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Journal Abstract Search

126 related items for PubMed ID: 38314877

  • 21. Markers associated with inborn errors of metabolism of branched-chain amino acids and their relevance to upper levels of intake in healthy people: an implication from clinical and molecular investigations on maple syrup urine disease.
    Mitsubuchi H, Owada M, Endo F.
    J Nutr; 2005 Jun; 135(6 Suppl):1565S-70S. PubMed ID: 15930470
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  • 22. MR diffusion imaging and MR spectroscopy of maple syrup urine disease during acute metabolic decompensation.
    Jan W, Zimmerman RA, Wang ZJ, Berry GT, Kaplan PB, Kaye EM.
    Neuroradiology; 2003 Jun; 45(6):393-9. PubMed ID: 12736767
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  • 26. Thiamine response in maple syrup urine disease.
    Fernhoff PM, Lubitz D, Danner DJ, Dembure PP, Schwartz HP, Hillman R, Bier DM, Elsas LJ.
    Pediatr Res; 1985 Oct; 19(10):1011-6. PubMed ID: 3903643
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  • 28. Domino liver transplantation in maple syrup urine disease: a case report and review of the literature.
    Badell IR, Hanish SI, Hughes CB, Hewitt WR, Chung RT, Spivey JR, Knechtle SJ.
    Transplant Proc; 2013 Mar; 45(2):806-9. PubMed ID: 23267808
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  • 29. Long-term results of liver transplantation for maple syrup urine disease: A single-center experience in Turkey.
    Aras A, Avanaz A, Inan Aydemir N, Kayaalp E, Ulgen Tekerek N, Kisaoglu A, Demiryilmaz I, Soyucen E, Dursun O, Yilmaz A, Artan R, Aydinli B.
    Pediatr Transplant; 2023 May; 27(3):e14464. PubMed ID: 36588190
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  • 31. Organic acids and branched-chain amino acids in body fluids before and after multiple exchange transfusions in maple syrup urine disease.
    Shigematsu Y, Kikuchi K, Momoi T, Sudo M, Kikawa Y, Nosaka K, Kuriyama M, Haruki S, Sanada K, Hamano N.
    J Inherit Metab Dis; 1983 May; 6(4):183-9. PubMed ID: 6422161
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  • 32. Elective liver transplantation for the treatment of classical maple syrup urine disease.
    Strauss KA, Mazariegos GV, Sindhi R, Squires R, Finegold DN, Vockley G, Robinson DL, Hendrickson C, Virji M, Cropcho L, Puffenberger EG, McGhee W, Seward LM, Morton DH.
    Am J Transplant; 2006 Mar; 6(3):557-64. PubMed ID: 16468966
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  • 34. Diagnosis and treatment of maple syrup disease: a study of 36 patients.
    Morton DH, Strauss KA, Robinson DL, Puffenberger EG, Kelley RI.
    Pediatrics; 2002 Jun; 109(6):999-1008. PubMed ID: 12042535
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  • 37. Pathophysiology of maple syrup urine disease: Focus on the neurotoxic role of the accumulated branched-chain amino acids and branched-chain α-keto acids.
    Amaral AU, Wajner M.
    Neurochem Int; 2022 Jul; 157():105360. PubMed ID: 35577033
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  • 39. Clearance of branched chain amino acids by peritoneal dialysis in maple syrup urine disease.
    McMahon Y, MacDonnell RC.
    Adv Perit Dial; 1990 Jul; 6():31-4. PubMed ID: 1982835
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  • 40. Apoptotic signaling pathways induced by acute administration of branched-chain amino acids in an animal model of maple syrup urine disease.
    Vilela TC, Scaini G, Furlanetto CB, Pasquali MA, Santos JP, Gelain DP, Moreira JC, Schuck PF, Ferreira GC, Streck EL.
    Metab Brain Dis; 2017 Feb; 32(1):115-122. PubMed ID: 27510712
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