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abortion, spontaneous

acetylcholine receptor

acetylcholine receptor antibody

acetylcholinesterase

acetylcholinesterase deficiency

acquired immunodeficiency syndrome

acute disseminated encephalomyelitis

adolescent medicine

advances in neurology

adverse drug reaction

affective disorders

airway obstruction

alcohol intolerance

alpha-fetoprotein

Alzheimer's disease

Alzheimer's disease, familial

amyloid angiopathy, cerebral

amyotrophic chorea-acanthocytosis

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, bulbar

amyotrophic lateral sclerosis, childhood

amyotrophic lateral sclerosis, familial

amyotrophic lateral sclerosis, juvenile

amyotrophic lateral sclerosis, Parkinson-dementia-complex

amyotrophic lateral sclerosis, post-encephalitic

analgesic overuse

anesthesia, general

anesthesia, local

anterior horn cell disease

antibiotics, neurologic complications with

anticholinergic drugs

anticonvulsants, cognitive function with

anticonvulsants, discontinuation in seizure-free epileptics

anticonvulsants, effectiveness

anticonvulsants, untoward effects of

apraxia of eyelid opening

arthrogryposis multiplex

arylsulfatase A

aspartate aminotransferase

asthma, poliomyelitis-like syndrome with

ataxia, cerebellar

ataxia, hereditary

athetosis, causes of

atidarsagene autotemcel

atlanto axial dislocation, congenital

atypical lymphocytes

auditory evoked brainstem potentials

autoimmune disease

automobile accidents

autonomic dysfunction

axonal spheroid

basal ganglia, degeneration

basal ganglia, lesion of

basal ganglia, lesion, bilateral

behavioral disorder

benign essential tremor

bicaudate index

biologic markers

biopterin deficiency

biotin deficiency

biotin deficiency, juvenile form

biotin-responsive basal ganglia disease

body mass index

bone marrow transplantation

brain transplantation

Brueghel's syndrome

bulbar palsy, acute

bulbar palsy, juvenile

bulbar palsy, progressive

calf amyotrophy

CAT scan, abnormal

CAT scan, emission

CAT scan, emission, abnormal

CAT scan, false negative

caudate nucleus

caudate nucleus, atrophy

caudate nucleus, lesion of

cavernous sinus, syndrome

central nervous system, infection of

cerebellar degeneration

cerebellar lesion

cerebellum, disease of

cerebral blood flow

cerebral cortex

cerebral cortical atrophy

cerebral glucose metabolism

cerebrospinal fluid

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, gamma amino butyric acid

cerebrospinal fluid, gammaglobulin of

cerebrovascular accident

cerebrovascular accident, young adult

cerebrovascular disease

cerebrovascular disease, risk factors in

cervical collar

cesarean section

chorea, causes of

chorea, treatment of

choreoathetosis

chromosomal abnormality

cingulate gyrus

Clinical Pathologic Conference(C.P.C.)

clubbing of fingers

cogwheel rigidty

cold temperature

collagen vascular disease

congenital birth defects

congenital infection, CNS

congenital malformation

congenital myasthenic syndromes

congenital paresis

controversies in neurology

corpus callosum, lesion of

cortical muscular atrophy

crawl regression

cryopyrin-associated periodic syndrome

decision analysis

deep gray nuclei

degenerative diseases of CNS

delay in diagnosis

delivery, complicated

dementia, childhood

dementia, frontotemporal

dementia, presenile

dementia, subcortical

dentatorubral-pallidoluysian atrophy

developmental milestones

developmental milestones, loss of

developmental retardation

diabetes mellitus

diagnostic criteria

differential diagnosis

difficulty climbing stairs

distal muscle atrophy

distal muscle weakness

dopa responsive dystonia

dopamine agonist

dropped head syndrome

drug abuse, adolescent

drug induced neurologic disorders

dyskinesia, causes of

dyskinesia, drug induced

dystonia musculorum deformens

dystonia, painful

dystonia, treatment of

edema, periorbital

electrical sensation

electroencephalogram

electroencephalogram, abnormalities of

electromyogram, decremental response

electron microscopy

encephalitis, viral

encephalopathy, neonatal

epidemiology of neurology

episodic neurologic deficits

Epstein-Barr virus

ethics in neurology

evoked potentials

exercise-induced neurologic dysfunction

extremity, cold

eye movement, disorders of

facial weakness

facial weakness, bilateral

flaccid paralysis

fragile-X syndrome

Friedreich's ataxia

frontal lobe, behavior with disease of

frontal lobe, pathologic signs of

gamma amino butyric acid

gamma amino butyric acid-mimetic drug

gammaglobulin therapy, intravenous

genetic counselling

genetic diagnosis

genetic diagnosis, prenatal

genetic linkage

genetic neurologic disorders

genetic screening

genetic testing

genu of corpus callosum

Gilles de la Tourette syndrome

gyrus, abnormal

Hallervorden Spatz disease

headache, children

headache, chronic

headache, drug induced

headache, icepick

headache, severe

headache, treatment of

headache, unilateral

health insurance

hepatolenticular degeneration(Wilson's disease)

