-
1
-
-
0034700807
-
Mitochondrial respiratory chain disorders I: Mitochondrial DNA defects
-
DOI 10.1016/S0140-6736(99)05225-3
-
Leonard JV, Schapira AHV. Mitochondrial respiratory chain disorders in: Mitochondrial DNA defects. The Lancet 2000; 355: 299-304. (Pubitemid 30068529)
-
(2000)
Lancet
, vol.355
, Issue.9200
, pp. 299-304
-
-
Leonard, J.V.1
Schapira, A.H.V.2
-
2
-
-
33748089976
-
Approaches to the treatment of mitochondrial diseases
-
DOI 10.1002/mus.20598
-
DiMauro S, Hirano M, Schon EA. Approaches to the treatment of mitochondrial diseases. Muscle & nerve 2006; 34: 265-83. (Pubitemid 44300157)
-
(2006)
Muscle and Nerve
, vol.34
, Issue.3
, pp. 265-283
-
-
DiMauro, S.1
Hirano, M.2
Schon, E.A.3
-
3
-
-
33750305666
-
Dynamic subcompartmentalization of the mitochondrial inner membrane
-
DOI 10.1083/jcb.200605138
-
Vogel F, Bornhovd C, Neupert W, Reichert AS. Dynamic subcompartmentalization of the mitochondrial inner membrane. J. Cell Biol. 2006; 175: 237-47. (Pubitemid 44631418)
-
(2006)
Journal of Cell Biology
, vol.175
, Issue.2
, pp. 237-247
-
-
Vogel, F.1
Bornhovd, C.2
Neupert, W.3
Reichert, A.S.4
-
5
-
-
9644274004
-
The epidemiology of mitochondrial disorders - Past, present and future
-
DOI 10.1016/j.bbabio.2004.09.005, PII S0005272804002713, Euromit 6
-
Schaefer AM, Taylor RW, Turnbull DM, Chinnery PF. The epidemiology of mitochondrial disorders - past, present and future. Biochim Biophys Acta 2004; 1659: 115-20. (Pubitemid 39575497)
-
(2004)
Biochimica et Biophysica Acta - Bioenergetics
, vol.1659
, Issue.2-3
, pp. 115-120
-
-
Schaefer, A.M.1
Taylor, R.W.2
Turnbull, D.M.3
Chinnery, P.F.4
-
6
-
-
33748377123
-
Central nervous system manifestations of mitochondrial disorders
-
DOI 10.1111/j.1600-0404.2006.00671.x
-
Finsterer J. Central nervous system manifestations of mitochondrial disorders. Acta Neurologica Scandinavica 2006; 114: 217-38. (Pubitemid 44337240)
-
(2006)
Acta Neurologica Scandinavica
, vol.114
, Issue.4
, pp. 217-238
-
-
Finsterer, J.1
-
7
-
-
33644816856
-
Retrospective, multicentric study of 180 children with cytochrome c oxidase deficiency
-
Bohm M, Pronicka E, Karczmarewicz E, Pronicki M, Piekutowska-Abramczuk D, Sykut-Cegielska J, Mierzewska H, Hansikova H, Vesela K, Tesarova M, Houstkova H, Houstek J, Zeman J. Retrospective, multicentric study of 180 children with cytochrome c oxidase deficiency. Pediatr Res 2006; 59: 21-6.
-
(2006)
Pediatr Res
, vol.59
, pp. 21-26
-
-
Bohm, M.1
Pronicka, E.2
Karczmarewicz, E.3
Pronicki, M.4
Piekutowska-Abramczuk, D.5
Sykut-Cegielska, J.6
Mierzewska, H.7
Hansikova, H.8
Vesela, K.9
Tesarova, M.10
Houstkova, H.11
Houstek, J.12
Zeman, J.13
-
8
-
-
34250302680
-
Mitochondrial hepatopathies: Advances in genetics and pathogenesis
-
DOI 10.1002/hep.21710
-
Lee WS, Sokol RJ. Mitochondrial hepatopathies: Advances in genetics and pathogenesis. Hepatology (Baltimore), Md 2007; 45: 1555-65. (Pubitemid 46918340)
-
(2007)
Hepatology
, vol.45
, Issue.6
, pp. 1555-1565
-
-
Lee, W.S.1
Sokol, R.J.2
-
9
-
-
0034951326
-
Clinical spectrum and diagnosis of mitochondrial disorders
-
Munnich A, Rustin P. Clinical spectrum and diagnosis of mitochondrial disorders. Am J Med Genet 2001; 106: 4-17.
