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Journal Abstract Search

200 related items for PubMed ID: 7207707

  • 1. Intermittent neurological symptoms in a girl with a maple syrup urine disease (MSUD) variant.
    Holmgren G, Brundin A, Gustavson KH, Sjögren S, Kleijer WJ, Niermeijer MF.
    Neuropediatrics; 1980 Nov; 11(4):377-83. PubMed ID: 7207707
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  • 3. Intermittent maple syrup urine disease: two case reports.
    Axler O, Holmquist P.
    Pediatrics; 2014 Feb; 133(2):e458-60. PubMed ID: 24394677
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  • 4. Diagnosis of MSUD by newborn screening allows early intervention without extraneous detoxification.
    Heldt K, Schwahn B, Marquardt I, Grotzke M, Wendel U.
    Mol Genet Metab; 2005 Apr; 84(4):313-6. PubMed ID: 15781191
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  • 5. Variant maple syrup urine disease in mother and daughter.
    Zaleski LA, Dancis J, Cox RP, Hutzler J, Zaleski WA, Hill A.
    Can Med Assoc J; 1973 Aug 18; 109(4):299-300 passim. PubMed ID: 4730202
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  • 6. Management of maple syrup urine disease in Canada. Committee for improvement of Hereditary Disease Management.
    Can Med Assoc J; 1976 Nov 20; 115(10):1005-13. PubMed ID: 1032577
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  • 7. Ophthalmoplegia and bulbar palsy in variant form of maple syrup urine disease.
    Chhabria S, Tomasi LG, Wong PW.
    Ann Neurol; 1979 Jul 20; 6(1):71-2. PubMed ID: 507761
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  • 8. Mild variant of maple syrup urine disease.
    Kovács J, Kiss P.
    Acta Paediatr Acad Sci Hung; 1978 Jul 20; 19(2):137-43. PubMed ID: 707084
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  • 10. [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 20; 19(5):393-400. PubMed ID: 6660657
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  • 11. Maple syrup urine disease in Thai infants.
    Pangkanon S, Charoensiriwatana W, Sangtawesin V.
    J Med Assoc Thai; 2008 Oct 20; 91 Suppl 3():S41-4. PubMed ID: 19255991
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  • 13. Maple syrup urine disease: case report of 2 Thai infants.
    Chiemchanya S, Suthutvoravut U, Visudhiphan P.
    J Med Assoc Thai; 1989 Jan 20; 72 Suppl 1():116-20. PubMed ID: 2732631
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  • 14. Maple syrup urine disease in a Bedouin tribe: pre- and postnatal diagnosis.
    Potashnik R, Carmi R, Sofer S, Bashan N, Abeliovich D.
    Isr J Med Sci; 1987 Aug 20; 23(8):886-9. PubMed ID: 3679791
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  • 15. [Heterogeneity of leucinosis. Correlations between clinical manifestations, protein tolerance and enzyme deficiency].
    Saudubray JM, Amédée-Manesme O, Munnich A, Ogier H, Depondt E, Charpentier C, Coudé FX, Rey F, Frézal J.
    Arch Fr Pediatr; 1982 Dec 20; 39 Suppl 2():735-40. PubMed ID: 6897702
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  • 16. Clues and challenges in the diagnosis of intermittent maple syrup urine disease.
    Pode-Shakked N, Korman SH, Pode-Shakked B, Landau Y, Kneller K, Abraham S, Shaag A, Ulanovsky I, Daas S, Saraf-Levy T, Reznik-Wolf H, Vivante A, Pras E, Almashanu S, Anikster Y.
    Eur J Med Genet; 2020 Jun 20; 63(6):103901. PubMed ID: 32151765
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  • 20. Glucose and alanine metabolism in children with maple syrup urine disease.
    Haymond MW, Ben-Galim E, Strobel KE.
    J Clin Invest; 1978 Aug 20; 62(2):398-405. PubMed ID: 670400
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