Zobrazeno 1 - 10
of 36
pro vyhledávání: '"Fabian Speth"'
Autor:
Till Joscha Demal, Tasja Scholz, Helke Schüler, Jakob Olfe, Anja Fröhlich, Fabian Speth, Yskert von Kodolitsch, Thomas S. Mir, Hermann Reichenspurner, Christian Kubisch, Maja Hempel, Georg Rosenberger
Publikováno v:
Scientific Reports, Vol 12, Iss 1, Pp 1-12 (2022)
Abstract MASS phenotype is a connective tissue disorder clinically overlapping with Marfan syndrome and caused by pathogenic variants in FBN1. We report four patients from three families presenting with a MASS-like phenotype consisting of tall statur
Externí odkaz:
https://doaj.org/article/9abe0c60c92645cdb0f0b6565cf5ba06
Autor:
Jasmin K. Lalia, Raphael Schild, Marc Lütgehetmann, Gabor A. Dunay, Tilmann Kallinich, Robin Kobbe, Mona Massoud, Jun Oh, Leonora Pietzsch, Ulf Schulze-Sturm, Catharina Schuetz, Freya Sibbertsen, Fabian Speth, Sebastian Thieme, Mario Witkowski, Reinhard Berner, Ania C. Muntau, Søren W. Gersting, Nicole Toepfner, Julia Pagel, Kevin Paul
Publikováno v:
Viruses, Vol 15, Iss 7, p 1553 (2023)
The situation of limited data concerning the response to COVID-19 mRNA vaccinations in immunocom-promised children hinders evidence-based recommendations. This prospective observational study investigated humoral and T cell responses after primary BN
Externí odkaz:
https://doaj.org/article/aa64e7f7d916470e82f44df7aafbfaa6
Autor:
Julia Hildebrandt, Anja Rahn, Anja Kessler, Fabian Speth, Dagmar-Christiane Fischer, Manfred Ballmann
Publikováno v:
Pediatric Rheumatology Online Journal, Vol 19, Iss 1, Pp 1-5 (2021)
Abstract Background In adults with rheumatic diseases pulmonary complications are relevant contributors to morbidity and mortality. In these patients diffusion capacity for CO (DLCO) is an established method to detect early pulmonary impairment. Pilo
Externí odkaz:
https://doaj.org/article/fdec98a772b24a72b24a3cba40d84ec1
Autor:
Kristina Vollbach, Catharina Schuetz, Christian M. Hedrich, Fabian Speth, Kirsten Mönkemöller, Jürgen Brunner, Ulrich Neudorf, Christoph Rietschel, Anton Hospach, Tilmann Kallinich, Claas Hinze, Norbert Wagner, Burkhard Tönshoff, Lutz T. Weber, Kay Latta, Julia Thumfart, Martin Bald, Dagobert Wiemann, Hildegard Zappel, Klaus Tenbrock, Dieter Haffner
Publikováno v:
Frontiers in Pediatrics, Vol 10 (2022)
BackgroundTo describe treatment practices for juvenile proliferative lupus nephritis (LN) class III and IV of pediatric rheumatologists and nephrologists in Germany and Austria in preparation for a treat-to-target treatment protocol in LN.MethodsSurv
Externí odkaz:
https://doaj.org/article/16220893982b49f6a06d76e8ae04d4e6
Autor:
Paul Keenan, Jürgen Brunner, Angela S. Quan, Martin Smitka, Gabriele Hahn, Clare E. Pain, Renate Häfner, Fabian Speth, Lucia Gerstl, Christian M. Hedrich
Publikováno v:
Frontiers in Pediatrics, Vol 9 (2021)
Childhood primary angiitis of the Central Nervous System (cPACNS) is a rare autoimmune and inflammatory disease. It can result in significant neuronal damage, neurodevelopmental delay and potentially death. Childhood PACNS is divided into subcategori
Externí odkaz:
https://doaj.org/article/7b0ef60d9f0a4d16a26d5c147efb62e7
Autor:
Angela S. Quan, Jürgen Brunner, Benjamin Rose, Martin Smitka, Gabriele Hahn, Clare E. Pain, Renate Häfner, Fabian Speth, Lucia Gerstl, Christian M. Hedrich
Publikováno v:
Frontiers in Pediatrics, Vol 9 (2021)
Childhood Primary Angiitis of Central Nervous System (cPACNS) is rare, but can cause significant damage and result in disability or even death. Because of its rarity, the sometimes acute and variable presentation, limited awareness, and the absence o
Externí odkaz:
https://doaj.org/article/da6bbf417cad433bb5a00a6aff9b5ec3
Autor:
Claas H. Hinze, Prasad T. Oommen, Frank Dressler, Andreas Urban, Frank Weller-Heinemann, Fabian Speth, Elke Lainka, Jürgen Brunner, Heike Fesq, Dirk Foell, Wolfgang Müller-Felber, Ulrich Neudorf, Christoph Rietschel, Tobias Schwarz, Ulrike Schara, Johannes-Peter Haas
Publikováno v:
Pediatric Rheumatology Online Journal, Vol 16, Iss 1, Pp 1-9 (2018)
Abstract Background Juvenile dermatomyositis (JDM) is the most common inflammatory myopathy in childhood and a major cause of morbidity among children with pediatric rheumatic diseases. The management of JDM is very heterogeneous. The JDM working gro
Externí odkaz:
https://doaj.org/article/b9db04a85f274305a15ce4e6ffeebd37
Publikováno v:
Pediatric Rheumatology Online Journal, Vol 16, Iss 1, Pp 1-8 (2018)
Abstract Background Juvenile Dermatomyositis (JDM) is a rare pediatric autoimmune disease with broad variations of the individual course. Data on the optimal management are mostly lacking. Currently treatment decisions are often based on experts’ o
Externí odkaz:
https://doaj.org/article/0bbb06954dde409ca2b90111ff55414b
Publikováno v:
Pediatric Rheumatology Online Journal, Vol 16, Iss 1, Pp 1-10 (2018)
Abstract Background The goal of this study was to apply the varicella zoster virus (VZV) vaccine to patients with pediatric rheumatic diseases (PRD) at risk for severe chickenpox, without interrupting their current immunosuppression, including biolog
Externí odkaz:
https://doaj.org/article/cf63e488048646ac96affe41aa897b31
Autor:
Claas H. Hinze, Dirk Holzinger, Elke Lainka, Johannes-Peter Haas, Fabian Speth, Tilmann Kallinich, Nikolaus Rieber, Markus Hufnagel, Annette F. Jansson, Christian Hedrich, Hanna Winowski, Thomas Berger, Ivan Foeldvari, Gerd Ganser, Anton Hospach, Hans-Iko Huppertz, Kirsten Mönkemöller, Ulrich Neudorf, Elisabeth Weißbarth-Riedel, Helmut Wittkowski, Gerd Horneff, Dirk Foell, PRO-KIND SJIA project collaborators
Publikováno v:
Pediatric Rheumatology Online Journal, Vol 16, Iss 1, Pp 1-14 (2018)
Abstract Background Systemic juvenile idiopathic arthritis (SJIA) is an autoinflammatory disease associated with chronic arthritis. Early diagnosis and effective therapy of SJIA is desirable, so that complications are avoided. The PRO-KIND initiative
Externí odkaz:
https://doaj.org/article/64103f490e774a9b8a7cd7b21dfddc8c