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Differential
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abdominal muscle paralysis

acid maltase deficiency

acid maltase deficiency, adult

acquired immunodeficiency syndrome

activities of daily living scale

addiction, heroin-neurologic complications with

adenosine deaminase deficiency

adult polyglucosan body disease

advances in neurology

adverse drug reaction

alcohol, neurologic complications with

alpha glucosidase

altered states of consciousness

alveolar hypoventilation

aminoacidopathies

aminoacylase 1 deficiency

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, treatment of

anemia, hemolytic

anemia, megaloblastic

angina pectoris

angiography, neurologic complications with

angiotensin-converting enzyme

animal exposure

anterior horn cell disease

anti signal recognition particle antibody

anticholinergic drugs

anticoagulant, complications of

anticonvulsants

anticonvulsants, hypersensitivity syndrome

anticonvulsants, untoward effects of

antiphospholipid antibodies

antithyroid antibodies

antiviral agents

aromatic amino acid decarboxylase deficiency

arrhythmia, cardiac

arteritis, temporal

ascending paralysis

aspartate aminotransferase

ataxia, cerebellar

atherosclerosis, generalized

atrial fibrillation

atrioventricular block

autoimmune disease

autonomic dysfunction

B 12 deficiency

bacterial infection

bacterial infection, CNS

basal ganglia, lesion of

basal ganglia, lesion, bilateral

basophilic stippling of red blood cells

behavioral disorder

biotin deficiency

biotinidase deficiency

bladder dysfunction

blindness, monocular

blood dyscrasias, neurologic findings with

bone demineralization

bone marrow infarction

bone marrow necrosis

bone marrow suppression

bone marrow transplantation

Borrelia burgdorferi infection

brachial neuritis

brachial plexus neuropathy

brain biopsy, false negative

brain natriuretic peptide

brainstem, lesion of

bulimia nervosa

burning paresthesia

calcification, liver

calcification, lymph node

calf hypertrophy

campylobacter infection

Canavan's disease

cardiac enzymes

cardiac surgery, neurologic complications with

cardiovascular disease

carnitine deficiency myopathy

CAT scan, abnormal

CAT scan, chest

CAT scan, emission, abnormal

cauda equina, lesion of

central nervous system, infection of

central nuclei, muscle

cerebellar atrophy, secondary

cerebellar degeneration

cerebellar infarction

cerebellar lesion

cerebellar vermis

cerebral cortical atrophy

cerebral embolism

cerebral embolism, cardiac origin

cerebral infarction, hemorrhagic

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, gammaglobulin of

cerebrospinal fluid, gold sol.curve of

cerebrospinal fluid, oligoclonal IgG in

cerebrospinal fluid, proteincytologic dissociation

cerebrovascular accident

cerebrovascular accident, complications with

cerebrovascular accident, multiple

cerebrovascular accident, prognosis in

cerebrovascular accident, seizure with

cerebrovascular disease, cardiovascular disease with

ceruloplasmin, serum

chelation therapy

chemotherapy, CNS treatment and complications with

cherry red spot

cherry red spot-myoclonus syndrome

chest x-ray, abnormal

choreoathetosis

chorioretinitis

chromosomal abnormality

cirrhosis, infancy

Clinical Pathologic Conference(C.P.C.)

