-
1
-
-
1842567157
-
Conversion de l'énergie: Mitochondries et chloroplastes
-
Flammarion, Paris
-
Alberts B, Bray D, Lewis J, Raff M, Roberts K, Watson JD. Conversion de l'énergie: mitochondries et chloroplastes. In: Biologie moléculaire de la cellule. Deuxième édition. Flammarion, Paris, 1990; 341-404.
-
(1990)
Biologie Moléculaire de la Cellule. Deuxième Édition
, pp. 341-404
-
-
Alberts, B.1
Bray, D.2
Lewis, J.3
Raff, M.4
Roberts, K.5
Watson, J.D.6
-
2
-
-
0034700807
-
Mitochondrial respiratory chain disorders. I: Mitochondrial DNA defects
-
Leonard JV, Schapira AH. Mitochondrial respiratory chain disorders. I: mitochondrial DNA defects. Lancet 2000; 355: 299-304.
-
(2000)
Lancet
, vol.355
, pp. 299-304
-
-
Leonard, J.V.1
Schapira, A.H.2
-
3
-
-
0034728096
-
Mitochondrial respiratory chain disorders. II: Neurodegenerative disorders and nuclear gene defects
-
Leonard JV, Schapira AH. Mitochondrial respiratory chain disorders. II: neurodegenerative disorders and nuclear gene defects Lancet 2000; 355: 389-94.
-
(2000)
Lancet
, vol.355
, pp. 389-394
-
-
Leonard, J.V.1
Schapira, A.H.2
-
4
-
-
0031822037
-
Prenatal diagnosis of Friedreich ataxia
-
Pandolfo M, Montermini L. Prenatal diagnosis of Friedreich ataxia. Prenat Diagn 1998; 18: 831-3.
-
(1998)
Prenat Diagn
, vol.18
, pp. 831-833
-
-
Pandolfo, M.1
Montermini, L.2
-
5
-
-
0033604060
-
Persistent mitochondrial dysfunction and perinatal exposure to antiretroviral nucleoside analogues
-
Blanche S, Tardieu M, Rustin P, Slama A, Barret B, Firtion G, et al. Persistent mitochondrial dysfunction and perinatal exposure to antiretroviral nucleoside analogues. Lancet 1999; 354: 1084-9.
-
(1999)
Lancet
, vol.354
, pp. 1084-1089
-
-
Blanche, S.1
Tardieu, M.2
Rustin, P.3
Slama, A.4
Barret, B.5
Firtion, G.6
-
6
-
-
0033547598
-
HIV-1 therapy and fetal mitochondrial dysfunction
-
Poulton J, Lyall H, Taylor G, Williams GT. HIV-1 therapy and fetal mitochondrial dysfunction. Lancet 1999; 354: 2081-2.
-
(1999)
Lancet
, vol.354
, pp. 2081-2082
-
-
Poulton, J.1
Lyall, H.2
Taylor, G.3
Williams, G.T.4
-
7
-
-
0034319154
-
Nucleoside exposure in the children of HIV-infected women receiving antiretroviral drugs: Absence of clear evidence for mitochondrial disease in children who died before 5 years of age in five United States cohorts
-
The Perinatal Safety Review Working Group. Nucleoside exposure in the children of HIV-infected women receiving antiretroviral drugs: absence of clear evidence for mitochondrial disease in children who died before 5 years of age in five United States cohorts. J Acquir Immune Defic Syndr 2000; 25: 261-8.
-
(2000)
J Acquir Immune Defic Syndr
, vol.25
, pp. 261-268
-
-
-
8
-
-
0036155708
-
Diagnosis and management of mitochondrial diseases
-
Gillis L, Kaye E. Diagnosis and management of mitochondrial diseases. Pediatr Clin North Am 2002; 49: 203-19.
-
(2002)
Pediatr Clin North Am
, vol.49
, pp. 203-219
-
-
Gillis, L.1
Kaye, E.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
-
-
1842462549
-
Cytopathies mitochondriales: Diagnostic postnatal et diagnostic prénatal
-
Rötig A. Cytopathies mitochondriales: diagnostic postnatal et diagnostic prénatal. Med fœt Echogr Gynecol 2002; 50: 19-24.
