Individual red blood cell fetal hemoglobin quantification allows to determine protective thresholds in sickle cell disease-Reference-Cited by-同舟云学术

Individual red blood cell fetal hemoglobin quantification allows to determine protective thresholds in sickle cell disease

Published:2020-08-25 Issue:11 Volume:95 Page:1235-1245
ISSN:0361-8609
Container-title:American Journal of Hematology
language:en
Short-container-title:Am J Hematol

Author:

Hebert Nicolas¹²³^ORCID,Rakotoson Marie Georgine¹,Bodivit Gwellaouen¹²,Audureau Etienne³,Bencheikh Laura¹³,Kiger Laurent¹³,Oubaya Nadia⁴,Pakdaman Sadaf¹²,Sakka Mehdi⁴,Di Liberto Gaetana¹²,Chadebech Philippe¹²^ORCID,Vingert Benoit¹²^ORCID,Pirenne France¹²^ORCID,Galactéros Frédéric¹³,Cambot Marie⁵,Bartolucci Pablo¹³

Affiliation:

1. Institut Mondor de Recherche Biomédicale, Unité 955, team Pirenne, INSERM, EFS, UPEC, Laboratory of excellence LABEX GRex Créteil France

2. Etablissement Français du Sang, Île‐de‐France, Hôpital Henri Mondor Créteil France

3. Sickle cell referral center, UMGGR Plateforme d'expertise Maladies Rares Grand Paris Est, UPEC Hôpitaux Universitaires Henri Mondor, APHP Créteil France

4. Hôpital Henri Mondor Assistance Publique‐Hôpitaux De Paris (APHP), Université Paris‐Est Créteil Créteil France

5. UMR_S1134, Université Sorbonne Paris Cité, Université Paris Diderot, Inserm, INTS, Unité Biologie Intégrée du Globule Rouge, Laboratory of excellence LABEX GRex Paris France

Publisher

Wiley

Subject

Hematology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ajh.25937

Reference50 articles.

1. Hydroxyurea for the Treatment of Sickle Cell Anemia

2. The effect of prolonged administration of hydroxyurea on morbidity and mortality in adult patients with sickle cell syndromes: results of a 17-year, single-center trial (LaSHS)

3. Lack of influence of fetal hemoglobin levels or erythrocyte indices on the severity of sickle cell anemia.

4. The Senegal DNA haplotype is associated with the amelioration of anemia in African-American sickle cell anemia patients

5. Is there a threshold level of fetal hemoglobin that ameliorates morbidity in sickle cell anemia?

Cited by 19 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Oxygen gradient ektacytometry–derived biomarkers are associated with acute complications in sickle cell disease;Blood Advances;2024-01-10

2. High-throughput quantification of red blood cell deformability and oxygen saturation to probe mechanisms of sickle cell disease;Proceedings of the National Academy of Sciences;2023-11-20

3. C2H2 Zinc Finger Transcription Factors Associated with Hemoglobinopathies;Journal of Molecular Biology;2023-11

4. Exploration de l’hémolyse associée à la drépanocytose et perspectives thérapeutiques spécifiques;La Revue de Médecine Interne;2023-11

5. Genetic reversal of the globin switch concurrently modulates both fetal and sickle hemoglobin and reduces red cell sickling;Nature Communications;2023-09-20