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Results: 1 to 20 of 373

1.

Maternally inherited diabetes and deafness: a multicenter study.

Guillausseau PJ, Massin P, Dubois-LaForgue D, Timsit J, Virally M, Gin H, Bertin E, Blickle JF, Bouhanick B, Cahen J, Caillat-Zucman S, Charpentier G, Chedin P, Derrien C, Ducluzeau PH, Grimaldi A, Guerci B, Kaloustian E, Murat A, Olivier F, Paques M, Paquis-Flucklinger V, Porokhov B, Samuel-Lajeunesse J, Vialettes B.

Ann Intern Med. 2001 May 1;134(9 Pt 1):721-8.

PMID:
11329229
[PubMed - indexed for MEDLINE]
2.

Heterogeneity of diabetes phenotype in patients with 3243 bp mutation of mitochondrial DNA (Maternally Inherited Diabetes and Deafness or MIDD).

Guillausseau PJ, Dubois-Laforgue D, Massin P, Laloi-Michelin M, Bellanné-Chantelot C, Gin H, Bertin E, Blickle JF, Bauduceau B, Bouhanick B, Cahen-Varsaux J, Casanova S, Charpentier G, Chedin P, Derrien C, Grimaldi A, Guerci B, Kaloustian E, Lorenzini F, Murat A, Olivier F, Paques M, Paquis-Flucklinger V, Tielmans A, Vincenot M, Vialettes B, Timsit J; GEDIAM, Mitochondrial Diabetes French Study Group.

Diabetes Metab. 2004 Apr;30(2):181-6.

PMID:
15223991
[PubMed - indexed for MEDLINE]
Free Article
3.

Prevalence of macular pattern dystrophy in maternally inherited diabetes and deafness. GEDIAM Group.

Massin P, Virally-Monod M, Vialettes B, Paques M, Gin H, Porokhov B, Caillat-Zucman S, Froguel P, Paquis-Fluckinger V, Gaudric A, Guillausseau PJ.

Ophthalmology. 1999 Sep;106(9):1821-7.

PMID:
10485557
[PubMed - indexed for MEDLINE]
4.

Retinal and renal complications in patients with a mutation of mitochondrial DNA at position 3,243 (maternally inherited diabetes and deafness). A case-control study.

Massin P, Dubois-Laforgue D, Meas T, Laloi-Michelin M, Gin H, Bauduceau B, Bellanné-Chantelot C, Bertin E, Blickle JF, Bouhanick B, Cahen-Varsaux J, Casanova S, Charpentier G, Chedin P, Dupuy O, Grimaldi A, Guerci B, Kaloustian E, Lecleire-Collet A, Lorenzini F, Murat A, Narbonne H, Olivier F, Paquis-Flucklinger V, Virally M, Vincenot M, Vialettes B, Timsit J, Guillausseau PJ; GEDIAM (Mitochondrial Diabetes French Study Group).

Diabetologia. 2008 Sep;51(9):1664-70. doi: 10.1007/s00125-008-1073-1. Epub 2008 Jun 26.

PMID:
18581092
[PubMed - indexed for MEDLINE]
5.

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
[PubMed - indexed for MEDLINE]
6.

Progressive sensorineural hearing impairment in maternally inherited diabetes mellitus and deafness (MIDD).

Hendrickx JJ, Mudde AH, 't Hart LM, Huygen PL, Cremers CW.

Otol Neurotol. 2006 Sep;27(6):802-8.

PMID:
16788417
[PubMed - indexed for MEDLINE]
7.

Does mitochondrial genome mutation in subjects with maternally inherited diabetes and deafness decrease severity of diabetic retinopathy?

Holmes-Walker DJ, Mitchell P, Boyages SC.

Diabet Med. 1998 Nov;15(11):946-52.

PMID:
9827849
[PubMed - indexed for MEDLINE]
8.

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
[PubMed - indexed for MEDLINE]
9.

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
[PubMed - indexed for MEDLINE]
10.

Gastrointestinal tract symptoms in Maternally Inherited Diabetes and Deafness (MIDD).

Narbonne H, Paquis-Fluckinger V, Valero R, Heyries L, Pellissier JF, Vialettes B.

Diabetes Metab. 2004 Feb;30(1):61-6.

PMID:
15029099
[PubMed - indexed for MEDLINE]
Free Article
11.

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
[PubMed - indexed for MEDLINE]
12.

Macular pattern retinal dystrophy, adult-onset diabetes, and deafness: a family study of A3243G mitochondrial heteroplasmy.

Harrison TJ, Boles RG, Johnson DR, LeBlond C, Wong LJ.

Am J Ophthalmol. 1997 Aug;124(2):217-21.

PMID:
9262546
[PubMed - indexed for MEDLINE]
13.

Prevalence and clinical characteristics of maternally inherited diabetes and deafness caused by the mt3243A > G mutation in young adult diabetic subjects in Sri Lanka.

Katulanda P, Groves CJ, Barrett A, Sheriff R, Matthews DR, McCarthy MI, Gloyn AL.

Diabet Med. 2008 Mar;25(3):370-4. doi: 10.1111/j.1464-5491.2007.02377.x. Epub 2008 Feb 13.

PMID:
18279408
[PubMed - indexed for MEDLINE]
14.

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
[PubMed - indexed for MEDLINE]
15.

Prevalence of 15 mitochondrial DNA mutations among type 2 diabetic patients with or without clinical characteristics of maternally inherited diabetes and deafness.

Crispim D, Estivalet AA, Roisenberg I, Gross JL, Canani LH.

Arq Bras Endocrinol Metabol. 2008 Nov;52(8):1228-35.

PMID:
19169474
[PubMed - indexed for MEDLINE]
Free Article
16.

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
[PubMed - indexed for MEDLINE]
17.

HLA-DQ polymorphism and degree of heteroplasmy of the A3243G mitochondrial DNA mutation in maternally inherited diabetes and deafness.

van Essen EH, Roep BO, 't Hart LM, Jansen JJ, Van den Ouweland JM, Lemkes HH, Maassen JA.

Diabet Med. 2000 Dec;17(12):841-7.

PMID:
11168326
[PubMed - indexed for MEDLINE]
18.

Involvement of nervous system in maternally inherited diabetes and deafness (MIDD) with the A3243G mutation of mitochondrial DNA.

Lien LM, Lee HC, Wang KL, Chiu JC, Chiu HC, Wei YH.

Acta Neurol Scand. 2001 Mar;103(3):159-65.

PMID:
11240563
[PubMed - indexed for MEDLINE]
19.

Mitochondrial diabetes mellitus: prevalence and clinical characterization of diabetes due to mitochondrial tRNA(Leu(UUR)) gene mutation in Japanese patients.

Katagiri H, Asano T, Ishihara H, Inukai K, Anai M, Yamanouchi T, Tsukuda K, Kikuchi M, Kitaoka H, Ohsawa N, et al.

Diabetologia. 1994 May;37(5):504-10.

PMID:
8056189
[PubMed - indexed for MEDLINE]
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
[PubMed - indexed for MEDLINE]
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