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Subject Areas on Research
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A defect in myoblast fusion underlies Carey-Fineman-Ziter syndrome.
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A splice junction mutation in a new myopathic variant of phosphoglycerate kinase deficiency (PGK North Carolina).
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A system to monitor statin-induced myopathy in individual engineered skeletal muscle myobundles.
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AAV9 gene replacement therapy for respiratory insufficiency in very-long chain acyl-CoA dehydrogenase deficiency.
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Ablation of steroid receptor coactivator-3 resembles the human CACT metabolic myopathy.
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Abnormal postnatal maintenance of elevated DLK1 transcript levels in callipyge sheep.
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Adaptive immune response to therapy in hmgcr autoantibody myopathy.
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American College of Rheumatology Guidance for COVID-19 Vaccination in Patients With Rheumatic and Musculoskeletal Diseases: Version 4.
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Amyloid myopathy presenting with respiratory failure.
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Analysis of amplitude and area of concentric needle EMG motor unit action potentials.
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Anesthetic management of a ventilator-dependent parturient with the King-Denborough syndrome.
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Angiopoietin-1 enhances skeletal muscle regeneration in mice.
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Are hepatic and muscle T2 values different at 0.5 and 1.5 Tesla?
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Automatic analysis of the electromyographic interference pattern using the turns: amplitude ratio.
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BAG3 (Bcl-2-Associated Athanogene-3) Coding Variant in Mice Determines Susceptibility to Ischemic Limb Muscle Myopathy by Directing Autophagy.
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Bedside ultrasound measurement of skeletal muscle.
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Biomarker Profile of Left Atrial Myopathy in Heart Failure With Preserved Ejection Fraction: Insights From the RELAX Trial.
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Cholesterol rethink for high-risk patients.
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Chronic myopathy due to immunoglobulin light chain amyloidosis.
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Collagenolytic activity of the skin associated with neuromuscular diseases including amyotrophic lateral sclerosis.
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Combination drug therapy for combined hyperlipidemia.
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Comparison of transurethral versus periurethral collagen injection in women with intrinsic sphincter deficiency.
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Cross-sectional imaging of abnormalities of the abdominal wall in pediatric patients.
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Delayed myonecrosis in a leukemic patient with invasive group A streptococcal disease.
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Diagnosis of late-onset Pompe disease and other muscle disorders by next-generation sequencing.
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Dislocating medial triceps and ulnar neuropathy in three generations of one family.
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Distal vacuolar myopathy with complete heart block.
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Early detection measures and triage procedures for suicide ideation in chronic pain patients.
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Effect of oxidative stress on homer scaffolding proteins.
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Efficacy and Tolerability of Evolocumab vs Ezetimibe in Patients With Muscle-Related Statin Intolerance: The GAUSS-3 Randomized Clinical Trial.
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Efficacy and tolerability of lovastatin in 3390 women with moderate hypercholesterolemia.
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Electrophysiological findings in X-linked myopathy with excessive autophagy.
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Enzyme elevation in patients with juvenile dermatomyositis and steroid myopathy.
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Evaluation of a course for general practitioners on muscles and joints.
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Evaluation of an automatic method of measuring features of motor unit action potentials.
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Exercise attenuates the weight-loss-induced reduction in muscle mass in frail obese older adults.
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Expression quantitative trait locus analysis identifies novel genes for statin myopathy.
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Extranodal Castleman disease of the extremities: a case report and review of the literature.
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Familial X-linked myalgia and cramps: a nonprogressive myopathy associated with a deletion in the dystrophin gene.
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Familial visceral myopathy.
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Final conclusions and recommendations of the National Lipid Association Statin Safety Assessment Task Force.
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Functional problems and treatment solutions after total hip arthroplasty.
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Glycogen storage disease type III (glycogen debranching enzyme deficiency): correlation of biochemical defects with myopathy and cardiomyopathy.
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Granular cell tumors of the extremities.
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Health care utilization for musculoskeletal back disorders, Washington State union carpenters, 1989-2003.
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Identification of the single base change causing the callipyge muscle hypertrophy phenotype, the only known example of polar overdominance in mammals.
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Imaging of recurrent intramuscular granulomatous masses induced by depot injection of leuprorelin.
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Impaired growth and force production in skeletal muscles of young partially pancreatectomized rats: a model of adolescent type 1 diabetic myopathy?
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In patients at high CV risk receiving simvastatin, the Myopathy Risk Score predicted statin-related myopathy.
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Intermittent nondaily dosing strategies in patients with previous statin-induced myopathy.
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Intramuscular myxoma. Radiographic and computed tomographic findings with pathologic correlation.
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Lean body mass should not be used as a surrogate measurement of muscle mass in malnourished men and women: Comment on Compher et al.
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Levator ani abnormality 6 weeks after delivery persists at 6 months.
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Levator ani denervation and reinnervation 6 months after childbirth.