cogwheel rigidty

collagen vascular disease

congenital infection, CNS

congenital infection, viral

congenital myopathy

congestive heart failure

conjunctival injection

contractures, joint

coronary artery bypass

corpus callosum, infarction of

corpus callosum, lesion of

cranial nerve palsies

cranial neuropathy

cranial neuropathy, multiple

C-reactive protein, elevated

creatine kinase

creatine phosphokinase isoenzyme elevation

creatine phosphokinase MB isoenzyme elevation

creatine phosphokinase(CPK)elevated

critical care unit

cultured skin fibroblasts

cyclophosphamide

cystoisospora belli

cytochrome c oxidase

cytochrome c oxidase, deficiency

cytomegalic inclusion disease

cytomegalovirus infection

cytomegalovirus infection, congenital

decerebrate posture

deep gray nuclei

degenerative diseases of CNS

delay in diagnosis

dentate nuclei, lesion of

dermatomyositis

developmental disability

developmental milestones, loss of

developmental retardation

dexterity, impaired

diabetes insipidus

diagnostic criteria

diaphragmatic paralysis

differential diagnosis

difficulty climbing stairs

dilantin, hypersensitivity to

disability, neurological

distal muscle atrophy

distal muscle weakness

dopa responsive dystonia

dropped head syndrome

drug induced neurologic disorders

drug interactions

dysdiadochokinesia

dyskinesia, buccal lingual facial

dysostosis multiplex

dystonia, children

dystrophic calcification

eating disorder

echocardiogram, transesophageal

edema, periorbital

ejection fraction

ejection fraction, abnormal

electrocardiogram, abnormal

electroencephalogram, abnormalities of

electron microscopy

embolism, atheromatous

embolism, cholesterol

embolism, retinal

embolism, systemic

embolism, tumor

emergencies, neurologic

emotional lability

encephalitis, autoimmune

encephalitis, etiology

encephalitis, viral

encephalomyelitis

encephalopathy, acute

encephalopathy, Hashimoto's

encephalopathy, neonatal

encephalopathy, progressive

enzyme activity

enzyme inhibition

enzyme treatment

enzyme, muscle disease

eosinophilia-myalgia syndrome

epidemiology of neurology

Epstein-Barr virus

Epstein-Barr virus, negative

erythema migrans

esophageal varices

evoked potentials

exercise intolerance

extraocular muscle enlargement

extraocular muscle lesion

eye movement, disorders of

face, numbness of

facial appearance, abnormal

facial expression abnormality

facial nerve palsy

facial nerve palsy, bilateral

facial nerve palsy, recurrent

facial weakness

failure to thrive

feeding disorder

femoral artery catheterization

femoral neuropathy

ferritin, elevated

fine motor function, impaired

fingernails, abnormal

Fisher's syndrome

flaccid paralysis

flu-like illness

fundus, abnormality of

gammaglobulin therapy, intravenous

gangliosidosis GM1

gangliosidosis GM2

gastroenteritis

gastrointestinal bleeding

genetic counselling

genetic diagnosis, prenatal

genetic neurologic disorders

genetic screening

genetic testing

geographic location

globus pallidus, lesion of

globus pallidus, lesion of, bilateral

glycogen debranching enzyme deficiency

glycogen storage disease

Gowers maneuver

gram negative rod

granulomatous disease

growth retardation

Guillain Barre syndrome

Guillain Barre syndrome, axonal form

Guillain Barre syndrome, differential diagnosis of

Guillain Barre syndrome, etiology of

Guillain Barre syndrome, prognosis of

Guillain Barre syndrome, sensory

Guillain Barre syndrome, variant forms of

Hallervorden Spatz disease

Hallervorden Spatz disease, late onset

headache, new onset

headache, persistent

headache, retro-orbital

hearing loss, unilateral

heart block, complete

heavy metal intoxication

hematuria, microscopic

hemoglobin abnormality, neurologic complications of

hemolytic-uremic syndrome

hemorrhagic diathesis

hepatic encephalopathy

hepatic failure

hepatitis B virus

hepatitis E virus

hepatolenticular degeneration(Wilson's disease)

hepatolenticular degeneration(Wilson's disease), presymptomatic

hepatosplenomegaly

herniation syndromes, intracranial

heterophile antibody test

hexosaminidase-A

hip flexor weakness

histochemistry of muscle

HMGcoA reductase inhibitors

human granulocytic anaplasmosis

human immunodeficiency virus type 1

human immunodeficiency virus type 1, acute infection

hyperamylasemia

hyperbilirubinemia

hyperparathyroidism, secondary

hyperphosphatasia

hypersegmented polys

hypersensitivity reaction

hypertensive encephalopathy

hypertrophic intracranial pachymeningitis

hypoalbuminemia

hypoglycorrhachia

hypokalemic paralysis

hypomyelination

hypoparathyroidism

hypoparathyroidism, idiopathic

hypothalamus, disturbance of

hypothalamus, lesion of

hypotonia, infants

iatrogenic neurologic disorders

ileus, paralytic

immunologic disease

immunosuppression

immunosuppressive agents

inappropriate antidiuretic(A.D.H.)hormone

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

inborn errors of metabolism

inclusion bodies

inclusion bodies, intracytopasmic

inclusion body myositis

infection, recurrent

infectious mononucleosis

intellectual deficit

intellectual deterioration

interferon antibodies

interferon beta 1-a

interferon beta 1-b

intracerebral hemorrhage

intracranial pressure, increased

intrauterine infection

intrauterine infection, viral

ischemic exercise test

jaw claudication

Kayser-Fleischer ring

Krabbe's disease

Kugelberg-Welander syndrome

kyphoscoliosis, neurologic causes of

lactic dehydrogenase(LDH)

