Neudle.com: tonic cerebellar fits

Differential
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abducens nerve paralysis

abscess, cerebellum

abscess, intracerebral

abscess, intracerebral, tuberculous

acanthocytosis

aciduria

acoustic nerve

acquired immunodeficiency syndrome

acute cerebellar ataxia

acute disseminated encephalomyelitis

advances in neurology

adverse drug reaction

alcohol, heart involvement with

alcohol, neurologic complications with

alcoholic polyneuropathy

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

altered states of consciousness

alternating hemiplegia

alternating hemiplegia of childhood

alternating rapid movement

Alzheimer's disease

Alzheimer's disease, early onset

Alzheimer's disease, familial

amenorrhea

amnesia

AMPA receptor antibodies

amyloid angiopathy, cerebral

aneurysm, anterior communicating

Angelman syndrome

angiography, cerebral

angiography, cerebral, false negative

angiokeratoma

angiotensin-converting enzyme

anterior commissure

anterior spinal artery infarction

anti GQ1b IgG antibody

antibiotics, neurologic complications with

antibodies to voltage-gated calcium channels

anticoagulant, complications of

anticoagulant, restarting

anticoagulant, reversal of

anticoagulant, treatment

anticoagulant, treatment in CVD

anticonvulsants

anticonvulsants, effectiveness

anticonvulsants, untoward effects of

aqueduct of Sylvius, stenosis

arteriovenous malformation

arteriovenous malformation, cerebral

arthralgia

asparginase

aspartate aminotransferase

autoimmune basal ganglia encephalitis

autoimmune disease

autonomic dysfunction

basal ganglia, calcification of

basal ganglia, degeneration

basal ganglia, hemorrhage

basal ganglia, lesion of

basal ganglia, lesion, bilateral

Bassen-Kornzweig syndrome

behavior, combative

behavioral disorder

bitemporal visual field defect

bladder dysfunction

blindness

blood dyscrasias, neurologic findings with

blood pressure

blood pressure, control

blood pressure, lowering

brainstem, infarction of

brainstem, lesion of

brainstem, vascular malformation of

calcification, intracranial

calcification, periventricular

calcium channel dysfunction

carbamazepine

carbamazepine, toxicity

CAT scan, contrast enhanced

CAT scan, disappearing lesion on

CAT scan, emission

CAT scan, emission, abnormal

CAT scan, false negative

central nervous system, infection of

central pontine myelinolysis

centrum semiovale

cephalosporins

cerebellar ataxia, children

cerebellar ataxia, primary

cerebellar atrophy, primary

cerebellar atrophy, secondary

cerebellar degeneration

cerebellar disease, eye movement disorder in

cerebellar hemorrhage

cerebellar hypoplasia

cerebellar infarction

cerebellar lesion

cerebellar plaques, amyloid

cerebellar pontine angle tumor

cerebellar stimulation

cerebellar stimulation for seizures

cerebellum, disease of

cerebellum, neoplasms of

cerebral autosomal recessive arteriopathy with subcortical infarction and leukoencephalopathy

cerebral cortex

cerebral cortical atrophy

cerebral cortical encephaliis

cerebral edema

cerebral edema, cytotoxic

cerebral edema, vasogenic

cerebral embolism

cerebral embolism, cardiac origin

cerebral folate deficiency syndrome

cerebral infarction, subcortical

cerebral palsy

cerebral peduncle

cerebral vasculature

cerebral venous thrombosis

cerebral venous thrombosis, deep

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, culture negative

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, gammaglobulin of

cerebrospinal fluid, lactic acid concentration

cerebrospinal fluid, oligoclonal IgG in

cerebrospinal fluid, pressure low

cerebrospinal fluid, proteincytologic dissociation

cerebrospinal fluid, xanthochromia of

cerebrovascular accident

cerebrovascular accident, acute management of

cerebrovascular accident, complications with

cerebrovascular accident, multiple

cerebrovascular disease, surgical treatment of

Charcot-Marie-Tooth

chemotherapy, CNS treatment and complications with

cherry red spot

chest x-ray, abnormal

children

chloride channel dysfunction

chromosomal abnormality

chronic progressive external ophthalmoplegia

Chvostek sign

cisterna magna, enlarged

Clinical Pathologic Conference(C.P.C.)

