Neudle.com: myopathy critically ill

Differential
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abdominal distention

abdominal protrusion

abducens nerve paralysis

abscess, intracerebral

acanthocytosis

acquired immunodeficiency syndrome

acquired immunodeficiency syndrome dementia complex

ACTH, ectopic syndrome of

acute disseminated encephalomyelitis

acute intermittant porphyria

acute necrotizing encephalitis

acute respiratory distress syndrome

addiction, heroin-neurologic complications with

Addison's disease

Adies pupil

adrenal crisis, acute

advances in neurology

adverse drug reaction

amaurosis fugax, unilateral vs.bilateral

amnesia

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, differential diagnosis

aneurysm, multiple intracranial

angiotensin-converting enzyme

anterior horn cell disease

anti signal recognition particle antibody

antibiotics

anticonvulsants, untoward effects of

antineutrophil cytoplasmic autoantibodies

antisynthetase syndrome

antiviral agents

aortic valve, insufficiency

aspartate aminotransferase

aspiration

aspirin

asthma

asthma, poliomyelitis-like syndrome with

automatic implantable cardioverter-defibrillator

autonomic dysfunction

autonomic nervous system

basal ganglia, calcification of

basal ganglia, lesion of

basal ganglia, lesion, bilateral

basophilic stippling of red blood cells

Bassen-Kornzweig syndrome

behavioral disorder

bent spine syndrome

bitemporal visual field defect

bone marrow suppression

bone marrow transplantation

bone pain

bone scanning

botulism

bovine spongiform encephalopathy

brachial neuritis

brachial plexus neuropathy

brain biopsy

brain fog

brain natriuretic peptide

brain scan, abnormal

brainstem

brainstem, infarction of

bulbar palsy, acute-causes of

burning skin

cachexia

cafe au lait spots

calcification, intracranial

carotid artery disease

carpal tunnel syndrome

CAT scan, false negative

cavernous sinus, expansion

cavernous sinus, lesion of

CD4 counts

celiac disease, childhood

Central America

central nervous system, infection of

central retinal artery occlusion

cerebellar atrophy, secondary

cerebellar degeneration

cerebellar lesion

cerebral cortex

cerebral cortical atrophy

cerebral edema

cerebral embolism

cerebral infarction

cerebral venous thrombosis

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, culture of, viral

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, gammaglobulin of

cerebrospinal fluid, gold sol.curve of

cerebrospinal fluid, lactic acid concentration

cerebrospinal fluid, oligoclonal IgG in

cerebrospinal fluid, pressure increased

cerebrospinal fluid, protein of

cerebrospinal fluid, xanthochromia of

cerebrovascular accident

cerebrovascular accident, atrial myxoma

cerebrovascular accident, familial occurrence

cerebrovascular accident, mimics

cerebrovascular accident, misdiagnosis

cerebrovascular accident, multiple

cerebrovascular accident, non atherosclerotic cause of

cerebrovascular accident, nonvascular territory

cerebrovascular accident, recurrent

cerebrovascular accident, young adult

cerebrovascular disease

chemotherapy, CNS treatment and complications with

chest pain

chest x-ray, abnormal

chronic fatigue syndrome

chronic graft versus host disease

chronic progressive external ophthalmoplegia

Churg-Strauss syndrome

Chvostek sign

cingulate gyrus

cirrhosis

Clinical Pathologic Conference(C.P.C.)

