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1دورية أكاديمية
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2دورية أكاديمية
المؤلفون: Futema, Marta, Ramaswami, Uma, Tichy, Lukas, Bogsrud, Martin P., Holven, Kirsten B., Roeters van Lennep, Jeanine, Wiegman, Albert, Descamps, Olivier S., De Leener, Anne, Fastre, Elodie, Vrablik, Michal, Freiberger, Tomas, Esterbauer, Harald, Dieplinger, Hans, Greber-Platzer, Susanne, Medeiros, Ana M., Bourbon, Mafalda, Mollaki, Vasiliki, Drogari, Euridiki, Humphries, Steve E.
المصدر: In Atherosclerosis February 2021 319:108-117
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3دورية أكاديمية
المؤلفون: Brouillard, Pascal, Schlögel, Matthieu J., Homayun Sepehr, Nassim, Helaers, Raphaël, Queisser, Angela, Fastré, Elodie, Boutry, Simon, Schmitz, SandraAff2, Aff3, Aff4, Clapuyt, PhilippeAff2, Aff3, Aff4, Hammer, FrankAff2, Aff3, Aff4, Dompmartin, Anne, Weitz-Tuoretmaa, Annamaria, Laranne, Jussi, Pasquesoone, Louise, Vilain, Catheline, Boon, Laurence M.Aff1, Aff3, Aff4, Vikkula, MiikkaAff1, Aff3, Aff4, Aff10
المصدر: Orphanet Journal of Rare Diseases. 16(1)
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4دورية أكاديمية
المؤلفون: Lantoine, Joséphine, Brysse, Anne, DIDEBERG, Vinciane, Claes, Kathleen, Symoens, Sofie, Coucke, Wim, Benoit, Valérie, Rombout, Sonia, De Rycke, Martine, Seneca, Sara, Van Laer, Lut, Wuyts, Wim, Corveleyn, Anniek, Van Den Bogaert, Kris, Rydlewski, Catherine, Wilkin, Françoise, Ravoet, Marie, Fastré, Elodie, Capron, Arnaud, Vandevelde, Nathalie Monique
المصدر: JMIR Medical Informatics, 9 (7), e27980 (2021)
مصطلحات موضوعية: algorithm, cost-effectiveness, external quality assessment, frequency, genetic testing, genetics, health informatics, human genetics, medical informatics, proficiency testing, public health, quality control, rare diseases, surveillance, public health authorities, Life sciences, Genetics & genetic processes, Sciences du vivant, Génétique & processus génétiques
Relation: urn:issn:2291-9694
URL الوصول: https://orbi.uliege.be/handle/2268/264695
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المؤلفون: Lantoine, Joséphine, Brysse, Anne, Dideberg, Vinciane, Claes, Kathleen B. M., Symoens, Sofie, Coucke, Wim, Benoit, Valérie, Rombout, Sonia, De Rycke, Martine, Seneca, Sara, Van Laer, Lut, Wuyts, Wim, Corveleyn, Anniek, Van den Bogaert, Kris, Rydlewski, Catherine, Wilkin, Françoise, Ravoet, Marie, Fastré, Elodie, Capron, Arnaud, Vandevelde, Nathalie M.
المساهمون: Basic (bio-) Medical Sciences, Medical Genetics, Reproduction and Genetics, Clinical sciences
URL الوصول: https://explore.openaire.eu/search/publication?articleId=od______3848::eb348ed3738acd9d666ae8d7d7cd17cb
https://hdl.handle.net/20.500.14017/d819c675-c7fe-4cac-be24-399b012fd56b -
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المؤلفون: Schlögel, Matthieu J, Mendola, Antonella, Fastré, Elodie, Vasudevan, Pradeep, Devriendt, Koen, de Ravel, Thomy Jl, Van Esch, Hilde, Casteels, Ingele, Arroyo Carrera, Ignacio, Cristofoli, Francesca, Fieggen, Karen, Jones, Katheryn, Lipson, Mark, Balikova, Irina, Singer, Ami, Soller, Maria, Mercedes Villanueva, María, Revencu, Nicole, Boon, Laurence M, Brouillard, Pascal, Vikkula, Miikka
المصدر: Orphanet Journal of Rare Diseases. 10(1)
مصطلحات موضوعية: Medicin och hälsovetenskap, Medicinska och farmaceutiska grundvetenskaper, Medicinsk genetik, Medical and Health Sciences, Basic Medicine, Medical Genetics
وصف الملف: electronic
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المؤلفون: Brouillard, Pascal, Schlögel, Matthieu J., Homayun Sepehr, Nassim, Helaers, Raphaël, Queisser, Angela, Fastré, Elodie, Boutry, Simon, Schmitz, Sandra, Clapuyt, Philippe, Hammer, Frank, Dompmartin, Anne, Weitz-Tuoretmaa, Annamaria, Laranne, Jussi, Pasquesoone, Louise, Vilain, Catheline, Boon, Laurence M., Vikkula, Miikka
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::27d86d2003173a6e0c08679046a98033
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8دورية أكاديمية
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9
المؤلفون: Leppänen, Veli-Matti, Brouillard, Pascal, Korhonen, Emilia A, Sipilä, Tuomas, Jha, Sawan Kumar, Revencu, Nicole, Labarque, Veerle, Fastré, Elodie, Schlögel, Matthieu, Ravoet, Marie, Singer, Amihood, Luzzatto, Claudia, Angelone, Donatella, Crichiutti, Giovanni, D'Elia, Angela, Kuurne, Jaakko, Elamaa, Harri, Koh, Gou Young, Saharinen, Pipsa, Vikkula, Miikka, Alitalo, Kari
المساهمون: UCL - SSS/DDUV - Institut de Duve, UCL - SSS/IREC/SLUC - Pôle St.-Luc, UCL - (SLuc) Centre de malformations vasculaires congénitales, UCL - (SLuc) Centre de génétique médicale UCL
المصدر: Science translational medicine, Vol. 12, no.560, p. 1-11 (2020)
مصطلحات موضوعية: Angiopoietin-2, Pregnancy, Mutation, Angiopoietin-1, Endothelial Cells, Humans, Female, Lymphedema, Lymphangiogenesis, Receptor, TIE-2, Signal Transduction
URL الوصول: https://explore.openaire.eu/search/publication?articleId=od______1493::9a4a011cb7d0d13d82717ea188b9ff16
https://hdl.handle.net/2078.1/263166 -
10دورية أكاديمية
لا يتم عرض هذه النتيجة على الضيوف.
تسجيل الدخول للوصول الكامل.