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Long-term Safety and Efficacy of Achieving Very Low Levels of Low-Density Lipoprotein Cholesterol : A Prespecified Analysis of the IMPROVE-IT Trial.
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MR features of soft-tissue abnormalities due to acute marrow infarction in five children with sickle cell disease.
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Measurement of ocular torsion after macular translocation: disc fovea angle and Maddox rod.
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Metabolic myopathies: clinical features and diagnostic approach.
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Modeling statin myopathy in a human skeletal muscle microphysiological system.
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Multivariate discriminant analysis of the electromyographic interference pattern: statistical approach to discrimination among controls, myopathies and neuropathies.
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Muscle Complaints or Events in Patients Randomized to Simvastatin or Ezetimibe/Simvastatin.
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Muscle giants: molecular scaffolds in sarcomerogenesis.
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Muscle stiffness and oral pentazocine.
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Musculoskeletal syndromes associated with malignancy.
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Myopathy in human immunodeficiency virus-infected children receiving long-term zidovudine therapy.
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Narrowing in on the causative defect of an intriguing X-linked myopathy with excessive autophagy.
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Natural Progression of Canine Glycogen Storage Disease Type IIIa.
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Nemaline myopathy associated with hypertrophic cardiomyopathy.
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Outcomes and Complications in Management of Congenital Myopathy Early-Onset Scoliosis.
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Pelvic muscle electromyography of levator ani and external anal sphincter in nulliparous women and women with pelvic floor dysfunction.
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Phenotype standardization for statin-induced myotoxicity.
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Posterior tibial tendon dysfunction in rheumatoid arthritis.
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Prevention of Reperfusion Injury in Skeletal Muscle.
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Previously unreported adverse reaction to encainide.
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Prognosis for psychophysiologic disorders in the naval service.
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Pseudometabolic presentation of dystrophinopathy due to a missense mutation.
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Pseudothyrotoxic myopathy: a complication of thionamide therapy in hyperthyroidism.
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Recent advances for measurement of protein synthesis rates, use of the 'Virtual Biopsy' approach, and measurement of muscle mass.
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Relationship between fat-to-fat-free mass ratio and decrements in leg strength after downhill running.
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Riboflavin-responsive multiple acyl coenzyme A dehydrogenase deficiency presenting as a proximal myopathy in a young adult.
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Self-reported pain and disability outcomes from an endogenous model of muscular back pain.
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Serum enzyme alterations in hypothyroidism before and after treatment.
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Simulation of myopathic motor unit action potentials.
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Simultaneous thigh muscle metastasis from lung cancer and Escherichia coli gas producing myonecrosis.
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Statin Safety and Associated Adverse Events: A Scientific Statement From the American Heart Association.
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Statin safety: an assessment using an administrative claims database.
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Statins, exercise, and skeletal muscle.
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Striated muscle function, regeneration, and repair.
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Synergizing Engineering and Biology to Treat and Model Skeletal Muscle Injury and Disease
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Systemic correction of the muscle disorder glycogen storage disease type II after hepatic targeting of a modified adenovirus vector encoding human acid-alpha-glucosidase.
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Targeted Re-Sequencing Emulsion PCR Panel for Myopathies: Results in 94 Cases.
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The 2011 ACR meeting: what's new in the Windy City.
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The Composition, Development, and Regeneration of Neuromuscular Junctions.
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The SLCO1B1*5 genetic variant is associated with statin-induced side effects.
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The clinical pharmacogenetics implementation consortium guideline for SLCO1B1 and simvastatin-induced myopathy: 2014 update.
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The clinical pharmacogenomics implementation consortium: CPIC guideline for SLCO1B1 and simvastatin-induced myopathy.
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The electrodiagnostic characteristics of Glycogen Storage Disease Type III.
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The etiology and reversibility of muscle dysfunction in the aged.
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The junctophilin family of proteins: from bench to bedside.
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The management of soft-tissue problems associated with calcaneal fractures.
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The more the merrier?
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The role of an autoantigen, histidyl-tRNA synthetase, in the induction and maintenance of autoimmunity.
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The standardization of terminology for researchers in female pelvic floor disorders.
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Tissue-Engineered Human Myobundle System as a Platform for Evaluation of Skeletal Muscle Injury Biomarkers.
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Tongue weakness and atrophy differentiates late-onset Pompe disease from other forms of acquired/hereditary myopathy.
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Weaning from mechanical ventilation.
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Wegener's granulomatosis: prospective clinical and therapeutic experience with 85 patients for 21 years.
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Winning the war against ICU-acquired weakness: new innovations in nutrition and exercise physiology.
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Keywords of People
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Dement, John McCray,
Professor Emeritus in Family Medicine and Community Health,
Family Medicine & Community Health,Occupational & Environmental Medicine
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Lagoo, Anand Shreeram,
Professor of Pathology,
Pathology
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Smith, Edward Clinton,
Professor of Pediatrics,
Pediatrics, Neurology