Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Georges Nouadje"'
Autor:
Randa Bittar, Alain Carrié, Georges Nouadje, Corinne Cherfils, Valérie Fesel-Fouquier, Laurence Barbot-Trystram, Philippe Giral, Dominique Bonnefont-Rousselot
Publikováno v:
Practical Laboratory Medicine, Vol 18, Iss , Pp - (2020)
A qualitative, semi-automatized method for apolipoprotein E (apoE) phenotyping by isoelectric focusing method has been evaluated on 40 serum samples from patients previously genotyped for apoE, especially as regards concordance with genotyping, but a
Externí odkaz:
https://doaj.org/article/befe669d18fb49a0abf8550989c4a3d6
Autor:
C. Cherfils, Laurence Barbot-Trystram, Georges Nouadje, Philippe Giral, Dominique Bonnefont-Rousselot, Randa Bittar, Valérie Fesel-Fouquier, Alain Carrié
Publikováno v:
Practical Laboratory Medicine
Practical Laboratory Medicine, Elsevier, 2020, 18, pp.e00150-. ⟨10.1016/j.plabm.2019.e00150⟩
Practical Laboratory Medicine, 2020, 18, pp.e00150. ⟨10.1016/j.plabm.2019.e00150⟩
Practical Laboratory Medicine, Vol 18, Iss, Pp-(2020)
Practical Laboratory Medicine, Elsevier, 2020, 18, pp.e00150-. ⟨10.1016/j.plabm.2019.e00150⟩
Practical Laboratory Medicine, 2020, 18, pp.e00150. ⟨10.1016/j.plabm.2019.e00150⟩
Practical Laboratory Medicine, Vol 18, Iss, Pp-(2020)
A qualitative, semi-automatized method for apolipoprotein E (apoE) phenotyping by isoelectric focusing method has been evaluated on 40 serum samples from patients previously genotyped for apoE, especially as regards concordance with genotyping, but a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0c6e94ea6828186e728a0eff66201e6b
https://hal.archives-ouvertes.fr/hal-03489268
https://hal.archives-ouvertes.fr/hal-03489268
Autor:
Sandrine Macé, Greg Finn, Marie-Thérèse Melki, Georges Nouadje, Samia Menad, Ruiyin Chu, Helgi van de Velde
Publikováno v:
Blood. 136:15-15
Introduction Evaluation of multiple myeloma (MM) response through quantification of M-protein, by serum protein electrophoresis (SPEP) and immuno-fixation electrophoresis (IFE) is challenging for clinical laboratories because therapeutic monoclonal a
Autor:
Galina Zemtsovskaja, Hector Bautista, Valdas Banys, Marika Pikta, Margus Viigimaa, Georges Nouadje, Timea Szanto
BackgroundThe von Willebrand factor (VWF) multimer test is required to correctly subtype qualitative type 2 von Willebrand disease (VWD). The current VWF multimer assays are difficult, nonstandardized, and time-consuming. The purpose of this study wa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ac07a212e1f7553e29e15b3044783579
https://europepmc.org/articles/PMC6816851/
https://europepmc.org/articles/PMC6816851/
Autor:
Pascal Philibert, Georges Nouadje, Sandrine Mary, Jérôme Vialaret, Constance Delaby, Audrey Gabelle, Pascale Benlian, Sylvain Lehmann, Susanna Schraen, Laurent Tiers, Christophe Hirtz, Pauline Bros
Publikováno v:
Clinica Chimica Acta
Clinica Chimica Acta, Elsevier, 2016, 454, pp.33-38. ⟨10.1016/j.cca.2015.12.020⟩
Clinica Chimica Acta, 2016, 454, pp.33-38. ⟨10.1016/j.cca.2015.12.020⟩
Clinica Chimica Acta, Elsevier, 2016, 454, pp.33-38. ⟨10.1016/j.cca.2015.12.020⟩
Clinica Chimica Acta, 2016, 454, pp.33-38. ⟨10.1016/j.cca.2015.12.020⟩
Background Apolipoprotein E (Apo E) is a 36 Kda glycoprotein involved in lipid transport. It exists in 3 major isoforms: E2, E3 and E4. ApoE status is known to be a major risk factor for late-onset Alzheimer's and cardiovascular diseases. Genotyping
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::18183345cec8bdd83577b2930bd06c9d
https://hal.umontpellier.fr/hal-01842388
https://hal.umontpellier.fr/hal-01842388
Autor:
Anita Vergne, Marie-Françoise Odou, Jean-Jacques Lafitte, Philippe Joly, Georges Nouadje, Denis Roche, Nicole Porchet, Philippe Beaune, Malika Balduyck, Colette Chapuis Cellier, Vincent Madelain, Farid Zerimech
Publikováno v:
Annales de Biologie Clinique
Annales de Biologie Clinique, John Libbey Eurotext, 2014, 72 (6), pp.689-704. ⟨10.1684/abc.2014.1004⟩
Annales de Biologie Clinique, John Libbey Eurotext, 2014, 72 (6), pp.689-704. ⟨10.1684/abc.2014.1004⟩
Alpha- 1-antitrypsin (A1AT) deficiency is a hereditary autosomal codominant genetic disorder resulting in low circulating levels of A1AT and leading to lung and/or liver disease. It remains underdiagnosed and only 5 to 10% of PIZZ patients, the most
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8636dc7c161b29c0906b7eefb440b5f0
https://hal.archives-ouvertes.fr/hal-02368056
https://hal.archives-ouvertes.fr/hal-02368056
Autor:
Georges Nouadje, Kate Sasser, Thomas Dejoie, Jason S. Simon, Alix Irimia, Hélène Caillon, Philippe Moreau, Thierry Ligneel, Matthew James Scullion, Amy Axel
Publikováno v:
Blood. 128:2063-2063
Background : Detection and quantification of monoclonal component (M-spike) by serum protein electrophoresis (SPE) and immunofixation (IFE) are essential for response evaluation in multiple myeloma (MM) according to the International Myeloma Working