Neudle.com: cerebellar ataxia hereditary

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Differential
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abdominal distention

abdominal reflex, absent

abducens nerve paralysis

achilles tendon, enlarged

acoustic neurinoma, bilateral

acquired immunodeficiency syndrome

acquired immunodeficiency syndrome myelopathy

Addison's disease

adrenoleukodystrophy

adrenoleukodystrophy, carrier

adrenomyeloneuropathy

adult-onset leukodystrophy, with neuroaxonal spheroids

advances in neurology

adverse drug reaction

alcohol intolerance

alcohol, neurologic complications with

Alexanders disease

Alexanders disease, adult onset

alkylating agents

alpha-fetoprotein

altered states of consciousness

alternating hemiplegia

alternating hemiplegia of childhood

alternating rapid movement

alternating rapid movement, impaired

Alzheimer's disease

aminoacidopathies

amyloid plaques

amyotrophic lateral sclerosis

Angelman syndrome

ankle reflex, absent

antibodies to voltage-gated calcium channels

anticholinesterase

anticonvulsants

anticonvulsants, effectiveness

apnea, primary central

apraxia of eye movements

Arnold Chiari malformation

arrhythmia, cardiac

arylsulfatase A

ataxia telangiectasia

ataxia, cerebellar

ataxia, congenital

ataxia, hereditary

ataxia, paroxysmal

ataxia, progressive

ataxia, sensory

ataxia, truncal

ataxic-dystonia syndromes

atherosclerosis, premature

attention deficit disorder with hyperactivity

auditory evoked brainstem potentials

autonomic dysfunction

autosomal dominant leukodystrophy

autosomal rcessive spastic ataxia of Charlevoix-Saguenay

axonal spheroid

B 12 deficiency

basal ganglia, calcification of

basal ganglia, degeneration

basal ganglia, lesion of

basal ganglia, lesion, bilateral

Bassen-Kornzweig syndrome

behavior, combative

behavioral disorder

biologic markers

biotin deficiency

biotinidase deficiency

bladder dysfunction

blood dyscrasias, neurologic findings with

bone marrow biopsy

brainstem, atrophy

brainstem, lesion of

brainstem, neoplasms of

cafe au lait spots

calcification, intracranial

calcium channel dysfunction

carcinoembryonic antigen

CAT scan, abnormal

CAT scan, emission

CAT scan, emission, abnormal

cataracts, congenital

caudate nucleus, lesion of, bilateral

celiac disease, adult

central core disease

cerebellar ataxia, autosomal recessive

cerebellar ataxia, children

cerebellar ataxia, children, differential diagnosis of

cerebellar ataxia, hereditary

cerebellar ataxia, neuropathy and vestibular areflexia syndrome

cerebellar ataxia, primary

cerebellar atrophy, primary

cerebellar atrophy, secondary

cerebellar degeneration

cerebellar hemangioma

cerebellar hypoplasia

cerebellar lesion

cerebellar plaques, amyloid

cerebellar vermis

cerebellum, disease of

cerebellum, neoplasms of

cerebral cortex

cerebral cortical atrophy

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, lactic acid concentration

cerebrospinal fluid, pressure low

cerebrospinal fluid, proteincytologic dissociation

cerebrospinal fluid, xanthochromia of

cerebrotendinous xanthomatosis

cerebrovascular accident

cerebrovascular accident, mimics

cerebrovascular accident, young adult

Charcot-Marie-Tooth

chemotherapy, CNS treatment and complications with

chenodeoxycholic acid

chewing movements

chloride channel dysfunction

chorea, familial

choreoathetosis

chromosomal abnormality

chronic progressive external ophthalmoplegia

ciguatera poisoning

cisterna magna, enlarged

Clinical Pathologic Conference(C.P.C.)

