Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Cécile A. Robinson"'
Publikováno v:
Respiratory Research, Vol 18, Iss 1, Pp 1-13 (2017)
Abstract The role of differential cytology patterns in peripheral blood and bronchoalveolar lavage samples is increasingly investigated as a potential adjunct to diagnose acute and chronic allograft dysfunction after lung transplantation. While these
Externí odkaz:
https://doaj.org/article/5abe0719a33e4faa8a32372c5f4ae78f
Publikováno v:
Jornal Brasileiro de Pneumologia, Vol 45, Iss 1 (2019)
ABSTRACT Objective: Bone disease is a common comorbidity in patients with cystic fibrosis (CF). We sought to determine risk factors and identify potential biochemical markers for CF-related bone disease (CFBD) in a unique cohort of CF patients with e
Externí odkaz:
https://doaj.org/article/d0ee24ad08984f04af9cead5f93c9c82
Publikováno v:
Journal of Clinical Apheresis. 36:186-188
Extra-corporeal photopheresis (ECP) is known as safe ultimate treatment option for chronic lung allograft dysfunction (CLAD). Here, we report the first case of ECP as "second-line" immunomodulatory therapy early post-transplant in an adult patient un
Publikováno v:
Infectious Diseases. 50:476-478
Autor:
Verena Tischler, Stephan Baumueller, Cécile A. Robinson, Lutz Freitag, Pascal Bezel, Daniel Franzen, Beata Bode-Lesniewska, Malcolm Kohler
Publikováno v:
Clinical Lung Cancer. 17:e151-e156
There is a paucity of data concerning the benefit of bronchoalveolar lavage (BAL) for the diagnosis of suspected peripheral lung cancer (PLC). The aim of this study was to investigate the diagnostic value of BAL for the diagnosis of suspected PLC.All
Autor:
Christian Murer, Astrid Hirt, Lars C. Huber, Cécile A. Robinson, Urs Bürgi, Christian Benden, Thomas Kurowski
AIMS OF THE STUDY Cystic fibrosis is the most common genetic disorder in Caucasians. The combination of the cystic fibrosis transmembrane conductance regulator (CFTR) corrector lumacaftor / potentiator ivacaftor (LUM/IVA) has been shown to increase f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::567b49fde1c1feca1de8b7c4f138fa55
https://www.zora.uzh.ch/id/eprint/160493/
https://www.zora.uzh.ch/id/eprint/160493/
Autor:
Cécile A. Robinson, Lars C. Huber, Thomas Kurowski, Urs Bürgi, Christian Murer, Astrid Hirt, Christian Benden
Publikováno v:
Cystic Fibrosis.
Objectives: Recently, the combination of CFTR potentiator ivacaftor and CFTR corrector lumacaftor (Orkambi®) has been shown to reduce acute exacerbation rate (AER) in Phe508del homozygous CF patients. Patients with a FEV1 Methods : Since 01/2016, we
Publikováno v:
Respiratory Research
Respiratory Research, Vol 18, Iss 1, Pp 1-13 (2017)
Respiratory Research, Vol 18, Iss 1, Pp 1-13 (2017)
The role of differential cytology patterns in peripheral blood and bronchoalveolar lavage samples is increasingly investigated as a potential adjunct to diagnose acute and chronic allograft dysfunction after lung transplantation. While these profiles
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::22d1b127d7368ad1466f3f848156ba25
https://doi.org/10.5167/uzh-147923
https://doi.org/10.5167/uzh-147923
Autor:
Lars C. Huber, Urs Buergi, Malcolm Kohler, Christian Benden, Bruno Isenring, Cécile A. Robinson, Macé M. Schuurmans
Publikováno v:
Clinical transplantation. 31(10)
Extracorporeal photophoresis (ECP) is an increasingly used therapy to address chronic lung allograft dysfunction (CLAD) following lung transplantation. In 2008, we reported the first single-center experience showing that ECP not only reduces lung fun