-
1
-
-
0025666322
-
Leu (UUR) gene associated with the MELAS subgroup of mitochondrial encephalomyopathies
-
Leu (UUR) gene associated with the MELAS subgroup of mitochondrial encephalomyopathies. Nature 1990; 348: 651-653
-
(1990)
Nature
, vol.348
, pp. 651-653
-
-
Goto, Y.1
Nonaka, I.2
Horai, S.3
-
2
-
-
0026906885
-
Leu (UUR) gene in a large pedigree with maternally transmitted type I diabetes mellitus and deafness
-
Leu (UUR) gene in a large pedigree with maternally transmitted type I diabetes mellitus and deafness. Nat Genet 1992; 1: 368
-
(1992)
Nat Genet
, vol.1
, pp. 368
-
-
Van Den Ouweland, J.M.W.1
Lemkes, H.H.P.J.2
Ruitenbeek, W.3
-
3
-
-
0026462744
-
Diabetes mellitus associated with a pathogenic point mutation in mitochondrial DNA
-
Readon W, Ross RJM, Sweeney MG, et al: Diabetes mellitus associated with a pathogenic point mutation in mitochondrial DNA. Lancet 1992; 340: 1376-1379
-
(1992)
Lancet
, vol.340
, pp. 1376-1379
-
-
Readon, W.1
Ross, R.J.M.2
Sweeney, M.G.3
-
4
-
-
0028328317
-
A subtype of diabetes mellitus associated with a mutation of mitochondrial DNA
-
Kadowaki T, Kadowaki H, Mori Y, Tobe K, Sakura R, Suzuki Y, et al: A subtype of diabetes mellitus associated with a mutation of mitochondrial DNA. N Engl J Med 1994; 330: 362-368
-
(1994)
N Engl J Med
, vol.330
, pp. 362-368
-
-
Kadowaki, T.1
Kadowaki, H.2
Mori, Y.3
Tobe, K.4
Sakura, R.5
Suzuki, Y.6
-
6
-
-
0028148863
-
Cardiomyopathy and angiopathy in patients with mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes
-
Sato W, Tanaka M, Sugiyama S, Nemoto T, Harada K, Miura Y, et al: Cardiomyopathy and angiopathy in patients with mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes. Am Heart J 1994; 128: 733-741
-
(1994)
Am Heart J
, vol.128
, pp. 733-741
-
-
Sato, W.1
Tanaka, M.2
Sugiyama, S.3
Nemoto, T.4
Harada, K.5
Miura, Y.6
-
7
-
-
0025641669
-
Mitochondrial cytopathy
-
Ito T, Hattori K, Tanaka M, Sugiyama S, Ozawa T: Mitochondrial cytopathy. Jpn Circ J 1990; 54: 1214-1220
-
(1990)
Jpn Circ J
, vol.54
, pp. 1214-1220
-
-
Ito, T.1
Hattori, K.2
Tanaka, M.3
Sugiyama, S.4
Ozawa, T.5
-
8
-
-
0019909046
-
Mitochondrial encephalomyopathies: Biochaimical studies in two cases revealing defects in the respiratory chain
-
Morgan-Hughes JA, Hayes DJ, Clark JB, Landon DN, Swash M, Stark RJ, et al: Mitochondrial encephalomyopathies: biochaimical studies in two cases revealing defects in the respiratory chain. Brain 1982; 105: 553-582
-
(1982)
Brain
, vol.105
, pp. 553-582
-
-
Morgan-Hughes, J.A.1
Hayes, D.J.2
Clark, J.B.3
Landon, D.N.4
Swash, M.5
Stark, R.J.6
-
9
-
-
0024433287
-
Pleiotropic molecular defects in energy-transducing complex in mitochondrial encephalomyopathy (MELAS)
-
Yoneda M, Tanaka M, Nishikimi M, Suzuki H, Tanaka K, Nishizawa M, et al: Pleiotropic molecular defects in energy-transducing complex in mitochondrial encephalomyopathy (MELAS). J Neurol Sci 1989; 92: 143-158