clubfoot as related to neurologic disease

Cockayne's syndrome

cognition, slowed

cogwheel rigidty

color vision, impaired

cone-rod dystrophy

congestive heart failure

conjunctival biopsy

contractures, joint

controversies in neurology

conus medullaris, lesion of

copper metabolism, abnormal

cornea, abnormal

corpus callosum

corpus callosum, atrophy of

corpus callosum, lesion of

corpus callosum, thinning

cortical blindness

cranial nerve palsies

cranial neuropathy, multiple

cranio-cervical junction

creatine phosphokinase(CPK)elevated

Creutzfeldt-Jakob disease, genetic

cultured skin fibroblasts

cyst, peritumoral

cyst, neoplastic cerebellum

deep gray nuclei

deep tendon reflexes

degenerative diseases of CNS

delay in diagnosis

delayed dentition

dementia, childhood

dementia, familial

dementia, frontotemporal

dementia, presenile

dementia, rapidly progressive

dementia, subcortical

dementia, transmissible

demyelinating disease

dentate nuclei, lesion of

dentatorubral-pallidoluysian atrophy

dermatoglyphics

developmental disability

developmental milestones

developmental milestones, loss of

developmental retardation

dexterity, impaired

diabetes insipidus

diabetes mellitus

diabetes mellitus, chemical

diabetes mellitus, neurologic manifestations of

diagnostic criteria

differential diagnosis

difficulty climbing stairs

disability, neurological

disease modifying agents

distal muscle atrophy

down-beat nystagmus

down-beat nystagmus, primary position of gaze

Dravet syndrome

drug abuse, inhalation

dysdiadochokinesia

dyssynergia cerebellaris myoclonica

eating disorder

electrical sensation

electrocardiogram, abnormal

electroencephalogram

electroencephalogram, abnormalities of

electron microscopy

electroretinograph

encephalopathy, progressive

epicanthal folds

epidemiology of neurology

episodic disorders

episodic neurologic deficits

erectile dysfunction

ethics in neurology

evoked potentials

executive dysfunction

exercise intolerance

exome sequencing

extraocular muscle lesion

eye movement, disorders of

facial appearance, abnormal

facial expression abnormality

facial nerve palsy, bilateral

failure to thrive

familial hemiplegic migraine

familial periodic ataxia

family planning

fatal familial insomnia

feeding disorder

finger nose finger test

fingerprint bodies

fluorescene in situ hybridization

fornix, lesion of

Fragile-X associated tremor/ataxia-syndrome

fragile-X syndrome

fragile-X syndrome, carrier

Friedreich's ataxia

Friedreich's ataxia, late onset

frontotemporal dementia, behavioral variant

fundus, abnormality of

gastrointestinal disease, neurologic complications

gastrointestinal motility

gaze palsy, supranuclear

gaze palsy, vertical

genetic counselling

genetic diagnosis, prenatal

genetic linkage

genetic neurologic disorders

genetic screening

genetic testing

genu of corpus callosum

Gerstmann-Straussler-Scheinker disease

Gillespie syndrome

globus pallidus, lesion of

globus pallidus, lesion of, bilateral

glucose tolerance test, abnormal

GLUT1 deficiency syndrome

glutamate dehydrogenase deficiency

granular osmiphilic material

growth hormone deficiency

growth retardation

Hallervorden Spatz disease

Hallgren's syndrome

hallucination, visual

hearing problems in children

heel-knee-shin test

hemangioblastoma

hematuria, gross

hemochromatosis

hemochromatosis, primary

hemophagocytic lymphohistiocytosis, cerebromeningeal

hemophagocytosis

hepatic encephalopathy

hepatic failure

hepatolenticular degeneration(Wilson's disease)

hepatolenticular degeneration(Wilson's disease), screening for

hepatolenticular degeneration, non-Wilsonian

hepatosplenomegaly

heralding manifestation

herniated disc, thoracic

hot cross bun sign

human T-lymphotropic virus type II(HTLV-II)

Huntington's chorea

Hurler's syndrome

hydroxytryptophan L-5(L-5 HTP)

