Neudle.com: progressive spinal muscular atrophy

Differential
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abiotrophy

acid maltase deficiency

acoustic neurinoma

acquired immunodeficiency syndrome

acquired immunodeficiency syndrome, heralded by neurologic invol

ACTH, ectopic syndrome of

acute intermittant porphyria

Addison's disease

adult polyglucosan body disease

advance directives

advances in neurology

adverse drug reaction

alcoholic polyneuropathy

algorithm

alpha-fetoprotein

alveolar hypoventilation

Alzheimer's disease

aminoacidopathies

aminoacidurias

amyloid angiopathy, cerebral

amyloidosis

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, bulbar

amyotrophic lateral sclerosis, atypical

amyotrophic lateral sclerosis, childhood

amyotrophic lateral sclerosis, cluster

amyotrophic lateral sclerosis, complications with

amyotrophic lateral sclerosis, conjugal

amyotrophic lateral sclerosis, diagnosis of

amyotrophic lateral sclerosis, differential diagnosis

amyotrophic lateral sclerosis, epidemiology of

amyotrophic lateral sclerosis, etiology of

amyotrophic lateral sclerosis, familial

amyotrophic lateral sclerosis, guamian type of

amyotrophic lateral sclerosis, hospitalization

amyotrophic lateral sclerosis, juvenile

amyotrophic lateral sclerosis, misdiagnosis

amyotrophic lateral sclerosis, myasthenic syndrome with

amyotrophic lateral sclerosis, Parkinson-dementia-complex

amyotrophic lateral sclerosis, post-encephalitic

amyotrophic lateral sclerosis, prognosis

amyotrophic lateral sclerosis, sensory symptoms in

amyotrophic lateral sclerosis, treatment of

amyotrophic lateral sclerosis, work up

amyotrophic lateral sclerosis-like syndrome

analgesic

anatomy of

aneurysm

aneurysm, cavernous sinus

aneurysm, internal carotid artery

animal exposure

ankle edema

ankle reflex, preserved

ankylosing spondylitis

anterior horn cell disease

anterior interosseous neuropathy

anterior spinal artery infarction

anterior tibial muscle weakness

anti citrullinated antibody

anti Hu antibody

anti IgLON5

antibodies to voltage-gated calcium channels

aphasia, progressive, primary

aphonia

apnea

apraxia

apraxia of eye movements

arterial dissection, aorta

arterial dissection, vertebral

arthrogryposis multiplex

ascending paralysis

aspiration

asthma

asthma, poliomyelitis-like syndrome with

asymptomatic

ataxia

ataxia telangiectasia

atlanto axial dislocation, congenital

autoantibodies

autoimmune disease

autonomic dysfunction

axonal degeneration

Babinski sign

basal ganglia, calcification of

basal ganglia, lesion of

behavioral disorder

Bence Jones protein

benign congenital hypotonia

benzodiazepine

biologic markers

BiPAP

bitemporal visual field defect

bladder dysfunction

bone marrow biopsy

botulinum toxin

botulinum toxin, complications of

botulism

brachial amyotrophic diplegia

brachial neuritis

brain atrophy

brain biopsy

brainstem, infarction of

brainstem, lesion of

bright tongue sign

Brown Sequard syndrome

Brugada syndrome

bulbar palsy

bulbar palsy, acute

bulbar palsy, childhood

bulbar palsy, progressive

C9orf72

cachexia

CAG repeats

calcification, intracranial

calcium channel dysfunction

calf hypertrophy

camptocormia

cane

carbon monoxide poisoning

carcinoembryonic antigen

CAT scan, emission, abnormal

cataracts

cauda equina

cavernous sinus, syndrome

CD4 counts

central core disease

central nervous system, infection of

cerebellar ataxia, children

cerebellar ataxia, hereditary

cerebellar atrophy, primary

cerebellar atrophy, secondary

cerebellar degeneration

cerebellar vermis

cerebellum, neoplasms of

cerebral cortex

cerebral cortical atrophy

cerebrospinal fluid, abnormal

cerebrospinal fluid, cell count

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, oligoclonal IgG in

cerebrospinal fluid, protein of

cerebrospinal fluid, proteincytologic dissociation

cerebrovascular accident

cerebrovascular accident, young adult

cerebrovascular disease, cardiovascular disease with

cervical collar

cervical osteoarthritis

cervical osteophyte

cervical rib

cervical spine

cervical spine injury

cervical spine injury, treatment of

cervical spondylosis

cervical spondylosis, differential diagnosis of

cervical spondylosis, misdiagnosis

Charcot-Marie-Tooth

chest x-ray, abnormal

chewing, impaired

children

chills

Chinese paralytic syndrome

chorea

chorea, Sydenham's

choreoathetosis

chromosomal abnormality

chromosome 11

chromosome 5

chronic polyneuritis, children

chronic progressive external ophthalmoplegia

Chvostek sign

ciguatera poisoning

climate change

Clinical Pathologic Conference(C.P.C.)