coenzyme Q10 deficiency

cognition

cognitive delay

cogwheel rigidty

collagen vascular disease

coma

complications

concentration, impaired

confusion

congenital infection, CNS

congenital infection, viral

congenital malformation

congestive heart failure

conjugate gaze, forced

conjunctival biopsy

consanguinity

contractures, joint

controversies in neurology

cornea, abnormal

corpus callosum

corpus callosum, atrophy of

corpus callosum, hypoplastic

corpus callosum, lesion of

corpus callosum, neoplasm of

cortical blindness

cortical vein thrombosis

cost

cranial nerve palsies

cranial neuropathy

cranial neuropathy, multiple

craniopharyngioma

creatine phosphokinase(CPK)elevated

cry, abnormal

crying, pathologic

cultured skin fibroblasts

degenerative diseases of CNS

delirium

delivery, complicated

delusion

dementia

dementia, familial

dementia, frontotemporal

dementia, presenile

demyelinating disease

dentate nuclei

dentate nuclei, lesion of

dentatorubral-pallidoluysian atrophy

dermatoglyphics

developmental milestones

developmental milestones, loss of

developmental retardation

developmental venous anomalies

diabetes insipidus

diabetes mellitus

diabetes mellitus, neurologic manifestations of

diagnostic criteria

diaschisis

differential diagnosis

distal muscle atrophy

drop attacks, differential diagnosis of

drowsiness

drug abuse

drug abuse, neurologic complications of

drug induced neurologic disorders

dural sinus thrombosis

dyssynergia cerebellaris myoclonica

dystonia

ear, abnormal

echocardiogram

echocardiogram, transesophageal

echolalia

eclampsia

eclampsia, postpartum

efficacy

electroencephalogram

electroencephalogram, abnormalities of

encephalitis, autoimmune

encephalitis, bacterial

encephalitis, brainstem

encephalitis, clinical picture and treatment of

encephalitis, diagnosis of

encephalitis, episodic

encephalitis, focal

encephalitis, paraneoplastic

encephalitis, recurrent

encephalitis, viral

encephalitis, viral-causes of

encephalomyelitis

encephalomyopathy

encephalopathy

encephalopathy, progressive

epidemiology of neurology

extralimbic encephalitis

eye movement, disorders of

facial appearance, abnormal

facial expression abnormality

facial nerve palsy

facial nerve palsy, bilateral

familial hemiplegic migraine

fetal alcohol syndrome

fluorescene in situ hybridization

fluorescent treponema antibody absorption/false positive

fluorouracil

flush syndrome

folic acid

folic acid deficiency

foot drop

forceps delivery

Friedreich's ataxia

frontal lobe, behavior with disease of

frontal lobe, pathologic signs of

frontotemporal brain sagging syndrome

fungal infection

fungal infection, CNS

gamma amino butyric acid receptor antibody

gammaglobulin therapy, intravenous

gargoylism

gastrointestinal bleeding

gastrointestinal disease, neurologic complications

gaze deviation

gaze palsy, supranuclear

gene

gene mutation

genetic neurologic disorders

globus pallidus, lesion of

glutamic acid

glutamic acid decarboxylase, antibody

GM antigen test

gram positive rod

granular osmiphilic material

granulomatous disease

grasping

gray matter

growth hormone deficiency

Guillain Barre syndrome

gyrus, abnormal

Hallgren's syndrome

hallucination

hallucination, auditory

hallucination, olfactory

hands, fisted

Hand-Schuller-Christian disease

headache, hypertensive

hemianopia, transient

hemiparesis

hemiplegia

hemorrhage, intracranial, newborn

hepatic encephalopathy

hepatic failure

hepatomegaly

hepatosplenomegaly

heralding manifestation

herniation syndromes, intracranial

herpes simplex encephalitis

herpes simplex virus

herpes virus

herpes zoster

herpes zoster, disseminated

hydrocephalus, non-communicating(obstructive)