hyperammonemic encephalopathy

hypertriglyceridemia

hypocholesterolemia

hypofibrinogenemia

hypogonadism, hypogonadotropic

hypokalemic periodic paralysis

hypomyelination

hypopigmentation of skin

hypotonia, infants

imbalance, postural

immunodeficiency

immunologic disease

immunosuppression

inappropriate antidiuretic(A.D.H.)hormone, CNS involvement with

inborn errors of metabolism

inclusion bodies

inclusion bodies, eosinophilic cytoplasmic

inclusion bodies, eosinophilic intranuclear

inclusion bodies, intranuclear

inclusion bodies, ubiquitin

incontinence, fecal

intellectual deficit

intellectual deterioration

intelligence quotient

internal capsule

internuclear ophthalmoplegia

internuclear ophthalmoplegia, bilateral

intestinal pseudoobstruction

intracranial pressure, increased

Jakob-Creutzfeldt disease

Jakob-Creutzfeldt disease, cerebellar variant

joint hypermobility

Kayser-Fleischer ring

Kearns-Sayre syndrome

Korsakoff's psychosis

kyphoscoliosis, neurologic causes of

lactic acidemia

laughing, pathologic

Laurence-Moon-Bardet-Biedl syndrome

Leber's hereditary optic neuropathy

leg weakness, bilateral

Leigh's disease

Leigh's disease, adult variety

lenticular nucleus, lesion of, bilateral

leukemia, neurologic findings assoc.with

leukoencephalopathy

leukoencephalopathy, adult onset, sporadic

leukoencephalopathy, differential diagnosis

leukoencephalopathy, hereditary diffuse

Lhermitte's sign

libido, decreased

life expectancy

lipid storage disorder of CNS

liver function enzymes

liver transplantation

lymphadenopathy

lysosomal storage disease

macular degeneration

malformation, CNS, congenital

malignant hyperpyrexia

maple syrup urine disease

marche a petits pas

Marinesco-Sjogren syndrome

memory, defect of recent

memory, impairment of

meningitis, carcinomatous

meningoencephalopathy

mental retardation

mesial temporal lobe

metabolic acidosis

metabolic disorder, primary

metachromatic leukodystrophy

metachromatic leukodystrophy, adult onset

metachromatic leukodystrophy, juvenile

methylhydrazine derivatives

microhemorrhage, intracerebral

midbrain, atrophy

middle cerebellar peduncle

middle cerebellar peduncle, lesion

middle cerebellar peduncle, lesion, bilateral

migraine, hemiplegic

Minamata disease

Mini Mental Status Examination

mitochondrial disease

mitochondrial disease, pathogenesis

mitochondrial encephalomyopathy

molecular genetics

monoamine oxidase inhibitors

motor neuron disease

movement disorder

movement disorder, extrapyramidal

movement disorder, hyperkinetic

MRI, CAT scan compared to

MRI, contrast enhanced

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, high signal intensity of basal ganglia

