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Differential
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abdominal distention

abdominal muscle paralysis

acid maltase deficiency

acid maltase deficiency, adult

acquired immunodeficiency syndrome

acquired immunodeficiency syndrome, infants and children

acquired immunodeficiency syndrome-related complex

acute coronary syndrome

addiction, heroin

advances in neurology

adverse drug reaction

alcohol, neurologic complications with

alcoholic withdrawal states, DT's, convulsions, etc.

alpha glucosidase

alveolar hypoventilation

amyotrophic chorea-acanthocytosis

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, bulbar

amyotrophic lateral sclerosis, differential diagnosis

anesthesia, general

aneurysm, intracranial, delayed cerebral ischemia with

angina pectoris

angiography, neurologic complications with

angiotensin-converting enzyme

animal exposure

anoctaminopathy

anterior horn cell disease

anterior tibial muscle weakness

anti HMGCR antibody

anti Jo1 antibody

anti Ku antibody

anti Mi2 antibody

anti signal recognition particle antibody

anticholinergic drugs

anticholinergic drugs, side effects of

anticoagulant, complications of

anticoagulant, treatment

anticonvulsants

anticonvulsants, hypersensitivity syndrome

anticonvulsants, untoward effects of

aphasia, global

arrhythmia, cardiac

aspartate aminotransferase

ataxia, cerebellar

atherosclerosis, generalized

atrial fibrillation

atrioventricular block

atypical lymphocytes

autoimmune disease

autonomic dysfunction

axonal degeneration

azidodeoxythymidine

bacterial endocarditis, neurologic manifestations of

bacterial infection

bacterial infection, CNS

basal ganglia, calcification of

basal ganglia, degeneration

behavioral disorder

Bence Jones protein

bent spine syndrome

bicaudate index

biologic markers

brain natriuretic peptide

Brugada syndrome

bulging of biceps

bulimia nervosa

calcification, intracranial

calcification, muscle

calf hypertrophy

carbon monoxide poisoning

carcinoma of esophagus

carcinoma of pancreas

cardiac arrest and resuscitation

cardiac enzymes

cardiac surgery, hypothermia and circulatory arrest for

cardiac surgery, neurologic complications with

cardiopulmonary bypass

cardiovascular disease

carnitine deficiency myopathy

carpal tunnel syndrome

CAT scan, abnormal

CAT scan, chest

CAT scan, contrast enhanced

CAT scan, emission, abnormal

CAT scan, gray matter enhancement

CAT scan, muscle

CAT scan, pelvis

catatonia, lethal

caudate nucleus

caudate nucleus, atrophy

central core disease

central nervous system, infection of

central pontine myelinolysis

cerebellar atrophy, secondary

cerebellar degeneration

cerebellar infarction

cerebellar lesion

cerebral edema, cytotoxic

cerebral embolism

cerebral embolism, cardiac origin

cerebral ischemia

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, enzymes in

cerebrospinal fluid, gammaglobulin of

cerebrospinal fluid, gold sol.curve of

cerebrospinal fluid, oligoclonal IgG in

cerebrospinal fluid, pressure increased

cerebrovascular accident

cerebrovascular accident, multiple

cerebrovascular disease, cardiovascular disease with

chemotherapy, CNS treatment and complications with

chest x-ray, abnormal

chewing, impaired

chlordiazepoxide

chorea, familial

chromosomal abnormality

chronic fatigue syndrome

Clinical Pathologic Conference(C.P.C.)

clorazepate dipotassium

clubfoot as related to neurologic disease

coenzyme Q10 deficiency

cold intolerance

cold temperature

compartment syndrome

compartment syndrome, gluteal

compression neuropathy

conduction block

congenital myopathy

congenital myopathy, inflammatory

congestive heart failure

Congo red stain

conjunctival injection

contractures, joint

contraindications

contusion, cerebral

conversion reaction

coronary artery bypass

cranial nerve palsies

creatine phosphokinase BB isoenzyme elevation

creatine phosphokinase isoenzyme elevation

creatine phosphokinase MB isoenzyme elevation

creatine phosphokinase(CPK)elevated

critical care unit

critical illness

cryoglobulinemia

cryptococcal meningitis

cultured skin fibroblasts

dantrolene sodium

deep gray nuclei

delay in diagnosis

delayed muscle relaxation

dermatomyositis

dermatomyositis, childhood

descending paralysis

developmental disability

developmental retardation

diabetes mellitus

diagnostic criteria

diamond on quadriceps

diaphragmatic paralysis

differential diagnosis

difficulty climbing stairs

dilantin, hypersensitivity to

disability, neurological

dislocated hip, congenital

disseminated intravascular coagulation(DIC)

