Neudle.com: SCA

Differential
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acanthocytosis

acetylcholine

acoustic neurinoma, bilateral

adrenoleukodystrophy

advances in neurology

adverse drug reaction

albinism

alcohol intolerance

alcohol, neurologic complications with

algorithm

alpha-fetoprotein

alternating rapid movement

Alzheimer's disease

amantadine

aminoacidopathies

amyotrophic lateral sclerosis

anemia

antibodies to voltage-gated calcium channels

anticholinesterase

anticonvulsants

anticonvulsants, selection of

antioxidant

apraxia of eye movements

areflexia

Arnold Chiari malformation

arrhythmia, cardiac

asymptomatic

ataxia

ataxia telangiectasia

ataxic-dystonia syndromes

ataxin

ataxin-2

atypical

auditory evoked brainstem potentials

autonomic dysfunction

Babinski sign

baclofen

bacterial infection

basal ganglia, degeneration

Bassen-Kornzweig syndrome

benign essential tremor

biologic markers

blindness

blood dyscrasias, neurologic findings with

calcium channel dysfunction

carcinoembryonic antigen

CAT scan, emission, abnormal

cataracts

celiac disease, adult

central core disease

cerebellar ataxia, autosomal recessive

cerebellar ataxia, children

cerebellar ataxia, children, differential diagnosis of

cerebellar ataxia, hereditary

cerebellar ataxia, primary

cerebellar atrophy, primary

cerebellar atrophy, secondary

cerebellar degeneration

cerebellar vermis

cerebral cortical atrophy

cerebral glucose metabolism

cerebro hepato renal syndrome

cerebrovascular accident

Chediak-Higashi syndrome

cherry red spot-myoclonus syndrome

children

chloride channel dysfunction

choking

chorea

choreoathetosis

chromosomal abnormality

Clinical Pathologic Conference(C.P.C.)

clonus

clubfoot as related to neurologic disease

congestive heart failure

consanguinity

controversies in neurology

conversion reaction

copper deficiency

cornea, abnormal

cranio-cervical junction

creatine phosphokinase(CPK)elevated

Cuba

cystic fibrosis, neurologic complications with

deafmute

deafness

deep tendon reflexes

degenerative diseases of CNS

delay in diagnosis

dementia

dentate nuclei, lesion of

dentatorubral-pallidoluysian atrophy

depression

dexterity, impaired

diabetes mellitus

diabetes mellitus, chemical

dilantin

diplopia

disability, neurological

distal muscle atrophy

DNA probes

down-beat nystagmus

down-beat nystagmus, primary position of gaze

drooling

drug induced neurologic disorders

electrocardiogram, abnormal

electrocardiogram, LVH

electroencephalogram, abnormalities of

electromyogram

electronystagmography

electronystagmography, abnormal

electroretinograph

endocardial fibrosis

enzyme, defect

epidemiology of neurology

episodic neurologic deficits

eye movement, disorders of

falling

familial

familial hemiplegic migraine

finger nose finger test

foot numbness

Fragile-X associated tremor/ataxia-syndrome

fragile-X syndrome

fragile-X syndrome, carrier

frataxin

Friedreich's ataxia

Friedreich's ataxia, late onset

fundus, abnormality of

gait disorder

gangliosidosis GM2

gargoylism

gastrectomy, neurologic complications following

gaze palsy

gaze palsy, supranuclear

genetic neurologic disorders

genetic screening

genetic testing

glaucoma

globus pallidus, lesion of

glutamate dehydrogenase deficiency

glutamic acid

glycogen storage disease

growth retardation

Guillain Barre syndrome

Hallervorden Spatz disease

hepatolenticular degeneration(Wilson's disease)

hexosaminidase-A and B

hydroxytryptophan L-5(L-5 HTP)