L-dopa, drug interactions with and side effects of

L-dopa, potentiators of

learning disability

learning disability, in children

leg weakness, bilateral

Legionella pneumophilia

Legionnaires'disease

Leigh's disease

leukocyte enzyme abnormality

leukoencephalitis

leukoencephalopathy

level of consciousness, decreased

life expectancy

limbic encephalitis

lipid lowering agent

lipid storage disorder of CNS

livedo reticularis

liver function enzymes

long bone lesion

Lowe's syndrome

lumbosacral plexopathy

lumbosacral plexus

lumbosacral plexus, neuritis

lymphadenopathy

lymphadenopathy, cervical

lymphadenopathy, hilar

lymphadenopathy, paraaortic

lymphocytic choriomeningitis

lymphoma involving CNS

lysosomal storage disease

lysosomes, abnoral

McArdle's disease

meconium staining

memory, impairment of

meningeal enhancement

meningitis, aseptic

meningitis, basilar

meningitis, chronic

meningitis, leptospira

meningitis, neutrophilic

meningitis, plasma cell

meningitis, recurrent

meningoencephalitis

meningomyelitis

menses, irregular

mental retardation

mental status, abnormal

metabolic acidosis

metabolic disorder, primary

metabolic disorder, primary-screening tests

methylmalonic acid, serum

microhemorrhage, intracerebral

migraine, seizures in

mitochondrial disease

molecular genetics

monoamine oxidase inhibitors

mononeuropathy multiplex

motor neuron disease

movement disorder

movement disorder, extrapyramidal

MRI, CAT scan compared to

MRI, contrast enhanced

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, eye of tiger sign

MRI, false negative

MRI, gradient-echo

MRI, hypointense signal foci on

MRI, paramagnetic effect

MRI, sulcal hyperintensity

MRI, susceptibility weighted

multinucleated giant cell

multiple sclerosis

multiple sclerosis, treatment of

muscle atrophy, progressive

muscle hypertrophy

muscle phosphofructokinase deficiency

muscle phosphorylase deficiency

muscle stiffness

muscle strength, testing

muscle tenderness

muscle wasting, diffuse

muscle weakness

muscle weakness, causes of

muscle weakness, insidious onset of

muscle weakness, intermediate onset of

muscle weakness, proximal

muscle weakness, sudden onset of

muscular dystrophy

muscular dystrophy, Becker

muscular dystrophy, central nervous system abnormality

muscular dystrophy, Duchenne

muscular dystrophy, Duchenne, carrier

muscular dystrophy, Duchenne, neonatal screening

muscular dystrophy, Duchenne, presymptomatic detection

myelitis, longitudinal

myeloneuropathy

myocardial infarction

myocardial infarction, acute

myocardial injury

myocardial ischemia

myoclonic jerks

myopathy, acute

myopathy, alcoholic

myopathy, centronuclear

myopathy, critically ill

myopathy, distal, vacuolar

myopathy, drug-induced

myopathy, genetic

myopathy, hypocalcemic

myopathy, hypokalemic

myopathy, inflammatory

myopathy, metabolic

myopathy, necrotizing

myopathy, necrotizing, autoimmune

myopathy, vacuolar

myotonic discharges

nausea and vomiting

neck tenderness

necrotizing granuloma

neonatal infection, viral

neonatal screening, genetic neurologic disorders

neoplastic angioendotheliosis

nerve conduction studies

neuraminidase deficiency

neuritis, heavy metals causing

neurogenic bladder

neurologic complications of, surgery

neurologic complications of, systemic disease

neurologic disease

neurologic disease, diagnoses of

neurologic examination

neurologic signs

neuromuscular disease, electrodiagnosis of

neuropathy, painful

neuropathy, peripheral

neuropathy, sensory

neuropathy, toxic

neurotransmitter

NMDA antagonists

nonsteroidal anti-inflammatory drug

nutritional deficiency

occupational neurologic disorders

oculogyric crisis

oculopharyngeal muscular dystrophy

ophthalmoplegia

optic chiasm, enlarged

optic disc edema

optic nerve, enlarged

optic nerve, lesion of

optic neuropathy

oral ulcerations

overlap syndrome

pain, abdominal

paralysis, acute

paralysis, acute areflexic

paraparesis, spastic

parasitic infection

parasitic infection, CNS

paraspinal muscle

paraspinal muscle weakness

paresthesias, feet

paresthesias, hands

Parkinson disease

Parkinson disease, on-off phenomena in

Parkinson disease, treatment of

