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PUBMED FOR HANDHELDS

Journal Abstract Search


274 related items for PubMed ID: 24838951

  • 1. Two novel missense mutations in nonketotic hyperglycinemia.
    Yilmaz BS, Kor D, Ceylaner S, Mert GG, Incecik F, Kartal E, Mungan NO.
    J Child Neurol; 2015 May; 30(6):789-92. PubMed ID: 24838951
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  • 3. Late-onset nonketotic hyperglycinemia caused by a novel homozygous missense mutation in the GLDC gene.
    Brunel-Guitton C, Casey B, Coulter-Mackie M, Vallance H, Hewes D, Stockler-Ipsiroglu S, Mercimek-Mahmutoglu S.
    Mol Genet Metab; 2011 Jun; 103(2):193-6. PubMed ID: 21411353
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  • 5. Glycine encephalopathy (nonketotic hyperglycinemia): comments and speculations.
    Applegarth DA, Toone JR.
    Am J Med Genet A; 2006 Jan 15; 140(2):186-8. PubMed ID: 16353254
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  • 6. Two novel missense mutations observed in nonketotic hyperglycinemia.
    Yoon IA, Lee NM, Yoo BH, Lee BS, Yoo HW.
    Pediatr Neurol; 2012 Jun 15; 46(6):401-3. PubMed ID: 22633639
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  • 17. d-Glyceric aciduria does not cause nonketotic hyperglycinemia: A historic co-occurrence.
    Swanson MA, Garcia SM, Spector E, Kronquist K, Creadon-Swindell G, Walter M, Christensen E, Van Hove JLK, Sass JO.
    Mol Genet Metab; 2017 Jun 15; 121(2):80-82. PubMed ID: 28462797
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  • 18. Biochemical and molecular predictors for prognosis in nonketotic hyperglycinemia.
    Swanson MA, Coughlin CR, Scharer GH, Szerlong HJ, Bjoraker KJ, Spector EB, Creadon-Swindell G, Mahieu V, Matthijs G, Hennermann JB, Applegarth DA, Toone JR, Tong S, Williams K, Van Hove JL.
    Ann Neurol; 2015 Oct 15; 78(4):606-18. PubMed ID: 26179960
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  • 20. Mild glycine encephalopathy (NKH) in a large kindred due to a silent exonic GLDC splice mutation.
    Flusser H, Korman SH, Sato K, Matsubara Y, Galil A, Kure S.
    Neurology; 2005 Apr 26; 64(8):1426-30. PubMed ID: 15851735
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