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Journal Article
European Journal of Pediatrics, ISSN 0340-6199, 1/2016, Volume 175, Issue 1, pp. 147 - 149
Journal Article
British Journal of Haematology, ISSN 0007-1048, 07/2019, Volume 186, Issue 1, pp. 125 - 129
Summary The role of mast cells has been questioned in sickle cell disease (SCD). We performed a prospective study evaluating plasma histamine and tryptase... 
vaso‐occlusive crisis | mast cell activation | histamine | tryptase | sickle cell disease | vaso-occlusive crisis | ACTIVATION | HEMATOLOGY | Histamine | Sickle cell anemia | Elevation | Cell activation | Tryptase | Mast cells | Volatile organic compounds--VOCs | Sickle cell disease | Steady state
Journal Article
PLoS ONE, ISSN 1932-6203, 2011, Volume 6, Issue 10, p. e24117
Journal Article
Journal of Clinical Medicine, ISSN 2077-0383, 09/2019, Volume 8, Issue 9, p. 1481
Hepatobiliary complications in children with sickle cell disease (SCD) are rarely reported but can be life-threatening. We retrospectively assessed their... 
cholangiopathy | acute hepatic crisis | cholelithiasis | sickle cell hepatopathy
Journal Article
Journal Article
Cochrane Database of Systematic Reviews, ISSN 1469-493X, 02/2016, Volume 2016, Issue 2, p. CD011199
Journal Article
Expert Review of Hematology, ISSN 1747-4086, 11/2017, Volume 10, Issue 11, pp. 1023 - 1028
Introduction: Anemia in children is a major public health problem throughout the world. It is often multifactorial, iron deficiency being the most frequent... 
iron deficiency | Hematology | children | anemia | hemoglobin | SYSTEMATIC ANALYSIS | IRON-DEFICIENCY ANEMIA | HEREDITARY SPHEROCYTOSIS | IMPACT | INFANTS | GROWTH | COMPLICATIONS | SICKLE-CELL-DISEASE | SOLUBLE TRANSFERRIN RECEPTOR | BETA-THALASSEMIA
Journal Article
Journal of medical genetics, ISSN 0022-2593, 2011, Volume 48, Issue 6, pp. 417 - 421
Journal Article