Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Nadia Leticee"'
Autor:
Nadia Leticee, Yves Ville, Jean-Marc Costa, Jean-Marie Jouannic, Sophie Delahaye, Alexandra Benachi
Publikováno v:
European Journal of Obstetrics & Gynecology and Reproductive Biology. 162:28-32
Objectives Fetal rhesus D ( RhD ) status determination using circulating cell-free fetal DNA from maternal plasma or serum is now recognized in Europe as a reliable and useful tool. A few countries are presently using this test in their management po
Publikováno v:
La Presse Médicale. 35:1467-1474
Resume Objectif Evaluer les effets de decisions de justice (arret Perruche et loi du 4 mars 2002) sur les pratiques relatives a l’echographie fœtale et la medecine fœtale. Methode Des questionnaires ont ete envoyes aux 186 echographistes des rese
Publikováno v:
Contraception. 85:425-427
Contraception for HIV-positive women is a complex issue. Although the use of condoms is recommended, complementary methods of contraception are often prescribed. Antiretroviral therapy can lead to drug interactions and modify the efficacy of hormonal
Autor:
Emilie Pateau, Nadia Leticee, Sophie Thomas, Louise Devisme, Maryse Bonnière, Marc Wessner, Peter J. Wookey, Stanislas Lyonnet, Christine Bole Feysot, Annie Laquerrière, Vincent Meyer, Patrick Nitschke, Bernard Foliguet, Nadia Elkhartoufi, Géraldine Goudefroye, Heather C. Etchevers, Pascale Marcorelle, Marie Gonzales, Jelena Martinovic, Philippe Parent, Tania Attié-Bitach, Bettina Bessieres-Grattagliano, Laurence Loeuillet, Sylvie Manouvrier, Muriel Holder, Gabor Gyapay, Soumaya Mougou-Zerelli, Arnold Munnich, Michel Vekemans, Amale Ichkou, Férechté Encha-Razavi, Joelle Roume
Publikováno v:
Human Mutation
Human Mutation, Wiley, 2010, 31 (10), pp.1134. ⟨10.1002/humu.21329⟩
Human Mutation, Wiley, 2010, 31 (10), pp.1134. 〈10.1002/humu.21329〉
Human Mutation, 2010, 31 (10), pp.1134. ⟨10.1002/humu.21329⟩
Human Mutation, Wiley, 2010, 31 (10), pp.1134. ⟨10.1002/humu.21329⟩
Human Mutation, Wiley, 2010, 31 (10), pp.1134. 〈10.1002/humu.21329〉
Human Mutation, 2010, 31 (10), pp.1134. ⟨10.1002/humu.21329⟩
International audience; Rare lethal disease gene identification remains a challenging issue, but it is amenable to new techniques in high-throughput sequencing (HTS). Cerebral proliferative glomeruloid vasculopathy (PGV), or Fowler syndrome, is a sev
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::269b8b7c6bf378beb538faac2c138772
https://hal.archives-ouvertes.fr/hal-00574003/document
https://hal.archives-ouvertes.fr/hal-00574003/document
Autor:
Thierry Dupré, Nadia El Khartoufi, Sandrine Vuillaumier-Barrot, Nathalie Seta, Pascale de Lonlay, Ferechté Razavi, Tania Attié-Bitach, Raymonde Bouvier, Nadia Leticee, Bettina Bessieres-Grattagliano, Michel Vekemans, Yves Ville
Publikováno v:
Molecular genetics and metabolism. 101(2-3)
Hydrops fetalis (HF) is characterized by an accumulation of fluid in the extracellular compartments and in body cavities. Non-immune HF (NIHF) is caused by a wide variety of disorders and overall, 20-25% of NIHF remain unexplained. Inborn errors of m
Autor:
S. Zrelli, Férechté Encha-Razavi, Bernard Foliguet, Jelena Martinovic, Annie Laquerrière, Tania Attié-Bitach, Louise Devisme, Laurence Loeuillet, Maryse Bonnière, Catherine Fallet-Bianco, Nadia Leticee, Pascale Marcorelles, V. Cayol, Heather C. Etchevers, Michel Vekemans, Bettina Bessieres-Grattagliano
Publikováno v:
European journal of medical genetics. 52(6)
Cerebral proliferative glomeruloid vasculopathy (PGV) is a severe disorder of brain angiogenesis, resulting in abnormally thickened and aberrant perforating vessels, forming glomeruloids with inclusion-bearing endothelial cells. This peculiar vascula