Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Bert Arets"'
Autor:
Tjomme van der Bruggen, Anna Kolecka, Bart Theelen, Johanna M. Kwakkel-van Erp, Bert Arets, Teun Boekhout
Publikováno v:
Medical Mycology Case Reports, Vol 22, Iss , Pp 18-20 (2018)
Cystic fibrosis (CF) patients are colonized with a multitude of bacteria and fungi. From respiratory samples of two CF patients in our institute, a difficult to identify yeast was isolated repeatedly. This yeast was eventually identified as Cutaneotr
Externí odkaz:
https://doaj.org/article/e4fdbb606af24c8ebd9dce9195f2db62
Autor:
Sanne Maria Henriette Zweijpfenning, Raphael Chiron, Sharon Essink, Jodie Schildkraut, Onno W. Akkerman, Stefano Aliberti, Josje Altenburg, Bert Arets, Eva van Braeckel, Bénédicte Delaere, Sophie Gohy, Eric Haarman, Natalie Lorent, Genevieve McKew, Lucy Morgan, Dirk Wagner, Jakko van Ingen, Wouter Hoefsloot
Publikováno v:
CHEST
Autor:
Maartje I Kristensen, Gerdien A. Tramper-Stranders, Bert Arets, Hettie M. Janssens, Cornelis K. van der Ent, Elisabeth A. M. Sanders, H.A.W.M. Tiddens, Debby Bogaert, Mireille van Westreenen, Raiza Hasrat, Gino Kalkman, Bart J. F. Keijser, Karin M. de Winter-de Groot, Sabine M. P. J. Prevaes
Publikováno v:
Journal of Cystic Fibrosis, 19(4), 553-561. Elsevier
Patients with Cystic Fibrosis (CF) suffer from pancreatic insufficiency, lipid malabsorption and gastrointestinal complaints, next to progressive pulmonary disease. Altered mucosal homoeostasis due to malfunctioning chloride channels results in an ad
Autor:
Sanne Maria, Henriette Zweijpfenning, Raphael, Chiron, Sharon, Essink, Jodie, Schildkraut, Onno W, Akkerman, Stefano, Aliberti, Josje, Altenburg, Bert, Arets, Eva, van Braeckel, Bénédicte, Delaere, Sophie, Gohy, Eric, Haarman, Natalie, Lorent, Genevieve, McKew, Lucy, Morgan, Dirk, Wagner, Jakko, van Ingen, Wouter, Hoefsloot
Publikováno v:
Chest. 162(1)
Autor:
Patrick A Flume, Reta Fischer Biner, Damian G Downey, Cynthia Brown, Manu Jain, Rainald Fischer, Kris De Boeck, Gregory S Sawicki, Philip Chang, Hildegarde Paz-Diaz, Jaime L Rubin, Yoojung Yang, Xingdi Hu, David J Pasta, Stefanie J Millar, Daniel Campbell, Xin Wang, Neil Ahluwalia, Caroline A Owen, Claire E Wainwright, Ronald L. Gibson, Steven M. Rowe, Noah Lechtzin, Richard C. Ahrens, Karen S. McCoy, Moira Aitken, Scott H. Donaldson, Kimberly Ann McBennett, Joseph M. Pilewski, Joanne Billings, Carlos Milla, Ronald Rubenstein, Daniel Brian Rosenbluth, Rachel Linnemann, Michael R. Powers, Christopher Fortner, Carla Anne Frederick, Theodore G. Liou, Philip Black, Janice Wang, John L. Colombo, Maria Berdella, Maria Veronica Indihar, Cynthia D. Brown, Michael Anstead, Lara Bilodeau, Leonard Sicilian, James Jerome Tolle, Kathryn Moffett, Samya Nasr, Jennifer Taylor-Cousar, Tara Lynn Barto, Nicholas Antos, John S. Rogers, Bryon Quick, Henry R. Thompson, Gregory Sawicki, Bruce Barnett, Robert L. Zanni, Thomas C. Smith, Karen D. Schultz, Claire Keating, Patrick Flume, Gregory J. Omlor, Alix Ashare, Karen Voter, Nighat Mehdi, Maria Gabriela Tupayachi Ortiz, Tonia E. Gardner, Steven R. Boas, Barbara Messore, Edith Zemanick, Raksha Jain, Michael McCarthy, Dana G. Kissner, Kapilkumar Patel, John McNamara, Julie Philley, Ariel Berlinski, Francisco J. Calimano, Terry Chin, Douglas Conrad, Cori Daines, Hengameh H. Raissy, Thomas G. Keens, Jorge E. Lascano, Bennie McWilliams, Brian Morrissey, Santiago Reyes, Subramanyam Chittivelu, Sabiha Hussain, Arvey Stone, James Wallace, Ross Klingsberg, Julie A. Biller, Stephanie Bui, Olaf Sommerburg, Elisabetta Bignamini, Mirella