compression neuropathy

concussion

conduction block

confusion

congenital heart disease

congenital myopathy

congestive heart failure

constipation

controversies in neurology

coxsackievirus, myopathy with

CPAP

cranial neuropathy

cranial neuropathy, multiple

craniopharyngioma

creatine phosphokinase(CPK)elevated

degenerative diseases of CNS

Dejerine-Sottas syndrome

delay in diagnosis

delusion

dementia

dementia, age at onset

dementia, cerebrovascular disease causing

dementia, frontal lobe type

dementia, frontotemporal

dementia, presenile

dementia, rapidly progressive

denervation of muscle

denervation potentials

dentatorubral-pallidoluysian atrophy

depression

dermatomyositis

developmental milestones

developmental milestones, loss of

developmental retardation

dexterity, impaired

diabetes mellitus

diabetes mellitus, neurologic manifestations of

diabetic mononeuropathy

diagnostic criteria

diaphragmatic paralysis

diaphragmatic paralysis, causes of

diarrhea

diet

differential diagnosis

difficulty climbing stairs

diphtheria

diplegia, atonic

diplegia, brachial

disability rating scale, neurological

disability, neurological

distal muscle atrophy

distal muscle weakness

DNA probes

dopamine

drooling

dropped head syndrome

electrical injury of nervous system

electrical sensation

electrocardiogram, abnormal

electromyogram

electromyogram, decremental response

electron microscopy

electrophoretic pattern, serum

emotional lability

encephalitis

encephalitis, autoimmune

encephalitis, brainstem

encephalitis, central European

encephalitis, paraneoplastic

encephalitis, Powassan

encephalitis, viral

encephalocele

encephalomyelitis

encephalomyeloneuritis

encephalopathy

encephalopathy, anoxic

encephalopathy, neonatal

encephalopathy, post anoxic

endocarditis, subacute bacterial

enterovirus

enterovirus infection of CNS

entrapment neuropathy

enzyme, defect

enzyme, muscle disease

epidemiology of neurology

episodic disorders

episodic neurologic deficits

episodic unconsciousness

ethics in neurology

euthanasia

evidence-based research

eye movement, disorders of

facial pain

facial weakness

facial weakness, bilateral

facioscapulohumeral syndrome

falling

familial

fasciculation

fasciculation, benign

fatigable chewing

fatigue

Fazio-Londe's disease

fever

fibrillations

fine motor function, impaired

football neurologic injuries

fragile-X syndrome

free radical

Friedreich's ataxia

frontal lobe, atrophy

frontal lobe, behavior with disease of

frontal lobe, lesion of

frontotemporal dementia, behavioral variant

F-wave response

gag reflex, depressed

gait disorder

gait, spastic

gait, waddling

gammaglobulin therapy, intravenous

ganglionitis

gangliosides

gangliosidosis GM2

gastrectomy, neurologic complications following

gastrostomy

gastrostomy, percutaneous endoscopic

gaze palsy

gaze palsy, horizontal

gaze palsy, supranuclear

genetic diagnosis, prenatal

genetic linkage

genetic neurologic disorders

glycogen storage disease

GM1 ganglioside

GM1 ganglioside antibodies

granular atrophy, cerebral cortex

growth retardation

guanidine

Guillain Barre syndrome

Guillain Barre syndrome, differential diagnosis of

Guillain Barre syndrome, variant forms of

hallucination, auditory

hand weakness

handlebar palsy

Hand-Schuller-Christian disease

heavy metal intoxication

hemiplegia, progressive

heralding manifestation

herniated disc

herpes simplex encephalitis

herpes simplex encephalitis, diagnosis of

herpes zoster

heterochromia iridis

highly active antiretroviral therapy

Hodgkin's disease, neurologic involvement with

Horner's syndrome

Horner's syndrome, etiologies of

hospice