Parkinsonism syndrome

PAS positive material in the brain

pediatric neurology

periarteritis nodosa

pericardial effusion

peripheral blood smear

peripheral blood smear, abnormal

pernicious anemia

personality change

phosphorylase b kinase deficiency

pigmentary retinopathy

pleocytosis of cerebrospinal fluid

pleural effusion

polyglucosan body

polyglucosan body disease

polymerase chain reaction

polymerase chain reaction, false negative

Pompe's disease of glycogen storage

position sensation, abnormal

positive sharp waves

postural abnormality

precipitating factors

pregnancy, neurologic complications in

prenatal diagnosis by amniocentesis

prevention of neurologic disorders

progressive multifocal leucoencephalopathy

progressive neurologic disorder

prolactin, elevated

proprioception, abnormal

protozoan infection

psychiatric disorder

psychiatric problems in neurologic disorders

psychomotor retardation

ptosis, unilateral

pulmonary embolism

pulmonary function tests

pulmonary hypertension

pulmonary infiltrates

pyloric stenosis

pyramidal tract

pyruvate dehydrogenase deficiency

pyruvate metabolism, abnormality of

radiculoneuritis

rapidly progressing neurologic illness

Raynaud's phenomenon

release phenomena

remote effect of cancer on the nervous system

renal failure, acute

reserpine and reserpine like drugs

respiratory distress syndrome, neurologic status with

respiratory failure

reticulum cell sarcoma

retinal degeneration

retro-orbital pain

rickettsial organism

risus sardonicus

Sabin-Feldman dye test

sarcoidosis, CNS

scalp tenderness

scoliosis, neurologic association with

second wind phenomena

sedimentation rate

sedimentation rate, elevated

seizure, children

seizure, neonatal

self-mutilation

semialdehyde dehydrogenase deficiency

sensorineural hearing loss

serologic testing

serologic testing of cerebrospinal fluid

serum alanine aminotransferase

serum gamma glutamyl transferase

serum glutamic oxaloacetic transaminase

serum glutamic pyruvic transaminase

serum lipase, elevated

severe acute respiratory syndrome

sex reassignment surgery

sexual behavior, disorder of

sickle cell disease

skin, lesions in neurologic disorders

sleep pathology and physiology

slit lamp examination

small for dates infant, problems in

speech disorder

speech disorder, childhood

speech, delayed development of

spinal cord, lesion of

spinal muscular atrophy

spinal muscular atrophy, adult onset

spirochete infection

spongy degeneration of brain

standing difficulty

startle reaction

steroid therapy, CNS treatment and complications with

subarachnoid hemorrhage

subcutaneous nodules

sweating, abnormality of

symmetric brain lesions

systemic illness

Tay-Sachs disease

temporal lobe, lesion

temporal lobe, lesion, bilateral

teratoma, ovarian

thalamus, infarction, bilateral

thalamus, lesion of

thalamus, lesion of-bilateral

thrombocytopenia

thrombophlebitis

tone, muscle, increased

tongue, enlarged

tongue, swelling

tongue, weakness

toxoplasma complement fixation test

toxoplasma gondii

toxoplasmosis, acquired

toxoplasmosis, CNS

toxoplasmosis, muscle

travel, foreign

treatment of neurologic disorder

tremor, intention

trientine dihydrochloride

trigeminal neuropathy

tumor necrosis factor inhibitor

type 2 muscle fiber

tyrosine hydroxylase deficiency

ultrasonography, head

uncal herniation

unconsciousness

urinary incontinence

urinary tract infection

urine test for metabolic disorders

urine test in toxic screen

vectors of infection

vertebral infarction

viral infection

viral infection, CNS

vision, blurred, monocular

visual acuity, decreased

visual acuity, decreased, monocular

visual evoked response

visual impairment

visual loss, sudden-unilateral

visual loss, transient

vitamin D deficiency

vitamin deficiency

vitamin, multiple

walking, difficulty with

weakness, generalized

weakness, progressive

weakness, proximal

weakness, severe

West Nile fever

Western immunoblot test

white matter disease

winging of scapula

X-linked myopathy

Showing articles 1700 to 1750 of 3508 << Previous Next >>

Ten Steps in Characterizing and Diagnosing Patients with Peripheral Neuropathy
Neurol 47:10-17, Dyck,P.J.,et al, 1996

