Zobrazeno 1 - 10
of 63
pro vyhledávání: '"Werner Stenzel"'
Autor:
Anne Schänzer, Leonie Rager, Iris Dahlhaus, Carsten Dittmayer, Corinna Preusse, Adela Della Marina, Hans-Hilmar Goebel, Andreas Hahn, Werner Stenzel
Publikováno v:
Cells, Vol 11, Iss 109, p 109 (2022)
Cells; Volume 11; Issue 1; Pages: 109
Cells
Cells; Volume 11; Issue 1; Pages: 109
Cells
Background: In juvenile idiopathic inflammatory myopathies (IIMs), morphological characteristic features of distinct subgroups are not well defined. New treatment strategies require a precise diagnosis of the subgroups in IIM, and, therefore, knowled
Autor:
Corinna Preuße, Carsten Dittmayer, Werner Stenzel, Elise Siegert, Jakob Höppner, Vincent Casteleyn, Hans-Hilmar Goebel, Udo Schneider, Rieke Alten, Gerd R Burmester, Felix Kleefeld, Akinori Uruha, Kathrin Hahn
Publikováno v:
Acta Neuropathologica. 141:917-927
Systemic sclerosis represents a chronic connective tissue disease featuring fibrosis, vasculopathy and autoimmunity, affecting skin, multiple internal organs, and skeletal muscles. The vasculopathy is considered obliterative, but its pathogenesis is
Autor:
David Süßmuth, Ellen Knierim, Claudia Castiglioni, Enrico Bertini, Laurie D. Smith, Omid Aryani, Markus Buelow, Werner Stenzel, Markus Schuelke
Publikováno v:
European Journal of Human Genetics
Neurodevelopmental disorder with hypotonia, neuropathy, and deafness (NEDHND, OMIM #617519) is an autosomal recessive disease caused by homozygous or compound heterozygous variants in SPTBN4 coding for type 4 βIV-spectrin, a non-erythrocytic member
Autor:
Sarah Guégan, Nathalie Costedoat-Chalumeau, Vincent Descamps, Emmanuel Bergot, G. Monseau, Yoland Schoindre, C. Martel, Stéphane Barete, Cristian Bulai Livideanu, Valérie Jooste, Aude Rigolet, Achille Aouba, Thierry Zenone, Hubert de Boysson, Emmanuelle Salort-Campana, Jean-Emmanuel Kahn, Sarah Leonard-Louis, Werner Stenzel, Baptiste Hervier, Sylvain Audia, Antoine Dossier, Nicolas Schleinitz, Eric Hachulla, Alain Meyer, Laurent Mortier, Marie Lacoste, Guillaume Moulis, Serge Madaule, Florian Perez, Kuberaka Mariampillai, Anne-Marie Bouvier, Yves Allenbach, Laurence Verneuil, Benjamin Terrier, Nicolas Champtiaux, Thomas Papo, Séverine Genot, Maxime Samson, Agathe Masseau, Thierry Maisonobe, Marie-Aleth Richard, Olivier Benveniste, Boris Bienvenu, François Maurier, Guillaume Lefèvre, Anne-Marie Piette, O. Landon-Cardinal
Publikováno v:
Journal of the American Academy of Dermatology. 83:1759-1763
Autor:
Andreas Meisel, Markus Schuelke, Jens-Carsten Rückert, Sarah Hoffmann, Lutz Harms, Werner Stenzel, Hans-Hilmar Goebel
Publikováno v:
Acta Neuropathologica
Autor:
Stylianos Tomaras, Yves Allenbach, Marc Pawlitzki, Christopher Nelke, Saskia Räuber, Liesa Regner, Anne Schänzer, Olivier Benveniste, Eugen Feist, Werner Stenzel, Corinna Preuße, Rebecca Hasseli, Tobias Ruck, Heinz Wiendl, Leoni Rolfes, Sven G. Meuth
Publikováno v:
Cells, Vol 10, Iss 2551, p 2551 (2021)
Cells
Cells, MDPI, 2021, 10 (10), pp.2551. ⟨10.3390/cells10102551⟩
Volume 10
Issue 10
Cells, 2021, 10 (10), pp.2551. ⟨10.3390/cells10102551⟩
Cells
Cells, MDPI, 2021, 10 (10), pp.2551. ⟨10.3390/cells10102551⟩
Volume 10