human immunodeficiency virus type 1

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

hyperpigmentation of skin

hypogammaglobulinemia

hypoglycemia

hypoglycemic coma

hypokalemia

hypokalemic alkalosis

hypokalemic periodic paralysis

hypotension, systemic

hypothalamus

hypothalamus, disturbance of

hypoxic encephalopathy

iatrogenic neurologic disorders

imbalance

immune complexes

immunodeficiency

immunoelectrophoresis, serum

immunohistochemistry

immunologic disease

immunosuppression

immunosuppressive agents

immunotherapy

impotence

inborn errors of metabolism

inclusion bodies

inclusion bodies, eosinophilic cytoplasmic

inclusion bodies, ubiquitin

inclusion body myositis

incontinentia pigmenti

infant, evaluation of

infantile neuronal degeneration

infantile tremor syndrome

infection

inflexibility, mental

insomnia

intellectual deficit

intellectual deterioration

intermittent positive pressure breathing

internal capsule

internet

intestinal pseudoobstruction

intrinsic hand muscles, wasting of

Jakob-Creutzfeldt disease

juvenile distal and segmental muscular atrophy

Kearns-Sayre syndrome

klippel feil syndrome

Klumpke palsy

Kugelberg-Welander syndrome

kyphoscoliosis, neurologic causes of

laboratory values, normal

lactic acidemia

laminectomy, cervical

lathyrism

laughing

laughing, pathologic

lead and the nervous system

lead poisoning

Leber's hereditary optic neuropathy

leg atrophy

leg weakness, bilateral

leg weakness, unilateral

Leigh's disease

leukemia

leukemia, neurologic findings assoc.with

leukodystrophy

leukoencephalopathy

level of consciousness, decreased

Lewy body disease, diffuse

Lhermitte's sign

lid closure, weakness of

life expectancy

life support, withdrawal of

life support, withholding of

life sustaining treatment

lymphadenopathy, hilar

lymphoma

lymphoma involving CNS

lysosomal storage disease

malformation, CNS, congenital

malformation, vascular

malformation, vascular, cerebral

Man-In-The-Barrel syndrome

masseter muscle wasting

masseter muscle weakness

median neuropathy

medical-legal aspects of neurology

MELAS syndrome

memory, defect of recent

memory, impairment of

meningismus

meningitis

mental retardation

mental status, abnormal

MERRF syndrome

metabolic disorder, primary

microinfarcts

Millard Gubler syndrome

Mills syndrome

mimics

minimally conscious state

miosis

misdiagnosis

misdirection

mitochondrial disease

mitochondrial encephalomyopathy

monoclonal antibodies

monoclonal gammopathy

monomelic amyotrophy

mononeuritis multiplex

mononeuropathy

mononeuropathy, motor

motor neuron disease, juvenile form

motor neuron disease, misdiagnosis

motor neuron disease, spontaneous recovery

motor system

movement disorder

movement disorder, extrapyramidal

MRI

MRI, abnormal

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, paramagnetic effect

MRI, spinal cord

MRI, spinal cord, increased intramedullary cord signal

MRI, spine

MRI, susceptibility weighted

MRS

multiple myeloma

multiple sclerosis

multiple sclerosis, diagnosis of

multiple sclerosis, differential diagnosis of

multiple sclerosis, misdiagnosis

multiple sclerosis, treatment of

multiple system atrophy

muscle atrophy, progressive

muscle atrophy, static

muscle biopsy

muscle cramp

muscle diseases, characteristics of

muscle wasting, diffuse

muscle weakness

muscle weakness, causes of

muscle weakness, proximal

muscle, metabolic disorders of

muscular dystrophy

muscular dystrophy, Becker

muscular dystrophy, Becker, carrier

muscular dystrophy, cardiovascular changes with

muscular dystrophy, differential diagnosis of

muscular dystrophy, Duchenne

muscular dystrophy, facioscapulohumeral

