Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Alexandra Lefebvre"'
Autor:
Roseline Vibert, Jasmine Hasnaoui, Alexandre Perrier, Alexandra Lefebvre, Chrystelle Colas, Marion Dhooge, Noémie Basset, Albain Chansavang, Camille Desseignes, Alex Duval, Solenne Farelly, Nadim Hamzaoui, Pierre Laurent-Puig, Julie Metras, Diane Moliere, Martine Muleris, Jeanne Netter, Mehdi Touat, Franck Bielle, Karim Labreche, Romain Nicolle, Géraldine Perkins, Mathilde Warcoin, Florence Coulet, Patrick R. Benusiglio
Publikováno v:
European Journal of Human Genetics.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8921497eb9c1a0e245ce99245c188f25
https://doi.org/10.1038/s41431-023-01367-z
https://doi.org/10.1038/s41431-023-01367-z
Autor:
Roseline VIBERT, Jasmine Hasnaoui, Alexandra Lefebvre, Chrystelle Colas, Marion Dhooge, Noemie Basset, Albain Chansavang, Camille Desseignes, Alex Duval, Solenne Farelly, Nadim Hamzaoui, Pierre Laurent-Puig, Julie Metras, Diane Moliere, Martine Muleris, Jeanne Netter, Romain Nicolle, Géraldine Perkins, Alexandre Perrier, Mathilde Warcoin, Florence Coulet, Patrick Benusiglio
Some patients with Lynch syndrome (LS) have extreme phenotypes, i.e. cancer before the recommended screening age, or cancer for which there are no screening guidelines. We made the hypothesis that additional germline variants in cancer susceptibility
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9a37a87cafff94066f032af60c65ae91
https://doi.org/10.21203/rs.3.rs-2159229/v1
https://doi.org/10.21203/rs.3.rs-2159229/v1
Autor:
Francis Houde, Alexandra Lefebvre, Pierre-François Tremblay Labrecque, Marie-Philippe Harvey, Guillaume Léonard, Francis Lamarche
Publikováno v:
Journal of Pain Research
Purpose Complex regional pain syndrome (CRPS) is a rare neuropathic pain condition characterized by sensory, motor and autonomic alterations. Previous investigations have shown that transcranial direct current stimulation (tDCS) and transcutaneous el
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f1277f6ce741d4edc348bfef714c00a8
http://europepmc.org/articles/PMC7060070
http://europepmc.org/articles/PMC7060070
Publikováno v:
Genetics in Medicine
Genetics in Medicine, Nature Publishing Group, 2020, 22 (8), pp.1422-1423. ⟨10.1038/s41436-020-0819-0⟩
Genetics in Medicine, 2020, 22 (8), pp.1422-1423. ⟨10.1038/s41436-020-0819-0⟩
Genetics in Medicine, Nature Publishing Group, 2020, 22 (8), pp.1422-1423. ⟨10.1038/s41436-020-0819-0⟩
Genetics in Medicine, 2020, 22 (8), pp.1422-1423. ⟨10.1038/s41436-020-0819-0⟩
International audience
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f1ae5b8203c3bc115a97a9a0ac031082
http://hdl.handle.net/20.500.12278/36422
http://hdl.handle.net/20.500.12278/36422
Publikováno v:
Computational and Mathematical Methods in Medicine
Computational and Mathematical Methods in Medicine, Hindawi Publishing Corporation, 2017
Computational and Mathematical Methods in Medicine, Vol 2017 (2017)
Computational and Mathematical Methods in Medicine, 2017
Computational and Mathematical Methods in Medicine, Hindawi Publishing Corporation, 2017
Computational and Mathematical Methods in Medicine, Vol 2017 (2017)
Computational and Mathematical Methods in Medicine, 2017
When considering a genetic disease with variable age at onset (e.g., familial amyloid neuropathy, cancers), computing the individual risk of the disease based on family history (FH) is of critical interest for both clinicians and patients. Such a ris
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::03a2f92d240f55bd2445aca9f30e2dcf
https://doi.org/10.1155/2017/9193630
https://doi.org/10.1155/2017/9193630
Publikováno v:
Revue d'Épidémiologie et de Santé Publique. 66:S125-S126
Introduction Un microsatellite est une sequence d’ADN composee de la repetition de un a six nucleotides. L’instabilite des microsatellites (MSI) se retrouve dans 15 % des cancers colorectaux (CRC), de l’estomac, de l’endometre et plus raremen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5ff670fa5213aa8fb9308b91bc01ca24
https://doi.org/10.1016/j.respe.2018.03.325
https://doi.org/10.1016/j.respe.2018.03.325
Publikováno v:
Journal of Clinical Oncology. 35:e13005-e13005
e13005 Background: Most of the BRCA1/2 and PALB2 analyses performed in patients with a personal and familial history (FH) of breast/ovarian cancer are negative. In this context, there is no targeted analysis available to identify relatives at high ri
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6d04d7e9233fd43845588cd64fa51091
https://doi.org/10.1200/jco.2017.35.15_suppl.e13005
https://doi.org/10.1200/jco.2017.35.15_suppl.e13005
Publikováno v:
Les troubles psychologiques
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2eba2b60d203dbdc6d164a64bb1c6b8f
https://doi.org/10.2307/j.ctv18ph48p.8
https://doi.org/10.2307/j.ctv18ph48p.8