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About 7,198 results

ALLMedicine™ Myopathies Center

Research & Reviews  3,539 results

Efficacy and safety of statins in ethnic differences: a lesson for application in Indig...
https://doi.org/10.2217/pgs-2020-0152
Pharmacogenomics Gebremichael LG, Suppiah V et. al.

Jun 14th, 2021 - Although statins are effective in treating high cholesterol, adverse effects do occur with their use. Efficacy and tolerability vary among statins in different ethnic groups. Indigenous Australians have a high risk for cardiovascular and kidney di...

Myositis autoantibodies in a racially diverse population of children with idiopathic in...
https://doi.org/10.1186/s12969-021-00574-6 10.1136/annrheumdis-2012-201483 10.1016/S0140-6736(08)60955-1 10.1002/art.11122 10.1097/MD.0b013e31829d08f9 10.1111/joim.12444 10.1186/ar4600 10.1016/j.jaut.2017.06.007 10.1093/rheumatology/kem359 10.1016/j.jpeds.2010.11.033 10.1093/rheumatology/keu259 10.1093/rheumatology/keq153 10.1002/acr.21992
Pediatric Rheumatology Online Journal; Perron MM, Vasquez-Canizares N et. al.

Jun 13th, 2021 - Juvenile idiopathic inflammatory myopathies (JIIMs) is a group of autoimmune disorders, including juvenile dermatomyositis (JDM), juvenile polymyositis (JPM) and overlap myositis, that are characterized by proximal muscle weakness, elevated levels...

Immune recognition of lysyl-tRNA synthetase and isoleucyl-tRNA synthetase by anti-OJ an...
https://doi.org/10.1016/j.jaut.2021.102680
Journal of Autoimmunity; Muro Y, Yamano Y et. al.

Jun 13th, 2021 - Anti-aminoacyl-tRNA synthetase (anti-ARS) antibodies are useful for identifying a clinical subset of patients with idiopathic inflammatory myopathies (IIMs). Anti-OJ antibodies, which recognize multi-enzyme synthetase complexes including isoleucyl...

A case report of malignant hyperthermia in a patient with myotonic dystrophy type I: A ...
https://doi.org/10.1097/MD.0000000000025859
Medicine Yoo SW, Baek SJ et. al.

Jun 11th, 2021 - Several hereditary myopathies that can predispose to malignant hyperthermia (MH) are reported. However, the risk of MH in myotonic dystrophy type I (DM1) has been suggested equal to general population, although the evidence is limited to only a fe...

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Guidelines  2 results

2017 European League Against Rheumatism/American College of Rheumatology classification...
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5736307
Annals of the Rheumatic Diseases; Lundberg IE, Tjärnlund A et. al.

Oct 28th, 2017 - To develop and validate new classification criteria for adult and juvenile idiopathic inflammatory myopathies (IIM) and their major subgroups. Candidate variables were assembled from published criteria and expert opinion using consensus methodolog...

EFNS guidelines for the molecular diagnosis of neurogenetic disorders: motoneuron, peri...
https://doi.org/10.1111/j.1468-1331.2010.03069.x
European Journal of Neurology; Burgunder JM, Schöls L et. al.

May 26th, 2010 - These EFNS guidelines on the molecular diagnosis of motoneuron disorders, neuropathies and myopathies are designed to summarize the possibilities and limitations of molecular genetic techniques and to provide diagnostic criteria for deciding when ...

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Clinicaltrials.gov  3,587 results

Efficacy and safety of statins in ethnic differences: a lesson for application in Indig...
https://doi.org/10.2217/pgs-2020-0152
Pharmacogenomics Gebremichael LG, Suppiah V et. al.

Jun 14th, 2021 - Although statins are effective in treating high cholesterol, adverse effects do occur with their use. Efficacy and tolerability vary among statins in different ethnic groups. Indigenous Australians have a high risk for cardiovascular and kidney di...