collagen vascular disease

color vision, impaired

coma

comorbidities

complications

concentration, impaired

conduction block

confusion

congenital birth defects

congestive heart failure

conjunctival injection

controversies in neurology

conversion reaction

Coombs test, positive

coxsackievirus, myopathy with

cranial nerve palsies

cranial neuropathy

cranial neuropathy, multiple

craniopharyngioma

C-reactive protein, elevated

creatine phosphokinase isoenzyme elevation

creatine phosphokinase(CPK)elevated

Creutzfeldt-Jakob disease, genetic

critical care unit

critical illness

cultured skin fibroblasts

Cushing's syndrome

cyst, bone

cytoid bodies

cytomegalovirus infection

degenerative diseases of CNS

dementia, frontotemporal

dementia, presenile

dementia, rapidly progressive

dementia, transmissible

demyelinating disease

developmental milestones, loss of

developmental retardation

diabetes mellitus

diabetes mellitus, chemical

diabetes mellitus, neurologic manifestations of

diagnostic criteria

diaphragmatic paralysis

diarrhea

diarrhea, bloody

differential diagnosis

difficulty climbing stairs

diphtheria

diplopia

disability, neurological

disorientation

distal muscle weakness

diurnal variation

dizziness

dopa responsive dystonia

doxycycline

drug abuse

drug induced neurologic disorders

dystonia, etiology of

Ehlers-Danlos syndrome

Ehlers-Danlos syndrome, classification

ehrlichiosis

ejection fraction

ejection fraction, abnormal

electrocardiogram, abnormal

electroencephalogram

electroencephalogram, abnormalities of

electroencephalogram, periodic complexes

emergencies, neurologic

Emery-Dreifuss muscular dystrophy

emotional lability

encephalitis

encephalitis, brainstem

encephalitis, eastern equine

encephalopathy, metabolic

encephalopathy, progressive

encephalopathy, septic

eosinophilic granulomatosis with polyangiitis

epidemic

epidemiology of neurology

epistaxis

Epstein-Barr virus

Epstein-Barr virus, negative

erythrocyte

evoked potentials

executive dysfunction

extraocular muscle lesion

eye movement, disorders of

facial nerve palsy, recurrent

facial pain

facial weakness

facial weakness, bilateral

fingernails, abnormal

fluorescent treponema antibody absorption/false positive

foam cells

foot drop

foot ulcer, neuropathic

Friedreich's ataxia

fundus, abnormality of

gadolinium

gag reflex, depressed

gammaglobulin therapy, intravenous

gargoylism

gastroenteritis

gastrointestinal disease, neurologic complications

gastrointestinal motility

gastrointestinal perforation

gastroparesis

gaze palsy

gaze palsy, supranuclear

genetic neurologic disorders

genetic screening

genetic testing

glaucoma

glucose tolerance test, abnormal

granulomatosis with polyangiitis

granulomatosis, allergic

granulomatous disease

Graves ophthalmopathy

growth hormone

Guillain Barre syndrome

Guillain Barre syndrome, differential diagnosis of

Guillain Barre syndrome, etiology of

Guillain Barre syndrome, variant forms of

Hallgren's syndrome

hallucination

hallucination, auditory

hallucination, visual

hand weakness

Hand-Schuller-Christian disease

heart block, complete

heart murmur

heart rhythm

heat intolerance

heavy metal intoxication

heliotrope rash

hematuria, microscopic

hemianopia, homonymous

hemiparesis

hemoglobinuria

hemolytic-uremic syndrome

heralding manifestation

herpes simplex encephalitis

herpes simplex encephalitis, differential diagnosis of

herpes virus

herpes virus infection

heterophile antibody test

highly active antiretroviral therapy

hip pain

hippocampus, hyperintense

hirsutism

histochemistry

histochemistry of muscle

human immunodeficiency virus type 1

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

hypercoagulable state

hypereosinophilic syndrome(HES)

hypergammaglobulinemia

hyperpigmentation of skin

hypertrophic intracranial pachymeningitis

hypertrophic spinal pachymeningitis

hypocalcemia

hypocomplementemia

hypokalemia

hypokalemic alkalosis

hypokalemic paralysis

hypokalemic periodic paralysis

hyponatremia

hypoosmolality of serum

hypotension, systemic

hypothalamus

hypothalamus, disturbance of

hypothyroidism

iatrogenic neurologic disorders

idiopathic CD4+lymphopenia

ileus, paralytic

imbalance

immune checkpoint inhibitors

immune-related adverse events

immunosuppressive agents

immunotherapy

impotence

impulsivity

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

inattention

inclusion bodies

inclusion body myositis

incoordination

India

infection

infectious mononucleosis

intellectual deterioration

intestinal biopsy

intestinal pseudoobstruction

intracerebral hemorrhage

intracranial hypertension, benign

intrauterine infection

intrauterine infection, viral

intrinsic hand muscles, wasting of

iritis

irritability

islet cell tumor

Jakob-Creutzfeldt disease

Jakob-Creutzfeldt disease, variant

jaundice

jaw pain

joint hypermobility

juvenile idiopathic inflammatory myopathy

Kearns-Sayre syndrome

keratitis

keratitis, interstitial

keratoconus

kyphoscoliosis, neurologic causes of

lactic dehydrogenase(LDH)