distal muscle atrophy

distal muscle weakness

dopamine antagonist

dropped head syndrome

drug abuse, neurologic complications of

drug abuse, toxic screen In

drug induced neurologic disorders

drug interactions

drug withdrawal

dysferlinopathy

dyskinesia, buccal lingual facial

dystonia, drug induced

dystroglycanopathies

dystrophic calcification

eating disorder

echocardiogram, transesophageal

eclampsia, postpartum

edema, periorbital

electrocardiogram, abnormal

electroencephalogram

electroencephalogram, abnormalities of

electroencephalogram, video monitoring with

electromyogram, decremental response

electron microscopy

embolism, atheromatous

embolism, cholesterol

embolism, paradoxical

embolism, retinal

embolism, source of

embolism, systemic

embolism, tumor

emergencies, neurologic

Emery-Dreifuss muscular dystrophy

encephalitis, brainstem

encephalitis, paraneoplastic

encephalomyopathy

encephalopathy, acute

endocarditis, acute bacterial

endocarditis, infectious

endocarditis, marantic

endocarditis, neurologic manifestations with

entrapment neuropathy

enzyme treatment

enzyme, muscle disease

eosinophilia-myalgia syndrome

eosinophilic fasciitis

epidemiology of neurology

episodic disorders

Epstein-Barr virus

ethics in neurology

exercise intolerance

extraocular muscle lesion

eye movement, disorders of

facial appearance, abnormal

facial expression abnormality

facial swelling

facial weakness

facial weakness, bilateral

facioscapulohumeral syndrome

failure to thrive

fatigable chewing

feeding disorder

femoral artery catheterization

ferritin, elevated

fine motor function, impaired

flu-like illness

foot drop, bilateral

gammaglobulin therapy, intravenous

gastrointestinal bleeding

gastrointestinal disease, neurologic complications

gastrointestinal motility

gastrointestinal perforation

genetic counselling

genetic diagnosis, prenatal

genetic neurologic disorders

genetic screening

genetic testing

glycogen storage disease

Gowers maneuver

gram negative rod

growth retardation

Gulf War syndrome

hallucination, visual

head injury, defibrination following

head injury, management of

headache, bilateral

headache, temporal

heart block, complete

heliotrope rash

hematuria, microscopic

hemidiaphragm, paralysis of

hemorrhagic diathesis

hepatic failure

hepatosplenomegaly

heralding manifestation

hereditary myopathy with early respiratory failure

herpes simplex encephalitis

heterophile antibody test

high arched palate

hip flexor weakness

histochemistry of muscle

HMGcoA reductase inhibitors

Horner's syndrome

H-reflex testing

human diploid cell rabies vaccine

human immunodeficiency virus type 1

hyperamylasemia

hyperbilirubinemia

hyperphosphatasia

hyperpigmentation of skin

hypersensitivity reaction

hypoglycorrhachia

hypoparathyroidism

hypoparathyroidism, idiopathic

hypotension, systemic

hypotonia, infants

iatrogenic neurologic disorders

idiopathic inflammatory myopathy

immune checkpoint inhibitors

immune-related adverse events

immunoelectrophoresis, serum

immunohistochemistry

immunologic disease

immunomodulation

immunosuppression

immunosuppressive agents

inability to sit up

inclusion bodies

inclusion body myositis

infectious mononucleosis

infectious mononucleosis, neurologic findings with

influenza A virus

influenza B virus

infusion-associated reaction

intellectual deficit

interferonopathy

interstitial pulmonary fibrosis

intestinal pseudoobstruction

intracranial pressure, increased

intrinsic hand muscles, wasting of

Isaacs syndrome

ischemic exercise test

jaw closure weakness

Kearns-Sayre syndrome

Kugelberg-Welander syndrome

lactic acidemia

lactic dehydrogenase(LDH)