hyperreflexia

hypertonia

hypokalemic periodic paralysis

inclusion bodies, intracytopasmic

inclusion bodies, ubiquitin

incoordination

intellectual deficit

internuclear ophthalmoplegia

internuclear ophthalmoplegia, bilateral

intestinal lymphangiectasia

jaw jerk, abnormal

Kearns-Sayre syndrome

keratoconus

kyphoscoliosis, neurologic causes of

kyphosis

Lafora's disease

Laurence-Moon-Bardet-Biedl syndrome

L-dopa

lecithin

leg weakness, bilateral

lipid storage disorder of CNS

lipid storage myopathy

malabsorption syndrome

malformation, CNS, congenital

malignant hyperpyrexia

malondialdehyde

Marinesco-Sjogren syndrome

memory, impairment of

mental retardation

MERRF syndrome

metabolic disorder, primary

Mexican

middle cerebellar peduncle

middle cerebellar peduncle, lesion

mitochondrial disease

movement disorder, extrapyramidal

mucopolysaccharidoses

multiple sclerosis

multiple sclerosis, differential diagnosis of

multiple sclerosis, misdiagnosis

multiple system atrophy

muscle biopsy

muscle cramp

muscle weakness

muscle weakness, proximal

muscular dystrophy

muscular dystrophy, Becker

muscular dystrophy, cardiovascular changes with

muscular dystrophy, Duchenne

myopathy, mitochondrial

myopia

myotonia congenita

myotonia dystrophica

neoplasm, primary intracranial

neoplasm, primary of CNS

nerve conduction studies

neuritis

neurocutaneous disease

neuroendocrinology

neurologic disease

neurologic disease, diagnoses of

neurologic signs

neuronal ceroid-lipofuscinosis

neuronal migration disorder

neuropathy, hereditary peripheral

neuropathy, peripheral

nystagmus, primary position of gaze

nystagmus, upbeating-in primary position of gaze

nystagmus, vertical

obesity

ocular motility, disorders of

ocular myopathy

old age, neurology of

ophthalmoplegia

ophthalmoplegia, progressive external

optic atrophy

optic nerve

optic neuropathy

optical coherence tomography

orbit, tomograms of

orthostatic hypotension

pain

pain, management of chronic

palatal myoclonus

pancytopenia

paramyotonia congenita

paraparesis, familial spastic

Parkinson disease

Parkinson disease, familial

Parkinsonism multiple-system atrophy

Parkinsonism syndrome

paroxysmal neurologic deficits

pigmentary retinopathy

polydactyly

polymerase chain reaction

polymyositis

polyneuropathy

pons, atrophy

pontocerebellar atrophy

posterior column disease

potassium channel antibodies

potassium channel dysfunction

prevention of neurologic disorders

progeria

prognosis

progressive myoclonic epilepsy

progressive neurologic disorder

proprioception, abnormal

pseudobulbar palsy

pseudoretinitis pigmentosa

psychiatric disorder

psychiatric problems in neurologic disorders

psychological testing

psychological testing, neurologic problems

Purkinje cell

putamen, lesion of

putamen, lesion of, bilateral

pyramidal tract

pyramidal tract dysfunction

radiation hypersensitivity

remote effect of cancer on the nervous system

saccadic eye movements, abnormal

seizure, treatment of

sensorineural hearing loss

skew deviation, alternating

skin, biopsy

skin, lesions in neurologic disorders

sleep apnea

sleep pathology and physiology

sodium channel dysfunction

spastic ataxia

spasticity

sphingolipodoses

Spielmeyer Vogt syndrome

spinal cord, cervical

spinal cord, lesion of

spinal cord, neoplasm

spinal cord, neoplasm, intramedullary

spinal muscular atrophy

spinocerebellar ataxia

spinocerebellar ataxia type 1

spinocerebellar ataxia type 10

spinocerebellar ataxia type 12

spinocerebellar ataxia type 14

spinocerebellar ataxia type 16

spinocerebellar ataxia type 17

spinocerebellar ataxia type 2

spinocerebellar ataxia type 28