Collura, Alexander Moller, Donatello Salvatore, Chantal Belleguic, Lea Bentur, Ori Efrati, Eitan Kerem, Dario Prais, Esther Quintana Gallego, Peter Barry, Galit Livnat-Levanon, Jose Ramon Villa Asensi, David Stuart Armstrong, Oscar Asensio de la Cruz, Francis Gilchrist, Diana Elizabeth Tullis, Bradley Quon, Larry C. Lands, Nancy Morrison, Annick Lavoie, Barry Linnane, Okan Elidemir, Felix Ringshausen, Matthias Kappler, Helge Hebestreit, Jochen Mainz, Alexander Kiefer, Cordula Koerner-Rettberg, Doris Staab, Wolfgang Gleiber, Tacjana Pressler, Florian Stehling, Andreas Hector, Sivagurunathan Sutharsan, Lutz Naehrlich, Damian Downey, Jane Carolyn Davies, Robert Ian Ketchell, Mary Patricia Carroll, Simon Doe, Gordon MacGregor, Edward Fairbairn Nash, Nicholas Withers, Daniel Gavin Peckham, Martin James Ledson, Sonal Kansra, Timothy William Rayner Lee, Bertrand Delaisi, Gilles Rault, Jean Le Bihan, Dominique Hubert, Isabelle Fajac, Isabelle Sermet-Gaudelus, Marleen Bakker, Bert Arets, Christiane De Boeck, Raphael Chiron, Philippe Reix, Catherine Mainguy, Eva van Braeckel, Anne Malfroot, Isabelle Durieu, Nadine Desmazes Dufeu, Anne Prevotat, Renske van der Meer, Petrus Merkus, E.J.M. Weersink, Isabel Barrio Gomez-Aguero, Silvia Gartner, Amparo Sole Jover, Antonio Alvarez Fernandez, Desmond William Cox, Edward F. McKone, Barry James Plant, Hiranjan Selvadurai, Simon David Bowler, Claire Elizabeth Wainwright, Daniel Smith, Peter Gordon Middleton, John William Wilson, Sonia Volpi, Carla Colombo, Benedetta Fabrizzi, Vincenzina Lucidi, Federico Cresta, Salvatore Cucchiara, Ernst Eber, Helmut Ellemunter, Isidor Huttegger, Lena Hjelte, Christina Krantz, Marita Gilljam
Publikováno v:
lancet. Respiratory medicine, 9(7), 733-746. Elsevier Limited
VX14-661-110 study group 2021, ' Long-term safety and efficacy of tezacaftor–ivacaftor in individuals with cystic fibrosis aged 12 years or older who are homozygous or heterozygous for Phe508del CFTR (EXTEND): an open-label extension study ', The Lancet Respiratory Medicine . https://doi.org/10.1016/S2213-2600(20)30510-5
VX14-661-110 study group 2021, ' Long-term safety and efficacy of tezacaftor–ivacaftor in individuals with cystic fibrosis aged 12 years or older who are homozygous or heterozygous for Phe508del CFTR (EXTEND): an open-label extension study ', The Lancet Respiratory Medicine . https://doi.org/10.1016/S2213-2600(20)30510-5
Summary Background Tezacaftor–ivacaftor is an approved cystic fibrosis transmembrane conductance regulator (CFTR) modulator shown to be efficacious and generally safe and well tolerated over 8–24 weeks in phase 3 clinical studies in participants
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bf49af3de3f90b3a65bf102dbba3756b
https://pure.amc.nl/en/publications/longterm-safety-and-efficacy-of-tezacaftorivacaftor-in-individuals-with-cystic-fibrosis-aged-12-years-or-older-who-are-homozygous-or-heterozygous-for-phe508del-cftr-extend-an-openlabel-extension-study(cc1b629c-44f6-4a77-aff2-ea80f4598819).html
https://pure.amc.nl/en/publications/longterm-safety-and-efficacy-of-tezacaftorivacaftor-in-individuals-with-cystic-fibrosis-aged-12-years-or-older-who-are-homozygous-or-heterozygous-for-phe508del-cftr-extend-an-openlabel-extension-study(cc1b629c-44f6-4a77-aff2-ea80f4598819).html
Autor:
Cornelis K. van der Ent, S. Schotman, Marit van Oirschot van de Ven, Firdaus Mohamed Hoesein, Inez Bronsveld, M.A. Kruijswijk, Sabine Michel, Regina W. Hofland, Harry G.M. Heijerman, Bente L. Aalbers, Karin de Winter-de Groot, Bert Arets, Cora de Kiviet