-
(2002)
Med Fœt Echogr Gynecol
, vol.50
, pp. 19-24
-
-
Rötig, A.1
-
11
-
-
0028242830
-
Carnitine palmitoyl transferase deficiency in pregnancy - A case report
-
Dreval D, Bernstein D, Zakut H. Carnitine palmitoyl transferase deficiency in pregnancy- a case report. Am J Obstet Gynecol 1994; 170: 1390-2.
-
(1994)
Am J Obstet Gynecol
, vol.170
, pp. 1390-1392
-
-
Dreval, D.1
Bernstein, D.2
Zakut, H.3
-
12
-
-
0032788521
-
Mitochondrial myopathy in a primigravid pregnancy
-
Blake LL, Shaw R.W. Mitochondrial myopathy in a primigravid pregnancy. Br J Obstet Gynaecol 1999; 106: 871-3.
-
(1999)
Br J Obstet Gynaecol
, vol.106
, pp. 871-873
-
-
Blake, L.L.1
Shaw, R.W.2
-
13
-
-
0030944009
-
Pregnancy in chronic progressive external ophtalmoplegia: A case report
-
Ewart RM, Burrows RF. Pregnancy in chronic progressive external ophtalmoplegia: a case report. Am J Perinatol 1997; 14: 293-5.
-
(1997)
Am J Perinatol
, vol.14
, pp. 293-295
-
-
Ewart, R.M.1
Burrows, R.F.2
-
14
-
-
0344417167
-
Pregnancy with mitochondrial encephalopathy, lactic acidosis, and stroke-like episodes syndrome
-
Kovilam OP, Cahill W, Siddiqi TA. Pregnancy with mitochondrial encephalopathy, lactic acidosis, and stroke-like episodes syndrome, Obstet Gynecol 1999; 93: 853
-
(1999)
Obstet Gynecol
, vol.93
, pp. 853
-
-
Kovilam, O.P.1
Cahill, W.2
Siddiqi, T.A.3
-
15
-
-
0344505239
-
Pregnancy and delivery complicated by mitochondrial myopathy, encephalopathy, lactic acidosis, and stoke-like episodes
-
Kokawa N, Ishii Y, Yamoto M, Nakano R. Pregnancy and delivery complicated by mitochondrial myopathy, encephalopathy, lactic acidosis, and stoke-like episodes. Obstet Gynecol 1998; 91: 865.
-
(1998)
Obstet Gynecol
, vol.91
, pp. 865
-
-
Kokawa, N.1
Ishii, Y.2
Yamoto, M.3
Nakano, R.4
-
16
-
-
0032151603
-
Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes with deterioration during pregnancy
-
Yanagawa T, Sakaguchi H, Nakao T, Sasaki H, Matsumoto G, Sanke T, et al. Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes with deterioration during pregnancy. Intem Med 1998; 37: 780-3.
-
(1998)
Intem Med
, vol.37
, pp. 780-783
-
-
Yanagawa, T.1
Sakaguchi, H.2
Nakao, T.3
Sasaki, H.4
Matsumoto, G.5
Sanke, T.6
-
18
-
-
0029985716
-
Leigh syndrome: Clinical features and biochemical and DNA abnormalities
-
Rahman S, Blok RB, Dahl HH, Danks DM, Kirby DM, Chow CW, et al. Leigh syndrome: clinical features and biochemical and DNA abnormalities. Ann Neurol 1996; 39: 343-51.
-
(1996)
Ann Neurol
, vol.39
, pp. 343-351
-
-
Rahman, S.1
Blok, R.B.2
Dahl, H.H.3
Danks, D.M.4
Kirby, D.M.5
Chow, C.W.6
-
19
-
-
0033646445
-
Practical problems in detecting abnormal mitochondrial function and genomes
-
Thorburn DR. Practical problems in detecting abnormal mitochondrial function and genomes. Hum Reprod 2000; 15: 57-67.
-
(2000)
Hum Reprod
, vol.15
, pp. 57-67
-
-
Thorburn, D.R.1
-
20
-
-
0034949930
-
Mitochondrial disorders: Genetics, counselling, prenatal diagnosis and reproductive options
-
Thorburn DR, Dahl HH. Mitochondrial disorders: genetics, counselling, 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
-
21
-
-
0032700777
-
Two cases of prenatal analysis for the pathogenic T to G substitution at nucleotide 8993 in mitochondrial DNA
-
White SL, Shanske S, Biros I, Warwick L, Dahl HM, Thorburn DR, et al. Two cases of prenatal analysis for the pathogenic T to G substitution at nucleotide 8993 in mitochondrial DNA. Prenat Diagn 1999; 19: 1165-8.
