Zobrazeno 1 - 10
of 22
pro vyhledávání: '"Elise Lammertyn"'
Autor:
Maxime Hautrive, Veerle Bulteel, Kate Hayes, F. Chedevergne, Elise Lammertyn, Emmanuelle Bardin, D. Hubert, Muriel Le Bourgeois, Andreas Hager, Anna Fonts, Hilde de Keyser, Trudy Havermans, Dominique Grenet, Paola de Carli, Pierre-Régis Burgel, Jutta Bend, Claire Bresnihan, Véronique Bontemps, Anne Calvert, Rosa Coucke, Diana Hofmann, Maya Kirszenbaum, I. Honoré, Audrey Chansard, Clémence Martin, Isabelle Sermet-Gaudelus
Publikováno v:
Journal of Cystic Fibrosis. 20:e108-e113
Background People with cystic fibrosis (pwCF) are central in the development of patient-led assessment tools. Qualitative analysis of a frequently used CF-specific patient-reported outcome measure (PROM) sought patient recommendations for development
Autor:
Kevin W. Southern, Carlo Castellani, Elise Lammertyn, Alan Smyth, Donald VanDevanter, Silke van Koningsbruggen-Rietschel, Jürg Barben, Amanda Bevan, Edwin Brokaar, Sarah Collins, Gary J. Connett, Thomas W.V. Daniels, Jane Davies, Dimitri Declercq, Silvia Gartner, Andrea Gramegna, Naomi Hamilton, Jenny Hauser, Nataliya Kashirskaya, Laurence Kessler, Jacqueline Lowdon, Halyna Makukh, Clémence Martin, Lisa Morrison, Dilip Nazareth, Jacquelien Noordhoek, Ciaran O'Neill, Elizabeth Owen, Helen Oxley, Karen S. Raraigh, Caroline Raynal, Karen Robinson, Jobst Roehmel, Carsten Schwarz, Isabelle Sermet, Michal Shteinberg, Ian Sinha, Constance Takawira, Peter van Mourik, Marieke Verkleij, Michael D. Waller, Alistair Duff
Publikováno v:
Journal of Cystic Fibrosis. Elsevier
Southern, K W, Castellani, C, Lammertyn, E, Smyth, A, VanDevanter, D, van Koningsbruggen-Rietschel, S, Barben, J, Bevan, A, Brokaar, E, Collins, S, Connett, G J, Daniels, T W V, Davies, J, Declercq, D, Gartner, S, Gramegna, A, Hamilton, N, Hauser, J, Kashirskaya, N, Kessler, L, Lowdon, J, Makukh, H, Martin, C, Morrison, L, Nazareth, D, Noordhoek, J, O'Neill, C, Owen, E, Oxley, H, Raraigh, K S, Raynal, C, Robinson, K, Roehmel, J, Schwarz, C, Sermet, I, Shteinberg, M, Sinha, I, Takawira, C, van Mourik, P, Verkleij, M, Waller, M D & Duff, A 2023, ' Standards of care for CFTR variant-specific therapy (including modulators) for people with cystic fibrosis ', Journal of Cystic Fibrosis, vol. 22, no. 1, pp. 17-30 . https://doi.org/10.1016/j.jcf.2022.10.002
Scientia
Southern, K W, Castellani, C, Lammertyn, E, Smyth, A, VanDevanter, D, van Koningsbruggen-Rietschel, S, Barben, J R, Bevan, A, Brokaar, E, Collins, S, Connett, G J, Daniels, T W V, Davies, J, Declercq, D, Gartner, S, Gramegna, A, Hamilton, N, Hauser, J, Kashirskaya, N, Kessler, L, Lowdon, J, Makukh, H, Martin, C, Morrison, L, Nazareth, D, Noordhoek, J, O'Neill, C, Owen, E, Oxley, H, Raraigh, K S, Raynal, C, Robinson, K, Roehmel, J, Schwarz, C, Sermet, I, Shteinberg, M, Sinha, I, Takawira, C, van Mourik, P, Verkleij, M, Waller, M D & Duff, A 2023, ' Standards of care for CFTR variant-specific therapy (including modulators) for people with cystic fibrosis ', Journal of Cystic Fibrosis, vol. 22, no. 1, pp. 17-30 . https://doi.org/10.1016/j.jcf.2022.10.002
JOURNAL OF CYSTIC FIBROSIS
Southern, K W, Castellani, C, Lammertyn, E, Smyth, A, VanDevanter, D, van Koningsbruggen-Rietschel, S, Barben, J, Bevan, A, Brokaar, E, Collins, S, Connett, G J, Daniels, T W V, Davies, J, Declercq, D, Gartner, S, Gramegna, A, Hamilton, N, Hauser, J, Kashirskaya, N, Kessler, L, Lowdon, J, Makukh, H, Martin, C, Morrison, L, Nazareth, D, Noordhoek, J, O'Neill, C, Owen, E, Oxley, H, Raraigh, K S, Raynal, C, Robinson, K, Roehmel, J, Schwarz, C, Sermet, I, Shteinberg, M, Sinha, I, Takawira, C, van Mourik, P, Verkleij, M, Waller, M D & Duff, A 2023, ' Standards of care for CFTR variant-specific therapy (including modulators) for people with cystic fibrosis ', Journal of Cystic Fibrosis, vol. 22, no. 1, pp. 17-30 . https://doi.org/10.1016/j.jcf.2022.10.002
