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Pubmed for Handhelds

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Journal Abstract Search

153 related items for PubMed ID: 17560505

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  • 4. A CLN5 mutation causing an atypical neuronal ceroid lipofuscinosis of juvenile onset.
    Pineda-Trujillo N, Cornejo W, Carrizosa J, Wheeler RB, Múnera S, Valencia A, Agudelo-Arango J, Cogollo A, Anderson G, Bedoya G, Mole SE, Ruíz-Linares A.
    Neurology; 2005 Feb 22; 64(4):740-2. PubMed ID: 15728307
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  • 5. Novel mutations in CLN8 in Italian variant late infantile neuronal ceroid lipofuscinosis: Another genetic hit in the Mediterranean.
    Cannelli N, Cassandrini D, Bertini E, Striano P, Fusco L, Gaggero R, Specchio N, Biancheri R, Vigevano F, Bruno C, Simonati A, Zara F, Santorelli FM.
    Neurogenetics; 2006 May 22; 7(2):111-7. PubMed ID: 16570191
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  • 6. A mutation in the CLN8 gene in English Setter dogs with neuronal ceroid-lipofuscinosis.
    Katz ML, Khan S, Awano T, Shahid SA, Siakotos AN, Johnson GS.
    Biochem Biophys Res Commun; 2005 Feb 11; 327(2):541-7. PubMed ID: 15629147
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  • 11. Two novel CLN6 mutations in variant late-infantile neuronal ceroid lipofuscinosis patients of Turkish origin.
    Siintola E, Topcu M, Kohlschütter A, Salonen T, Joensuu T, Anttonen AK, Lehesjoki AE.
    Clin Genet; 2005 Aug 11; 68(2):167-73. PubMed ID: 15996215
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  • 15. Gene symbol: CLN6. Disease: Neuronal ceroid lipofuscinosis, late Infantile.
    Cismondi IA, Kohan R, Ghio A, Ramirez AM, Halac IN.
    Hum Genet; 2008 Oct 11; 124(3):324. PubMed ID: 18846690
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  • 17. Impaired cell adhesion and apoptosis in a novel CLN9 Batten disease variant.
    Schulz A, Dhar S, Rylova S, Dbaibo G, Alroy J, Hagel C, Artacho I, Kohlschütter A, Lin S, Boustany RM.
    Ann Neurol; 2004 Sep 11; 56(3):342-50. PubMed ID: 15349861
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  • 20. Variant late infantile neuronal ceroid lipofuscinosis (CLN6 gene) in Saudi Arabia.
    Al-Muhaizea MA, Al-Hassnan ZN, Chedrawi A.
    Pediatr Neurol; 2009 Jul 11; 41(1):74-6. PubMed ID: 19520283
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