Zobrazeno 1 - 10
of 39
pro vyhledávání: '"Biervliet, Martine"'
Autor:
Storm, Katrien, Moens, Els, Vits, Lieve, De Vlieger, Haike, Delaere, Gino, D'Hollander, Maria, Wuyts, Wim, Biervliet, Martine, Van Schil, Lutgardis, Desager, Kristine, Nöthen, Markus M.
Publikováno v:
In Journal of Cystic Fibrosis 2007 6(6):371-375
Autor:
Van Hoorenbeeck, Kim, Storm, Katrien, van den Ende, Jenneke, Biervliet, Martine, Desager, Kristine N.
Publikováno v:
In Journal of Cystic Fibrosis 2007 6(3):220-222
Akademický článek
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Autor:
Peeters, Uschi, Daneels, Dorien, Biervliet, Martine, Caljon, Ben, Pappaert, Gudrun, Brugada, Pedro, Bonduelle, Mary-Louise, Van Dooren, Sonia
Secondary cardiac arrhythmias, or cardiomyopathies are characterized by structural abnormalities of the cardiac muscle. These diseases are associated with arrhythmias, heart failure and sudden cardiac death. The cardiomyopathies are a heterogeneous g
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3848::e0b00d613bd3d30c91e75f4ce0629e17
https://biblio.vub.ac.be/vubir/a-comprehensive-cardiomyopathy-gene-panel(752acec3-5ac7-49ea-9dfa-7f6d993d96f1).html
https://biblio.vub.ac.be/vubir/a-comprehensive-cardiomyopathy-gene-panel(752acec3-5ac7-49ea-9dfa-7f6d993d96f1).html
Autor:
Van Malderen, Sophie, Daneels, Dorien, Van Dooren, Sonia, Dirk, Kerkhove, Peeters, Uschi, Theuns, Damj, Meuwissen, Marije, Biervliet, Martine, Droogmans, Steven, Van Camp, Guy, Weytjens, Caroline, Bonduelle, Mary-Louise, Brugada, Pedro
Background Brugada Syndrome (BS) patients with a previous history of syncope or sustained ventricular arrhythmia have longer right ventricular ejection delays (RVED’s) when compared to asymptomatic BS patients. A genotype-phenotype relationship has
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3848::d1602e94dcfdaf04ba1dcd42834cd40b
https://biblio.vub.ac.be/vubir/prolonged-right-ventricular-ejection-delay-in-brugada-syndrome-depends-on-the-type-of-scn5a-mutation-a-bridge-between-tissue-velocity-imaging-and-genetics(b9e027a5-f601-4e38-a386-6081390516f7).html
https://biblio.vub.ac.be/vubir/prolonged-right-ventricular-ejection-delay-in-brugada-syndrome-depends-on-the-type-of-scn5a-mutation-a-bridge-between-tissue-velocity-imaging-and-genetics(b9e027a5-f601-4e38-a386-6081390516f7).html
Autor:
Daneels, Dorien, Peeters, Uschi, Brugada, Pedro, Bonduelle, Mary-Louise, Raimondi, Daniele, Tanyalcin, Ibrahim, Peirsman, Liszl, Timmermans, Inge, Pappaert, Gudrun, Van Malderen, Sophie, Biervliet, Martine, Verdonck, Daisy, Van Dooren, Sonia
Brugada syndrome (BrS) is a cardiac channelopathy manifesting in apparently structural normal hearts and inherited as an autosomal dominant trait with incomplete penetrance and variable expression. The clinical diagnosis is based on documented ventri
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3848::a3159b3c43a9e94138cc33c31de285be
https://biblio.vub.ac.be/vubir/mutation-analysis-of-the-scn5a-gene-in-147-brugada-syndrome-probands(0ae7ff22-e77f-4aad-844c-74bae819a36a).html
