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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
Phosphorus-31 magnetic resonance spectroscopy of skeletal muscle in maternally inherited diabetes and deafness A3243G mitochondrial mutation carriers.
van Elderen SG, Doornbos J, van Essen EH, Lemkes HH, Maassen JA, Smit JW, de Roos A. van Elderen SG, et al. Among authors: lemkes hh. J Magn Reson Imaging. 2009 Jan;29(1):127-31. doi: 10.1002/jmri.21620. J Magn Reson Imaging. 2009. PMID: 19097109
Impact of simultaneous pancreas and kidney transplantation on progression of coronary atherosclerosis in patients with end-stage renal failure due to type 1 diabetes.
Jukema JW, Smets YF, van der Pijl JW, Zwinderman AH, Vliegen HW, Ringers J, Reiber JH, Lemkes HH, van der Wall EE, de Fijter JW. Jukema JW, et al. Among authors: lemkes hh. Diabetes Care. 2002 May;25(5):906-11. doi: 10.2337/diacare.25.5.906. Diabetes Care. 2002. PMID: 11978689
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.
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. Among authors: lemkes h. 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.
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
Mitochondrial diabetes and its lessons for common Type 2 diabetes.
Maassen JA, 't Hart LM, Janssen GM, Reiling E, Romijn JA, Lemkes HH. Maassen JA, et al. Among authors: lemkes hh. Biochem Soc Trans. 2006 Nov;34(Pt 5):819-23. doi: 10.1042/BST0340819. Biochem Soc Trans. 2006. PMID: 17052206
[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.
[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.
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.
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