Twelfth-Nerve Palsy:Analysis of 100 Cases
Arch Neurol 53:561-566, Keane,J.R., 1996

Multifocal Motor Neuropathy
JNNP 60:599-603, Nobile-Orazio,E., 1996

Hereditary Spastic Paraplegia:Advances in Genetic Research
Neurol 46:1507-1514, Fink,J.K.,et al, 1996

Syringomyelia as a Cause of Body Hypertrophy
Lancet 347:1593-1595, Sudo,K.,et al, 1996

New Antiepileptic Drugs
NEJM 334:1583-1590, Dichter,M.A.&Brodie,M.J., 1996

Progressive Encephalomyelitis with Rigidity Responsive to Plasmapheresis and Immunosuppression
Ann Neurol 40:451-453, Fogan,L., 1996

Idiopathic Dysautonomia Treated with Intravenous Gammaglobulin
Lancet 347:28-29, Heafield,M.T.E.,et al, 1996

Brief Report:Deficiency of a Dystrophin-Assoc Glycoprotein (Adhalin) in Pt with Muscular Dystrophy & Cardiomyopathy
NEJM 334:362-366, Fadic,R.,et al, 1996

Bent Spine Syndrome
JNNP 60:51-54, Serratrice,G.,et al, 1996

Pilot Trial of Immunoglobulin Versus Plasma Exchange in Patients with Guillain-Barre Syndrome
Neurol 46:100-103, Bril,V.,et al, 1996

Clinicopath Conf
Chronic Schistosoma Mansoni Infection Involving Large Intestine and Spinal Cord, Case 4-1996, NEJM 3, 4:2-389,1996., 1996

Progressive Ataxia, Focal Seizures, and Malabsorption Syndrome in a 41 Year Old Woman
JNNP 60:225-230, Mumford,C.J.,et al, 1996

Management of Patients Receiving Interferon Beta-1b for MS:Report of a Consensus Conf
Neurol 46:12-18, Lublin,F.D.,et al, 1996

Delayed-Onset Progressive Movement Disorders after Static Brain Lesions
Neurol 46:68-74, Scott,B.L.,et al, 1996

Reversible Encephalopathy with Cerebral Vasospasm in a Guillain-Barre Syndrome Patient Treated with Intravenous Immunoglobulin
Neurol 46:250-251, Voltz,R.,et al, 1996

Pediatric Ulnar Mononeuropathy:Report of 21 Electromyography-Documented Cases & Review of Literature
J Child Neurol 11:116-120, Felice,K.J.&Jones,H.R., 1996

Needle Electromyography in the Thoracic Paraspinal Muscles of Motor Neuron Disease
No to Shinkei-Brain & Nerve 48:637-642996., Kyuno,K.,et al, 1996

Idiopathic Acute Transverse Myelitis:MR Imaging Findings
Radiology 201:661-669, Tartaglino,L.M.,et al, 1996

Diagnostic Test for the Prader-Willi Syndrome by SNRPN Expression in Blood
Lancet 348:1068-1069, Wevrick,R.&Francke,U., 1996

A Case of Creutzfeldt-Jakob Disease (CJD) Started with Monoparesis of the Left Arm
Rinshi Shinkeigaku 36:1245-1248, Obi, T.,et al, 1996

The Electrophysiological Study of Diff Dx Between ALS & Cervical Spondylotic Myelopathy
EMG & Clin Neurophysiology 35:231-238995., Kang,D.X.&Fan,D.S., 1995

Lambert-Eaton Myasthenic Syndrome:Clinical Diagnosis,Immune-Mediated Mechanisms,and Update on Therapies
Ann Neurol 37:S63-S73, Sanders,D.B., 1995

Myasthenic Symptoms in Patients with Mitochondrial Myopathies
Muscle & Nerve 18:1338-1340, LeForestier,N.,et al, 1995