hepatosplenomegaly

heralding manifestation

homovanillic acid

human parechovirus

Huntington's chorea

Huntington's chorea, age at onset

Huntington's chorea, akinetic-rigid form

Huntington's chorea, differential diagnosis

Huntington's chorea, genetic counselling

Huntington's chorea, late onset

Huntington's chorea, membrane abnormality

Huntington's chorea, misdiagnosis of

Huntington's chorea, presymptomatic detection of

Huntington's chorea, sporadic form

Huntington's disease, children

hydroxyindole acetic acid 5(5HIAA)

hyperthyroidism

hypotonia, infants

hypoxic encephalopathy

immunologic disease

immunosuppression

immunosuppressive agents

inclusion bodies, intranuclear

infantile tremor syndrome

infectious mononucleosis

infectious mononucleosis, neurologic findings with

intellectual deficit

intellectual deterioration

intracranial hypertension, benign

intranasal medication

intrauterine infection

intrauterine infection, viral of CNS

intrinsic hand muscles, wasting of

Jakob-Creutzfeldt disease

juvenile distal and segmental muscular atrophy

juvenile idiopathic inflammatory myopathy

juvenile myoclonus epilepsy

juvenile paresis

keratoconjunctivitis

Kluver-Bucy syndrome

Kugelberg-Welander syndrome

labor, complicated

leg weakness, unilateral

leukoencephalopathy

Lewy body disease, diffuse

Lhermitte's sign

liver function enzymes

lymphadenopathy

lymphadenopathy, axillary

lymphadenopathy, paraaortic

lymphocyte capping, diminished

lysosomal storage disease

magnesium sulfate

malformation, CNS, congenital

malformation, vascular

malformation, vascular, cerebral

manic-depressive

Mary Walker phenomenon

medical-legal aspects of neurology

memory, impairment of

meningitis, aseptic

meningitis, chronic

meningoencephalitis

mental retardation

metabolic acidosis

metabolic disorder, primary

metachromatic leukodystrophy

metachromatic leukodystrophy, adult onset

metachromatic leukodystrophy, juvenile

metachromatic leukodystrophy, late-infantile

migraine, children

migraine, seizures in

migraine, treatment of

mitochondrial disease

mitochondrial encephalomyopathy

molecular genetics

monomelic amyotrophy

motor neuron disease

motor neuron disease, juvenile form

movement disorder

movement disorder, extrapyramidal

movement disorder, extrapyramidal-treatment of

movement disorder, treatment of

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, functional

MRI, spinal cord

MRI, sunburst pattern

multiple sclerosis

multiple system atrophy

muscle atrophy, progressive

muscle atrophy, static

muscle twitching

muscle wasting, diffuse

muscle weakness

muscle weakness, proximal

muscular dystrophy

muscular dystrophy, Duchenne

myasthenia gravis

myasthenia gravis, classification

myasthenia gravis, congenital

myasthenia gravis, distal weakness

myasthenia gravis, etiology of

myasthenia gravis, familial incidence of

myasthenia gravis, infantile and juvenile

myasthenia gravis, limb-girdle

myasthenia gravis, misdiagnosis of

myasthenia gravis, neonatal

myasthenia gravis, neuromuscular junction in

myasthenia gravis, ocular

myasthenia gravis, passive transfer of

myasthenia gravis, presenting manifestations

myasthenia gravis, prognosis of

myasthenia gravis, receptor site in

myasthenia gravis, remission of

myasthenia gravis, seronegative

myasthenia gravis, thymectomy in

myasthenia gravis, treatment of

myasthenic crisis

myasthenic syndrome

myoclonic jerks

myoclonus, action

myoclonus, cortical

myoclonus, epilepsy

myoclonus, stimulus sensitive

myopathy inflammatory, classification

myopathy, inflammatory

myopathy, inflammatory, classification

myositis specific autoantibody

myositis, juvenile

myotonia dystrophica

neoplasm, intracranial

neoplasm, primary intracranial

neoplasm, primary of CNS

nerve conduction studies

neuroaxonal dystrophy

neuroaxonal dystrophy, infantile

neuroaxonal dystrophy, juvenile

neurofibrillary degeneration

neurofibromatosis 1

neurofibromatosis 2

neurologic complications of, systemic disease

neurologic disease

neurologic disease, diagnoses of

neurologic history

neuromuscular disease, electrodiagnosis of

neuromuscular junction

neuronal intranuclear inclusion disease

neuronal migration disorder

neuropathology, brain

neuropathy, amyloid

