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acute ataxia of childhood

acute cerebellar ataxia

advances in neurology

alcohol intolerance

alpha-fetoprotein

alternating hemiplegia

alternating hemiplegia of childhood

alternating rapid movement

Alzheimer's disease

AMPA receptor antibodies

amyotrophic lateral sclerosis

aneurysm, children

aneurysm, fusiform

aneurysm, vertebral basilar system

Angelman syndrome

angiography, cerebral

angiography, posterior fossa

angiotensin-converting enzyme

ankle reflex, absent

anti GQ1b IgG antibody

anticonvulsants

anticonvulsants, effectiveness

apraxia of eye movements

Arnold Chiari malformation

arterial dissection

arterial dissection, intracranial

arterial dissection, ruptured

arterial dissection, vertebral

ataxia telangiectasia

ataxia, acute onset

ataxia, cerebellar

ataxia, congenital

ataxia, hereditary

ataxia, paroxysmal

ataxia, progressive

ataxia, truncal

autoimmune basal ganglia encephalitis

autoimmune disease

autonomic dysfunction

autosomal rcessive spastic ataxia of Charlevoix-Saguenay

bacterial infection

bacterial infection, CNS

ballismus, bilateral

basal ganglia, calcification of

basal ganglia, lesion of

basal ganglia, lesion, bilateral

Bassen-Kornzweig syndrome

behavior, combative

behavioral disorder

behavioral disorder, acute

blood dyscrasias, neurologic findings with

brainstem, atrophy

brainstem, dysfunction

brainstem, glioma in children

brainstem, infarction of

brainstem, lesion of

brainstem, neoplasms of

calcification, intracranial

carcinoembryonic antigen

CAT scan, abnormal

CAT scan, emission

CAT scan, emission, abnormal

CAT scan, pelvis

cataracts, congenital

cauda equina, enhancement

celiac disease, adult

celiac disease, childhood

central nervous system, infection of

cerebellar ataxia, children

cerebellar ataxia, children, differential diagnosis of

cerebellar ataxia, hereditary

cerebellar ataxia, primary

cerebellar atrophy, primary

cerebellar atrophy, secondary

cerebellar degeneration

cerebellar disease, eye movement disorder in

cerebellar hypoplasia

cerebellar infarction

cerebellar lesion

cerebellar pontine angle

cerebellar pontine angle tumor

cerebellar vermis

cerebellitis, autoimmune

cerebellum, neoplasms of

cerebral cortical atrophy

cerebral folate deficiency syndrome

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, lactic acid concentration

cerebrospinal fluid, proteincytologic dissociation

cerebrospinal fluid, red cells in

cerebrovascular accident

cerebrovascular accident, bilateral

cerebrovascular accident, prognosis in

cerebrovascular accident, young adult

cerebrovascular disease, risk factors in

cerebrovascular disease, surgical treatment of

choreoathetosis

chromosomal abnormality

Clinical Pathologic Conference(C.P.C.)

