Results 91 to 100 of about 341,590 (292)

Újabb adatok a myositisspecifikus és -asszociált antitestekről juvenilis és felnőttkori myositisekben [PDF]

, 2016
Absztrakt Az idiopathiás inflammatorikus myopathiák ismeretlen etiológiájú heterogén betegségcsoportot képeznek. Az elmúlt évtizedekben a korai diagnózisnak és az azt követően elkezdett agresszív ...
Dankó, Katalin, Váncsa, Andrea
core   +1 more source

The Role of Repeat Skeletal Muscle Biopsy: Indications, Yield and Outcomes

Muscle &Nerve, Volume 72, Issue 2, Page 217-223, August 2025.
ABSTRACT Introduction/Aims Muscle biopsy performed to investigate weakness and/or pain may be nondiagnostic and prompt repeat biopsy. We determined the indications and yield of rebiopsy. Methods Patients who underwent > 1 muscle biopsy (South Australia, 2000–2023) were identified.
Thomas Khoo, Sarah Saxon, Barbara Koszyca, Bernice Gutschmidt, Vidya Limaye   +4 more
wiley   +1 more source

Siglec-1 expression on monocytes is associated with the interferon signature in juvenile dermatomyositis and can predict treatment response

Rheumatology, 2021
Objective JDM is a rare chronic immune-mediated inflammatory disease with a predominant role for type I IFN responses. We aimed to determine the potential of Siglec-1 expression on monocytes as a novel IFN-inducible biomarker for disease activity ...
Butsabong Lerkvaleekul, S. Veldkamp, M. M. van der Wal, E. Schatorjé, S. Kamphuis, J. M. van den Berg, P. Muller, W. Armbrust, S. Vastert, J. Wienke, M. Jansen, A. van Royen-Kerkhof, F. van Wijk   +12 more
semanticscholar   +1 more source

Superimposed segmental manifestation of juvenile amyopathic dermatomyositis in a 9-year-old boy

Indian Journal of Dermatology, 2017
Dermatomyositis is a well-known autoimmune disorder. On the other hand, juvenile amyopathic dermatomyositis (JADM) occurs rather rarely. Here, we report an unusual case in a 9-year-old Turkish boy showing a unilateral linear inflammatory skin lesion that
Isil Bulur, Hilal Kaya Erdogan, Zeynep Nurhan Saracoglu, Rudolf Happle, Funda Canaz   +4 more
doaj   +1 more source

Radiographic Patterns of Soft Tissue Calcinosis in Juvenile Dermatomyositis and its Clinical Implications [PDF]

Journal of Clinical and Diagnostic Research, 2014
Juvenile Dermatomyositis (JDM) is a rare autoimmune inflammatory disease of muscles affecting children and adolescents with soft tissue calcification and varying systemic involvement.
SHANTIRANJAN SANYAL, SWAPNDEEP SINGH ATWAL, DEBOPRIYO MONDAL, UMESH CHANDRA GARGA   +3 more
doaj   +1 more source

A juvenile dermatomyositis: demographics, characteristics and disease outcome in an Egyptian cohort.

Clinical and Experimental Rheumatology, 2021
OBJECTIVES To study the demographics, characteristics, management and disease outcome of Egyptian children with juvenile dermatomyositis (JDM). METHODS Retrospective analysis of the records of 134 JDM patients attending two centres in Cairo, Egypt from
K. El-Garf, A. El-Garf, S. Salah, Huda Marzouk, Y. Farag, Noha Mostafa   +5 more
semanticscholar   +1 more source

Unilateral Heliotrope Rash in Juvenile Dermatomyositis: An Unusual Presentation of an Underlying Serious Disease

Case Reports in Rheumatology, 2014
Background. Heliotrope rash is one of the characteristic skin manifestations of juvenile dermatomyositis. It is a reddish-purple rash on the upper eyelids that is usually bilateral. Case Presentation.
Ghada Al-Janobi, Hisham Alkhalidi, Mohammed A. Omair   +2 more
doaj   +1 more source

Macrophage activation syndrome due to juvenile amyopathic dermatomyositis with atypical onset

Turkderm Turkish Archives of Dermatology and Venereology, 2022
Macrophage activation syndrome (MAS) is a life-threatening condition associated with rheumatic diseases. It is rarely reported in juvenile dermatomyositis.
Esma İnan Yüksel, Betül Demir, Metin kaya Gürgöze, Ilknur Calik   +3 more
doaj   +1 more source

Patients With IgA Vasculitis and Kawasaki Disease Show Dysregulated Interferon Signature

International Journal of Rheumatic Diseases, Volume 28, Issue 7, July 2025.
ABSTRACT Objective IgA vasculitis (IgAV) and Kawasaki disease (KD) are the most common forms of childhood vasculitis. Although various factors such as viral infections, genetic factors, and environmental factors are involved in the development of both diseases, their pathogenesis remains unclear.
Sevki Erdem Varol, Cisem Cinar, Nihan Burtecene, Sezgin Sahin, Mehmet Yildiz, Kenan Barut, Haluk Cokugras, Sinem Firtina, Ozgur Kasapcopur, Ayca Kiykim   +9 more
wiley   +1 more source

[Juvenile dermatomyositis].

La Pediatria medica e chirurgica : Medical and surgical pediatrics, 1990
Juvenile dermatomyositis (JDM) is a chronic multisystem inflammatory disease that primarily involves skin and muscles. The clinical picture is mainly characterized by the typical cutaneous rash and by skeletal muscle weakness. Nevertheless the vasculitic process may extend in some cases to other organs such as lung, joints or gastrointestinal system ...
MARTINI, ALBERTO, RAVELLI, ANGELO, L. Aramini, B. Ramenghi   +3 more
openaire   +2 more sources