Maassen JA - Search Results

1

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. van Essen EH, et al. Among authors: maassen ja. Diabet Med. 2000 Dec;17(12):841-7. doi: 10.1046/j.1464-5491.2000.00379.x. Diabet Med. 2000. PMID: 11168326

2

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. Maassen JA, et al. Exp Clin Endocrinol Diabetes. 1996;104(3):205-11. doi: 10.1055/s-0029-1211444. Exp Clin Endocrinol Diabetes. 1996. PMID: 8817237 Review.

3

Heteroplasmy levels of a mitochondrial gene mutation associated with diabetes mellitus decrease in leucocyte DNA upon aging.

't Hart LM, Jansen JJ, Lemkes HH, de Knijff P, Maassen JA. 't Hart LM, et al. Among authors: maassen ja. Hum Mutat. 1996;7(3):193-7. doi: 10.1002/(SICI)1098-1004(1996)7:3<193::AID-HUMU2>3.0.CO;2-C. Hum Mutat. 1996. PMID: 8829651

4

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. Maassen JA, et al. Horm Metab Res. 1997 Feb;29(2):50-5. doi: 10.1055/s-2007-978984. Horm Metab Res. 1997. PMID: 9105898 Review.

5

Mutation in mitochondrial tRNA(Leu(UUR)) gene associated with progressive kidney disease.

Jansen JJ, Maassen JA, van der Woude FJ, Lemmink HA, van den Ouweland JM, t' Hart LM, Smeets HJ, Bruijn JA, Lemkes HH. Jansen JJ, et al. Among authors: maassen ja. J Am Soc Nephrol. 1997 Jul;8(7):1118-24. doi: 10.1681/ASN.V871118. J Am Soc Nephrol. 1997. PMID: 9219161

6

[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. Maassen JA, et al. Ned Tijdschr Geneeskd. 1998 Jan 31;142(5):229-33. Ned Tijdschr Geneeskd. 1998. PMID: 9557035 Dutch.

7

Functional and morphological abnormalities of mitochondria harbouring the tRNA(Leu)(UUR) mutation in mitochondrial DNA derived from patients with maternally inherited diabetes and deafness (MIDD) and progressive kidney disease.

van den Ouweland JM, Maechler P, Wollheim CB, Attardi G, Maassen JA. van den Ouweland JM, et al. Among authors: maassen ja. Diabetologia. 1999 Apr;42(4):485-92. doi: 10.1007/s001250051183. Diabetologia. 1999. PMID: 10230654

8

Molecular and clinical aspects of mitochondrial diabetes mellitus.

Maassen JA, van Essen E, van den Ouweland JM, Lemkes HH. Maassen JA, et al. Exp Clin Endocrinol Diabetes. 2001;109(3):127-34. doi: 10.1055/s-2001-14834. Exp Clin Endocrinol Diabetes. 2001. PMID: 11409293 Review.

9

[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. Maassen JA, et al. Ned Tijdschr Geneeskd. 2001 Jun 16;145(24):1153-4. Ned Tijdschr Geneeskd. 2001. PMID: 11433662 Review. Dutch.

10

Mitochondrial diabetes mellitus.

Maassen JA, Janssen GM, Lemkes HH. Maassen JA, et al. J Endocrinol Invest. 2002 May;25(5):477-84. doi: 10.1007/BF03344042. J Endocrinol Invest. 2002. PMID: 12035948 Review.

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