{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2022,4,4]],"date-time":"2022-04-04T17:23:18Z","timestamp":1649092998212},"reference-count":17,"publisher":"Springer Science and Business Media LLC","issue":"4","license":[{"start":{"date-parts":[[2007,3,31]],"date-time":"2007-03-31T00:00:00Z","timestamp":1175299200000},"content-version":"tdm","delay-in-days":0,"URL":"http:\/\/www.springer.com\/tdm"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["J Neurol"],"published-print":{"date-parts":[[2007,4]]},"DOI":"10.1007\/s00415-006-0399-1","type":"journal-article","created":{"date-parts":[[2007,3,30]],"date-time":"2007-03-30T17:48:52Z","timestamp":1175276932000},"page":"482-487","source":"Crossref","is-referenced-by-count":0,"title":["Investigation of the mitochondrial genome in patients with atypical motor neuron disease"],"prefix":"10.1007","volume":"254","author":[{"given":"Catherine","family":"Phoenix","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Geoffrey A.","family":"Taylor","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Judith","family":"Hartley","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Hannah","family":"Nixon","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Paul G.","family":"Ince","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Pamela J.","family":"Shaw","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Douglass M.","family":"Turnbull","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Robert W.","family":"Taylor","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"297","published-online":{"date-parts":[[2007,3,31]]},"reference":[{"key":"399_CR1","doi-asserted-by":"crossref","first-page":"1046","DOI":"10.1136\/jnnp.2004.048652","volume":"76","author":"Shaw","year":"2005","unstructured":"Shaw PJ (2005) Molecular and cellular pathways of neurodegeneration in motor neurone diseas. J Neurol Neurosurg Psychiatry 76:1046\u20131057","journal-title":"J Neurol Neurosurg Psychiatry"},{"key":"399_CR2","doi-asserted-by":"crossref","first-page":"77","DOI":"10.1016\/j.mito.2005.01.002","volume":"5","author":"Manfredi","year":"2005","unstructured":"Manfredi G, Xu Z (2005) Mitochondrial dysfunction and its role in motor neuron degeneration in ALS. Mitochondrion 5:77\u201387","journal-title":"Mitochondrion"},{"key":"399_CR3","doi-asserted-by":"crossref","first-page":"1870","DOI":"10.1093\/brain\/awh540","volume":"128","author":"Krasnianski","year":"2005","unstructured":"Krasnianski A, Deschauer M, Neudecker S, Gellerich FN, Muller T, Schoser BG, Krasnianski M, Zierz S (2005) Mitochondrial changes in skeletal muscle in amyotrophic lateral sclerosis and other neurogenic atrophies. Brain 128:1870\u20131876","journal-title":"Brain"},{"key":"399_CR4","doi-asserted-by":"crossref","first-page":"787","DOI":"10.1002\/1531-8249(199911)46:5<787::AID-ANA17>3.0.CO;2-8","volume":"46","author":"Borthwick","year":"1999","unstructured":"Borthwick GM, Johnson MA, Ince PG, Shaw PJ, Turnbull DM (1999) Mitochondrial enzyme activity in amyotrophic lateral sclerosis: implications for the role of mitochondria in neuronal cell death. Ann Neurol 46:787\u2013790","journal-title":"Ann Neurol"},{"key":"399_CR5","doi-asserted-by":"crossref","first-page":"389","DOI":"10.1038\/nrg1606","volume":"6","author":"Taylor","year":"2005","unstructured":"Taylor RW, Turnbull DM (2005) Mitochondrial DNA mutations in human disease. Nature Rev Genet 6:389\u2013402","journal-title":"Nature Rev Genet"},{"key":"399_CR6","doi-asserted-by":"crossref","first-page":"110","DOI":"10.1002\/ana.410430119","volume":"43","author":"Comi","year":"1998","unstructured":"Comi GP, Bordoni A, Salani S, Franceschina L, Sciacco M, Prelle A, Fortunato F, Zeviani M, Napoli L, Bresolin N, Moggio M, Ausenda CD, Taanman JW, Scarlato G (1998) Cytochrome c oxidase subunit I microdeletion in a patient with motor neuron disease. Ann Neurol 43:110\u2013116","journal-title":"Ann Neurol"},{"key":"399_CR7","doi-asserted-by":"crossref","first-page":"723","DOI":"10.1016\/j.nmd.2004.07.002","volume":"14","author":"Fetoni","year":"2004","unstructured":"Fetoni V, Briem E, Carrara F, Mora M, Zeviani M (2004) Monomelic amyotrophy associated with the 7472insC mutation in the mtDNA tRNASer(UCN) gene. Neuromuscul Disord 14:723\u2013726","journal-title":"Neuromuscul Disord"},{"key":"399_CR8","doi-asserted-by":"crossref","first-page":"570","DOI":"10.1002\/ana.20758","volume":"59","author":"Borthwick","year":"2006","unstructured":"Borthwick GM, Taylor RW, Walls TJ, Tonska K, Taylor GA, Shaw PJ, Ince PG, Turnbull DM (2006) Motor neuron