-
2
-
-
33645313021
-
Diabetes mellitus associated with a pathogenic point mutation in mitochondrial DNA
-
Reardon W, Ross RJ, Sweeney MG, et al. Diabetes mellitus associated with a pathogenic point mutation in mitochondrial DNA. Lancet. 1993;341:1291-1292.
-
(1993)
Lancet
, vol.341
, pp. 1291-1292
-
-
Reardon, W.1
Ross, R.J.2
Sweeney, M.G.3
-
3
-
-
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;30:962-968.
-
(1994)
N Engl J Med
, vol.30
, pp. 962-968
-
-
Kadowaki, T.1
Kadowaki, H.2
Mori, Y.3
-
5
-
-
0029875834
-
Clinical phenotypes, insulin secretion, and insulin sensitivity in kindreds with maternally inherited diabetes and deafness due to mitochondrial tRNALeu (UUR) gene mutation
-
Velho G, Byrne MM, Clèment C, et al. Clinical phenotypes, insulin secretion, and insulin sensitivity in kindreds with maternally inherited diabetes and deafness due to mitochondrial tRNALeu (UUR) gene mutation. Diabetes. 1995;45:478-487.
-
(1995)
Diabetes
, vol.45
, pp. 478-487
-
-
Velho, G.1
Byrne, M.M.2
Clèment, C.3
-
6
-
-
0029867177
-
Insulin resistance associated with maternally inherited diabetes and deafness
-
Gebhart SS, Shoffner JM, Koontz D, et al. Insulin resistance associated with maternally inherited diabetes and deafness. Metabolism. 1996;45:526-531.
-
(1996)
Metabolism
, vol.45
, pp. 526-531
-
-
Gebhart, S.S.1
Shoffner, J.M.2
Koontz, D.3
-
7
-
-
0003725206
-
-
for the World Health Organization, Geneva: WHO;, Report of a WHO Consultation
-
Alberti KGGM, Zimmet PZ, for the World Health Organization. Consultation, definition, diagnosis and classification of diabetes mellitus and its complications. Part 1: Diagnosis and classification of diabetes mellitus. Geneva: WHO; 1999. Report of a WHO Consultation.
-
(1999)
Consultation, definition, diagnosis and classification of diabetes mellitus and its complications. Part 1: Diagnosis and classification of diabetes mellitus
-
-
Alberti, K.G.G.M.1
Zimmet, P.Z.2
-
8
-
-
3042631694
-
-
Cesarini PR, Mendon0a E, Fernandes V, et al. Prevalence of immunologic markers (Anti-GAD and Anti-IA-2) in first-degree relatives of patients with type I diabetes in greater area of São Paulo. Rev Assoc Med Bras. 2003;49:395-400.
-
Cesarini PR, Mendon0a E, Fernandes V, et al. Prevalence of immunologic markers (Anti-GAD and Anti-IA-2) in first-degree relatives of patients with type I diabetes in greater area of São Paulo. Rev Assoc Med Bras. 2003;49:395-400.
-
-
-
-
9
-
-
0025742834
-
Relationship between first-phase insulin secretion and age, HLA, islet cell antibody status, and development of type 1 diabetes in 220 juvenile first-degree relatives of diabetic patients
-
Robert JJ, Deschamps I, Chevenne D, et al. Relationship between first-phase insulin secretion and age, HLA, islet cell antibody status, and development of type 1 diabetes in 220 juvenile first-degree relatives of diabetic patients. Diabetes. 1991;14:718-723.
-
(1991)
Diabetes
, vol.14
, pp. 718-723
-
-
Robert, J.J.1
Deschamps, I.2
Chevenne, D.3
-
10
-
-
0028997729
-
The b-cell and diabetes
-
Polonski KS. The b-cell and diabetes. Diabetes. 1995;45:705-717.
-
(1995)
Diabetes
, vol.45
, pp. 705-717
-
-
Polonski, K.S.1
-
11
-
-
0026941505
-
C-peptide used in the estimation of islet b-cell function in diabetes
-
Gjessing HJ. C-peptide used in the estimation of islet b-cell function in diabetes. Dan Med Bull. 1992;39:438-452.
-
(1992)
Dan Med Bull
, vol.39
, pp. 438-452
-
-
Gjessing, H.J.1
-
13
-
-
0021278601
-
Differential sensitivity to B-cell secretogogues in "early" type I diabetes mellitus
-
Ganda OP, Srikanta S, Brink SJ, et al. Differential sensitivity to B-cell secretogogues in "early" type I diabetes mellitus. Diabetes. 1984;33:516-521.
-
(1984)
Diabetes
, vol.33
, pp. 516-521
-
-
Ganda, O.P.1
Srikanta, S.2
Brink, S.J.3
-
14
-
-
0021224142
-
Pre-type I diabetes. Linear loss of beta cell response to intravenous glucose
-
Srikanta S, Ganda OP, Gleason RE, et al. Pre-type I diabetes. Linear loss of beta cell response to intravenous glucose. Diabetes. 1984;33:717-720.
