-
1
-
-
0026906885
-
Leu(UUR) gene in a large pedigree with maternally transmitted type II diabetes mellitus and deafness
-
Leu(UUR) gene in a large pedigree with maternally transmitted type II diabetes mellitus and deafness. Nat Genet 1992;1:368-71.
-
(1992)
Nat Genet
, vol.1
, pp. 368-371
-
-
Van Den Ouweland, J.M.W.1
Lemkes, H.H.P.J.2
Ruitenbeek, W.3
-
2
-
-
0026462744
-
Diabetes mellitus associated with a pathogenic point mutation in mitochondrial DNA
-
Reardon W, Ross RJM, Sweeney MG, et al. Diabetes mellitus associated with a pathogenic point mutation in mitochondrial DNA. Lancet 1992;340:1376-9.
-
(1992)
Lancet
, vol.340
, pp. 1376-1379
-
-
Reardon, W.1
Ross, R.J.M.2
Sweeney, M.G.3
-
3
-
-
0029129204
-
Macular pattern dystrophy associated with a mutation of mitochondrial DNA
-
Massin P, Guillausseau PJ, Vialettes B, et al. Macular pattern dystrophy associated with a mutation of mitochondrial DNA. Am J Ophthalmol 1995;120:247-8.
-
(1995)
Am J Ophthalmol
, vol.120
, pp. 247-248
-
-
Massin, P.1
Guillausseau, P.J.2
Vialettes, B.3
-
4
-
-
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;348:651-3.
-
(1990)
Nature
, vol.348
, pp. 651-653
-
-
Goto, Y.1
Nonaka, I.2
Horai, S.3
-
5
-
-
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;330:962-8.
-
(1994)
N Engl J Med
, vol.330
, pp. 962-968
-
-
Kadowaki, T.1
Kadowaki, H.2
Mori, Y.3
-
6
-
-
0029914927
-
Maternally inherited diabetes and deafness: A new diabetes subtype
-
Maassen JA, Kadowaki T. Maternally inherited diabetes and deafness: a new diabetes subtype. Diabetologia 1996;39:375-82.
-
(1996)
Diabetologia
, vol.39
, pp. 375-382
-
-
Maassen, J.A.1
Kadowaki, T.2
-
7
-
-
0027996170
-
Prevalence of maternally inherited diabetes and deafness in diabetic populations in The Netherlands
-
Hart LM, Lemkes HHPJ, Heine RJ, et al. Prevalence of maternally inherited diabetes and deafness in diabetic populations in The Netherlands. Diabetologia 1994;37:1169-70.
-
(1994)
Diabetologia
, vol.37
, pp. 1169-1170
-
-
Hart, L.M.1
Lemkes, H.H.P.J.2
Heine, R.J.3
-
8
-
-
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;79:768-71.
-
(1994)
J Clin Endocrinol Metab
, vol.79
, pp. 768-771
-
-
Otabe, S.1
Sakura, H.2
Shimokawa, K.3
-
10
-
-
0027369567
-
Prevalence of mitochondrial gene mutations in families with diabetes mellitus
-
Vionnet N, Passa P, Froguel P. Prevalence of mitochondrial gene mutations in families with diabetes mellitus [letter]. Lancet 1993;342:1429-30.
-
(1993)
Lancet
, vol.342
, pp. 1429-1430
-
-
Vionnet, N.1
Passa, P.2
Froguel, P.3
-
11
-
-
0031812303
-
Importance of searching for mt DNA defects in patients with diabetes and hearing deficit
-
Paquis-Fluckinger V, Vialettes B, Vague P, et al. Importance of searching for mt DNA defects in patients with diabetes and hearing deficit. Diabetologia 1998;41:740-4.