-
(1999)
Prenat Diagn
, vol.19
, pp. 1165-1168
-
-
White, S.L.1
Shanske, S.2
Biros, I.3
Warwick, L.4
Dahl, H.M.5
Thorburn, D.R.6
-
22
-
-
0033797760
-
Determination of enzyme activities for prenatal diagnosis of respiratory chain deficiency
-
Faivre L, Cormier-Daire V, Chrétien D, Von Kleist-Retzow JC, Amiel J, Dommergues M, et al. Determination of enzyme activities for prenatal diagnosis of respiratory chain deficiency. Prenat Diagn 2000; 20: 732-7.
-
(2000)
Prenat Diagn
, vol.20
, pp. 732-737
-
-
Faivre, L.1
Cormier-Daire, V.2
Chrétien, D.3
Von Kleist-Retzow, J.C.4
Amiel, J.5
Dommergues, M.6
-
23
-
-
0034873918
-
Prenatal diagnosis of respiratory chain deficiency by direct mutation screening
-
Amiel J, Gigarel N, Benacki A, Benit P, Valnot I, Parfait B, et al. Prenatal diagnosis of respiratory chain deficiency by direct mutation screening. Prenat Diagn 2001; 21: 602-4.
-
(2001)
Prenat Diagn
, vol.21
, pp. 602-604
-
-
Amiel, J.1
Gigarel, N.2
Benacki, A.3
Benit, P.4
Valnot, I.5
Parfait, B.6
-
24
-
-
0032231707
-
A high rate (20-30%) of parental consanguinity in cytochrome-oxidase deficiency
-
Von Kleist-Retzow JC, Cormier-Daire V, De Loulay P, Parfait B, Chrétien D, Rustin P, et al. A high rate (20-30%) of parental consanguinity in cytochrome-oxidase deficiency. Am J Hum Genet 1998; 63: 428-35.
-
(1998)
Am J Hum Genet
, vol.63
, pp. 428-435
-
-
Von Kleist-Retzow, J.C.1
Cormier-Daire, V.2
De Loulay, P.3
Parfait, B.4
Chrétien, D.5
Rustin, P.6
-
25
-
-
0033041968
-
Long-chain 3-hydroxyacyl-CoA deshydrogenase deficiency
-
Tyni T, Pihko H. Long-chain 3-hydroxyacyl-CoA deshydrogenase deficiency. Acta Paediatr 1999; 88: 237-45.
-
(1999)
Acta Paediatr
, vol.88
, pp. 237-245
-
-
Tyni, T.1
Pihko, H.2
-
26
-
-
0025189723
-
Mitochondrial myopathy and preeclampsia associated with pregnancy
-
Berkowitz K, Monteagudo A, Marks F, Jackson U, Baxi L. Mitochondrial myopathy and preeclampsia associated with pregnancy. Am J Obstet Gynecol 1990; 162: 146-7.
-
(1990)
Am J Obstet Gynecol
, vol.162
, pp. 146-147
-
-
Berkowitz, K.1
Monteagudo, A.2
Marks, F.3
Jackson, U.4
Baxi, L.5
-
28
-
-
0029901571
-
Mutations in mitochondrial transfer ribonucleic acid genes in preeclampsia
-
Folgero T, Storbakk N, Torbergsen T, Oian P. Mutations in mitochondrial transfer ribonucleic acid genes in preeclampsia. Am J Obstet Gynecol 1996; 174: 1626-30.
-
(1996)
Am J Obstet Gynecol
, vol.174
, pp. 1626-1630
-
-
Folgero, T.1
Storbakk, N.2
Torbergsen, T.3
Oian, P.4
-
29
-
-
0035181782
-
Contraindication of magnesium sulfate in a pregnancy complicated with late-onset diabetes mellitus and sensory deafness due to mitochondrial myopathy
-
Hosono T, Suzuki M, Chiba Y. Contraindication of magnesium sulfate in a pregnancy complicated with late-onset diabetes mellitus and sensory deafness due to mitochondrial myopathy. J Mareta Fetal Med 2001; 10: 355-6.
