Kolexia
Pissard Serge
Biologie médicale
Hôpital Henri Mondor
Créteil, France
89 Activités
9 Followers

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{{person.topmesh1.name}} Thalassémie Anémie Drépanocytose Bêta-Thalassémie Alpha-Thalassémie Hémoglobinopathies Déficit en glucose-6-phosphate-déshydrogénase Hémolyse Anémie hémolytique

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WorldOne
1 collaboration(s)
Dernière en 2020
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Dernières activités

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.
American journal of hematology   26 octobre 2023
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.
International journal of laboratory hematology   04 juillet 2023
Prenatal management of fetal anemia due to pyruvate kinase deficiency: A case report.
Transfusion   08 novembre 2022
Homozygosity for the hyperunstable hemoglobin variant Hb Agrinio (HBA2:c.89T>C) leads to severe antenatal anemia: Eight new cases in three families.
American journal of hematology   02 septembre 2022
Syndromes thalassémiques majeurs et intermédiaires
HAS Publications   29 juillet 2021
A new gene associated with a β-thalassemia phenotype: the observation of variants in SUPT5H.
Blood   14 juin 2021
HbF-promoting polymorphisms may specifically reduce the residual risk of cerebral vasculopathy in SCA children with alpha-thalassemia.
Clinical hemorheology and microcirculation   21 mai 2021
Le déficit en G6PD
Journal de pediatrie et de puericulture   19 mai 2021
Clinically relevant updates of the HbVar database of human hemoglobin variants and thalassemia mutations.
Nucleic acids research   28 janvier 2021
Hb Angers: A new α2-globin variant α2 (140)(HC2) Tyr → Ser; HBA2: C.422 A>C with increased oxygen affinity leading to erythrocytosis.
International journal of laboratory hematology   20 novembre 2020