MRI, paramagnetic effect

MRI, punctate pattern

MRI, spinal cord

MRI, T1 weighted high signal foci

mucopolysaccharidoses

multiple sclerosis

multiple sclerosis, misdiagnosis

multiple system atrophy

muscle atrophy, progressive

muscle weakness

muscle weakness, proximal

muscular dystrophy

myasthenic syndrome

myeloneuropathy

myelopathy, hepatic

myelopathy, vacuolar

myoclonic jerks

myoclonus, epilepsy

myopathy, mitochondrial

myotonia congenita

myotonia dystrophica

N-acetylcysteine

Native Americans

nausea and vomiting

neonatal screening, genetic neurologic disorders

neoplasm, metastatic to CNS

neoplasm, primary of CNS

neoplasm, primary of CNS-surgical treatment of

nerve conduction studies

nerve growth factor

neuroaxonal dystrophy

neuroaxonal dystrophy, infantile

neuroaxonal dystrophy, juvenile

neuroaxonal leukodystrophy

neurocutaneous disease

neuroendocrinology

neurofibrillary degeneration

neurofibromatosis 1

neurogenic bladder

neurologic complications of, systemic cancer

neurologic complications of, systemic disease

neurologic disease

neurologic disease, diagnoses of

neurologic examination, focal

neurologic signs

neurologic testing

neuronal ceroid-lipofuscinosis

neuronal intranuclear inclusion disease

neuronopathy, sensory

neuroophthalmology

neuropathology, brain

neuropathy, ataxic

neuropathy, demyelinating

neuropathy, hereditary peripheral

neuropathy, hypertrophic

neuropathy, onion bulb

neuropathy, peripheral

neuropathy, sensory

neurotransmitter

next-generation sequencing

Niemann-Pick disease

night blindness

nitrogen mustard

nutritional deficiency

nystagmus, gaze-evoked

nystagmus, gaze-paretic

nystagmus, hereditary

nystagmus, monocular

nystagmus, periodic

nystagmus, primary position of gaze

nystagmus, rotary

nystagmus, upbeating-in primary position of gaze

nystagmus, vertical

ocular dysmetria

ocular motility, disorders of

ocular myopathy

oculodentodigital dysplasia

old age, neurology of

ophthalmoplegia

ophthalmoplegia, progressive external

optic atrophy, hereditary

optic neuropathy

optical coherence tomography

optokinetic nystagmus, abnormal

orbit, tomograms of

orthostatic hypotension

ovarian dysgenesis

ovarian insufficiency

pain, abdominal

palatal myoclonus

paramyotonia congenita

paraparesis, familial spastic

paraparesis, familial spastic, classification

paraparesis, spastic

Parkinson disease

Parkinson disease, dystonia with

Parkinson disease, familial

Parkinsonism multiple-system atrophy

Parkinsonism syndrome

paroxysmal hemiplegia

paroxysmal neurologic deficits

PAS positive material in the brain

patient information and support

Pelizaeus Merzbacher

periodic paralysis

peroxisomal disease

Perrault syndrome

personality change

pheochromocytoma

photosensitivity, skin

pigmentary retinopathy

pleocytosis of cerebrospinal fluid

poison, mercury

poison, neurologic problems with

polymerase chain reaction

pons, lesion of

pontocerebellar atrophy

portal caval shunt

positional head-hanging test

postural abnormality

potassium channel antibodies

potassium channel dysfunction

Prader-Labhart-Willi syndrome

precipitating factors

pregnancy, neurologic complications in

prenatal diagnosis by amniocentesis

pretectal syndrome

prevention of neurologic disorders

primary episodic ataxia

prion protein gene

prisoners of war, neurologic complications in

progressive infantile poliodystrophy

progressive neurologic disorder

progressive pallidum atrophy

proprioception, abnormal

protein 14-3-3, cerebrospinal fluid

pseudobulbar palsy

pseudoretinitis pigmentosa

psychiatric disorder

psychiatric problems in neurologic disorders

psychological testing

psychological testing, neurologic problems

psychomotor retardation

ptosis, bilateral

pulmonary infection

pursuit eye movements, abnormal

putamen, lesion of

putamen, lesion of, bilateral

pyramidal tract

pyramidal tract dysfunction

pyruvate dehydrogenase deficiency

pyruvate metabolism, abnormality of

radiation hypersensitivity

radiation therapy, CNS treatment and complications with

radiation therapy, stereotactic

ragged-red fibers

rapid onset dystonia parkinsonism

rapidly progressing neurologic illness

reading disorder, acquired

real-time quaking-induced conversion

Refsum's disease

rehabilitation for neurologic disorders

release phenomena

remote effect of cancer on the nervous system

respiratory failure

respiratory tract infection

retina, abnormal

retinal degeneration

retinal hemangioma

retinitis pigmentosa

Rett's syndrome

reversible neurologic disorder

Riley-Day syndrome

Rosenthal fibers

saccadic eye movements, abnormal

salivation, excessive

seizure, children

seizure, familial

seizure, febrile

seizure, intractable

seizure, laughing as manifestation

seizure, neonatal

seizure, paradoxical

seizure, photosensitive

seizure, psychomotor-temporal lobe

