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7. Congenital defect in intracellular cobalamin metabolism resulting in homocysteinuria and methylmalonic aciduria. I. Case report and histopathology. Baumgartner ER; Wick H; Maurer R; Egli N; Steinmann B Helv Paediatr Acta; 1979; 34(5):465-82. PubMed ID: 528229 [TBL] [Abstract][Full Text] [Related]
8. [Selective malabsorption of vitamin B 12 (Imerslund's disease) and its treatment. Apropos of 2 cases]. Odievre M; Pigot JY Arch Fr Pediatr; 1975 Feb; 32(2):185-9. PubMed ID: 1217951 [TBL] [Abstract][Full Text] [Related]
9. [A case of metabolic encephalopathy caused by vitamin B 12-dependent methylmalonicaciduria]. Capece G; Giliberti P; Militerni R; Pignero A Acta Neurol Quad (Napoli); 1981; 42():254-9. PubMed ID: 7270059 [No Abstract] [Full Text] [Related]
10. Cobalamin C mutation (methylmalonic aciduria and homocystinuria) in adolescence. A treatable cause of dementia and myelopathy. Shinnar S; Singer HS N Engl J Med; 1984 Aug; 311(7):451-4. PubMed ID: 6749192 [No Abstract] [Full Text] [Related]
11. [Methylmalonic aciduria. Study of its occurrence in clinical material]. Kastrup KW Ugeskr Laeger; 1968 Jun; 130(25):1056-8. PubMed ID: 4302991 [No Abstract] [Full Text] [Related]
12. Management of megaloblastic anaemia in the very young. Chanarin I Br J Haematol; 1983 Jan; 53(1):1-3. PubMed ID: 6848114 [No Abstract] [Full Text] [Related]
13. Participation of vitamin B 12 in enzymatic regulation. Excretion of methylmalonic acid in vitamin B 12 deficiency. Wysocki K; Hansz J; Fenrych W Pol Med J; 1969; 8(1):62-6. PubMed ID: 5782171 [No Abstract] [Full Text] [Related]
14. [Megaloblastic anemia of the Imerslund-Naiman-Grasbeck type]. Burdzińska-Golowin J; Matheisel K; Sadowska L; Wojakiewicz R Pediatr Pol; 1975 Jan; 50(1):87-90. PubMed ID: 1110851 [No Abstract] [Full Text] [Related]