lacunar infarction

laminar necrosis, cortical

laminopathies

Laurence-Moon-Bardet-Biedl syndrome

L-dopa

Leber's hereditary optic neuropathy

leg spasms

leg spasms, painful

leg weakness, bilateral

leg weakness, unilateral

Leigh's disease

lenticular nucleus, lesion of, bilateral

leukemia

leukemia, neurologic findings assoc.with

leukocytosis

leukodystrophy

leukopenia

level of consciousness, decreased

lid closure, weakness of

life expectancy

limbic encephalitis

linear lesion

lipid storage disorder of CNS

lipoma of skin

lipomatosis

lipomatosis, multiple symmetrical

lissencephaly

livedo reticularis

liver disease

liver function enzymes

liver transplantation

lymphocytic choriomeningitis

lymphocytosis

lymphoma

lymphoma involving CNS

lymphopenia

lysosomal storage disease

malaise

malformation, CNS, congenital

Melkersson's syndrome

memory, impairment of

meningeal biopsy

meningeal enhancement

meningitis, neutrophilic

meningoencephalitis

mental retardation

mental status, abnormal

MERRF syndrome

microcephaly

microscopic polyangiitis

middle cerebral artery, occlusion of

mitochondrial disease

mitochondrial disease, pathogenesis

mitochondrial encephalomyopathy

mitral valve prolapse

MNGIE syndrome

molecular genetics

monoclonal antibodies

monoclonal gammopathy

monoclonal gammopathy of uncertain significance

mononeuritis multiplex

mononeuropathy

mononeuropathy multiplex

MRI, CAT scan compared to

MRI, contrast enhanced

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, sulcal hyperintensity

MRI, susceptibility weighted

MRS

mucopolysaccharidoses

multinucleated giant cell

multiple organ failure

multiple sclerosis

muscle atrophy, progressive

muscle wasting, diffuse

muscle weakness

muscle weakness, causes of

muscle weakness, pattern

muscle weakness, proximal

muscle weakness, sudden onset of

muscular dystrophy

muscular dystrophy, cardiovascular changes with

muscular dystrophy, central nervous system abnormality

muscular dystrophy, classification

muscular dystrophy, congenital

muscular dystrophy, Duchenne

muscular dystrophy, facioscapulohumeral

muscular dystrophy, limb-girdle

myelopathy, carcinomatous

myelopathy, chronic progressive

myocardial infarction

myoclonus, stimulus sensitive

myoedema

myoglobinuria

myopathy

myopathy inflammatory, classification

myopathy, critically ill

myopathy, drug-induced

myopathy, glycogen storage

myopathy, inclusion body

myopathy, inclusion body with Paget's disease

myopathy, inflammatory

myopathy, inflammatory, classification

myopathy, metabolic

myopathy, mitochondrial

myopathy, necrotizing

myopathy, necrotizing, autoimmune

myopathy, necrotizing, immune-mediated

myopathy, proximal

myopathy, scleromyxedema

myopathy, steroid induced

myopathy, thyroid disease causing

myositis specific autoantibody

myositis, acute of childhood

myositis, juvenile

myositis, ocular

myositis, overlap

myositis, post infectious

myotonia dystrophica

myxedema coma

myxedema, neurologic manifestations of

nasal septum, perforation of

necrotizing vasculitis

nemaline rod myopathy

nemaline rod myopathy, adult onset

neoplasm, hormone producing

neoplasm, hormone producing, ectopic

neoplasm, metastatic

neoplasm, pituitary

neoplasm, primary of CNS

neoplastic angioendotheliosis

Nepal

nephritis

nerve biopsy

nerve conduction studies

neuritis

neuritis, heavy metals causing

neurocutaneous disease

neuroendocrinology

neurofibrillary degeneration

neurofibromatosis 2