Systemic Sclerosis Sine Scleroderma:An Unusual Presentation in Scleroderma Renal Crisis
J Rheumatol 22:557-560, Molina,J.F.,et al, 1995

Acquired Neuromyotonia:Evidence for Autoantibodies Directed Against K+Channels of Peripheral Nerves
Ann Neurol 38:714-722, 7011995., Shillito,P.,et al, 1995

Neuromuscular Effects of Papuan Taipan Snake Venom
Ann Neurol 38:916-920, Connolly,S.,et al, 1995

Clinicopath Conf
Progressive Muscular Atrophy, Case 36-1995, NEJM 333:1406-1412995., , 1995

Neurodegeneration and Diabetes:UK Nationwide Study of Wolfram (DIDMOAD) Syndrome
Lancet 1458-1463, Barrett,T.G.,et al, 1995

Apolipoprotein E E4 in Inclusion Body Myositis
Ann Neurol 38:957-959, Garlepp,M.J.,et al, 1995

Detection of Borrelia Burgdorferi-Specific Antigen in Antibody-Negative Cerebrospinal Fluid in Neurologic Lyme Disease
Neurol 45:2010-2015, Coyle,P.K.,et al, 1995

Inclusion Body Myositis and Myopathies
Ann Neurol 38:705-713, Griggs,R.C.,et al, 1995

Myasthenic Symptoms in Patients with Mitochondrial Myopathies
Muscle & Nerve 18:1338-1340995., Forestier,N.L.,et al, 1995

Clinicopath Conf
Multiple Myeloma with Bilateral Carpal Tunnel Syndrome Probably Due to Secondary Amyloid Deposit, Ca, e38-1995,NEJM 333:1625-1630,1995., 1995

Prognosis for Survival After an Initial Stroke
Stroke 26:2011-2015, Lai,S.M.,et al, 1995

Clinicopath Conf
Intravascular Lymphomatosis, Case 31-1995, NEJM 333:992-999995., , 1995

Familial Hemiplegic Migraine and Autosomal Dominant Arteriopathy with Leukoencephalopathy (CADASIL)
Ann Neurol 38:817-824, Hutchinson,M.,et al, 1995

Neurological Correlated of Fetal Cocaine Exposure:Transient Hypertonia of Infancy and Early Childhood
Pediatrics 96:1070-1077, Chiriboga,C.A.,et al, 1995

Lambert-Eaton Myasthenic Syndrome (LEMS) in Association with Lymphoproliferative Disorders
Muscle & Nerve 18:715-719995., Argov,Z.,et al, 1995

Genotype-Phenotype Correlation in Adult-Onset Acid Maltase Deficiency
Ann Neurol 38:450-454, Wokke,J.H.J.,et al, 1995

Sarin Poisoning in Matsumoto, Japan
Lancet 346:290-293, Morita,H.,et al, 1995

The Use of Sumatriptan in Patients with Monoamine Oxidase Inhibitors
Neurol 45:1039-1040, Diamond,S., 1995

Cardiac Arrest Following the Use of Sumatriptan
Neurol 45:1211-1213, Kelly,K.M., 1995

Extreme Eyelid Swelling as an Unusual Presentation of Dysthyroid Orbitopathy
J Neuro-Ophthalmol 15:84-89, Rosen,C.E.&Kennerdell,J.S., 1995

Clinicopath Conf
Ganglioneuroblastoma of Adrenal Gland, Opsoclonus-Myoclonus-Ataxia Syndrome, Paraneoplastic, Case 27, 199EJM 333:579-586,1995., 1995

Dopamine, Dystonia, and the Deficient Co-Factor
Lancet 345:1130, Williams,A.C., 1995

Bilateral Ulnar Handcuff Neuropathies with Segmental Conduction Block
Muscle & Nerve 18:1021-1023995., Satkunam,L.&Zochodne,D., 1995

Neurological Multisystem Manifestation in Multiple Symmetric Lipomatosis:A Clinical and Electrophysiological Study
Muscle & Nerve 18:693-698995., Naumann,M.,et al, 1995

Multifocal Motor Neuropathy with Conduction Block:A Study of 24 Patients
JNNP 59:38-44, Bouche,P.,et al, 1995

X-Linked Pure Familial Spastic Paraparesis
Arch Neurol 52:665-669, Cambi,F.,et al, 1995

Showing articles 1700 to 1750 of 3508 << Previous Next >>