muscular dystrophy, limb-girdle

muscular dystrophy, neurogenic hypothesis of

mutism

myasthenia gravis

myasthenia gravis, distal weakness

myasthenia gravis, drug induced

myasthenia gravis, limb-girdle

myasthenia gravis, treatment of

myasthenic crisis

myasthenic syndrome

myelitis

myelitis, longitudinal

myelopathy, carcinomatous

myelopathy, chronic progressive

myelopathy, necrotizing

myelopathy, radiation induced

myeloradiculitis

myeloradiculopathy

myocardial infarction

myopathy, carcinomatous

myopathy, centronuclear

myopathy, distal

myopathy, mitochondrial

myopathy, neurogenic hypothesis of

myopathy, quadriceps

myopathy, thyroid disease causing

myxedema, neurologic manifestations of

N-acetyl-L-aspartic acid

nemaline rod myopathy

nemaline rod myopathy, adult onset

neoplasm, hormone producing

neoplasm, hormone producing, ectopic

neoplasm, pituitary

neoplasm, primary intracerebral

neoplasm, primary intracranial

neoplasm, primary of CNS

nerve biopsy

nerve conduction studies

nerve conduction studies, motor

nerve growth factor

neuritis, causes of

neurocutaneous disease

neuroendocrinology

neurofibrillary degeneration

neurofibromatosis 1

neurofibromatosis 2

neurogenic bladder

neurogenic vs.myopathic atrophy

neurologic complications

neurologic complications of, surgery

neurologic complications of, systemic cancer

neurologic complications of, systemic disease

neurologic consultation

neurologic disease

neurologic disease, diagnoses of

neurologic disease, incurable

neurologic evaluation

neurologic signs

neurologic symptoms

neurologic testing

neuromuscular blockade

neuromuscular disease, electrodiagnosis of

neuromuscular junction

neuromuscular junction, abnormality of

neuromyotonia

neuronal ceroid-lipofuscinosis

neuronal degeneration

neuronal migration disorder

neuronopathy

neuronopathy, sensory

neuroophthalmology

neuropathology

neuropathology, brain

neuropathy, diphtheritic

neuropathy, hereditary peripheral

neuropathy, motor

neuropathy, motor, multifocal

neuropathy, multifocal

neuropathy, painful

neuropathy, paraneoplastic

neuropathy, peripheral

neuropathy, peripheral, treatment

neuropathy, sensory

neuropathy, short-fiber

neuroprotective agents

newborn, evaluation of

next-generation sequencing

nystagmus, primary position of gaze

nystagmus, rotary

occupational neurologic disorders

occupational neuropathies

ocular motility, disorders of

old age, neurology of

olivary degeneration, hypertrophic

Onufrowicz nucleus

ophthalmoplegia

ophthalmoplegia, painful

ophthalmoplegia, progressive external

ophthalmoplegia, total

opiate

Oppenheim muscular dystrophy

otitis, neurologic complications with

owl's eye sign of spinal cord

pain, increased response

pain, management of chronic

paralysis, acute areflexic

paralysis, asymmetric

paralysis, use-related

paraneoplastic ganglionopathy

paranoia

paraoxonase

paraparesis

paraparesis, familial spastic

paraparesis, familial spastic, classification

paratrigeminal syndrome

paresthesias

Parkinson disease

Parkinson disease, motor neuron disease with

Parkinson disease, treatment of

Parkinsonism syndrome

Parkinsonism-dementia complex

paroxysmal neurologic deficits

pathology

patient information and support

penicillamine

periodic paralysis

periodic paralysis, thyrotoxic

peripheral vascular disease

peroneal muscle atrophy, causes of

peroxisomal disease

persistent vegetative state

phrenic nerve pacemaker

physical activity

physical therapy

physician assisted suicide

Pick's disease

pigmentary retinopathy

placebo

plasma cell dyscrasia

pleocytosis of cerebrospinal fluid

pneumoencephalogram(PEG)

