Zobrazeno 1 - 10
of 47
pro vyhledávání: '"Urs Widmer"'
Autor:
Marco Scortichini, Stefania Loreti, Nicoletta Pucci, Valeria Scala, Giuseppe Tatulli, Dimitri Verweire, Michael Oehl, Urs Widmer, Josep Massana Codina, Peter Hertl, Gianluigi Cesari, Monica De Caroli, Federica Angilè, Danilo Migoni, Laura Del Coco, Chiara Roberta Girelli, Giuseppe Dalessandro, Francesco Paolo Fanizzi
Publikováno v:
Pathogens, Vol 10, Iss 6, p 668 (2021)
Xylella fastidiosa subsp. pauca is the causal agent of “olive quick decline syndrome” in Salento (Apulia, Italy). On April 2015, we started interdisciplinary studies to provide a sustainable control strategy for this pathogen that threatens the m
Externí odkaz:
https://doaj.org/article/568e12d05dbd4039b7cec2936bd0df77
Autor:
Urs Widmer
Publikováno v:
Forum Médical Suisse ‒ Swiss Medical Forum.
Autor:
Urs Widmer
Publikováno v:
Swiss Medical Forum ‒ Schweizerisches Medizin-Forum.
Autor:
Urs Widmer
Publikováno v:
Controlling. 28:743-750
Autor:
Josee Kaulich-Bartz, Amanda Mocroft, Ard van Sighem, François Dabis, Suzanne M Ingle, Margaret T May, Antonella d'Arminio Monforte, Santiago Moreno, Andrew N. Phillips, Ramón Teira, Sophie Grabar, Josep Vilaro, Bruno Lederberger, Wayne Dam, Urs Widmer, Jonathan A C Sterne
Publikováno v:
AIDS; Vol 27
AIDS (London, England)
AIDS (London, England)
Objective: To increase equitable access to life insurance for HIV-positive individuals by identifying subgroups with lower relative mortality. Design: Collaborative analysis of cohort studies. Methods: We estimated relative mortality from 6 months af
Autor:
Markus Cybulla, K. N. Walter, M. Schärer, Urs Widmer, T. Jansen, Gere Sunder-Plassmann, Mathias Beck, Hartmut P. H. Neumann, A. Rolfs
Publikováno v:
DMW - Deutsche Medizinische Wochenschrift. 132:1505-1509
Background and objective Fabry's disease is a rare, X-chromosome linked recessive lysosomal storage disorder. In its course multiple organ damage occurs, e.g. in skin, nerves, kidneys and heart. The disease not only markedly impairs the quality of li
Autor:
Uma Ramaswami, Guillem Pintos-Morell, R. Parini, Catharina Whybra, Michael Beck, Urs Widmer, Atul Mehta, Gere Sunder-Plassmann
Publikováno v:
Acta Paediatrica. 95:86-92
Autor:
Julia Kleinert, Gunnar Houge, Gere Sunder-Plassmann, Uma Ramaswami, Aleš Linhart, Atul Mehta, Andreas Schwarting, Urs Widmer, Andreas Gal, Roberta Ricci, F Dehout, Christoph Kampmann, Michael Beck, Abelardo García de Lorenzo
Publikováno v:
American Journal of Hypertension. 19:782-787
Background Fabry disease is a rare X-linked disease arising from deficiency of α-galactosidase A. It results in early death related to renal, cardiac, and cerebrovascular disease, which are also important outcomes in patients with elevated blood pre
Autor:
Gere Sunder-Plassmann, Roberta Ricci, Atul Mehta, F Dehout, Andreas Schwarting, Gunnar Houge, Christoph Kampmann, Abelardo García de Lorenzo, Michael Beck, Aleš Linhart, Julia Kleinert, Urs Widmer, Andreas Gal, Uma Ramaswami
Publikováno v:
Kidney International. 67(5):1955-1960
Anemia is a new complication in Fabry disease: Data from the Fabry Outcome Survey.BackgroundThe prevalence and causes of anemia among patients with Fabry disease are unknown.MethodsIn a cross-sectional study we examined hemoglobin concentrations of p
Autor:
Uma Ramaswami, Atul Mehta, F Dehout, Christoph Kampmann, Gere Sunder-Plassmann, A. García de Lorenzo, Gunnar Houge, Mathias Beck, Aleš Linhart, Urs Widmer, Andreas Gal, Roberta Ricci
Publikováno v:
European Journal of Clinical Investigation. 34:838-844
Background Fabry disease is a rare X-linked disorder caused by deficient activity of the lysosomal enzyme α-galactosidase A. Progressive accumulation of the substrate globotriaosylceramide in cells throughout the body leads to major organ failure an