Lehto M - Search Results

1

Chronic diabetic complications in patients with MODY3 diabetes.

Isomaa B, Henricsson M, Lehto M, Forsblom C, Karanko S, Sarelin L, Häggblom M, Groop L. Isomaa B, et al. Among authors: lehto m. Diabetologia. 1998 Apr;41(4):467-73. doi: 10.1007/s001250050931. Diabetologia. 1998. PMID: 9562352

2

Insulin secretion and insulin sensitivity in diabetic subgroups: studies in the prediabetic and diabetic state.

Tripathy D, Carlsson AL, Lehto M, Isomaa B, Tuomi T, Groop L. Tripathy D, et al. Among authors: lehto m. Diabetologia. 2000 Dec;43(12):1476-83. doi: 10.1007/s001250051558. Diabetologia. 2000. PMID: 11151756

3

Human hexokinase II gene: exon-intron organization, mutation screening in NIDDM, and its relationship to muscle hexokinase activity.

Lehto M, Huang X, Davis EM, Le Beau MM, Laurila E, Eriksson KF, Bell GI, Groop L. Lehto M, et al. Diabetologia. 1995 Dec;38(12):1466-74. doi: 10.1007/BF00400608. Diabetologia. 1995. PMID: 8786021

4

Characterization of the MODY3 phenotype. Early-onset diabetes caused by an insulin secretion defect.

Lehto M, Tuomi T, Mahtani MM, Widén E, Forsblom C, Sarelin L, Gullström M, Isomaa B, Lehtovirta M, Hyrkkö A, Kanninen T, Orho M, Manley S, Turner RC, Brettin T, Kirby A, Thomas J, Duyk G, Lander E, Taskinen MR, Groop L. Lehto M, et al. J Clin Invest. 1997 Feb 15;99(4):582-91. doi: 10.1172/JCI119199. J Clin Invest. 1997. PMID: 9045858 Free PMC article.

5

High frequency of mutations in MODY and mitochondrial genes in Scandinavian patients with familial early-onset diabetes.

Lehto M, Wipemo C, Ivarsson SA, Lindgren C, Lipsanen-Nyman M, Weng J, Wibell L, Widén E, Tuomi T, Groop L. Lehto M, et al. Diabetologia. 1999 Sep;42(9):1131-7. doi: 10.1007/s001250051281. Diabetologia. 1999. PMID: 10447526

6

Hepatocyte nuclear factor-1 beta (MODY5) gene mutations in Scandinavian families with early-onset diabetes or kidney disease or both.

Weng JP, Lehto M, Forsblom C, Huang X, Li H, Groop LC. Weng JP, et al. Among authors: lehto m. Diabetologia. 2000 Jan;43(1):131-2. doi: 10.1007/s001250050018. Diabetologia. 2000. PMID: 10672455 No abstract available.

7

Characterization of a naturally occurring mutation (L107I) in the HNF1 alpha (MODY3) gene.

Cervin C, Orho-Melander M, Ridderstråle M, Lehto M, Barg S, Groop L, Cilio CM. Cervin C, et al. Among authors: lehto m. Diabetologia. 2002 Dec;45(12):1703-8. doi: 10.1007/s00125-002-0977-4. Epub 2002 Oct 19. Diabetologia. 2002. PMID: 12488960

8

Functional consequences of mutations in the MODY4 gene (IPF1) and coexistence with MODY3 mutations.

Weng J, Macfarlane WM, Lehto M, Gu HF, Shepherd LM, Ivarsson SA, Wibell L, Smith T, Groop LC. Weng J, et al. Among authors: lehto m. Diabetologia. 2001 Feb;44(2):249-58. doi: 10.1007/s001250051608. Diabetologia. 2001. PMID: 11270685

9

Decreased plasma kallikrein activity is associated with reduced kidney function in individuals with type 1 diabetes.

Härma MA, Dahlström EH, Sandholm N, Forsblom C, Groop PH, Lehto M; FinnDiane Study Group. Härma MA, et al. Among authors: lehto m. Diabetologia. 2020 Jul;63(7):1349-1354. doi: 10.1007/s00125-020-05144-1. Epub 2020 Apr 8. Diabetologia. 2020. PMID: 32270254 Free PMC article.

10

Lack of association between the Gly40Ser polymorphism in the glucagon receptor gene and NIDDM in Finland.

Huang X, Orho M, Lehto M, Groop L. Huang X, et al. Among authors: lehto m. Diabetologia. 1995 Oct;38(10):1246-8. doi: 10.1007/BF00422376. Diabetologia. 1995. PMID: 8690179

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