-
(2001)
J Mareta Fetal Med
, vol.10
, pp. 355-356
-
-
Hosono, T.1
Suzuki, M.2
Chiba, Y.3
-
30
-
-
0028365102
-
Maternally inherited diabetes and deafness is a distinct subtype of diabetes and associates with a single point mutation in the mitochondrial tRNA Leu (UUR) gene
-
Van den Ouweland JM, Lemkes HH, Trembath RC, Ross R, Velho G, Cohen D, et al. Maternally inherited diabetes and deafness is a distinct subtype of diabetes and associates with a single point mutation in the mitochondrial tRNA Leu (UUR) gene. Diabetes 1994; 43: 746-51.
-
(1994)
Diabetes
, vol.43
, pp. 746-751
-
-
Van Den Ouweland, J.M.1
Lemkes, H.H.2
Trembath, R.C.3
Ross, R.4
Velho, G.5
Cohen, D.6
-
31
-
-
0028328317
-
A subtype of diabetes mellitus associated with a mutation of mitochondrial DNA
-
Kadowaki T, Kadowaki H, Mori Y, Tobe K, Sakuta R, Suzuki Y, et al. A subtype of diabetes mellitus associated with a mutation of mitochondrial DNA. N Engl J Med 1994; 330: 962-8.
-
(1994)
N Engl J Med
, vol.330
, pp. 962-968
-
-
Kadowaki, T.1
Kadowaki, H.2
Mori, Y.3
Tobe, K.4
Sakuta, R.5
Suzuki, Y.6
-
32
-
-
0029745044
-
Genetic counselling and prenatal diagnosis in disorders of the mitochondrial energy metabolism
-
Ruitenbeek W, Wendel U, Hamel BCJ, Trijbels JMF. Genetic counselling and prenatal diagnosis in disorders of the mitochondrial energy metabolism. J Inher Metab Dis 1996; 19: 581-7.
-
(1996)
J Inher Metab Dis
, vol.19
, pp. 581-587
-
-
Ruitenbeek, W.1
Wendel, U.2
Hamel, B.C.J.3
Trijbels, J.M.F.4
-
33
-
-
0031768035
-
Prenatal diagnosis of pyruvate carboxylase deficiency by direct measurement of catalytic activity on chorionic villi samples
-
Van Coster RN, Janssens S, Misson JP, Verloes A, Leroy JG. Prenatal diagnosis of pyruvate carboxylase deficiency by direct measurement of catalytic activity on chorionic villi samples. Prenat Diagn 1998; 18: 1041-4.
-
(1998)
Prenat Diagn
, vol.18
, pp. 1041-1044
-
-
Van Coster, R.N.1
Janssens, S.2
Misson, J.P.3
Verloes, A.4
Leroy, J.G.5
-
34
-
-
0028239213
-
Prenatal diagnosis of pyruvate dehydrogenase E1α subunit deficiency
-
Brown RM, Brown GK. Prenatal diagnosis of pyruvate dehydrogenase E1α subunit deficiency. Prenat Diagn 1994; 14: 435-42.
-
(1994)
Prenat Diagn
, vol.14
, pp. 435-442
-
-
Brown, R.M.1
Brown, G.K.2
-
35
-
-
0032700776
-
First prenatal diagnosis of defects in the HsPDX1 gene encoding protein X, an additional lipoyl-containing subunit of the human pyruvate dehydrogenase complex
-
Rouillac C, Aral B, Fouque F, Marchant D, Saudubray JM, Dumez Y, et al. First prenatal diagnosis of defects in the HsPDX1 gene encoding protein X, an additional lipoyl-containing subunit of the human pyruvate dehydrogenase complex. Prenat Diagn 1999; 19: 1160-4.
-
(1999)
Prenat Diagn
, vol.19
, pp. 1160-1164
-
-
Rouillac, C.1
Aral, B.2
Fouque, F.3
Marchant, D.4
Saudubray, J.M.5
Dumez, Y.6
-
36
-
-
0026533834
-
Lack of transmission of deleted mtDNA from a woman with Kearns-Sayre syndrome to her child
-
Larsson NG, Eiken HG, Boman H, Holme E, Oldfors A, Tulinius MH. Lack of transmission of deleted mtDNA from a woman with Kearns-Sayre syndrome to her child. Am J Hum Genet 1992; 50: 360-3.