-
(2001)
Am J Med Genet
, vol.106
, pp. 4-17
-
-
Munnich, A.1
Rustin, P.2
-
10
-
-
0014310131
-
Biochemical studies of skeletal muscle mitochondria
-
Microanalysis of cytochrome content, oxidative and phosphorylative activities of mammalian skeletal muscle mitochondria
-
Makinen MW, Lee CP. Biochemical studies of skeletal muscle mitochondria. In. Microanalysis of cytochrome content, oxidative and phosphorylative activities of mammalian skeletal muscle mitochondria. Arch Biochem Biophys 1968; 126: 75-82.
-
(1968)
Arch Biochem Biophys
, vol.126
, pp. 75-82
-
-
Makinen, M.W.1
Lee, C.P.2
-
11
-
-
0027931039
-
Biochemical and molecular investigations in respiratory chain deficiencies
-
DOI 10.1016/0009-8981(94)90055-8
-
Rustin P, Chretien D, Bourgeron T, Gerard B, Rotig A, Saudubray JM, Munnich A. Biochemical and molecular investigations in respiratory chain deficiencies.ClinChimActa1994;228: 35-51. (Pubitemid 24231224)
-
(1994)
Clinica Chimica Acta
, vol.228
, Issue.1
, pp. 35-51
-
-
Rustin, P.1
Chretien, D.2
Bourgeron, T.3
Gerard, B.4
Rotig, A.5
Saudubray, J.M.6
Munnich, A.7
-
14
-
-
0036254695
-
Mitochondrial energy metabolism in very premature neonates
-
DOI 10.1159/000056753
-
Wenchich L, Zeman J, Hansikova H, Plavka R, Sperl W, Houstek J. Mitochondrial energy metabolism in very premature neonates. Biol Neonate 2002; 81: 229-35. (Pubitemid 34507590)
-
(2002)
Biology of the Neonate
, vol.81
, Issue.4
, pp. 229-235
-
-
Wenchich, L.1
Zeman, J.2
Hansikova, H.3
Plavka, R.4
Sperl, W.5
Houstek, J.6
-
15
-
-
0028832212
-
Analysis of oxidative phosphorylation complexes in cultured human fibroblastsand amniocytes by blue-native-electrophoresis using mitoplasts isolated with the help of digitonin
-
Klement P, Nijtmans LG, Van den Bogert C, Houstek J. Analysis of oxidative phosphorylation complexes in cultured human fibroblastsand amniocytes by blue-native-electrophoresis using mitoplasts isolated with the help of digitonin. Anal Biochem 1995; 231: 218-24.
-
(1995)
Anal Biochem
, vol.231
, pp. 218-224
-
-
Klement, P.1
Nijtmans, L.G.2
Van Den Bogert, C.3
Houstek, J.4
-
17
-
-
0033568447
-
Defective kinetics of cytochrome c oxidase and alteration of mitochondrial membrane potential in fibroblasts and cytoplasmic hybrid cells with the mutation for myoclonus epilepsy with ragged-red fibres ('MERRF') at position 8344 nt
-
DOI 10.1042/0264-6021:3420537
-
Antonicka H, Floryk D, Klement P, Stratilova L, Hermanska J, Houstkova H, Kalous M, Drahota Z, Zeman J, Houstek J. Defective kinetics of cytochrome c oxidase and alteration of mitochondrial membrane potential in fibroblastsand cytoplasmic hybrid cells with the mutation for myoclonus epilepsy with ragged-red fibres(merrf) at position 8344 nt. Biochem J 1999; 342 (3): 537-44. (Pubitemid 29452638)
-
(1999)
Biochemical Journal
, vol.342
, Issue.3
, pp. 537-544
-
-
Antonicka, H.1
Floryk, D.2
Klement, P.3
Stratilova, L.4
Hermanska, J.5
Houstkova, H.6
Kalous, M.7
Drahota, Z.8
Zeman, J.9
Houstek, J.10
-
18
-
-
0025802951
-
Evolutionary aspects of cytochrome c oxidase
-
Kadenbach B, Stroh A, Huther FJ, Reimann A, Steverding D. Evolutionary aspects of cytochrome c oxidase. J Bioenerg Biomembr 1991; 23: 321-34.