hydroxyglutaric aciduria

hypertension, cerebrovascular disease with

hypertensive encephalopathy

hypokalemic periodic paralysis

hypomyelination

hyponatremia

hypoparathyroidism

hypopigmentation of skin

hypopituitarism

hypopituitarism, aneurysm causing

hyposmia

hypothalamus

hypothalamus, disturbance of

iatrogenic neurologic disorders

imbalance

immunization, neurologic complications with

immunocompetent

immunosuppression

immunosuppressive agents

immunotherapy

impotence

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

inborn errors of metabolism

incidence

incidental finding

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 immunization

intellectual deficit

intellectual deterioration

interpeduncular cistern, compressed

intracerebral hemorrhage

intracerebral hemorrhage, bilateral

intracerebral hemorrhage, causes of

intracerebral hemorrhage, clot evacuation

intracerebral hemorrhage, incidence of

intracerebral hemorrhage, lobar

intracerebral hemorrhage, location of

intracerebral hemorrhage, multiple

intracerebral hemorrhage, pathophysiology

intracerebral hemorrhage, progression of

intracerebral hemorrhage, recurrent

intracerebral hemorrhage, treatment of

intracranial hemorrhage

intracranial hypertension, benign

intracranial pressure monitoring

intracranial pressure, increased

intrathecal medication

intrauterine

intrauterine infection, viral

intrauterine infection, viral of CNS

intravenous drug abuse

intraventricular hemorrhage

intraventricular hemorrhage, clot evacuation

intraventricular hemorrhage, treatment

intrinsic hand muscles, wasting of

Jakob-Creutzfeldt disease

Jakob-Creutzfeldt disease, cerebellar variant

Kearns-Sayre syndrome

keratoconus

Korsakoff's psychosis

lactic dehydrogenase(LDH)