disease in a patient with a mitochondrial tRNAIle mutation. Ann Neurol 59:570\u2013574","journal-title":"Ann Neurol"},{"key":"399_CR9","doi-asserted-by":"crossref","first-page":"e74","DOI":"10.1093\/nar\/29.15.e74","volume":"29","author":"Taylor","year":"2001","unstructured":"Taylor RW, Taylor GA, Durham SE, Turnbull DM (2001) The determination of complete human mitochondrial DNA sequences in single cells: implications for the study of somatic mitochondrial DNA point mutations. Nucleic Acids Res 29:e74","journal-title":"Nucleic Acids Res"},{"key":"399_CR10","unstructured":"MITOMAP: A Human Mitochondrial Genome Database. http:\/\/www.mitomap.org, 2005"},{"key":"399_CR11","doi-asserted-by":"crossref","first-page":"D749","DOI":"10.1093\/nar\/gkj010","volume":"34","author":"Ingman","year":"2003","unstructured":"Ingman M, Gyllensten U (2006) mtDB: Human Mitochondrial Genome Database, a resource for population genetics and medical sciences. Nucleic Acids Res 34:D749\u2013D751","journal-title":"Nucleic Acids Res"},{"key":"399_CR12","doi-asserted-by":"crossref","first-page":"583","DOI":"10.1016\/j.tig.2005.08.012","volume":"21","author":"Howell","year":"2005","unstructured":"Howell N, Elson JL, Chinnery PF, Turnbull DM (2005) mtDNA mutations and common neurodegenerative disorders. Trends Genet 21:583\u2013586","journal-title":"Trends Genet"},{"key":"399_CR13","doi-asserted-by":"crossref","first-page":"135","DOI":"10.1006\/exnr.1998.6866","volume":"153","author":"Swerdlow","year":"1998","unstructured":"Swerdlow RH, Parks JK, Cassarino DS, Trimmer PA, Miller SW, Maguire DJ, Sheehan JP, Maguire RS, Pattee G, Juel VC, Phillips LH, Tuttle JB, Bennett JP Jr, Davis RE, Parker WD Jr (1998) Mitochondria in sporadic amyotrophic lateral sclerosis. Exp Neurol 153:135\u2013142","journal-title":"Exp Neurol"},{"key":"399_CR14","doi-asserted-by":"crossref","first-page":"229","DOI":"10.1016\/S0014-4886(02)00022-5","volume":"179","author":"Gajewski","year":"2003","unstructured":"Gajewski CD, Lin MT, Cudkowicz ME, Beal MF, Manfredi G (2003) Mitochondrial DNA from platelets of sporadic ALS patients restores normal respiratory functions in p 0 cells. Exp Neurol 179:229\u2013235","journal-title":"Exp Neurol"},{"key":"399_CR15","doi-asserted-by":"crossref","first-page":"515","DOI":"10.1038\/ng1769","volume":"38","author":"Bender","year":"2006","unstructured":"Bender A, Krishnan KJ, Morris CM, Taylor GA, Reeve AK, Perry RH, Jaros E, Hersheson JS, Betts J, Klopstock T, Taylor RW, Turnbull DM (2006) High levels of mitochondrial DNA deletions in substantia nigra neurons in aging and Parkinson disease. Nat Genet 38:515\u2013517","journal-title":"Nat Genet"},{"key":"399_CR16","doi-asserted-by":"crossref","first-page":"591","DOI":"10.1016\/j.tig.2004.09.014","volume":"20","author":"McFarland","year":"2004","unstructured":"McFarland R, Elson JL, Taylor RW, Howell N, Turnbull DM (2004) Assigning pathogenicity to mitochondrial tRNA mutations: when \u201cdefinitely maybe\u201d is not good enough. Trends Genet 20:591\u2013596","journal-title":"Trends Genet"},{"key":"399_CR17","doi-asserted-by":"crossref","first-page":"175","DOI":"10.1136\/jmg.2005.032474","volume":"43","author":"Mitchell","year":"2006","unstructured":"Mitchell AL, Elson JL, Howell N, Taylor RW, Turnbull DM (2006) Sequence variation in mitochondrial complex I genes: mutation or polymorphism? J Med Genet 43:175\u2013179","journal-title":"J Med Genet"}],"container-title":["Journal of Neurology"],"original-title":[],"language":"en","link":[{"URL":"http:\/\/link.springer.com\/content\/pdf\/10.1007\/s00415-006-0399-1.pdf","content-type":"application\/pdf","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/link.springer.com\/article\/10.1007\/s00415-006-0399-1\/fulltext.html","content-type":"text\/html","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/link.springer.com\/content\/pdf\/10.1007\/s00415-006-0399-1","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2019,5,28]],"date-time":"2019-05-28T15:04:13Z","timestamp":1559055853000},"score":1,"resource":{"primary":{"URL":"http:\/\/link.springer.com\/10.1007\/s00415-006-0399-1"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2007,3,31]]},"references-count":17,"journal-issue":{"issue":"4","published-print":{"date-parts":[[2007,4]]}},"alternative-id":["399"],"URL":"https:\/\/doi.org\/10.1007\/s00415-006-0399-1","relation":{},"ISSN":["0340-5354","1432-1459"],"issn-type":[{"value":"0340-5354","type":"print"},{"value":"1432-1459","type":"electronic"}],"subject":[],"published":{"date-parts":[[2007,3,31]]}}}