poison, mercury

poison, neurologic problems with

poliomyelitis

poliomyelitis, provocation

poliomyelitis-like illness

polyclonal gammopathy

polyglucosan body

polyglucosan body disease

polymerase chain reaction

polymyositis

polyneuropathy

polyneuropathy, chronic inflammatory demyelinating

porphyria

positive sharp waves

post polio syndrome

posterior fossa, differential diagnosis of lesions of

posterior inferior cerebellar artery syndrome

posterior interosseous neuropathy

practice guidelines

preclinical

pregnancy, neurologic complications in

pressure sores

prevention of neurologic disorders

primary aldosteronism

primary lateral sclerosis

progeria

prognosis

progranulin

progressive muscular dystrophy

progressive neurologic disorder

progressive spinal muscular atrophy

proprioception

proprioception, abnormal

proximal muscle atrophy

pseudoathetosis

pseudobulbar palsy

pseudohypertrophy

psychiatric problems in neurologic disorders

psychomotor retardation

pulmonary function tests

pupil

pupil, abnormality in neurologic disorders

pyramidal tract

pyramidal tract dysfunction

rabies, nervous system involvement with

radiation hypersensitivity

radiation therapy, CNS treatment and complications with

radiation therapy, salivary gland

radiculitis

radiculopathy

ragged-red fibers

rapidly progressing neurologic illness

REM sleep behavior disorder

remote effect of cancer on the nervous system

renal cell carcinoma

renal stones

repetitive nerve stimulation

respirator

respiratory arrest

respiratory depression

respiratory failure

respiratory tract infection

retinitis pigmentosa

retinopathy

retrograde axonal flow

retrovirus

reverse split hand sign

review article

RFLPs

rheumatoid arthritis

rheumatoid arthritis, neurologic complications of

risk-benefit assessment

rodents

Roussy Levy syndrome

saccadic eye movements, abnormal

safety

salivation, excessive

sarcoidosis

scleroderma

scoliosis

scoliosis, neurologic association with

scooters

screening

sedation

segmental demyelination

seizure

seizure, children

seizure, treatment of

sensorineural hearing loss

sensory ganglia

sensory ganglia, abnormal

serologic testing of cerebrospinal fluid

serologic testing, false negative

serum alanine aminotransferase

shell fish poisoning

short stature

shoulder, subluxation

single photon emission computed tomography

skin, biopsy

skin, lesions in neurologic disorders

sleep

sleep apnea

sleep pathology and physiology

smell

Smell Identification Test

SMN1 gene

solvent

somatosensory evoked potentials

somatosensory evoked potentials, dermatomal

spinal cord degeneration

spinal cord, cervical

spinal cord, compression of

spinal cord, infarction of

spinal cord, injury of

spinal cord, injury, management of

spinal cord, ischemic lesion of

spinal cord, lesion of

spinal cord, neoplasm

spinal cord, neoplasm, extramedullary

spinal cord, neoplasm, intramedullary

spinal cord, pathologic exam of

spinal muscular atrophy

spinal muscular atrophy, adult onset

spinal muscular atrophy, classification

spinal muscular atrophy, intermediate form

spinocerebellar ataxia

spinocerebellar ataxia type 1

spinocerebellar degeneration

spirometry

spondylosis

sports medicine, neurology of

standing difficulty

stem cell tourism

stem cell transplantation

stereotyped behavior

sternocleidomastoid muscle

subacute myelo-opticoneuropathy(S.M.O.N.)complex

subacute sclerosing panencephalitis(S.S.P.E.)Dawson's disease

subarachnoid hemorrhage

survival motor neuron gene

symptomatic

syphilis, neurologic complications with

temporal lobe, atrophy

temporalis muscle wasting

tensilon test

tensilon test, false positive

thoracic outlet syndromes

