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Journal Abstract Search

359 related items for PubMed ID: 9377079

  • 21. The neuronal ceroid-lipofuscinoses. Recent advances.
    Goebel HH, Sharp JD.
    Brain Pathol; 1998 Jan; 8(1):151-62. PubMed ID: 9458173
    [Abstract] [Full Text] [Related]

  • 22. Current state of clinical and morphological features in human NCL.
    Goebel HH, Wisniewski KE.
    Brain Pathol; 2004 Jan; 14(1):61-9. PubMed ID: 14997938
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  • 23. Alterations in ROS activity and lysosomal pH account for distinct patterns of macroautophagy in LINCL and JNCL fibroblasts.
    Vidal-Donet JM, Cárcel-Trullols J, Casanova B, Aguado C, Knecht E.
    PLoS One; 2013 Jan; 8(2):e55526. PubMed ID: 23408996
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    Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, Mole SE, Williams RE.
    ; 1993 Jan. PubMed ID: 20301601
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  • 27. An Australasian diagnostic service for the neuronal ceroid lipofuscinoses.
    Muller VJ, Paton BC, Fietz MJ.
    Eur J Paediatr Neurol; 2001 Jan; 5 Suppl A():197-201. PubMed ID: 11588997
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  • 31. A function retained by the common mutant CLN3 protein is responsible for the late onset of juvenile neuronal ceroid lipofuscinosis.
    Kitzmüller C, Haines RL, Codlin S, Cutler DF, Mole SE.
    Hum Mol Genet; 2008 Jan 15; 17(2):303-12. PubMed ID: 17947292
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  • 33. Neuronal ceroid lipofuscinoses: a clinical and morphological study of 17 patients from southern Brazil.
    Puga AC, Jardim LB, Chimelli L, De Souza CF, Clivati M.
    Arq Neuropsiquiatr; 2000 Sep 15; 58(3A):597-606. PubMed ID: 10973097
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  • 39. A mouse mutant deficient in both neuronal ceroid lipofuscinosis-associated proteins CLN3 and TPP1.
    Sleat DE, Banach-Petrosky W, Larrimore KE, Nemtsova Y, Wiseman JA, Najafi A, Johnson D, Poole TA, Takahashi K, Cooper JD, Lobel P.
    J Inherit Metab Dis; 2023 Jul 15; 46(4):720-734. PubMed ID: 37078466
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  • 40. CLN-encoded proteins do not interact with each other.
    Zhong NA, Moroziewicz DN, Ju W, Wisniewski KE, Jurkiewicz A, Brown WT.
    Neurogenetics; 2000 Sep 15; 3(1):41-4. PubMed ID: 11085596
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