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Journal Abstract Search

164 related items for PubMed ID: 34153280

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  • 2. Changes in branched-chain amino acids in an infant with maple syrup urine disease during perioperative pediatric liver transplant: A case report.
    Saeyup P, Tubjaroen C, Kamolvisit W, Chongsrisawat V, Thaveepunsan W.
    Paediatr Anaesth; 2024 Apr; 34(4):366-370. PubMed ID: 38314877
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  • 4. Branched-chain α-ketoacid dehydrogenase deficiency (maple syrup urine disease): Treatment, biomarkers, and outcomes.
    Strauss KA, Carson VJ, Soltys K, Young ME, Bowser LE, Puffenberger EG, Brigatti KW, Williams KB, Robinson DL, Hendrickson C, Beiler K, Taylor CM, Haas-Givler B, Chopko S, Hailey J, Muelly ER, Shellmer DA, Radcliff Z, Rodrigues A, Loeven K, Heaps AD, Mazariegos GV, Morton DH.
    Mol Genet Metab; 2020 Mar; 129(3):193-206. PubMed ID: 31980395
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  • 7. 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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  • 8. Treatment of maple syrup urine disease: Benefits, risks, and challenges of liver transplantation.
    Deon M, Guerreiro G, Girardi J, Ribas G, Vargas CR.
    Int J Dev Neurosci; 2023 Oct; 83(6):489-504. PubMed ID: 37340513
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  • 9. Long-Term Amino Acid Homeostasis, Neurodevelopmental and Growth Profiles Following Liver Transplantation in Maple Syrup Urine Disease.
    Vasudevan AK, Shanmugam N, Rammohan A, Balakrishnan U, Menon J, Iqbal MAUH, Mohammed GMO, Kaliamoorthy I, Rela M.
    Pediatr Transplant; 2024 Sep; 28(6):e14845. PubMed ID: 39158064
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  • 13. 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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  • 14. Outcomes from a Single Transplant Center of 5 Pediatric Cases of Domino Liver Transplantation from Live Donors with Maple Syrup Urine Disease.
    Zhang JP, Zhu ZJ, Sun LY, Wei L, Qu W, Zeng ZG, Zhang HM, Liu Y.
    Ann Transplant; 2023 May 30; 28():e939893. PubMed ID: 37248682
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  • 18. Liver transplantation for classical maple syrup urine disease: long-term follow-up in 37 patients and comparative United Network for Organ Sharing experience.
    Mazariegos GV, Morton DH, Sindhi R, Soltys K, Nayyar N, Bond G, Shellmer D, Shneider B, Vockley J, Strauss KA.
    J Pediatr; 2012 Jan 30; 160(1):116-21.e1. PubMed ID: 21839471
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  • 19. The need of essential amino acids in children. An evaluation based on the intake of phenylalanine, tyrosine, leucine, isoleucine, and valine in children with phenylketonuria, tyrosine amino transferase defect, and maple syrup urine disease.
    Kindt E, Halvorsen S.
    Am J Clin Nutr; 1980 Feb 30; 33(2):279-86. PubMed ID: 6101930
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  • 20. Evaluation of branched-chain amino acid intake in children with maple syrup urine disease and methylmalonic aciduria.
    Parsons HG, Carter RJ, Unrath M, Snyder FF.
    J Inherit Metab Dis; 1990 Feb 30; 13(2):125-36. PubMed ID: 2116544
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