spinocerebellar ataxia type 3/Machado Joseph disease

spinocerebellar ataxia type 5

spinocerebellar ataxia type 6

spinocerebellar ataxia type 7

spinocerebellar ataxia type 8

spinocerebellar degeneration

spinopontine atrophy, dominant

staggering

steatorrhea

striatonigral degeneration

syphilis, neurologic complications with

tandem gait, ataxic

tapetoretinal degeneration

telangiectases

thalamus

thyrotropin-releasing hormone

tinnitus

trazodone

treatment of neurologic disorder

tremor

tremor, cerebellar

tremor, intention

trimethoprim-sulfamethoxazole

trinucleotide repeats

Unverricht-Lundborg disease

vibratory sensation, abnormal

visual acuity, decreased

visual evoked response

visual field defect

visual fields, constricted

visual loss

visual loss, progressive

vitamin supplementation

Von Hippel Lindau

walking, difficulty with

X-linked bulbospinal neuronopathy

Showing articles 50 to 100 of 159 << Previous Next >>

Progressive Atrophy of Cerebellum & Brainstem, Age & Size of Expanded CAG Repeats in the MJDI Gene in Machado-Joseph Dis
Ann Neurol 43:288-296, Onokera,O.,et al, 1998

Friedreich's Ataxia GAA Repeat Expansion in Pts with Recessive or sporadic Ataxia
Neurol 49:1004-1009, Geschwind,D.H.,et al, 1997

Broadened Friedreich's Ataxia Phenotype after Gene Cloning, Minimal GAA Expan Causes Late Spastic Ataxia
Neurol 49:1617-1620, Ragno,M.,et al, 1997

Atrophy of Cerebellum & Brainstem in Dentatorubral Pallidoluysian Atrophy, CAG Repeat Size on MRI Findings
Neurol 49:1605-1612, Koide,R.,et al, 1997

Multiple-System Atrophy is Genet Distinct from Ident Inherited Causes of Spinocerebellar Degen
Neurol 49:1598-1604, Brandmann,O.,et al, 1997

Machado-Joseph Disease in 4 Chinese Pedigrees:Molecular Analysis of 15 Pts
Neurol 48:482-485, Zhou,Y.X.,et al, 1997

Phenotypic Variability in Friedreich Ataxia:Role of the Associated GAA Triplet Repeat Expansion
Ann Neurol 41:675-682, Montermini,L.,et al, 1997

Frataxin Gene of Friedreich's Ataxia is Targeted to Mitochondria
Ann Neurol 42:265-269, Priller,J.,et al, 1997

Calcium Channels in Neurological Disease
Ann Neurol 42:275-282, Greenberg,D.A., 1997

The Expansion of the CAG Repeat in Ataxin-2 is a Frequent Cause of Autosomal Dominant Spinocerebellar Ataxia
Neurol 49:1009-1013, Lorenzetti,D.,et al, 1997

Spinocerebellar Ataxia Type 6, Molecular & Clin Features of 35 Japanese Pts (1 Homozygous for CAG Repeat Expan)
Neurol 49:1238-1243, 11961997., Matsumura,R.,et al, 1997

Clinical and Molecular Features of Spinocerebellar Ataxia Type 6
Neurol 49:1243-1246, 11961997., Stevanin,G.,et al, 1997

Spinocerebellar Ataxia Type 6, Frequency of the Mutation & Genotype-Phenotype Correl
NEurol 49:1247-1251, Geschwind,D.H.,et al, 1997

Age on Onset, Sex, & Cardiomyopathy as Predictors of Disability and Survival in Friedreich's Disease
Neurol 47:1260-1264, DeMichele,G.,et al, 1996

Clinical and Genetic Abnormalities in Patients with Friedreich's Ataxia
NEJM 335:1169-1175, 12221996., Durr,A.,et al, 1996

Isolated Vitamin E Deficiency
Muscle & Nerve 19:1161-1165996., Jackson,C.E.,et al, 1996

The Inherited Ataxias and the New Genetics
JNNP 61:327-332, Hammans,S.R., 1996

Machado Joseph Disease Maps to Same Region of Chromosome 14 as Spinocerebellar Ataxia Type 3 Locus
J Med Genet 32:25-31, Twist,E.C.,et al, 1995

Clinicopathological Study of 35 Cases of Multiple System Atrophy
JNNP 58:160-166, Wenning,G.K.,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

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

Dentatorubral-Pallidoluysian Atrophy:Clin Features Closely Related to Unstable Expansion of Trinucleotide (CAG) Repeat
Ann Neurol 37:769-775, Ikeuchi,T.,et al, 1995

