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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 550 to 600 of 4245 << Previous Next >>

Traumatic Vertebrobasilar Occlusive Disease in Childhood
Neurol 28:185, Zimmerman,A.W.,et al, 1978

Combined Congenital Vascular Anomalies & Neuroepithelial (Colloid) Cysts
Neurol 28:552, Shuangshoti,S.,et al, 1978

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

Dominant Spinopontine Atrophy
Arch Neurol 35:156, Pogacar,S.,et al, 1978

Lecithin in Neurologic Disorders
NEJM 299:200, 1978 (Letter) ., Barbeau,A., 1978

Persistent Cerebellar Ataxia after Exposure to Toluene
Ann Neurol 2:440, Boor,J.W.,et al, 1977

The Spectrum of Mild X-Linked Recessive Muscular Dystrophy
Arch Neurol 34:408, Ringer,S.P.,et al, 1977

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

Physostigmine in Familial Ataxias
Neurol 27:70, Kark,R.A.,et al, 1977

Spinocerebellar Ataxia & HLA Linkage:Risk Prediction by HLA Typing
NEJM 296:1138, Jackson,J.F.,et al, 1977

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

Cerebrovascular diseases
In Harrison's Principles of Internal Medicine, 1977. McGraw-Hill Book Co. , p1., , 1977

Downbeating Nystagmus & Hereditary Cerebellar Degeneration, Levin DB, et al, In Neuro-ophthalmology Update
Masson Publishing USA, INC. 1977 P 337-338., Smith,J.L., 1977

Ocular Motor Abnormalities in Hereditary Cerebellar Ataxia
Brain 99:207-234, Zee,D.S.,et al, 1976

Normocalcemic Tetany
Neurol 26:825, Isgreen,W.P., 1976

Chronic Meningitis
Medicine 55:341, Ellner,J.J.,et al, 1976

The Thyroid Gland:Its Relationship to Neurology
In Handbook of Clin Neurol, Vinken & Bruyn (Ed) , North Holland Publ Co, Amsterdam 27:255, Greene,R., 1976

MGH-CPC-Gliomatosis Cerebri of Cerebellum & Brainstem
NEJM 292:852, , 1975

Adult Toxoplasmosis Presenting as Polymyositis & Cerebellar Ataxia
Ann Int Med 82:367, Greenlee,J.,et al, 1975

Chronic Progressive Panencephalitis due to Rubella Virus Simulating Subacute Sclerosing Panencephalitis
NEJM 292:994-998,1023, Weil, M.L.,et al, 1975

Progressive Rubella Panencephalitis
NEJM 292:990-993,1023, Townsend,J.,et al, 1975

Neurotoxicity of Commonly Used Antineoplastic Agents
NEJM 291:75, 1271974., Weiss,H.,et al, 1974

Infiltration of the Leptomeninges by Systemic Cancer:a Clinical & Pathologic Study
Arch Neurol 30:122, Olson,M.E.,et al, 1974

Acquired Pendular Nystagmus with Oscillopsia in Multiple Sclerosis:A Sign of Cerebellar Nuclei Disease
JNNP 37:570, Aschoff,J.C.,et al, 1974

Neuro Complica of Coeliac Disease & Trop Sprue, Neurology of GI Disease
1974, Major Problems in Neurology V-3, W. B. Saunders Co, Ltd., Pallis,C.A.&Lewis,P.D., 1974

Case Records of MGH-NEJM 287:1291
1972, 289:1039, 1973 Arterio-Venous Malformation of Cerebellum., , 1973

Effects of Viral Infection on the Developing Nervous System
Seminars in Medicine of the Beth Israel Hosp, Boston NEJM 287:5991972., Johnson,R., 1972

Genetic Counseling in Retinitis Pigmentosa
MCV Quart 8:283, Noah,V., 1972

Neurological Problems in Endocrine Diseases
Med Clin North Am 56:1029, Dale,A., 1972

"Idiopathic"Thrombosis in the Vertebrobasilar Arterial System in Young Men
BMJ 1:26, Graham,D.I., 1972

Mollaret's Meningitis & Differential Diagnosis of Recurrent Meningitis
Am J Med 52:128, Hermans,P.,et al, 1972

Olivopontocerebellar Atrophies:A Review
Medicine 49:227, Konigsmark,B., 1970

Treatment of Strokes
NEJM 281:594, 1969,, Browne,T.,et al, 1969

Huntington's Chorea
Bruyn, G. W. In Vinken & Bruyn, Handbk of Clin Neurol, North-Holland Publ Co, Amsterdam, 6:298, , 1968

The Uveomeningoencephalitic Syndrome
Neurol 16, 6031966., Riehl,J.L.,et al, 1966

Neurological Disorders Associated with Adult Celiac Disease
Brain 89:683, Cooke,W.T.,et al, 1966

Acute Cerebellar Syndrome Secondary to Infectious Mononucleosis in a Fifty-Two Yealr Old Man
Ann Int Med 55:147-149, Bennett,D.R.&Peters,H.A., 1961

Basilar Artery Migraine
Lancet 1:15-17, Bickerstaff,E.R., 1961

A Case of Cerebellar Ataxia, with a Discussion of Classification
Arch Neurol 3:71, Locke,S.,et al, 1960

Neuro CPC of MGH
Congenital Vascular Malfor. of Spinal Cord, NEJM 258:949-954958., , 1958

An Acute Syndrome of Ocular Oscillations & Truncal Ataxis
p. 96-99., Winkler,G.,et al, 1850

Alcoholism
Clin Neurol Chap 22 p. 1084, A. B. Baker Text Book of Neurology., Victor,M., 1850

Hereditary Ataxias
Genetics & the Inheritance of Integrated Neurol & Psych. Patterns-Vol 33, Proceed. Assoc. for Resear, h in NerSchut, J., 1850

Spectrum of Intracranial Hemorrhages in Cerebral Venous Thrombosis, A Pictorial Case Series and Review of Pathophysiology and Management
Neurologist 30:45-51, Jha,S.,et al, 2025

A 62-Year-Old Woman with Progressive Spasticity, Weakness,and Gait Instability
Neurol 104:e210290, Voloshyna-Farber, E.Y.,et al, 2025

Spontaneous Spinal Cord Infarction in a Young Patient: An Overview of Clinical Features and Management
Stroke 56:58-61, Chornay,C.,et al, 2025

A 68-YEar-Old Man with Progressive Numbness, Vertigo, and Cognitive Decline
Neurol 104:e213437, Regan,S.M. & Davalos,L.F., 2025

Spontaneous Intracranial Hypotension Associated with Vascular Malformations
AJNR 46:426-432, Mamlouk,M.D.,et al, 2025

Rapidly Progressive Frontotemporal Dementia with Amytrophic Lateral Sclerosis in an Elderly Female
Cureus doi:10.7759/CUREUS.32182, Sweedan,Y.G.,et al, 2025

Abnormal and Persistent Mineralization of Globi Pallidi in GAMT Deficiency
Neurol 104:e213636, Chanda,G.,et al, 2025

Showing articles 550 to 600 of 4245 << Previous Next >>