Neudle.com: chorea familial

Differential
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acanthocytosis

advances in neurology

akathisia

alcohol

alcohol, neurologic complications with

algorithm

alpha-fetoprotein

alternating hemiplegia

alternating hemiplegia of childhood

Alzheimer's disease

Alzheimer's disease, familial

aminoacidopathies

aminoacidurias

amyotrophic chorea-acanthocytosis

amyotrophic lateral sclerosis

apraxia of eye movements

areflexia

asymptomatic

ataxia

ataxia telangiectasia

autonomic dysfunction

Babinski sign

baclofen

basal ganglia

basal ganglia, calcification of

basal ganglia, degeneration

basal ganglia, lesion of

basal ganglia, lesion, bilateral

behavioral disorder

benign essential tremor

bicaudate index

biotin

blindness

blood dyscrasias, neurologic findings with

calcification, intracranial

carbamazepine

carcinoembryonic antigen

CAT scan, emission, abnormal

catalepsy

cataracts

caudate nucleus

caudate nucleus, atrophy

caudate nucleus, lesion of

cerebellar ataxia, children

cerebellar ataxia, hereditary

cerebellar atrophy, primary

cerebellar atrophy, secondary

cerebellar degeneration

cerebellar lesion

cerebral cortical atrophy

cerebrovascular accident

chorea, familial benign

chorea, senile

chorea, treatment of

choreoathetosis

choreoathetosis, paroxysmal

chromosomal abnormality

cirrhosis, causes of childhood

Clinical Pathologic Conference(C.P.C.)

copper metabolism, abnormal

cortical blindness

creatine phosphokinase(CPK)elevated

cultured skin fibroblasts

deafness

degenerative diseases of CNS

delay in diagnosis

dementia

dementia, presenile

dementia, rapidly progressive

dentate nuclei, lesion of

dentatorubral-pallidoluysian atrophy

depression

developmental disability

developmental retardation

diabetes mellitus

diagnostic criteria

differential diagnosis

disease modifying agents

distal muscle atrophy

dyskinesia, buccal lingual facial

dyskinesia, causes of

dyskinesia, drug induced

dysphagia

dysphasia

dyssynergia cerebellaris myoclonica

dystonia

dystonia musculorum deformens

dystonia, cervical

dystonia, face

dystonia, paroxysmal

dystonia, treatment of

dystonic reaction, acute

electroencephalogram, abnormalities of

epileptic encephalopathy

episodic neurologic deficits

eye movement, disorders of

fatal familial insomnia

gaze palsy, supranuclear

genetic diagnosis, prenatal

genetic linkage

genetic neurologic disorders

genetic screening

genetic testing

Gilles de la Tourette syndrome

gliosis

globus pallidus

globus pallidus, lesion of

globus pallidus, lesion of, bilateral

Hallervorden Spatz disease

hepatolenticular degeneration(Wilson's disease)

