Diagnostic Utility of Next-Generation Sequencing for Unconjugated Hyperbilirubinemia in Children. [PDF]
Pediatr Gastroenterol Hepatol NutrKim HJ.
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Correction: Identification of a novel <i>ANK1</i> gene variant c.1504-9G>A and its mechanism of intron retention in hereditary spherocytosis. [PDF]
Front GenetXiong T +6 more
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Case Report: Abnormally low hemoglobin A1c in a diabetic patient with <i>SLC4A1</i> gene mutation. [PDF]
Front Endocrinol (Lausanne)Ye L, Ren Q, Ba T, Wu J, Han X, Ji L.
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Moyamoya syndrome associated with hereditary spherocytosis: pathogenesis, management, and an illustrative case with rapid radiological progression. [PDF]
Childs Nerv SystYan L, Lu X, Yang B, Ma Y.
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Editorial: Recent advances in pediatric red blood cells disorders
Frontiers in PediatricsGabriele Canciani +6 more
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De novo mutations in ANK1 and SPTB cause hereditary spherocytosis: three case reports and literature review. [PDF]
Ann HematolQin Y +6 more
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Hereditary Spherocytosis: Linking Ion Transport Defects to Osmotic Gradient Ektacytometry Profiles-A Review. [PDF]
Int J Mol SciVives-Corrons JL, Krishnevskaya E.
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From Splenectomy to Partial Splenic Embolization, Which is Better for Hereditary Spherocytosis? [PDF]
J Blood MedSi M, Yang S, Chen Z, Dou A.
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Optimal Corticosteroid Therapy Based on Liver Biopsy for Severe Immune-Mediated Hepatitis During Pembrolizumab Treatment: A Case Report. [PDF]
CureusEsaki K +4 more
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Parvovirus B19-Induced Aplastic Crisis and Hemophagocytic Lymphohistiocytosis in a Child With Hereditary Spherocytosis. [PDF]
CureusOyama M +4 more
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