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Journal Abstract Search

268 related items for PubMed ID: 564423

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  • 11. Definition of the mutation responsible for maple syrup urine disease in Poll Shorthorns and genotyping Poll Shorthorns and Poll Herefords for maple syrup urine disease alleles.
    Dennis JA, Healy PJ.
    Res Vet Sci; 1999 Aug; 67(1):1-6. PubMed ID: 10425233
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  • 12. Amino acids levels and lipid peroxidation in maple syrup urine disease patients.
    Barschak AG, Sitta A, Deon M, Busanello EN, Coelho DM, Cipriani F, Dutra-Filho CS, Giugliani R, Wajner M, Vargas CR.
    Clin Biochem; 2009 Apr; 42(6):462-6. PubMed ID: 19121297
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  • 13. [3 patients with maple syrup urine disease].
    Merinero B, del Valle JA, García MJ, García Miguel MJ, Barrio MI, García Hortelano J, Morales E, González F, García Aparicio J, Sáez Pérez E.
    An Esp Pediatr; 1983 Nov; 19(5):393-400. PubMed ID: 6660657
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  • 14. Synaptic plasma membrane Na(+), K (+)-ATPase activity is significantly reduced by the alpha-keto acids accumulating in maple syrup urine disease in rat cerebral cortex.
    Wajner A, Bürger C, Dutra-Filho CS, Wajner M, de Souza Wyse AT, Wannmacher CM.
    Metab Brain Dis; 2007 Mar; 22(1):77-88. PubMed ID: 17295076
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  • 18. Clinical consequences of disorders in the intermediate metabolism of branched chain amino acids (valine, leucine and isoleucine).
    Mogoş T, Cheţa CP, Mincu IT.
    Rom J Intern Med; 1994 Mar; 32(1):57-61. PubMed ID: 8081313
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  • 20. Combined nutritional support and continuous extracorporeal removal therapy in the severe acute phase of maple syrup urine disease.
    Jouvet P, Jugie M, Rabier D, Desgrès J, Hubert P, Saudubray JM, Man NK.
    Intensive Care Med; 2001 Nov; 27(11):1798-806. PubMed ID: 11810125
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