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2. Methylmalonic aciduria (1 case report). Yuan LF, Zhao SM, Luo HY, Huang XH, Guo YZ, Xu JZ, Xu YY. Proc Chin Acad Med Sci Peking Union Med Coll; 1987 May; 2(3):183-5. PubMed ID: 3444838 [No Abstract] [Full Text] [Related]
3. [Methylmalonic aciduria - diagnosis and therapy using as example 2 cases of this genetic metabolic disorder]. Lubs H, Seidlitz G, Pfau E. Padiatr Grenzgeb; 1982 May; 21(4):319-26. PubMed ID: 7177670 [No Abstract] [Full Text] [Related]
4. [Pharmacologic and dietetic treatment of 2 siblings with atypical methylmalonic aciduria]. Duillo MT, Poggi L, Cortese M, de Toni T, Di Rocco M. Minerva Pediatr; 1984 Oct 31; 36(20):999-1002. PubMed ID: 6531009 [No Abstract] [Full Text] [Related]
5. Corneal involvement in methylmalonic aciduria. Haney ML, Jeffrey CP, Cavanagh HD. Ann Ophthalmol; 1981 Jan 31; 13(1):81-3. PubMed ID: 7247163 [No Abstract] [Full Text] [Related]
6. [Carnitine in the treatment of methylmalonic aciduria (MMA)]. Penn D, Schmidt H, Otten A, Schmidt-Sommerfeld E. Monatsschr Kinderheilkd; 1986 Oct 31; 134(10):758-61. PubMed ID: 2879226 [Abstract] [Full Text] [Related]
16. Methylmalonic aciduria in a black female child with congenital short femur on the right side. Meiring JL, Strydom AJ. J Inherit Metab Dis; 1981 Mar 31; 4(2):107-8. PubMed ID: 6790839 [No Abstract] [Full Text] [Related]
18. 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 16; 311(7):451-4. PubMed ID: 6749192 [No Abstract] [Full Text] [Related]