lateral medullary syndrome

lateral sinus thrombosis

lateropulsion

lateropulsion, ocular

laughing, pathologic

Laurence-Moon-Bardet-Biedl syndrome

learning disability, in children

Leigh's disease

lethargy

leucine rich glioma inactivated 1 antibodies

leukemia

leukemia, neurologic findings assoc.with

leukocyte enzyme abnormality

leukodystrophy

leukodystrophy, 4H

leukoencephalitis, acute necrotizing hemorrhagic

leukoencephalopathy

leukopenia

level of consciousness

level of consciousness, decreased

life expectancy

life support, withdrawal of

limbic encephalitis

limbic system

lip biopsy

lipid storage disorder of CNS

liver function enzymes

low back pain

lung biopsy

lymphadenopathy, hilar

lymphocytic choriomeningitis

lymphoma

lymphomatoid granulomatosis

lysosomal storage disease

macrocephaly

macrognathia

macular degeneration

malformation, CNS, congenital

malformation, vascular

malformation, vascular, cerebral

malformation, vascular, cryptic

malformation, vascular, treatment of

malignancy screen

malignant hyperpyrexia

mania

marche a petits pas

Marchiafava-Bignami disease

meconium staining

medulla oblongata, infarction of

medulla oblongata, lesion of

MELAS syndrome

memory, impairment of

meningismus

meningitis

meningitis, aseptic

meningitis, aspergillus

meningitis, bacterial

meningitis, basilar

meningitis, carcinomatous

meningitis, chronic

meningitis, elderly

meningitis, fungal

meningitis, fungal-negative CSF culture

meningitis, granulomatous

meningitis, neutrophilic

meningitis, neutrophilic, persistent

meningitis, nocardia

meningitis, recurrent

meningitis, spinal fluid smear and culture-negative

meningoencephalitis

meningoencephalopathy

mental retardation

mental status, abnormal

mesial temporal lobe

metabolic disorder, primary

methotrexate

methylhydrazine derivatives

microhemorrhage, intracerebral

midbrain, lesion of

midbrain, swollen

middle cerebellar peduncle

middle cerebellar peduncle, lesion

middle cerebellar peduncle, lesion, bilateral

mitochondrial disease

mitochondrial encephalomyopathy

molecular genetics

monoamine oxidase inhibitors

monoclonal antibodies

movement disorder, drug induced

movement disorder, extrapyramidal

movement disorder, hyperkinetic

MRI

MRI, abnormal

MRI, abnormal, seizure causing

MRI, cardiac

MRI, CAT scan compared to

MRI, contrast enhanced

MRI, cortical enhancement

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, FLAIR

MRI, gray matter enhancement

MRI, hypointense signal foci on

MRI, incidental finding

MRI, negative

MRI, ring sign

MRI, serial

MRI, sulcal hyperintensity

MRI, susceptibility weighted

MRS

mucopolysaccharidoses

multiple system atrophy

muscle weakness, causes of

mutism

myasthenia gravis

mycoplasma

mycoplasma pneumoniae

myelitis

myelitis, longitudinal

myelitis, transverse

myelogram, thoracic

myelopathy

myelopathy, chronic progressive

myocardial infarction

myocardial infarction, acute

myopathy, mitochondrial

myxedema, neurologic manifestations of

nausea and vomiting

negative

neoplasm, pituitary

neoplasm, primary intracerebral

neoplasm, primary intracranial

neoplasm, primary of CNS

nephrotic syndrome

nerve conduction studies

neuraminidase deficiency

neuritis

neuroaxonal dystrophy

neuroaxonal dystrophy, juvenile

neuroendocrinology

neurologic complications

neurologic complications of, systemic cancer

neurologic disease

neurologic disease, diagnoses of

neurologic examination

neurologic examination, focal

neurologic history

neurologic signs

neurological intensive care

neuronal cell surface antigen

neuronal ceroid-lipofuscinosis

neuronal intranuclear inclusion disease

neuronal migration disorder

neuropathology

neuropathology, brain

neuropathy

neuropathy, painful

neuropathy, peripheral

nutritional deficiency

nystagmus

nystagmus, monocular

nystagmus, primary position of gaze

nystagmus, rotary

nystagmus, upbeating-in primary position of gaze

nystagmus, vertical

obesity

obstetric neurologic injuries

occipital lobe, lesion of

ocular myopathy

oculodentodigital dysplasia

old age, neurology of

ophelia syndrome

ophthalmoplegia

ophthalmoplegia, progressive external

ophthalmoplegia, total

opisthotonus

opportunistic infection

opportunistic infection, CNS

opsoclonus

optic atrophy

optic chiasm, enlarged

optic disc edema

optic nerve

optic nerve, enlarged

optic nerve, lesion of

optic neuritis

optic neuritis, bilateral

optic neuritis, recurrent

optic neuropathy

optic neuropathy, nutritional

organ transplantation

orthostatic hypotension

paramyotonia congenita

paranoia

paraparesis

paraparesis, spastic

parasitic infection, CNS

parathyroid adenoma

paratonia

paresthesias

Parkinson disease, dystonia with

Parkinsonism syndrome

paroxysmal hemiplegia

paroxysmal neurologic deficits

paroxysmal nonkinesigenic dyskinesia

PAS positive

PAS positive material in the brain

pediatric autoimmune neuropsychiatric disorders associated with streptococcal infection

pedicles of vertebrae, erosion of

peripheral nerve, lesion of

personality change

pheochromocytoma

pigmentary retinopathy

pituitary, lesion of

PLEDs

pleocytosis of cerebrospinal fluid

pneumoencephalogram(PEG)

