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24. Deterioration of mitochondrial bioenergetics and ultrastructure impairment in skeletal muscle of a transgenic minipig model in the early stages of Huntington's disease. Rodinova M; Krizova J; Stufkova H; Bohuslavova B; Askeland G; Dosoudilova Z; Juhas S; Juhasova J; Ellederova Z; Zeman J; Eide L; Motlik J; Hansikova H Dis Model Mech; 2019 Jul; 12(7):. PubMed ID: 31278192 [TBL] [Abstract][Full Text] [Related]
25. Biological abnormalities of peripheral A(2A) receptors in a large representation of polyglutamine disorders and Huntington's disease stages. Varani K; Bachoud-Lévi AC; Mariotti C; Tarditi A; Abbracchio MP; Gasperi V; Borea PA; Dolbeau G; Gellera C; Solari A; Rosser A; Naji J; Handley O; Maccarrone M; Peschanski M; DiDonato S; Cattaneo E Neurobiol Dis; 2007 Jul; 27(1):36-43. PubMed ID: 17512749 [TBL] [Abstract][Full Text] [Related]
27. Inherited CAG.CTG allele length is a major modifier of somatic mutation length variability in Huntington disease. Veitch NJ; Ennis M; McAbney JP; ; Shelbourne PF; Monckton DG DNA Repair (Amst); 2007 Jun; 6(6):789-96. PubMed ID: 17293170 [TBL] [Abstract][Full Text] [Related]
28. Diminished hippocalcin expression in Huntington's disease brain does not account for increased striatal neuron vulnerability as assessed in primary neurons. Rudinskiy N; Kaneko YA; Beesen AA; Gokce O; Régulier E; Déglon N; Luthi-Carter R J Neurochem; 2009 Oct; 111(2):460-72. PubMed ID: 19686238 [TBL] [Abstract][Full Text] [Related]
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30. Yugoslav HD phenocopies analyzed on the presence of mutations in PrP, ferritin, and Jp-3 genes. Keckarević M; Savić D; Svetel M; Kostić V; Vukosavić S; Romac S Int J Neurosci; 2005 Feb; 115(2):299-301. PubMed ID: 15764008 [TBL] [Abstract][Full Text] [Related]
31. Nortriptyline delays disease onset in models of chronic neurodegeneration. Wang H; Guan Y; Wang X; Smith K; Cormier K; Zhu S; Stavrovskaya IG; Huo C; Ferrante RJ; Kristal BS; Friedlander RM Eur J Neurosci; 2007 Aug; 26(3):633-41. PubMed ID: 17686041 [TBL] [Abstract][Full Text] [Related]
32. [Mechanisms of neuronal death in Huntington's disease. Second part: therapeutic challenges]. Bantubungi K; Blum D Rev Med Brux; 2007; 28(6):487-94. PubMed ID: 18265808 [TBL] [Abstract][Full Text] [Related]
33. Normal electrical properties of hippocampal neurons modelling early Huntington disease pathogenesis. Shelbourne P; Coote E; Dadak S; Cobb SR Brain Res; 2007 Mar; 1139():226-34. PubMed ID: 17291464 [TBL] [Abstract][Full Text] [Related]
34. Abnormal morphology of peripheral cell tissues from patients with Huntington disease. Squitieri F; Falleni A; Cannella M; Orobello S; Fulceri F; Lenzi P; Fornai F J Neural Transm (Vienna); 2010 Jan; 117(1):77-83. PubMed ID: 19834779 [TBL] [Abstract][Full Text] [Related]
36. Homozygosity for CAG mutation in Huntington disease is associated with a more severe clinical course. Squitieri F; Gellera C; Cannella M; Mariotti C; Cislaghi G; Rubinsztein DC; Almqvist EW; Turner D; Bachoud-Lévi AC; Simpson SA; Delatycki M; Maglione V; Hayden MR; Donato SD Brain; 2003 Apr; 126(Pt 4):946-55. PubMed ID: 12615650 [TBL] [Abstract][Full Text] [Related]
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38. Mitochondrial organization and structure are compromised in fibroblasts from patients with Huntington's disease. Vanisova M; Stufkova H; Kohoutova M; Rakosnikova T; Krizova J; Klempir J; Rysankova I; Roth J; Zeman J; Hansikova H Ultrastruct Pathol; 2022 Sep; 46(5):462-475. PubMed ID: 35946926 [TBL] [Abstract][Full Text] [Related]
39. Impairment of energy metabolism and excitotoxic cell death in Huntington disease. Young AB Rev Neurol (Paris); 1997 Sep; 153(8-9):496-8. PubMed ID: 9683998 [TBL] [Abstract][Full Text] [Related]
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