Sphérocytose héréditaire : recommandations pour le diagnostic et la prise en charge chez l’enfant
Author:
Publisher
Elsevier BV
Subject
Pediatrics, Perinatology, and Child Health
Reference57 articles.
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1. Genetic mutation analysis of hereditary spherocytosis in Guangxi Zhuang Autonomous Region;Journal of Hematopathology;2023-05-05
2. Screening for hereditary spherocytosis in daily practice: what is the best algorithm using erythrocyte and reticulocyte parameters?;Annals of Hematology;2022-04-22
3. Case 1: Rapidly Rising Bilirubin Level in a 3-day-old Term Infant;NeoReviews;2020-10-01
4. Expression néonatale d’un trait bêta-thalassémique associé à une sphérocytose héréditaire chez deux jumelles monozygotes;Archives de Pédiatrie;2017-02
5. Hereditary Spherocytosis - Diagnosis, Surgical Treatment and Outcomes. A Literature Review;Chirurgia;2017
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