Scientia
Southern, K W, Castellani, C, Lammertyn, E, Smyth, A, VanDevanter, D, van Koningsbruggen-Rietschel, S, Barben, J R, Bevan, A, Brokaar, E, Collins, S, Connett, G J, Daniels, T W V, Davies, J, Declercq, D, Gartner, S, Gramegna, A, Hamilton, N, Hauser, J, Kashirskaya, N, Kessler, L, Lowdon, J, Makukh, H, Martin, C, Morrison, L, Nazareth, D, Noordhoek, J, O'Neill, C, Owen, E, Oxley, H, Raraigh, K S, Raynal, C, Robinson, K, Roehmel, J, Schwarz, C, Sermet, I, Shteinberg, M, Sinha, I, Takawira, C, van Mourik, P, Verkleij, M, Waller, M D & Duff, A 2023, ' Standards of care for CFTR variant-specific therapy (including modulators) for people with cystic fibrosis ', Journal of Cystic Fibrosis, vol. 22, no. 1, pp. 17-30 . https://doi.org/10.1016/j.jcf.2022.10.002
JOURNAL OF CYSTIC FIBROSIS
Cystic fibrosis; Guidelines; Variant-specific therapy Fibrosis quística; Pautas; Terapia variante específica Fibrosi quística; Pautes; Teràpia variant específica Cystic fibrosis (CF) has entered the era of variant-specific therapy, tailored to t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7c6ded04c482379180be18ea1ab6cf12
https://research.vumc.nl/en/publications/6fa8f077-49b9-4675-b900-f20dc3826455
https://research.vumc.nl/en/publications/6fa8f077-49b9-4675-b900-f20dc3826455
Autor:
Halyna Makukh, Andrea Dugac Vukic, Meir Mei-Zahav, Tsitsino Parulava, Harriet Corvol, Godfrey Fletcher, Rita Padoan, S. Fustik, Silke van Koningsbruggen-Rietschel, Fiona Dunlevy, Andreas Jung, Hana Kayserova, Satenik Harutyunyan, Siobhán B. Carr, Domenique Zomer-van Ommen, Łukasz Woźniacki, Svetlana Keegan, Elena Kondratyeva, Jacqui G. van Rens, Elpis Hatziagorou, Carla Colombo, Pedro Mondejar-Lopez, Vincent Gulmans, Anita Senstad Wathne, María Dolores Pastor-Vivero, Milan Macek, Egil Bakkeheim, Milan Rodić, Sevgi Pekcan, Filia Diamantea, Elliott McClenaghan, Géraldine Daneau, Guergana Petrova, Kęstutis Malakauskas, Marko Krasnyk, Yasemin Gokdemir, Panayiotis K. Yiallouros, Elise Lammertyn, Marc Schlesser, Edward F. McKone, Andreas Pfleger, Olga I. Simonova, Luísa Pereira, Elena Zhekaite, Anders Lindblad, Oxana Turcu, Andrea Párniczky, Isabelle de Monestrol, Duška Tješić-Drinković, Elina Aleksejeva, Uro Krivecs, Lutz Naehrlich, Elena Amelina, A. Zolin, Pierre-Régis Burgel, Vladimir Bobrovnichy, Annalisa Orenti, Alena Bilkova, Deniz Dogru, Liviu Pop, Marco Salvatore, Nataliya Kashirskaya, Irena Kasmi, Keith G. Brownlee, Pavel Drevinek, Hanne Vebert Olesen, Rebecca Cosgriff, Lydie Lemonnier-Videau, A. Fox, Ivan Bambir
Publikováno v:
Naehrlich, L, Orenti, A, Dunlevy, F, Kasmi, I, Harutyunyan, S, Pfleger, A, Keegan, S, Daneau, G, Petrova, G, Tješić-Drinković, D, Yiallouros, P, Bilkova, A, Olesen, H V, Burgel, P R, Parulava, T, Diamantea, F, Párniczky, A, McKone, E F, Mei-Zahav, M, Salvatore, M, Colombo, C, Aleksejeva, E, Malakauskas, K, Schlesser, M, Fustik, S, Turcu, O, Zomer-van Ommen, D, Wathne, A S, Woźniacki, Ł, Pereira, L, Pop, L, Kashirskaya, N, Rodić, M, Kayserova, H, Krivecs, U, Mondejar-Lopez, P, de Monestrol, I, Dogru, D, Makukh, H, Cosgriff, R, van Koningsbruggen-Rietschel, S, Jung, A & European Cystic Fibrosis COVID project group 2021, ' Incidence of SARS-CoV-2 in people with cystic fibrosis in Europe between February and June 2020 ', Journal of Cystic Fibrosis, vol. 20, no. 4, pp. 566-577 . https://doi.org/10.1016/j.jcf.2021.03.017
Journal of Cystic Fibrosis
Journal of Cystic Fibrosis
Background: Viral infections can cause significant morbidity in cystic fibrosis (CF). The current Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) pandemic could therefore have a serious impact on the health of people with CF (pwCF). Meth
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::890c3cc12ea4caf2f33deed43b74c782
https://pure.au.dk/ws/files/275030134/1_s2.0_S1569199321000990_main.pdf
