Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Marie Biard"'
Autor:
Zangbéwendé Guy Ouedraogo, Caroline Janel, Alexandre Janin, Gilles Millat, Sarah Langlais, Bénédicte Pontier, Marie Biard, Mathis Lepage, Christine Francannet, Fanny Laffargue, Isabelle Creveaux
Publikováno v:
Genes, Vol 15, Iss 2, p 225 (2024)
Skeletal dysplasia, also called osteochondrodysplasia, is a category of disorders affecting bone development and children’s growth. Up to 552 genes, including fibroblast growth factor receptor 3 (FGFR3), have been implicated by pathogenic variation
Externí odkaz:
https://doaj.org/article/f113b77975634845af32fb9cd3de0b68
Autor:
Marie Biard, Philippe Vago, Hélène Laurichesse, Charles Rouzade, Andrei Tchirkov, Carole Goumy, Laetitia Gouas, Christine Francannet, Mathilde Gay-Bellile, Stephan Kemeny, Philippe Vanlieferinghen, Gaelle Salaun, Céline Pebrel-Richard, Eleonore Eymard-Pierre
Publikováno v:
Birth Defects Research Part A: Clinical and Molecular Teratology. 106:793-797
Background Microdeletions encompassing chromosome bands 2q14.1q14.3 are rare. To date, eight reports of relatively large deletions of this region (∼20 Mb) but only two small deletions (
Publikováno v:
CardioVascular and Interventional Radiology. 27:637-642
We evaluated immediate and long-term results of percutaneous transluminal angioplasty (PTA) and stent placement to treat stenotic and occluded arteries in patients with chronic mesenteric ischemia. Fourteen patients were treated by 3 exclusive celiac
Autor:
Jean-Louis Stephan, Etienne Merlin, Marie Biard, Eric Doré, Alain Marques-Verdier, Stéphane Chabrier
Publikováno v:
Journal of child neurology. 27(10)
The few cases of antiphospholipid syndrome that have been reported in neonates are believed to have resulted from a transplacental transfer of antiphospholipid antibodies. Here we report on a boy with a neonatal stroke revealing a de novo primary ant
Autor:
Placide, Emmanuel
Publikováno v:
Sciences du Vivant [q-bio]. 2019
Objectifs : Principal : Évaluer dans le cadre de l’interruption médicale de grossesse (IMG), l’apport de la virtopsie fœtale par IRM comparativement au gold standard qu’est l’autopsie pour l’établissement d’un diagnostic génétique.S
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::615a887b99106cd83547478e56a2096d
https://dumas.ccsd.cnrs.fr/dumas-02191306
https://dumas.ccsd.cnrs.fr/dumas-02191306
Autor:
Cotton de Bennetot, Grégoire
Publikováno v:
Sciences du Vivant [q-bio]. 2019
Contexte : La maturation de l’encéphale de l’enfant suit un schéma bien connu. La myélinisation progressive de la substance blanche débutant dès la vie in-utéro jusqu’à l’âge de deux ans a été largement décrite dès l’avènement
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::bd0597925b4169d481d7fa2e06eecd77
https://dumas.ccsd.cnrs.fr/dumas-02442437/document
https://dumas.ccsd.cnrs.fr/dumas-02442437/document