
Neurol 46:1499-1507, Lesser,R.P., 1996

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