learning disability

learning disability, in children

leg weakness, bilateral

leg weakness, unilateral

Legionella pneumophilia

Legionnaires'disease

leukoencephalopathy

leukoencephalopathy, toxic

level of consciousness, decreased

lid closure, weakness of

life expectancy

limb-girdle weakness

limbic encephalitis

lipid lowering agent

liver function enzymes

Lowe's syndrome

lysosomal storage disease

lysosomes, abnoral

malabsorption syndrome

malignant hyperpyrexia

malignant papulosis

manic-depressive

marathon running

masseter muscle weakness

McArdle's disease

McLeod syndrome

mediastinum, mass of

memory, defect of recent

memory, impairment of

meningitis, aseptic

meningitis, bacterial

meningitis, carcinomatous

meningitis, CSF findings in

meningitis, fungal

meningitis, leptospira

meningitis, predisposing factors in

meningitis, spinal fluid smear and culture of

meningoencephalitis

meningoencephalitis, amoebic

meningoencephalitis, mumps

meningoencephalopathy

mental retardation

mental status, abnormal

metabolic acidosis

middle cerebral artery, occlusion of

mitochondrial disease

mitochondrial encephalomyopathy

mitral valve vegetation

molecular genetics

mononeuritis multiplex

monospot slide test

motor neuron disease

movement disorder

movement disorder, extrapyramidal

MRI, contrast enhanced

multiple sclerosis

muscle atrophy, focal

muscle atrophy, progressive

muscle atrophy, static

muscle hypertrophy

muscle phosphorylase deficiency

muscle relaxant

muscle stiffness

muscle strength, testing

muscle swelling

muscle swelling, focal

muscle tenderness

muscle twitching

muscle wasting, diffuse

muscle weakness

muscle weakness, insidious onset of

muscle weakness, proximal

muscle weakness, sudden onset of

muscle-eye-brain disease

muscular dystrophy

muscular dystrophy, Becker

muscular dystrophy, Becker, carrier

muscular dystrophy, cardiovascular changes with

muscular dystrophy, central nervous system abnormality

muscular dystrophy, classification

muscular dystrophy, congenital

muscular dystrophy, congenital, Fukuyama type

muscular dystrophy, differential diagnosis of

muscular dystrophy, distal, Miyoshi

muscular dystrophy, Duchenne

muscular dystrophy, Duchenne, carrier

muscular dystrophy, Duchenne, neonatal screening

muscular dystrophy, Duchenne, presymptomatic detection

muscular dystrophy, dystrophin normal

muscular dystrophy, facioscapulohumeral

muscular dystrophy, female occurrence of

muscular dystrophy, LAMA2

muscular dystrophy, limb-girdle

muscular dystrophy, neurogenic hypothesis of

muscular dystrophy, pattern of muscle involvement

myasthenia gravis

myasthenia gravis, distal weakness

myasthenia gravis, drug induced

myasthenia gravis, limb-girdle

myasthenia gravis, non motor symptoms

myocardial biopsy

myocardial infarction

myocardial infarction, acute

myocardial injury

myocardial ischemia

myopathy, acute

myopathy, alcoholic

myopathy, amyloid

myopathy, autoimmune

myopathy, centronuclear

myopathy, critically ill

myopathy, desmin

myopathy, distal

myopathy, distal Laing

myopathy, distal, vacuolar

myopathy, drug-induced

myopathy, genetic

myopathy, hereditary

myopathy, hypocalcemic

myopathy, hypokalemic

myopathy, inflammatory

myopathy, metabolic

myopathy, mitochondrial

myopathy, necrotizing

myopathy, necrotizing, autoimmune

myopathy, necrotizing, immune-mediated

myopathy, proximal

myopathy, quadriceps

myopathy, steroid induced

myopathy, steroid responsive

myopathy, thyroid disease causing

myopathy, toxic

myopathy, vacuolar

myositis, acute of childhood

myositis, bacterial

myositis, focal

myositis, post infectious

myotonia congenita

myotonia dystrophica

myotonic discharges

myxedema, neurologic manifestations of

nausea and vomiting

nemaline rod myopathy

nemaline rod myopathy, adult onset

neonatal screening, genetic neurologic disorders

neoplasm, intracranial

nephrotic syndrome

nerve conduction studies

nerve conduction studies, motor

neurocardiology

neuroendocrinology

neuroleptic malignant syndrome

