Lemkes HH - Search Results

1

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

2

Mitochondrial diabetes: molecular mechanisms and clinical presentation.

Maassen JA, 'T Hart LM, Van Essen E, Heine RJ, Nijpels G, Jahangir Tafrechi RS, Raap AK, Janssen GM, Lemkes HH. Maassen JA, et al. Among authors: lemkes hh. Diabetes. 2004 Feb;53 Suppl 1:S103-9. doi: 10.2337/diabetes.53.2007.s103. Diabetes. 2004. PMID: 14749274 Review.

3

A rare mitochondrial DNA BstNI polymorphism in a family with type II diabetes.

van den Ouweland JM, Lemkes H, Maassen JA. van den Ouweland JM, et al. Nucleic Acids Res. 1991 Apr 25;19(8):1962. doi: 10.1093/nar/19.8.1962-a. Nucleic Acids Res. 1991. PMID: 1674376 Free PMC article.

4

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: lemkes hh. J Am Soc Nephrol. 1997 Jul;8(7):1118-24. doi: 10.1681/ASN.V871118. J Am Soc Nephrol. 1997. PMID: 9219161

5

[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.

6

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

7

Molecular and clinical aspects of mitochondrial diabetes mellitus.

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

8

[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.

9

Mutation in mitochondrial tRNA(Leu)(UUR) gene in a large pedigree with maternally transmitted type II diabetes mellitus and deafness.

van den Ouweland JM, Lemkes HH, Ruitenbeek W, Sandkuijl LA, de Vijlder MF, Struyvenberg PA, van de Kamp JJ, Maassen JA. van den Ouweland JM, et al. Among authors: lemkes hh. Nat Genet. 1992 Aug;1(5):368-71. doi: 10.1038/ng0892-368. Nat Genet. 1992. PMID: 1284550

10

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.

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