-
(1991)
J Bioenerg Biomembr
, vol.23
, pp. 321-334
-
-
Kadenbach, B.1
Stroh, A.2
Huther, F.J.3
Reimann, A.4
Steverding, D.5
-
19
-
-
0032104133
-
Assembly of cytochrome-c oxidase in cultured human cells
-
DOI 10.1046/j.1432-1327.1998.2540389.x
-
Nijtmans LG, Taanman JW, Muijsers AO, Speijer D, Van den Bogert C. Assembly of cytochrome-c oxidase in cultured human cells. Eur. J. Biochem. 1998; 254: 389-94. (Pubitemid 28289396)
-
(1998)
European Journal of Biochemistry
, vol.254
, Issue.2
, pp. 389-394
-
-
Nijtmans, L.G.J.1
Taanman, J.-W.2
Muijsers, A.O.3
Speijer, D.4
Van Den, B.C.5
-
20
-
-
29644440471
-
Tissue-specific cytochrome c oxidase assembly defects due to mutations in SCO2 and SURF1
-
DOI 10.1042/BJ20050807
-
Stiburek L, Vesela K, Hansikova H, Pecina P, Tesarova M, Cerna L, Houstek J, Zeman J. Tissue-specific cytochrome c oxidase assembly defects due to mutations in sco2 and surf1. Biochem J. 2005; 392: 625-32. (Pubitemid 43022743)
-
(2005)
Biochemical Journal
, vol.392
, Issue.3
, pp. 625-632
-
-
Stiburek, L.1
Vesela, K.2
Hansikova, H.3
Pecina, P.4
Tesarova, M.5
Cerna, L.6
Houstek, J.7
Zeman, J.8
-
21
-
-
0033766123
-
Human cytochrome oxidase deficiency
-
Robinson BH. Human cytochrome oxidase deficiency. Pediatr Res 2000; 48: 581-5.
-
(2000)
Pediatr Res
, vol.48
, pp. 581-585
-
-
Robinson, B.H.1
-
22
-
-
0037458031
-
Identification of a gene causing human cytochrome c oxidase deficiency by integrative genomics
-
DOI 10.1073/pnas.242716699
-
Mootha VK, Lepage P, Miller K, Bunkenborg J, Reich M, Hjerrild M, Delmonte T, Villeneuve A, Sladek R, Xu F, Mitchell GA, Morin C, Mann M, Hudson TJ, Robinson B, Rioux JD, Lander ES. Identification of a gene causing human cytochrome c oxidase deficiency by integrative genomics. Proc. Natl. Acad. Sci. USA. 2003; 100: 605-10. (Pubitemid 36126099)
-
(2003)
Proceedings of the National Academy of Sciences of the United States of America
, vol.100
, Issue.2
, pp. 605-610
-
-
Mootha, V.K.1
Lepage, P.2
Miller, K.3
Bunkenborg, J.4
Reich, M.5
Hjerrild, M.6
Delmonte, T.7
Villeneuve, A.8
Sladek, R.9
Xu, F.10
Mitchell, G.A.11
Morin, C.12
Mann, M.13
Hudson, T.J.14
Robinson, B.15
Rioux, J.D.16
Lander, E.S.17
-
23
-
-
0038230469
-
Supercomplexes in the respiratory chains of yeast and mammalian mitochondria
-
Schagger H, Pfeiffer K. Supercomplexes in the respiratory chains of yeast and mammalian mitochondria. Embo J 2000; 19: 1777-83. (Pubitemid 30204389)
-
(2000)
EMBO Journal
, vol.19
, Issue.8
, pp. 1777-1783
-
-
Schagger, H.1
Pfeiffer, K.2
-
24
-
-
41649106228
-
Activities of respiratory chain complexes and pyruvate dehydrogenase in isolated muscle mitochondria in premature neonates
-
DOI 10.1016/j.earlhumdev.2006.07.008, PII S0378378207001120
-
Honzik T, Wenchich L, Bohm M, Hansikova H, Pejznochova M, Zapadlo M, Plavka R, Zeman J. Activities of respiratory chain complexes and pyruvate dehydrogenase in isolated muscle mitochondria in premature neonates. Early human development 2008; 84: 269-76. (Pubitemid 351484183)
-
(2008)
Early Human Development
, vol.84
, Issue.4
, pp. 269-276
-
-
Honzik, T.1
Wenchich, L.2
Bohm, M.3
Hansikova, H.4
Pejznochova, M.5
Zapadlo, M.6
Plavka, R.7
Zeman, J.8
-
25
-
-
82455161803
-
Mitochondrial energy generating system in liver during foetal development
-
Hansikova H, Havlickova V, Stiburek L, Pejznochova M, Honzik T, Magner M, Bohm M, Hulkova H, Zeman J. Mitochondrial energy generating system in liver during foetal development. J Inherit Metab Dis 2007; 30 (1): 68.
