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Serge Pissard

Explore the profile of Serge Pissard including associated specialties, affiliations and a list of published articles. Areas
Snapshot
Articles 76
Citations 607
Followers 0
Related Specialties
Hematology
Biochemistry
Biology
Top 10 Co-Authors
Frederic Galacteros
Philippe Joly
Henri Wajcman
Catherine Badens
Michel Goossens
Christian Rose
Patricia Aguilar-Martinez
Cecile Arnaud
Veronique Baudin-Creuza
Mariane De Montalembert
Published In
Hemoglobin
Am J Hematol
Haematologica
Blood
Br J Haematol
Affiliations
Soon will be listed here.
Recent Articles
1.
Marked microcytosis and increased transferrin saturation: Think about variants in SLC11A2 (DMT1)
Raynor A, Peoch K, Boi C, Manceau H, Pissard S, Diallo K, et al.
Blood Cells Mol Dis . 2024 Nov; 110:102898. PMID: 39531753
Congenital microcytic anemias are rare diseases associated with decreased hemoglobin synthesis and red blood cells of low corpuscular volume. DMT1/NRAMP2 is a highly conserved divalent cation transporter encoded by the...
2.
Prognostic significance of early acute splenic sequestration in children with severe sickle cell genotypes: A comprehensive longitudinal neonatal cohort study
Soulie A, Arnaud C, Pissard S, Hau I, Shum M, Madhi F, et al.
Am J Hematol . 2024 Nov; 100(1):176-179. PMID: 39487586
No abstract available.
3.
High risk of progression for chronic major organ complications of sickle cell disease in adolescents and young adults: A long-term neonatal cohort study
Borgey M, Genty I, Habibi A, Arlet J, Dhedin N, Lionnet F, et al.
Am J Hematol . 2024 Apr; 99(8):1601-1605. PMID: 38686944
No abstract available.
4.
Clinical events in a long-term prospective neonatal cohort of children with sickle cell disease: Evidence for a high disease burden without systematic preventive intensification with hydroxyurea
Soulie A, Kamdem A, Neumann F, Hau I, Madhi F, Delestrain C, et al.
Am J Hematol . 2023 Oct; 98(12):E395-E398. PMID: 37883505
No abstract available.
5.
A high level of Hb F unmasks a new case of Hb Wanjiang (β (F3-F4) Ala87_Thr88delinsSer_Gln (HBB:c.255_264 delinsTTTTTCTCAG)) in a pregnant woman of African ancestry
Pissard S, Moyrand C, Peron A, Bodereau V, Bichr A, El Osta M, et al.
Int J Lab Hematol . 2023 Jul; 45(6):990-994. PMID: 37402598
No abstract available.
6.
Prenatal management of fetal anemia due to pyruvate kinase deficiency: A case report
Maisonneuve E, Sohier Lepine M, Maurice P, Pissard S, Lafon B, Mailloux A, et al.
Transfusion . 2022 Nov; 63(1):257-262. PMID: 36349479
Background: Pyruvate Kinase (PK) deficiency is the most common enzyme defect of glycolysis, leading to congenital hemolytic anemia, which can occur during the neonatal period. Study Design And Methods: We...
7.
Homozygosity for the hyperunstable hemoglobin variant Hb Agrinio (HBA2:c.89T>C) leads to severe antenatal anemia: Eight new cases in three families
Szepetowski S, Berger C, Joly P, Baron-Joly S, Huguenin Y, Cantais A, et al.
Am J Hematol . 2022 Sep; 97(11):E393-E395. PMID: 36052950
No abstract available.
8.
Hb Angers: A new α2-globin variant [α2 (140)(HC2) Tyr → Ser; HBA2: C.422 A>C] with increased oxygen affinity leading to erythrocytosis
Orvain C, Kiger L, Peronet I, Peron A, Galacteros F, Wajcman H, et al.
Int J Lab Hematol . 2020 Nov; 43(3):e114-e117. PMID: 33217156
No abstract available.
9.
HbF-promoting polymorphisms may specifically reduce the residual risk of cerebral vasculopathy in SCA children with alpha-thalassemia
Joly P, Bonello-Palot N, Badens C, Pissard S, Chamouine A, Bernaudin F, et al.
Clin Hemorheol Microcirc . 2020 Nov; 77(3):267-272. PMID: 33216016
Sickle cell anemia (SCA) is a disease characterized by abnormal red blood cell rheology. Because of their effects on HbS polymerization and red blood cell deformability, alpha-thalassemia and the residual...
10.
Clinically relevant updates of the HbVar database of human hemoglobin variants and thalassemia mutations
Giardine B, Joly P, Pissard S, Wajcman H, Chui D, Hardison R, et al.
Nucleic Acids Res . 2020 Oct; 49(D1):D1192-D1196. PMID: 33125055
HbVar (http://globin.bx.psu.edu/hbvar) is a widely-used locus-specific database (LSDB) launched 20 years ago by a multi-center academic effort to provide timely information on the numerous genomic variants leading to hemoglobin variants...