Zobrazeno 1 - 10
of 89
pro vyhledávání: '"Juvenile Polymyositis"'
Autor:
Jessica Perfetto, Donna A. Yoo, Carolina Y. Tamashiro, Megan M. Perron, Natalia Vasquez-Canizares, Dawn M. Wahezi
Publikováno v:
Pediatric Rheumatology Online Journal, Vol 21, Iss 1, Pp 1-8 (2023)
Abstract Background Growing evidence suggests that infection with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) may trigger idiopathic inflammatory myopathies (IIM). Few studies have described individual juvenile IIM (JIIM) cases follo
Externí odkaz:
https://doaj.org/article/531252050c624cf49378f0fe9e436a75
Akademický článek
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Publikováno v:
Pediatric Rheumatology Online Journal, Vol 19, Iss 1, Pp 1-6 (2021)
Abstract Background 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
Externí odkaz:
https://doaj.org/article/1cbcf985ca3849409fcfa27f39ba0c60
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
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Autor:
Alberto Cappellari, Francesca Minoia, Dario Consonni, Isabella Picca, Antonella Petaccia, Giovanni Filocamo
Publikováno v:
Pediatric Neurology. 124:6-10
Introduction We performed a pilot study in order to investigate the feasibility of an electromyography (EMG)-scoring protocol for the assessment of disease activity in juvenile idiopathic inflammatory myopathies (JIIM). Methods Children with JIIM fol
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7218b50551793e46e763babe10c7965e
https://doi.org/10.1016/j.pediatrneurol.2021.07.017
https://doi.org/10.1016/j.pediatrneurol.2021.07.017
Autor:
Ana Fernández Pérez, Patricia Carreira, Raquel Almodóvar, María Carmen Barbadillo, Francisco Javier López-Longo, Laura Nuño-Nuño, Beatriz Joven, Tatiana Cobo-Ibáñez, L. Ruiz, Eva Tomero, Carmen Larena, M. Ángeles Blázquez, María Jesús García-De Yébenes, Indalecio Monteagudo, Juan Carlos López-Robledillo, Leticia Lojo Oliveira, Henry Moruno, Paloma García de la Peña, Julia Martínez-Barrio, Jesús Loarce-Martos, I. Llorente
Publikováno v:
JCR: Journal of Clinical Rheumatology. 28:e195-e202
Few studies have been published focusing on the differences between juvenile idiopathic inflammatory myopathy (JIIM) and adult IIM. This study aimed to describe the characteristics of JIIM main subgroups (juvenile dermatomyositis [JDM] and juvenile p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::19fda89f16216a6a04572300b70dca4b
https://doi.org/10.1097/rhu.0000000000001696
https://doi.org/10.1097/rhu.0000000000001696
Autor:
Ciro Matsui-Júnior, Umbertina Conti Reed, Rodrigo de Holanda Mendonça, Clara Gontijo Camelo, Adriana Maluf Elias, Edmar Zanoteli, Clovis A. Silva, Lucia M.A. Campos, André Macedo Serafim da Silva
Publikováno v:
Neurology. 96:e1383-e1386
A 4-year-old girl, the first child of nonconsanguineous parents, with normal motor development, presented with frequent falls, difficulty getting up from the floor, and muscle pain for several months. Her initial serum creatine kinase (CK) level was
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6435c2272aec426b2c8f3c572fc08e22
https://doi.org/10.1212/wnl.0000000000011320
https://doi.org/10.1212/wnl.0000000000011320
Publikováno v:
Pediatric Rheumatology Online Journal
Pediatric Rheumatology Online Journal, Vol 19, Iss 1, Pp 1-6 (2021)
Pediatric Rheumatology Online Journal, Vol 19, Iss 1, Pp 1-6 (2021)
Background 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, elevate
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f772e4c179a776bbb7df425abeb5691d
https://doi.org/10.1186/s12969-021-00574-6
https://doi.org/10.1186/s12969-021-00574-6
Publikováno v:
Cureus
Idiopathic inflammatory myopathy encompasses a group of acquired, heterogeneous, systemic diseases of the skeletal muscle, including adult polymyositis, adult dermatomyositis, juvenile dermatomyositis, juvenile polymyositis, inclusion body myositis,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::94852b1786a505d2f1c999a9d483eea0
https://doi.org/10.7759/cureus.14507
https://doi.org/10.7759/cureus.14507
Autor:
Adam M. Huber
Publikováno v:
Managing Myositis ISBN: 9783030158194
Juvenile idiopathic inflammatory myopathies (JIIM) are rare, autoimmune myositis syndromes affecting children. These disorders have much in common with their adult counterparts, but there are important differences that should be appreciated. These in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b348796a5dca7c44b1b86fe6269b971b
https://doi.org/10.1007/978-3-030-15820-0_10
https://doi.org/10.1007/978-3-030-15820-0_10