-
(2007)
J Inherit Metab Dis
, vol.30
, Issue.1
, pp. 68
-
-
Hansikova, H.1
Havlickova, V.2
Stiburek, L.3
Pejznochova, M.4
Honzik, T.5
Magner, M.6
Bohm, M.7
Hulkova, H.8
Zeman, J.9
-
26
-
-
0034951707
-
Cytochrome c oxidase deficiency
-
Shoubridge EA. Cytochrome c oxidase deficiency. Am J Med Genet 2001; 106: 46-52.
-
(2001)
Am J Med Genet
, vol.106
, pp. 46-52
-
-
Shoubridge, E.A.1
-
27
-
-
0037972522
-
Mitochondrial respiratory-chain diseases
-
DOI 10.1056/NEJMra022567
-
DiMauro S, Schon EA. Mitochondrial respiratory-chain diseases. N Engl J Med 2003; 348: 2656-68. (Pubitemid 36741594)
-
(2003)
New England Journal of Medicine
, vol.348
, Issue.26
, pp. 2656-2668
-
-
DiMauro, S.1
Schon, E.A.2
-
28
-
-
0033766123
-
Human cytochrome oxidase deficiency
-
Robinson BH. Human cytochrome oxidase deficiency.PediatrRes2000;48:581- 85.
-
(2000)
PediatrRes
, vol.48
, pp. 581-585
-
-
Robinson, B.H.1
-
29
-
-
0034949930
-
Mitochondrial disorders: Genetics, counseling, prenatal diagnosis and reproductive options
-
Thorburn DR, Dahl HH. Mitochondrial disorders: Genetics, counseling, prenatal diagnosis and reproductive options. Am J Med Genet 2001; 106: 102-14.
-
(2001)
Am J Med Genet
, vol.106
, pp. 102-114
-
-
Thorburn, D.R.1
Dahl, H.H.2
-
30
-
-
33947362946
-
Defects in cytochrome oxidase assembly in humans: Lessons from yeast
-
DOI 10.1139/O06-201
-
Zee JM, Glerum DM. Defects in cytochrome oxidase assembly in humans: Lessons from yeast. Biochem Cell Biol 2006; 84: 859-69. (Pubitemid 46450686)
-
(2006)
Biochemistry and Cell Biology
, vol.84
, Issue.6
, pp. 859-869
-
-
Zee, J.M.1
Glerum, D.M.2
-
31
-
-
4644221272
-
Clinical, biochemical and molecular analyses of six patients with isolated cytochrome c oxidase deficiency due to mutations in the SCO2 gene
-
DOI 10.1080/08035250410008761
-
Vesela K, Hansikova H, Tesarova M, Martasek P, Elleder M, Houstek J, Zeman J. Clinical, biochemical and molecular analyses of six patients with isolated cytochrome c oxidase deficiency due to mutations in the sco2 gene. Acta Paediatr 2004; 93: 1312-7. (Pubitemid 39273902)
-
(2004)
Acta Paediatrica, International Journal of Paediatrics
, vol.93
, Issue.10
, pp. 1312-1317
-
-
Vesela, K.1
Hansikova, H.2
Tesarova, M.3
Martasek, P.4
Elleder, M.5
Houstek, J.6
Zeman, J.7
-
32
-
-
0023883150
-
Deletions of muscle mitochondrial DNA in patients with mitochondrial myopathies
-
DOI 10.1038/331717a0
-
Holt IJ, Harding AE, Morgan-Hughes JA. Deletions of muscle mitochondrial DNA in patients with mitochondrial myopathies. Nature 1988; 331: 717-9. (Pubitemid 18062238)
-
(1988)
Nature
, vol.331
, Issue.6158
, pp. 717-719
-
-
Holt, I.J.1
Harding, A.E.2
Morgan-Hughes, J.A.3
-
33
-
-
45449121006
-
Severe infantile encephalomyopathy caused by a mutation in cox6b1, a nucleus-encoded subunit of cytochrome c oxidase
-
Massa V, Fernandez-Vizarra E, Alshahwan S, Bakhsh E, Goffrini P, Ferrero I, Mereghetti P, D'Adamo P, Gasparini P, Zeviani M. Severe infantile encephalomyopathy caused by a mutation in cox6b1, a nucleus-encoded subunit of cytochrome c oxidase. Am J Hum Genet 2008; 82: 1281-9.
