Redefining phenotypes associated with mitochondrial DNA single deletion-Reference-Cited by-同舟云学术

Redefining phenotypes associated with mitochondrial DNA single deletion

Published:2015-03-26 Issue:5 Volume:262 Page:1301-1309
ISSN:0340-5354
Container-title:Journal of Neurology
language:en
Short-container-title:J Neurol

Author:

Mancuso Michelangelo,Orsucci Daniele,Angelini Corrado,Bertini Enrico,Carelli Valerio,Comi Giacomo Pietro,Donati Maria Alice,Federico Antonio,Minetti Carlo,Moggio Maurizio,Mongini Tiziana,Santorelli Filippo Maria,Servidei Serenella,Tonin Paola,Toscano Antonio,Bruno Claudio,Bello Luca,Caldarazzo Ienco Elena,Cardaioli Elena,Catteruccia Michela,Da Pozzo Paola,Filosto Massimiliano,Lamperti Costanza,Moroni Isabella,Musumeci Olimpia,Pegoraro Elena,Ronchi Dario,Sauchelli Donato,Scarpelli Mauro,Sciacco Monica,Valentino Maria Lucia,Vercelli Liliana,Zeviani Massimo,Siciliano Gabriele

Publisher

Springer Science and Business Media LLC

Subject

Clinical Neurology,Neurology

Link

http://link.springer.com/content/pdf/10.1007/s00415-015-7710-y.pdf

Reference24 articles.

1. DiMauro S, Schon EA (2003) Mitochondrial respiratory-chain diseases. N Engl J Med 348:2656–2668

2. Filosto M, Mancuso M (2007) Mitochondrial diseases: a nosological update. Acta Neurol Scand 115:211–221

3. Mancuso M, Orsucci D, Angelini CI, Bertini E, Carelli V, Comi GP, Minetti C, Moggio M, Mongini T, Servidei S, Tonin P, Toscano A, Uziel G, Bruno C, Caldarazzo Ienco E, Filosto M, Lamperti C, Martinelli D, Moroni I, Musumeci O, Pegoraro E, Ronchi D, Santorelli FM, Sauchelli D, Scarpelli M, Sciacco M, Spinazzi M, Valentino ML, Vercelli L, Zeviani M, Siciliano G (2013) Phenotypic heterogeneity of the 8344A>G mtDNA “MERRF” mutation. Neurology 80:2049–2054

4. Mancuso M, Orsucci D, Angelini C, Bertini E, Carelli V, Comi GP, Donati A, Minetti C, Moggio M, Mongini T, Servidei S, Tonin P, Toscano A, Uziel G, Bruno C, Ienco EC, Filosto M, Lamperti C, Catteruccia M, Moroni I, Musumeci O, Pegoraro E, Ronchi D, Santorelli FM, Sauchelli D, Scarpelli M, Sciacco M, Valentino ML, Vercelli L, Zeviani M, Siciliano G (2014) The m.3243A>G mitochondrial DNA mutation and related phenotypes. A matter of gender? J Neurol 261:504–510

5. Bernier FP, Boneh A, Dennett X, Chow CW, Cleary MA, Thorburn DR (2002) Diagnostic criteria for respiratory chain disorders in adults and children. Neurology 59:1406–1411

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