poison, mercury

poison, neurologic problems with

POLG1 gene

polydactyly

polymerase chain reaction

pontocerebellar atrophy

post hemorrhagic hydrocephalus

posterior fossa, differential diagnosis of lesions of

posterior fossa, lesion of

posterior inferior cerebellar artery syndrome

posterior leukoencephalopathy syndrome

posterior leukoencephalopathy syndrome, location

postpartum

posttransplant lymphoproliferation disorder

postural abnormality

potassium channel antibodies

potassium channel dysfunction

practice guidelines

precipitating factors

pre-eclampsia

pregnancy, neurologic complications in

prepontine cistern, effaced

prevention of neurologic disorders

primary aldosteronism

primary intracranial hypotension

progressive infantile poliodystrophy

progressive multifocal leucoencephalopathy

progressive neurologic disorder

progressive pallidum atrophy

pseudoretinitis pigmentosa

psychiatric disorder

psychiatric problems in neurologic disorders

psychomotor retardation

pulmonary infiltrates

pulmonary nodules

pupil, abnormality in neurologic disorders

putamen, lesion of, bilateral

pyramidal tract

pyramidal tract dysfunction

pyruvate metabolism, abnormality of

quadriparesis

quadriplegia

race

radiation therapy, stereotactic

radiculitis

radiculopathy

Ramsay Hunt syndrome

rapid onset dystonia parkinsonism

rapidly fatal neurologic illness

rapidly progressing neurologic illness

remote effect of cancer on the nervous system

reversible cerebral vasoconstrictive syndromes

reversible neurologic disorder

rubella encephalitis, progressive

sedimentation rate, elevated

seizure

seizure, children

seizure, drug-induced

seizure, laughing as manifestation

seizure, neonatal

seizure, paradoxical

seizure, photosensitive

seizure, prevention of

seizure, psychomotor-temporal lobe

seizure, surgical treatment of

seizure, tonic-clonic

seizure, treatment of

seizure, withdrawal

sensorineural hearing loss

serologic testing

serologic testing of cerebrospinal fluid

serologic testing, false negative

single photon emission computed tomography

Sjogren's syndrome

Sjogren's syndrome, neurologic manifestations of

skew deviation

skin, biopsy

skin, lesions in neurologic disorders

skull x-ray

skull x-ray, abnormal

sleep pathology and physiology

slow virus infection of CNS

smiling

sodium channel dysfunction

somnolence

spasticity

speech disorder

speech disorder, childhood

speech, delayed development of

speech, loss of

Spielmeyer Vogt syndrome

spinal cord

spinal cord, compression of

spinal cord, lesion of

spinal cord, metastasis to

spinocerebellar ataxia

spinocerebellar ataxia type 1

spinocerebellar ataxia type 10

spinocerebellar ataxia type 6

splenium of corpus callosum

splenium of corpus callosum, displaced

steroid therapy, CNS treatment and complications with

stiff man syndrome

storage disease of CNS

striatal encephalitis

striatonigral degeneration

striatonigral degeneration, infantile

stuttering

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

subarachnoid hemorrhage

subarachnoid hemorrhage, cerebral convexity

subcortical U fibers

subdural hematoma

superior cerebellar artery infarction

superior sagittal sinus thrombosis

symmetric brain lesions

syncope

syndactyly

systemic illness

systemic lupus erythematosus

systemic lupus erythematosus, neurologic complications with

systemic lupus erythematosus, skin changes in

tabes dorsalis

teeth, abnormal

teeth, wide-spaced

temporal lobe, lesion

temporal lobe, lesion, bilateral