hepatomegaly

hepatosplenomegaly

heralding manifestation

huntingtin

Huntington's chorea

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

inborn errors of metabolism

incoordination

infantile bilateral striatal necrosis

insight, loss

insomnia

intellectual deficit

intellectual deterioration

internet

iron, brain

Jakob-Creutzfeldt disease

jaundice

karyotyping

Kayser-Fleischer ring

lactic acidemia

lenticular nucleus, lesion of, bilateral

lipid storage disorder of CNS

liver disease

liver function enzymes

liver transplantation

lymphocyte capping, diminished

lymphoma

lysosomal storage disease

manic-depressive

McLeod syndrome

memory, defect of recent

memory, impairment of

meningitis, carcinomatous

mental retardation

mental status, abnormal

metabolic disorder, primary

microcephaly

middle cerebellar peduncle, lesion

middle cerebellar peduncle, lesion, bilateral

Minamata disease

misdiagnosis

mitochondrial disease

movement disorder, extrapyramidal

movement disorder, hyperkinetic

movement disorder, paroxysmal

movement disorder, treatment of

MRI

MRI, abnormal

MRI, eye of tiger sign

MRI, FLAIR

MRI, gradient-echo

MRI, paramagnetic effect

MRI, susceptibility weighted

multiple system atrophy

muscle stiffness

muscle weakness

muscular dystrophy

muscular dystrophy, Duchenne

neoplasm, primary intracranial

neoplasm, primary of CNS

neurocutaneous disease

neurodegeneration with brain iron accumulation

neurologic disease, diagnoses of

neurologic history

neurologic testing

neuronal migration disorder

neuronopathy, sensory

neuropathology

neuropathology, brain

neuropathy

neuropathy, amyloid

neuropathy, peripheral

neurotoxin

neurotransmitter

next-generation sequencing

Niemann-Pick disease

nystagmus

nystagmus, gaze-evoked

nystagmus, monocular

ocular motility, disorders of

old age, neurology of

opened mouth

ophthalmoplegia

optic atrophy

optokinetic nystagmus, abnormal

Parkinson disease, dystonia with

Parkinsonism syndrome

paroxysmal dystonic choreoathetosis

paroxysmal hemiplegia

paroxysmal kinesigenic dyskinesia

paroxysmal neurologic deficits

photosensitivity, skin

poison, mercury

poison, neurologic problems with

POLG1 gene

polymerase chain reaction

pons, atrophy

pontocerebellar atrophy

precipitating factors

prevention of neurologic disorders

prion disease

progeria

prognosis

progressive neurologic disorder

progressive pallidum atrophy

psychiatric disorder

psychiatric problems in neurologic disorders

psychomotor retardation

psychosis

putamen, lesion of

pyramidal tract

pyramidal tract dysfunction

quadriplegia

radiation hypersensitivity

rapid onset dystonia parkinsonism

rapidly progressing neurologic illness

salivation, excessive

seizure, stimulus sensitive

self-mutilation

sensorineural hearing loss

short stature

single photon emission computed tomography

skin, lesions in neurologic disorders

sleep pathology and physiology

slit lamp examination

spasticity

speech disorder

speech disorder, childhood

spinal muscular atrophy

spinocerebellar ataxia

spinocerebellar ataxia type 1

spinocerebellar ataxia type 16

spinocerebellar degeneration

striatum, lesion of, bilateral

striopallidodentate calcifications, familial idiopathic

thalamus, lesion of-bilateral

toxins, nervous system

transient neurologic deficit

treatment of neurologic disorder

tremor

tremor, wing beating

trinucleotide repeats

urea-cycle enzymopathies

uric acid, low

visual evoked response

walking, difficulty with

X-linked bulbospinal neuronopathy

Showing articles 1750 to 1800 of 2019 << Previous Next >>

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

Diagnosis & Treatment, Physiologic & Pathologic Tremors
Ann Int Med 93:460-465, Jankovic,J.,et al, 1980

Metoprolol in Essential Tremor
Arch Neurol 37:596-597, Newman,R.R.,et al, 1980

Lafora Disease:Diagnosis by Liver Biopsy
Ann Neurol 8:409-415, Nishimura,R.N.,et al, 1980

Chorea Gravidarum, Report of a Fatal Case With Neuro-pathological Observations
Arch Neurol 37:429-432, Ichikawa,K.,et al, 1980

Evidence For & Against the Transmissibility of Alzheimer Disease
Neurol 30:945-950, Goudsmit,J.,et al, 1980

Presenile Alzheimer Disease:Amyloid Plaques in the Cerebellum
Neurol 30:820-825, Pro,J.D.,et al, 1980

Generalized Chorea Associated with Chronic Subdural Hematomas
Ann Neurol 8:449-450, Bae,S.H.,et al, 1980

Abetalipoproteinemia, Report of Two Cases & Review of Therapy
Arch Neurol 37:659-662, Illingworth,D.R.,et al, 1980

An Autosomal Dominant Syndrome of Hemiplegic Migraine, Nystagmus, & Tremor
Ann Neurol 8:329-332, Zifkin,B.,et al, 1980

Congenital Myotonic Dystrophy
Arch Neurol 37:693-696, Argov,Z.,et al, 1980

Cylindrical Spirals in a Familial Neuromuscular Disorder
Ann Neurol 7:550-556, Bove,K.E.,et al, 1980

Osteopetrosis, Renal Tubular Acidosis & Basal Ganglia Calcification in Three Sisters
Am J Med 69:64-74, Whythe,M.P.,et al, 1980

Progressive Supranuclear Palsy & Hyperkalemic Periodic Paralysis
Arch Neurol 37:461-462, Foster,N.L.,et al, 1980

Leber's Optic Neuropathy
Editorial, BMJ 280:1097-10981980., , 1980

Amelioration Of Neurologic Abnormalities After"Enzyme Replacement"In Adenosine Deaminase Deficiency
NEJM 303:377-380, Hirschhorn,R.,et al, 1980

Perinatal Neuropathy as an Early Manifestation of Krabbe's Disease
Arch Neurol 37:446-447, Lieberman,J.S.,et al, 1980