neurologic complications

neurologic complications of, chronic pulmonary disease

neurologic complications of, surgery

neurologic complications of, systemic cancer

neurologic complications of, systemic disease

neurologic disease

neurologic disease, diagnoses of

neurologic examination, focal

neurologic signs

neurologic symptoms

neuromuscular blockade

neuromuscular disease, electrodiagnosis of

neuromuscular junction, abnormality of

neurons

neuroophthalmology

neuropathology

neuropathology, brain

neuropathy

neuropathy, acute

neuropathy, diphtheritic

neuropathy, medication induced

neuropathy, motor, multifocal

neuropathy, peripheral

neuropathy, toxic

neuropathy, vasculitic, systemic

next-generation sequencing

obsessive-compulsive disorder

ocular myopathy

old age, neurology of

olfactory bulb

ophthalmoplegia

ophthalmoplegia, progressive external

ophthalmoplegia, total

opportunistic infection

opportunistic infection, CNS

optic neuritis, bilateral

optic neuropathy

oral contraceptives

organ transplantation

organomegaly

otitis, neurologic complications with

pacemaker, cardiac-transvenous

paralysis, acute areflexic

paraspinal muscle weakness

Parkinsonism syndrome

partial thromboplastin time, prolonged

PAS positive

patient information and support

periodic paralysis, thyrotoxic

peripheral blood smear

peripheral blood smear, abnormal

photosensitivity, skin

pigmentary retinopathy

pituitary, hormones of

plasmapheresis

PLEDs

PLEDs, bilateral independent

PLEDs, etiology of

pleocytosis of cerebrospinal fluid

poliomyelitis vaccine

poliomyelitis-like illness

polycythemia, primary

polydactyly

polymerase chain reaction

polymerase chain reaction, false negative

polymerase chain reaction, false positive

polymyositis

polymyositis, eosinophilic

polyneuropathy

polyneuropathy, chronic inflammatory demyelinating

polyneuropathy, critically ill

polyneuropathy, critically ill, children

Pompe's disease of glycogen storage

Pompe's disease, infantile

pons, lesion of

porphyria

position sensation, abnormal

positive sharp waves

post infectious polyneuropathy

posterior inferior cerebellar artery syndrome

postinfectious

postural abnormality

postviral fatigue syndrome

precipitating factors

pregnancy, neurologic complications in

prenatal diagnosis by amniocentesis

prevention of neurologic disorders

primary aldosteronism

prion disease

progeria

prognosis

progressive multifocal leucoencephalopathy

progressive neurologic disorder

proprioception, abnormal

protease inhibitor, HIV-1

protein 14-3-3, cerebrospinal fluid

proteinuria

proximal muscle atrophy

pseudoretinitis pigmentosa

psychiatric disorder

psychiatric problems in neurologic disorders

psychological testing

psychomotor retardation

pulmonary function tests

pulmonary infiltrates

pupil, abnormality in neurologic disorders

rapidly progressing neurologic illness

rash

rash, hand

Raynaud's phenomenon

real-time quaking-induced conversion

recurrent

regional enteritis

rehabilitation for neurologic disorders

remote effect of cancer on the nervous system

renal failure

renal failure, acute

renal stones

repetitive nerve stimulation

respirator

respiratory distress syndrome, neurologic status with

respiratory failure

respiratory tract infection

reticulum cell sarcoma

retina, abnormal

retinal artery occlusion

reversible neurologic disorder

review article

Reye's syndrome

Reye's syndrome, adult

rhabdomyolysis

rheumatoid arthritis

rheumatoid arthritis factor(R.A.factor)

