Neudle.com: Huntington s chorea

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acanthocytosis

acetylcholine

acquired immunodeficiency syndrome

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

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anxiety

apomorphine

apraxia

apraxia of eyelid opening

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basal ganglia

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benign essential tremor

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CAT scan, emission, abnormal

CAT scan, false negative

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

cerebrospinal fluid

cerebrospinal fluid, gamma amino butyric acid

cerebrovascular accident

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chromosomal abnormality

cingulate gyrus

Clinical Pathologic Conference(C.P.C.)

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clozapine

cognition

congenital birth defects

controversies in neurology

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dentatorubral-pallidoluysian atrophy

depression

differential diagnosis

dropped head syndrome

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dyskinesia, causes of

dyskinesia, drug induced

dysphagia

dysphasia

dystonia

dystonia musculorum deformens

efficacy

electroencephalogram

electroencephalogram, abnormalities of

eye movement, disorders of

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

hepatolenticular degeneration(Wilson's disease)

hiccoughs

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

hyperreflexia

hypotonia

hypoxia

hypoxic encephalopathy

imbalance

intellectual deficit

intellectual deterioration

internet

isoniazid

Jakob-Creutzfeldt disease

Kluver-Bucy syndrome

L-dopa

lecithin

Lewy body disease, diffuse

lipoma of CNS

lymphocyte capping, diminished

manic-depressive

medical-legal aspects of neurology

memory, impairment of

misdiagnosis

mitochondrial disease

mitochondrial encephalomyopathy

movement disorder, extrapyramidal

movement disorder, extrapyramidal-treatment of

movement disorder, treatment of

multiple system atrophy

muscimol

muscular dystrophy

muscular dystrophy, Duchenne

myoclonus

myoclonus, action

myoclonus, cortical

myoclonus, stimulus sensitive

myopathy

myotonia dystrophica

neoplasm, intracranial

neoplasm, primary intracranial

neoplasm, primary of CNS

neurofibrillary degeneration

neurologic disease, diagnoses of

neurologic history

neuronal migration disorder

neuropathology

neuropathology, brain

old age, neurology of

Parkinson disease

Parkinson disease, drug induced

peptides, brain

persistent vegetative state

personality change

Pick's disease

piracetam

pneumoencephalogram(PEG)

pneumonia

polymerase chain reaction

polymerase chain reaction, false negative

polymerase chain reaction, false positive

postural abnormality

practice guidelines

preclinical

prevention of neurologic disorders

prognosis

progressive neurologic disorder

progressive supranuclear palsy

psychiatric disorder

psychiatric problems in neurologic disorders

psychological testing

psychological testing, neurologic problems

psychomotor retardation

psychosis

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

striatum, lesion of

striatum, lesion of, bilateral

tardive dyskinesia, treatment of

treatment of neurologic disorder

tremor

trinucleotide repeats

viral infection, CNS

visual evoked response

visuospatial disturbance

walking

walking, difficulty with

weight loss

writers cramp

X-linked bulbospinal neuronopathy

Showing articles 50 to 100 of 430 << Previous Next >>

Molecular Genetics in Neurology
Ann Neurol 34:757-773, Martin,J.B., 1993

The Polymerase Chain Reaction:Application to Nervous System Disease
Ann Neurol 34:513-523, Darnell,R.B., 1993

Clinical and Magnetic Resonance Features of the Classic & Akinetic-Rigid Variants of Huntington's Dis
Arch Neurol 50:17-19, Oliva,D.,et al, 1993

Clinical Consequences of Isolating the Gene for Huntington's Disease
BMJ 307:397-398, Harper,P.S., 1993

Serial Changes of Cerebral Glucose Metab & Caudate Size in Persons at Risk for Huntington's Dis
Arch Neurol 49:1161-1167, Grafton,S.T.,et al, 1992

The Psychological Consequences of Predictive Testing for Huntington's Disease
NEJM 327:1401-1405, 14491992., Wiggins,S.,et al, 1992

Putamen Volume Reduction on Magnetic Resonance Imaging Exceeds Caudate Changes in Mild Huntington's Disease
Ann Neurol 31:69-75, Harris,G.J.,et al, 1992