tetany

thalamus, lesion of

thalamus, lesion of-bilateral

thrombocytopenia

thrombotic thrombocytopenia purpura

tongue, protrusion of

tonic cerebellar fits

tonsillar herniation of cerebellum

topiramate

toxins, nervous system

toxoplasma complement fixation test

toxoplasmosis, acquired

toxoplasmosis, CNS

transient ischemic attack

transient neurologic deficit

travel history

treatment delay

treatment of neurologic disorder

trigeminal neuropathy

trimethyltin

trinucleotide repeats

trisomes

trisomy 9p

Trousseau's sign

tuberculin skin test, positive

varicella zoster virus

varicella zoster virus, encephalitis

vasculopathy

vectors of infection

Venereal Disease Research Laboratory test

ventriculostomy

ventriculostomy, endoscopic

vertebral-basilar insufficiency

vertigo

vinblastine

vincristine neurotoxicity

vision, failure of in childhood

visual acuity, decreased

visual field defect

visual fields, constricted

visual impairment

visual loss

visual loss, progressive

visual loss, slow

vocal cord paralysis

voriconazole

walking, difficulty with

weakness

weakness, progressive

weight loss

Wernicke's encephalopathy

x-linked mental retardation

Showing articles 50 to 100 of 3983 << Previous Next >>

Clinical Features and ATTCT Repeat Expansion in Spinocerebellar Ataxia Type 10
Arch Neurol 59:1285-1290, Grewal,R.P.,et al, 2002

Glutamic Acid Decarboxylase Autoantibodies and Neurological Disorders
Neurol Sci 23:145-151, Vianello,M.,et al, 2002

Posterior Leukoencephalopathy Syndrome
Postgrad Med J 77:24-28, Garg,R.K., 2001

Spontaneous Intracerebral Hemorrhage
NEJM 344:1450-1460, Qureshi,A.I.,et al, 2001

Marchiafava-Bignami Disease
Merrit's Neurology, L.P. Rowland Ed., Lippincott, Phila.:792, Miller,J.R., 2000

Fluid Attenuation Inversion Recovery (FLAIR) Images of Dentatorubropalliodoluysian Atrophy:Case Report
JNNP 65:396-399, Yoshii,F.,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

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

Gliomatosis Cerebri
Radiology 198:831-835, delCarpio-O'Donovan,R.,et al, 1996

The Epilepsy of Trisomy 9p
Neurol 47:821-824, Stern,J.M., 1996

The Synd of Autosomal Recessive Pontocerbellar Hypoplasia, Microcephaly, & Extrapyr Dyskinesia (Pontocereb Hypopl Type 2)
Neurol 45:311-317, Barth,P.G.,et al, 1995

Cerebellar Atrophy in Patients with Long-Term Phenytoin Exposure and Epilepsy
Arch Neurol 51:767-771, Ney,G.C.,et al, 1994

Phenotype of Chromosome 14-Linked Familial Alzheimer's Disease in a Large Kindred
Ann Neurol 36:368-378, Lampe,T.H.,et al, 1994

Methylmercury Poisoning:Long-Term Clinical, Radiological, Toxicological, and Pathological Studies of an Affected Family
Ann Neurol 35:680-688, Davis,L.E.,et al, 1994

Clinicopath Conf
Spongiform Encephalopathy (Creutzfeldt-Jakob Disease) , with Amyloid (KURU) Plaques, Case 17-1993, N, JM 328:66,1993., 1993

Toxoplasma Encephalitis in Patients with the Acquired Immunodeficiency Syndrome
Medicine 71:224-239, Renold,C.,et al, 1992

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

Hypertensive Encephalopathy:Findings on CT, MR Imaging, and SPECT Imaging in 14 Cases
AJR 159:379-383, Schwartz,R.B.,et al, 1992

Wolfram Syndrome:Evidence of a Diffuse Neurodegenerative Disease by Magnetic Resonance Imaging
Neurol 42:1220-1224, 1992,, Rando,T.A.,et al, 1992

Toxoplasmosis of the Central Nervous System in the Acquired Immunodeficiency Syndrome
NEJM 327:1643-1648, Porter,S.B.&Sande,M.A., 1992

Angelman Syndrome: Clinical Profile
J Child Neurol 7:270-280, Zori,R.T.,et al, 1992