coenzyme Q10 deficiency

cognitive delay

conjunctival biopsy

corpus callosum, thinning

counterimmunoelectrophoresis

cranial nerve palsies

cranial neuropathy

cranial neuropathy, multiple

creatine phosphokinase(CPK)elevated

cultured skin fibroblasts

cyst, parenchymal

cyst, subcortical

deep gray nuclei

degenerative diseases of CNS

delayed dentition

dementia, childhood

dentate nuclei, lesion of

dentatorubral-pallidoluysian atrophy

dermatitis herpetiformis

developmental disability

developmental milestones

developmental milestones, loss of

developmental retardation

diabetes insipidus

diabetes mellitus

diagnostic criteria

differential diagnosis

Dravet syndrome

drug induced neurologic disorders in children

dysdiadochokinesia

electroencephalogram, abnormalities of

electron microscopy

encephalitis, autoimmune

encephalitis, brainstem

encephalitis, paraneoplastic

encephalitis, viral

encephalomyelitis, postinfectious

encephalomyopathy

epicanthal folds

Epstein-Barr virus

evoked potentials

exercise intolerance

exome sequencing

eye movement, disorders of

facial appearance, abnormal

facial expression abnormality

facial nerve palsy

feeding disorder

finger nose finger test

fingerprint bodies

Fisher's syndrome

fluorescene in situ hybridization

folic acid deficiency

fourth ventricle, enlargement of

fourth ventricle, neoplasm of

fragile-X syndrome

Friedreich's ataxia

fundus, abnormality of

gamma amino butyric acid receptor antibody

gammaglobulin therapy, intravenous

gastrointestinal disease, neurologic complications

gaze palsy, supranuclear

genetic counselling

genetic linkage

genetic neurologic disorders

genetic testing

Gillespie syndrome

glioblastoma multiforme(astrocytoma Gr.III)

glutamic acid decarboxylase, antibody

gluten sensitivity

gluten-free diet

granulomatous disease

growth retardation

Guillain Barre syndrome

Guillain Barre syndrome, etiology of

Guillain Barre syndrome, variant forms of

Hartnup's disease

headache, severe

headache, sudden onset of

heel-knee-shin test

hemosiderosis of CNS, superficial

hepatolenticular degeneration(Wilson's disease)

hepatosplenomegaly

heralding manifestation

Hodgkin's disease

Hodgkin's disease, neurologic involvement with

Huntington's chorea

hydroxyglutaric aciduria

hyperosmolality

hypertension, cerebrovascular disease with

hypomyelination

hypopigmentation of skin

hypothalamus, disturbance of

hypotonia, infants

iatrogenic neurologic disorders

immunization, neurologic complications with

immunodeficiency

immunosuppression

inborn errors of metabolism

inclusion bodies

infectious mononucleosis, neurologic findings with

intellectual deficit

intellectual deterioration

intracranial pressure, increased

intrathecal medication

Jakob-Creutzfeldt disease

lactic acidemia

laughing, pathologic

learning disability

learning disability, in children

leg weakness, bilateral

Leigh's disease

leucine rich glioma inactivated 1 antibodies

limbic encephalitis

lipid storage disorder of CNS

lysosomal storage disease

macular degeneration

marche a petits pas

Marinesco-Sjogren syndrome

mediastinum, mass of

memory, impairment of

meningitis, carcinomatous

meningoencephalitis, mumps

meningovascular syphilis

mental retardation

mental status, abnormal

metabolic acidosis

metabolic disorder, primary

middle cerebellar peduncle

middle cerebellar peduncle, lesion

middle cerebellar peduncle, lesion, bilateral

migraine, children

mitochondrial disease

molecular genetics

monoclonal antibodies

movement disorder

movement disorder, extrapyramidal

movement disorder, hyperkinetic

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, high signal foci on

multiple sclerosis

multiple system atrophy

muscle weakness

mycoplasma pneumoniae

myelinolysis, extrapontine

myoclonic jerks

myoclonus, epilepsy

myotonia dystrophica

neoplasm, posterior fossa

neoplasm, primary of CNS

neoplasm, primary of CNS-children

neoplasm, primary of CNS-treatment of

nephrotic syndrome

neuroaxonal dystrophy

neuroaxonal dystrophy, infantile

neurocutaneous disease

neuroendocrinology

neurologic disease

neurologic disease, diagnoses of

neurologic disease, tempo

neuronal ceroid-lipofuscinosis

neuropathy, acute

neurotransmitter

Niemann-Pick disease

NMDA antagonists

nystagmus, hereditary

nystagmus, monocular

nystagmus, periodic

nystagmus, rotary

ocular motility, disorders of

oculodentodigital dysplasia

ophelia syndrome

ophthalmoplegia

opsoclonus-myoclonus syndrome

optic disc edema

optic neuropathy

optical coherence tomography

oral ulcerations

osmotic demyelination syndrome

ovary, enlarged

paraparesis, spastic

Parkinson disease

Parkinson disease, dystonia with

Parkinsonism syndrome

paroxysmal hemiplegia

paroxysmal neurologic deficits

pediatric autoimmune neuropsychiatric disorders associated with streptococcal infection

personality change

pleocytosis of cerebrospinal fluid

pneumoencephalogram(PEG)