https://biblio.vub.ac.be/vubir/mutation-analysis-of-the-scn5a-gene-in-147-brugada-syndrome-probands(0ae7ff22-e77f-4aad-844c-74bae819a36a).html
Autor:
Van Dooren, Sonia, Brugada, Pedro, Daneels, Dorien, Peeters, Uschi, Peirsman, Liszl, Timmermans, Inge, Kindermans, Kiliana, Biervliet, Martine, Pappaert, Gudrun, Bonduelle, Mary-Louise
Brugada syndrome is one of common inheritable arrhythmogenic disorders in apparently structurally normal hearts, inherited as an autosomal dominant trait with incomplete penetrance and variable expression. Clinical diagnosis is based on documented ve
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3848::1212ef6cd0e9fdd65cfd17f8c12fe176
https://biblio.vub.ac.be/vubir/genotypephenotype-discrepancies-in-brugada-syndrome(77006b5a-0cb6-4fc0-ab0c-59ed73652015).html
https://biblio.vub.ac.be/vubir/genotypephenotype-discrepancies-in-brugada-syndrome(77006b5a-0cb6-4fc0-ab0c-59ed73652015).html
Akademický článek
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Autor:
Roll, Patrice, Roca, Elisa, Lacroix, Romaric, Judicone, Coralie, Laroumagne, Sophie, Robert, Stéphane, Cointe, Sylvie, Muller, Alexandre, Kaspi, Elise, Brisson, Alain, Tantucci, Claudio, Astoul, Philippe, Dignat-George, Françoise, Barthélémy, Florian, Navarro, Claire, Fayek, Racha, Da Silva, Nathalie, Sigaudy, Sabine, Oshima, Junko, Bonne, Gisèle, Papadopoulou-Legbelou, Kyriaki, Evangeliou, Athanasios, Spilioti, Martha, LeMerrer, Martine, Wevers, Ron, Morava, Eva, Robaglia-Schlupp, Andrée, Lévy, Nicolas, Bartoli, Marc, De Sandre-Giovannoli, Annachiara, Hadj-Rabia, Smail, Mashiah, Jacob, Boyer, Amandine, Bourgeois, Patrice, Van Kien, Philippe Khau, Bodemer, Christine, Navarro, Claire Laure, Esteves-Vieira, Vera, Courrier, Sébastien, Duong Nguyen, Thuy, Huong, Le Thi Thanh, Meinke, Peter, Schröder, Winnie, Cormier-Daire, Valérie, Sznajer, Yves, Amor, David, Lagerstedt, Kristina, Biervliet, Martine, van den Akker, Peter, Cau, Pierre, BADENS, Catherine, Wehnert, Manfred, Sakr, Lama, Payan, Marie-José, Liprandi, Agnès, Dutau, Hervé, Loundou, Anderson, Barlesi, Fabrice
Publikováno v:
Lung Cancer
Lung Cancer, Elsevier, 2012, 75 (3), pp.293-299. ⟨10.1016/j.lungcan.2011.09.001⟩
Lung Cancer, Elsevier, 2012, 75 (3), pp.293-299. ⟨10.1016/j.lungcan.2011.09.001⟩
Accurate distinction of lung cancer types has become increasingly important as recent trials have shown differential response to chemotherapy among non-small cell lung carcinoma (NSCLC) subtypes. Cytological procedures are frequently used but their d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6ebe027d7e9e477a29f0cbc3ba42155b
https://hal-amu.archives-ouvertes.fr/hal-03508616
https://hal-amu.archives-ouvertes.fr/hal-03508616
Autor:
Storm, Katrien, Moens, Els, Vits, Lieve, Wuyts, Wim, Biervliet, Martine, Desager, Kristine, Nöthen, Markus
Publikováno v:
Journal of cystic fibrosis
We have analyzed 143 unrelated Belgian patients with a positive diagnosis of cystic fibrosis (CF) for mutations in the cystic fibrosis transmembrane conductance regular:or (CFTR) gene. An initial screening for 29 CFTR mutations led to mutation identi