Objective: To verify if the extent of structural lung damage visible on chest CT is correlated with change in ppFEV1 after start of CFTR modulating therapy in CF patients. Methods: In our retrospective observational study, we included patients aged
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e65180aabf68b95f12b783a2e100a752
https://doi.org/10.22541/au.160439592.20308162/v1
https://doi.org/10.22541/au.160439592.20308162/v1
Autor:
Marianne Nuijsink, Bert Arets, Daan J Touw, Els C. van der Wiel-Kooij, Erik M. van Maarseveen, Bas Pullens, Gijsbert A. van Zanten, Hettie M. Janssens, Harry G.M. Heijerman, J.W.F. Uges, Annelies J van Velzen
Publikováno v:
British Journal of Clinical Pharmacology, 85(9), 1984-1993. Wiley
British Journal of Clinical Pharmacology
British Journal of Clinical Pharmacology. Wiley-Blackwell Publishing Ltd
British Journal of Clinical Pharmacology, 85(9), 1984. Wiley-Blackwell
British Journal of Clinical Pharmacology
British Journal of Clinical Pharmacology. Wiley-Blackwell Publishing Ltd
British Journal of Clinical Pharmacology, 85(9), 1984. Wiley-Blackwell
Aims: We aimed to compare the pharmacokinetics (PK) and safety profile of tobramycin inhalation solution (TIS) using the I-neb device to the standard PARI-LC Plus nebulizer in children with cystic fibrosis. Methods: A randomized, open-label, crossove
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9c4098d085c7fa5ba8dc2f40b630a84d
https://dspace.library.uu.nl/handle/1874/392026
https://dspace.library.uu.nl/handle/1874/392026
Autor:
Teun Boekhout, Tjomme van der Bruggen, Bert Arets, Anna Kolecka, Johanna M. Kwakkel-van Erp, Bart Theelen
Publikováno v:
MEDICAL MYCOLOGY CASE REPORTS, 22, 18-20. Elsevier
Medical Mycology Case Reports, 22, 18-20. Elsevier B.V.
Medical Mycology Case Reports, Vol 22, Iss, Pp 18-20 (2018)
Medical Mycology Case Reports, 22, 18. Elsevier BV
Medical Mycology Case Reports
Medical Mycology Case Reports, 22, 18-20. Elsevier B.V.
Medical Mycology Case Reports, Vol 22, Iss, Pp 18-20 (2018)
Medical Mycology Case Reports, 22, 18. Elsevier BV
Medical Mycology Case Reports
Cystic fibrosis (CF) patients are colonized with a multitude of bacteria and fungi. From respiratory samples of two CF patients in our institute, a difficult to identify yeast was isolated repeatedly. This yeast was eventually identified as Cutaneotr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4a432d616b1c6db287ebf8104bc8efdd
https://dare.uva.nl/personal/pure/en/publications/cutaneotrichosporon-cryptococcus-cyanovorans-a-basidiomycetous-yeast-isolated-from-the-airways-of-cystic-fibrosis-patients(8134e12f-7c03-40b4-8e3d-dab06c8139d3).html
https://dare.uva.nl/personal/pure/en/publications/cutaneotrichosporon-cryptococcus-cyanovorans-a-basidiomycetous-yeast-isolated-from-the-airways-of-cystic-fibrosis-patients(8134e12f-7c03-40b4-8e3d-dab06c8139d3).html
Autor:
Jeroen A. L. Jeneson, Rutger A.J. Nievelstein, Birgitta K. Velthuis, Bert Arets, Tim Takken, Maarten S. Werkman, Kors van der Ent, Paul J. M. Helders, Erik H. J. Hulzebos
Publikováno v:
Experimental Physiology. 101:421-431
What is the central question of this study? Do intrinsic abnormalities in oxygenation and/or muscle oxidative metabolism contribute to exercise intolerance in adolescents with mild cystic fibrosis? What is the main finding and its importance? This st
Autor:
S. Schotman, M.A. Kruijswijk, H.G.M. Heijerman, Bente L. Aalbers, K.M. de Winter-de Groot, Bert Arets, Inez Bronsveld, C. de Kiviet, F. Mohammed Hoessein, S. Michel, Regina W. Hofland, M van de Ven, K. van der Ent
Publikováno v:
Journal of Cystic Fibrosis. 19:S115