-
1
-
-
0029638664
-
Mitochondrial DNA and disease
-
Johns D.R. Mitochondrial DNA and disease N Engl J Med 333 1995 638 644
-
(1995)
N Engl J Med
, vol.333
, pp. 638-644
-
-
Johns, D.R.1
-
2
-
-
0013665453
-
Mitochondrial hepatopathies
-
Sokol R.J. Narkewicz M.R. Mitochondrial hepatopathies Suchy F.J. Liver disease in children 1994 Mosby St. Louis 888 896
-
(1994)
, pp. 888-896
-
-
Sokol, R.J.1
Narkewicz, M.R.2
-
3
-
-
0027497228
-
Identical mitochondrial DNA deletion in mother with progressive external ophthalmoplegia and son with Pearson marrow-pancreas syndrome
-
Bernes S.M. Bacino C. Prezant T.R. Identical mitochondrial DNA deletion in mother with progressive external ophthalmoplegia and son with Pearson marrow-pancreas syndrome J Pediatr 123 1993 598 602
-
(1993)
J Pediatr
, vol.123
, pp. 598-602
-
-
Bernes, S.M.1
Bacino, C.2
Prezant, T.R.3
-
5
-
-
0028301915
-
Mitochondrial neurogastrointestinal encephaohnyopathy (MNGIE): clinical, biochemical, and genetic features of an autosomal recessive mitochondrial disorder
-
Hirano M. Silvestri G. Blake D.M. Mitochondrial neurogastrointestinal encephaohnyopathy (MNGIE): clinical, biochemical, and genetic features of an autosomal recessive mitochondrial disorder Neurology 44 1994 721 727
-
(1994)
Neurology
, vol.44
, pp. 721-727
-
-
Hirano, M.1
Silvestri, G.2
Blake, D.M.3
-
6
-
-
0027477946
-
Do defects in mitochondrial energy metabolism underlie the pathology of neurodegenerative diseases?
-
Beal M.F. Hyman B.T. Koroshetz W. Do defects in mitochondrial energy metabolism underlie the pathology of neurodegenerative diseases? Trends Neurosci 16 1993 125 131
-
(1993)
Trends Neurosci
, vol.16
, pp. 125-131
-
-
Beal, M.F.1
Hyman, B.T.2
Koroshetz, W.3
-
7
-
-
0026587335
-
Mitochondrial genetics: a paradigm for aging and degenerative diseases?
-
Wallace D.M. Mitochondrial genetics: a paradigm for aging and degenerative diseases? Science 256 1992 628 632
-
(1992)
Science
, vol.256
, pp. 628-632
-
-
Wallace, D.M.1
-
8
-
-
0028156783
-
Mitochondrial DNA rearrangements with onset as chronic diarrhea with villous atrophy
-
Cormier-Daire V. Bonnefont J.-P. Rustin P. Mitochondrial DNA rearrangements with onset as chronic diarrhea with villous atrophy J Pediatr 124 1994 63 70
-
(1994)
J Pediatr
, vol.124
, pp. 63-70
-
-
Cormier-Daire, V.1
Bonnefont, J.-P.2
Rustin, P.3
-
9
-
-
0027679504
-
Fatal neonatal liver failure and mitochondrial cytopathy (oxidative phosphorylation deficiency): a light and electron microscopic study of the liver
-
Bioulac-Sage P. Parrot-Roulaud F. Mazat J.P. Fatal neonatal liver failure and mitochondrial cytopathy (oxidative phosphorylation deficiency): a light and electron microscopic study of the liver Hepatology 18 1993 839 846
-
(1993)
Hepatology
, vol.18
, pp. 839-846
-
-
Bioulac-Sage, P.1
Parrot-Roulaud, F.2
Mazat, J.P.3
-
10
-
-
0025784069
-
Fatal hepatic failure with lactic acidaemia, Fanconi syndrome and defective activity of succinate:cytochrome c reductase
