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Serge Pissard

Showing results (11-20 of 63) with videos related to

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Haematologica|September 12, 2006
Beta-thalassemia in the indigenous population of Brittany: identification of three rare mutationsDéborah Jamet, Serge Pissard, Marie-Thérèse Blouch, et al.
Hemoglobin|February 1, 2019
Short in-Frame Insertions/Deletions in the Coding Sequence of the α-Globin Gene. Consequences of the 3D Structure and Resulting Phenotypes: Hb Choisy as an ExampleHenri Wajcman, Alexandre G de Brevern, Jean Riou, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|September 18, 2012
Characterization of three new deletions in the β-globin gene cluster during a screening survey in two French urban areasSerge Pissard, Valérie Raclin, Philippe Lacan, et al.
Blood|August 25, 2012
Erythrocyte density in sickle cell syndromes is associated with specific clinical manifestations and hemolysisPablo Bartolucci, Carlo Brugnara, Armando Teixeira-Pinto, et al.
Blood Cells, Molecules & Diseases|November 12, 2024
Marked microcytosis and increased transferrin saturation: Think about variants in SLC11A2 (DMT1)Alexandre Raynor, Katell Peoc'h, Camille Boi, et al.
Blood Advances|March 21, 2018
Biological impact of α genes, β haplotypes, and G6PD activity in sickle cell anemia at baseline and with hydroxyureaFrançoise Bernaudin, Cécile Arnaud, Annie Kamdem, et al.
Hemoglobin|August 21, 2015
Congenital Recessive Methemoglobinemia Revealed in Adulthood: Description of a New Mutation in Cytochrome b5 Reductase GeneAlexandra Forestier, Serge Pissard, Justine Cretet, et al.
Hemoglobin|August 24, 2005
Two French Caucasian families with dominant thalassemia-like phenotypes due to hyper unstable hemoglobin variants: Hb Sainte Seve [codon 118 (-T)] and codon 127 [CAG-->TAG (Gln-->stop])Claude Préhu, Serge Pissard, Maha Al-Sheikh, et al.
Hematology (Amsterdam, Netherlands)|December 21, 2011
First reported case of prenatal diagnosis for pyruvate kinase deficiency in a Chinese familyChi-Chiu So, Mary Tang, Chak-Ho Li, et al.
Fetal and Pediatric Pathology|May 21, 2014
Hemolytic anemia and progressive neurologic impairment: think about triosephosphate isomerase deficiencyKhaoula Aissa, Fatma Kamoun, Lamia Sfaihi, et al.
Pageof 7

Showing results (11-20 of 63) with videos related to

Sort By:
Pageof 7
Haematologica|September 12, 2006
Beta-thalassemia in the indigenous population of Brittany: identification of three rare mutationsDéborah Jamet, Serge Pissard, Marie-Thérèse Blouch, et al.
Hemoglobin|February 1, 2019
Short in-Frame Insertions/Deletions in the Coding Sequence of the α-Globin Gene. Consequences of the 3D Structure and Resulting Phenotypes: Hb Choisy as an ExampleHenri Wajcman, Alexandre G de Brevern, Jean Riou, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|September 18, 2012
Characterization of three new deletions in the β-globin gene cluster during a screening survey in two French urban areasSerge Pissard, Valérie Raclin, Philippe Lacan, et al.
Blood|August 25, 2012
Erythrocyte density in sickle cell syndromes is associated with specific clinical manifestations and hemolysisPablo Bartolucci, Carlo Brugnara, Armando Teixeira-Pinto, et al.
Blood Cells, Molecules & Diseases|November 12, 2024
Marked microcytosis and increased transferrin saturation: Think about variants in SLC11A2 (DMT1)Alexandre Raynor, Katell Peoc'h, Camille Boi, et al.
Blood Advances|March 21, 2018
Biological impact of α genes, β haplotypes, and G6PD activity in sickle cell anemia at baseline and with hydroxyureaFrançoise Bernaudin, Cécile Arnaud, Annie Kamdem, et al.
Hemoglobin|August 21, 2015
Congenital Recessive Methemoglobinemia Revealed in Adulthood: Description of a New Mutation in Cytochrome b5 Reductase GeneAlexandra Forestier, Serge Pissard, Justine Cretet, et al.
Hemoglobin|August 24, 2005
Two French Caucasian families with dominant thalassemia-like phenotypes due to hyper unstable hemoglobin variants: Hb Sainte Seve [codon 118 (-T)] and codon 127 [CAG-->TAG (Gln-->stop])Claude Préhu, Serge Pissard, Maha Al-Sheikh, et al.
Hematology (Amsterdam, Netherlands)|December 21, 2011
First reported case of prenatal diagnosis for pyruvate kinase deficiency in a Chinese familyChi-Chiu So, Mary Tang, Chak-Ho Li, et al.
Fetal and Pediatric Pathology|May 21, 2014
Hemolytic anemia and progressive neurologic impairment: think about triosephosphate isomerase deficiencyKhaoula Aissa, Fatma Kamoun, Lamia Sfaihi, et al.
Pageof 7