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Journal Abstract Search

374 related items for PubMed ID: 19686300

  • 1. Stabilization of blood methylmalonic acid level in methylmalonic acidemia after liver transplantation.
    Chen PW, Hwu WL, Ho MC, Lee NC, Chien YH, Ni YH, Lee PH.
    Pediatr Transplant; 2010 May; 14(3):337-41. PubMed ID: 19686300
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  • 2. Current role of liver transplantation for methylmalonic acidemia: a review of the literature.
    Kasahara M, Horikawa R, Tagawa M, Uemoto S, Yokoyama S, Shibata Y, Kawano T, Kuroda T, Honna T, Tanaka K, Saeki M.
    Pediatr Transplant; 2006 Dec; 10(8):943-7. PubMed ID: 17096763
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  • 3. [Analysis of propionylcarnitine in blood and methylmalonic acid in urine of 162 patients with methylmalonic acidemia].
    Wu SN, Han LS, Ye J, Qiu WJ, Zhang HW, Gao XL, Wang Y, Li XY, Xu H, Gu XF.
    Zhonghua Yi Xue Za Zhi; 2013 Feb 26; 93(8):561-5. PubMed ID: 23663331
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  • 4. [Carnitine in the treatment of methylmalonic aciduria (MMA)].
    Penn D, Schmidt H, Otten A, Schmidt-Sommerfeld E.
    Monatsschr Kinderheilkd; 1986 Oct 26; 134(10):758-61. PubMed ID: 2879226
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  • 5. Brain damage by mild metabolic derangements in methylmalonic acidemia.
    Lee NC, Chien YH, Peng SF, Huang AC, Liu TT, Wu AS, Chen LC, Hsu LW, Tseng SC, Hwu WL.
    Pediatr Neurol; 2008 Nov 26; 39(5):325-9. PubMed ID: 18940555
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  • 6. [Analysis of the MUT gene mutations in patients with methylmalonic acidemia].
    Wang F, Han L, Ye J, Qiu W, Zhang Y, Gao X, Wang Y, Yang Y, Gu X.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2009 Oct 26; 26(5):485-9. PubMed ID: 19806564
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  • 10. Simultaneous quantification of acylcarnitine isomers containing dicarboxylic acylcarnitines in human serum and urine by high-performance liquid chromatography/electrospray ionization tandem mass spectrometry.
    Maeda Y, Ito T, Suzuki A, Kurono Y, Ueta A, Yokoi K, Sumi S, Togari H, Sugiyama N.
    Rapid Commun Mass Spectrom; 2007 Oct 26; 21(5):799-806. PubMed ID: 17279485
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  • 13. Clinical presentation, molecular analysis and follow-up of patients with mut methylmalonic acidemia in Shandong province, China.
    Han B, Nie W, Sun M, Liu Y, Cao Z.
    Pediatr Neonatol; 2020 Apr 26; 61(2):148-154. PubMed ID: 31466887
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  • 15. Progressive neurologic disability in methylmalonic acidemia despite transplantation of the liver.
    Nyhan WL, Gargus JJ, Boyle K, Selby R, Koch R.
    Eur J Pediatr; 2002 Jul 26; 161(7):377-9. PubMed ID: 12111189
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  • 16. Preoperative dialysis for liver transplantation in methylmalonic acidemia.
    Kamei K, Ito S, Shigeta T, Sakamoto S, Fukuda A, Horikawa R, Saito O, Muguruma T, Nakagawa S, Iijima K, Kasahara M.
    Ther Apher Dial; 2011 Oct 26; 15(5):488-92. PubMed ID: 21974703
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  • 17. Methylmalonic semialdehyde dehydrogenase deficiency: psychomotor delay and methylmalonic aciduria without metabolic decompensation.
    Roe CR, Struys E, Kok RM, Roe DS, Harris RA, Jakobs C.
    Mol Genet Metab; 1998 Sep 26; 65(1):35-43. PubMed ID: 9787093
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  • 19. Molecular basis of methylmalonyl-CoA mutase apoenzyme defect in 40 European patients affected by mut(o) and mut- forms of methylmalonic acidemia: identification of 29 novel mutations in the MUT gene.
    Acquaviva C, Benoist JF, Pereira S, Callebaut I, Koskas T, Porquet D, Elion J.
    Hum Mutat; 2005 Feb 26; 25(2):167-76. PubMed ID: 15643616
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