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Differential
(Click to cross reference)
creatine phosphokinase(CPK)elevated
difficulty climbing stairs
electromyogram
familial
gene mutation
muscle biopsy
muscle weakness
myopathy
myopathy, hereditary
myopathy, vacuolar
myotonic discharges
proximal muscle atrophy
standing difficulty
weakness
weakness, progressive
weakness, proximal
X-linked myopathy
x-linked myopathy with excessive autophagy
Showing articles 1150 to 1200 of 1704 << Previous Next >>

Headache
Mental Status Changes, and Death in a 36-Year Old Woman with Lupus, Clinicopath Conf, Am J Med 86:94, 10289., 1989

Molecular Genetics of Amyloid Neuropathy in Europe
Lancet 1:524-526, Holt,I.J.,et al, 1989

Polymyositis and HTLV-I Antibodies
Ann Neurol 25:311, Francis,D.A.&Hughes,R.A.C., 1989

Mitochondrial Myopathies, Mechanisms Now Better Understood
BMJ 298:1127-1128, Schapira,A.H.V., 1989

Mitochondrial DNA Deletions in Progressive External Ophthalmoplegia and Kearns-Sayre Syndrome
NEJM 320:1293-1299, Moraes,C.T.,et al, 1989

Mitochondrial Encephalomyopathy with Associated Aminoacidopathy in a Male Sibship
J Pediatr 115:81-88, Sooth,F.A.,et al, 1989

Cardiac Transplantation in a Patient with Muscular Dystrophy and Cardiomyopathy
Arch Neurol 46:705-707, Donofrio,P.D.,et al, 1989

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

Pyomyositis in a Child with Acquired Immunodeficiency Syndrome
Am J Dis Child 143:779-781, Raphael,S.A.,et al, 1989

Nicotinic Acid-Associated Myopathy:A Report of Three Cases
Am J Med 86:481-483, Litin,S.C.&Snderson,C.G., 1989

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

Compression Syndromes Due to Hypertrophic Nerve Roots in Hereditary Motor Sensory Neuropathy Type I
Neurol 39:1173-1177, Rosen,S.A.,et al, 1989

Brain Metastases from Undiagnosed Systemic Neoplasms
Arch Int Med 149:1076-1080, Merchut,M.P., 1989

A Mitochondrial DNA Mutation as a Cause of Leber's Hereditary Optic Neuropathy
NEJM 320:1300-1305, Singh,G.,et al, 1989

Orbital Myositis and Giant Cell Myocarditis
Neurol 39:988-990, Klein,B.R.,et al, 1989

Dopa Responsive Dystonia:A Treatable Condition Misdiagnosed as Cerebral Palsy
BMJ 298:1019-1020, Boyd,K.&Patterson,V., 1989

Clozapine in the Treatment of Psychosis in Parkinson's Disease
Neurol 39:1219-1221, Friedman,J.H.&Lannon,M.C., 1989

Clinicopath Conf
Metastatic Adenocarcinoma Compatible with Breast Origin of Mastoid and Temporal Bone, Case Record 14, 189,NEJM 320:924-930,1989., 1989

Chronic Inflammatory Demyelinating Polyradiculoneuropathy, Clin Characteristics, Course, & Diag Criteria
Arch Neurol 46:878-884, Barohn,R.J.,et al, 1989

Intracranial Injury after Moderate Head Trauma in Children
J Pediatr 115:346-350, Rosenthal,B.W.&Bergman,I., 1989

Phenytoin-Induced Acute Respiratory Failure with Pulmonary Eosinophilia
Am J Med 87:93-94, Mahatma,M.,et al, 1989

Cerebral Erdheim-Chester Disease:Persistent Enhancement with Gd-DTPA on Mr Images
Radiology 172:791-792, Tien,R.D.,et al, 1989

Headaches, In Clinical Symposia
Ciba Co, 1989, Vol 41, p 2-32., Diamond,S.&Medina,J.L., 1989

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

Clinicopath Conf
Chronic Osteomyelitis of Spine, with Intervertebral Diskitis (T3-T4) & Epidural Abscess (Staph Aureu, ) , Cas9,NEJM 320:1610-1618,1989., 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

Duchenne Muscular Dystrophy:Patterns of Clinical Progression and Effects of Supportive Therapy
Neurol 39:475-481, Brooke,M.H.,et al, 1989

Genetic Abnormalities in Duchenne and Becker Dystrophies:Clinical Correlations
Neurol 39:461-465, 584-5851989., Medori,R.,et al, 1989

Molecular and Clinical Correlations of Deletions Leading to Duchenne and Becker Muscular Dystrophies
Neurol 39:465-474, 584-5851989., Baumbach,L.L.,et al, 1989

Selective Criteria May Increase Lumbosacral Spine Roentgenogram Use in Acute-Low-Back Pain
Arch Int Med 149:47-50, 271989., Frazier,L.M.,et al, 1989

Short-Term Outcomes of Skull Fracture:A Population-Based Study of Survival and Neurologic Complications
Neurol 39:96-102, Wiederholt,W.C.,et al, 1989

Ethanol and the Nervous System
NEJM 321:442-454, Charness,M.E.,et al, 1989

Comatose Patients Smelling of Alcohol, All Need Measurements of Blood Alcohol Concentrations and Skull Radiography
BMJ 299:410, Quaghebeur,G.&Richards,P., 1989

Brain-Stem Tuberculoma, An Analysis of 11 Patients
Arch Neurol 46:529-535, Talamas,O.,et al, 1989

Adrenoleukodystrophy
JAMA 262:1504-1506, Ladenson,P.W., 1989

Diagnosis of Gerstmann-Straussler Syndrome in Familial Dementia with Prion Protein Gene Analysis
Lancet 2:15-17, Collinge,J.,et al, 1989

AIDS and the Nervous System
JAMA 261:2396-2399, Dalakas,M.,et al, 1989

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

HTLV-I Polymyositis in a Patient Also Infected with the Human Immunodeficiency Virus
NEJM 320:992-995, Wiley,C.A.,et al, 1989

Computeritis, Who's Responsible When PCs Make Employees Sick?
Infoworld 11:51-54, Flynn,L., 1989

The Chronic Fatigue Syndrome-One Entity or Many?
NEJM 319:1726-1728, Swartz,M.N., 1989

Clinical Indicators of Intracranial Lesion on Computed Tomographic Scan in Children with Parietal Skull Fracture
Am J Dis Child 143:194-196, Bonadio,W.A.,et al, 1989

The Peroxisome:Nervous System Role of a Previously Underrated Organelle, The 1987 Robert Wartenberg Lecture
Neurol 38:1617-1627, Moser,H.W., 1988

Suxamethonium Myalgia
Editorial, Lancet 2:945-9461988., , 1988

Genetic Markers for Neurofibromatosis
Editorial, Lancet 2:719-7201988., , 1988

Intracerebral Cavernous Angiomas
Neurol 38:1699-1704, Farmer,J.P.,et al, 1988

Brain Metabolism in Mitochondrial Encephalomyopathy:A PET Study
J Comput Assist Tomogr 12:854-857, DeVolder,A.,et al, 1988

The Neuromuscular Manifestations of Human Immunodeficiency Virus Infections
Arch Neurol 45:1084-1088, Lange,D.J.,et al, 1988

Dysphagia in Inclusion Body Myositis
JNNP 51:1542-1545, Wintzen,A.R.,et al, 1988

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



Showing articles 1150 to 1200 of 1704 << Previous Next >>