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Shibuya A. Congenital hemolytic anemia. Shonika Rinsho (Japanese Journal of Pediatrics) 62: 321-328, 2009 (in Japanese)."},{"key":"2","doi-asserted-by":"crossref","unstructured":"2. Perrotta S, Gallagher PG, Mohandas N. Hereditary spherocytosis. Lancet 372: 1411-1426, 2008.","DOI":"10.1016\/S0140-6736(08)61588-3"},{"key":"3","doi-asserted-by":"crossref","unstructured":"3. Tamary H, Aviner S, Freud E, et al. High incidence of early cholelithiasis detected by ultrasonography in children and young adults with hereditary spherocytosis. J Pediatr Hematol Oncol 25: 952-954, 2003.","DOI":"10.1097\/00043426-200312000-00009"},{"key":"4","doi-asserted-by":"crossref","unstructured":"4. Ruparel RK, Bogert JN, Mori CR, et al. Synchronous splenectomy during cholecystectomy for hereditary spherocytosis: is it really necessary? J Pediatr Surg 49: 433-435, 2014.","DOI":"10.1016\/j.jpedsurg.2013.05.012"},{"key":"5","unstructured":"5. Krueger HC, Burgert EO Jr. Hereditary spherocytosis in 100 children. Mayo Clin Proc 41: 821-830, 1966."},{"key":"6","doi-asserted-by":"crossref","unstructured":"6. Guarnone R, Centenara E, Zappa M, Zanella A, Barosi G. Erythropoietin production and erythropoiesis in compensated and anaemic states of hereditary spherocytosis. Br J Haematol 92: 150-154, 1996.","DOI":"10.1046\/j.1365-2141.1996.00285.x"},{"key":"7","doi-asserted-by":"crossref","unstructured":"7. Eber S, Lux SE. Hereditary spherocytosis: defects in proteins that connect the membrane skeleton to the lipid bilayer. Semin Hematol 41: 118-141, 2004.","DOI":"10.1053\/j.seminhematol.2004.01.002"},{"key":"8","doi-asserted-by":"crossref","unstructured":"8. Jensson O, Jónasson JL, Magnússon S. Studies on hereditary spherocytosis in Iceland. Acta Med Scand 201: 187-195, 1977.","DOI":"10.1111\/j.0954-6820.1977.tb15680.x"},{"key":"9","doi-asserted-by":"crossref","unstructured":"9. del Giudice EM, Perrotta S, Nobili B, Specchia C, d'Urzo G, Iolascon A. 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Iolascon A, Faienza MF, Moretti A, Perrotta S, Miraglia del Giudice E. UGT1 promoter polymorphism accounts for increased neonatal appearence of hereditary spherocytosis. Blood 91: 1093, 1998.","DOI":"10.1182\/blood.V91.3.1093"},{"key":"14","doi-asserted-by":"crossref","unstructured":"14. Owens D, Evans J. Population studies on Gilbert's syndrome. J Med Genet 12: 152-156, 1975.","DOI":"10.1136\/jmg.12.2.152"},{"key":"15","doi-asserted-by":"crossref","unstructured":"15. Lee MJ, Chang YH, Kang SH, et al. A case of hereditary spherocytosis coexisting with Gilbert's syndrome. Korean J Gastroenterol 61: 166-169, 2013.","DOI":"10.4166\/kjg.2013.61.3.166"},{"key":"16","doi-asserted-by":"crossref","unstructured":"16. Bader-Meunier B, Gauthier F, Archambaud F, et al. Long-term evaluation of the beneficial effect of subtotal splenectomy for management of hereditary spherocytosis. 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