rheumatoid arthritis, neurologic complications of

Rocky Mountain spotted fever

scleroderma, neurologic involvement with

sedimentation rate, elevated

seizure

seizure, focal

seizure, laughing as manifestation

sensorineural hearing loss

serologic testing of cerebrospinal fluid

seronegative

serum alanine aminotransferase

serum lipase, elevated

serum sickness

severe acute respiratory syndrome

short stature

sicca syndrome

sinemet

single photon emission computed tomography

single-fiber electromyography

Sjogren's syndrome, neurologic manifestations of

skin, biopsy

skin, darkening of

skin, hyperextensible

skin, lesions in neurologic disorders

skin, thin

skin, translucent

slit lamp examination

Spielmeyer Vogt syndrome

spinal cord

spinal cord, compression of

spinal cord, lesion of

spinal pachymeningitis

spinal stenosis

spinal stenosis, cervical canal

splenomegaly

splinter hemorrhages

spongy degeneration of brain

status asthmaticus

stem cell transplantation

steroid

steroid psychosis

steroid therapy, CNS treatment and complications with

stiff man syndrome

Still's disease

stooped posture

storage disease of CNS

strokelike episodes

subarachnoid hemorrhage

subcutaneous edema

subcutaneous nodules

sudden death

sweating, abnormality of

Sweet's syndrome

syncope

systemic illness

systemic lupus erythematosus

systemic lupus erythematosus, neurologic complications with

tachycardia

Takayasu's arteritis

tandem gait, ataxic

temporal artery, biopsy

temporal lobe, lesion

temporal lobe, lesion, bilateral

tenderness

tensilon test, false positive

thalamus, infarction, bilateral

thalamus, lesion of

thalamus, lesion of-bilateral

transient ischemic attack

transient neurologic deficit

transverse smile

travel, foreign

treatment of neurologic disorder

tremor

trigeminal neuralgia

trigeminal neuropathy

trigeminal neuropathy, sensory

trinucleotide repeats

tropical disease

Trousseau's sign

ulcerative colitis

ultrasonography, head

ultrasonography, head, fetus-neonate

urine osmolality, elevated

urine test in toxic screen

visual acuity, decreased

visual field defect

visual fields, constricted

visual loss

walking, difficulty with

Watson-Schwartz reaction

weakness

weakness, acute

weakness, focal

weakness, generalized

weakness, progressive

weakness, proximal

weakness, rapidly progressive

weakness, severe

weaning from respirator, failure to

web sites

weight loss

West Nile fever

Western immunoblot test

whole genome sequencing

Showing articles 1750 to 1800 of 2740 << Previous Next >>

Immunologic Aspects of Neurological and Neuromuscular Diseases
JAMA 268:2918-2922, Zweiman,B.&Levinson,A.I., 1992

Glycogen Storage Disease Type III (Glucogen Debranching Enzyme Def) :Biochem Defects & Myopathy & Cardiomyopathy
Ann Int Med 116:896-900, Coleman,R.A.,et al, 1992

The Dropped Head Syndrome
Neurol 42:1625-1627, Suarez,G.A.&Kelly,J.J., 1992

Duplication of Part of Chromosome 17 is Commonly Associated with HMSN Type I (Charcot-Marie-Tooth Disease Type 1)
Ann Neurol 31:570-572, Hallam,P.J.,et al, 1992

De-Novo Mutation in Hereditary Motor and Sensory Neuropathy Type I
Lancet 339:1081-1082, Hoogendijk,J.E.,et al, 1992

Genetic Diagnosis of Gaucher's Disease
Lancet 339:889-892, Mistry,P.K.,et al, 1992

Wolfram Syndrome:Evidence of a Diffuse Neurodegenerative Disease by Magnetic Resonance Imaging
Neurol 42:1220-1224, 1992,, Rando,T.A.,et al, 1992

Chronic Limb-Girdle Myasthenia Gravis
Neurol 42:1153-1156, Oh,S.J.&Kuruoglu,R., 1992

Clinical and Electrophysiologic Improvement in Lambert-Eaton Syndrome with Intravenous Immunoglobulin Therapy
Neurol 42:1422-1423, Bird,S.J., 1992

Neurolymphomatosis:A Clinicopathologic Syndrome Re-emerges
Neurol 42:1136-1141, Diaz-Arrastia,R.,et al, 1992

Causal Heterogeneity in Isolated Lissencephaly
Neurol 42:1375-1388, Dobyns,W.B.,et al, 1992

Population Screening for Fragile X
Lancet 339:1210-1213, Turner,G.,et al, 1992

Role of MR Imaging in the Management of Spinal Infections
AJR 158:1333-1345, Sharif,H.S., 1992

Epilepsy and Stress, Time for Proper Studies of the Association
BMJ 305:378-379, Betts,T., 1992

Anosognosia in Patients with Cerebrovascular Lesions, A Study of Causative Factors
Stroke 23:1446-1453, Starkstein,S.E.,et al, 1992

Coma Assoc with Bursts of Abnor Movements & Cognitive Disturb:Acute Encephalopathy of Obscure Origin
J Pediatr 121:845-851, Sebire,G.,et al, 1992

Plasma-Cell Dyscrasia with Polyneuropathy, The Spectrum of POEMS Syndrome
NEJM 327:1919-1923, Miralles,G.D.,et al, 1992

High Frequency of Hemorrhage Strokes in Jerusalem During the Persian Gulf War
Neurol 42:2225-2226, Kleinman,Y.,et al, 1992

The Psychological Consequences of Predictive Testing for Huntington's Disease
NEJM 327:1401-1405, 14491992., Wiggins,S.,et al, 1992

Hysteria Following Brain Injury
JNNP 55:1046-1053, Eames,P., 1992

Evaluation and Management of the Patient with Syncope
JAMA 268:2553-2560, Kapoor,W.N., 1992