neuropathy, peripheral

neurotransmitter

newborn, evaluation of

next-generation sequencing

obesity, childhood

old age, neurology of

ophthalmoplegia

ophthalmoplegia, painful

optic atrophy, bilateral

palpebral erythema

paraparesis, spastic

parechovirus encephalitis

parietal lobe, lesion of

parietal lobe, syndromes of

Parkinson disease

Parkinson disease, drug induced

Parkinson disease, dystonia with

Parkinson disease, juvenile

Parkinson disease, treatment of

Parkinsonism syndrome

peptides, brain

periodic paralysis

periodic paralysis, thyrotoxic

persistent vegetative state

personality change

personality disorder

photosensitivity, skin

pleocytosis of cerebrospinal fluid

pneumoencephalogram(PEG)

poliomyelitis-like illness

polymerase chain reaction

polymerase chain reaction, false negative

polymerase chain reaction, false positive

postural abnormality

practice guidelines

pregnancy, neurologic complications in

prevention of neurologic disorders

progressive neurologic disorder

progressive supranuclear palsy

psychiatric disorder

psychiatric problems in neurologic disorders

psychological testing

psychological testing, neurologic problems

psychomotor retardation

psychosis, acute

ptosis, bilateral

putamen, lesion of

putamen, lesion of, bilateral

quality of life

recombinant DNA

repetitive nerve stimulation

respiratory depression

respiratory failure

reverse split hand sign

rheumatoid arthritis

rheumatoid arthritis, neurologic complications of

rubella encephalitis

rubella encephalitis, progressive

rubella syndrome

saccadic eye movements

saccadic eye movements, abnormal

sedimentation rate, elevated

seizure, classification of

seizure, diagnosis of

seizure, differential diagnosis of

seizure, familial

seizure, neonatal

seizure, paradoxical

seizure, prognosis in adults

seizure, stimulus sensitive

seizure, treatment of

serologic testing

serologic testing, false negative

single photon emission computed tomography

skin, lesions in neurologic disorders

sodium valproate

speech disorder

speech disorder, childhood

spinal cord, cervical

spinal cord, compression of

spinal cord, enlargement

spinal cord, ischemic lesion of

spinal cord, lesion of

spinal muscular atrophy

spinocerebellar ataxia

spinocerebellar ataxia type 1

spinocerebellar degeneration

splenium of corpus callosum

sports medicine, neurology of

stem cell transplantation

steroid therapy, CNS treatment and complications with

striatum, lesion of

striatum, lesion of, bilateral

subacute myelo-opticoneuropathy(S.M.O.N.)complex

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

subarachnoid hemorrhage

symmetric brain lesions

syphilis, congenital

syphilis, neurologic complications with

systemic illness

systemic juvenile idiopathic arthritis

systemic lupus erythematosus

systemic lupus erythematosus, neonatal

systemic lupus erythematosus, neurologic complications with

tardive dyskinesia

tardive dyskinesia, treatment of

tardive dystonia

Tay-Sachs disease

temporal lobe, lesion

temporal lobe, lesion, bilateral

tensilon test, false negative

thalamus, lesion of

thalamus, lesion of-bilateral

thymus and neuromuscular function

Tolosa Hunt syndrome

tongue, atrophy

tongue, fasciculations of

tongue, weakness

tonic foot response

transplacental virus infections

treatment of neurologic disorder

tremor, postural

trigeminal autonomic cephalgia

trinucleotide repeats

varicella zoster virus

varicella zoster virus, encephalitis

viral infection

viral infection, CNS

viral isolation

visual evoked response

visual loss, progressive

visuospatial disturbance

vocal cord paralysis

walking, difficulty with

weakness, fatiguable

weakness, generalized

weaning from respirator, failure to

West Nile fever

white matter disease

X-linked bulbospinal neuronopathy

Showing articles 200 to 237 of 237 << Previous

Juvenile Huntington Chorea:Clinical, Ultrastructural, & Biochemical Studies
Neurol 28:23, Goebel,H.H.,et al, 1978

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

Juvenile Type of Distal & Segmental Muscular Atrophy of Upper Extremities
Ann Neurol 3:429, Sobue,I.,et al, 1978

Juvenile Parkinsonism:A Patient with Possible Primary Striatal Dysfunction
Ann Neurol 3:453, Naidu,S.,et al, 1978

