Zobrazeno 1 - 10
of 27
pro vyhledávání: '"Werner Stenzel"'
Autor:
Falk Hiepe, Lydia Zorn-Pauly, Udo Schneider, Gerd R Burmester, Thomas Buttgereit, Thomas Rose, Nadine Unterwalder, Akinori Uruha, Martin Krusche, Robert Biesen, Christian Meisel, Tilman Kallinich, Werner Stenzel, Manuel Graf, Jens Klotsche, Sae Lim von Stuckrad
ObjectiveTo evaluate SIGLEC1 expression on monocytes by flow cytometry as a type I interferon biomarker in idiopathic inflammatory myopathies (IIM).MethodsWe performed a retrospective analysis of adult and pediatric patients with the diagnosis of IIM
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::32eb4421889d7fa3992797fb1fcd921a
https://doi.org/10.1101/2021.09.13.21263325
https://doi.org/10.1101/2021.09.13.21263325
Autor:
Josefine Radke, Anja von Renesse, Carsten Dittmayer, Udo Schneider, Helena Radbruch, Akinori Uruha, Werner Stenzel, Lutz Harms, Markus Schuelke, Florence Pache, Felix Kleefeld, Hans-Hilmar Goebel
Publikováno v:
Neuropathology and Applied Neurobiology. 48
Lipid myopathies are rare and heterogeneous multi-systemic diseases that may be hereditary or acquired and affect the skeletal muscle [1]. Four types usually demonstrate accumulation of lipids in muscle biopsy specimens that can be visualised using O
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:
Lutz Harms, Felix Kleefeld, Werner Stenzel, Florence Pache, Hans-Hilmar Goebel, Markus Schuelke, Josefine Radke, Anja von Renesse, Carsten Dittmayer, Uruha Akinori, Udo Schneider, Helena Radbruch
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::35b7851046e9645efd209c9b552d5998
https://doi.org/10.1111/nan.12731/v2/response1
https://doi.org/10.1111/nan.12731/v2/response1
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
Autor:
Selina Greuel, Franziska Scheibe, Christian Meisel, Helena Radbruch, Sefer Elezkurtaj, Jenny Meinhardt, Julia Schneider, Tom Aschman, Werner Stenzel, Ivana Büttnerova, Simon Streit, Frank L. Heppner, Victor M. Corman, Christian Drosten, Hans H. Goebel, Josefine Radke
Publikováno v:
JAMA neurology 78(8), 948-(2021). doi:10.1001/jamaneurol.2021.2004
Myalgia, increased levels of creatine kinase, and persistent muscle weakness have been reported in patients with COVID-19.To study skeletal muscle and myocardial inflammation in patients with COVID-19 who had died.This case-control autopsy series was
Autor:
Thomas Buttgereit, M. Graf, Nadine Unterwalder, Falk Hiepe, A. S. L. Von Stuckrad, Thomas Rose, Jens Klotsche, Tilmann Kallinich, G.-R. Burmester, Robert Biesen, Martin Krusche, L. Zorn-Pauly, Christian Meisel, A. Uruha, Werner Stenzel, Udo Schneider
Publikováno v:
Annals of the Rheumatic Diseases. 80:305.1-305
Background:Idiopathic inflammatory myopathies (IIM) are autoimmune diseases that mainly affect skeletal muscle, lung, skin and joints. IIM can be separated into dermatomyositis (DM), inclusion body myositis (IBM), antisynthetase syndrome (AS) and imm
Autor:
Arpad von Moers, M. Radke, Hans H. Goebel, Werner Stenzel, Angela Abicht, Josefine Radke, Mona Dreesmann
Publikováno v:
Seminars in Pediatric Neurology. 26:56-58
A 6-year-old girl had reduced fetal movements, numerous apneic spells, muscle hypotonia, and developmental motor delay. Her muscle biopsy tissue showed variation in myofiber diameters, small minicores by electron microscopy, and near-uniformity of ty
Autor:
Martin Lammens, Hans-Hilmar Goebel, Teresinha Evangelista, Benno Küsters, Caroline Sewry, Norma B. Romero, Anders Oldfors, Werner Stenzel, Montse Olivé, Bjarne Udd
Publikováno v:
Neuromuscular disorders
Neuromuscular Disorders, 29, 483-485
Neuromuscular Disorders, 29, 6, pp. 483-485
Neuromuscular Disorders, 29, 483-485
Neuromuscular Disorders, 29, 6, pp. 483-485
Contains fulltext : 208457.pdf (Publisher’s version ) (Closed access)
Autor:
Susanne Morales-Gonzalez, Gajja S. Salomons, Esther Gill, Anja von Renesse, Markus Schuelke, Werner Stenzel
Publikováno v:
JIMD Reports, 27-35
STARTPAGE=27;ENDPAGE=35;TITLE=JIMD Reports
von Renesse, A, Morales-Gonzalez, S, Gill, E, Salomons, G S, Stenzel, W & Schuelke, M 2019, Muscle weakness, cardiomyopathy, and l-2-hydroxyglutaric aciduria associated with a novel recessive SLC25A4 mutation . in JIMD Reports . JIMD Reports, vol. 43, Springer, pp. 27-35 . https://doi.org/10.1007/8904_2018_93
JIMD Reports ISBN: 9783662586136
STARTPAGE=27;ENDPAGE=35;TITLE=JIMD Reports
von Renesse, A, Morales-Gonzalez, S, Gill, E, Salomons, G S, Stenzel, W & Schuelke, M 2019, Muscle weakness, cardiomyopathy, and l-2-hydroxyglutaric aciduria associated with a novel recessive SLC25A4 mutation . in JIMD Reports . JIMD Reports, vol. 43, Springer, pp. 27-35 . https://doi.org/10.1007/8904_2018_93
JIMD Reports ISBN: 9783662586136
Background: Mutations in SLC25A4 (syn. ANT1, Adenine nucleotide translocase, type 1) are known to cause either autosomal dominant progressive external ophthalmoplegia (adPEO) or recessive mitochondrial myopathy, hypertrophic cardiomyopathy, and lacti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4bbc2994f9d7d12e08645d292ec753d3
https://research.vumc.nl/en/publications/b567a572-4252-423c-aa1e-b208b0e86f96
https://research.vumc.nl/en/publications/b567a572-4252-423c-aa1e-b208b0e86f96