-
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 348: 651-653.
-
(1990)
Nature
, vol.348
, pp. 651-653
-
-
Goto, Y.1
-
2
-
-
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. 1: 368-371.
-
(1992)
Nat. Genet.
, vol.1
, pp. 368-371
-
-
Van Den Ouweland, J.M.W.1
-
3
-
-
0028328317
-
A subtype of diabetes mellitus associated with a mutation of mitochondrial DNA
-
KADOWAKI, T. et al. 1994. A subtype of diabetes mellitus associated with a mutation of mitochondrial DNA. N. Engl. J. Med. 330: 962-968.
-
(1994)
N. Engl. J. Med.
, vol.330
, pp. 962-968
-
-
Kadowaki, T.1
-
4
-
-
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 37: 818-825.
-
(1994)
Diabetologia
, vol.37
, pp. 818-825
-
-
Suzuki, S.1
-
5
-
-
0028318758
-
Non-Mendelian mitochondrial inheritance as a cause of progressive genetic sensorineural hearing loss
-
GOLD, M. et al. 1994. Non-Mendelian mitochondrial inheritance as a cause of progressive genetic sensorineural hearing loss. Int. J. Pediatr. Otorhinolaryngol. 30: 91-104.
-
(1994)
Int. J. Pediatr. Otorhinolaryngol.
, vol.30
, pp. 91-104
-
-
Gold, M.1
-
6
-
-
0028918471
-
Cardiac involvement in mitochondrial diseases. A study on 17 patients with documented mitochondrial DNA defects
-
ANAN, R. et al. 1995. Cardiac involvement in mitochondrial diseases. A study on 17 patients with documented mitochondrial DNA defects. Circulation 91: 955-961.
-
(1995)
Circulation
, vol.91
, pp. 955-961
-
-
Anan, R.1
-
8
-
-
0035205506
-
Identification of mtDNA mutation in a pedigree with gestational diabetes, deafness, Wolff-Parkinson-White syndrome and placenta accreta
-
AGGARWAL, P. et al. 2001. Identification of mtDNA mutation in a pedigree with gestational diabetes, deafness, Wolff-Parkinson-White syndrome and placenta accreta. Hum. Hered. 51: 114-116.
-
(2001)
Hum. Hered.
, vol.51
, pp. 114-116
-
-
Aggarwal, P.1
-
9
-
-
0029024548
-
Mitochondrial diabetes mellitus: A review
-
GERBITZ, K.D. et al. 1995. Mitochondrial diabetes mellitus: a review. Biochim. Biophys. Acta 1271: 253-260.
-
(1995)
Biochim. Biophys. Acta
, vol.1271
, pp. 253-260
-
-
Gerbitz, K.D.1
-
11
-
-
0037365908
-
Clinical features of diabetes mellitus with the mitochondrial DNA 3243 (A-G) mutation in Japanese: Maternal inheritance and mitochondria-related complications
-
SUZUKI, S. et al. 2003. Clinical features of diabetes mellitus with the mitochondrial DNA 3243 (A-G) mutation in Japanese: maternal inheritance and mitochondria-related complications. Diabetes Res. Clin. Pract. 59: 207-217.
-
(2003)
Diabetes Res. Clin. Pract.
, vol.59
, pp. 207-217
-
-
Suzuki, S.1
-
12
-
-
0035341093
-
Maternally inherited diabetes and deafness: A multicenter study
-
GUILLAUSSEAU, P.J. et al. 2001. Maternally inherited diabetes and deafness: a multicenter study. Ann. Intern. Med. 134: 721-728.
-
(2001)
Ann. Intern. Med.
, vol.134
, pp. 721-728
-
-
Guillausseau, P.J.1
-
13
-
-
0030138871
-
Polyneuropathy in the mtDNA base pair 3243 point mutation
-
FANG, W. 1996. Polyneuropathy in the mtDNA base pair 3243 point mutation. Neurology 46: 1494-1495.
-
(1996)
Neurology
, vol.46
, pp. 1494-1495
-
-
Fang, W.1
-
14
-
-
0028004279
-
Prevalence of chronic complications in Japanese diabetic patients
-
KUZUYA, T. et al. 1994. Prevalence of chronic complications in Japanese diabetic patients. Diabetes Res. Clin. Pract. 24 (Suppl.): S159-S164.
-
(1994)
Diabetes Res. Clin. Pract.
, vol.24
, Issue.SUPPL.
-
-
Kuzuya, T.1
-
15
-
-
17844362448
-
(Leu(UUR)) gene in Japanese patients with diabetes mellitus and end stage renal disease
-
(Leu(UUR)) gene in Japanese patients with diabetes mellitus and end stage renal disease. J. Hum. Genet. 46: 330-334.
-
(2001)
J. Hum. Genet.
, vol.46
, pp. 330-334
-
-
Iwasaki, N.1
-
16
-
-
0035072946
-
Leu(UUR) gene mutation
-
Leu(UUR) gene mutation. Kidney Int. 59: 1236-1243.
-
(2001)
Kidney Int.
, vol.59
, pp. 1236-1243
-
-
Hotta, O.1
-
17
-
-
0036119350
-
Maternal transmission of diabetes
-
ALCOLADO, J.C. et al. 2002. Maternal transmission of diabetes. Diabetic Med. 19: 89-98.
-
(2002)
Diabetic Med.
, vol.19
, pp. 89-98
-
-
Alcolado, J.C.1
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