Neudle.com: SCA

Differential
(Click to cross reference)

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 100 to 150 of 159 << Previous Next >>

Spinocerebellar Degeneration:Qualitative & Quantitative MR Analysis of Atrophy
J Comput Assist Tomogr 12:298-303, Nabatame,H.,et al, 1988

Sleep Apnea in Olivopontocerebellar Degeneration:Treatment with Trazodone
Ann Neurol 23:399-401, Salazar-Grueso,E.F.,et al, 1988

The Treatment of Friedreich's Ataxia with Amantadine Hydrochloride
Neurol 38:1478-1480, Peterson,P.L.,et al, 1988

Adult-Onset Spinocerebellar Syndrome with Idiopathic Vitamin E Deficiency
Ann Neurol 22:84-87, Yokota,T.,et al, 1987

Frequency of Cerebral Infarction in Patients with Inherited Neuromuscular Disease
Stroke 18:805-807, Biller,J.,et al, 1987

The Aetiology of Mirror Writing:A New Hypothesis
JNNP 50:1572-1578, Tashiro,K.,et al, 1987

Multiple Sclerosis, The Problem of Incorrect Diagnosis
Arch Neurol 43:578-583, Rudick,R.A.,et al, 1986

The Heart in Friedreich's Ataxia
Arch Neurol 43:189-192, Brumback,R.A.,et al, 1986

Vitamin E-Deficient Spinocerebellar Syndrome Due to Intestinal Lymphangiectasia
Neurol 36:554-556, Gutmann,L.,et al, 1986

Vitamin E Deficiency
Editorial, Lancet 1:423-4241986., , 1986

Tobacco Intolerance in Multiple System Atrophy
Neurol 36:986-988, Johnsen,J.A.,et al, 1986

Neuro-Ophthalmologic Findings in Vestibulocerebellar Ataxia
Arch Neurol 43:1050-1053, Farris,B.K.,et al, 1986

The Role of Glutamate in Neurotransmission & in Neurologic Disease
Arch Neurol 43:1058-1063, Greenamyre,J.T., 1986

Blind Loop Syndrome, Vitamin E Malabsorption, & Spinocerebellar Degeneration
Neurol 35:338-342, Brin,M.F.,et al, 1985

Olivopontocerebellar Atrophy with Dementia, Blindness, & Chorea, Response to Baclofen
Arch Neurol 42:757-758, Trauner,D.A., 1985

Spinocerebellar Degeneration Associated with a Selective Defect of Vitamin E Absorption
NEJM 313:32-35, Harding,A.E.,et al, 1985

Celiac Disease & Spinocerebellar Degeneration with Normal Vitamin E Status
Neurol 35:1199-1201, Ward,M.E.,et al, 1985

Chediak-Higashi Syndrome
Arch Neurol 41:1001-1002, Pettit,R.E.,et al, 1984

Neurological Disorders Associated with Deficiency of Glutamate Dehydrogenase
Ann Neurol 15:144-153, Plaitakis,A.,et al, 1984

Autonomic Dysfunction & Sleep Apnea in Olivoponto Cerebellar Degeneration
Arch Neurol 41:926-931, Chokroverty,S.,et al, 1984

Machado-Joseph-Azorean Disease
Arch Neurol 41:921-925, Fowler,H.L., 1984

Small Bowel Resection with Vitamin E Deficiency & Progressive Spinocerebellar Syndrome
Neurol 34:1046-1052, Bertoni,J.M.,et al, 1984

Dominant Spinopontine Atrophy
Arch Neurol 40:259-260, Pogacar,S.,et al, 1983

Joseph Disease in a Non-Portuguese Family
Neurol 33:74-80, Sakai,T.,et al, 1983

Eye Movements in Friedreich's Ataxia
Arch Neurol 40:343-346, Furman,J.M.,et al, 1983

Primary Position Vertical Nystagmus & Cerebellar Ataxia
Arch Neurol 40:310-314, Kattah,J.C.,et al, 1983

Evoked Potentials in Olivopontocerebellar Atrophy
Arch Neurol 40:366-369, Hammond,E.J.,et al, 1983

Glutamate Dehydrogenase Deficiency in Patients with Olivopontocerebellar Atrophy
Neurol 33:1322-1326, Duvoisin,R.C.,et al, 1983

Electro-oculographic Findings in Machado-Joseph Disease
Neurol 32:1272-1276, Dawson,D.M.,et al, 1982

Spinocerebellar Degeneration Secondary to Chronic Intestinal Malabsorption:A Vitamin E Deficiency Syndrome
Ann Neurol 12:419-424, Harding,A.E.,et al, 1982

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

Lecithin Treatment in Friedreich's Ataxia
BMJ 282:1197-1198, Pentland,B.,et al, 1981

Visual involvement in Friedreich's Ataxia & Hereditary Spastic Ataxia
Arch Neurol 38:75-79, Livingstone,I.R.,et al, 1981

Effect Of Thyrotropin-Releasing Hormone On Ataxia Of Spinocerebellar Degeneration
Lancet 1:418-419, Sobue,I.,et al, 1981

Olivopontocerebellar Atrophy in Children:A Report of Seven Cases in Two Families
Ann Neurol 10:355-363, Colan,R.V.,et al, 1981

Association Of Spinocerebellar Disorders With Cystic Fibrosis Or Chronic Childhood Cholestasis & Very Low Serum Vit. E
Lancet 2:1319-1321, Elias,E.,et al, 1981

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

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

Remission of Cerebellar Dysfunction After Pneumonectomy For Bronchogenic Carcinoma
NEJM 302:156, Paone,J.F.,et al, 1980

Clin. Path. Conference
Olivopontocerebellar atrophy, sporadic form. Case Record 39-1980, NEJM 303:803-80980., , 1980

Spinocerebellar Degeneration:Hexosaminidase A & B Deficiency in Two Adult Sisters
Neurol 29:380-384, Oonk,J.G.W.,et al, 1979

Jaw Reflex in Friedreich Ataxia
Neurol 29:1049-1050, Salisachs,P., 1979

Cranial Computerized Tomography & Marie's Ataxia
Arch Neurol 35:55, Aita,J.F., 1978

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

Computerized Tomography & Auditory-evoked Potentials:Use in the Diagnosis of Olivopontocerebellar Degeneration
Arch Neurol 35:143, Gilroy,J.,et al, 1978

Downbeating Nystagmus & Hereditary Cerebellar Degeneration, Levin DB, et al, In Neuro-ophthalmology Update
Masson Publishing USA, INC. 1977 P 337-338., Smith,J.L., 1977

Physostigmine in Familial Ataxias
Neurol 27:70, Kark,R.A.,et al, 1977

Showing articles 100 to 150 of 159 << Previous Next >>