Myositis autoantibodies in a racially diverse population of children with idiopathic in...
https://doi.org/10.1186/s12969-021-00574-6 10.1136/annrheumdis-2012-201483 10.1016/S0140-6736(08)60955-1 10.1002/art.11122 10.1097/MD.0b013e31829d08f9 10.1111/joim.12444 10.1186/ar4600 10.1016/j.jaut.2017.06.007 10.1093/rheumatology/kem359 10.1016/j.jpeds.2010.11.033 10.1093/rheumatology/keu259 10.1093/rheumatology/keq153 10.1002/acr.21992
Pediatric Rheumatology Online Journal; Perron MM, Vasquez-Canizares N et. al.

Jun 13th, 2021 - Juvenile idiopathic inflammatory myopathies (JIIMs) is a group of autoimmune disorders, including juvenile dermatomyositis (JDM), juvenile polymyositis (JPM) and overlap myositis, that are characterized by proximal muscle weakness, elevated levels...

Immune recognition of lysyl-tRNA synthetase and isoleucyl-tRNA synthetase by anti-OJ an...
https://doi.org/10.1016/j.jaut.2021.102680
Journal of Autoimmunity; Muro Y, Yamano Y et. al.

Jun 13th, 2021 - Anti-aminoacyl-tRNA synthetase (anti-ARS) antibodies are useful for identifying a clinical subset of patients with idiopathic inflammatory myopathies (IIMs). Anti-OJ antibodies, which recognize multi-enzyme synthetase complexes including isoleucyl...

A case report of malignant hyperthermia in a patient with myotonic dystrophy type I: A ...
https://doi.org/10.1097/MD.0000000000025859
Medicine Yoo SW, Baek SJ et. al.

Jun 11th, 2021 - Several hereditary myopathies that can predispose to malignant hyperthermia (MH) are reported. However, the risk of MH in myotonic dystrophy type I (DM1) has been suggested equal to general population, although the evidence is limited to only a fe...

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News  63 results

Congenital myasthenic syndrome diagnosed best with repetitive stimulation and jitter analysis
https://www.mdedge.com/neurology/article/210304/neuromuscular-disorders/congenital-myasthenic-syndrome-diagnosed-best?channel=53
Tara Haelle

Oct 17th, 2019 - AUSTIN, TEX. – The use of both repetitive stimulation (RS) and jitter analysis are important for accurate diagnosis of congenital myasthenic syndrome (CMS) suggests newly presented research.

New System Classifies Idiopathic Inflammatory Myopathies
https://www.mdedge.com/neurology/article/175874/rare-diseases/new-system-classifies-idiopathic-inflammatory-myopathies

Sep 27th, 2018 - A new system that incorporates clinical and serologic data may help classify idiopathic inflammatory myopathies, according to an analysis published online ahead of print September 10 in JAMA Neurology. By analyzing the patterns of relationships be.

Idiopathic inflammatory myopathies: Muscle biopsy no longer needed?
https://www.mdedge.com/neurology/article/174324/neuromuscular-disorders/idiopathic-inflammatory-myopathies-muscle-biopsy-no
Andrew D. Bowser

Sep 10th, 2018 - A new classification system that incorporates clinical and serologic data may be useful in the classification of idiopathic inflammatory myopathies, results of a recent analysis suggest. By analyzing the patterns of relationships between 47 variab.

Stroke Risk Doubled in Myopathy
https://www.medpagetoday.com/rheumatology/generalrheumatology/74089

Jul 18th, 2018 - Action Points Be aware that patients with idiopathic inflammatory myopathies have double the risk of both ischemic and hemorrhagic stroke compared to the general population, according to a Swedish population-based cohort study. Note that the idiop...

Rare paraneoplastic dermatomyositis secondary to high-grade bladder cancer
https://www.mdedge.com/hematology-oncology/article/164487/genitourinary-cancer/rare-paraneoplastic-dermatomyositis
Kase et al

Apr 29th, 2018 - The clinical presentation of bladder cancer typically presents with hematuria; changes in voiding habits such as urgency, frequency, and pain; or less commonly, obstructive symptoms. Rarely does bladder cancer first present as part of a paraneopla.

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Patient Education  7 results see all →