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Journal Abstract Search

254 related items for PubMed ID: 20157158

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  • 4. Clinical and molecular analysis of Japanese patients with neuronal ceroid lipofuscinosis.
    Oishi K, Ida H, Kurosawa K, Eto Y.
    Mol Genet Metab; 1999 Apr; 66(4):344-8. PubMed ID: 10191127
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  • 6. A mutation in canine CLN5 causes neuronal ceroid lipofuscinosis in Border collie dogs.
    Melville SA, Wilson CL, Chiang CS, Studdert VP, Lingaas F, Wilton AN.
    Genomics; 2005 Sep; 86(3):287-94. PubMed ID: 16033706
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  • 7. Linkage analysis of late-infantile neuronal ceroid-lipofuscinosis.
    Sharp J, Savukoski M, Wheeler RB, Harris J, Järvelä I, Peltonen L, Gardiner M, Williams R.
    Am J Med Genet; 1995 Jun 05; 57(2):348-9. PubMed ID: 7668361
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  • 9. The clinical and genetic epidemiology of neuronal ceroid lipofuscinosis in Newfoundland.
    Moore SJ, Buckley DJ, MacMillan A, Marshall HD, Steele L, Ray PN, Nawaz Z, Baskin B, Frecker M, Carr SM, Ives E, Parfrey PS.
    Clin Genet; 2008 Sep 05; 74(3):213-22. PubMed ID: 18684116
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  • 16. Alport syndrome. Molecular genetic aspects.
    Hertz JM.
    Dan Med Bull; 2009 Aug 05; 56(3):105-52. PubMed ID: 19728970
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  • 17. Neuronal ceroid lipofuscinoses in Scandinavia. Epidemiology and clinical pictures.
    Uvebrant P, Hagberg B.
    Neuropediatrics; 1997 Feb 05; 28(1):6-8. PubMed ID: 9151309
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  • 18. [Neuronal ceroid lipofuscinosis: diagnostic algorithm and clinical description of the Finnish (CLN5) and Turkish (CLN7) variants late infantile].
    Pérez-Poyato M S, Milà-Recasens M, Ferrer-Abizanda I, Cusí-Sánchez V, Vázquez-López M, Camino-León R, Coll-Rosell MJ, Gort L, Pineda-Marfà M.
    Rev Neurol; 2012 May 01; 54(9):544-50. PubMed ID: 22532218
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