neuroleptic, atypical

neurologic complications of, surgery

neurologic complications of, systemic cancer

neurologic complications of, systemic disease

neurologic disease

neurologic disease, diagnoses of

neurologic evaluation

neurologic examination

neurologic symptoms

neurological intensive care

neuromuscular blockade

neuromuscular disease, electrodiagnosis of

neuromuscular junction, abnormality of

neuromyotonia and axonal neuropathy

neuron specific enolase

neuroophthalmology

neuropathology, brain

neuropathy, acute

neuropathy, cryoglobulinemic

neuropathy, medication induced

neuropathy, motor

neuropathy, motor, multifocal

neuropathy, multifocal

neuropathy, peripheral

neuropathy, vasculitic, systemic

neurosis, treatment of

next-generation sequencing

NMDA antagonists

noncommunicative

occupational neurologic disorders

ocular motility, disorders of

ocular myopathy

oculopharyngeal muscular dystrophy

old age, neurology of

ophthalmoplegia

ophthalmoplegia, progressive external

ophthalmoplegic migraine

opportunistic infection

orange peel appearance of skin

overlap syndrome

pacemaker, cardiac-transvenous

pain, abdominal

paralysis, asymmetric

paramyotonia congenita

paraspinal muscle

paraspinal muscle weakness

paresthesias, feet

paresthesias, hands

Parkinson disease

Parkinson disease, drug induced

Parkinsonism syndrome

percussion induced muscle contraction

periarteritis nodosa

pericardial effusion

periodic paralysis

peripheral blood smear

peripheral blood smear, abnormal

personality change

phosphorylase b kinase deficiency

pleocytosis of cerebrospinal fluid

pleural effusion

poison, neurologic problems with

polyclonal gammopathy

polymerase chain reaction

polymyositis, eosinophilic

polyneuropathy, critically ill

polyneuropathy, critically ill, children

Pompe's disease of glycogen storage

positive sharp waves

post polio syndrome

posterior leukoencephalopathy syndrome

posterior leukoencephalopathy syndrome, location

postural abnormality

potassium channel antibodies

precipitating factors

pregnancy, neurologic complications in

prenatal diagnosis by amniocentesis

prevention of neurologic disorders

progressive multifocal leucoencephalopathy

progressive neurologic disorder

protozoan infection

proximal muscle atrophy

proximal myotonic myopathy

pseudohypertrophy

pseudostatus epilepticus

psychiatric disorder

psychiatric problems in neurologic disorders

psychological testing

psychomotor retardation

ptosis, bilateral

ptosis, familial

pulmonary edema

pulmonary hypertension

pulmonary infiltrates

pupil, abnormality in neurologic disorders

quadriceps atrophy

quadriceps weakness

quality of life

radioimmunoassay

ragged-red fibers

Raynaud's phenomenon

remote effect of cancer on the nervous system

renal failure, acute

repetitive nerve stimulation

respiratory distress syndrome, neurologic status with

respiratory failure

respiratory tract infection

retina, abnormal

reversible cerebral vasoconstrictive syndromes

reversible neurologic disorder

rickettsial organism

rigid spine syndrome

rippling muscle disease

risk-benefit assessment

Sabin-Feldman dye test

salivation, excessive

sarcoglycanopathy

sciatic neuropathy

second wind phenomena

sedimentation rate

sedimentation rate, elevated

seizure, differential diagnosis of

seizure, hysterical

seizure, nonepileptic

selective serotonin reuptake inhibitors

self-mutilation

sensorineural hearing loss

sensory nerve action potentials

serologic testing

serotonin syndrome

serum alanine aminotransferase

serum glutamic oxaloacetic transaminase

serum glutamic pyruvic transaminase

serum lipase, elevated

severe acute respiratory syndrome

sex reassignment surgery

shoulder-girdle wasting

single photon emission computed tomography

Sjogren's syndrome

skin, lesions in neurologic disorders

skin, thickened

slit lamp examination

small vessel disease

sodium channel dysfunction

speech disorder, childhood

speech, delayed development of

spinal muscular atrophy

spinal muscular atrophy, adult onset

