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Differential
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abdominal protrusion
acid maltase deficiency
acquired immunodeficiency syndrome
acquired immunodeficiency syndrome, medical precautions with
acquired immunodeficiency syndrome-related complex
advances in neurology
amyotrophic lateral sclerosis
ankle clonous
anterior tibial muscle weakness
areflexia
arthrogryposis multiplex
bulbar palsy
bulbar palsy, progressive
camptocormia
cardiomyopathy
CAT scan
CAT scan, muscle
central core disease
central nuclei, muscle
children
cholelithiasis
Coats syndrome
congenital myopathy
congenital myopathy, inflammatory
contractures, joint
creatine phosphokinase(CPK)elevated
delivery, complicated
developmental disability
developmental retardation
differential diagnosis
difficulty climbing stairs
distal muscle weakness
dropped head syndrome
drug induced neurologic disorders
dysphagia
dyspnea
electromyogram
electron microscopy
encephalopathy
encephalopathy, anoxic
encephalopathy, neonatal
eye closure
face, elongated
facial appearance, abnormal
facial weakness
facial weakness, bilateral
facioscapulohumeral syndrome
false negative
familial
feeding disorder
fibrillations
floppy infant
foot drop
gait disorder
gait, waddling
gene mutation
genetic neurologic disorders
Guillain Barre syndrome
high arched palate
highly active antiretroviral therapy
histochemistry of muscle
human immunodeficiency virus type 1
hyperreflexia
hypotonia
hypotonia, infants
hypoxic encephalopathy
immunohistochemistry
immunomodulation
immunosuppressive agents
inclusion body myositis
joint hypermobility
leg weakness, bilateral
lid closure, weakness of
life expectancy
liver function enzymes
lordosis
malignant hyperpyrexia
melphalan
microcephaly
misdiagnosis
molecular genetics
monoclonal gammopathy
monoclonal gammopathy of uncertain significance
mononeuritis multiplex
mortality
motor neuron disease
MRI
MRI, muscle
multicore myopathy
multiminicore disease
muscle atrophy, progressive
muscle biopsy
muscle hypertrophy
muscle hypertrophy, congenital
muscle pain
muscle weakness
muscle weakness, proximal
muscular dystrophy
muscular dystrophy, Becker
muscular dystrophy, differential diagnosis of
muscular dystrophy, Duchenne
muscular dystrophy, facioscapulohumeral
muscular dystrophy, limb-girdle
myasthenia gravis
myasthenia gravis, distal weakness
myasthenia gravis, limb-girdle
myoglobinuria
myopathy
myopathy, acquired
myopathy, amyloid
myopathy, centronuclear
myopathy, drug-induced
myopathy, focal
myopathy, glycogen storage
myopathy, mitochondrial
myopathy, monomelic
myopathy, scleromyxedema
myositis
myotonia congenita
myotonia dystrophica
myotubularin
neck extension
neck weakness
nemaline rod myopathy
nemaline rod myopathy, adult onset
nerve conduction studies
neurologic complications of, systemic disease
neurologic disease, diagnoses of
neurologic evaluation
neuropathy
neuropathy, ataxic
neuropathy, painful
neuropathy, peripheral
newborn, evaluation of
old age, neurology of
ophthalmoplegia
ophthalmoplegia, progressive external
ophthalmoplegia, total
paraspinal muscle
paraspinal muscle weakness
periodic paralysis
polymyositis
polyneuropathy, chronic inflammatory demyelinating
positive sharp waves
pregnancy, neurologic complications in
prognosis
progressive neurologic disorder
pseudohypertrophy
ptosis
ptosis, bilateral
pyloric stenosis
respiratory failure
review article
rhabdomyolysis
scoliosis
serum alanine aminotransferase
sloped shoulders
spinal muscular atrophy
standing difficulty
stem cell transplantation
stooped posture
systemic illness
transverse smile
treatment of neurologic disorder
type 1 muscle fiber
viral myopathy
weakness
weakness, generalized
weakness, progressive
weakness, proximal
weight loss
wheelchair
whistle, inability to
winging of scapula
workup
X-linked myopathy
Showing articles 700 to 750 of 1027 << Previous Next >>

