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152 related items for PubMed ID: 7668327
21. Different patterns of hydrophobic protein storage in different forms of neuronal ceroid lipofuscinosis (NCL, Batten disease). Palmer DN, Jolly RD, van Mil HC, Tyynelä J, Westlake VJ. Neuropediatrics; 1997 Feb; 28(1):45-8. PubMed ID: 9151321 [Abstract] [Full Text] [Related]
22. Adult onset thalamocerebellar degeneration in dogs associated to neuronal storage of ceroid lipopigment. Sisó S, Navarro C, Hanzlícek D, Vandevelde M. Acta Neuropathol; 2004 Nov; 108(5):386-92. PubMed ID: 15365721 [Abstract] [Full Text] [Related]
24. Submitochondrial distribution and delayed proteolysis of subunit c of the H+-transporting ATP-synthase in ovine ceroid-lipofuscinosis. Hughes SM, Moroni-Rawson P, Jolly RD, Jordan TW. Electrophoresis; 2001 May; 22(9):1785-94. PubMed ID: 11425233 [Abstract] [Full Text] [Related]
26. Motor neuron degeneration of mice is a model of neuronal ceroid lipofuscinosis (Batten's disease). Bronson RT, Lake BD, Cook S, Taylor S, Davisson MT. Ann Neurol; 1993 Apr; 33(4):381-5. PubMed ID: 7683855 [Abstract] [Full Text] [Related]
27. Autosomal dominant adult neuronal ceroid lipofuscinosis: a novel form of NCL with granular osmiophilic deposits without palmitoyl protein thioesterase 1 deficiency. Nijssen PC, Ceuterick C, van Diggelen OP, Elleder M, Martin JJ, Teepen JL, Tyynelä J, Roos RA. Brain Pathol; 2003 Oct; 13(4):574-81. PubMed ID: 14655761 [Abstract] [Full Text] [Related]
31. Specific delay in the degradation of mitochondrial ATP synthase subunit c in late infantile neuronal ceroid lipofuscinosis is derived from cellular proteolytic dysfunction rather than structural alteration of subunit c. Ezaki J, Wolfe LS, Kominami E. J Neurochem; 1996 Oct; 67(4):1677-87. PubMed ID: 8858953 [Abstract] [Full Text] [Related]
34. Morphological alterations in neocortical and cerebellar GABAergic neurons in a canine model of juvenile Batten disease. March PA, Wurzelmann S, Walkley SU. Am J Med Genet; 1995 Jun 05; 57(2):204-12. PubMed ID: 7668331 [Abstract] [Full Text] [Related]
36. A mouse model for Finnish variant late infantile neuronal ceroid lipofuscinosis, CLN5, reveals neuropathology associated with early aging. Kopra O, Vesa J, von Schantz C, Manninen T, Minye H, Fabritius AL, Rapola J, van Diggelen OP, Saarela J, Jalanko A, Peltonen L. Hum Mol Genet; 2004 Dec 01; 13(23):2893-906. PubMed ID: 15459177 [Abstract] [Full Text] [Related]
37. Progress in neuropathology of the neuronal ceroid lipofuscinoses. Goebel HH, Schochet SS, Jaynes M, Brück W, Kohlschütter A, Hentati F. Mol Genet Metab; 1999 Apr 01; 66(4):367-72. PubMed ID: 10191130 [Abstract] [Full Text] [Related]