spinal muscular atrophy, intermediate form

spinocerebellar degeneration

spirochete infection

sports medicine, neurology of

standing difficulty

staphylococcus aureus

statin therapy, discontinuation

statin therapy, dose

status asthmaticus

status epilepticus

status epilepticus, nonconvulsive

status epilepticus, psychogenic

steroid therapy, CNS treatment and complications with

stooped posture

stress, emotional

striatum, lesion of

strychnine poisoning

subarachnoid hemorrhage

subdural hematoma

subdural hematoma, metastatic carcinoma deposits causing

survival motor neuron gene

syphilis, neurologic complications with

systemic illness

systemic lupus erythematosus

telangiectases, periungual

temporalis muscle hypertrophy

temporalis muscle swelling

temporalis muscle wasting

temporalis muscle weakness

temporomandibular joint, dislocation

teratoma, ovarian

thrombocytopenia

toilet seat neuropathy

tone, muscle, increased

tongue, enlarged

tongue, fasciculations of

tongue, weakness

toxoplasma complement fixation test

toxoplasma gondii

toxoplasmosis, acquired

toxoplasmosis, CNS

toxoplasmosis, muscle

transient ischemic attack

treatment of neurologic disorder

tremor, intention

trifluoperazine

trinucleotide repeats

type 1 muscle fiber

unconsciousness

urine test in toxic screen

vasospasm, cerebral

viral infection

viral infection, CNS

vision, blurred

vitamin deficiency

vitamin E deficiency

walking, difficulty with

weakness, acute

weakness, congenital

weakness, fatiguable

weakness, generalized

weakness, progressive

weakness, proximal

weakness, severe

weaning from respirator, failure to

whistle, inability to

white matter disease

wide based gait

winging of scapula

X-linked bulbospinal neuronopathy

X-linked myopathy

x-linked myopathy with excessive autophagy

yersinia enterocolitica

Showing articles 150 to 200 of 249 << Previous Next >>

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

Diagnostic Tests for Choreoacanthocytosis
Neurol 41:1000-1006, Feinberg,T.E.,et al, 1991

Myopathy Associated with Ketoconazole Treatment
Am J Dis Child 145:970-971, Garty,B-Z.,et al, 1991

Envenomation by the Scorpion Centruroides Exilicauda (C Sculpturatus) :Severe and Unusual Manifestations
Pediatrics 87:930-933, Berg,R.A.&Tarantino,M.D., 1991

Prognosis in AZT Myopathy
Neurol 41:1181-1184, Chalmers,A.C.,et al, 1991

Myopathy in Human Immunodeficiency Virus-Infected Children Receiving Long-Term Zidovudine Therapy
J Pediatr 119:152-155, Walter,E.B.,et al, 1991

Autosomal Recessive Distal Dystrophy
Neurol 41:1365-1370, Barohn,R.J.,et al, 1991

Pyomyositis Presenting as Rapidly Progressive Generalized Weakness
Neurol 41:944-945, Felice,K.,et al, 1991

Late Effects of Paralytic Poliomyelitis in Olmsted County, Minnesota
Neurol 41:501-507, Windebank,A.J.,et al, 1991

Clinical & Laboratory Findings in the Oculocerebrorenal Syndrome of Lowe, with Special Ref to Growth & Renal Function
NEJM 324:1318-1325, Charnas,L.R.,et al, 1991

Polymyositis, Dermatomyositis, and Inclusion-Body Myositis
NEJM 325:1487-1498, Dalakas,M.C., 1991

Clinicopath Conf
Case 40-1991, Inclusion-Body Myositis, NEJM 325:1026-1035991., , 1991

Clinicopath Conf
Eosinophilic Fasciitis, Case Study 4-1990, NEJM 322:252-261, 93190., , 1990

Mitochondrial Myopathy Caused by Long-Term Ziduvudine Therapy
NEJM 322:1098-1105, Dalakas,M.C.,et al, 1990

Attitudes of Mothers to Neonatal Screening for Duchenne Muscular Dystrophy
BMJ 300:1112, Smith,R.A.,et al, 1990

Congenital Inflammatory Myopathy
Neurol 40:1111-1114, Shevell,M.,et al, 1990

Adult Phosphorylase b Kinase Deficiency
Ann Neurol 28:529-538, Clemens,P.R.,et al, 1990

Hypothyroidism
In Neurologic Clinics, W. B. Saunders Co, Phila, 7:492-493., Kaminski,H.J.&Ruff,R.L., 1989

Human Leptospirosis-A Review of 50 Cases
Infection 17:10-14, Lecour,H.,et al, 1989

Familial X-linked Myalgia and Cramps:A Nonprogressive Myopathy Associated with a Deletion in the Dystrophin Gene
Neurol 39:1277-1280, Gospe,S.M.,et al, 1989

Abnormal Blood Clotting after Head Injury
Editorial, Lancet 2:957-9581989., , 1989