-
(1984)
Diabetes
, vol.33
, pp. 717-720
-
-
Srikanta, S.1
Ganda, O.P.2
Gleason, R.E.3
-
15
-
-
0017236889
-
Relationships between fasting plasma glucose levels and insulin secretion during intravenous glucose tolerance tests
-
Brunzell JD, Robertson RP, Lerner RL, et al. Relationships between fasting plasma glucose levels and insulin secretion during intravenous glucose tolerance tests. J Clin Endocrinol Metab. 1976;42:222-229.
-
(1976)
J Clin Endocrinol Metab
, vol.42
, pp. 222-229
-
-
Brunzell, J.D.1
Robertson, R.P.2
Lerner, R.L.3
-
16
-
-
0020490209
-
Characterization of the adenine nucleotide translocase of pancreatic islet mitochondria
-
Yousufzai SYK, Bradford MW, Shirago E, et al. Characterization of the adenine nucleotide translocase of pancreatic islet mitochondria. FEBS Lett. 1982;137:205-208.
-
(1982)
FEBS Lett
, vol.137
, pp. 205-208
-
-
Yousufzai, S.Y.K.1
Bradford, M.W.2
Shirago, E.3
-
17
-
-
0033569992
-
Leu(UUR) gene causes severe mitochondrial dysfunction without a strong decrease in protein synthesis rate
-
Leu(UUR) gene causes severe mitochondrial dysfunction without a strong decrease in protein synthesis rate. J Biol Chem. 1999;274:29744-29748.
-
(1999)
J Biol Chem
, vol.274
, pp. 29744-29748
-
-
Janssen, G.M.C.1
Maassen, J.A.2
van den Ouweland, J.M.W.3
-
18
-
-
0026457825
-
Marked replicative advantage of human mtDNA carrying a point mutation that causes the MELAS encephalomyopathy
-
Yoneda M, Chomyn A, Martinuzzi A, et al. Marked replicative advantage of human mtDNA carrying a point mutation that causes the MELAS encephalomyopathy. Proc Natl Acad Sci U S A. 1992;89:11164-11168.
-
(1992)
Proc Natl Acad Sci U S A
, vol.89
, pp. 11164-11168
-
-
Yoneda, M.1
Chomyn, A.2
Martinuzzi, A.3
-
19
-
-
0029056559
-
A case of diabetic amyotrophy associated with 3243 mitochondrial tRNA(leu; UUR) mutation and successful therapy with Coenzyme Q10
-
Suzuki S, Kadowaki H, Atsumi Y, et al. A case of diabetic amyotrophy associated with 3243 mitochondrial tRNA(leu; UUR) mutation and successful therapy with Coenzyme Q10. Endocr J. 1995;42:141-145.
-
(1995)
Endocr J
, vol.42
, pp. 141-145
-
-
Suzuki, S.1
Kadowaki, H.2
Atsumi, Y.3
-
20
-
-
0031596402
-
The effects of coenzyme Q10 treatment on maternally inherited diabetes mellitus and deafness, and mitochondrial DNA 3243 (A to G) mutation
-
Suzuki S, Hinokio Y, Ohtomo M, et al. The effects of coenzyme Q10 treatment on maternally inherited diabetes mellitus and deafness, and mitochondrial DNA 3243 (A to G) mutation. Diabetologia. 1998;41:584-588.
-
(1998)
Diabetologia
, vol.41
, pp. 584-588
-
-
Suzuki, S.1
Hinokio, Y.2
Ohtomo, M.3
-
21
-
-
0030823104
-
Leu (UUR) mutation: Clinical features and coenzyme Q10 treatment
-
Leu (UUR) mutation: clinical features and coenzyme Q10 treatment. Mol Aspects Med. 1997;18(suppl 1):s181-s188.
-
(1997)
Mol Aspects Med
, vol.18
, Issue.SUPPL. 1
-
-
Suzuki, Y.1
Taniyama, M.2
Muramatsu, T.3
-
22
-
-
0028802967
-
Could coenzyme Q10 and L-carnitine be a treatment for diabetes secondary to 3243 mutation of mtDNA?
-
Silvestre-Aillaud P, BenDahan D, Pasquis-Fluckinger V, et al. Could coenzyme Q10 and L-carnitine be a treatment for diabetes secondary to 3243 mutation of mtDNA? Diabetes Care. 1995;38:1485-1486.
-
(1995)
Diabetes Care
, vol.38
, pp. 1485-1486
-
-
Silvestre-Aillaud, P.1
BenDahan, D.2
Pasquis-Fluckinger, V.3
-
23
-
-
0033970418
-
Correction of pancreatic B-cell dysfunction with coenzyme Q10 in a patient with mitochondrial encephalomyopathy, lactic acidosis and stroke-like episodes syndrome and diabetes mellitus
-
Liou CW, Huang CH, Lin TK, et al. Correction of pancreatic B-cell dysfunction with coenzyme Q10 in a patient with mitochondrial encephalomyopathy, lactic acidosis and stroke-like episodes syndrome and diabetes mellitus. Eur Neurol. 2000;43:54-56.
-
(2000)
Eur Neurol
, vol.43
, pp. 54-56
-
-
Liou, C.W.1
Huang, C.H.2
Lin, T.K.3
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