-
(1992)
Am J Hum Genet
, vol.50
, pp. 360-363
-
-
Larsson, N.G.1
Eiken, H.G.2
Boman, H.3
Holme, E.4
Oldfors, A.5
Tulinius, M.H.6
-
37
-
-
0030665556
-
Segregation of the G8993 mutant mitochondrial DNA through generation and embryonic tissues in a family at risk of Leigh syndrome
-
Ferlin T, Landrieu P, Rambaud C, Fernandez H, Dumoulin R, Rustin P, et al. Segregation of the G8993 mutant mitochondrial DNA through generation and embryonic tissues in a family at risk of Leigh syndrome. J Pediatr 1997; 131: 447-9.
-
(1997)
J Pediatr
, vol.131
, pp. 447-449
-
-
Ferlin, T.1
Landrieu, P.2
Rambaud, C.3
Fernandez, H.4
Dumoulin, R.5
Rustin, P.6
-
38
-
-
0033652899
-
Towards reliable prenatal diagnosis of mtADN point mutations: Studies of nt8993 mutations in oocytes, fetal tissues, children and adults
-
Dahl HH, Thorburn DR, White SL. Towards reliable prenatal diagnosis of mtADN point mutations: studies of nt8993 mutations in oocytes, fetal tissues, children and adults. Hum Reprod 2000; 15: 246-55.
-
(2000)
Hum Reprod
, vol.15
, pp. 246-255
-
-
Dahl, H.H.1
Thorburn, D.R.2
White, S.L.3
-
39
-
-
0028286775
-
Familial mitochondrial encephalopathy with fetal ultrasonographic ventriculomegaly and intracerebral calcifications
-
Samson JF, Barth PG, de Vries JI, Menko FH, Ruitenbeek W, van Oost BA, et al. Familial mitochondrial encephalopathy with fetal ultrasonographic ventriculomegaly and intracerebral calcifications. Eur J Pediatr 1994; 153: 510-6.
-
(1994)
Eur J Pediatr
, vol.153
, pp. 510-516
-
-
Samson, J.F.1
Barth, P.G.2
De Vries, J.I.3
Menko, F.H.4
Ruitenbeek, W.5
Van Oost, B.A.6
-
40
-
-
0035687821
-
Prenatal diagnosis of pyruvate dehydrogenase deficiency using magnetic resonance imaging
-
Robinson JN, Norwitz ER, Mulkern R, Brown SA, Rybicki F, Tempany CM. Prenatal diagnosis of pyruvate dehydrogenase deficiency using magnetic resonance imaging. Prenat Diagn 2001; 21: 1053-6.
-
(2001)
Prenat Diagn
, vol.21
, pp. 1053-1056
-
-
Robinson, J.N.1
Norwitz, E.R.2
Mulkern, R.3
Brown, S.A.4
Rybicki, F.5
Tempany, C.M.6
-
41
-
-
0035218325
-
Congenital hydranencephalic-hydrocephalic syndrome with proliferative vasculopathy: A possible relation with mitochondrial dysfunction
-
Castro-Gago M, Pintos-Martinez E, Forteza-Vila J, Iglesias-Diz M, Ucieda-Somoza R, Silva-Villar I, et al. Congenital hydranencephalic-hydrocephalic syndrome with proliferative vasculopathy: a possible relation with mitochondrial dysfunction. J Child Neurol 2001; 16: 858-62.
-
(2001)
J Child Neurol
, vol.16
, pp. 858-862
-
-
Castro-Gago, M.1
Pintos-Martinez, E.2
Forteza-Vila, J.3
Iglesias-Diz, M.4
Ucieda-Somoza, R.5
Silva-Villar, I.6
-
42
-
-
0030005502
-
Anaesthetic management of labour and delivery in the parturient with mitochondrial myopathy
-
Rosaeg OP, Morrison S, MacLeod J.P. Anaesthetic management of labour and delivery in the parturient with mitochondrial myopathy. Can J Anaesth 1996; 43: 403-7.
-
(1996)
Can J Anaesth
, vol.43
, pp. 403-407
-
-
Rosaeg, O.P.1
Morrison, S.2
MacLeod, J.P.3
-
43
-
-
0034296915
-
Prise en charge anesthésique du travail obstétrical chez une parturiente atteinte d'un déficit musculaire en carnitine palmitoyl transférase
-
Moundras JM, Wattrisse G, Leroy B, Decocq J, Krivosic-Horber R. Prise en charge anesthésique du travail obstétrical chez une parturiente atteinte d'un déficit musculaire en carnitine palmitoyl transférase. Ann Fr Anesth Reanim 2000; 19: 611-6.
