Archives of neurology

(Arch Neurol) ISSNs: 0003-9942,

References in Archives of neurology:

Title Authors Year
A novel POLG gene mutation in 4 children with Alpers-like hepatocerebral syndromes. Kurt B, Jaeken J, Van Hove J, Lagae L, Löfgren A, Everman DB, Jayakar P, Naini AB, Wierenga KJ, Van Goethem G, Copeland WC, DiMauro S 2010
Clinical and genetic heterogeneity in progressive external ophthalmoplegia due to mutations in polymerase gamma. Filosto M, Mancuso M, Nishigaki Y, Pancrudo J, Harati Y, Gooch C, Mankodi A, Bayne L, Bonilla E, Shanske S, Hirano M, DiMauro S 2003
A novel polymerase gamma mutation in a family with ophthalmoplegia, neuropathy, and Parkinsonism. Mancuso M, Filosto M, Oh SJ, DiMauro S 2004
Juvenile Alpers disease. Wiltshire E, Davidzon G, DiMauro S, Akman HO, Sadleir L, Haas L, Zuccollo J, McEwen A, Thorburn DR 2008
POLG1 mutations manifesting as autosomal recessive axonal Charcot-Marie-Tooth disease. Harrower T, Stewart JD, Hudson G, Houlden H, Warner G, O'Donovan DG, Findlay LJ, Taylor RW, De Silva R, Chinnery PF 2008
Mutation of the linker region of the polymerase gamma-1 (POLG1) gene associated with progressive external ophthalmoplegia and Parkinsonism. Hudson G, Schaefer AM, Taylor RW, Tiangyou W, Gibson A, Venables G, Griffiths P, Burn DJ, Turnbull DM, Chinnery PF 2007
Association of novel POLG mutations and multiple mitochondrial DNA deletions with variable clinical phenotypes in a Spanish population. González-Vioque E, Blázquez A, Fernández-Moreira D, Bornstein B, Bautista J, Arpa J, Navarro C, Campos Y, Fernández-Moreno MA, Garesse R, Arenas J, Martín MA 2006
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