-
(1989)
J Neurol Sci
, vol.92
, pp. 143-158
-
-
Yoneda, M.1
Tanaka, M.2
Nishikimi, M.3
Suzuki, H.4
Tanaka, K.5
Nishizawa, M.6
-
10
-
-
0023117240
-
Two cases of NADH-coenzyme Q reductase deficiency: Relationship to MELAS syndrome
-
Kobayashi M, Morishita H, Sugiyama N, Yokochi K, Nakano M, Wada Y, et al: Two cases of NADH-coenzyme Q reductase deficiency: relationship to MELAS syndrome. J Pediatr 1987; 110: 223-227
-
(1987)
J Pediatr
, vol.110
, pp. 223-227
-
-
Kobayashi, M.1
Morishita, H.2
Sugiyama, N.3
Yokochi, K.4
Nakano, M.5
Wada, Y.6
-
11
-
-
0002441667
-
Cardiac involvement in four cases of MELAS (mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes)
-
in Japanese with English abstract
-
Nemoto T, Satoh W, Harada K, Komatsu K, Gotoh A, Matsuno K, et al: Cardiac involvement in four cases of MELAS (mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes). Jpn J Pediatr 1989; 93: 1416-1421 [in Japanese with English abstract]
-
(1989)
Jpn J Pediatr
, vol.93
, pp. 1416-1421
-
-
Nemoto, T.1
Satoh, W.2
Harada, K.3
Komatsu, K.4
Gotoh, A.5
Matsuno, K.6
-
12
-
-
0024790162
-
Mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes with special reference to the mechanism of cerebral manifestations
-
Seyama K, Suzuki K, Mizuno Y, Yoshida M, Tanaka M, Ozawa T: Mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes with special reference to the mechanism of cerebral manifestations. Acta Neurol Scand 1989; 80: 561-568
-
(1989)
Acta Neurol Scand
, vol.80
, pp. 561-568
-
-
Seyama, K.1
Suzuki, K.2
Mizuno, Y.3
Yoshida, M.4
Tanaka, M.5
Ozawa, T.6
-
14
-
-
0026736770
-
Left ventricular function and dimensions in newly diagnosed non-insulin-dependent diabetes mellitus
-
Vanninen E, Mustonen J, Vainio P, Lansimies E, Uusitupa M: Left ventricular function and dimensions in newly diagnosed non-insulin-dependent diabetes mellitus. Am J Cardiol 1992; 70: 371-378
-
(1992)
Am J Cardiol
, vol.70
, pp. 371-378
-
-
Vanninen, E.1
Mustonen, J.2
Vainio, P.3
Lansimies, E.4
Uusitupa, M.5
-
15
-
-
0023879355
-
Echocardiographically detected left ventricular hypertrophy: Prevalence and risk factors. the Framingham Heart Study
-
Levy D, Anderson KM, Savage DD, Kannel WB, Christiansen JC, Castelli WP: Echocardiographically detected left ventricular hypertrophy: prevalence and risk factors. The Framingham Heart Study. Ann Intern Med 1988; 108: 7-13
-
(1988)
Ann Intern Med
, vol.108
, pp. 7-13
-
-
Levy, D.1
Anderson, K.M.2
Savage, D.D.3
Kannel, W.B.4
Christiansen, J.C.5
Castelli, W.P.6
-
16
-
-
0022656337
-
Uptake of meta-iodobenzylguanidine by bovine chromaffin granule membranes
-
Gasnier B, Roisin MP, Scherman D, Coornaert S, Desplanches, Henry JP: Uptake of meta-iodobenzylguanidine by bovine chromaffin granule membranes. Mol Pharmacol 1986; 29: 275-280
-
(1986)
Mol Pharmacol
, vol.29
, pp. 275-280
-
-
Gasnier, B.1
Roisin, M.P.2
Scherman, D.3
Coornaert, S.4
Desplanches5
Henry, J.P.6
|