Confounding Factors in the Diagnosis of Hereditary Spherocytosis and Gallstone Formation in Related Hemolytic Disorders From a Tertiary Care Center in North India. [PDF]
Athar R, Kashyap R, Gupta J.
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Case Report: Identification and functional characterization of a novel heterozygous splice-donor (c.647+1G>A) site mutation in the <i>SPTB</i> gene that causes hereditary spherocytosis with hemolytic anemia. [PDF]
Cao K +6 more
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Hereditary Spherocytosis: Review of Presentation at Birth. [PDF]
Achenjang NS +3 more
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Effect of case-based learning biochemistry among first-year medical students. [PDF]
Singh M, Singh G.
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A flow cytometric assay of murine erythrocyte osmotic fragility. [PDF]
Zhang P +6 more
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SPTA1-Related Hereditary Spherocytosis: Novel Compound Heterozygous Mutations With Severe Clinical Manifestation. [PDF]
Khor J, Boo YL.
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Editorial: Anemia in children: from nutritional deficits to genetic disorders. [PDF]
Mettananda S, Songdej D, Yasara N.
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Pediatric acute cholecystitis: Risk factors and outcomes. [PDF]
Burjonrappa SC, Blamon F, Hurley SP.
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Caught by Whole-Exome Sequencing: Hemoglobin Sun Prairie in a Patient With Unexplained Hemolytic Anemia From Nepal. [PDF]
Upadhaya P, Shrestha A.
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Association between hereditary spherocytosis and gallstone disease: Pathophysiology, diagnosis, and management. [PDF]
Cong S, Wang YN, Wang JR, Duan RH.
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