Kühnen P - Search Results

1

An Integrated Understanding of the Molecular Mechanisms of How Adipose Tissue Metabolism Affects Long-term Body Weight Maintenance.

Mai K, Li L, Wiegand S, Brachs M, Leupelt V, Ernert A, Kühnen P, Hübner N, Robinson P, Chen W, Krude H, Spranger J. Mai K, et al. Among authors: kuhnen p. Diabetes. 2019 Jan;68(1):57-65. doi: 10.2337/db18-0440. Epub 2018 Nov 2. Diabetes. 2019. PMID: 30389745 Clinical Trial.

2

Diabetes caused by insulin gene (INS) deletion: clinical characteristics of homozygous and heterozygous individuals.

Raile K, O'Connell M, Galler A, Werther G, Kühnen P, Krude H, Blankenstein O. Raile K, et al. Among authors: kuhnen p. Eur J Endocrinol. 2011 Aug;165(2):255-60. doi: 10.1530/EJE-11-0208. Epub 2011 May 12. Eur J Endocrinol. 2011. PMID: 21566073

3

New pathogenic thyrotropin receptor mutations decipher differentiated activity switching at a conserved helix 6 motif of family A GPCR.

Biebermann H, Winkler F, Handke D, Teichmann A, Gerling B, Cameron F, Eichhorst J, Grüters A, Wiesner B, Kühnen P, Krude H, Kleinau G. Biebermann H, et al. Among authors: kuhnen p. J Clin Endocrinol Metab. 2012 Feb;97(2):E228-32. doi: 10.1210/jc.2011-2106. Epub 2011 Nov 23. J Clin Endocrinol Metab. 2012. PMID: 22112806

4

Glucose-dependent insulinotropic polypeptide reduces fat-specific expression and activity of 11β-hydroxysteroid dehydrogenase type 1 and inhibits release of free fatty acids.

Gögebakan Ö, Andres J, Biedasek K, Mai K, Kühnen P, Krude H, Isken F, Rudovich N, Osterhoff MA, Kintscher U, Nauck M, Pfeiffer AF, Spranger J. Gögebakan Ö, et al. Among authors: kuhnen p. Diabetes. 2012 Feb;61(2):292-300. doi: 10.2337/db10-0902. Epub 2011 Dec 16. Diabetes. 2012. PMID: 22179810 Free PMC article. Clinical Trial.

5

The neuroendocrine circuitry controlled by POMC, MSH, and AGRP.

Biebermann H, Kühnen P, Kleinau G, Krude H. Biebermann H, et al. Among authors: kuhnen p. Handb Exp Pharmacol. 2012;(209):47-75. doi: 10.1007/978-3-642-24716-3_3. Handb Exp Pharmacol. 2012. PMID: 22249810 Review.

6

Long-term lanreotide treatment in six patients with congenital hyperinsulinism.

Kühnen P, Marquard J, Ernert A, Meissner T, Raile K, Wannenmacher G, Blankenstein O. Kühnen P, et al. Horm Res Paediatr. 2012;78(2):106-12. doi: 10.1159/000341525. Epub 2012 Aug 14. Horm Res Paediatr. 2012. PMID: 22907123 Clinical Trial.

7

Two novel GATA6 mutations cause childhood-onset diabetes mellitus, pancreas malformation and congenital heart disease.

Gong M, Simaite D, Kühnen P, Heldmann M, Spagnoli F, Blankenstein O, Hübner N, Hussain K, Raile K. Gong M, et al. Among authors: kuhnen p. Horm Res Paediatr. 2013;79(4):250-6. doi: 10.1159/000348844. Epub 2013 Apr 26. Horm Res Paediatr. 2013. PMID: 23635550

8

Identification of PENDRIN (SLC26A4) mutations in patients with congenital hypothyroidism and "apparent" thyroid dysgenesis.

Kühnen P, Turan S, Fröhler S, Güran T, Abali S, Biebermann H, Bereket A, Grüters A, Chen W, Krude H. Kühnen P, et al. J Clin Endocrinol Metab. 2014 Jan;99(1):E169-76. doi: 10.1210/jc.2013-2619. Epub 2013 Dec 20. J Clin Endocrinol Metab. 2014. PMID: 24248179

9

Recessive mutations in PCBD1 cause a new type of early-onset diabetes.

Simaite D, Kofent J, Gong M, Rüschendorf F, Jia S, Arn P, Bentler K, Ellaway C, Kühnen P, Hoffmann GF, Blau N, Spagnoli FM, Hübner N, Raile K. Simaite D, et al. Among authors: kuhnen p. Diabetes. 2014 Oct;63(10):3557-64. doi: 10.2337/db13-1784. Epub 2014 May 21. Diabetes. 2014. PMID: 24848070 Free article.

10

Treatment of congenital thyroid dysfunction: Achievements and challenges.

Krude H, Kühnen P, Biebermann H. Krude H, et al. Among authors: kuhnen p. Best Pract Res Clin Endocrinol Metab. 2015 Jun;29(3):399-413. doi: 10.1016/j.beem.2015.04.004. Epub 2015 Apr 26. Best Pract Res Clin Endocrinol Metab. 2015. PMID: 26051299 Review.

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