DNA Restriction Fragment Length Polymorphisms in Diff Dx of Genetic Disease:Appl in Neuromusc Dis
Hum Genet 82:55-58, Defesche,J.C.,et al, 1989

Neurological Outcome after Out-of-Hospital Cardiac Arrest, Prediction by Cerebrospinal Fluid Enzyme Analysis
Arch Neurol 46:753-756, Roine,R.O.,et al, 1989

Zidovudine-Associated Myopathy
Am J Med 86:814-818, Gertner,E.,et al, 1989

Flaccid Quadriparesis Associated with Yersinia Enterocolitis-Induced Hypokalemia
Arch Int Med 149:1193-1194, Orman,R.A.&Lewis,J.B., 1989

Current Concepts in the Idiopathic Inflammatory Myopathies:Polymyositis, Dermatomyositis, and Related Disorders
Ann Int Med 111:143-157, Plotz,P.H.,et al, 1989

Improved Diagnosis of Becker Muscular Dystrophy by Dystrophin Testing
Neurol 39:1011-1017, Hoffman,E.P.,et al, 1989

Inclusion Body Myositis, Observations in 40 Patients
Brain 112:727-747, Lotz,B.P.,et al, 1989

Rippling Muscle Disease
Arch Neurol 46:405-408, Ricker,K.,et al, 1989

Congenital Muscular Dystrophy
J Pediatr 115:214-221, Leyten,Q.H.,et al, 1989

Clinicopath Conf
Polyarteritis Nodosa, Disseminated Obsolescent and Chronic, with Invol of Gallbladder & Muscle of Ex, rem, 42-1989,NEJM 321:1103-1118,1989., 1989

Human Immunodeficiency Virus-Associated Myopathy:Analysis of 11 Pts
Ann Neurol 24:79-84, Simpson,D.M.&Bender,A.N., 1988

Gene Studies in Newborn Males with Duchenne Muscular Dystrophy Detected by Neonatal Screening
Lancet 2:425-427, Greenberg,C.R.,et al, 1988

McArdle's Disease:Biochemical and Molecular Genetic Studies
Ann Neurol 24:774-781, Servidei,S.,et al, 1988

Emery-Dreifuss Muscular Dystrophy:Disease Spectrum and Differential Diagnosis
Neuropediatrics 19:62-71, Voit,T.,et al, 1988

Hypoparathyroidism
Cecil Textbook of Medicine 18th Ed, W B Saunders Co, Phila, p149688., Arnaud,C.D., 1988

Facioscapulohumeral Muscular Dystrophy, in Neuromuscular Disease
Springer-Verlag, NY, p289988., Swash,M.&Schwartz,M.S., 1988

Cholesterol Crystal Embolization:A Review of 221 Cases in the English Literature
Angiology 38:769-784, Fine,M.J.,et al, 1987

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

Clinicopath Conf
Kearns-Sayre Syndrome (Oculocraniosomatic Neuromuscular Disease with Mitochondrial Myopathy) , Case, 4-1,NEJM 317:493-501,1987., 1987

Neuroleptic Malignant Syndrome:Review and Analysis of 115 Cases
Biol Psychiatry 22:1004-1020, Addonizio,G.,et al, 1987

Detection of Cerebral Injury After Total Circulatory Arrest & Hypothermia by Specific CK Isoenzyme Levels
Am J Cardiol 58:1236-1241, Rossi,R.,et al, 1987

Multifocal Central Nervous System Lesions in Three Patients with Trichinosis
Arch Neurol 44:432-434, Ellrodt,A.,et al, 1987

Clinicopath Conf
Myopathy Due to Adult Acid Maltase Deficiency, 36-1986, NEJM 315:694-701986., , 1986

Phenytoin Hypersensitivity:A Case of Severe Acute Rhabdomyolysis
Am J Med 81:928-930, Engel,J.N.,et al, 1986

The Neuroleptic Malignant Syndrome:Agent and Host Interaction
Acta Psychiatr Scand 73:337-347, Shaley,A.&Munitz,H., 1986

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

Acid Maltase Deficiency
Engel, A. G. in Engel and Banker, Myology, McGraw-Hill Co, New York, Ch 55, p. 1629-1651, , 1986

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

Serum Creatine Kinase B Concentrations in Acute Cerebrovascular Diseases
Arch Neurol 41:1175-1178, Pfeiffer,F.E.,et al, 1984

Showing articles 150 to 200 of 249 << Previous Next >>