Neudle.com: Huntington s disease children

Differential
(Click to cross reference)

acanthocytosis

acetylcholine

acquired immunodeficiency syndrome

activated protein C resistance

adoption

advances in neurology

adverse drug reaction

affective disorders

algorithm

Alzheimer's disease

Alzheimer's disease, familial

amantadine

amnesia

amyloid angiopathy, cerebral

amyotrophic chorea-acanthocytosis

amyotrophic lateral sclerosis

anticardiolipin antibodies

anticoagulant, treatment

antiphospholipid antibodies

antithrombin III deficiency

anxiety

apomorphine

apraxia

apraxia of eyelid opening

autonomic dysfunction

basal ganglia

basal ganglia, degeneration

basal ganglia, lesion of

basal ganglia, lesion, bilateral

benign essential tremor

bicaudate index

biologic markers

blood dyscrasias, neurologic findings with

brain biopsy

brain transplantation

CAT scan, delta sign, empty

CAT scan, emission

CAT scan, emission, abnormal

CAT scan, false negative

CAT scan, venography

caudate nucleus

caudate nucleus, atrophy

caudate nucleus, lesion of

central nervous system, infection of

cerebral blood flow

cerebral cortical atrophy

cerebral death

cerebral glucose metabolism

cerebral infarction

cerebral venous infarction

cerebral venous thrombosis

cerebral venous thrombosis, deep

cerebral venous thrombosis, etiology

cerebral venous thrombosis, recurrent

cerebrospinal fluid

cerebrospinal fluid, gamma amino butyric acid

cerebrovascular accident

cerebrovascular accident, acute management of

cerebrovascular accident, cost of

cerebrovascular accident, familial occurrence

cerebrovascular accident, infancy and childhood

cerebrovascular accident, prevention of

cerebrovascular accident, recurrent

cerebrovascular accident, thrombolytic agents in treatment

cerebrovascular accident, work up for

cerebrovascular accident, young adult

cerebrovascular disease

chromosomal abnormality

cingulate gyrus

Clinical Pathologic Conference(C.P.C.)

congenital birth defects

controversies in neurology

cost effectiveness

craniectomy, decompressive

D-dimer

degenerative diseases of CNS

dementia

dementia, childhood

dementia, frontotemporal

dementia, presenile

dementia, subcortical

dentatorubral-pallidoluysian atrophy

depression

differential diagnosis

dropped head syndrome

drug induced neurologic disorders

drug overdose

dural sinus thrombosis

dying

dysarthria

dyskinesia

dyskinesia, causes of

dyskinesia, drug induced

dysphagia

dysphasia

dystonia

dystonia musculorum deformens

efficacy

electroencephalogram

electroencephalogram, abnormalities of

epidemiology of neurology

equinovarus

erythrocyte

ethics in neurology

evidence-based research

evoked potentials

excitotoxin

extrapyramidal

eye movement, disorders of

fibrinolytic agents, intra-venous local infusion

gamma amino butyric acid

gamma amino butyric acid-mimetic drug

genetic diagnosis, prenatal

genetic linkage

genetic neurologic disorders

genetic screening

genetic testing

Gilles de la Tourette syndrome

head injury, pediatric

hemoglobin abnormality, neurologic complications of

hepatolenticular degeneration(Wilson's disease)

hiccoughs

human immunodeficiency virus type 1

huntingtin

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

hypoxic encephalopathy

intellectual deterioration

internet

interobserver agreement

intracranial pressure, increased

isoniazid

Jakob-Creutzfeldt disease

Kluver-Bucy syndrome

L-dopa

lecithin

level of consciousness, decreased

Lewy body disease, diffuse

lipoma of CNS

lupus anticoagulant

lymphocyte capping, diminished

manic-depressive

medical-legal aspects of neurology

memory, impairment of

meningitis

middle cerebral artery territory infarction

middle cerebral artery, occlusion of

misdiagnosis

mitochondrial disease

mitochondrial encephalomyopathy

movement disorder, extrapyramidal

movement disorder, extrapyramidal-treatment of

movement disorder, treatment of

MRI

MRI, abnormal

MRI, CAT scan compared to

MRI, contrast enhanced

multiple system atrophy

muscimol

muscular dystrophy

muscular dystrophy, Duchenne

myoclonus

myoclonus, action

myoclonus, cortical

myoclonus, stimulus sensitive

myopathy

myotonia dystrophica

nausea and vomiting

neoplasm, intracranial

neoplasm, primary intracranial

neoplasm, primary of CNS

neurofibrillary degeneration

neurofibromatosis 1

neurofibromatosis 2

neuroleptic

neurologic complications of, systemic disease

neurologic disease

neurologic disease, diagnoses of

neurologic examination, focal

neurologic history

neuronal migration disorder

neuropathology

neuropathology, brain

old age, neurology of

oral contraceptives

Parkinson disease

Parkinson disease, drug induced

peptides, brain

persistent vegetative state

pneumoencephalogram(PEG)

