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582 results

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Page 1
Current Classification and Management of Inflammatory Myopathies.
Schmidt J. Schmidt J. J Neuromuscul Dis. 2018;5(2):109-129. doi: 10.3233/JND-180308. J Neuromuscul Dis. 2018. PMID: 29865091 Free PMC article. Review.
Inflammatory disorders of the skeletal muscle include polymyositis (PM), dermatomyositis (DM), (immune mediated) necrotizing myopathy (NM), overlap syndrome with myositis (overlap myositis, OM) including anti-synthetase syndrome (ASS), and inclusion body myositis (IBM). .. …
Inflammatory disorders of the skeletal muscle include polymyositis (PM), dermatomyositis (DM), (immune mediated) necrotizing myopathy …
Diagnosis and Management of Myositis-Associated Lung Disease.
Hallowell RW, Danoff SK. Hallowell RW, et al. Chest. 2023 Jun;163(6):1476-1491. doi: 10.1016/j.chest.2023.01.031. Epub 2023 Feb 9. Chest. 2023. PMID: 36764512 Free article. Review.
We propose alternative nomenclature to facilitate research on this unique patient population. Additionally, evidence supporting the various therapies used in the treatment of myositis-associated ILD is reviewed. The classification and treatment of patients with myositis-as …
We propose alternative nomenclature to facilitate research on this unique patient population. Additionally, evidence supporting the various …
Current diagnosis and treatment of polymyositis and dermatomyositis.
Sasaki H, Kohsaka H. Sasaki H, et al. Mod Rheumatol. 2018 Nov;28(6):913-921. doi: 10.1080/14397595.2018.1467257. Epub 2018 May 9. Mod Rheumatol. 2018. PMID: 29669460 Review.
Polymyositis, dermatomyositis, and inclusion body myositis are major IIM subsets. Immune-mediated necrotizing myopathy became recognized as a potentially new IIM subset. Since the new classification criteria published by the International Myositis Classification Criteria P …
Polymyositis, dermatomyositis, and inclusion body myositis are major IIM subsets. Immune-mediated necrotizing myopathy became recogni …
Proximal myopathy: diagnostic approach and initial management.
Suresh E, Wimalaratna S. Suresh E, et al. Postgrad Med J. 2013 Aug;89(1054):470-7. doi: 10.1136/postgradmedj-2013-131752. Epub 2013 Apr 17. Postgrad Med J. 2013. PMID: 23596213 Review.
Proximal myopathy presents as symmetrical weakness of proximal upper and/or lower limbs. ...Management depends on underlying cause, and includes measures, such as removal of offending agent, correction of endocrine or metabolic problem, corticosteroids and immunosuppressiv …
Proximal myopathy presents as symmetrical weakness of proximal upper and/or lower limbs. ...Management depends on underlying cause, a …
Consensus on the diagnosis, treatment and follow-up of patients with Duchenne muscular dystrophy.
Nascimento Osorio A, Medina Cantillo J, Camacho Salas A, Madruga Garrido M, Vilchez Padilla JJ. Nascimento Osorio A, et al. Neurologia (Engl Ed). 2019 Sep;34(7):469-481. doi: 10.1016/j.nrl.2018.01.001. Epub 2018 Mar 9. Neurologia (Engl Ed). 2019. PMID: 29526319 Free article. English, Spanish.
INTRODUCTION: Duchenne muscular dystrophy (DMD) is the most common myopathy in children, with a worldwide prevalence of approximately 0.5 cases per 10,000 male births. ...Genetic studies play a key role in the management of the disease, both in detecting cases and potentia …
INTRODUCTION: Duchenne muscular dystrophy (DMD) is the most common myopathy in children, with a worldwide prevalence of approximately …
Classification and management of adult inflammatory myopathies.
Selva-O'Callaghan A, Pinal-Fernandez I, Trallero-Araguás E, Milisenda JC, Grau-Junyent JM, Mammen AL. Selva-O'Callaghan A, et al. Lancet Neurol. 2018 Sep;17(9):816-828. doi: 10.1016/S1474-4422(18)30254-0. Lancet Neurol. 2018. PMID: 30129477 Review.
Five main types of inflammatory myopathies are now widely recognised: dermatomyositis, immune-mediated necrotising myopathy, sporadic inclusion-body myositis, overlap myositis (including antisynthetase syndrome), and polymyositis. ...Treatment is still largely based on exp …
Five main types of inflammatory myopathies are now widely recognised: dermatomyositis, immune-mediated necrotising myopathy, sporadic …
MELAS syndrome: Clinical manifestations, pathogenesis, and treatment options.
El-Hattab AW, Adesina AM, Jones J, Scaglia F. El-Hattab AW, et al. Mol Genet Metab. 2015 Sep-Oct;116(1-2):4-12. doi: 10.1016/j.ymgme.2015.06.004. Epub 2015 Jun 15. Mol Genet Metab. 2015. PMID: 26095523 Review.
MELAS syndrome is a multi-organ disease with broad manifestations including stroke-like episodes, dementia, epilepsy, lactic acidemia, myopathy, recurrent headaches, hearing impairment, diabetes, and short stature. ...Management is largely symptomatic and should involve a …
MELAS syndrome is a multi-organ disease with broad manifestations including stroke-like episodes, dementia, epilepsy, lactic acidemia, my …
Management of Atrial Fibrillation Across the Spectrum of Heart Failure With Preserved and Reduced Ejection Fraction.
Reddy YNV, Borlaug BA, Gersh BJ. Reddy YNV, et al. Circulation. 2022 Jul 26;146(4):339-357. doi: 10.1161/CIRCULATIONAHA.122.057444. Epub 2022 Jul 25. Circulation. 2022. PMID: 35877831 Review.
Preliminary data also show a close relationship among AF, left atrial myopathy, mitral regurgitation, and HF with preserved ejection, with potential clinical benefits to catheter ablation therapy. The modern management of AF in HF also requires consideration of the …
Preliminary data also show a close relationship among AF, left atrial myopathy, mitral regurgitation, and HF with preserved ejection, …
Juvenile Dermatomyositis: Advances in Pathogenesis, Assessment, and Management.
Leung AKC, Lam JM, Alobaida S, Leong KF, Wong AHC. Leung AKC, et al. Curr Pediatr Rev. 2021;17(4):273-287. doi: 10.2174/1573396317666210426105045. Curr Pediatr Rev. 2021. PMID: 33902423 Review.
In the absence of muscle biopsy, a definite diagnosis of idiopathic inflammatory myopathy can be made if the total score is 7.5. Patients whose age at onset of symptoms is less than 18 years and who meet the above criteria for idiopathic inflammatory myopathy and ha …
In the absence of muscle biopsy, a definite diagnosis of idiopathic inflammatory myopathy can be made if the total score is 7.5. Pati …
582 results