Case Report: Clinical and genetic analysis of a family with hereditary spherocytosis combined with familial chylomicronemia syndrome. [PDF]
Qin Y +10 more
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Clinical Characteristics and Gene Mutations of Hereditary Spherocytosis in 59 Chinese Children. [PDF]
Li Y +7 more
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Hereditary Spherocytosis due to an SPTA1 Nonsense Mutation Coinherited With α spectrin<sup>LELY</sup> in Trans. [PDF]
Molina-Arrebola MA, Bain BJ.
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A novel <i>ANK1</i> frameshift mutation associated with neonatal hereditary spherocytosis: a case report. [PDF]
Qing X +5 more
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Molecular surprises in evaluations of red cell disorders. [PDF]
Elgammal Y, Zhang W, Kalfa TA.
europepmc +1 more source
Hereditary spherocytosis concomitant with JAK2V617F-positive primary myelofibrosis: a case report. [PDF]
Qiu CE, Lei L, Jiang G, Huang X, Li Y.
europepmc +1 more source
Genotype clinical phenotype analysis of 35 cases of hereditary spherocytosis in children. [PDF]
Duowen H, Xia G, Ju G.
europepmc +1 more source
Cognitive impairment in hereditary spherocytosis. [PDF]
Tartaglione I +12 more
europepmc +1 more source
In silico analysis of the invasion mechanics and invasiveness of the Plasmodium falciparum merozoite. [PDF]
Msosa C, Abdalrahman T, Franz T.
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A case report of hereditary spherocytosis complicated by massive splenomegaly and cholelithiasis. [PDF]
Sun Q, Yu Y, Song L, Liang L.
europepmc +1 more source

