Results 31 to 40 of about 10,614 (207)

Developmentally appropriate transitional care during the Covid-19 pandemic for young people with juvenile-onset rheumatic and musculoskeletal diseases: the rationale for a position statement

Pediatric Rheumatology Online Journal, 2021
Background The importance of developmentally appropriate transitional care in young people with juvenile-onset rheumatic and musculoskeletal disease is well recognised.
Janet E. McDonagh, Rachel Tattersall, Jacqui Clinch, Joanne Swan, Helen E. Foster, Liza McCann   +5 more
doaj   +1 more source

Clinical phenotypes and biologic treatment use in juvenile dermatomyositis-associated calcinosis [PDF]

, 2018
Background Few risk factors have been identified for the development of calcinosis among patients with Juvenile Dermatomyositis, and currently no clinical phenotype has been associated with its development.
Al-Hammadi, Noor, Baszis, Kevin W, CARRA Legacy Registry Investigators,, Dharnidharka, Vikas R, Orandi, Amir B   +4 more
core   +2 more sources

Juvenile Dermatomyositis

Kinder- und Jugendmedizin, 2015
ZusammenfassungDie juvenile Dermatomyositis ist die häufigste chronisch-entzündliche Myopathie des Kindesalters, charakterisiert durch Haut- und Gefäßveränderungen und Muskelschwäche, am häufigsten im frühen Schulalter auftre-tend. Die pathognomonische Befundkonstellation erlaubt prinzipiell eine frühe klinische Diagnose.
M. FROSCH, F. DRESSLER
  +6 more sources

Banker Type of Juvenile Dermatomyositis

Indian Journal of Dermatology
Sunil K. Gupta, Ratnakar Shukla
doaj   +2 more sources

Biomarkers in Inflammatory Myopathies – An Expanded Definition [PDF]

, 2019
Biomarkers as parameters of pathophysiological conditions can be of outmost relevance for inflammatory myopathies. They are particularly warranted to inform about diagnostic, prognostic, and therapeutic questions.
Benveniste, Olivier, Goebel, Hans-Hilmar, Stenzel, Werner   +2 more
core   +3 more sources

A Cause of High Creatine Kinase: A Case of Juvenile Dermatomyositis

Haseki Tıp Bülteni, 2014
Although juvenile dermatomyositis is rare, it is the most common idiopathic nonsupurrative inflammatory myositis in childhood. Skin lesions, proximal muscle weakness, elevated levels of muscle enzymes, electromyography, and muscle biopsy findings are ...
İsmail Yıldız, Özge Umur, Muhammet Ali Varkal, Alev Yılmaz, Gökçen Gündoğdu, Ayşe Kılıç, Fatma Oğuz, Emin Ünüvar   +7 more
doaj   +1 more source

Plasma exosomes from children with juvenile dermatomyositis are taken up by human aortic endothelial cells and are associated with altered gene expression in those cells [PDF]

, 2019
BACKGROUND: The pathology of juvenile dermatomyositis (JDM) is characterized by prominent vessel wall and perivascular inflammation. This feature of the disease has remained unexplained and under-investigated. We have hypothesized that plasma exosomes,
Chen, Yanmin, Holmes, Lucy, Hu, Zihua, Jarvis, James N., Jiang, Kaiyu, Karasawa, Rie, O’Neil, Kathleen M.   +6 more
core   +1 more source

Skeletal muscle major histocompatibility complex class I and II expression differences in adult and juvenile dermatomyositis

Clinics, 2012
OBJECTIVE: To analyze major histocompatibility complex expression in the muscle fibers of juvenile and adult dermatomyositis. METHOD: In total, 28 untreated adult dermatomyositis patients, 28 juvenile dermatomyositis patients (Bohan and Peter's criteria)
Samuel Katsuyuki Shinjo, Adriana Maluf Elias Sallum, Clovis Artur Silva, Suely Kazue Nagahashi Marie   +3 more
doaj   +1 more source

A national registry for juvenile dermatomyositis and other paediatric idiopathic inflammatory myopathies: 10 years' experience; the Juvenile Dermatomyositis National (UK and Ireland) Cohort Biomarker Study and Repository for Idiopathic Inflammatory Myopathies [PDF]

, 2011
Objectives: The paediatric idiopathic inflammatory myopathies (IIMs) are a group of rare chronic inflammatory disorders of childhood, affecting muscle, skin and other organs.
Bohan, Bohan, Brown, Chinoy, Chinoy, Christen-Zaech, Clarissa A. Pilkington, Constantin, Elst, Gunawardena, Gunawardena, Huber, Huber, Huber, Huber, Isenberg, Joyce E. Davidson, Kevin Murray, Kim, Li, Li, Lovell, Lowry, Lucy R. Wedderburn, Maillard, Maillard, Marhaug, McCann, McCann, McCann, Mendez, Miller, Neil Martin, Pachman, Pachman, Petra Krol, Ravelli, Rider, Rider, Rider, Rider, Riley, Riley, Sally Smith, Salomonsson, Stringer, Symmons, Varsani, Wedderburn, Wedderburn, Wedderburn   +50 more
core   +1 more source

Features distinguishing clinically amyopathic juvenile dermatomyositis from juvenile dermatomyositis [PDF]

Rheumatology, 2018
We examined features of clinically amyopathic JDM (CAJDM), in which patients have characteristic rashes with little to no evidence of muscle involvement, to determine whether this is a distinct phenotype from JDM.Demographic, clinical, laboratory and treatment data from 12 (9 hypomyopathic, 3 amyopathic) patients meeting modified Sontheimer criteria ...
Gulnara Mamyrova, Takayuki Kishi, Ira N Targoff, Alison Ehrlich, Rodolfo V Curiel, Lisa G Rider, Leslie S Abramson, Bita Arabshahi, Victoria Cartwright, Elizabeth J Chalom, Barbara Anne Eberhardt, William Hannan, Gloria C Higgins, Robert C Fuhlbrigge, Jerry C Jacobs, Lawrence Jung, Yukiko Kimura, Carol B Lindsley, Alan L Martin, Frederick W Miller, Diana Milojevic, Barbara E Ostrov, Maria D Perez, Rafael F Rivas-Chacon, Margalit Rosenkranz, David D Sherry, Jennifer Soep, Sangeeta Sule, Scott A Vogelgesang   +28 more
openaire   +2 more sources