seizure, tonic-clonic

seizure, treatment of

self-mutilation

semialdehyde dehydrogenase deficiency

sensorineural hearing loss

sensory ganglia

sensory ganglia, abnormal

sensory loss, leg

serologic testing

Shy-Drager syndrome

skin, darkening of

skin, lesions in neurologic disorders

sleep pathology and physiology

sodium channel dysfunction

somatosensory evoked potentials

spastic paraplegia, type 7

speech disorder

speech disorder, childhood

speech disorder, non aphasic

speech, delayed development of

speech, loss of

Spielmeyer Vogt syndrome

spinal cord, lesion of

spinal cord, neoplasm

spinal cord, pathologic exam of

spinal muscular atrophy

spinocerebellar ataxia

spinocerebellar ataxia type 1

spinocerebellar ataxia type 10

spinocerebellar ataxia type 12

spinocerebellar ataxia type 14

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

splenium of corpus callosum

spongy degeneration of brain

startle myoclonus

status epilepticus

stereotaxic surgery

stereotyped behavior

steroid therapy, CNS treatment and complications with

storage disease of CNS

stress, emotional

striatonigral degeneration

striatonigral degeneration, infantile

striopallidodentate calcifications, familial idiopathic

strokelike episodes

subcortical U fibers

superior cerebellar peduncle

symmetric brain lesions

syphilis, neurologic complications with

systemic illness

tandem gait, ataxic

teeth, abnormal

teeth, number of in infants

teeth, wide-spaced

temper tantrums

temporal lobe, lesion

testicular enlargement

thalamus, lesion of

thalamus, lesion of-bilateral

thrombocytopenia

tongue, protrusion of

toxins, nervous system

transient neurologic deficit

treatment of neurologic disorder

tremor, cerebellar

tremor, intention

trinucleotide repeats

Unverricht-Lundborg disease

upgaze, paralysis of

urea-cycle enzymopathies

urinary frequency

urinary incontinence

urinary urgency

urine test for metabolic disorders

Usher's syndrome

vertigo, episodic

vertigo, treatment of

vestibular areflexia

vibratory sensation, abnormal

vincristine neurotoxicity

viral isolation

vision, failure of in childhood

visual acuity, decreased

visual field defect

visual fields, constricted

visual loss, progressive

visual loss, slow

visuospatial disturbance

vitamin deficiency

vitamin E deficiency

vitamin supplementation

vocal cord paralysis

voice, abnormality of

Von Hippel Lindau

walking, difficulty with

walking, difficulty with in dark

weakness, generalized

weakness, progressive

weaning from respirator, failure to

Western immunoblot test

white matter disease

whole genome sequencing

wide based gait

Wolfram syndrome

xanthoma, tendon

xeroderma pigmentosa

X-linked bulbospinal neuronopathy

x-linked intellectual deficit

x-linked mental retardation

Showing articles 850 to 900 of 3337 << Previous Next >>

Mitral Valve Prolapse & Ophthalmoplegia:A Progressive, Cardioneurologic Syndrome
Ann Int Med 92:735-741, Darsee,J.R.,et al, 1980

Clin. Path. Conference
Creutzfeldt-Jakob Disease, Ataxic Type, with Kuru Plaques, Case Record 45-1980, NEJM 303:1162-11710., , 1980

Central Nervous System Toxicity Associated With Metronidazole Therapy
Ann Int Med 93:59-60, Kusumi,R.K.,et al, 1980

Legionnaires'Disease With Profound Cerebellar Involvement
Arch Neurol 37:379-380, Shetty,K.R.,et al, 1980

Alcoholic Downbeat Nystagmus
Ann Ophthalmol 1127-1131, October 1980., Costin,J.A.,et al, 1980

Paroxysmal Symptoms as the First Manifestations of Multiple Sclerosis
JNNP 43:296-304, Twomey,J.A.,et al, 1980

Adult Celiac Disease Presenting as Cerebellar Syndrome
Neurol 30:245-249 1980., Finelli,P.F.,et al, 1980

Fusiform Basilar Artery Aneurysm in a Child
Neurol 29:1045-1049, Read,D.,et al, 1979

Optic Neuropathy & Ophthalmoplegia in Herpes Zoster Oticus
Neurol 29:726-729, Carroll,W.M.,et al, 1979

Neurologic Disturbances in Pagets Disease of Bone:Response to Calcitonin
Neurol 29:448-457, Chen,J.R.,et al, 1979

Hydrocephalic Dementia in Pagets Disease of the Skull:Treatment by Ventriculoatrial Shunt
Neurol 29:513-516, Goldhammer,Y.,et al, 1979

Acute Transitory Cerebellar Dysfunction Associated with Piperazine Adipate
Arch Neurol 36:180-181, Berger,J.R.,et al, 1979

Beneficial Effect of Propranolol in Familial Ataxia
Ann Neurol 5:207, Braham,J.,et al, 1979

Self-Limited Granulomatous Angiitis of the Cerebellum
Ann Neurol 5:490-492, Beresford,H.R.,et al, 1979

Helper & Suppressor T-Lymphocyte Leukemia In Ataxia Telangiectasia
NEJM 300:700-704, Saxon,A.,et al, 1979

Neurologic Abnormalities of Lyme Disease
Medicine 58:281-294, Reik,L.,et al, 1979

Familial Inverted Choreoathetosis
Neurol 29:1627-1631, Fisher,M.,et al, 1979

Adult Type Neuronal Storage Disease with Neuraminidase Deficiency
Ann Neurol 6:232-244, Miyatake,T.,et al, 1979

Neurological Manifestations & Mycoplasma Pneumoniae Infection
BMJ 2:832-833, Hodges,G.R.,et al, 1979

