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Revue du Praticien, ISSN 0035-2640, 10/2014, Volume 64, Issue 8, pp. 457 - 468
Journal Article
La Revue du praticien, ISSN 0035-2640, 10/2014, Volume 64, Issue 8, pp. 1110 - 1111
Journal Article
Revue du Praticien, ISSN 0035-2640, 10/2014, Volume 64, Issue 8, p. 1222
Journal Article
La Revue du praticien, ISSN 0035-2640, 10/2014, Volume 64, Issue 8, pp. 1108 - 1109
Journal Article
La Revue du praticien, ISSN 0035-2640, 10/2014, Volume 64, Issue 8, p. 1108
Journal Article
The New England Journal of Medicine, ISSN 0028-4793, 03/2017, Volume 376, Issue 9, pp. 848 - 855
Journal Article
Revue du Praticien, ISSN 0035-2640, 10/2014, Volume 64, Issue 8, pp. 1120 - 1126
Journal Article
La Revue du praticien, ISSN 0035-2640, 10/2014, Volume 64, Issue 8, p. 1120
Chronic complications of sickle cell disease take an increasing role in the management of patients due to their morbidity and mortality impact. The prevalence... 
Cardiovascular Diseases - etiology | Anemia, Sickle Cell - complications | Humans | Female | Male | Chronic Disease | Cerebrovascular Disorders - etiology
Journal Article
Clinical Science, ISSN 0143-5221, 08/2013, Volume 125, Issue 4, pp. 199 - 210
Journal Article
Journal Article
American Journal of Hematology, ISSN 0361-8609, 05/2019, Volume 94, Issue 5, pp. 522 - 527
Sickle cell disease (SCD) is the most common monogenic disorder in the world. Notably, there is extensive clinical heterogeneity in SCD that cannot be fully... 
RISK-FACTORS | PAIN | ACUTE CHEST SYNDROME | GENETIC INFLUENCES | HEREDITARY PERSISTENCE | HEMATOLOGY | CHILDREN | Medical research | Sickle cell anemia | Medicine, Experimental | Hemoglobin | Kidney diseases | Research institutes | Blood cell count | Risk factors
Journal Article
British Journal of Haematology, ISSN 0007-1048, 11/2017, Volume 179, Issue 4, pp. 627 - 634
Journal Article
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