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 1700 to 1750 of 2019 << Previous Next >>

Optic Neuritis in Familial MS
Neurol 31:1138-1142, Ebers,G.C.,et al, 1981

Pathogenesis of Pseudotumor Cerebri Syndromes
Neurol 31:877-880, Donaldson,J.O., 1981

Primary Empty Sella & Rieger's Anomaly Of The Anterior Chamber Of The Eye
NEJM 304:90-93, Kleinmann,R.E.,et al, 1981

Twin Study of Parkinson Disease
Neurol 31:77-80, Duvoisin,R.C.,et al, 1981

Familial Recurrent Peripheral Facial Palsy
Arch Neurol 38:463-464, Auerbach,S.H.,et al, 1981

Ataxia with Aniridia of Gillespie:A Case Report
Neurol 31:95-97, Lechtenberg,R.,et al, 1981

Von Recklinghausen Neurofibromatosis
NEJM 305:1617-1627, Riccardi,V.M., 1981

Dominant Inheritance of Intracranial Berry Aneurysm
BMJ 283:824-825, Evans,T.W.,et al, 1981

Benign Familial Tremor Treated with Primidone
BMJ 282:178-180, O'Brien,M.D.,et al, 1981

Blepharospasm & Oromandibular Dystonia (Meige's Syndrome) in Sisters
Ann Neurol 9:189-191, Nutt,J.G.,et al, 1981

Double-blind, Triple-crossover Trial of Low Doses of Oral Physostigmine in Inherited Ataxias
Neurol 31:288-292, Kark,R.A.P.,et al, 1981

Progressive Pontobulbar Palsy With Deafness
Arch Neurol 38:186-190, Brucher,J.M.,et al, 1981

Familial Spastic Paraplg, Peroneal Neuropathy, & Crural Hypopig, A New Neurocut Synd
Neurol 31:754-757, Stewart,R.M.,et al, 1981

Biologic Distinction Between Sporadic & Familial Alzheimer Disease by an in vitro Cell Fusion Test
Neurol 31:323-325, Dubois-Moreau,M.C.,et al, 1981

Lipomembranous Polycystic Osteodysplasia with Progressive Dementia
J Comput Assist Tomogr 5:580-582, Laasonen,E.M.,et al, 1981

Cerebellar Atrophy Demonstrated by Computed Tomography
Neurol 31:405-412, Koller,W.C.,et al, 1981

Familial Arteriovenous Malformation of the Brain
Neurol 31:184-186, Aberfeld,D.C.,et al, 1981

The Adrenoleukomyeloneuropathy Complex:Expression in Four Generations
Neurol 31:151-156, O'Neill,B.P.,et al, 1981

Familial Association of Giant Cell Arteritis
Arch Int Med 141:115-117, Granato,J.E.,et al, 1981

Hemichorea-hemiballism & Lacunar Infarction in the Basal Ganglia
Neurol 31:452-455, Kase,C.S.,et al, 1981

Pemoline-induced Chorea
Neurol 31:356-360, Nausieda,P.A.,et al, 1981

Amyotrophic Lateral Sclerosis & its Association with Dementia, Parkinsonism & Other Neurological Disorders:A Review
Brain 104:217-247, Hudson,A.J., 1981

Benign Paroxysmal Torticollis in Infancy
Arch Dis Child 56:956-959, Deonna,T.,et al, 1981

Familial Hemiplegic Migraine:EEG & CT Scan Study of Two Cases
Ann Neurol 10:392-295, Gastaut,J.L.,et al, 1981

Placement Of Ventriculo-Amniotic Shunt For Hydrocephalus In A Fetus
NEJM 305:955, Clewell,W.H.,et al, 1981

Biochemical Genetics Of Neurologic Disease
NEJM 305:1181-1193, Rosenberg,R.N., 1981

Tetrabenazine & Movement Disorders
Neurol 31:1051-1054, Asher,S.W., 1981

Neurologic Complications of Hyperthyroidism
Arch Neurol 38:669-670, Bulens,C., 1981

A Family Affected with Intestinal Polyposis & Gliomas
Ann Neurol 10:390-392, Todd,D.W.,et al, 1981

Intensive Evaluation of Referred Unclassified Neuropathies Yields Improved Diagnosis
Ann Neurol 10:222-226, Dyck,P.J.,et al, 1981

Bilateral Vocal Cord Paralysis in a Patient With Familial Hypertrophic Neuropathy
Arch Neurol 38:532, Johnson,J.A.,et al, 1981

Valproic Acid in Sydenham's Chorea
BMJ 283:274-275, McLachlam,R.S., 1981

Pattern Reversal Visual Evoked Potentials
Arch Neurol 38:739-741, Bird,T.D.,et al, 1981

Successful Treatment of Paramyotonia Congenita (Eulenburg) Muscle Stiffness & Weakness Prevented by Tocainide
JNNP 43:268-271, Ricker,K.,et al, 1980

Familial Trigeminal Neuralgia
Arch Neurol 37:285-286, Herzberg,L., 1980

Dejerine-Sottas Disease Revisited
Arch Neurol 37:67-68, Stran,R., 1980

Sydenham Chorea:An Update
Neurol 30:331-334, Nausieda,P.A.,et al, 1980

Multiple Vertebral Hemangiomas Resembling Metastases with Spinal Cord Compression
Arch Neurol 37:247-248, Zito,G.,et al, 1980

Benign Familial Neonatal Seizures
E. , Arch Neurol 37:47-48980., Pettit,R., 1980

Agenesis of the Corpus Callosum
Arch Neurol 37:444-445, Lynn,R.B.,et al, 1980

Use of Adrenal Biopsy in Diagnosing Adreno-leukomyeloneuropathy
Arch Neurol 37:634-636, Weiss,G.M.,et al, 1980

Adrenoleukodystrophy. Report of Two Cases With Relapsing & Remitting Courses
Arch Neurol 37:448-450, Walsh,R., 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

Choreic Movements Induced by the Use of Methadone
Arch Neurol 37:727-728, Wasserman,S.,et al, 1980

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

Neurological Disease In Ex-Far-East Prisoners Of War
Lancet 2:135-137, Gibberd,F.B.,et al, 1980

A Family with Hereditary Ataxia:HLA Typing
Neurol 30:12-20, Nino,H.E.,et al, 1980

Clinical Criteria for Diagnosis of Machado-Joseph Disease:Report of a Non-Azorean Portuguese Family
Neurol 30:319-322, Lima,L.,et al, 1980

Juvenile Metachromatic Leukodystrophy
Arch Neurol 37:42-46, Haltia,T.,et al, 1980

Familial Stroke Syndrome Associated with Mitral Valve Prolapse
Ann Neurol 7:130-134, Rice,G.P.A.,et al, 1980

Showing articles 1700 to 1750 of 2019 << Previous Next >>