Sarcoidosis of the Nervous System, A Clinical Approach
Arch Int Med 151:1317-1321, Sharma,Om.P.&Sharma,A.D., 1991

MR of Progressive Neurodegenerative Change in Treated Menkes'Kinky Hair Disease
Neuroradiology 33:181-182, Johnsen,D.E.,et al, 1991

Progressive Myoclonic Ataxia (The Ramsay Hunt Syndrome)
Arch Neurol 47:1121-1125, Marsden,C.D.,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

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

Intracerebral Cavernous Angiomas
Neurol 38:1699-1704, Farmer,J.P.,et al, 1988

Neurologic Complications of Cocaine Abuse
Neurol 38:1189-1193, Mody,C.K.,et al, 1988

Hereditary Dentatorubral-Pallidoluysian Atrophy:Clinical and Pathologic Variants in a Family
Neurol 38:1065-1070, Takahashi,H.,et al, 1988

Carbamazepine Side Effects in Children and Adults
Pellock. J. M. , Epilepsia 28:S64-S707., , 1987

CT in Ceroid Lipofuscinosis
Neurol 37:1025-1026, Dunn,D.W., 1987

Acute Trimethyltin Limbic-Cerebellar Syndrome
Neurol 37:945-950, Besser,R.,et al, 1987

The Role of Glutamate in Neurotransmission & in Neurologic Disease
Arch Neurol 43:1058-1063, Greenamyre,J.T., 1986

Lateropulsion & Upbeat Nystagmus are Manifestations of Central Vestibular Dysfunction
Arch Neurol 43:962-964, Benjamin,E.E.,et al, 1986

Cerebral Toxoplasmosis Complicating the Acquired Immune Deficiency Syndrome
Ann Neurol 19:224-238, Navia,B.A.,et al, 1986

Central Nervous System Toxicity with High-Dose Ara-C
Neurol 35:1475-1479, Hwang,T.,et al, 1985

Mitochondrial Encephalomyopathy:Fluctuating Symptoms & CT
Neurol 34:1456-1460, Yamamoto,T.,et al, 1984

Intracranial Hemorrhage in the Term Newborn
Arch Neurol 41:30-34, Fenichel,G.M.,et al, 1984

Epilepsy, the Cerebellum, & Cerebellar Stimulation
Lancet 2:1122-1123, Hetzel,B.S.,et al, 1983

Herpes Zoster-Associated Encephalitis:Clinicopathologic Report of 12 Cases and Review of the Literature
Medicine 62:81-95, Jemsek,J.,et al, 1983

Neurologic Complications of Primary Sjogren's Syndrome
Medicine 61:247-257, Alexander,E.L.,et al, 1982

Cerebellar Atrophy in Epilepsy & Headache:Lack of Relationship to Phenytoin
Neurol 32:910-912, Ballenger,C.E.,et al, 1982

Neurological Complications of Swine Influenza Vaccination
Acat Neurologica Scandinavica 66:413-431, Poser,C.M., 1982

Eye Movements in Patients with Wallenberg's Syndrome
Ann NY Acad Sci 374:600-613, Baloh,R.W.,et al, 1981

Olivopontocerebellar Atrophy in Children:A Report of Seven Cases in Two Families
Ann Neurol 10:355-363, Colan,R.V.,et al, 1981

Central Nervous System Toxicity Associated With Metronidazole Therapy
Ann Int Med 93:59-60, Kusumi,R.K.,et al, 1980

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

Adult Type Neuronal Storage Disease with Neuraminidase Deficiency
Ann Neurol 6:232-244, Miyatake,T.,et al, 1979

Intracranial Arteriovenous Malformations in Childhood
Ann Neurol 3:338, Kelly,J.J.,et al, 1978

Familial Chorea & Myoclonus Epilepsy
Neurol 28:913-919, Takahata,N.,et al, 1978

Showing articles 50 to 100 of 3983 << Previous Next >>