Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Julie Lachenaud"'
Autor:
Yoann Vial, Julie Lachenaud, Alain Verloes, Marianne Besnard, Odile Fenneteau, Elodie Lainey, Alice Marceau-Renaut, Claude Preudhomme, André Baruchel, Hélène Cavé, Séverine Drunat
Publikováno v:
Haematologica, Vol 103, Iss 6 (2018)
Externí odkaz:
https://doaj.org/article/723277150dca49f68f5261c3f38a4ad2
Autor:
Odile Fenneteau, Yoann Vial, Claude Preudhomme, Alice Marceau-Renaut, Julie Lachenaud, Hélène Cavé, Marianne Besnard, Séverine Drunat, Alain Verloes, André Baruchel, Elodie Lainey
Cornelia de Lange Syndrome (CdLS) is a rare autosomal dominant developmental disorder characterized by a distinctive facial dysmorphism and variable developmental anomalies including prenatal and postnatal growth delay, microcephaly, intellectual dis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::48e9664240a08aeaab22c83a2560a890
https://europepmc.org/articles/PMC6058797/
https://europepmc.org/articles/PMC6058797/
Autor:
Isabelle Guellec, Dalila Adjaoud, Marion Strullu, Hélène Cavé, Nicolas Sirvent, Christine Chomienne, Yves Bertrand, Steven Gazal, Julie Lachenaud, Clarisse Baumann, Bruno Cassinat, André Baruchel, Corinne Alberti, Martin Zenker, Francoise Mechinaud, Sabrina Pereira, Nathalie Pouvreau, Audrey Contet, Odile Fenneteau, Aurélie Caye, Catherine Paillard, Alain Verloes
Publikováno v:
Journal of Medical Genetics. 51:689-697
Background Infants with Noonan syndrome (NS) are predisposed to developing juvenile myelomonocytic leukaemia (JMML) or JMML-like myeloproliferative disorders (MPD). Whereas sporadic JMML is known to be aggressive, JMML occurring in patients with NS i
Publikováno v:
Bulletin du Cancer. 101:302-313
Juvenile myelomonocytic leukemias (JMML) are rare but severe myelodysplastic and myeloproliferative neoplasms of infancy. They represent about 10 new cases per year in France and preferentially affect males. JMML are all stem cell diseases the common
Autor:
Christine Chomienne, Yves Bertrand, Bruno Cassinat, Julie Lachenaud, Olivier Kosmider, André Baruchel, Hélène Cavé, Aline Renneville, Benoîte Pérez, Claude Preudhomme, Sophie Kaltenbach, Michaela Fontenay
Publikováno v:
British Journal of Haematology. 151:460-468
JMML and CMML are rare myelodysplastic/myeloproliferative neoplasms occurring at both ends of life. To investigate relationships between JMML and CMML, genes recently involved in CMML were studied in 68 JMML patients. Mutations in TET2, RUNX1 and JAK
Autor:
Mohammad Reza Ahmadian, Dieter Häussinger, Brigitte Nelken, Francoise Mechinaud, Marion Strullu, André Baruchel, Steven Gazal, Marilyne Poirée, Nicolas Sirvent, Jocelyne Vivent, Catherine Paillard, Radovan Dvorsky, Sabrina Pereira, Capucine Picard, Jean-Hugues Dalle, Emmanuelle Verger, Odile Fenneteau, Bruno Cassinat, Hélène Cavé, Yves Reguerre, Saeideh Nakhaei-Rad, Elodie Lainey, Aurélie Caye, Yves Bertrand, Fabien Guidez, Audrey Contet, Arnaud Petit, Kazem Nouri, Dominique Vidaud, Claire Galambrun, Julie Lachenaud, Christine Chomienne, Dalila Adjaoud
Publikováno v:
Nature Genetics
Nature Genetics, Nature Publishing Group, 2015, 47 (11), pp.1334-1340. ⟨10.1038/ng.3420⟩
Nature Genetics, Nature Publishing Group, 2015, 47 (11), pp.1334-1340. ⟨10.1038/ng.3420⟩
International audience; Juvenile myelomonocytic leukemia (JMML) is a rare and severe myelodysplastic and myeloproliferative neoplasm of early childhood initiated by germline or somatic RAS-activating mutations. Genetic profiling and whole-exome seque
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2f00f01cc3d98c8561ac6971cae84245
https://hal.umontpellier.fr/hal-01938513
https://hal.umontpellier.fr/hal-01938513
Autor:
Davood Mansouri, Caroline Galeotti, Parvaneh Adimi, Olivier Lortholary, Laurent Abel, Sébastien Héritier, Mahin Jamshidi, Valeska Bidault, Marie-Elisabeth Bougnoux, Capucine Picard, Jean-Laurent Casanova, Luyan Liu, Elisa Barbati, Stéphane Blanche, Maryline Chomton, Serge Romana, Emmanuel Jacquemin, Vincent Pedergnana, Seyed Alireza Mahdaviani, Fanny Lanternier, Julie Lachenaud, Marie-Louise Frémond, Danielle Canioni, Adela Angoulvant, Ulrich Meinzer, Emmanuel Gonzales, Mélanie Migaud, Anne Puel, Nahal Mansouri
Publikováno v:
Journal of Infectious Diseases
Journal of Infectious Diseases, 2015, 211 (8), pp.1241-1250. ⟨10.1093/infdis/jiu412⟩
Journal of Infectious Diseases, Oxford University Press (OUP), 2015, 211 (8), pp.1241-1250. ⟨10.1093/infdis/jiu412⟩
Journal of Infectious Diseases, 2015, 211 (8), pp.1241-1250. ⟨10.1093/infdis/jiu412⟩
Journal of Infectious Diseases, Oxford University Press (OUP), 2015, 211 (8), pp.1241-1250. ⟨10.1093/infdis/jiu412⟩
International audience; Background. Exophiala species are mostly responsible for skin infections. Invasive Exophiala dermatitidis disease is a rare and frequently fatal infection, with 42 cases reported. About half of these cases had no known risk fa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5eeb04160bc7fea1c6b201ce232274ca
https://hal.inrae.fr/hal-02634252
https://hal.inrae.fr/hal-02634252
Publikováno v:
Bulletin du cancer. 101(3)
Juvenile myelomonocytic leukemias (JMML) are rare but severe myelodysplastic and myeloproliferative neoplasms of infancy. They represent about 10 new cases per year in France and preferentially affect males. JMML are all stem cell diseases the common
Autor:
Isabelle Radford-Weiss, Julie Lachenaud, Pierre Brousset, Florence Nguyen-Khac, Stéphanie Struski, Christine J. Harrison, Hélène Cavé, Olivier Bernard, Véronique Della Valle, Elise Chapiro, Lisa J. Russell
Publikováno v:
Leukemia. 24:1362-1364
A new recurrent translocation t(11;14)(q24;q32) involving IGH@ and miR-125b-1 in B-cell progenitor acute lymphoblastic leukemia
Autor:
Patricia Mariani-Kurkdjian, Albert Faye, Véronique Houdouin, Antoine Bourrillon, Edouard Bingen, Guillaume Aubertin, Laure de Los Angeles, Julie Lachenaud, François Angoulvant, Mathie Lorrot
Publikováno v:
Journal of Clinical Microbiology. 44:4285-4287
We describe two cases of aseptic meningitis occurring some time after pneumococcal meningitis. Both cases may have resulted from an inflammatory response to persistent pneumococcal cell membrane components, as the cerebrospinal fluid samples were pos