Neudle.com: spinocerebellar ataxia

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 1000 to 1050 of 1208 << Previous Next >>

Biotinidase Deficiency:Initial Clinical Features & Rapid Diagnosis
Ann Neurol 18:614-617, Wolf,B.,et al, 1985

Cerebellar Dysfunction & Nephrotic Syndrome in a 50-Year-Old Man, Clinicopath. Conference
Am J Med 79:621-628, Klahr,S., 1985

Adrenoleukomyeloneuropathy with Onset in Early Childhood
Ann Neurol 17:311-312, Rosen,N.L.,et al, 1985

Long-Term Treatment of Cerebrotendinous Xanthomatosis with Chenodeoxycholic Acid
NEJM 311:1649-1652, Berginer,V.M.,et al, 1984

Ataxic Hemiparesis from Small Capsular Hemorrhage
Arch Neurol 41:1050-1053, Mori,E.,et al, 1984

Neurological Complications of Thyrotoxicosis in the Elderly
Ann Neurol 15:608, Florin,T., 1984

Severe Neurological Disease Associated with Hyperparathyroidism
Ann Neurol 15:453-456, Patten,B.M.,et al, 1984

Frequent Neurologic Toxicity Associated with Amiodarone Therapy
Neurol 34:669-671, Charness,M.E.,et al, 1984

Cyclosporine-Associated Central-Nervous-System Toxicity after Allogeneic Bone-Marrow Transplantation
NEJM 310:527, Atkinson,K.,et al, 1984

Positional Vertigo & the Cerebellar Vermis
Neurol 34:527-529, Kattah,J.C.,et al, 1984

Ataxic-Hemiparesis, Localization & Clinical Features
Stroke 15:363-365, Huang,C.Y.,et al, 1984

Long-Lasting Neurological Sequelae After Lithium Intoxication
Acta Psychiatr Scand 70:594-602, Schou,M., 1984

Pneumococcal Meningitis
Arch Neurol 41:1045-1049, Bohr,V.,et al, 1984

Reversible Central Nervous System Dysfunction Due to Tamoxifen in a Patient with Breast Cancer
Ann Int Med 101:652, Pluss,J.L.,et al, 1984

Association Between Cyclosporin Neurotoxicity & Hypomagnesaemia
Lancet 2:1116-1120, Thompson,C.B.,et al, 1984

Cerebellar Ataxia Due to Procainamide Toxicity
Arch Int Med 144:2260-2261, Schwartz,A.B.,et al, 1984

Ataxia-Telangiectasia:A Multisystem Hereditary Disease with Immunodeficiency
Ann Int Med 99:367-379, Waldmann,T.A.,et al, 1983

Ataxia Hemiparesis in Patients with Primary Pontine Hemorrhage
Stroke 14:762-764, Kobatake,K.,et al, 1983

Improvement of Ataxic Hemiparesis with Trihexyphenidyl
Neurol 33:1627-1628, Jabbari,B.,et al, 1983

Complications of Intravenous Phenytoin for Acute Treatment of Seizures
JAMA 249:762-765, Earnest,M.P.,et al, 1983

Signs & Symptoms from a Cerebral Lesion that Suggest Cerebellar Dysfunction
Jr. , Arch Neurol 40:422-423983., Montgomery,E.B., 1983

Clin. Path. Conference
Multiple-System Atrophy with Parkinsonism, Case 28-13, NEJM 308:1406-1414983., , 1983

Myeloneuropathy & Macrocytosis Associated with Nitrous Oxide Abuse
Arch Neurol 40:416-418, Bianco,G.,et al, 1983

Sensory Neuropathy from Pyridoxine Abuse
NEJM 309:445-448, Schaumburg,H.,et al, 1983

Acetazolamide-Responsive Episodic Ataxia Syndrome
Neurol 33:1212-1214, Zasorin,N.L.,et al, 1983

