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Items: 1 to 20 of 320

1.

Clinical features of diabetes mellitus with the mitochondrial DNA 3243 (A-G) mutation in Japanese: maternal inheritance and mitochondria-related complications.

Suzuki S, Oka Y, Kadowaki T, Kanatsuka A, Kuzuya T, Kobayashi M, Sanke T, Seino Y, Nanjo K; Research Committee or Specific Types of Diabetes Mellitus with Gene Mutations of the Japan Diabetes Society.

Diabetes Res Clin Pract. 2003 Mar;59(3):207-17.

PMID:
12590018
2.

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, Hirai M, Hirai A, Chiba M, Kasuga S, Satoh Y, Akai H, Toyota T.

Diabetologia. 1998 May;41(5):584-8.

PMID:
9628277
3.

Diabetes mellitus with mitochondrial gene mutations in Japan.

Suzuki S.

Ann N Y Acad Sci. 2004 Apr;1011:185-92.

PMID:
15126296
4.
5.

Novel mitochondrial DNA mutation in tRNA(Lys) (8296A-->G) associated with diabetes.

Kameoka K, Isotani H, Tanaka K, Azukari K, Fujimura Y, Shiota Y, Sasaki E, Majima M, Furukawa K, Haginomori S, Kitaoka H, Ohsawa N.

Biochem Biophys Res Commun. 1998 Apr 17;245(2):523-7.

PMID:
9571188
6.

Pigmentary retinal dystrophy and the syndrome of maternally inherited diabetes and deafness caused by the mitochondrial DNA 3243 tRNA(Leu) A to G mutation.

Smith PR, Bain SC, Good PA, Hattersley AT, Barnett AH, Gibson JM, Dodson PM.

Ophthalmology. 1999 Jun;106(6):1101-8.

PMID:
10366077
7.

Maternally inherited diabetes mellitus: the role of mitochondrial DNA defects.

Alcolado JC, Thomas AW.

Diabet Med. 1995 Feb;12(2):102-8. Review.

PMID:
7743754
8.

Maternally inherited diabetes and deafness: a diabetic subtype associated with a mutation in mitochondrial DNA.

Maassen JA, van den Ouweland JM, t Hart LM, Lemkes HH.

Horm Metab Res. 1997 Feb;29(2):50-5. Review.

PMID:
9105898
9.

The mitochondrial tRNA[Leu(UUR)] A to G 3243 mutation is associated with insulin-dependent and non-insulin-dependent diabetes in a Chinese population.

Smith PR, Dronsfield MJ, Mijovic CH, Hattersley AT, Yeung VT, Cockram C, Chan JC, Barnett AH, Bain SC.

Diabet Med. 1997 Dec;14(12):1026-31.

PMID:
9455929
10.
11.

A subtype of diabetes mellitus associated with a mutation of mitochondrial DNA.

Kadowaki T, Kadowaki H, Mori Y, Tobe K, Sakuta R, Suzuki Y, Tanabe Y, Sakura H, Awata T, Goto Y, et al.

N Engl J Med. 1994 Apr 7;330(14):962-8.

12.

The molecular basis and clinical characteristics of Maternally Inherited Diabetes and Deafness (MIDD), a recently recognized diabetic subtype.

Maassen JA, Jansen JJ, Kadowaki T, van den Ouweland JM, 't Hart LM, Lemkes HH.

Exp Clin Endocrinol Diabetes. 1996;104(3):205-11. Review.

PMID:
8817237
13.

A novel mitochondrial DNA missense mutation at G3421A in a family with maternally inherited diabetes and deafness.

Chen FL, Liu Y, Song XY, Hu HY, Xu HB, Zhang XM, Shi JH, Hu J, Shen Y, Lu B, Wang XC, Hu RM.

Mutat Res. 2006 Dec 1;602(1-2):26-33. Epub 2006 Sep 1.

PMID:
16949108
14.

High prevalence of mitochondrial diabetes mellitus in Japanese patients with major risk factors.

Fukui M, Nakano K, Obayashi H, Kitagawa Y, Nakamura N, Mori H, Kajiyama S, Wada S, Fujii M, Yoshimori K, Kanaitsuka T, Shigeta H, Kondo M.

Metabolism. 1997 Jul;46(7):793-5.

PMID:
9225833
15.

[Diabetes mellitus associated with the mitochondrial mutation A3243G: frequency and clinical presentation].

Salles JE, Kalinin LB, Ferreira SR, Kasamatsu T, Moisés RS.

Arq Bras Endocrinol Metabol. 2007 Jun;51(4):559-65. Portuguese.

PMID:
17684616
16.

A pilot study of mitochondrial DNA point mutation A3243G in a sample of Croatian patients having type 2 diabetes mellitus associated with maternal inheritance.

Martin-Kleiner I, Pape-Medvidović E, Pavlić-Renar I, Metelko Z, Kusec R, Gabrilovac J, Boranić M.

Acta Diabetol. 2004 Dec;41(4):179-84.

PMID:
15660201
17.

Search for mitochondrial DNA mutation at position 3243 in German patients with a positive family history of maternal diabetes mellitus.

Klemm T, Neumann S, Trülzsch B, Pistrosch F, Hanefeld M, Paschke R.

Exp Clin Endocrinol Diabetes. 2001;109(5):283-7.

PMID:
11507652
18.

Mitochondrial DNA point mutation at nucleotide pair 3316 in a Japanese family with heterogeneous phenotypes of diabetes.

Nakano S, Fukuda M, Hotta F, Ito T, Ishii T, Kitazawa M, Nishizawa M, Kigoshi T, Kakinuma H, Takahashi H, Uchida K.

Endocr J. 1998 Oct;45(5):625-30.

PMID:
10395242
19.

A patient with diabetes mellitus, cardiomyopathy, and a mitochondrial gene mutation: confirmation of a gene mutation in cardiac muscle.

Kitaoka H, Kameoka K, Suzuki Y, Sasaki E, Majima M, Takada K, Katagiri H, Oka Y, Ohsawa N.

Diabetes Res Clin Pract. 1995 Jun;28(3):207-12.

PMID:
8529500
20.

[A new subtype of diabetes mellitus: maternally inherited diabetes and deafness (MIDD)].

Maassen JA, Jansen JJ, van den Ouweland JM, Hart LM, van Essen EH, Lemkes HH.

Ned Tijdschr Geneeskd. 1998 Jan 31;142(5):229-33. Dutch.

PMID:
9557035

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