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

Aseptic Meningitis Complicating Adult Kawasaki Disease:Case Report and Review of the Literature
Am J Med 87:106-110, McIlroy,M.A.,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

Molecular Biology of Duchenne and Becker's Muscular Dystrophy:Clinical Applications
Ann Neurol 26:189-194, Gutmann,D.H.&Fischbeck,K.H., 1989

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

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

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

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

HTLV-1 and Polymyositis in Jamaica
Lancet 2:1184-1187, Morgan,O.S.,et al, 1989

HTLV-1 Associated Myelopathy and Polymyositis in a US Native
Neurol 39:1572-1575, Evans,B.K.,et al, 1989

Thyrotoxic Periodic Paralysis
Arch Int Med 149:2597-2600, Kelley,D.E.,et al, 1989

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

Antecollis in Parkinsonism
Lancet 1:1320-1321, Jorens,P.G.,et al, 1989

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

Life-Threatening Cranial Dystonia Following Trihexyphenidyl Withdrawal
Movement Disorders 4:349-353, Gimenez-Roldan,S.,et al, 1989

Rigid Spine Syndrome and Rigid Spine Sign in Myopathies
J Child Neurol 4:273-282, Merlini,L.,et al, 1989

The Effects of Alcoholism on Skeletal and Cardiac Muscle
NEJM 320:409-415, 458-4601989., Urbano-Marquez,A.,et al, 1989

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

Von Hippel-Lindau Disease Affecting 43 Members of a Single Kindred
Medicine 68:1-29, Lamiell,J.M.,et al, 1989

Predictive Testing for Huntington's Disease, Progress and Problems
BMJ 298:404-405, 1989, Harper,P.S.&Morris,M.J., 1989

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

Mitochondrial DNA and Genetic Disease
Editorial, Lancet 1:250-2511989., , 1989

Distinction of Becker from Limb-Girdle Muscular Dystrophy by Means of Dystrophin cDNA Probes
Lancet 1:466-468, Norman,A.,et al, 1989

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

Pyogenic Myositis:CT Evaluation
J Comput Assist Tomogr 12:1002-1005, Tumeh,S.S.,et al, 1988

Anderson-Fabray Disease, A Commonly Missed Diagnosis
BMJ 297:872-873, Morgan,S.H.&Crawfurd,M., 1988

Myopathy and Cystine Storage in Muscles in a Patient with Nephropathic Cystinosis
NEJM 392:1461-1464, Gahl,W.A.,et al, 1988

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

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

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

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

Severe Polymyositis-Like Syndrome Associated with Zidovudine Therapy of AIDS & ARC
NEJM 318:708, Bessen,L.J.,et al, 1988

Neurofibromatosis 2 (Bilateral Acoustic Neuro-fibromatosis)
NEJM 318:684-688, Martuza,R.L.&Eldridge,R., 1988

Autoantibodies to Glutamic Acid Decarboxylase in Pt with Stiff-Man Syndr, Epilepsy & Type I Diabetes Mellitus
NEJM 318:1012-1020, Solimena,M.,et al, 1988

Lyme Myositis:Muscle Invasion by Borrelia Burgdorferi
Ann Int Med 109:245-246, Atlas,E.,et al, 1988

Fatal Adult Respiratory Distress Syndrome in a Patient with Lyme Disease
JAMA 259:2737-2739, Kirsch,M.,et al, 1988

Early-Onset Benign Autosomal Dominant Limb-Girdle with Contractures (Bethlem Myopathy)
Neurol 38:573-580, Mohire,M.D.,et al, 1988



Showing articles 700 to 750 of 1027 << Previous Next >>