Neudle.com: chorea familial

Differential
(Click to cross reference)

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 1850 to 1900 of 2019 << Previous Next >>

Autosomal Dominant Neurological Disorders
Ann Neurol 4:548-552, Brady,R.O.,et al, 1978

Hereditary Paroxysmal Ataxia:Response to Acetazolamide
Neurol 28:1259-1264, Griggs,R.C.,et al, 1978

Clinical Pathological Conference, Reticulum Cell Sarcoma of Brain
NEJM 299:1349-1359, Case Record 49-1978,Mass.Gen.Hosp., 1978

Phenyton & Choreic Movements
NEJM 298:1093, Nausieda,P.A.,et al, 1978

Malignant Hyperthermia & Central Core Disease in a Child with Congenital Dislocating Hips
Arch Neurol 35:189, Eng,G.D.,et al, 1978

Pseudoxanthoma Elasticum:A Review of Neurological Complications
Ann Neurol 4:18, Iqbal,A.,et al, 1978

Clinical pathological conference
Von Hippel-Lindau disease, Case Record 1-1978, NEJM 298:95978., , 1978

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

Aggravation of Tardive Dyskinesia by Phenytoin
NEJM 298:457, DeVeaugh-Geiss,J., 1978

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

Autosomal Dominant System Degeneration in Portugese Families of the Azores Islands
Neurol 28:703, Coutinho,P.,et al, 1978

Clinical Aspects of Spasmodic Dysphonia
JNNP 41:361, Aminoff,M.J.,et al, 1978

Cervical Myelopathy Due to Ossification of the Posterior Longitudinal Ligament
Arch Neurol 35:33, Murakami,N., 1978

Late Adult-onset Metachromatic Leukodystrophy
Arch Neurol 35:475, Bosch,E.P., 1978

Familial Vascular Malformation or Chance Occurrence
Neurol 28:98, Barre,R.G.,et al, 1978

Supratentorial Leptomeningeal Hemangioblastoma
Neurol 28:727, Lee,K.R.,et al, 1978

Transient Spastic Paraparesis Following Abdominal Aortography:Management with Cerebrospinal Fluid Lavage
Ann Neurol 3:185, Morariu,M.A., 1978

Blue Rubber Bleb Nevus Syndrome with CNS Involvement & Thrombosis of a Vein of Galen Malformation
Ann Neurol 3:464, Waybright,E.A.,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

Extreme Insulin Resistance in Ataxia Telangiectasia
NEJM 298:1164, Bar,R.S.,et al, 1978

Clinical Syndromes of Myasthenia in Infancy & Childhood
Arch Neurol 35:97, Fenichel,G.M., 1978

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

Corticosteroids in the Treatment of Sydenham's Chorea
Arch Neurol 35:53, Green,L.N., 1978

Globoid cells, Glial nodules, & Peculiar Fibrillary Changes in the cerebro-hepato-renal Syndrome of Zellweger
Ann Neurol 2:473, deLeon,G.A.,et al, 1977

CT Scanning & Diagnosis of Adrenoleukodystrophy
Neurol 27:884, Greenberg,H.S.,et al, 1977

Spinal Cord Compression Due to Pseudomonas in a Heroin Addict
Neurol 27:1034, Jabbari,B.,et al, 1977

Nerve Growth Factor (three parts)
NEJM 297:1096, 1149, 1211977., Mobley,W.C.,et al, 1977

Spinal Cord Compression in Thalassaemia
JNNP 40:1120 1977., Cross,J.N.,et al, 1977

The Central Nervous System in a Case of Neurolathyrism
Neurol 27:1176, Striefler,M.,et al, 1977

CNS Lesions in Cystinuria
Arch Neurol 34:638, Blackburn,C.R.B.,et al, 1977

Reversible Corticospinal Tract Disease Due to Hyperthyrodisim
Arch Neurol 34:647, Garcia,C.A.,et al, 1977

Neuroectodermal Tumors in the Cerebellum in Two Sisters
JNNP 40:886, Thomas,M.,et al, 1977

Clinical Neurogenetics
Neurol 27:1057, Bird,T.D.,et al, 1977

Neurologic Manifestations in Sarcoidosis
Ann Int Med 87:336, Delaney,P., 1977

Prenatal Diagnosis of Duchenne's Muscular Dystrophy
NEJM 297:968, Mahoney,M.J.,et al, 1977

X-linked Muscular Dystrophy
Ann Neurol 2:414, Furukawa,T.,et al, 1977

Chronic Hexosaminidase A & B Deficiency
et al. , Ann Neurol 2:156977., Goldie,W.D., 1977

Juvenile Diabetes Mellitus & Optic Atrophy
Arch Neurol 34:759, Lessell,S.,et al, 1977

An unusual Cause of Apparent Epilepsy:ECG & EEG Findings in a Case of Jervell Lange-Neilson Syndrome
JNNP 40:1102, Selby,P.J.,et al, 1977

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

Paroxysmal Choreoathetosis Following Head Injury
Ann Neurol 2:447, Robin,J.J., 1977

Paroxysmal Choreoathetosis as a Presenting Symptom in Idiopathic Hypoparathyroidism
JNNP 40:692, Soffer,D.,et al, 1977

Duane Syndrome & Congential Upper-Limb Anomalies:A Familial Occurrence
Arch Neurol 34:174, Okihiro,M.M.,et al, 1977

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

Cervical Myelographic Changes in Hypertrophic Interstitial Polyneuropathy
Ann Neurol 2:83, Hammerschlag,S.B.,et al, 1977

Spinal Cord Involvement by C4-C5 Vertebral Subluxation in Rheumatoid Arthritis:A Description of Two Cases Examined at Necropsy
Ann Neurol 1:575, Hughes,J.T., 1977

Neurologic Aspects of Hereditary Hemorrhagic Telangiectasia
Arch Neurol 34:101, Adams,H.P.,et al, 1977

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

Showing articles 1850 to 1900 of 2019 << Previous Next >>