Heterozygous Expression Of X-Linked Mental Retardation & X-chromosome Marker fra (X) (q27)
NEJM 303:662-664, Turner,G.,et al, 1980

Computed tomography in Hallervorden-Spatz disease
Neurol 30:1128-1130, Dooling,E.C.,et al, 1980

Enlarged Cerebral Ventricular System in Infant Achondroplastic Dwarf
Neurol 30:767-769, Mueller,S.M., 1980

Peripheral Neuropathy in the Cherry-Red Spot-Myoclonus Syndrome (Sialidosis Type I)
Ann Neurol 7:450-456, Steinman,L.,et al, 1980

Myotonic Dystrophy
In Harrison's Principles of Internal Medicine, 9th Ed, McGraw-Hill Book Co, NY 206180., Adams,R.D.,et al, 1980

Paroxysmal Choreoathetosis Associated with Thyrotoxicosis
Ann Neurol 6:453-454, Fischblek,K.H.,et al, 1979

A Form of Chorea That Responds to Dantrolene Sodium
Neurol 29:163l-1632, Feit,H., 1979

Chorea Induced by Oral Contraceptives
Neurol 29:1605-1609, Nausieda,A.,et al, 1979

Prenatal Genetic Diagnosis in 3000 Amniocenteses
NEJM 300:157-163, Golbus,M.S.,et al, 1979

Clinical & Biochemical Aspects of Trichopoliodystrophy
Ann Neurol 5:65-71, Grover,W.D.,et al, 1979

CT Scans in Menkes Disease
Neurol 29:304-312, Seay,A.R.,et al, 1979

Fusiform Basilar Artery Aneurysm in a Child
Neurol 29:1045-1049, Read,D.,et al, 1979

Familial Arteriovenous Malformation
Ann Neurol 5:585-587, Snead,O.C.III.,et al, 1979

Famillial Carpal Tunnel Syndrome
Arch Neurol 36:727, Massey,E.W., 1979

Gyrate Atrophy of the Choroid & Retina with Hyperornithinemia:Tubular Aggreg. & Type 2 Fiber Atrophy
Neurol 29:966, Sipila,I.,et al, 1979

Familial Tapetorentinal Degeneration & Epilepsy
Arch Neurol 36:544-546, Cohan,S.L.,et al, 1979

Chronic Progressive Myelopathy:Investigation with CSF Electrophoresis, Evoked Potentials, & CT Scan
Ann Neurol 6:419-424, Patty,D.W.,et al, 1979

Hereditary Myoclonus & Progressive Distal Muscular Atrophy
Ann Neurol 6:227-231, Jankovic,J.,et al, 1979

Familial Fatal Parkinsonism with Alveolar Hypoventilation & Mental Depression
Ann Neurol 6:523-531, Purdy,A.,et al, 1979

Abnormalties In Cultured Muscle & Periphral Nerve Of A Patient With Adrenomyeloneuropathy
NEJM 301:588-590, Askanas,V.,et al, 1979

Peripheral Neuropathy in Cerebrotendinous Xanthomatosis
Neurol 29:880-881, Kuritzky,A.,et al, 1979

Studies in Aging of the Brain:IV. Familial Alzheimer Dis. :Relat. to Transmiss. Demetia, Aneuploidy, & Microtubular Defects
Neurol 29:1402, Book,R.H.,et al, 1979

Familial Tourette Syndrome
Ann Neurol 5:104, Guggenheim,M.A., 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

Progressive Myelopathy Due to Extramedullary Hematopoiesis:Case Report & Review of the Literature
Ann Neurol 5:485-489, Stahl,S.M.,et al, 1979

Postvaccinial Encephalomyelitis Without Cutaneous Vaccination Reaction
Ann Neurol 5:99-101, Rockoff,A.,et al, 1979

Marfan Syndrome
NEJM 300:772-777, Pyeritz,R.E.,et al, 1979

Metopropol For Essential Tremor
NEJM 301:331, Britt,C.W.Jr.,et al, 1979

Treatment Of Essential Tremor With Metopropol
NEJM 301:1005, Ljung,O., 1979

Familial Periodic Ataxia
Arch Neurol 36:568-569, Donat,J.R.,et al, 1979

Chorea:A Late Complication of a Subdural Hematoma
Neurol 29:1044-1045, Gilmore,P.C.,et al, 1979

Marfan's Syndrome
NEJM 301:273, Barr,M., 1979

Showing articles 1750 to 1800 of 2019 << Previous Next >>