-
1
-
-
0031869732
-
Incidence and Prevalence of ESRD; USRDS 1998 Annual Data Report
-
Incidence and Prevalence of ESRD; USRDS 1998 Annual Data Report. Am J Kidney Dis 1998; 32 [Suppl. 1]: S38-S49
-
(1998)
Am J Kidney Dis
, vol.32
, Issue.SUPPL. 1
-
-
-
2
-
-
0343898370
-
An overview of regular dialysis treatment in Japan (as of Dec. 31, 1998)
-
An overview of regular dialysis treatment in Japan (as of Dec. 31, 1998). Jpn Soc Dial Ther 1999; 64
-
(1999)
Jpn Soc Dial Ther
, pp. 64
-
-
-
3
-
-
0028279885
-
Mitochondrial gene defects in patients with NIDDM
-
Alcolado JC, Majid A, Brockington M, Sweeney MG, Morgan R, Rees A, Harding AE, Barnett AH. Mitochondrial gene defects in patients with NIDDM. Diabetologia 1994; 37: 372-376
-
(1994)
Diabetologia
, vol.37
, pp. 372-376
-
-
Alcolado, J.C.1
Majid, A.2
Brockington, M.3
Sweeney, M.G.4
Morgan, R.5
Rees, A.6
Harding, A.E.7
Barnett, A.H.8
-
4
-
-
0028328317
-
A subtype of diabetes mellitus associated with a mutation of mitochondrial DNA
-
Kadowaki T, Kadowaki H, Mori Y et al. A subtype of diabetes mellitus associated with a mutation of mitochondrial DNA. N Engl J Med 1994; 330: 962-968
-
(1994)
N Engl J Med
, vol.330
, pp. 962-968
-
-
Kadowaki, T.1
Kadowaki, H.2
Mori, Y.3
-
5
-
-
0028966152
-
Mitochondrial mutation in diabetic patient with gastrointestinal symptoms
-
Letter
-
Kishimoto M, Hashiramoto M, Kanda F, Tanaka M, Kasuga M. Mitochondrial mutation in diabetic patient with gastrointestinal symptoms. Lancet 1995; 345: 452 (Letter)
-
(1995)
Lancet
, vol.345
, pp. 452
-
-
Kishimoto, M.1
Hashiramoto, M.2
Kanda, F.3
Tanaka, M.4
Kasuga, M.5
-
6
-
-
0027968580
-
The high prevalence of the diabetic patients with a mutation in the mitochondrial gene in Japan
-
Otabe S, Sakura H, Shimokawa K et al. The high prevalence of the diabetic patients with a mutation in the mitochondrial gene in Japan. J Clin Endocrinol Metab 1994; 79: 768-771
-
(1994)
J Clin Endocrinol Metab
, vol.79
, pp. 768-771
-
-
Otabe, S.1
Sakura, H.2
Shimokawa, K.3
-
8
-
-
0030799145
-
LEU(UUR) gene associated with progressive kidney disease
-
LEU(UUR) gene associated with progressive kidney disease. J Am Soc Nephrol 1997; 8: 1118-1124
-
(1997)
J Am Soc Nephrol
, vol.8
, pp. 1118-1124
-
-
Jansen, J.J.1
Maassen, J.A.2
Van Der Woude, F.J.3
Lemmink, H.A.4
Van Den Ouweland, J.M.5
'T Hart, L.M.6
Smeets, H.J.7
Bruijn, J.A.8
Lemkes, H.H.9
-
9
-
-
0019423856
-
Sequence and organization of the human mitochondrial genome
-
Anderson S, Bankier AT, Barrell BG et al. Sequence and organization of the human mitochondrial genome. Nature 1981; 290: 457-465
-
(1981)
Nature
, vol.290
, pp. 457-465
-
-
Anderson, S.1
Bankier, A.T.2
Barrell, B.G.3
-
10
-
-
0025666322
-
LEU(UUR) gene associated with the MELAS subgroup in mitochondrial encephalomyopathies
-
LEU(UUR) gene associated with the MELAS subgroup in mitochondrial encephalomyopathies. Nature 1990; 348: 651-653
-
(1990)
Nature
, vol.348
, pp. 651-653
-
-
Goto, Y.1
Nonaka, I.2
Horai, S.3
-
14
-
-
0028818655
-
Clinical spectrum of the MELAS mutation in a large pedigree
-
Damian MS, Seibel P, Reichmann H et al. Clinical spectrum of the MELAS mutation in a large pedigree. Acta Neurol Scand 1995; 92: 409-415
-
(1995)
Acta Neurol Scand
, vol.92
, pp. 409-415
-
-
Damian, M.S.1
Seibel, P.2
Reichmann, H.3
-
17
-
-
0343461873
-
An autopsy case of mitochondrial encepharlopathy (MELAS) with special reference to extra-neuromuscular abnormalities
-
Ban S, Mori N, Saito K, Mizukami K, Suzuki T, Shiraishi H. An autopsy case of mitochondrial encepharlopathy (MELAS) with special reference to extra-neuromuscular abnormalities. J Neurol Sci 1992; 92: 818-825
-
(1992)
J Neurol Sci
, vol.92
, pp. 818-825
-
-
Ban, S.1
Mori, N.2
Saito, K.3
Mizukami, K.4
Suzuki, T.5
Shiraishi, H.6
-
18
-
-
0006288487
-
An autopsy case of mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes (MELAS) undergoing long-term hemodialysis
-
Tomonari H, Yoshida H, Omura K et al. An autopsy case of mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes (MELAS) undergoing long-term hemodialysis. J Jpn Soc Dial Ther 1996; 29: 1097-1102
-
(1996)
J Jpn Soc Dial Ther
, vol.29
, pp. 1097-1102
-
-
Tomonari, H.1
Yoshida, H.2
Omura, K.3
-
19
-
-
0027996170
-
Prevalence of maternally inherited diabetes and deafness in diabetic populations in the Netherlands
-
't Hart LM, Lemkes HH, Heine RJ et al. Prevalence of maternally inherited diabetes and deafness in diabetic populations in The Netherlands. Diabetologia 1994; 37: 1169-1170
-
(1994)
Diabetologia
, vol.37
, pp. 1169-1170
-
-
'T Hart, L.M.1
Lemkes, H.H.2
Heine, R.J.3
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