thrombophlebitis

thyrotoxicosis

thyrotropin-releasing hormone

tick bite

tick paralysis

tick-borne encephalitis

Tolosa Hunt syndrome

tongue, atrophy

tongue, enlarged

tongue, fasciculations of

tongue, impaired movements of

treatment of neurologic disorder

tremor

tremor, postural

triangle of Guillain and Mollaret

tricresylphosphate

trigger finger

trinucleotide repeats

ulnar nerve, deep palmar branch of

ulnar neuropathy

unconsciousness

unconsciousness, episodic

unconsciousness, transient

upgaze, paralysis of

urea-cycle enzymopathies

urinary incontinence

valium

vasculopathy

venous thrombosis, non-cerebral

vestibular function, tests of

Waldenstrom's macroglobulinemia

walking frame

walking, difficulty with

weakness, generalized

weakness, infant

weakness, progressive

weaning from respirator, failure to

web sites

Weber's syndrome

weight loss

Werdnig-Hoffman disease

West disease

West Nile fever

wheelchair

whistle, inability to

white matter disease

winging of scapula

word-finding difficulty

workup

xerostomia

X-linked bulbospinal neuronopathy

Showing articles 1350 to 1400 of 7468 << Previous Next >>

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

Paraneoplastic Syndromes Involving the Eyes
In Walsh & Hoyt's Clin Neuro-ophthal, 4th ed, Williams & Wilkins, Vol 3, p 1735-1746, Miller,N.R., 1988

Mineralization of the Basal Ganglia Detected by CT in Hallervorden-Spatz Syndrome
Neurol 38:154-155, Tennison,M.B.,et al, 1988

Life Spans of Duchenne Muscular Dystrophy Patients in the Hospital Care Program in Japan
J Neurol Sci 81:155-158, Mukoyama,M.,et al, 1987

Practical Problems in the Respiratory Care of Patients with Muscular Dystrophy
NEJM 316:1197-1205, Smith,P.E.M.,et al, 1987

Cerebral Ventricular Dilation in Congenital Myotonic Dystrophy
J Pediatr 111:372-376, Regev,R.,et al, 1987

Tropical Spastic Paraparesis in the Seychelles Islands:A Clinical & Case-Control Neuroepidemiologic Study
Neurol 37:1323-1328, Roman,G.C.,et al, 1987

Progressive Multifocal Leukoencephalopathy Associated with Human Immunodeficiency Virus Infection
Ann Int Med 107:78-87, Berger,J.R., 1987

Neurologic Manifestations of AIDS
Medicine 66:407-437, McArthur,J.C., 1987

Reflex Sympathetic Dystrophy, A Review
Arch Neurol 44:555-561, Schwartzman,R.J.&McLellan,T.L., 1987

Retrovirus-Associated Myelopathies
Arch Neurol 44:659-663, Roman,G.C., 1987

Human T-Lymphotropic Virus Type I Antibodies in The Serum of Pts with Tropical Spastic Paraparesis in the Seychelles
Arch Neurol 44:605-607, Roman,G.C.,et al, 1987

Disseminated Cholesterol Embolism Presenting as Neuromyelitis Optica
BMJ 295:697, Goldman,M.,et al, 1987

Cranial Magnetic Resonance Imaging in the Evaluation of Myelopathy of Undetermined Etiology
Neurol 37:840-843, Miska,R.M.,et al, 1987

Late Denervation in Patients with Antecedent Paralytic Poliomyelitis
NEJM 317:7-12, Cashman,N.R.,et al, 1987

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

Spectrum of Inclusion Body Myositis
Arch Neurol 44:1154-1157, Ringel,S.P.,et al, 1987

Computed Tomography Abnormalities in Hanging
Neuroradiology 29:297-298, Bianco,F.&Floris,R., 1987

MR Imaging in a Case of Hallervorden-Spatz Disease
J Comput Assist Tomogr 11:1057-1058, Tanfani,G.,et al, 1987

Magnetic Resonance Imaging in Isolated Noncompressive Spinal Cord Syndromes
Ann Neurol 22:714-723, Miller,D.H.,et al, 1987

Effective Strategy for Prenatal Prediction of Duchenne & Becker Muscular Dystrophy
Lancet 2:1294-1296, Forrest,S.M.,et al, 1987

Progressive Nemaline (Rod) Myopathy Associated with HIV Infection
NEJM 317:1602-1603, Dalakas,M.C.,et al, 1987

Carbon Monoxide Toxicity:MR Imaging in the Brain
Radiology 162:787-788, Horowitz,A.L.,et al, 1987