-
(2008)
Am J Hum Genet
, vol.82
, pp. 1281-1289
-
-
Massa, V.1
Fernandez-Vizarra, E.2
Alshahwan, S.3
Bakhsh, E.4
Goffrini, P.5
Ferrero, I.6
Mereghetti, P.7
D'Adamo, P.8
Gasparini, P.9
Zeviani, M.10
-
34
-
-
0032470811
-
Mutations of surf-1 in leigh disease associated with cytochrome c oxidase deficiency
-
Tiranti V, Hoertnagel K, Carrozzo R, Galimberti C, Munaro M, Granatiero M, Zelante L, Gasparini P, Marzella R, Rocchi M, Bayona-Bafaluy MP, Enriquez JA, Uziel G, Bertini E, Dionisi-Vici C, Franco B, Meitinger T, Zeviani M. Mutations of surf-1 in leigh disease associated with cytochrome c oxidase deficiency. Am J Hum Genet 1998; 63: 1609-21.
-
(1998)
Am J Hum Genet
, vol.63
, pp. 1609-1621
-
-
Tiranti, V.1
Hoertnagel, K.2
Carrozzo, R.3
Calimberti, C.4
Munaro, M.5
Granatiero, M.6
Zelante, L.7
Gasparini, P.8
Marzella, R.9
Rocchi, M.10
Bayona-Bafaluy, M.P.11
Enriquez, J.A.12
Uziel, G.13
Bertini, E.14
Dionisi-Vici, C.15
Franco, B.16
Meitinger, T.17
Zeviani, M.18
-
35
-
-
17344362021
-
SURF1, encoding a factor involved in the biogenesis of cytochrome c oxidase, is mutated in Leigh syndrome
-
DOI 10.1038/3804
-
Zhu Z, Yao J, Johns T, Fu K, De Bie I, Macmillan C, Cuthbert AP, Newbold RF, Wang J, Chevrette M, Brown GK, Brown RM, Shoubridge EA. Surf1, encoding a factor involved in the biogenesis of cytochrome c oxidase, is mutated in leigh syndrome. Nat Genet 1998; 20: 337-43. (Pubitemid 28541630)
-
(1998)
Nature Genetics
, vol.20
, Issue.4
, pp. 337-343
-
-
Zhu, Z.1
Yao, J.2
Johns, T.3
Fu, K.4
De Bie, I.5
Macmillan, C.6
Cuthbert, A.P.7
Newbold, R.F.8
Wang, J.-C.9
Chevrette, M.10
Brown, G.K.11
Brown, R.M.12
Shoubridge, E.A.13
-
36
-
-
0032699506
-
Fatal infantile cardioencephalomyopathy with cox deficiency and mutations in sco2, a cox assembly gene
-
Papadopoulou LC, Sue CM, Davidson MM, Tanji K, Nishino I, Sadlock JE, Krishna S, Walker W, Selby J, Glerum DM, Coster RV, Lyon G, Scalais E, Lebel R, Kaplan P, Shanske S, De Vivo DC, Bonilla E, Hirano M, DiMauro S, Schon EA. Fatal infantile cardioencephalomyopathy with cox deficiency and mutations in sco2, a cox assembly gene. Nat Genet 1999; 23: 333-7.
-
(1999)
Nat Genet
, vol.23
, pp. 333-337
-
-
Papadopoulou, L.C.1
Sue, C.M.2
Davidson, M.M.3
Tanji, K.4
Nishino, I.5
Sadlock, J.E.6
Krishna, S.7
Walker, W.8
Selby, J.9
Glerum, D.M.10
Coster, R.V.11
Lyon, G.12
Scalais, E.13
Lebel, R.14
Kaplan, P.15
Shanske, S.16
De Vivo, D.C.17
Bonilla, E.18
Hirano, M.19
DiMauro, S.20
Schon, E.A.21
more..