Delayed Neurologic Sequelae in Carbon Monoxide Intoxication
Arch Neurol 40:433-435, Choi,I.I.S., 1983

Phytanic Acid Storage Disease:Hearing Maintained After 15 Years of Dietary Treatment
Neurol 33:237-240, Djupesland,G.,et al, 1983

Gait Disorders Among Elderly Patients
Arch Neurol 40:740-743, Sudarsky,L.,et al, 1983

Idiopathic Hemochromatosis (IHC) :Dementia & Ataxia as Presenting Signs
Neurol 33:1479-1483, Royden,H.,et al, 1983

Acute Cerebellar Ataxia & Hearing Loss as Initial Symptoms of Infectious Mononucleosis
Arch Neurol 40:760-762, Erzurum,S.,et al, 1983

Cerebellar Degeneration Caused by High-Dose Cytosine Arabinoside:A Clinicopathological Study
Ann Neurol 14:520-527, Winkelman,M.D.,et al, 1983

Cerebellar Dysfunction after Acute Carbon Tetrachloride Poisoning
Lancet 2:968, Forster,S.H.,et al, 1983

Gerstmann-Straussler-Scheinker Disease with Coincidental Familial Onset
Ann Neurol 14:670-678, Hudson,A.J.,et al, 1983

Persisting Neurologic Sequelae of Lithium Carbonate Therapy
Arch Neurol 40:747-751, MacDonaldson,I.,et al, 1983

Unrecognized Chronic Lithium Neurotoxic Reactions
JAMA 250:2029-2030, Lewis,D.A., 1983

A Progressive Syndrome of Autism, Dementia, Ataxia, & Loss of Purposeful Hand Use in Girls:Rett's Syndrome
Ann Neurol 14:471-491, Hagberg,B., 1983

Permanent Neurological Deficits Due to Lithium Toxicity
Ann Neurol 13:453-455, Apte,S.N.,et al, 1983

Nervous System Complications of Relapsing Polychondritis
Neurol 33:513-515, Sundaram,M.B.M.,et al, 1983

Supranuclear Gaze Palsy in Familial Creutzfeldt-Jakob Disease
Arch Neurol 40:618-622, Bertoni,J.M.,et al, 1983

Sensory Ataxia, A Residual Disability of Guillain-Barre Syndrome
Arch Neurol 40:86-89, Sobue,G.,et al, 1983

Ataxic Hemiparesis from Lesions of the Corona Radiata
Arch Neurol 40:449-450, Sage,J.L.,et al, 1983

Progressive Supranuclear Palsy:Clinical Features & Response to Treatment in 16 Patients
Ann Neurol 13:273-278, Jackson,J.A.,et al, 1983

Herpes Zoster-Associated Encephalitis:Clinicopathologic Report of 12 Cases and Review of the Literature
Medicine 62:81-95, Jemsek,J.,et al, 1983

Peripheral Neuropathy & Starvation After Gastric Partitioning for Morbid Obesity
Ann Int Med 96:453-455, Feit,H.,et al, 1982

Truncal Ataxia in Terminal Bronchial Carcinoma
Arch Neurol 39:787-788, Puvanendran,K., 1982

Neuroaxonal Dystrophy in Young Adults:A Clinicopathological Study of Two Unrelated Cases
Ann Neurol 11:335-343, Williamson,K.,et al, 1982

Abnormal Brainstem Auditory Evoked Potentials in Chronic Paint Sniffers
Ann Neurol 12:553-556, Metrick,S.A.,et al, 1982

Neurologic Complications of Primary Sjogren's Syndrome
Medicine 61:247-257, Alexander,E.L.,et al, 1982

Hydrocephalus as a Cause of Disturbances of Gait in the Elderly
Neurol 32:1358-1363, Fisher,C.M., 1982

Brainstem Encephalitis & The Syndrome Of Miller Fisher
Brain 105:481-495, Al-Din,A.N.,et al, 1982

Showing articles 1000 to 1050 of 1208 << Previous Next >>