Issue 10
Cells, 2021, 10 (10), pp.2551. ⟨10.3390/cells10102551⟩
Background: Pulmonary affection (PA) is associated with a substantial increase in morbidity and mortality in patients with idiopathic inflammatory myopathies (IIM). However, the underlying immune mechanisms of PA remain enigmatic and prompt deeper im
Autor:
Randi Koll, Pascale Eede, Anne Schänzer, Kiara Freitag, Hans-Hilmar Goebel, C. Preusse, Lucie Heinzeling, Udo Schneider, Werner Stenzel, Waltraud Froehlich, Josefine Radke, Olivier Benveniste, Yves Allenbach
Publikováno v:
Brain Pathology
Brain Pathology, Wiley, 2021, 31 (3), ⟨10.1111/bpa.12957⟩
Brain pathology 31(3), e12957 (2021). doi:10.1111/bpa.12957
Brain Pathology, Wiley, 2021, 31 (3), ⟨10.1111/bpa.12957⟩
Brain pathology 31(3), e12957 (2021). doi:10.1111/bpa.12957
Dermatomyositis (DM) is a systemic idiopathic inflammatory disease affecting skeletal muscle and skin, clinically characterized by symmetrical proximal muscle weakness and typical skin lesions. Recently, myositis‐specific autoantibodies (MSA) becam
Autor:
Carsten Dittmayer, Jantima Tanboon, Ichizo Nishino, Yukie Arahata, Hans-Hilmar Goebel, Leonille Schweizer, Akinori Uruha, Werner Stenzel
Publikováno v:
Brain Pathology
Sporadic late‐onset nemaline myopathy (SLONM) is a rare adult‐onset non‐hereditary disease with subacute proximal muscle and often axial muscle weakness, characterized by the presence of nemaline bodies in skeletal muscle biopsies. Considering
Autor:
Gizem Inak, Agnieszka Rybak-Wolf, Pawel Lisowski, Tancredi M. Pentimalli, René Jüttner, Petar Glažar, Karan Uppal, Emanuela Bottani, Dario Brunetti, Christopher Secker, Annika Zink, David Meierhofer, Marie-Thérèse Henke, Monishita Dey, Ummi Ciptasari, Barbara Mlody, Tobias Hahn, Maria Berruezo-Llacuna, Nikos Karaiskos, Michela Di Virgilio, Johannes A. Mayr, Saskia B. Wortmann, Josef Priller, Michael Gotthardt, Dean P. Jones, Ertan Mayatepek, Werner Stenzel, Sebastian Diecke, Ralf Kühn, Erich E. Wanker, Nikolaus Rajewsky, Markus Schuelke, Alessandro Prigione
Publikováno v:
Nature Communications
Nature Communications, Vol 12, Iss 1, Pp 1-22 (2021)
Nature Communications, Vol 12, Iss 1, Pp 1-22 (2021)
Leigh syndrome (LS) is a severe manifestation of mitochondrial disease in children and is currently incurable. The lack of effective models hampers our understanding of the mechanisms underlying the neuronal pathology of LS. Using patient-derived ind
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::15507fdc618a46e7b1a2eaf9b3df8030
http://edoc.mdc-berlin.de/20132/1/20132oa.pdf
http://edoc.mdc-berlin.de/20132/1/20132oa.pdf
Autor:
Sarah Leonard-Louis, Olivier Boyer, K. Mariampillai, Thierry Maisonobe, C. Rasmussen, L. Bolko, Shigeaki Suzuki, O. Landon-Cardinal, L. Musset, Akinori Uruha, Yves Allenbach, Werner Stenzel, J.L. Charuel, Ichizo Nishino, A. Aussy, Olivier Benveniste
Publikováno v:
Neuropathology and Applied Neurobiology. 45:513-522
Aims To elucidate the diagnostic value of sarcoplasmic expression of myxovirus resistance protein A (MxA) for dermatomyositis (DM) specifically analysing different DM subforms, and to test the superiority of MxA to other markers. Methods Immunohistoc