Psychosis with Disulfiram Prescribed Under Probation Order
BMJ 305:763, Rossiter,S.K., 1992

Attention-Deficit Hyperactivity Disorder in Adults
Clinical Therapeutics 14:138-147, Bellak,L.&Black,R.B., 1992

Risk FActors for Central Nervous System Manifest of Gastroenteritis-Associated Hemolytic-Uremic Syndrome
Pediatrics 90:616-621, Cimolai,N.,et al, 1992

Travel and Ciguatera Fish Poisoning
Arch Int Med 152:2049-2053, Lange,W.R.,et al, 1992

The Postpolio Syndrome:No Evidence for Poliovirus Persistence
Ann Neurol 32:728-732, Melchers,W.,et al, 1992

Severe Phenytoin Hypersensitivity with Myopathy:A Case Report
Neurol 42:2303, Barclay,C.L.,et al, 1992

McArdle's Disease with Late-Onset Symptoms:Case Report & Review of the Literature
JNNP 55:407-408, Felice,K.J.,et al, 1992

Behavior Changes Following Temporal Lobectomy, With Special Reference to Psychosis
JNNP 55:89-91, Trimble,M.R., 1992

The First Decade of Molecular Genetics in Neurology:Changing Clinical Thought and Practice
Ann Neurol 32:207-214, Rowland,L.P., 1992

Lyme Disease Associated with Fibromyalgia
Ann Int Med 117:281-285, Dinerman,H.&Steere,A.C., 1992

Controlled Trial of Plasma Exchange and Leukapheresis in Polymyositis and Dermatomyositis
NEJM 326:1380-1384, Miller,F.W.,et al, 1992

Dystrophinopathy in Isolated Cases of Myopathy in Females
Neurol 42:967-975, Hoffman,E.P.,et al, 1992

Unstable DNA Sequence in Myotonic Dystrophy
Lancet 339:1125-1128, Harley,H.G.,et al, 1992

Generalized Myositis in Behcet Disease:TReatment with Cyclosporine
Ann Int Med 116:651-653, Lingenfelser,T.,et al, 1992

Cerebrovascular Complications of Primary Herpes Varicella-Zoster Infection
Editorial, Lancet 339:1449-14501992., , 1992

Familial Inclusion Body Myositis:Evidence for Autosomal Dominant Inheritance
Neurol 42:897-902, Nevile,H.E.,et al, 1992

Clinicopath Conf
Emery-Dreifus Muscular Dystrophy, NEJM 327:548-5571992., , 1992

Pravastatin-Associated Inflammatory Myopathy
NEJM 327:649-650, Schalke,B.B.,et al, 1992

Psychiatric Disturbances in Metachromatic Leukodystrophy
Arch Neurol 49:401-406, Hyde,T.M.,et al, 1992

Clinicopath Conf
Churg-Strauss Syndrome, Case 18-1992, NEJM 326:1204-1212992., , 1992

Small Infarctions of Cochlear, Retinal, and Encephalic Tissue in Young Women
Stroke 23:903-907, Schwitter,J.,et al, 1992

Wilson Disease
Medicine 71:139-164, Brewer,G.J.&Yuzbasiyan-Gurkan,V., 1992

Wilson's Disease:Current Status
Am J Med 92:643-654, Yarze,J.C.,et al, 1992

Wilson's Disease:The Problem of Delayed Diagnosis
JNNP 55:692-696, Walshe,J.M.&Yealland,M., 1992

Relapsing Acue Disseminated Encephalomyelitis Assoc with Chronic E. B. Virus Infection:MRI Findings
Neuroradiology 34:340-342, Shoji,H.,et al, 1992

Clinical and NEuroradiol Findings of Congen Hydroceph in Infant Born to Mother with HTLV-I-Assoc Myelopathy
Neurol 42:1406-1408, Tohyama,J.,et al, 1992

Thyrotoxic Periodic Paralysis in the US, Report of 7 Cases & Review of the Literature
Medicine 71:109-120, Ober,K.P., 1992

Fibromyalgia:The Copenhagen Declaration
Lancet 340:663-664, Csillag,C., 1992

Human Herpesvirus-6:Clinical Implications of a Recently Discovered, Ubiquitous Agent
J Pediatr 121:173-181, Leach,C.T.,et al, 1992

Showing articles 1750 to 1800 of 2740 << Previous Next >>