https://pure.au.dk/ws/files/275030134/1_s2.0_S1569199321000990_main.pdf
Autor:
Pavel Drevinek, Halyna Makukh, Muriel Thomas Sciensano, Rita Ujhelyi, Godfrey Fletcher, Vincent Gulmans, Milan Macek, Kris De Boeck, Elise Lammertyn, Hanne Vebert Olesen, Luísa Pereira, Isabelle de Monestrol, Siobhán B. Carr, Rebecca Cosgriff, Simona Mosescu, Anne Farge, Kęstutis Malakauskas, Oxana Turcu, Carlos Vazquez-Cordero, R. Padoan, Nataliya Kashirskaya, Lutz Naehrlich, Andreas Pfleger, Meir Mei-Zahav, S. Fustik, Annalisa Orenti, Zane Timpare, A. Zolin, Milan Rodić, Anders Lindblad, Elpis Hatziagorou, Uros Krivec, Hana Kayserova, Andreas Jung
Publikováno v:
Hatziagorou, E, Orenti, A, Drevinek, P, Kashirskaya, N, Mei-Zahav, M, De Boeck, K & on behalf of the ECFSPR 2020, ' Changing epidemiology of the respiratory bacteriology of patients with cystic fibrosis–data from the European cystic fibrosis society patient registry ', Journal of Cystic Fibrosis, vol. 19, no. 3, pp. 376-383 . https://doi.org/10.1016/j.jcf.2019.08.006
Background Monitoring changes in the epidemiology of cystic fibrosis (CF) pathogens is essential for clinical research, quality improvement, and clinical management. Methods We analyzed data reported to the European Cystic Fibrosis Society Patient Re
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ed305916495c8bb64a88a9330ca6c302
https://pure.au.dk/portal/da/publications/changing-epidemiology-of-the-respiratory-bacteriology-of-patients-with-cystic-fibrosisdata-from-the-european-cystic-fibrosis-society-patient-registry(0673c2da-a0bc-44a1-a1e8-5cda02c08994).html
https://pure.au.dk/portal/da/publications/changing-epidemiology-of-the-respiratory-bacteriology-of-patients-with-cystic-fibrosisdata-from-the-european-cystic-fibrosis-society-patient-registry(0673c2da-a0bc-44a1-a1e8-5cda02c08994).html
Publikováno v:
Journal of Cystic Fibrosis. 20:S101-S102
Publikováno v:
Journal of Cystic Fibrosis. 20:S61
Autor:
François Vermeulen, Marc Decramer, Geert Verleden, Kris De Boeck, Barbara Bosch, Elise Lammertyn, Joel D. Cooper, Johny Verschakelen, Erik Verbeken, Mariette Kemner-van de Corput, Bart M. Vanaudenaerde, Lieven Dupont, John E. McDonough, Marijke Proesmans, Dirk Van Raemdonck, Cindy Mai, Mieke Boon, Stijn E. Verleden, Harm A.W.M. Tiddens, James C. Hogg
Publikováno v:
American journal of respiratory and critical care medicine
American Journal of Respiratory and Critical Care Medicine, 193(5), 516-526. American Thoracic Society
American Journal of Respiratory and Critical Care Medicine, 193(5), 516-526. American Thoracic Society
RATIONALE: After repeated cycles of lung infection and inflammation, patients with cystic fibrosis (CF) evolve to respiratory insufficiency. Although histology and imaging have provided descriptive information, a thorough morphometric analysis of end
Publikováno v:
Journal of Cystic Fibrosis. 19:S49
Autor:
Kate Hayes, R. Coucke, I. Sermet, H. de Keyser, Elise Lammertyn, A. Chansard, P. de Carli, V. Bontemps
Publikováno v:
Journal of Cystic Fibrosis. 19:S51
Autor:
Elise Lammertyn, Robin Vos, Wim A. Wuyts, Bart M. Vanaudenaerde, Naftali Kaminski, Laurens J. De Sadeleer, Karen Maes, Stijn E. Verleden, John E. McDonough, Roel Goldschmeding, Tim S. Nawrot, Coline H.M. van Moorsel, Geert Verleden, Ghislaine Gayan-Ramirez, Lieven Dupont, Stephanie Everaerts, James C. Hogg, Aernoud A. van Batenburg, Dries S. Martens, Wim Janssens
Publikováno v:
Respiratory Research, Vol 19, Iss 1, Pp 1-10 (2018)
Respiratory Research
Respiratory research, 19(1). BioMed Central
Respiratory research
Respiratory Research
Respiratory research, 19(1). BioMed Central
Respiratory research
Background: Telomere shortening has been associated with several lung diseases. However, telomere length is generally measured in peripheral blood leucocytes rather than in lung tissue, where disease occurs. Consequently, telomere dynamics have not b