Zobrazeno 1 - 10
of 19
pro vyhledávání: '"S. W. J. Terheggen-Lagro"'
Autor:
Deborah Snijders, Matthias Griese, Nural Kiper, Larissa Schwarzkopf, Joanna Lange, Boglárka Szentes, Andrew Bush, Steve Cunningham, S. W. J. Terheggen-Lagro, Nicolaus Schwerk, Reiner Leidl, Sabine Witt
Publikováno v:
Paediatric bronchology.
Objectives: Childhood Interstitial lung disease (chILD) is an umbrella term for more than 200 rare disease entities for which there is no evidence on optimal medications and clinical outcomes. We hypothesised that there would be wide variations acros
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::be02bcb5344bd1dddaf9be88fa2bc84f
https://doi.org/10.1183/13993003.congress-2018.pa634
https://doi.org/10.1183/13993003.congress-2018.pa634
Autor:
Marije Lammers, Renate Kos, Rianne De Vries, Paul Brinkman, J. W. F. Dagelet, Niels W. Rutjes, C. J. Majoor, S. W. J. Terheggen-Lagro, E.J.M. Weersink, Lieuwe D. J. Bos, Peter J. Sterk, Anke-Hilse Maitland-Van Der Zee, Anne H. Neerincx & The Amsterdam Cf Research Group
Publikováno v:
Cystic fibrosis.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::66486be81baa4bf595cdf4f36ac1a470
https://doi.org/10.1183/13993003.congress-2018.pa3412
https://doi.org/10.1183/13993003.congress-2018.pa3412
Autor:
Andreas Günther, Meike Hengst, Joerg Grosse-Onnebrink, Poornima Mahavadi, Matthias Griese, Lutz Naehrlich, S. W. J. Terheggen-Lagro
Publikováno v:
7.7 Paediatric Bronchology.
Background Hermansky-Pudlak Syndrome (HPS) is a rare hereditary multisystem disorder, characterized by oculocutaneous albinism, bleeding diathesis, pulmonary fibrosis, neutropenia and granulomatous colitis. Based on the responsible genes, nine types
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6eadb9b22003a8fe27c263816062dd70
https://doi.org/10.1183/13993003.congress-2016.oa1496
https://doi.org/10.1183/13993003.congress-2016.oa1496
Autor:
D. P. Hoytema van Konijnenburg, P. A. de Jong, Elisabeth A. M. Sanders, Marianne Boes, S. W. J. Terheggen-Lagro, O. A. M. Kessels, A. A. J. M. van de Ven, J. M. van Montfrans
Publikováno v:
Clinical and Experimental Immunology. 165:235-242
Summary Common variable immunodeficiency (CVID) is a common primary immune deficiency, caused by undefined defects in lymphocyte function, and is treated routinely by immunoglobulin substitution. CVID complications include airway disease (AD) and int
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::020c4f73824e3847d7cee8fe2d726d71
https://doi.org/10.1111/j.1365-2249.2011.04425.x
https://doi.org/10.1111/j.1365-2249.2011.04425.x
Autor:
O. A. M. Kessels, Laurens Hogeweg, P. A. de Jong, B. van Ginneken, S. W. J. Terheggen-Lagro, Frederik J. A. Beek, Jens A. Achterberg
Publikováno v:
European Radiology
European Radiology, 21, 722-9
European Radiology, 21, 4, pp. 722-9
European Radiology, 21, 722-9
European Radiology, 21, 4, pp. 722-9
Contains fulltext : 96114.pdf (Publisher’s version ) (Open Access) OBJECTIVE: To test observer agreement and two strategies for possible improvement (consensus meeting and reference images) for the modified Chrispin-Norman score for children with c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::671ab5fa844b180b904b02960129e179
http://europepmc.org/articles/PMC3047050
http://europepmc.org/articles/PMC3047050
Autor:
Joris M. van Montfrans, Catharina M L Touw, Annick A. J. M. van de Ven, Erik Beek, Pim A de Jong, Elisabeth A. M. Sanders, S. W. J. Terheggen-Lagro
Publikováno v:
Pediatric Allergy and Immunology. 21:793-805
Touw CML, van de Ven AA, de Jong PA, Terheggen-Lagro S, Beek E, Sanders EAM, van Montfrans JM. Detection of pulmonary complications in common variable immunodeficiency. Pediatr Allergy Immunol 2010: 21: 793-805. (c) 2009 John Wiley & Sons A/S Pulmona
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::47ce5ecc1ccd3d2e98bdc894d4556d1c
https://doi.org/10.1111/j.1399-3038.2009.00963.x
https://doi.org/10.1111/j.1399-3038.2009.00963.x
Publikováno v:
Journal of Cystic Fibrosis. 4:15-23
Cystic fibrosis (CF) is caused by mutations in the CF transmembrane conductance regulator (CFTR) gene, which accounts for the cAMP-modulated chloride conductance of airway epithelial cells. CFTR also regulates other membrane proteins like the negativ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f87cf7c7ce8cd4ff28d104c1a162c717
Publikováno v:
American Journal of Respiratory and Critical Care Medicine. 168:1227-1231
Several factors influence levels of end-tidal carbon monoxide (ETCO). We studied determinants of ETCO corrected for inhaled CO (ETCOc) levels in healthy control subjects and compared ETCOc levels and determinants between healthy control subjects and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8e2e95e9183d09642e2dd23b62cf066f
https://doi.org/10.1164/rccm.200302-248oc
https://doi.org/10.1164/rccm.200302-248oc
Autor:
V. A. M. Gulmans, Johan van der Laag, Noor van Poppel, Neeltje Truijens, Cornelis K. van der Ent, S. W. J. Terheggen-Lagro
Publikováno v:
Pediatric Pulmonology. 35:441-445
In past decades, several chest radiograph scoring systems for cystic fibrosis were developed. This study was performed to compare interobserver variability of six different radiograph scores and to correlate them with clinical parameters. Thirty ches
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4da1585eed74fb2fca5c3c94b3ebedea
https://doi.org/10.1002/ppul.10280
https://doi.org/10.1002/ppul.10280
Publikováno v:
Tijdschrift voor kindergeneeskunde. 71:29-34
Het respiratoire distressbeeld van de a terme neonaat kan zich op diverse manieren presenteren en berust op een uitgebreide differentiaaldiagnose. De meest voorkomende oorzaken op pulmonaal gebied zijn pneumonie en/of sepsis, transient tachypnoe of t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::19959a7e46c65a67af52e674bbb75018
https://doi.org/10.1007/bf03061421
https://doi.org/10.1007/bf03061421