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 900 to 950 of 2019 << Previous Next >>

Delayed-Onset Progressive Movement Disorders after Static Brain Lesions
Neurol 46:68-74, Scott,B.L.,et al, 1996

Apolipoprotein E Genotype in Patients with Alzheimer's Disease:Implications for Risk of Dementia Among Relatives
Ann Neurol 38:797-808, Farrer,L.A.,et al, 1995

Hereditary Hemorrhagic Telangiectasia
NEJM 333:918-924, Guttmacher,A.E.,et al, 1995

Screening Family Members of Patients with Hereditary Hemorrhagic Telangiectasia
Am J Med 99:519-524, Haitjema,T.,et al, 1995

Adult-Onset Spinocerebellar Dysfunction Caused by a Mutation in the Gene for the a-Tocopherol-Transfer Protein
NEJM 333:1313-1318, 13511995., Gotoda,T.,et al, 1995

Cerebrovascular Complications in Ehlers-Danlos Syndrome Type IV
Ann Neurol 38:960-964, North,K.N.,et al, 1995

Familial Acephalgic Migraine
Neurol 45:2293-2294, Ziegler,D.K., 1995

Clinical Significance of Fetal Choroid Plexus Cysts
Lancet 346:724-729, Gupta,J.K.,et al, 1995

Spinocerebellar Ataxias and Ataxins
NEJM 333:1351-1353, Rosenberg,R.N., 1995

Familial Aorto-Cervicocephalic Arterial Dissections and Congenitally Bicuspid Aortic Valve
Stroke 26:1935-1940, Schievink,W.I.&Mokri,B., 1995

Familial Subarachnoid Hemorrhage:Distinctive Features and Patterns of Inheritance
Ann Neurol 38:929-934, Bromberg,J.E.C.,et al, 1995

Postoperative Neurologic Complications after Open Heart Surgery on Young Infants
Arch Pediatr Adolesc Med 149:764-768, Miller,G.,et al, 1995

Autosomal Dominant, Familial Spastic Paraplegia, Type I:Clinical and Genetic Analysis of a Large North American Family
Neurol 45:325-331, Fink,J.K.,et al, 1995

Charcot-Marie-Tooth Neuropathies:From Clinical Description to Molecular Genetics
Muscle & Nerve 18:267-275995., Ionasecu,V.V., 1995

Parkinsonism-Recognition and Differential Diagnosis
BMJ 310:447-452, Quinn,N., 1995

Familial Autoimmune Myasthenia Gravis:Report of Four Families
JNNP 58:729-731, Evoli,A.,et al, 1995

Genotype-Phenotype Correlation in Adult-Onset Acid Maltase Deficiency
Ann Neurol 38:450-454, Wokke,J.H.J.,et al, 1995

Clinical Variability in Adult-Onset Acid Maltase Deficiency:Report of Affected Sibs and Review of Literature
Medicine 74:131-135, Felice,K.J.,et al, 1995

Kindreds of Dominantly Inherited Parkinson's Disease:Keys to the Riddle
Ann Neurol 38:355-356, Duvoisin,R.C.&Golbe,L.I., 1995

A Greek-American Kindred with Autosomal Dominant, Levodopa-Responsive Parkinsonism and Anticipation
Ann Neurol 38:373-378, 3551995., Markopoulou,K.,et al, 1995

Combined System Disease after Nitrous Oxide Anesthesia:A Case Report
Neurol 45:1224-1225, McMorrow,A.M.,et al, 1995

Hereditary Sensory and Autonomic Neuropathy with Cataracts, Mental Retardation, and Skin Lesions:Five Cases
Neurol 45:1405-1408, Heckmann,J.M.,et al, 1995

Predictors of Neonatal Encephalopathy in Full Term Infants
BMJ 331:598-602, Adamson,S.J.,et al, 1995

X-Linked Pure Familial Spastic Paraparesis
Arch Neurol 52:665-669, Cambi,F.,et al, 1995

Rapid Antibody Test for Fragile X Syndrome
Lancet 345:1147-1148, Willemsen,R.,et al, 1995

