Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Valérie Ortonne"'
Autor:
Valérie Ortonne, Quentin Lucas, Olivia Garrigou, Alexandre Soulier, Dominique Challine, Jean-Michel Pawlotsky, Vincent Leroy, Stéphane Chevaliez
Publikováno v:
mSphere, Vol 7, Iss 3 (2022)
ABSTRACT The International Liver Association recommends the use of accurate and sensitive molecular methods for determination of hepatitis B virus (HBV) DNA levels in plasma or serum of chronic HBsAg carriers. The level of HBV replication represents
Externí odkaz:
https://doaj.org/article/e18fe2fc5e2749cca3d81d24ffe0ad6d
Autor:
Lamisse Mansour-Hendili, Abdelrazak Aissat, Bouchra Badaoui, Mehdi Sakka, Christine Gameiro, Valérie Ortonne, Orianne Wagner-Ballon, Serge Pissard, Véronique Picard, Khaldoun Ghazal, Michel Bahuau, Corinne Guitton, Ziad Mansour, Mylène Duplan, Arnaud Petit, Nathalie Costedoat-Chalumeau, Marc Michel, Pablo Bartolucci, Stéphane Moutereau, Benoît Funalot, Frédéric Galactéros
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 15, Iss 1, Pp 1-15 (2020)
Abstract Background Congenital hemolytic anemia constitutes a heterogeneous group of rare genetic disorders of red blood cells. Diagnosis is based on clinical data, family history and phenotypic testing, genetic analyses being usually performed as a
Externí odkaz:
https://doaj.org/article/6f893e2c9cf14483b312306ba68dde60
Autor:
Lucie Tosca, Loïc Drévillon, Aurélie Mouka, Laure Lecerf, Audrey Briand, Valérie Ortonne, Virginie Benoit, Sophie Brisset, Lionel Van Maldergem, Quitterie Laudouar, Solveig Heide, Michel Goossens, Irina Giurgea, Gérard Tachdjian, Corinne Métay
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 9, Iss 11, Pp n/a-n/a (2021)
Abstract Background Terminal deletions of the long arm of chromosome 7 are well known and frequently associated with syndromic holoprosencephaly due to the involvement of the SHH (aliases HHG1, SMMCI, TPT, TPTPS, and MCOPCB5) gene region. However, in
Externí odkaz:
https://doaj.org/article/ce89b36c62a24af3a9382758b4baf3e7
Autor:
Valérie Ortonne, Mélanie Wlassow, Magali Bouvier-Alias, Giovana Melica, Jean-Dominique Poveda, Syria Laperche, Jean-Michel Pawlotsky, Stephane Chevaliez
Publikováno v:
Microorganisms, Vol 9, Iss 3, p 573 (2021)
(1) Background: Sensitive and accurate nucleic acid amplification technologies are now recommended for hepatitis B virus (HBV) DNA detection and quantification in clinical practice to diagnose and monitor hepatitis B infection. The aim of this study
Externí odkaz:
https://doaj.org/article/21c47e1e5b6a46fdae53f00a5f439aef
Autor:
Fabbio Marcuccilli, Stephane Chevaliez, Thomas Muller, Luna Colagrossi, Giulia Abbondanza, Kurt Beyser, Mélanie Wlassow, Valérie Ortonne, Carlo Federico Perno, Marco Ciotti
Publikováno v:
Diagnostics, Vol 11, Iss 2, p 297 (2021)
Accurate measurement of the hepatitis B virus (HBV) DNA is important for the management of patients with chronic HBV infection. Here, the performance of the Xpert® HBV Viral Load test (Xpert HBV Viral Load) versus the Roche COBAS® Ampliprep/COBAS®
Externí odkaz:
https://doaj.org/article/d3b6518861c84a899d00d0451a17006f
Autor:
Laure Lecerf, Irina Giurgea, Quitterie Laudouar, Audrey Briand, Sophie Brisset, Solveig Heide, Aurélie Mouka, G Tachdjian, Lionel Van Maldergem, Michel Goossens, Corinne Metay, Loïc Drévillon, Valérie Ortonne, Lucie Tosca, Virginie Benoit
Publikováno v:
Molecular Genetics & Genomic Medicine
Molecular Genetics & Genomic Medicine, Wiley Periodicals, Inc. In press, pp.e1645. ⟨10.1002/mgg3.1645⟩
Molecular Genetics & Genomic Medicine, Vol 9, Iss 11, Pp n/a-n/a (2021)
Molecular Genetics & Genomic Medicine, Wiley Periodicals, Inc. In press, pp.e1645. ⟨10.1002/mgg3.1645⟩
Molecular Genetics & Genomic Medicine, Vol 9, Iss 11, Pp n/a-n/a (2021)
Background Terminal deletions of the long arm of chromosome 7 are well known and frequently associated with syndromic holoprosencephaly due to the involvement of the SHH (aliases HHG1, SMMCI, TPT, TPTPS, and MCOPCB5) gene region. However, interstitia
Autor:
Aurélie Gourgeon, Valérie Ortonne, Oriane Picard, Clair Mills, Dominique Challine, Céline Langendorf, Etienne Audureau, Nada Malou, Alexandre Soulier, Nazim Ahnou, François Hemery, Justine Michel, Stéphane Chevaliez, Jean-Michel Pawlotsky, Claire Rieux, Isaac Désveaux, Slim Fourati
Publikováno v:
Journal of Clinical Virology
Background Direct detection of SARS-CoV-2 viral proteins in nasopharyngeal swabs using lateral flow immunoassays is a simple, fast and cheap approach to diagnose the infection. Aims and Methods The performance of 6 SARS-CoV-2 antigen rapid diagnostic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dfa0634217868734f27ec7ba88f0eabb
http://hdl.handle.net/10144/619949
http://hdl.handle.net/10144/619949
Dried blood spot sampling for hepatitis C virus infection: A new tool to simplify testing algorithms
Publikováno v:
Journal of clinical virology : the official publication of the Pan American Society for Clinical Virology. 141
Autor:
Abdelrazak Aissat, Marc Michel, Corinne Guitton, Michel Bahuau, Benoît Funalot, Pablo Bartolucci, Arnaud Petit, Orianne Wagner-Ballon, Stéphane Moutereau, Véronique Picard, Serge Pissard, Christine Gameiro, Ziad Mansour, Valérie Ortonne, Khaldoun Ghazal, Mylène Duplan, Lamisse Mansour-Hendili, Bouchra Badaoui, Mehdi Sakka, Frédéric Galactéros, Nathalie Costedoat-Chalumeau
Publikováno v:
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases, Vol 15, Iss 1, Pp 1-15 (2020)
Orphanet Journal of Rare Diseases, Vol 15, Iss 1, Pp 1-15 (2020)
Background Congenital hemolytic anemia constitutes a heterogeneous group of rare genetic disorders of red blood cells. Diagnosis is based on clinical data, family history and phenotypic testing, genetic analyses being usually performed as a late step
Autor:
Murielle François, Isabelle Rosa, Valérie Ortonne, Mélanie Wlassow, Christophe Hézode, Stéphane Chevaliez, Jean-Michel Pawlotsky
Publikováno v:
Journal of Clinical Virology. 141:104873