poison, mercury

pons, lesion of

Poretti-Boltshauser syndrome

postural abnormality

potassium channel antibodies

practice guidelines

precipitating factors

pregnancy, neurologic complications in

progressive multifocal leucoencephalopathy

progressive neurologic disorder

psychiatric problems in neurologic disorders

psychomotor retardation

puberty, delayed

pulmonary infection

putamen, lesion of

putamen, lesion of, bilateral

pyramidal tract dysfunction

pyruvate dehydrogenase deficiency

pyruvate metabolism, abnormality of

radiation hypersensitivity

radiation therapy, CNS treatment and complications with

rapid onset dystonia parkinsonism

rapidly progressing neurologic illness

Refsum's disease

remote effect of cancer on the nervous system

respiratory failure

respiratory tract infection

retina, abnormal

retinal degeneration

retinitis pigmentosa

sarcoidosis, CNS

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

serologic testing

serologic testing, false negative

Sjogren's syndrome

Sjogren's syndrome, neurologic manifestations of

skin, lesions in neurologic disorders

skull x-ray, abnormal

sleep pathology and physiology

sodium channel dysfunction

speech disorder

speech disorder, childhood

speech, delayed development of

speech, loss of

spinal cord, lesion of

spinal muscular atrophy

spinocerebellar ataxia

spinocerebellar ataxia type 1

spinocerebellar ataxia type 7

spinocerebellar degeneration

spongy degeneration of brain

startle myoclonus

status epilepticus

steroid therapy, CNS treatment and complications with

striatal encephalitis

striatonigral degeneration

striatonigral degeneration, infantile

subarachnoid hemorrhage

subarachnoid hemorrhage, recurrent

symmetric brain lesions

syphilis, diagnosis and treatment

syphilis, neurologic complications with

systemic illness

tandem gait, ataxic

teeth, abnormal

teeth, number of in infants

teeth, wide-spaced

teratoma, ovarian

tongue, protrusion of

toxins, nervous system

transient ischemic attack

treatment of neurologic disorder

tremor, cerebellar

tremor, intention

trinucleotide repeats

upgaze, paralysis of

urinary incontinence

urinary retention

vertebral-basilar insufficiency

vertigo, episodic

viral infection

viral infection, CNS

vision, failure of in childhood

visual acuity, decreased

visual evoked response

visual impairment

visual loss, progressive

visual loss, slow

Von Hippel Lindau

walking, difficulty with

white matter disease

wide based gait

Wolfram syndrome

X-linked bulbospinal neuronopathy

Showing articles 400 to 450 of 4245 << Previous Next >>

Clinicopath Conf
Subacute Bacterial Endocarditis with Multiple Cerebral Emboli and Mycotic Aneurysm, Case 10-1993, NE, M 8:717-725,1993., 1993

Paraneoplastic Cerebellar Degener II, Clin & Immunologic Find in 21 Pts with Hodgkin's Disease
Neurol 42:1938-1943, Hammack,J.,et al, 1992

Paraneoplastic Cerebellar Degener I A Clinical Analysis of 55 Anti-Yo Antibody-Positive Pts
Neurol 42:1931-1937, Peterson,K.,et al, 1992

Cerebellar and Cerebral Abnormalities in Rett Syndrome:A Quantitative MR Analysis
AJR 159:177-183, Murakami,J.W.,et al, 1992

Cerebellar Symptoms as Presenting Manifest of Bilirubin Encephal in Children with Crigler-Najjar Type I Disease
Pediatrics 89:768-770, Labrune,P.H.,et al, 1992

Chiari I Malformations:Clinical and Radiologic Reappraisal
Radiology 183:347-353, Elster,A.D.&Chen,M.Y.M., 1992

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

CT & MR Imaging Findings in Adults with Cerebellar Medulloblastoma:Comparison with Findings in Children
AJR 159:609-612, Bourgouin,P.M.,et al, 1992

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

MR Imaging Features of Medulloblastoma
AJR 158:859-865, Meyers,S.P.,et al, 1992

Cerebellar Infarction in the Young
Stroke 23:763-766, Rosman,N.P.,et al, 1992

Chronic Neurodegenerative Disease Associated with HTLV-II Infection
Lancet 339:645-646, Hjelle,B.,et al, 1992