-
(2000)
Ann Fr Anesth Reanim
, vol.19
, pp. 611-616
-
-
Moundras, J.M.1
Wattrisse, G.2
Leroy, B.3
Decocq, J.4
Krivosic-Horber, R.5
-
44
-
-
0037159183
-
Ubiquinone and nicotinamide treatment of patients with the 3243 A-G mtDNA mutation
-
Remes AM, Liimatta EV, Winqvist S, Tolonen U, Ranua JA, Reinikainen K, et al. Ubiquinone and nicotinamide treatment of patients with the 3243 A-G mtDNA mutation. Neurology 2002; 59: 1275-7.
-
(2002)
Neurology
, vol.59
, pp. 1275-1277
-
-
Remes, A.M.1
Liimatta, E.V.2
Winqvist, S.3
Tolonen, U.4
Ranua, J.A.5
Reinikainen, K.6
-
45
-
-
0036398010
-
Coenzyme Q (10) and idebenone in the therapy of respiratory chain diseases: Rationale and comparative benefits
-
Geromel V, Darin N, Chretien D, Benit P, DeLonlay P, Rötig A, et al. Coenzyme Q (10) and idebenone in the therapy of respiratory chain diseases: rationale and comparative benefits. Mol Genet Metab 2002; 77: 21.
-
(2002)
Mol Genet Metab
, vol.77
, pp. 21
-
-
Geromel, V.1
Darin, N.2
Chretien, D.3
Benit, P.4
DeLonlay, P.5
Rötig, A.6
-
46
-
-
0030730874
-
Mitochondrial myopathy with tRNA (Leu (UUR)) mutation and complex I deficiency responsive to riboflavin
-
Ogle RF, Christodoulou J, Fagan E, Blok RB, Kirby DM, Seller KL, et al. Mitochondrial myopathy with tRNA (Leu (UUR)) mutation and complex I deficiency responsive to riboflavin. J Pediatr 1997; 130: 138-45.
-
(1997)
J Pediatr
, vol.130
, pp. 138-145
-
-
Ogle, R.F.1
Christodoulou, J.2
Fagan, E.3
Blok, R.B.4
Kirby, D.M.5
Seller, K.L.6
-
47
-
-
0036347518
-
Effects of oral creatine supplementation in a patient with MELAS phenotype and associated nephropathy
-
Barisic N, Bernert G, Ipsiroglu O, Stromberger C, Muller T, Gruber S, et al. Effects of oral creatine supplementation in a patient with MELAS phenotype and associated nephropathy. Neuropediatrics 2002; 33: 157-61.
-
(2002)
Neuropediatrics
, vol.33
, pp. 157-161
-
-
Barisic, N.1
Bernert, G.2
Ipsiroglu, O.3
Stromberger, C.4
Muller, T.5
Gruber, S.6
-
49
-
-
0034308261
-
Progress in genetic counselling and prenatal diagnosis of maternally inherited mtDNA diseases
-
Poulton JR, Marchington D. Progress in genetic counselling and prenatal diagnosis of maternally inherited mtDNA diseases. Neuromuscul Disord 2000; 10: 484-7.
-
(2000)
Neuromuscul Disord
, vol.10
, pp. 484-487
-
-
Poulton, J.R.1
Marchington, D.2
-
50
-
-
0037015695
-
Mitochondrial respiratory rates and activities of respiratory chain complexes correlate linearly with heteroplasmy of deleted mtDNA without threshold and independently of deletion size
-
Gellerich FN, Deschauer M, Chen Y, Muller T, Neudecker S, Zierz S. Mitochondrial respiratory rates and activities of respiratory chain complexes correlate linearly with heteroplasmy of deleted mtDNA without threshold and independently of deletion size. Biochim Biophys Acta 2002; 1556: 41-52
-
(2002)
Biochim Biophys Acta
, vol.1556
, pp. 41-52
-
-
Gellerich, F.N.1
Deschauer, M.2
Chen, Y.3
Muller, T.4
Neudecker, S.5
Zierz, S.6
|