Lemkes HH - Search Results

1

Prevalence of maternally inherited diabetes and deafness in diabetic populations in The Netherlands.

t Hart LM, Lemkes HH, Heine RJ, Stolk RP, Feskens EJ, Jansen JJ, van der Does FE, Grobbee DE, Kromhout D, van den Ouweland JM, et al. t Hart LM, et al. Among authors: lemkes hh. Diabetologia. 1994 Nov;37(11):1169-70. doi: 10.1007/BF00418385. Diabetologia. 1994. PMID: 7867892 No abstract available.

2

[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. Among authors: lemkes hh. Ned Tijdschr Geneeskd. 1998 Jan 31;142(5):229-33. Ned Tijdschr Geneeskd. 1998. PMID: 9557035 Dutch.

3

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: lemkes hh. Diabet Med. 2000 Dec;17(12):841-7. doi: 10.1046/j.1464-5491.2000.00379.x. Diabet Med. 2000. PMID: 11168326

4

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. van den Ouweland JM, et al. Among authors: lemkes hh. Muscle Nerve Suppl. 1995;3:S124-30. doi: 10.1002/mus.880181425. Muscle Nerve Suppl. 1995. PMID: 7603513 Review.

5

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. Among authors: lemkes hh. Exp Clin Endocrinol Diabetes. 1996;104(3):205-11. doi: 10.1055/s-0029-1211444. Exp Clin Endocrinol Diabetes. 1996. PMID: 8817237 Review.

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

7

[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. Among authors: lemkes hh. Ned Tijdschr Geneeskd. 2001 Jun 16;145(24):1153-4. Ned Tijdschr Geneeskd. 2001. PMID: 11433662 Review. Dutch.

8

Maternally inherited diabetes and deafness is a distinct subtype of diabetes and associates with a single point mutation in the mitochondrial tRNA(Leu(UUR)) gene.

van den Ouweland JM, Lemkes HH, Trembath RC, Ross R, Velho G, Cohen D, Froguel P, Maassen JA. van den Ouweland JM, et al. Among authors: lemkes hh. Diabetes. 1994 Jun;43(6):746-51. doi: 10.2337/diab.43.6.746. Diabetes. 1994. PMID: 7910800

9

Absence of the Gly40-Ser mutation in the glucagon receptor among diabetic patients in the Netherlands.

Hart LM, Stolk RP, Jansen JJ, Grobbee DE, Lemkes HH, Maassen JA. Hart LM, et al. Among authors: lemkes hh. Diabetes Care. 1995 Oct;18(10):1400-1. doi: 10.2337/diacare.18.10.1400. Diabetes Care. 1995. PMID: 8721949 No abstract available.

10

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: lemkes hh. 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

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