Juvenile Neuroaxonal Dystrophy:Clinical, Electrophysiological, & Neuropathological Features
Ann Neurol 3:419, Dorfman,L.J.,et al, 1978

Huntington's Disease, CSF GABA Level in at-risk Individuals
Arch Neurol 35:728-730, Manyam,N.V.B.,et al, 1978

Huntington's Disease:Treatment with Muscimol, a GABA-Mimetic Drug
Ann Neurol 4:279-284, Shoulson,I.,et al, 1978

Bicaudate Index in Computerized Tomography of Huntington Disease & Cerebral atrophy
Neurol 28:1196-1200, Barr,A.N.,et al, 1978

Identification of GABA in Human CSF by Gas Liquid Chromatography & Mass Spectrometry
NEJM 296:692, Huizinga,J.D.,et al, 1977

Anti-Acetylcholine Receptor Antibody in Neonatal Myasthenia Gravis
NEJM 296:55, Keesey,J.,et al, 1977

Anti-Acetylcholine Receptor IgG in Neonatal Masthenia Gravis
NEJM 297:169, Nakao,K., 1977

Effective Treatment of Infantile Myasthenia Gravis by Combined Prednisone & Thymectomy
Neurol 27:550, Sarnat,H.B.,et al, 1977

Juvenile Parkinsonism Treated with Levodopa
Arch Neurol 34:244, Sachdev,K.K.,et al, 1977

Treatment of Huntington's Chorea with Isoniazid
NEJM 297:840, 1977. (Letter), Perry,T.L.,et al, 1977

Huntington's Chorea, Changes in Neurotransmitter Receptors in the Brain
NEJM 294:1305, Enna,S.J.,et al, 1976

Computerized Axial Tomography-Use in the Dx. of Dementia
JAMA 234:754, Menzer,L.,et al, 1975

Huntington's Chorea-Deficiency of Y-Aminobutynic Acid in Brain
NEJM 288:337, 1973, 289:104, 1973, 292:10295., Perry,T.,et al, 1975

Progressive Rubella Encephalitis
NEJM 292:990-993, 994-998, 1023-1024975., Townsend,J.J., 1975

Clinical Neuropathological Conference
(Ed) , Dis Ner Sys 34:124, 1973, Pick's Disease., Aronson,S.&Aronson,B., 1973

Huntington's Disease in Children
Neurol 23:561, Byers,R.,et al, 1973

Clinical Diagnosis of the Dyskinesias
Med Clin of North Am 56:1321, Duvoisin,R., 1972

Presymptomatic Detection of Huntington's Chorea
BMJ 540, 1972 Sept., , 1972

Huntington's Disease-Newspaper Article-Boston Globe
May 7, 1972, , 1972

Use of L-Dopa in the Detection of Presymptomatic Huntington's Chorea
NEJM 286:1332, Klawans,H.,et al, 1972

Huntington's Chorea, Effect of Serotonin Depletion
Arch Neurol 26:282, Chase,T.,et al, 1972

Drug Use within an Adolescent Treatment Center
Psych Ann 2:26, 1972 May., Crabtree,L.,et al, 1972

Psychiatry in the Schools
Psych Ann 2, 1972 May., Balser,B.H., 1972

The Geography of Neurology
BMJ 2:506, Spillane,J.D., 1972

The EEG in Huntington's Chorea:A Clinical & Neuropathological Study
JNNP 35:97-102, Scott,D.F.,et al, 1972

Cholinergic & Dopaminergic Mechanisms in Huntington's Chorea
Life Sciences 10:405 1971., Aquilonius,S.,et al, 1971

Diseases of the Extrapyramidal System
Disease-a-month-Jan 1970., Klawans,H.,et al, 1970

Metachromatic Leukodystrophy
in Handbook of Clinical Neurology, Vinken, P. J. & Bruyn, G. W. , (Ed) , Vol 10, North-Holland Publ, o, Amsterdam, Peiffer, J., 1970

How to Talk Sense to Adolescent Rebels
Hosp Physician, Sept 1969, p. 143., Bates,R., 1969

Parietal Lobe Syndromes
In Handbk of Clinical Neurology, Vinken & Bruyn, Ed, North-Holland Publ Co, Amsterdam, V2, Ch21, p., 84wesbury,E.C.O., 1969

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

Pneumoencephalographic Findings in Huntington's Chorea
Neurol 18:991, Gath,I.,et al, 1968

Diseases of the Basal Ganglia-Their Relation to Disorders of Movement
Lancet 1099, 1960, Nov., Denny-Brown,D., 1960

Electric Shocks and Weakness of the Right Hand in a Young Man:Hirayama Disease
, Witiw,C.D.&OToole,J.E.,

Showing articles 200 to 237 of 237 << Previous