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6. A Thai boy with hereditary enzymopenic methemoglobinemia type II. Shotelersuk V; Tosukhowong P; Chotivitayatarakorn P; Pongpunlert W J Med Assoc Thai; 2000 Nov; 83(11):1380-6. PubMed ID: 11215870 [TBL] [Abstract][Full Text] [Related]
7. Enzymopenic hereditary methemoglobinemia: a clinical/biochemical classification. Jaffé ER Blood Cells; 1986; 12(1):81-90. PubMed ID: 3539237 [TBL] [Abstract][Full Text] [Related]
12. A rare cause of mental motor retardation: recessive congenital methemoglobinemia type II. Yüksel D; Senbil N; Yilmaz D; Yarali N; Gürer YK Turk J Pediatr; 2009; 51(2):187-9. PubMed ID: 19480335 [TBL] [Abstract][Full Text] [Related]
13. Congenital methemoglobinemia due to NADH-methemoglobin reductase deficiency in three Indian families. Kedar PS; Colah RB; Ghosh K; Mohanty D Haematologia (Budap); 2002; 32(4):543-9. PubMed ID: 12803131 [TBL] [Abstract][Full Text] [Related]
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19. Generalized deficiency of the NADH-methemoglobin reductase in congenital methemoglobinemia with neurological symptoms. Jabłońska-Skwiecińska E; Holtorp-Tyszkiewiczowa J; Staniszewska K Biomed Biochim Acta; 1984; 43(6):S98-100. PubMed ID: 6487287 [TBL] [Abstract][Full Text] [Related]
20. [Hereditary methemoglobinemia with mental retardation and neurologic disorders. Clinical and biochemical study of a case]. Beauvais P; Leroux A; Kaplan JC Nouv Presse Med; 1976 Dec; 5(41):2793-5. PubMed ID: 995609 [No Abstract] [Full Text] [Related] [Next] [New Search]