Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Mohammed Nashawi"'
Publikováno v:
Clinical Epidemiology and Global Health, Vol 26, Iss , Pp 101562- (2024)
Background: The importance of transition of care for adolescents with rheumatological illnesses from pediatric to adult rheumatology is increasing as the childhood rheumatologic diseases continue to adulthood. Despite that, transition practice in Sau
Externí odkaz:
https://doaj.org/article/a426e1beefe14e5cabaf87f20039c257
Publikováno v:
Saudi Journal of Kidney Diseases and Transplantation, Vol 34, Iss 6, Pp 576-591 (2023)
Renal involvement of systemic lupus erythematosus needs aggressive treatment. Despite the development of multiple international guidelines, differences in practices exist. This study aimed to explore the current practices of pediatric rheumatologists
Externí odkaz:
https://doaj.org/article/f6a30dba4b3b44d8972f1664f2f64c6a
Autor:
Anita Heinkele, Friederike Blankenburg, Mohammed Nashawi, Anton Hospach, Carsten Speckmann, Stephan Ehl
Publikováno v:
Arthritis und Rheuma. 42:351-352
Publikováno v:
Pädiatrie. 33:21-23
Autor:
Anita Heinkele, Kirsten Timmermann, Toni Hospach, Friederike Blankenburg, Christian Stirnkorb, Friedrich Reichert, Mohammed Nashawi, Felix Noll
Publikováno v:
Arthritis und Rheuma. 41:148-150
ZUSAMMENFASSUNGEinleitung: Das Kawasaki-Syndrom (KS) ist eine systemische Vaskulitis, die mittelgroße Arterien betrifft. Obwohl Diagnose- und Klassifizierungskriterien existieren, kann die Abgrenzung von anderen Krankheiten schwierig sein.Falldarste
Autor:
Alexandru Anton Sabo, Anita Heinkele, Frederike Blankenburg, Clemens Wurz, Hans-Jürgen Pander, Toni Hospach, Mohammed Nashawi
Publikováno v:
Arthritis und Rheuma. 42:193-194
Autor:
Felix Noll, Kirsten Timmermann, Toni Hospach, Mohammed Nashawi, Christian Stirnkorb, Friederike Blankenburg, Friedrich Reichert, Anita Heinkele
Background: Kawasaki disease (KD) is a systemic vasculitis which affects medium-sized arteries. Although diagnostic and classification criteria exist, differentiation from other diseases can be difficult.Case Presentation: We present a 3-year old pat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::39b9e71229366f9a2376d19ea847df92
https://doi.org/10.21203/rs.3.rs-76944/v1
https://doi.org/10.21203/rs.3.rs-76944/v1
Autor:
Mohammed Nashawi, Stefan Kölker, Markus Bettendorf, Georg F. Hoffmann, Andreas Ziegler, Jan Henje Döring
Publikováno v:
Abstracts Accepted for Publication.
Background Fibrodysplasia ossificans progressiva (FOP) caused by mutations in the ACVR1 gene, which codes for activin receptor IA, a type I receptor of the bone morphogenetic protein (BMP) pathway. FOP is a very rare disease which usually begins in t