Irradiation of Meningiomas of the Intracranial Anterior Visual Pathway
Ann Neurol 21:131-137, Kupersmith,M.J.,et al, 1987

Prenatal Diagnosis & Detection of Carriers with DNA Probes in Duchenne's Muscular Dystrophy
NEJM 316:985-993, 1018-10201987., Darras,B.T.,et al, 1987

Myelopathies & Retroviral Infections
Ann Neurol 21:113-115, Johnson,R.T.&McArthur,J.C., 1987

Tropical Spastic Paraparesis:HTLV-I Antibodies in Patients from the Seychelles
NEJM 316:51, Roman,G.C.,et al, 1987

Endemic Tropical Spastic Paraparesis Associated with HTLV-I:A Clinical & Seroepidem Study of 25 Cases
Ann Neurol 21:123-130, Vernant,J.C.,et al, 1987

Chronic Progressive Myelopathy Associated with Elevated Antibodies to HTLV-I & Adult T-Cell Leukemialike Cells
Ann Neurol 21:117-121, Osame,M.,et al, 1987

Antibody to Human T-Lymphotropic Virus Type I In West-Indian-Born UK Residents with Spastic Paraparesis
Lancet 1:415-416, Newton,M.,et al, 1987

Optico-Cerebral Syndrome:Simultaneous Hemodynamic Infarction of Optic Nerve & Brain
Neurol 37:263-268, Bogousslavsky,J.,et al, 1987

Tuberculous Meningitis:Role of CT in Management and Prognosis
JNNP 50:30-36, Kingsley,D.P.E.,et al, 1987

Radiculomeningeal Vascular Malformations of the Spine:MR Imaging
Radiology 164:845-849, Nasaryk,T.J.,et al, 1987

Bilateral Lucency of the Globus Pallidus Complicating Methylmalonic Acidemia
Ann Neurol 20:364-366, Korf,B.,et al, 1986

Brain Abscess, A Study of 45 Consecutive Cases
Medicine 65:415-431, Chun,C.H.,et al, 1986

Adult-Onset Autosomal Dominant Limb-Girdle Muscular Dystrophy
Ann Neurol 20:240-248, Chutkow,J.G.,et al, 1986

Hydrocephalic Dementia & Spinal Cord Tumor, Report of a Case & Review of the Literature
Arch Neurol 43:714-718, Feldmann,E.,et al, 1986

CT Myelography in Spinal Cysticercosis
J Comput Assist Tomogr 10:195-198, Zee,C.,et al, 1986

Causalgia as a Complication of Meningococcal Meningitis
BMJ 292:1710, McLelland,J.&Ellis,S.J., 1986

Segmental Myoclonus Clinical and Pharmacologic Study
Arch Neurol 43:1025-1031, Jankovic,J.&Pardo,R., 1986

Phosphorylase Deficiency
In Englel & Banker, Myology, McGraw-Hill Book Co, Ch 52, 1585-1601, DiMauro,S.&Bresolin,N., 1986

Facioscapulohumeral Dystrophy, in Myology, Basic & Clinical
McGraw-Hill Book Co, NY, p1251986., Munsat,T.L., 1986

Facioscapulohumeral Dystrophy Presenting in Infancy with Facial Diplegia & Sensorineural Deafness
Ann Neurol 17:513-516, Korf,B.R.,et al, 1985

Portal-Systemic Myelopathy after Portacaval Shunt Surgery
Arch Int Med 145:1921-1922, Lebovics,E.,et al, 1985

Vacuolar Myelopathy Pathologically Resembling Subacute Combined Degeneration in Patients with AIDS
NEJM 312:874-879, Petito,C.K.,et al, 1985

Sarcoidosis & Its Neurological Manifestations
Arch Neurol 42:909-917, Stern,B.J.,et al, 1985

Neurosyphilis
Arch Neurol 42:606-613, Simon,R.P., 1985

Prenatal Diagnosis & Carrier Detection of Duchenne Muscular Dystrophy with Closely Linked RFLPs
Lancet 1:655-658, Bakker,E.,et al, 1985

McArdle's Disease in the 1980s
NEJM 312:370-371, Layzer,R.B., 1985

Showing articles 1350 to 1400 of 7468 << Previous Next >>