Similar articles

• Maple syrup urine disease: two different forms within a single family.

  Frézal J, Amédée-Manesme O, Mitchell G, Heuertz S, Rey F, Rey J, Saudubray JM. Frézal J, et al. Hum Genet. 1985;71(1):89-91. doi: 10.1007/BF00295676. Hum Genet. 1985. PMID: 4029957
• Complementation analysis in lymphoid cells from five patients with different forms of maple syrup urine disease.

  Jinno Y, Akaboshi I, Matsuda I. Jinno Y, et al. Hum Genet. 1984;68(1):54-6. doi: 10.1007/BF00293872. Hum Genet. 1984. PMID: 6500555
• [Maple syrup urine disease].

  Rokkones T. Rokkones T. Tidsskr Nor Laegeforen. 1970 Jan 25;90(2):239-42. Tidsskr Nor Laegeforen. 1970. PMID: 5430195 Norwegian. No abstract available.
• [Maple syrup urine disease: molecular pathology of the branched chain alpha-keto acid dehydrogenase complex].

  Nobukuni Y, Mitsubuchi H, Indo Y, Endo F, Matsuda I. Nobukuni Y, et al. Seikagaku. 1992 Feb;64(2):67-82. Seikagaku. 1992. PMID: 1593184 Review. Japanese. No abstract available.
• [MAPLE SYRUP URINE DISEASE].

  SCARABICCHI S. SCARABICCHI S. Minerva Dietol. 1963 Oct-Dec;3:212-4. Minerva Dietol. 1963. PMID: 14115937 Review. Italian. No abstract available.