-
(1998)
Diabetologia
, vol.41
, pp. 740-744
-
-
Paquis-Fluckinger, V.1
Vialettes, B.2
Vague, P.3
-
14
-
-
0030837435
-
Macular pattern retinal dystrophy, adult-onset diabetes, and deafness: A family study of A3243G mitochondrial heteroplasmy
-
Harrison TJ, Boles RG, Johnson DR, et al. Macular pattern retinal dystrophy, adult-onset diabetes, and deafness: a family study of A3243G mitochondrial heteroplasmy. Am J Ophthalmol 1997;124:217-21.
-
(1997)
Am J Ophthalmol
, vol.124
, pp. 217-221
-
-
Harrison, T.J.1
Boles, R.G.2
Johnson, D.R.3
-
15
-
-
0030967074
-
Macular pattern dystrophy in patients with deafness and diabetes
-
Bonte CA, Matthijs GL, Cassiman JJ, Leys AM. Macular pattern dystrophy in patients with deafness and diabetes. Retina 1997;17:216-21.
-
(1997)
Retina
, vol.17
, pp. 216-221
-
-
Bonte, C.A.1
Matthijs, G.L.2
Cassiman, J.J.3
Leys, A.M.4
-
16
-
-
0030715313
-
Pigmentary retinopathy associated with the mitochondrial DNA 3243 point mutation
-
Sue CM, Mitchell P, Crimmins DS, et al. Pigmentary retinopathy associated with the mitochondrial DNA 3243 point mutation. Neurology 1997;49:1013-7.
-
(1997)
Neurology
, vol.49
, pp. 1013-1017
-
-
Sue, C.M.1
Mitchell, P.2
Crimmins, D.S.3
-
18
-
-
0031742026
-
Does mitochondrial genome mutation in subjects with maternally inherited diabetes and deafness decrease severity of diabetic retinopathy?
-
Holmes-Walker DJ, Mitchell P, Boyages SC. Does mitochondrial genome mutation in subjects with maternally inherited diabetes and deafness decrease severity of diabetic retinopathy? Diabet Med 1998;15:946-52.
-
(1998)
Diabet Med
, vol.15
, pp. 946-952
-
-
Holmes-Walker, D.J.1
Mitchell, P.2
Boyages, S.C.3
-
19
-
-
0027939581
-
LEU(UUR) gene: A study in seven families with mitochondrial encephalomyopathy, lactic acidosis and stroke-like episodes (MELAS)
-
LEU(UUR) gene: a study in seven families with mitochondrial encephalomyopathy, lactic acidosis and stroke-like episodes (MELAS). Diabetologia 1994;37:818-25.
-
(1994)
Diabetologia
, vol.37
, pp. 818-825
-
-
Suzuki, S.1
Hinokio, Y.2
Hirai, S.3
-
20
-
-
0021191759
-
The Wisconsin Epidemiologic Study of Diabetic Retinopathy. III. Prevalence and risk of diabetic retinopathy when age at diagnosis is 30 or more years
-
Klein R, Klein BEK, Moss SE, et al. The Wisconsin Epidemiologic Study of Diabetic Retinopathy. III. Prevalence and risk of diabetic retinopathy when age at diagnosis is 30 or more years. Arch Ophthalmol 1984;102:527-32.
-
(1984)
Arch Ophthalmol
, vol.102
, pp. 527-532
-
-
Klein, R.1
Klein, B.E.K.2
Moss, S.E.3
-
21
-
-
0022970769
-
Relationship of duration and onset of diabetes to prevalence of diabetic retinopathy
-
Jerneld B, Algvere P. Relationship of duration and onset of diabetes to prevalence of diabetic retinopathy. Am J Ophthalmol 1986;102:431-7.
-
(1986)
Am J Ophthalmol
, vol.102
, pp. 431-437
-
-
Jerneld, B.1
Algvere, P.2
-
22
-
-
0022344135
-
The retinal manifestations of mitochondrial myopathy. A study of 22 cases
-
Mullie MA, Hording AE, Petty RKH, et al. The retinal manifestations of mitochondrial myopathy. A study of 22 cases. Arch Ophthalmol 1985;103:1825-30.
