Lemkes HH - Search Results

1

[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.

2

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

3

[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.

4

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

5

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.

6

[From gene to disease; 'maturity-onset diabetes of the young' (MODY), monogenetic inheritable forms of diabetes mellitus].

Maassen JA, Lemkes HH, Losekoot M. Maassen JA, et al. Among authors: lemkes hh. Ned Tijdschr Geneeskd. 2001 Jul 14;145(28):1352-3. Ned Tijdschr Geneeskd. 2001. PMID: 11484433 Review. Dutch.

7

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

8

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.

9

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

10

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.

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