Current WSES-AAST guidelines on anorectal emergencies—Summary and comments

Autor: F. Bender, A. Tarasconi, F. Catena, M. Sartelli, F. Coccolini, J. Liese, W. Padberg, M. Reichert, A. Hecker

Publikováno v: Die Chirurgie. 94:333-341

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::a6449ae637d5cf9d0d3de914b9080c2b
https://doi.org/10.1007/s00104-023-01826-9

When to operate after SARS-CoV-2 infection? A review on the recent consensus recommendation of the DGC/BDC and the DGAI/BDA

Autor: J. Noll, M. Reichert, M. Dietrich, J. G. Riedel, M. Hecker, W. Padberg, M. A. Weigand, A. Hecker

Publikováno v: Langenbeck's Archives of Surgery. 407:1315-1332

Abstract Since the eruption of the worldwide SARS-CoV-2 pandemic in late 2019/early 2020, multiple elective surgical interventions were postponed. Through pandemic measures, elective operation capacities were reduced in favour of intensive care treat

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::8ab1e97bc0a70ad4fa3289dd97eac501
https://doi.org/10.1007/s00423-022-02495-8

Chromosome 10q-linked FSHD identifies DUX4 as principal disease gene

Autor: Nicol C. Voermans, Silvère M. van der Maarel, George W. Padberg, Richard J.L.F. Lemmers, Patrick J. van der Vliet, Rianne J.M. Goselink, Ana Blatnik, Janez Zidar, Stephen J. Tapscott, Don Henderson, Rabi Tawil, Judit Balog, Baziel G.M. van Engelen

Publikováno v: Journal of Medical Genetics, 59, 2, pp. 180-188
Journal of Medical Genetics, 59(2), 180-188. BMJ PUBLISHING GROUP
J Med Genet
Journal of Medical Genetics, 59, 180-188

BackgroundFacioscapulohumeral dystrophy (FSHD) is an inherited muscular dystrophy clinically characterised by muscle weakness starting with the facial and upper extremity muscles. A disease model has been developed that postulates that failure in som

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e56b44f3f32ec1f700036846de44cb09
https://repository.ubn.ru.nl/handle/2066/248853

Distinct disease phases in muscles of facioscapulohumeral dystrophy patients identified by MR detected fat infiltration.

Autor: Barbara H Janssen, Nicoline B M Voet, Christine I Nabuurs, Hermien E Kan, Jacky W J de Rooy, Alexander C Geurts, George W Padberg, Baziel G M van Engelen, Arend Heerschap

Publikováno v: PLoS ONE, Vol 9, Iss 1, p e85416 (2014)

Facioscapulohumeral muscular dystrophy (FSHD) is an untreatable disease, characterized by asymmetric progressive weakness of skeletal muscle with fatty infiltration. Although the main genetic defect has been uncovered, the downstream mechanisms causi

Externí odkaz: https://doaj.org/article/9c41ae2c80b64b588942b7eadbec58ea

Characterizing the face in facioscapulohumeral muscular dystrophy

Autor: Karlien Mul, George W. Padberg, C. H. G. Beurskens, S. Knuijt, B.G.M. van Engelen, Thomas J.J. Maal, T. G. J. Loonen, Jeffrey Statland, Nicol C. Voermans, Corinne G.C. Horlings, Sanne C. C. Vincenten

Publikováno v: Journal of neurology, 268(4), 1342-1350. D. Steinkopff-Verlag
Journal of Neurology, 268, 1342-1350
Journal of Neurology, 268, 4, pp. 1342-1350
Journal of Neurology

ObjectiveTo evaluate facial weakness in patients with FSHD to better define clinical signs, and pilot a facial weakness severity score.Methods87 FSHD patients and 55 controls were video recorded while performing seven facial tasks. The videos were as

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2f3d6b2d0411a26843eb88ea2d949a1b
https://pure.amc.nl/en/publications/characterizing-the-face-in-facioscapulohumeral-muscular-dystrophy(05f3aef3-918b-416e-9560-19e5a00bebcc).html