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PUBMED FOR HANDHELDS

Journal Abstract Search

255 related items for PubMed ID: 9930336

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  • 4. Aspartylglucosaminidase (AGA) is efficiently produced and endocytosed by glial cells: implication for the therapy of a lysosomal storage disorder.
    Harkke S, Laine M, Jalanko A.
    J Gene Med; 2003 Jun; 5(6):472-82. PubMed ID: 12797112
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  • 6. Overgrowth of oral mucosa and facial skin, a novel feature of aspartylglucosaminuria.
    Arvio P, Arvio M, Kero M, Pirinen S, Lukinmaa PL.
    J Med Genet; 1999 May; 36(5):398-404. PubMed ID: 10353787
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  • 8. Correction of deficient enzyme activity in a lysosomal storage disease, aspartylglucosaminuria, by enzyme replacement and retroviral gene transfer.
    Enomaa N, Danos O, Peltonen L, Jalanko A.
    Hum Gene Ther; 1995 Jun; 6(6):723-31. PubMed ID: 7548272
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  • 13. Identification of a novel mutation causing aspartylglucosaminuria reveals a mutation hotspot region in the aspartylglucosaminidase gene.
    Isoniemi A, Hietala M, Aula P, Jalanko A, Peltonen L.
    Hum Mutat; 1995 Jun; 5(4):318-26. PubMed ID: 7627186
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  • 20. Monitoring the CNS pathology in aspartylglucosaminuria mice.
    Tenhunen K, Uusitalo A, Autti T, Joensuu R, Kettunen M, Kauppinen RA, Ikonen S, LaMarca ME, Haltia M, Ginns EI, Jalanko A, Peltonen L.
    J Neuropathol Exp Neurol; 1998 Dec; 57(12):1154-63. PubMed ID: 9862638
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