Multiple sclerosis-like disorder in OPA1-related autosomal dominant optic atrophy

被引：47

作者：

Verny, C. ^{[2
]}

Loiseau, D. ^{[1
]}

Scherer, C. ^{[2
]}

Lejeune, P. ^{[2
]}

Chevrollier, A. ^{[1
]}

Gueguen, N. ^{[1
]}

Guillet, V. ^{[1
]}

Dubas, F. ^{[2
]}

Reynier, P. ^{[1
]}

Amati-Bonneau, P. ^{[1
]}

Bonneau, D. ^{[1
]}

机构：

[1] Ctr Hosp Univ, Dept Biochim & Genet, INSERM, U 694, F-49933 Angers, France

[2] Ctr Hosp Univ, Dept Neurol, INSERM, U 694, F-49933 Angers, France

来源：

NEUROLOGY | 2008年 / 70卷 / 13期

关键词：

D O I：

10.1212/01.wnl.0000289194.89359.a1

中图分类号：

R74 [神经病学与精神病学];

学科分类号：

摘要：

[No abstract available]

引用

页码：1152 / 1153

页数：2

共 8 条

[1] OPA1 R445H mutation in optic atrophy associated with sensorineural deafness [J].

Amati-Bonneau, P ;

Guichet, A ;

Olichon, A ;

Chevrollier, A ;

Viala, F ;

Miot, S ;

Ayuso, C ;

Odent, S ;

Arrouet, C ;

Verny, C ;

Calmels, MN ;

Simard, G ;

Belenguer, P ;

Wang, J ;

Puel, JL ;

Hamel, C ;

Malthièry, Y ;

Bonneau, D ;

Lenaers, G ;

Reynier, P .

ANNALS OF NEUROLOGY, 2005, 58 (06) :958-963

[2] Dissecting mitochondrial fusion [J].

Chan, David C. .

DEVELOPMENTAL CELL, 2006, 11 (05) :592-594

[3] Nuclear gene OPA1, encoding a mitochondrial dynamin-related protein, is mutated in dominant optic atrophy [J].

Delettre, C ;

Lenaers, G ;

Griffoin, JM ;

Gigarel, N ;

Lorenzo, C ;

Belenguer, P ;

Pelloquin, L ;

Grosgeorge, J ;

Turc-Carel, C ;

Perret, E ;

Astarie-Dequeker, C ;

Lasquellec, L ;

Arnaud, B ;

Ducommun, B ;

Kaplan, J ;

Hamel, CP .

NATURE GENETICS, 2000, 26 (02) :207-210

[4] Mitochondrial dysfunction as a cause of axonal degeneration in multiple sclerosis patients [J].

Dutta, R ;

McDonough, J ;

Yin, XG ;

Peterson, J ;

Chang, A ;

Torres, T ;

Gudz, T ;

Macklin, EB ;

Lewis, DA ;

Fox, RJ ;

Rudick, R ;

Mirnics, K ;

Trapp, BD .

ANNALS OF NEUROLOGY, 2006, 59 (03) :478-489

[5] OPA1 controls apoptotic cristae remodeling independently from mitochondrial fusion [J].

Frezza, Christian ;

Cipolat, Sara ;

de Brito, Olga Martins ;

Micaroni, Massimo ;

Beznoussenko, Galina V. ;

Rudka, Tomasz ;

Bartoli, Davide ;

Polishuck, Roman S. ;

Danial, Nika N. ;

De Strooper, Bart ;

Scorrano, Luca .

CELL, 2006, 126 (01) :177-189

[6] OCCURRENCE OF A MULTIPLE SCLEROSIS-LIKE ILLNESS IN WOMEN WHO HAVE A LEBERS HEREDITARY OPTIC NEUROPATHY MITOCHONDRIAL-DNA MUTATION [J].

HARDING, AE ;

SWEENEY, MG ;

MILLER, DH ;

MUMFORD, CJ ;

KELLARWOOD, H ;

MENARD, D ;

MCDONALD, WI ;

COMPSTON, DAS .

BRAIN, 1992, 115 :979-989

[7] Deficit of in vivo mitochondrial ATP production in OPA1-related dominant optic atrophy [J].

Lodi, R ;

Tonon, C ;

Valentino, ML ;

Lotti, S ;

Clementi, V ;

Malucelli, E ;

Barboni, P ;

Longanesi, L ;

Schimpf, S ;

Wissinger, B ;

Baruzzi, A ;

Barbiroli, B ;

Carelli, V .

ANNALS OF NEUROLOGY, 2004, 56 (05) :719-723

[8] Mitochondrial coupling defect in Charcot-Marie-Tooth type 2A disease [J].

Loiseau, Dominique ;

Chevrollier, Arnaud ;

Verny, Christophe ;

Guillet, Virginie ;

Gueguen, Naig ;

de Crescenzo, Marie-Anne Pou ;

Ferre, Marc ;

Malinge, Marie-Claire ;

Guichet, Agnes ;

Nicolas, Guillaume ;

Amati-Bonneau, Patrizia ;

Malthiery, Yves ;

Bonneau, Dominique ;

Reynier, Pascal .

ANNALS OF NEUROLOGY, 2007, 61 (04) :315-323

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