Restoring balance to ataxia with coenzyme Q10 deficiency

被引:4
作者
Hirano, Michio [1 ]
Quinzii, Catarina M. [1 ]
DiMauro, Salvatore [1 ]
机构
[1] Columbia Univ, Med Ctr, Dept Neurol, New York, NY 10032 USA
关键词
D O I
10.1016/j.jns.2006.03.017
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
引用
收藏
页码:11 / 12
页数:2
相关论文
共 15 条
[1]  
ARTUCH R, 2006, J NEUROL SCI
[2]   Progression despite replacement of a myopathic form of coenzyme Q10 defect [J].
Auré, K ;
Benoist, JF ;
de Baulny, HO ;
Romero, NB ;
Rigal, O ;
Lombès, A .
NEUROLOGY, 2004, 63 (04) :727-729
[3]   Coenzyme Q10 reverses pathological phenotype and reduces apoptosis in familial CoQ10 deficiency [J].
Di Giovanni, S ;
Mirabella, M ;
Spinazzola, A ;
Crociani, P ;
Silvestri, G ;
Broccolini, A ;
Tonali, P ;
Di Mauro, S ;
Servidei, S .
NEUROLOGY, 2001, 57 (03) :515-518
[4]   Coenzyme Q10 deficiency and isolated myopathy [J].
Horvath, R ;
Schneiderat, P ;
Schoser, BGH ;
Gempel, K ;
Neuen-Jacob, E ;
Plöger, H ;
Müller-Höcker, J ;
Pongratz, DE ;
Naini, A ;
DiMauro, S ;
Lochmüller, H .
NEUROLOGY, 2006, 66 (02) :253-255
[5]   Familial cerebellar ataxia with muscle coenzyme Q10 deficiency [J].
Musumeci, O ;
Naini, A ;
Slonim, AE ;
Skavin, N ;
Hadjigeorgiou, GL ;
Krawiecki, N ;
Weissman, BM ;
Tsao, CY ;
Mendell, JR ;
Shanske, S ;
De Vivo, DC ;
Hirano, M ;
DiMauro, S .
NEUROLOGY, 2001, 56 (07) :849-855
[6]   Primary coenzyme Q10 deficiency and the brain [J].
Naini, A ;
Lewis, VJ ;
Hirano, M ;
DiMauro, S .
BIOFACTORS, 2003, 18 (1-4) :145-152
[7]   MUSCLE COENZYME-Q DEFICIENCY IN FAMILIAL MITOCHONDRIAL ENCEPHALOMYOPATHY [J].
OGASAHARA, S ;
ENGEL, AG ;
FRENS, D ;
MACK, D .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (07) :2379-2382
[8]   A mutation in para-hydroxybenzoate-polyprenyl transferase (COQ2) causes primary coenzyme Q10 deficiency [J].
Quinzii, C ;
Naini, A ;
Salviati, L ;
Trevisson, E ;
Navas, P ;
DiMauro, S ;
Hirano, M .
AMERICAN JOURNAL OF HUMAN GENETICS, 2006, 78 (02) :345-349
[9]   Coenzyme Q deficiency and cerebellar ataxia associated with an aprataxin mutation [J].
Quinzii, CM ;
Kattah, AG ;
Naini, A ;
Akman, HO ;
Mootha, VK ;
DiMauro, S ;
Hirano, M .
NEUROLOGY, 2005, 64 (03) :539-541
[10]   Neonatal presentation of coenzyme Q10 deficiency [J].
Rahman, S ;
Hargreaves, I ;
Clayton, P ;
Heales, S .
JOURNAL OF PEDIATRICS, 2001, 139 (03) :456-458