Photo by Gije Cho on Pexels
Anemia Defisiensi Vitamin B12 akibat Malabsorpsi Selektif dengan Proteinuria (ICD-10: D51.1)
📚 Daftar Pustaka (APA 7)
[1]
Imerslund O. Idiopathic chronic megaloblastic anemia in children. Acta Paediatr Scand. 1960;49(Suppl 119):1-115.
[2]
Gräsbeck R, Gordin R, Kantero I, et al. Selective vitamin B12 malabsorption and proteinuria in young people. A nosological entity. Acta Med Scand. 1970;187(5):431-434.
[3]
Aminoff M, Carter JE, Chadwick RB, et al. Mutations in CUBN, encoding the intrinsic factor-vitamin B12 receptor, cubilin, cause hereditary megaloblastic anemia. Am J Hum Genet. 1999;65(1):180-185.
[4]
Heil SG, Lievers KJ, Beijers AM, et al. Vitamin B12 deficiency in African Americans with megaloblastic anemia. Ned Tijdschr Geneeskd. 2000;144(49):2333-2338.
[5]
WHO. Haemoglobin concentrations for the diagnosis of anaemia and assessment of severity. Geneva: World Health Organization; 2011.
[6]
Stabler SP. Vitamin B12 deficiency. N Engl J Med. 2013;368(2):149-160.