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

A Follow-Up Study of Isolated Cases of Suspected Huntington's Disease
Ann Neurol 31:293-298, Bateman,D.,et al, 1992

Postural Stability in Patients with Huntington's Disease
Neurol 42:1232-1238, Tian,J.,et al, 1992

Presymptomatic Testing for Huntington's Disease in the United Kingdom
BMJ 304:1593-1596, Tyler,A.,et al, 1992

Ideomotor Apraxia in Huntington's Disease
Arch Neurol 48:35-41, Shelton,P.A.&Knopman,D.S., 1991

Myoclonus in Adult Huntington's Disease
Ann Neurol 29:213-215, Vogel,C.M.,et al, 1991

Genetic Testing for Huntington's Disease
BMJ 300:1089-1090, Harper,P.,et al, 1990

Abnormalities of Striatal Projection Neurons and n-Methyl-d-Aspartate Receptors in Presymptomatic Huntington's Disease
NEJM 322:1293-1298, Albin,R.L.,et al, 1990

Predictive Testing for Huntington's Disease, Progress and Problems
BMJ 298:404-405, 1989, Harper,P.S.&Morris,M.J., 1989

Predictive Testing for Huntington's Disease with Linked DNA Markers
Lancet 2:463-466, Brock,D.J.H.,et al, 1989

Problems in Genetic Prediction for Huntington's Disease
Lancet 2:601-603, Morris,M.J.,et al, 1989

Uptake of Presymptomatic Predictive Testing for Huntington's Disease
Lancet 2:603-605, Craufurd,D.,et al, 1989

Clinical-Pathologic Correlation in Huntington's Disease:A Neuropsychological and Computed Tomography Study
Neurol 39:796-801, Bamford,K.A.,et al, 1989

Adoption and Genetic Prediction for Huntington's Disease
Lancet 2:1069-1070, Morris,M.,et al, 1988

The Molecular Genetic Revolution, Its Impact on Clinical Neurology
Arch Neurol 45:1366-1376, Payne,C.S.&Roses,A.D., 1988

Autonomic Nervous Function in Huntington's Disease
Arch Neurol 45:309-312, DenHeijer,J.C.,et al, 1988

Predictive Testing for Huntington's Disease with Use of a Linked DNA Marker
NEJM 318:535-542, Meissen,G.J.,et al, 1988

Tetrabenazine Therapy of Dystonia, Chorea, Tics, & Other Dyskinesias
Neurol 38:391-394, Jankovic,J.&Orman,J., 1988

Huntington's Disease Mortality in the United States
Neurol 38:769-772, Lanska,D.J.,et al, 1988

Presymptomatic Neuropsychological Impairment in Huntington's Disease
Arch Neurol 45:769-773, Jason,G.W.,et al, 1988

Huntington's Disease:Deterioration in Clinical State During Treatment with ACE Inhibitor
BMJ 294:1659-1660, Goldblatt,J.&Bryer,A., 1987

The Combined Use of Positron Emission Tomography & DNA Polymorphisms for Preclinical Detection of Huntington's Disease
Neurol 37:1441-1447, Hayden,M.R.,et al, 1987

First-Trimester Prenatal Diagnosis for Huntington's Disease with DNA Probes
et al Lancet 1:1284-1285, Hayden,M.R., 1987

Normal Caudate Glucose Metabolism in Persons at Risk for Huntington's Disease
Arch Neurol 44:254-257, Young,A.B.,et al, 1987

Reduced Cerebral Glucose Metabolism in Asymptomatic Subjects at Risk for Huntington's Disease
NEJM 316:357-362, Mazziotta,J.C.,et al, 1987

Genetic Linkage in Neurologic Diseases
Editorial, NEJM 316:1018-10201987., Martin,J.B., 1987

Positron Emission Tomography in the Early Diagnosis of Huntington's Disease
Neurol 36:888-894, Hayden,M.R.,et al, 1986

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

PET Scan Investigations of Huntington's Disease:Cerebral Metabolic Corr. of Neuro & Funct Decline
Ann Neurol 20:296-303, Young,A.B.,et al, 1986

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

Neuropeptides in Neurological Disease
Ann Neurol 20:547-565, Beal,M.F.&Martin,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

Showing articles 50 to 100 of 430 << Previous Next >>