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 |