Juvenile Huntington Disease:CT and MR Features
AJNR 16:1405-1412, Ho,V.B.,et al, 1995

Panic Attacks and Panic Disorder:The Great Neurologic Imposters
Semin Neurol 15:126-132, Stahl,S.M.&Soefje,S., 1995

Involuntary Movement Disorders Associated with Felbamate
Neurol 45:185-187, Kerrick,J.M.,et al, 1995

Clinical, Neuropath & Genetic Studies of Large Spinocerebellar Ataxia Type 1 (SCA1) Kindred: (CAG) n Early Premonitory Signs & Symp
Neurol 45:24-30, Genis,D.,et al, 1995

Autosomal Dominant Cerebellar Phenotypes:The Genotype has Settled the Issue
Neurol 45:1-5, Rosenberg,R.N., 1995

Intracranial Aneurysms:MR Angiographic Screening in 400 Asymptomatic Individuals with Increased Familial Risk
Radiology 195:35-40, Ronkainen,A.,et al, 1995

Familial Occurrence of Cluster Headache
JNNP 58:341-343, Russell,M.B.,et al, 1995

Proximal Myotonic Myopathy, Clin Features of Disorder Similar to Myotonic Dystrophy
Arch Neurol 52:25-31, Ricker,K.,et al, 1995

Outcome in Familial Subarachnoid Hemorrhage
Stroke 26:961-963, Bromberg,J.E.C.,et al, 1995

Autosomal Dominant Migraine with MRI White-Matter Abnormalities Mapping to the CADASIL Locus
Neurol 45:1086-1091, Chabriat,H.,et al, 1995

Ischemic Stroke in Young Pts with Activated Protein C Resistance:Rpt of Three Cases Belonging to Three Different Kindreds
Stroke 26:885-890, Simioni,P.,et al, 1995

Correlations Between Triplet Repeat Expansion and Clinical Features in Huntington's Disease
Arch Neurol 113:749-753, Claes,S.,et al, 1995

Levorotatory Form of 5-Hydroxytryptophan in Friedreich's Ataxia
Arch Neurol 52:456-460, Trouillas,P.,et al, 1995

Double-Blind Study with Levorotatory form of Hydroxytryptophan in Pts with Degen Cerebellar Dis
Arch Neurol 52:451-455, 4401995., Wessel,K.,et al, 1995

Botulinum Toxin Treatment of Essential Head Tremor
Neurol 45:822-824, Pahwa,R.,et al, 1995

The Effect of Nimodipine on Essential Tremor
Neurol 45:1523-1525, Biary,N.,et al, 1995

Clinical and Genetic Studies of Fatal Familial Insomnia
Neurol 45:1068-1075, Reder,A.T.,et al, 1995

Tourette's Syndrome:A Model Neuropsychiatric Disorder
JAMA 273:498-501, Hyde,T.M.&Weinberger,D.R., 1995

A Gene for Hereditary Paroxysmal Cerebellar Ataxia Maps to Chromosome 19p
Ann Neurol 37:289-293, 2851995., Vahedi,K.,et al, 1995

Familial Cerebral Cavernous Angiomas:Clinical and Radiologic Studies
Neurol 45:492-497, Kattapong,V.J.,et al, 1995

Subarachnoid Hemorrhage and Family History:A Population-Based Case-Control Study
Arch Neurol 52:202-204, Wang,P.S.,et al, 1995

A Positron Emission Tomography Study of Cerebral Activation Associated with Essential and Writing Tremor
Arch Neurol 52:299-305, Wills,A.J.,et al, 1995

Hereditary Leukoencephalopathy and Palmoplantar Keratoderma:A New Disorder with Increased Skin Collagen Content
Neurol 45:331-337, Lossos,A.,et al, 1995

Gene Analysis of L1 Neural Cell Adhesion Molecule in Prenatal Diagnosis of Hydrocephalus
Lancet 345:161-162, Jouet,M.&Kenwrick,S., 1995

Postvaricella Basal Ganglia Infarction in Children
AJNR 16:449-452, Silverstein,F.S.&Brunberg,J.A., 1995

Showing articles 900 to 950 of 2019 << Previous Next >>