Results 51 to 60 of about 10,614 (207)

Nuclear matrix protein 2 antibody-positive adult dermatomyositis: a case report and review of the literature [PDF]

, 2020
Dermatomyositis is a clinically heterogenous inflammatory myopathy with unique cutaneous features. Myositis-specific antibodies can aid in diagnosis and anticipation of patient prognosis.
Cartron, Alexander M, Chung, Catherine, Osler, Montana, Trinidad, John C   +3 more
core  

Update in juvenile myositis. [PDF]

, 2013
This update on childhood idiopathic inflammatory myopathies (IIMs) reviews recent progress in the field of translational science and clinical research over the past 12-18 ...
Nistala, K, Wedderburn, LR
core   +1 more source

Cardiac involvement in adult and juvenile idiopathic inflammatory myopathies [PDF]

, 2016
Idiopathic inflammatory myopathies (IIM) include the main subgroups polymyositis (PM), dermatomyositis (DM), inclusion body myositis (IBM) and juvenile DM (JDM).
Diederichsen, L. P., Lundberg, Ingrid E., Sanner, Helga, Schwartz, TThomas W, Sjaastad, Ivar   +4 more
core   +1 more source

Juvenile amyopathic dermatomyositis

Dermatology Online Journal, 2005
A 3-year-old girl presented with a 6-month history of multiple, light-pink, flat-topped papules over the dorsal aspects of the metacarpophalangeal and interphalangeal joints of the hands and feet. Nailfold telangiectases, ragged cuticles, and a heliotrope color of the upper eyelids were also evident, but there was no clinical evidence of muscle ...
Henning, J Scott, Witkiewicz, Agnieszka, Schaffer, Julie V, Orlow, Seth J   +3 more
openaire   +4 more sources

Respiratory symptoms as initial manifestations of interstitial lung disease in clinically amyopathic juvenile dermatomyositis: a case report with literature review

BMC Pediatrics, 2021
Background Clinically amyopathic juvenile dermatomyositis (CAJDM) is a clinical subgroup of juvenile dermatomyositis (JDM), characterized by JDM rashes with little or no clinically evident muscle weakness.
Jingyi Xia, Gaoli Jiang, Tingting Jin, Quanli Shen, Yangyang Ma, Libo Wang, Liling Qian   +6 more
doaj   +1 more source

Assessment of the trophological status of children with rheumatic diseases

Zdorovʹe Rebenka, 2021
Background. Analyzing modern medical literature, it can be noted that in pediatric rheumatology, insufficient attention is paid to assessing the trophological status of sick children.
L.I. Omelchenko, O.M. Mukvich, E.A. Belskaya, I.V. Dudka, T.A. Ludvik   +4 more
doaj   +1 more source

Juvenile dermatomyositis (JDM) and severe pulmonary involvement: case report [PDF]

, 2009
Juvenile dermatomyositis (JDM) is an inflammatory, non-pustular disorder of skeletal muscles and skin. Other organs, such as the lungs, can be involved.
Bugni, Vanessa Monteiro, Castro, Márcia Helena de Oliveira, Hilário, Maria Odete Esteves, Ishigai, Márcia Marcelino de Souza, Silva, Érika Cristina Carneiro da, Terreri, Maria Teresa Ramos Ascensão   +5 more
core   +2 more sources

Comparison between treatment naive juvenile and adult dermatomyositis muscle biopsies: difference of inflammatory cells phenotyping

Advances in Rheumatology, 2018
Background Different inflammatory cells (i.e., CD4, CD8, CD20 and CD68) are involved in pathogenesis of DM muscle. In this context, the aim of this study was to assess and compare these inflammatory cell phenotyping in muscle samples of treatment naive ...
Samuel Katsuyuki Shinjo, Adriana Maluf Elias Sallum, Sueli Mieko Oba-Shinjo, Marilda Guimarães Silva, Clovis Artur Silva, Suely Kazue Nagahashi Marie   +5 more
doaj   +1 more source

A juvenilis és felnőttkori dermatomyositises betegek klinikai jellemzői [PDF]

, 2015
Absztrakt Bevezetés: A juvenilis és felnőttkori dermatomyositisek szisztémás autoimmun megbetegedések, jellegzetességük a proximális végtagizomzat szimmetrikus gyengesége és típusos bőrtünetek ...
Dankó, Katalin, Farkas, Flóra, Nagy-Vince, Melinda, Szalmás, Orsolya   +3 more
core   +1 more source

Case Report: IVIG causing bilateral papilledema and increased intracranial hypertension in patients with anti-TIF-1γ antibody-positive JDM

Frontiers in Pediatrics
Juvenile dermatomyositis is a systemic autoimmune disease characterized by progressive proximal muscle weakness, pathognomonic rashes, and often the presence of myositis-specific antibodies.
Sarah Baluta, Ivana Stojkic, Kyla Driest, Christina Schutt   +3 more
doaj   +1 more source