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Items: 1 to 20 of 187

1.

New insights in the molecular pathogenesis of the maternally inherited diabetes and deafness syndrome.

Maassen JA, Jahangir Tafrechi RS, Janssen GM, Raap AK, Lemkes HH, 't Hart LM.

Endocrinol Metab Clin North Am. 2006 Jun;35(2):385-96, x-xi. Review.

PMID:
16632100
2.

Mitochondrial diabetes and its lessons for common Type 2 diabetes.

Maassen JA, 't Hart LM, Janssen GM, Reiling E, Romijn JA, Lemkes HH.

Biochem Soc Trans. 2006 Nov;34(Pt 5):819-23.

PMID:
17052206
3.

Maternally inherited diabetes and deafness (MIDD): a distinct subtype of diabetes associated with a mitochondrial tRNA(Leu)(UUR) gene point mutation.

van den Ouweland JM, Lemkes HH, Gerbitz KD, Maassen JA.

Muscle Nerve Suppl. 1995;3:S124-30. Review.

PMID:
7603513
4.

D-glucose metabolism in lymphocytes of patients with mitochondrial point mutation of the tRNALeu(UUR) gene.

Malaisse WJ, Pueyo ME, Nadi AB, Malaisse-Lagae F, Froguel P, Velho G.

Biochem Mol Med. 1995 Apr;54(2):91-5.

PMID:
8581364
5.

Mitochondrial 3243 BP mutation: a case report.

Rigoli L, Caruso RA, Zuccarello D, Rigoli M, Barberi I.

Diabetes Nutr Metab. 2001 Dec;14(6):343-8.

PMID:
11853367
6.

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
7.

Mitochondrial DNA variations in patients with maternally inherited diabetes and deafness syndrome.

Perucca-Lostanlen D, Narbonne H, Hernandez JB, Staccini P, Saunieres A, Paquis-Flucklinger V, Vialettes B, Desnuelle C.

Biochem Biophys Res Commun. 2000 Nov 2;277(3):771-5.

PMID:
11062027
8.

[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
9.

Clinical aspects of mitochondrial diabetes.

Vialettes B, Paquis-Flucklinger V, Bendahan D.

Diabetes Metab. 1997 Mar;23 Suppl 2:52-6. Review.

PMID:
9105784
10.

[From gene to disease; mutation in mitochondrial DNA and maternally inherited diabetes mellitus with deafness (MIDD)].

Maassen JA, van den Ouweland JM, Losekoot M, Lemkes HH.

Ned Tijdschr Geneeskd. 2001 Jun 16;145(24):1153-4. Review. Dutch.

PMID:
11433662
11.

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
12.

Mitochondrial diabetes: pathophysiology, clinical presentation, and genetic analysis.

Maassen JA.

Am J Med Genet. 2002 May 30;115(1):66-70. Review.

PMID:
12116179
13.

The effect on mitochondrial function of the tRNA Ser(UCN)/COI A7445G mtDNA point mutation associated with maternally-inherited sensorineural deafness.

Hyslop SJ, James AM, Maw M, Fischel-Ghodsian N, Murphy MP.

Biochem Mol Biol Int. 1997 Jul;42(3):567-75.

PMID:
9247714
14.

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
15.

Cardiomyopathy and kidney disease in a patient with maternally inherited diabetes and deafness caused by the 3243A>G mutation of mitochondrial DNA.

Azevedo O, Vilarinho L, Almeida F, Ferreira F, Guardado J, Ferreira M, Lourenço A, Medeiros R, Almeida J.

Cardiology. 2010;115(1):71-4. doi: 10.1159/000252811. Epub 2009 Oct 27.

PMID:
19864902
16.

Genetic factors related to mitochondrial function and risk of diabetes mellitus.

Cho YM, Park KS, Lee HK.

Diabetes Res Clin Pract. 2007 Sep;77 Suppl 1:S172-7. Epub 2007 Apr 23. Review.

PMID:
17451836
17.

Mitochondrial DNA mutations and pathogenesis.

Schon EA, Bonilla E, DiMauro S.

J Bioenerg Biomembr. 1997 Apr;29(2):131-49. Review.

PMID:
9239539
18.

[A pedigree with maternally transmitted diabetes mellitus, deafness and cardiomyopathy].

Kuzuya N, Noda M, Fujii M, Kanazawa Y.

Nihon Rinsho. 1994 Oct;52(10):2611-5. Japanese.

PMID:
7983786
19.

Diabetes-associated mitochondrial DNA mutation A3243G impairs cellular metabolic pathways necessary for beta cell function.

de Andrade PB, Rubi B, Frigerio F, van den Ouweland JM, Maassen JA, Maechler P.

Diabetologia. 2006 Aug;49(8):1816-26. Epub 2006 May 31.

PMID:
16736129
20.

Diabetes mellitus, deafness, muscle weakness and hypocalcemia in a patient with an A3243G mutation of the mitochondrial DNA.

Tanaka K, Takada Y, Matsunaka T, Yuyama S, Fujino S, Maguchi M, Yamashita S, Yuba I.

Intern Med. 2000 Mar;39(3):249-52.

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