Zobrazeno 1 - 10
of 72
pro vyhledávání: '"Françoise, Petit"'
Autor:
Fabrice Kwiatkowski, Mathilde Gay-Bellile, Pascal Dessenne, Claire Laquet, Véronique Boussion, Marie Béguinot, Marie-Françoise Petit, Anne-Sophie Grémeau, Céline Verlet, Charlotte Chaptal, Marilyn Broult, Sylvie Jouvency, Martine Duclos, Yves-Jean Bignon
Publikováno v:
Hereditary Cancer in Clinical Practice, Vol 17, Iss 1, Pp 1-9 (2019)
Abstract Background In families with high risk of hereditary breast/ovarian cancer (HBOC), women before age 30 do not yet undergo clinical screening, but they are exposed to contradictory information from diverse sources. They may be presented with s
Externí odkaz:
https://doaj.org/article/59e5953435484fc6a190314a37ec1036
Autor:
Marion Marro, Audrey Françoise Petit, Céline Falaise, Martine Roche, Sophie Gensollen, Nathalie Hezard, Mohamed Boucekine, Pascal Auquier, Hervé Chambost, Paul Saultier
Publikováno v:
Haemophilia
Haemophilia, 2022, ⟨10.1111/hae.14724⟩
Haemophilia, 2022, ⟨10.1111/hae.14724⟩
International audience
Autor:
Paul Saultier, Nour El Riachy, Yves Bertrand, Marie-Dominique Tabone, Guy Leverger, Jean-Hugues Dalle, Andre Baruchel, Cecile Pochon, Catherine Paillard, Stephane Ducassou, Marilyne Poiree, Dominique Plantaz, Justyna Kanold, Virginie Gandemer, Nicolas Sirvent, Genevieve Plat, Isabelle Pellier, Yves Reguerre, Sandrine Thouvenin, Audrey Françoise Petit, Pascal Auquier, Julie Berbis, Gerard Michel
Publikováno v:
Blood. 140:2187-2189
Autor:
Audrey Françoise Petit, Bénédicte Neven, Victoria Min, Nizar Mahlaoui, Despina Moshous, Martin Castelle, Maya Allouche, Arthur Stérin, Sandrine Visentin, Mohamed Boucekine, Alaa Mustafa Shawket, Capucine Picard, Pascal Auquier, Gérard Michel, Alain FISCHER, Vincent Barlogis
Hematopoietic stem cell transplantation (HSCT) for Inborn Errors of Immunity (IEI) survival outcome has improved considerably and the indications have broadened. Subsequently, the issue of long-term quality of live (HRQoL) has become crucial. Our stu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f85ba8d68de6c9f6c865b85707de6fad
https://doi.org/10.21203/rs.3.rs-2324771/v1
https://doi.org/10.21203/rs.3.rs-2324771/v1
Autor:
Audrey Françoise Petit, Austin G. Kulasekararaj, Dirk‐Jan Eikema, Alexey Maschan, Dalila Adjaoud, Alexander Kulagin, Anna Grassi, Franca Fagioli, Laimonas Griskevicius, John A. Snowden, Jan‐Erik J. Johansson, Jean‐Hugues Dalle, Jenny Byrne, Antonio M. Risitano, Régis Peffault de Latour, Carlo Dufour
Publikováno v:
American journal of hematologyREFERENCES. 97(1)
Autor:
Kwiatkowski, Fabrice, Gay-Bellile, Mathilde, Dessenne, Pascal, Laquet, Claire, Boussion, Véronique, Béguinot, Marie, Marie-Françoise Petit, Anne-Sophie Grémeau, Verlet, Céline, Chaptal, Charlotte, Broult, Marilyn, Jouvency, Sylvie, Duclos, Martine, Yves-Jean Bignon
Table S1. Detail of scores by questionnaire and by completion time. (DOCX 21 kb)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5a387f9b5d3a6fc65f37d1cec085368a
Autor:
Anne-Sophie Grémeau, Charlotte Chaptal, Marie Beguinot, Céline Verlet, Mathilde Gay-Bellile, Sylvie Jouvency, Claire Laquet, Pascal Dessenne, Yves-Jean Bignon, Marilyn Broult, Marie-Françoise Petit, Fabrice Kwiatkowski, Véronique Boussion, Martine Duclos
Publikováno v:
Hereditary Cancer in Clinical Practice
Hereditary Cancer in Clinical Practice, BioMed Central, 2019, 17, ⟨10.1186/s13053-019-0107-7⟩
Hereditary Cancer in Clinical Practice, 2019, 17, ⟨10.1186/s13053-019-0107-7⟩
Hereditary Cancer in Clinical Practice (17), . (2019)
Hereditary Cancer in Clinical Practice, Vol 17, Iss 1, Pp 1-9 (2019)
Hereditary Cancer in Clinical Practice, BioMed Central, 2019, 17, ⟨10.1186/s13053-019-0107-7⟩
Hereditary Cancer in Clinical Practice, 2019, 17, ⟨10.1186/s13053-019-0107-7⟩
Hereditary Cancer in Clinical Practice (17), . (2019)
Hereditary Cancer in Clinical Practice, Vol 17, Iss 1, Pp 1-9 (2019)
Background In families with high risk of hereditary breast/ovarian cancer (HBOC), women before age 30 do not yet undergo clinical screening, but they are exposed to contradictory information from diverse sources. They may be presented with surgical p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3fc3946871ba1f9b8012c6cee1d9c7dc
https://hal.archives-ouvertes.fr/hal-02076059/document
https://hal.archives-ouvertes.fr/hal-02076059/document
Publikováno v:
European Journal of Human Genetics
How long counselees retain the information given during their genetic consultation is of major importance. To address this issue, we conducted a survey among the 3500 families that have been offered genetic counseling at our Center since 1988. In Aug
Autor:
Alexandra Ducancelle, Marie-Christine Mazeron, Marie-José Sanson-Le Pors, Françoise Petit, Sophie Alain
Publikováno v:
Journal of Virological Methods
Journal of Virological Methods, Elsevier, 2007, 141 (2), pp.212-215. ⟨10.1016/j.jviromet.2006.11.039⟩
Journal of Virological Methods, Elsevier, 2007, 141 (2), pp.212-215. ⟨10.1016/j.jviromet.2006.11.039⟩
International audience; Phenotypic characterisation of the human cytomegalovirus (HCMV) pUL54 DNA polymerase is a useful tool for testing for mutations in the UL54 gene thought to render HCMV resistant to foscarnet. In this study, an in-house non-iso
Autor:
M.-J. Sanson-Le Pors, S. Alain, Alexandra Ducancelle, Françoise Petit, Marie-Christine Mazeron, Anne-Marie Fillet, C. Scieux
Publikováno v:
Pathologie Biologie. 53:551-555
We described a colorimetric method to determine the biochemical phenotype of wild-type and mutated cytomegalovirus (HCMV) DNA polymerases by measuring the incorporation of digoxigenin-labelled nucleotides into the growing DNA chain. Mutations V715M a