[Analysis of 12 cases with methylmalonicacidemia cblA type].
E H, Han L, Ye J, Qiu W, Zhang H, Liang L, Wang Y, Wang J, Ji W, Chen T, Xu F, Gu X.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2020 Feb 10;37(2):101-105. doi: 10.3760/cma.j.issn.1003-9406.2020.02.001.
Methylmalonicacidemia: biochemical heterogeneity in defects of 5'-deoxyadenosylcobalamin synthesis.
Mahoney MJ, Hart AC, Steen VD, Rosenberg LE.
Proc Natl Acad Sci U S A. 1975 Jul;72(7):2799-803. doi: 10.1073/pnas.72.7.2799.
[13C]Valine metabolism in methylmalonicacidemia using nuclear magnetic resonance: propinonate as an obligate intermediate.
Tanaka K, Armitage IM, Ramsdell HS, Hsia YE, Lipsky SR, Rosenberg LE.
Proc Natl Acad Sci U S A. 1975 Sep;72(9):3692-6. doi: 10.1073/pnas.72.9.3692.
Pregnancy in a methylmalonic acidemia patient with kidney transplantation: a case report.
Lubrano R, Bellelli E, Gentile I, Paoli S, Carducci C, Carducci C, Santagata S, Pérez B, Ugarte M, Labriola D, Elli M.
Am J Transplant. 2013 Jul;13(7):1918-22. doi: 10.1111/ajt.12282. Epub 2013 May 24.
Inborn errors of cobalamin metabolism: effect of cobalamin supplementation in culture on methylmalonyl CoA mutase activity in normal and mutant human fibroblasts.
Willard HF, Rosenberg LE.
Biochem Genet. 1979 Feb;17(1-2):57-75. doi: 10.1007/BF00484474.
Genetic complementation in heterokaryons of human fibroblasts defective in cobalamin metabolism.
Gravel RA, Mahoney MJ, Ruddle FH, Rosenberg LE.
Proc Natl Acad Sci U S A. 1975 Aug;72(8):3181-5. doi: 10.1073/pnas.72.8.3181.
Rapid prenatal and postnatal detection of inborn errors of propionate, methylmalonate, and cobalamin metabolism: a sensitive assay using cultured cells.
Willard HF, Ambani LM, Hart AC, Mahoney MJ, Rosenberg LE.
Hum Genet. 1976 Dec 15;34(3):277-83. doi: 10.1007/BF00295291.
Effects of postnatal methylmalonate administration on neurobehavioral development of rats.
Mello CF, Somer JE, Tavaroni V, Graciolli R, Wu V, Torres G, Aguiar F, Wajner M, Wannmacher CM.
Braz J Med Biol Res. 1994 Mar;27(3):655-61.