-
Vilaseca M.A. Briones P. Ribes A. Fatal hepatic failure with lactic acidaemia, Fanconi syndrome and defective activity of succinate:cytochrome c reductase J Inher Metab Dis 14 1991 285 288
-
(1991)
J Inher Metab Dis
, vol.14
, pp. 285-288
-
-
Vilaseca, M.A.1
Briones, P.2
Ribes, A.3
-
12
-
-
0025807180
-
Mitochondrial encephalomyopathies in childhood. I. Biochemical and morphologic investigations
-
Tulinius M.H. Holme E. Kristiansson B. Larsson N.-G. Oldfors A. Mitochondrial encephalomyopathies in childhood. I. Biochemical and morphologic investigations J Pediatr 119 1991 242 250
-
(1991)
J Pediatr
, vol.119
, pp. 242-250
-
-
Tulinius, M.H.1
Holme, E.2
Kristiansson, B.3
Larsson, N.-G.4
Oldfors, A.5
-
13
-
-
0029869935
-
Depletion of mitochondrial DNA in a family with fatal neonatal liver disease
-
Bakker H.D. Scholte H.R. Dingemans K.P. Depletion of mitochondrial DNA in a family with fatal neonatal liver disease J Pediatr 128 1996 683 687
-
(1996)
J Pediatr
, vol.128
, pp. 683-687
-
-
Bakker, H.D.1
Scholte, H.R.2
Dingemans, K.P.3
-
14
-
-
0029980584
-
Depletion of mitochondrial DNA in the liver of a patient with lactic acidemia and hypoketotic hypoglycemia
-
Maaswinkel-Mooij P.D. Van den Bogert C. Scholte H.R. Depletion of mitochondrial DNA in the liver of a patient with lactic acidemia and hypoketotic hypoglycemia J Pediatr 128 1996 679 683
-
(1996)
J Pediatr
, vol.128
, pp. 679-683
-
-
Maaswinkel-Mooij, P.D.1
Van den Bogert, C.2
Scholte, H.R.3
-
15
-
-
0026480006
-
Fatal infantile liver failure associated with mitochondrial DNA depletion
-
Mazziotta M.R.M. Ricci E. Bertini E. Fatal infantile liver failure associated with mitochondrial DNA depletion J Pediatr 121 1992 896 901
-
(1992)
J Pediatr
, vol.121
, pp. 896-901
-
-
Mazziotta, M.R.M.1
Ricci, E.2
Bertini, E.3
-
16
-
-
0028817865
-
Hepatic failure and lactic acidosis due to fialuridine (FIAU), an investigational nucleoside analogue for chronic hepatitis B
-
McKenzie R. Fried M.W. Sallie R. Hepatic failure and lactic acidosis due to fialuridine (FIAU), an investigational nucleoside analogue for chronic hepatitis B N Engl J Med 333 1995 1099 1105
-
(1995)
N Engl J Med
, vol.333
, pp. 1099-1105
-
-
McKenzie, R.1
Fried, M.W.2
Sallie, R.3
-
17
-
-
0027177530
-
Abnormal hepatic mitochondrial respiration and cytochrome c oxidase activity in rats with long-term copper overload
-
Sokol R.J. Devereaux M.W. O'Brien K. Khandwala R.A. Loehr J.P. Abnormal hepatic mitochondrial respiration and cytochrome c oxidase activity in rats with long-term copper overload Gastroenterology 105 1993 178 187
-
(1993)
Gastroenterology
, vol.105
, pp. 178-187
-
-
Sokol, R.J.1
Devereaux, M.W.2
O'Brien, K.3
Khandwala, R.A.4
Loehr, J.P.5
-
18
-
-
0018130269
-
Reye syndrome: a metabolic response to an acute mitochondrial insult?
-
De Vivo D.C. Reye syndrome: a metabolic response to an acute mitochondrial insult? Neurology 28 1978 105 108
-
(1978)
Neurology
, vol.28
, pp. 105-108
-
-
De Vivo, D.C.1
|