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Differential
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abdominal muscle paralysis
acid maltase deficiency
acid maltase deficiency, adult
activities of daily living scale
adverse drug reaction
alpha glucosidase
aminoacidopathies
aneurysm
anterior horn cell disease
aspartate aminotransferase
asymptomatic
bright tongue sign
bulbar palsy
calf hypertrophy
cardiomegaly
cardiomyopathy
CAT scan, abnormal
children
chromosomal abnormality
chromosome 11
Clinical Pathologic Conference(C.P.C.)
compartment syndrome
complications
congenital myopathy
congestive heart failure
consanguinity
creatine phosphokinase(CPK)elevated
cultured skin fibroblasts
delay in diagnosis
developmental retardation
diaphragmatic paralysis
differential diagnosis
difficulty climbing stairs
distal muscle atrophy
distal muscle weakness
dysarthria
dysphagia
dyspnea
efficacy
electrocardiogram, abnormal
electromyogram
electron microscopy
encephalopathy
encephalopathy, anoxic
encephalopathy, neonatal
enzyme treatment
enzyme, defect
enzyme, muscle disease
exercise
exercise intolerance
exercise-related muscle strength increase
facial weakness
falling
familial
fatigue
fibrillations
floppy infant
gene
gene mutation
gene therapy
genetic diagnosis, prenatal
genetic neurologic disorders
genetic testing
glycogen debranching enzyme deficiency
glycogen storage disease
Gowers maneuver
hepatomegaly
heralding manifestation
hip flexor weakness
histochemistry of muscle
hypoglycemia
hypotonia
hypotonia, infants
hypoxia
hypoxic encephalopathy
iatrogenic neurologic disorders
imbalance
immunohistochemistry
immunomodulation
immunosuppressive agents
inborn errors of metabolism, screening
ischemic exercise test
leg weakness, bilateral
leukocytes
limb-girdle weakness
lipid storage myopathy
low back pain
lysosomal storage disease
lysosomes, abnoral
McArdle's disease
McArdle's disease, adult onset
misdiagnosis
molecular genetics
monoclonal gammopathy
monoclonal gammopathy of uncertain significance
mortality
MRI
MRI, abnormal
MRI, muscle
mucopolysaccharidoses
muscle atrophy, progressive
muscle atrophy, static
muscle biopsy
muscle cramp
muscle hypertrophy
muscle pain
muscle phosphofructokinase deficiency
muscle phosphorylase deficiency
muscle stiffness
muscle strength, testing
muscle wasting, diffuse
muscle weakness
muscle weakness, insidious onset of
muscle weakness, proximal
muscular dystrophy
myoglobinuria
myopathy
myopathy, acquired
myopathy, amyloid
myopathy, distal, vacuolar
myopathy, genetic
myopathy, glycogen storage
myopathy, metabolic
myopathy, necrotizing
myopathy, scleromyxedema
myopathy, vacuolar
myositis
myotonia congenita
myotonic discharges
neck weakness
nemaline rod myopathy
nemaline rod myopathy, adult onset
nerve biopsy
neurologic complications of, systemic disease
neurologic disease
neurologic disease, diagnoses of
neurologic evaluation
neuropathy
newborn, evaluation of
next-generation sequencing
old age, neurology of
orthopnea
pain
pain, arm
pain, back
paraspinal muscle
paraspinal muscle weakness
PAS positive
patient in waiting
phosphorylase b kinase deficiency
polymerase chain reaction
Pompe's disease of glycogen storage
Pompe's disease, infantile
preclinical
prenatal diagnosis by amniocentesis
prevention of neurologic disorders
prognosis
proximal muscle atrophy
pseudomyotonia
pulmonary function tests
pulmonary hypertension
renal failure
respiratory failure
respiratory tract infection
review article
RFLPs
screening
second wind phenomena
seizure
short stature
sphingolipodoses
spinal muscular atrophy
spinocerebellar degeneration
stem cell transplantation
storage disease of CNS
subarachnoid hemorrhage
systemic illness
tongue, enlarged
tongue, weakness
treatment of neurologic disorder
urine, dark
vital capacity
walking, difficulty with
weakness
weakness, generalized
weakness, progressive
weakness, proximal
weight loss
winging of scapula
workup
Showing articles 650 to 700 of 1146 << Previous Next >>

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

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

Facioscapulohumeral Dystrophy, In Skeletal Muscle Pathology
Churchhill Livingstone, NY, p285, 30392., Mastaglia,F.L.&Walton,J., 1992

Acute Quadriplegic Myopathy:A Complic of Treat with Steroids, Nondepolarizing Blocking Agents, or Both
Neurol 42:2082-2087, Hirano,M.,et al, 1992

Ipecac Myopathy and Cardiomyopathy
JNNP 56:560-562, Dresser,L.P.,et al, 1992

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

Evaluation of Cerebral Biopsies for the Diagnosis of Dementia
Arch Neurol 49:28-31, Hulette,C.M.,et al, 1992