PET Studies on the Dopaminergic Sys & Striatal Opioid Binding in the OPCA Variant of Multiple System Atrophy
Ann Neurol 37:568-573, Rinne,J.O.,et al, 1995

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

Dopa-Responsive parkinsonism Phenotype of Machado-Jospeh Disease:Confirmation of 14q CAG Expansion
Ann Neurol 48:684-687, Tuite,P.J.,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

Structural and Functional Brain Imaging in Friedreich's Ataxia
Arch Neurol 51:349-355, Junck,L.,et al, 1994

Friedreich's Ataxia:MR Findings Involving the Cervical Portion of the Spinal Cord
AJR 163:187-191, Mascalchi,M.,et al, 1994

Trinucleotide Repeat Length and Rate of Progression of Huntington's Disease
Ann Neurol 36:630-635, Illarioshkin,S.N.,et al, 1994

Trinucleotide Repeat Expansion in Neurological Disease
Ann Neurol 36:814-822, LaSpada,A.R.,et al, 1994

Magnetic Resonance Imaging in Hereditary and Idiopathic Ataxia
Neurol 43:318-325, Wullner,U.,et al, 1993

Late-Onset Friedreich's Ataxia, Molecular Genetics, Clinical Neurophysiology, and Magnetic Resonance Imaging
Arch Neurol 50:803-806, Klockgether,T.,et al, 1993

The Neurologic Syndrome of Vitamin E Deficiency:A Significant Cause of Ataxia
Neurol 43:2167-2169, Kayden,H.J., 1993

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

Ataxia-Telangiectasia:An Interdisciplinary Approach to Pathogenesis
Medicine 70:99-117, Gatti,R.A.,et al, 1991

Presynaptic Parkinsonism in Olivopontocerebellar Atrophy:Clinical, pathological, and Neurochemical Evidence
Ann Neurol 30:425-428, Pascual,J.,et al, 1991

Olivopontocerebellar Atrophy:MR Diagnosis and Relationahip to Multisystem Atrophy
Radiology 174:693-696, Savoiardo,M.,et al, 1990

Idiopathic Cerebellar Ataxia of Late Onset:Natural History and MRI Morphology
JNNP 53:297-305, Klockgether,T.,et al, 1990

Neuropsychological Changes in Olivopontocerebellar Atrophy
Arch Neurol 47:997-1001, Berent,S.,et al, 1990

A Quantitative Evaluation of Pontine Volume by Computed Tomography in Patients with Cerebral Degeneration
Neurol 40:1241-1245, Chida,K.,et al, 1990

Cerebral Glucose Hypermetabolism in Friedreich's Ataxia Detected with Positron Emission Tomography
Ann Neurol 28:750-757, Gilman,S.,et al, 1990

Friedreich Ataxia
In Rowland, L. P. Merritt's Textbook of Neurology, 8th Ed, Lea & Febiger, Phila, Ch 13, p627, Rosenberg,R.N., 1989

Primary Progressive Cerebellar Ataxia
Neuroradiology 31:16-18, Bradac,G.B.,et al, 1989

Hereditary Dentatorubral-Pallidoluysian Atrophy:Clinical and Pathologic Variants in a Family
Neurol 38:1065-1070, Takahashi,H.,et al, 1988

Retinitis Pigmentosa
Surv Ophthalmol 33:137-177, Pagon,R.A., 1988

Effect of Sulfamethoxazole & Trimethoprim on Neurologic Dysfunction in a Patient with Joseph's Disease
Arch Neurol 45:210-213, Mello,K.A.&Abbott,B.P., 1988

Alternating Skew on Lateral Gaze (Bilateral Abducting Hypertropia)
Ann Neurol 23:190-192, Moster,M.L.,et al, 1988

Cerebellar & Brainstem Hypometabolism in Olivo-pontocerebellar Atrophy Detected with Positron Emission Tomography
Ann Neurol 23:223-230, Gilman,S.,et al, 1988

Showing articles 50 to 100 of 159 << Previous Next >>