Acute & Chronic Progressive Encephalopathy Due to Gasoline Sniffing
Neurol 28:507-510, Valpey,R.,et al, 1978

Kearns-Sayre Syndrome with Hypoparathyroidism
Ann Neurol 3:513, Horwitz,S.J.,et al, 1978

Adult Onset of the Dandy-Walker Syndrome
Arch Neurol 35:672-674, Lipton,H.L.,et al, 1978

Varicella & Acute Cerebellar Ataxia
Arch Neurol 35:769-771, Peters,A.C.B.,et al, 1978

Clinical pathological conference
Von Hippel-Lindau disease, Case Record 1-1978, NEJM 298:95978., , 1978

Extreme Insulin Resistance in Ataxia Telangiectasia
NEJM 298:1164, Bar,R.S.,et al, 1978

Ataxic Hemiparesis
Arch Neurol 35:126, Fisher,C.M., 1978

Persistent Cerebellar Ataxia after Exposure to Toluene
Ann Neurol 2:440, Boor,J.W.,et al, 1977

Case Record of the M. G. H.
Glioblastoma Multiforme of Pons, NEJM 296:8651977., , 1977

Supratentorial Arachnoid Cysts in Adults:A Discussion of Two Cases from a Pathophysiologic & Surgical Perspective
Arch Neurol 34:276, Dyck,P.,et al, 1977

More about Poisoning by Phencyclidine ("PCP, ""Angel Dust")
NEJM 297:1405, 1977. (Letter), Herskowitz,J.,et al, 1977

Tonic Pupils with Acute Ophthalmoplegic Polyneuritis
Ann Neurol 2:393, Keane,J.R., 1977

Reversible Corticospinal Tract Disease Due to Hyperthyrodisim
Arch Neurol 34:647, Garcia,C.A.,et al, 1977

Neuroectodermal Tumors in the Cerebellum in Two Sisters
JNNP 40:886, Thomas,M.,et al, 1977

Cerebrovascular diseases
In Harrison's Principles of Internal Medicine, 1977. McGraw-Hill Book Co. , p1., , 1977

Fisher's Syndrome:A Pharmacological Study of the Pupils
Ann Neurol 2:63, Okajima,T.,et al, 1977

The Spectrum of Mild X-Linked Recessive Muscular Dystrophy
Arch Neurol 34:408, Ringer,S.P.,et al, 1977

Pellagra
In Brain's Diseases of the Nervous System, 8th Ed. 1977, p 849-851, Oxford University Press., , 1977

Progressive Rubella Panencephalitis
Arch Neurol 33:722, Wolinsky,J.S.,et al, 1976

Neurologic Complications After Treatment for Whipple's Disease:A Report of Four Patients
Medicine 55:467, Knox,D.L.,et al, 1976

Chronic Meningitis
Medicine 55:341, Ellner,J.J.,et al, 1976

Normocalcemic Tetany
Neurol 26:825, Isgreen,W.P., 1976

Progressive Spastic Paraparesis & Adrenal Insufficiency
Arch Neurol 33:678, Gumbinas,M.,et al, 1976

Hypophosphatemia Mimicking Acute Guillain-Barre-Strohl Syndrome
JAMA 235:1040-1041, Weintraub,M.I., 1976

The Thyroid Gland:Its Relationship to Neurology
In Handbook of Clin Neurol, Vinken & Bruyn (Ed) , North Holland Publ Co, Amsterdam 27:255, Greene,R., 1976

MGH-CPC-Gliomatosis Cerebri of Cerebellum & Brainstem
NEJM 292:852, , 1975

Progressive Rubella Encephalitis
NEJM 292:990-993, 994-998, 1023-1024975., Townsend,J.J., 1975

MGH-CPC-Ataxic Telangiectasia & Left Frontal Lobe Glioma
NEJM 292:1231, , 1975

Adult Toxoplasmosis Presenting as Polymyositis & Cerebellar Ataxia
Ann Int Med 82:367, Greenlee,J.,et al, 1975

Ataxia, Vertigo, & Hearing Loss
Arch Otolarygn l00:l30, Healy,G.B.,et al, 1974

Pseudointernuclear Ophthalmoplegia in Acute Idiopathic Polyneuritis (Fisher's Syndrome)
Am J Ophthalmol 77:725, Swick,H.M., 1974

Showing articles 850 to 900 of 3337 << Previous Next >>