-
37
-
-
0034192365
-
A mutation in the human heme A:farnesyltransferase gene (COX10) causes cytochrome c oxidase deficiency
-
Valnot I, von Kleist-Retzow JC, Barrientos A, Gorbatyuk M, Taanman JW, Mehaye B, Rustin P, Tzagoloff A, Munnich A, Rotig A. A mutation in the human heme a: Farnesyltransferase gene (cox10) causes cytochrome c oxidase deficiency. Hum Mol Genet 2000; 9:1245-9. (Pubitemid 30248611)
-
(2000)
Human Molecular Genetics
, vol.9
, Issue.8
, pp. 1245-1249
-
-
Valnot, I.1
Von Kleist-Retzow, J.-C.2
Barrientos, A.3
Gorbatyuk, M.4
Taanman, J.-W.5
Mehaye, B.6
Rustin, P.7
Tzagoloff, A.8
Munnich, A.9
Rotig, A.10
-
38
-
-
0037221950
-
Mutations in COX15 produce a defect in the mitochondrial heme biosynthetic pathway, causing early-onset fatal hypertrophic cardiomyopathy
-
DOI 10.1086/345489
-
Antonicka H, Mattman A, Carlson CG, Glerum DM, Hoffbuhr KC, Leary SC, Kennaway NG, Shoubridge EA. Mutations in cox15 produce a defect in the mitochondrial heme biosynthetic pathway, causing early-onset fatal hypertrophic cardiomyopathy. Am J Hum Genet 2003; 72: 101-14. (Pubitemid 36056846)
-
(2003)
American Journal of Human Genetics
, vol.72
, Issue.1
, pp. 101-114
-
-
Antonicka, H.1
Mattman, A.2
Carlson, C.G.3
Glerum, D.M.4
Hoffbuhr, K.C.5
Leary, S.C.6
Kennaway, N.G.7
Shoubridge, E.A.8
-
39
-
-
0033754154
-
Mutations of the sco1 gene in mitochondrial cytochrome c oxidase deficiency with neonatal-onset hepatic failure and encephalopathy
-
Valnot I, Osmond S, Gigarel N, Mehaye B, Amiel J, Cormier-Daire V, Munnich A, Bonnefont JP, Rustin P, Rotig A. Mutations of the sco1 gene in mitochondrial cytochrome c oxidase deficiency with neonatal-onset hepatic failure and encephalopathy. Am J Hum Genet 2000; 67: 1104-9.
-
(2000)
Am J Hum Genet
, vol.67
, pp. 1104-1109
-
-
Valnot, I.1
Osmond, S.2
Gigarel, N.3
Mehaye, B.4
Amiel, J.5
Cormier-Daire, V.6
Munnich, A.7
Bonnefont, J.P.8
Rustin, P.9
Rotig, A.10
-
40
-
-
0142154270
-
Mutations in COX10 result in a defect in mitochondrial heme A biosynthesis and account for multiple, early-onset clinical phenotypes associated with isolated COX deficiency
-
DOI 10.1093/hmg/ddg284
-
Antonicka H, Leary SC, Guercin GH, Agar JN, Horvath R, Kennaway NG, Harding CO, Jaksch M, Shoubridge EA. Mutations in cox10 result in a defect in mitochondrial heme a biosynthesis and account for multiple, early-onset clinical phenotypes associated with isolated cox deficiency.HumMolGenet2003;12:2693-702. (Pubitemid 37304691)
-
(2003)
Human Molecular Genetics
, vol.12
, Issue.20
, pp. 2693-2702
-
-
Antonicka, H.1
Leary, S.C.2
Guercin, G.-H.3
Agar, J.N.4
Horvath, R.5
Kennaway, N.G.6
Harding, C.O.7
Jaksch, M.8
Shoubridge, E.A.9
-
41
-
-
4944260285
-
Mitochondrial disorders
-
DOI 10.1093/brain/awh259
-
Zeviani M, Di Donato S. Mitochondrial disorders. Brain 2004; 127: 2153-72. (Pubitemid 39382225)
-
(2004)
Brain
, vol.127
, Issue.10
, pp. 2153-2172
-
-
Zeviani, M.1
Di, D.S.2
-
42
-
-
34250676955
-
Mitochondrial diseases: Therapeutic approaches
-
DOI 10.1007/s10540-007-9041-4
-
DiMauro S, Mancuso M. Mitochondrial diseases: Therapeutic approaches. Bioscience reports 2007; 27: 125-37. (Pubitemid 46940941)
-
(2007)
Bioscience Reports
, vol.27
, Issue.1-3
, pp. 125-137
-
-
DiMauro, S.1
Mancuso, M.2
|