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Differential
(Click to cross reference)
alcohol, neurologic complications with
aneurysm, intracranial, delayed cerebral ischemia with
aortitis
arrhythmia, cardiac
bacteremia
bacterial endocarditis, neurologic manifestations of
boxing
cardiac arrest
cardiac arrest and resuscitation
cardiac output
cardiac surgery, hypothermia and circulatory arrest for
cardiac surgery, neurologic complications with
cardiopulmonary bypass
cerebral ischemia
cerebrospinal fluid
cerebrospinal fluid, abnormal
cerebrospinal fluid, enzymes in
cerebrovascular accident
children
Clinical Pathologic Conference(C.P.C.)
confusion
contractures, joint
creatine phosphokinase BB isoenzyme elevation
creatine phosphokinase isoenzyme elevation
creatine phosphokinase MB isoenzyme elevation
creatine phosphokinase(CPK)elevated
disseminated intravascular coagulation(DIC)
doxycycline
echocardiogram
ehrlichiosis
electrocardiogram, abnormal
electroencephalogram
electromyogram
Emery-Dreifuss muscular dystrophy
endocarditis
endocarditis, acute bacterial
endocarditis, infectious
enolase
enzyme, muscle disease
fever
fibrillations
flu-like illness
head injury
head injury, defibrination following
head injury, management of
hematuria, microscopic
hypocalcemia
hypoparathyroidism, idiopathic
hypotension, systemic
hypothermia
imbalance
infection
Janeway spots
jogging
lactic dehydrogenase(LDH)
leg weakness, bilateral
leukopenia
liver function enzymes
marathon running
meningoencephalitis
mental status, abnormal
mortality
muscle biopsy
muscle pain
muscle tenderness
muscle weakness
muscular dystrophy
muscular dystrophy, cardiovascular changes with
myocardial injury
myocardial ischemia
myocytolysis
myopathy, alcoholic
myositis
neck weakness
neoplasm, intracranial
neurocardiology
neuromuscular disease, electrodiagnosis of
neuron specific enolase
oculopharyngeal muscular dystrophy
pain, leg
pain, thigh
peripheral blood smear, abnormal
polymerase chain reaction
prognosis
psychological testing
pulmonary edema
quinidine
radioimmunoassay
rash
rash, hand
renal failure
rhabdomyolysis
rickettsial organism
seizure
serologic testing
skin, lesions in neurologic disorders
sports medicine, neurology of
staphylococcus aureus
subarachnoid hemorrhage
tachycardia
tachypnea
thrombocytopenia
tick bite
transient ischemic attack
treatment of neurologic disorder
vasculitides
vasospasm, cerebral
weakness
weakness, generalized
Showing articles 150 to 200 of 250 << Previous Next >>

Acute Rhabdomyolysis in Patients Infected by Human Immunodeficiency Virus
Neurol 44:1692-1696, Chariot,P.,et al, 1994

Benign Familial Disease with Muscle Mounding and Rippling
JNNP 57:344-347, Burns,R.J.,et al, 1994

The Nondystrophic Myotonias
In Myology, McGraw-Hill, 2nd Ed, Ch49, p1291-13024., Rudel,R.,et al, 1994

How"Malignant"is the Neuroleptic Malignant Syndrome
BMJ 307:1223-1224, Bristow,M.F.&Kohen,D., 1993

Cardiomyopathy May Be the Only Clinical Manifestation in Female Carriers of Duchenne Muscular Dystrophy
Neurol 43:2342-2345, Mirabella,M.,et al, 1993

Sudden Onset of Profound Weakness in a Toddler
J Pediatr 122:663-667, Carraccio,C.,et al, 1993

Myopathy in the Elderly:Evaluation of the Histopathologic Spectrum and the Accuracy of Clinical Diagnosis
Neurol 43:825-828, Lacomis,D.,et al, 1993

Brief Report:Deletion of the Dystrophin Muscle-Promoter Region Associated with X-Linked Dilated Cardiomyopathy
NEJM 329:921-925, 9601993., Muntoni,F.,et al, 1993

Diag of Occult Muscular Dystrophy:"Chance"Finding of Elevated Serum Aminotransferase Act
J Pediatr 122:254-256, Morse,R.P.&Rosman,N.P., 1993

Experience with Screening Newborns for Duchenne Muscular Dystrophy in Wales
BMJ 306:357-360, 3491993., Bradley,D.M.,et al, 1993

Missed Neuroleptic Malignant Syndrome
BMJ 304:831-832, Renwick,D.S.,et al, 1992

Skeletal Muscle Toxoplasmosis in Patients with Acquired Immunodeficiency Syndrome:A Clinicopath Study
Ann Neurol 32:535-542, Gherardi,R.,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

Myopathy in Severe Asthma
Am Rev Respir Dis 146:517-519, Douglass,J.A.,et al, 1992

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

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

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



Showing articles 150 to 200 of 250 << Previous Next >>