Zobrazeno 1 - 10
of 53
pro vyhledávání: '"Annie Levy"'
Autor:
Meryl Darlington, Bruno Carbonne, Agnès Mailloux, Yves Brossard, Annie Levy-Mozziconacci, Anne Cortey, Hassani Maoulida, Tabassome Simon, Alexandra Rousseau, Isabelle Durand-Zaleski, the GENIFERH1 Study Group
Publikováno v:
BMC Pregnancy and Childbirth, Vol 18, Iss 1, Pp 1-10 (2018)
Abstract Background The determination of foetal Rhesus D (RHD) status allows appropriate use of IgRh prophylaxis by restricting its use to cases of RHD feto-maternal incompatibilities. There is a degree of uncertainty about the cost-effectiveness of
Externí odkaz:
https://doaj.org/article/108e177f8eb141b8bbd5a479f444f3c6
Autor:
Coralie Zumelzu, Marina Alexandre, Christelle Le Roux, Patricia Weber, Alexis Guyot, Annie Levy, Françoise Aucouturier, Sabine Mignot-Grootenboer, Frédéric Caux, Eve Maubec, Catherine Prost-Squarcioni
Publikováno v:
Frontiers in Medicine, Vol 5 (2018)
An 83-year-old patient developed erosions and a blister of the gingival mucous membrane, 6 months after discontinuation of the anti-programmed death-1 (anti PD-1) pembrolizumab therapy administered for 10 months for a metastatic melanoma. A diagnosis
Externí odkaz:
https://doaj.org/article/6af666eae4fd4a6d80703bbf6a75993d
Autor:
Sophie Brun, Coralie Zumelzu, Mai Ba Hoanganh, Annie Levy, Dea Garcia-Hermoso, Liliane Laroche, Arezki Izri
Publikováno v:
Medical Mycology Case Reports, Vol 11, Iss C, p 27 (2016)
Externí odkaz:
https://doaj.org/article/f4ae8fcf698945f7859512f8194438d7
Autor:
Simon Barbieux, Anne Tallet, Christine Collin, Matthias Tallegas, Flore Delalande, Guido Bens, Annie Levy, Athanasios Kalampokas, David Schrama, Roland Houben, Antoine Touzé, Jeremy Garcia, Nicolas Macagno, Romain Appay, Mahtab Samimi, Serge Guyétant, Thibault Kervarrec
Publikováno v:
Journal of the European Academy of Dermatology and Venereology. 37
Autor:
Lydia Deschamps, Silke Appenzeller, Serge Guyétant, Anne Tallet, Patricia Berthon, Thibault Kervarrec, Guilhem Bousquet, Annie Levy, David Schrama, Mahtab Samimi, Eva-Maria Sarosi, Bernard Cribier, Eve Maubec, Bhavishya Sarma, Mohanad Aljundi, Roland Houben, Antoine Touzé
Publikováno v:
Journal of Investigative Dermatology
Journal of Investigative Dermatology, Nature Publishing Group, 2020, 140 (5), pp.976-985. ⟨10.1016/j.jid.2019.09.026⟩
Journal of Investigative Dermatology, Nature Publishing Group, 2020, 140 (5), pp.976-985. ⟨10.1016/j.jid.2019.09.026⟩
International audience; Merkel cell carcinoma (MCC), an aggressive neuroendocrine carcinoma of the skin, is to date the only human cancer known to be frequently caused by a polyomavirus. However, it is a matter of debate which cells are targeted by t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::048f9884ba4e5bd43393b66d5ed24c19
https://hal.inrae.fr/hal-02621965
https://hal.inrae.fr/hal-02621965
Autor:
Linda Akloul, Véronique David, Clarisse Baumann, Sylvie Odent, Laurent Pasquier, Christèle Dubourg, Houda Hamdi-Rozé, Daniel Amram, Charlotte Mouden, Pierre Sarda, Sophie Naudion, Amélie Poidvin, Marie Gonzales, Nicolas Chassaing, Valérie Dupé, Fabienne Prieur, Joelle Roume, Marie de Tayrac, Benmansour Abdelmajid, Annie Levy-Mozziconacci, Christine Coubes, Wilfrid Carré, Annick Toutain, Laurence Faivre-Olivier, Emmanuelle Ginglinger, Sally-Ann Lynch
