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Journal Abstract Search

287 related items for PubMed ID: 16733455

  • 1. [Acrodermatitis enteropathica-like syndrome secondary to branched-chain amino acid deficiency during treatment of maple syrup urine disease].
    Templier I, Reymond JL, Nguyen MA, Boujet C, Lantuejoul S, Beani JC, Leccia MT.
    Ann Dermatol Venereol; 2006 Apr; 133(4):375-9. PubMed ID: 16733455
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  • 2. Acrodermatitis dysmetabolica in an infant with maple syrup urine disease.
    Flores K, Chikowski R, Morrell DS.
    Clin Exp Dermatol; 2016 Aug; 41(6):651-4. PubMed ID: 27334242
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  • 3. Acrodermatitis enteropathica-like syndrome secondary to isoleucine deficiency during treatment of maple syrup urine disease.
    Giacoia GP, Berry GT.
    Am J Dis Child; 1993 Sep; 147(9):954-6. PubMed ID: 8362810
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  • 4. [Iatrogenic acrodermatitis enteropathica-like syndrome in leucinosis].
    Puzenat E, Durbise E, Fromentin C, Humbert P, Aubin F.
    Ann Dermatol Venereol; 2004 Sep; 131(8-9):801-4. PubMed ID: 15505548
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  • 6. Acrodermatitis enteropathica-like cutaneous lesions in organic aciduria.
    De Raeve L, De Meirleir L, Ramet J, Vandenplas Y, Gerlo E.
    J Pediatr; 1994 Mar; 124(3):416-20. PubMed ID: 8120711
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  • 10. Iatrogenic isolated isoleucine deficiency as the cause of an acrodermatitis enteropathica-like syndrome.
    Bosch AM, Sillevis Smitt JH, Van Gennip AH, Abeling NG, Schutgens RB, Bakker HD, Wijburg FA.
    Br J Dermatol; 1998 Sep; 139(3):488-91. PubMed ID: 9767296
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  • 11. [Isolated isoleucine deficiency in diet therapy of a case of maple syrup urine disease].
    Sanjurjo P, Centeno C, Vallo A, Ojembarrena E, Rodríguez Soriano J.
    An Esp Pediatr; 1983 Nov; 19(5):389-92. PubMed ID: 6660656
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  • 12. Acrodermatitis enteropathica-like eruption in metabolic disorders: acrodermatitis dysmetabolica is proposed as a better term.
    Tabanlioğlu D, Ersoy-Evans S, Karaduman A.
    Pediatr Dermatol; 2009 Nov; 26(2):150-4. PubMed ID: 19419460
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  • 13. Acrodermatitis dysmetabolica secondary to isoleucine deficiency in infant with maple syrup urine disease.
    Alkhayal FA, Al Haddad S, Bakraa RM, Alqahtani A.
    Dermatol Reports; 2023 Dec 01; 15(4):9750. PubMed ID: 38327590
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  • 14. 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 01; 109(6):999-1008. PubMed ID: 12042535
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  • 16. Plasma amino acid analyses in two cases of maple syrup urine disease.
    Surarit R, Srisomsap C, Wasant P, Svasti J, Suthatvoravut U, Chokchaichamnankit D, Liammongkolkul S.
    Southeast Asian J Trop Med Public Health; 1999 Jun 01; 30 Suppl 2():138-9. PubMed ID: 11400750
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  • 18. DIETARY TREATMENT OF A CHILD WITH MAPLE SYRUP URINE DISEASE (BRANCHED-CHAIN KETOACIDURIA).
    WESTALL RG.
    Arch Dis Child; 1963 Oct 01; 38(201):485-91. PubMed ID: 14065992
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  • 19. Quantification of Branched-Chain Amino Acids in Plasma by High-Performance Liquid Chromatography-Tandem Mass Spectrometry (LC-MS/MS).
    Piri-Moghadam H, Miller A, Pronger D, Vicente F, Charrow J, Haymond S, Lin DC.
    Methods Mol Biol; 2022 Oct 01; 2546():65-81. PubMed ID: 36127579
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  • 20. Maple syrup urine disease: branched-chain amino acid concentrations and metabolism in cultured human lymphoblasts.
    Skaper SD, Molden DP, Seegmiller JE.
    Biochem Genet; 1976 Aug 01; 14(7-8):527-39. PubMed ID: 985377
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