-
(1985)
Arch Ophthalmol
, vol.103
, pp. 1825-1830
-
-
Mullie, M.A.1
Hording, A.E.2
Petty, R.K.H.3
-
23
-
-
0031964692
-
Macular dystrophy, diabetes, and deafness associated with a large mitochondrial DNA deletion
-
Souied EH, Salès MJ, Soubrane G, et al. Macular dystrophy, diabetes, and deafness associated with a large mitochondrial DNA deletion. Am J Ophthalmol 1998;125:100-3.
-
(1998)
Am J Ophthalmol
, vol.125
, pp. 100-103
-
-
Souied, E.H.1
Salès, M.J.2
Soubrane, G.3
-
24
-
-
0030832950
-
Phenotypic expression of diabetes secondary to a T14709C mutation of mitochondrial DNA
-
Vialettes BH, Paquis-Flucklinger V, Pelissier JF, et al. Phenotypic expression of diabetes secondary to a T14709C mutation of mitochondrial DNA. Diabetes Care 1997;20:1731-7.
-
(1997)
Diabetes Care
, vol.20
, pp. 1731-1737
-
-
Vialettes, B.H.1
Paquis-Flucklinger, V.2
Pelissier, J.F.3
-
26
-
-
0027213773
-
Ocular clinicopathologic study of the mitochondrial encephalomyopathy overlap syndromes
-
Chang TS, Johns DR, Walker D, et al. Ocular clinicopathologic study of the mitochondrial encephalomyopathy overlap syndromes. Arch Ophthalmol 1993;111:1254-62.
-
(1993)
Arch Ophthalmol
, vol.111
, pp. 1254-1262
-
-
Chang, T.S.1
Johns, D.R.2
Walker, D.3
-
27
-
-
0027131293
-
Ocular pathology of MELAS syndrome with mitochondrial DNA nucleotide 3243 point mutation
-
Rummelt V, Folberg R, Ionasescu V, et al. Ocular pathology of MELAS syndrome with mitochondrial DNA nucleotide 3243 point mutation. Ophthalmology 1993;100:1757-66.
-
(1993)
Ophthalmology
, vol.100
, pp. 1757-1766
-
-
Rummelt, V.1
Folberg, R.2
Ionasescu, V.3
-
28
-
-
0027526665
-
Deletion of mitochondrial DNA in a case of early-onset diabetes mellitus, optic atrophy, and deafness (Wolfram syndrome? MIM 222300)
-
Rötig A, Cormier V, Chatelain P, et al. Deletion of mitochondrial DNA in a case of early-onset diabetes mellitus, optic atrophy, and deafness (Wolfram syndrome? MIM 222300). J Clin Invest 1993;91:1095-8.
-
(1993)
J Clin Invest
, vol.91
, pp. 1095-1098
-
-
Rötig, A.1
Cormier, V.2
Chatelain, P.3
-
29
-
-
0028802967
-
Could coenzyme Q10 and L-carnitine be a treatment for diabetes secondary to 3243 mutation of mtDNA?
-
Silvestre-Aillaud P, BenDahan D, Paquis-Fluckinger V, et al. Could coenzyme Q10 and L-carnitine be a treatment for diabetes secondary to 3243 mutation of mtDNA? Diabetologia 1995;38:1485-6.
-
(1995)
Diabetologia
, vol.38
, pp. 1485-1486
-
-
Silvestre-Aillaud, P.1
Bendahan, D.2
Paquis-Fluckinger, V.3
-
30
-
-
0031596402
-
10 treatment on maternally inherited diabetes mellitus and deafness, and mitochondrial DNA 3243 (A to G) mutation
-
10 treatment on maternally inherited diabetes mellitus and deafness, and mitochondrial DNA 3243 (A to G) mutation. Diabetologia 1998;41:584-8.
-
(1998)
Diabetologia
, vol.41
, pp. 584-588
-
-
Suzuki, S.1
Hinokio, Y.2
Ohtomo, M.3
|