pneumonia

polymerase chain reaction

polymerase chain reaction, false negative

polymerase chain reaction, false positive

postural abnormality

practice guidelines

preclinical

pregnancy, neurologic complications in

prethrombotic state

prevention of neurologic disorders

prognosis

progressive neurologic disorder

progressive supranuclear palsy

protein C deficiency

protein S deficiency

psychiatric disorder

psychiatric problems in neurologic disorders

psychological testing

psychological testing, neurologic problems

psychomotor retardation

psychosis

pulmonary embolism

putamen, lesion of

putamen, lesion of, bilateral

saccadic eye movements

saccadic eye movements, abnormal

screening

seizure

serotonin

single photon emission computed tomography

spinal muscular atrophy

spinocerebellar ataxia

spinocerebellar ataxia type 1

spinocerebellar degeneration

straight sinus

striatum, lesion of

striatum, lesion of, bilateral

stuttering

substance P

suicide

superior sagittal sinus thrombosis

tardive dyskinesia

tardive dyskinesia, treatment of

tissue plasminogen activator, intravenous

torticollis

treatment of neurologic disorder

tremor

trinucleotide repeats

viral infection, CNS

visual evoked response

visuospatial disturbance

walking

walking, difficulty with

weight loss

workup

writers cramp

X-linked bulbospinal neuronopathy

Showing articles 100 to 150 of 2671 << Previous Next >>

The Diagnosis of Huntington's Disease
Neurol 36:1279-1283, Folstein,S.E.,et al, 1986

Huntington's Disease, Pathogenesis & Management
NEJM 315:1267-1276, Martin,J.B.&Gusella,J.F., 1986

Subcortical Dementia
BMJ 292:1035-1036, Foster,J.B., 1986

The Gait Abnormality of Huntington's Disease
Neurol 35:1450-1454, Koller,W.C.&Trimble,J., 1985

Presymptomatic Testing for Huntington's Disease
JAMA 253:3286-3291, Bird,S.J., 1985

Genetic Prediction & Family Structure in Huntington's Chorea
BMJ 290:1929-1931, Harper,P.S.,et al, 1985

Dysphagia in Huntington's Disease
Arch Neurol 42:57-60, Leopold,N.A.,et al, 1985

A DNA Polymorphism for Huntington's Disease Marks the Future
Arch Neurol 42:20-24, Wexler,N.S.,et al, 1985

Genetic Testing in Huntington's Disease
Ann Neurol 16:511-513, Koller,W.C.,et al, 1984

Evoked Potentials in Huntington's Disease
Arch Neurol 41:379-382, Ehle,A.L.,et al, 1984

Parental Transmission in Huntington's Disease
Lancet 1:1100-1102, Went,L.N.,et al, 1984

Apraxia of Eyelid Opening in Progressive Supranuclear Palsy
Ann Neurol 15:115-116, Dehaene,I., 1984

Increased Rate of Suicide Among Patients with Huntington's Disease
JNNP 47:1283-1287, Schoenfeld,M.,et al, 1984

A Genetic Marker for Huntington's Chorea
BMJ 287:1567-1568, Harper,P.S., 1983

Huntington's Chorea:Neglected Opportunities for Preventive Medicine
Lancet 1:634-636, Martindale,B.,et al, 1983

Maternal Transmission in Huntington's Disease
Lancet 1:208-210, Myers,R.H.,et al, 1983

Positron Computed Tomography for Studies of Myocardial & Cerebral Function
Ann Int Med 98:339-359, Phelps,M.E.,et al, 1983

Treatment of Hyperkinetic Movement Disorders with Tetrabenazine:A Double-blind Crossover Study
Ann Neurol 11:41-47, Jankovic,J., 1982

False-Negative Results With Levodopa For Early Detection Of Huntington's Disease
NEJM 307:561-562, Myers,R.H.,et al, 1982

Attitudes Of Those At Risk For Huntington's Disease Toward Presymptomatic Provocative Testing
NEJM 307:1406, McCormack,M.K., 1982

Neurotransmitters & CNS Disease, Basal Ganglia Disease
Lancet 2:1141-1147, Marsden,C.D., 1982

Neuroleptics & Abnormal Movements
BMJ 285:463-464, Lader,M.H., 1982

Levodopa & Presymptomatic Detection of Huntington's Disease-Eight-Year Follow-Up
NEJM 302:1090, Klawans,H.L.,et al, 1980

Presymptomatic & Early Detection in Huntington's Disease
Ann Neurol 8:343-347, Klawans,H.L.,et al, 1980

Levels of y-Aminobutyric Acid in Cerebrospinal Fluid in Various Neurologic Disorders
Arch Neurol 37:352-355, Manyam,N.V.B.,et al, 1980

Huntington's Disease:Abnormality of Lymphocyte Capping
Ann Neurol 6:447-450, Noronha,A.B.C.,et al, 1979

Studies of the Fluorescence of Fibroblasts From Huntington's Disease:Evidence of a Membrane Abnormality
NEJM 300:678, Pettegrew,J.,et al, 1979

Isoniazid Therapy of Huntington Disease
Neurol 29:370-375, Perry,T.L.,et al, 1979

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

Huntington Disease Associated with Alzheimer Disease
Ann Neurol 3:545, McIntosh,G.C.,et al, 1978

The Visually Evoked Potential in Huntington disease
Neurol 28:95, Ellenberger,C.,et al, 1978

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

Apomorphine Hydrochloride-Induced Improvement in Huntington's Chorea
Arch Neurol 35:27, Corsini,G.U.,et al, 1978

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

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

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 Chorea, Effect of Serotonin Depletion
Arch Neurol 26:282, Chase,T.,et al, 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

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

Showing articles 100 to 150 of 2671 << Previous Next >>