Publikováno v:
Human Mutation. 37:1329-1339
Holoprosencephaly (HPE) is the most common congenital cerebral malformation in humans, characterized by impaired forebrain cleavage and midline facial anomalies. It presents a high heterogeneity, both in clinics and genetics. We have developed a nove
Publikováno v:
Revue de médecine périnatale. 8:62-66
Nous rapportons notre experience de l’analyse du genotypage non invasif du RHD, RHCE et KEL1 fœtal sur sang maternel, effectuee en routine hospitaliere dans l’Unite Fonctionnelle de Biologie Materno-Fœtale du Service de Biochimie et Biologie Mo
Autor:
Fabien Stenard, Pascal de Lagausie, Florence Bretelle, Nicole Philip, Pascale Hoffmann, Anderson Loundou, Pierre Mace, Isabelle Mortier, Jonathan Lopater, Marie Christine Pellissier, Sabine Sigaudy, Claude D'Ercole, M. Capelle, Thierry Merrot, Candice Ronin, Annie Levy
Publikováno v:
European Journal of Obstetrics & Gynecology and Reproductive Biology
European Journal of Obstetrics & Gynecology and Reproductive Biology, Elsevier, 2017, 212, pp.166-170. ⟨10.1016/j.ejogrb.2017.01.060⟩
European Journal of Obstetrics & Gynecology and Reproductive Biology, 2017, 212, pp.166-170. ⟨10.1016/j.ejogrb.2017.01.060⟩
European Journal of Obstetrics & Gynecology and Reproductive Biology, Elsevier, 2017, 212, pp.166-170. ⟨10.1016/j.ejogrb.2017.01.060⟩
European Journal of Obstetrics & Gynecology and Reproductive Biology, 2017, 212, pp.166-170. ⟨10.1016/j.ejogrb.2017.01.060⟩
International audience; Objective: The aim of this study was to identify antenatal prognostic factors of neonatal outcomes in cases of fetal echogenic bowel (FEB). Study design: A retrospective study in three tertiary referral centers including fetal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d912013385082880572ff6fa56fcb931
https://hal.archives-ouvertes.fr/hal-01573807
https://hal.archives-ouvertes.fr/hal-01573807
Autor:
Marie Dominique Vignon-Pennamen, Annie Levy, Stéphane Dalle, Valérie Costes-Martineau, Philippe Courville, Andrew Mitchell, Béatrice Vergier, Anne de Muret, Fanny Julia, Laurence Lamant, Gérard Duru, Agnès Carlotti, Nicolas Ortonne, Pierre Dechelotte, Claire Delattre, Tony Petrella, Sylvie Fraitag, Sophie Dalac, Brigitte Balme
Publikováno v:
American Journal of Surgical Pathology. 38:673-680
Blastic plasmacytoid dendritic cell neoplasm is a rare clinicopathologic entity, characterized by strong skin tropism and a poor prognosis. The diagnosis is generally made by skin biopsy with appropriate immunohistochemical studies. To identify poten
Autor:
S. Jridi, Slama Hmida, Hajer Moussa, Annie Levy-Mozziconacci, Monique Silvy, Pascal Bailly, T. Chakroun, Marthe Tsochandaridis, Jean Gabert, B. Abdelneji, Saloua Jemni-Yacoub
Publikováno v:
Transfusion Medicine. 22:192-198
Background: Most studies of the molecular basis of Rhesus D-negative phenotype have been conducted in Caucasian and African populations. A comprehensive survey of RHD alleles was lacking in people from North Africa (Tunisians, Moroccans and Algerians