Brain MRI and Electrophysiologic Abnormalities in Preclinical and Clinical Adrenomyeloneuropathy
Neurol 42:85-91, Aubourg,P.,et al, 1992

MR Imaging of the Spinal Cord in 23 Subjects with ALD-AMN Complex
AJR 158:413-416, Snyder,R.D.,et al, 1992

Clinicopath Conf
Huntington's Diseae, Case2-1992, NEJM 326:117-125992., , 1992

Vertebral Artery Occlusion and Stroke from Cervical Self-Manipulation
Neurol 41:1696-1697, Rothrock,J.F.,et al, 1991

Wallenberg's Syndrome Following Self-Induced Manipulation
Cook. J. W. & Sanstead, J. K. , Neurol 41:1695-1696, , 1991

Dissection of the Extracranial Vertebral Artery:Report of Four Cases and Review of the Literature
JNNP 54:863-869, Hinse,P.,et al, 1991

Reversal of a Neurologic Paraneoplastic Syndrome with Octreotide (Sandostatin) in a Pt with Glucagonoma
Am J Med 91:434-436, Holmes,A.,et al, 1991

Hallervorden-Spatz Syndrome and Brain Iron Metabolism
Arch Neurol 48:1285-1293, Swaiman,K.F., 1991

Clinicopath Conf
Radiation Induced Cerebellar Astrocytoma, Case 23-1991, NEJM 324:1651-1659991., , 1991

Presynaptic Parkinsonism in Olivopontocerebellar Atrophy:Clinical, pathological, and Neurochemical Evidence
Ann Neurol 30:425-428, Pascual,J.,et al, 1991

The Spectrum of Cerebellar Infarctions
Neurol 41:973-979, Amarenco,P., 1991

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

Neurological Conversion Disorders in Childhood
Lancet 337:889-890, , 1991

Infarction in the Anterior Rostral Cerebellum (the Territory of the Lateral Branch of the Superior Cerebellar Artery)
Neurol 41:253-258, Amarenco,P.,et al, 1991

Central Nervous System Involvement in Von Hippel-Lindau Disease
Neurol 41:41-46, Filling-Katz,M.R.,et al, 1991

Lateral Medullary Infarction:Prognosis in an Unselected Series
Neurol 41:244-248, Norrving,B.&Cronqvist,S., 1991

Cat Scratch Disease, Acute Encephalopathy & Other Neurologic Manifestations
Am J Dis Child 145:98-101, Carithers,H.A.&Margileth,A.M., 1991

Short-Lasting Unilateral Neuralgiform Headache Atacks with Tearing & Conjunctival Injection:First"Symptomatic"Case
Cephalalgia 11:123-127, Bussone,G.,et al, 1991

Recurrent Intraparenchymal Hemorrhages from Angiographically Occult Vascular Malformations
J Neurosurg 73:174-180, Tung,H.,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

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

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

Avoidable Factors Contributing to Death of Children with Head Injury
BMJ 300:87-91, Sharples,P.M.,et al, 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

Progressive Myoclonic Ataxia (The Ramsay Hunt Syndrome)
Arch Neurol 47:1121-1125, Marsden,C.D.,et al, 1990

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

Gerstmann-Straussler-Scheinker Disease, I, Extending the Clinical Spectrum
Neurol 39:1446-1452, Farlow,M.R.,et al, 1989

Human T-Lymphotropic Virus Type I-Associated Myelopathy Presenting as Spinocerebellar Syndrome
Ann Neurol 25:419-420, Iwasaki,Y.,et al, 1989

Histological Verification of Microaneurysms as a Cause of Cerebral Haemorrhage in Surgical Specimens
JNNP 52:595-599, Wakai,S.&Nagai,M., 1989

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

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

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

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

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

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

MR Imaging of a Group I Case of Hallervorden-Spatz Disease
J Comput Assist Tomogr 12:851-853, Mutoh,K.,et al, 1988

Showing articles 400 to 450 of 4245 << Previous Next >>