GM-1 Ganglioside for Spinal-Cord Injury
NEJM 326:493, Schonhofer,P.S., 1992

A Chronic Illness of Fatigue, Neurologic and Immunologic Disorders, & Active Human Herpesvirus Type 6 Infection
Ann Int Med 116:103-113, Buchwald,D.,et al, 1992

Polymyalgia Rheumatica and Mitochondrial Myopathy:Clinicopathologic and Biochemical Studies in Five Cases
Am J Med 92:167-172, Harle,J.,et al, 1992

Headaches in Children Younger than 7 Years of Age
Arch Neurol 49:79-82, Chu,M.L.&Chinnar,S., 1992

Cardioskeletal Mitochondrial Myopathy Associated with Chronic Magnesium Deficiency
Neurol 42:128-130, Riggs,J.E.,et al, 1992

Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes (MELAS) :Clin Features & DNA Mutation
Neurol 42:545-550, Goto,Y.,et al, 1992

The Neuropsychological Features of Mitochondrial Myopathies and Encephalomyopathies
Arch Neurol 49:158-160, Kartsounis,L.D.,et al, 1992

GM1 Gangliosidosis in Adults:Clinical and Molecular Analysis of 16 Japanese Patients
Ann Neurol 31:328-332, Yoshida,K.,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

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

Clinical Genetics and Genetic Counseling in Alzheimer Disease
Ann Int Med 115:601-606, Breitner,J.C.S., 1991

NEurologic Complications of Nonneuronopathic Gaucher's Disease
Arch Neurol 48:1271-1272, Grewal,R.P.,et al, 1991

The Bruns-Garland Syndrome (Diabetic Amyotrophy) , Revisited 100 Years Later
Arch Neurol 48:1130-1135, Barohn,R.J.,et al, 1991

Stroke-Like Syndrome, Mineralizing Microangiopathy, and Neuroaxonal Dyst with Intrathecal Methotrexate
Neurol 41:1847-1848, Phanthumchinda,K.,et al, 1991

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

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

Cyclosporin in the Management of Polymyositis and Dermatomyositis
JNNP 54:1007-1008, Lueck,C.J.,et al, 1991

Myopathy and Prolonged Neuromuscular Blockade after Lung Transplant
Crit Care Med 19:1580-1582, 14571991., Subramony,S.H.,et al, 1991

Fatigue and Myalgia in AIDS Patients
Neurol 41:1603-1607, Miller,R.G.,et al, 1991

Complete Ophthalmoplegia as a Complication of Acute Corticosteroid-and Pancuronium-Associated Myopathy
Neurol 41:921-922, Sitwell,L.D.,et al, 1991

Recovery of Motor Function after Spinal-cord Injury-A Randomized, Placebo-Contrlled Trial with GM-1 Ganglioside
NEJM 324:1829-1838, 1885-18871991., Geisler,F.H.,et al, 1991

Congenital Monomelic Hypertrophy with Progressive Myopathy
Arch Neurol 48:107-110, Shukla,A.,et al, 1991

Glucose-Induced Exertional Fatigue in Muscle Phosphofructokinase Deficiency
NEJM 324:364-369, 4111991., Haller,R.G.&Lewis,S.F., 1991

Depletion of Muscle Mitochondrial DNA in AIDS Patients with Zidovudine-Induced Myopathy
Lancet 337:508-510, Arnaudo,E.,et al, 1991

Response to Treatment with Antihistamines in a Family with Myotonia Congenita
Lancet 337:28-30, Hughes,E.F.&Wilson,J., 1991

N-Isopropyl-p- (123I) Iodoamphetamine SPECT in MELAS Syndrome:Comparison with CT & MR Imaging
J Comput Assist Tomogr 15:77-82, Satoh,M.,et al, 1991

Eosinophilia-Myalgia Syndrome, A Clinical Case Series of 21 Patients
Arch Int Med 151:533-537, Philen,R.M.,et al, 1991

Polymyositis Mediated by T Lymphocytes that Express the y/8 Receptor
NEJM 324:877-881, Hohlfeld,R.,et al, 1991

Lisch Nodules in Neurofibromatosis Type I
NEJM 324:1264-1266, 1283-12851991., Lubs,M-L.E.,et al, 1991

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

Cervical Dystonia:Clinical Findings and Associated Movement Disorders
Neurol 41:1088-1091, Jankovic,J.,et al, 1991

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

Cramp-Fasciculation Syndrome:A Treatable Hyperexcitable Peripheral Nerve Disorder
Neurol 41:1021-1024, Tahmoush,A.J.,et al, 1991

Poliomyelitis-Like paralysis During Recovery from Acute Bronchial Asthma:Possible Etiology and Risk Fators
Pediatrics 88:276-279, Shahar,E.M.,et al, 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

Zidovudine Myopathy:A Distinctive Disorder Associated with Mitochondrial Dysfunction
Ann Neurol 29:606-614, Mhiri,C.,et al, 1991



Showing articles 650 to 700 of 1146 << Previous Next >>