Karges B - Search Results

1

Elucidating the underlying molecular pathogenesis of NR3C2 mutants causing autosomal dominant pseudohypoaldosteronism type 1.

Riepe FG, Finkeldei J, de Sanctis L, Einaudi S, Testa A, Karges B, Peter M, Viemann M, Grötzinger J, Sippell WG, Fejes-Toth G, Krone N. Riepe FG, et al. Among authors: karges b. J Clin Endocrinol Metab. 2006 Nov;91(11):4552-61. doi: 10.1210/jc.2006-1161. Epub 2006 Sep 5. J Clin Endocrinol Metab. 2006. PMID: 16954160

2

Metabolic control during the first two years of the COVID-19 pandemic in pediatric patients with type 1 diabetes: results from the German DPV initiative.

Hammersen J, Tittel SR, Khodaverdi S, Reschke F, Flury M, Menzel U, Mönkemöller K, Meissner T, Karges B, Holl RW. Hammersen J, et al. Among authors: karges b. Acta Diabetol. 2023 Jun;60(6):757-766. doi: 10.1007/s00592-023-02050-x. Epub 2023 Mar 4. Acta Diabetol. 2023. PMID: 36871116 Free PMC article.

3

Satisfaction with genital surgery and sexual life of adults with XY disorders of sex development: results from the German clinical evaluation study.

Köhler B, Kleinemeier E, Lux A, Hiort O, Grüters A, Thyen U; DSD Network Working Group. Köhler B, et al. J Clin Endocrinol Metab. 2012 Feb;97(2):577-88. doi: 10.1210/jc.2011-1441. Epub 2011 Nov 16. J Clin Endocrinol Metab. 2012. PMID: 22090272

4

Five novel mutations in the SCNN1A gene causing autosomal recessive pseudohypoaldosteronism type 1.

Welzel M, Akin L, Büscher A, Güran T, Hauffa BP, Högler W, Leonards J, Karges B, Kentrup H, Kirel B, Senses EE, Tekin N, Holterhus PM, Riepe FG. Welzel M, et al. Among authors: karges b. Eur J Endocrinol. 2013 Apr 15;168(5):707-15. doi: 10.1530/EJE-12-1000. Print 2013 May. Eur J Endocrinol. 2013. PMID: 23416952

5

Mutation Ala(171)Thr stabilizes the gonadotropin-releasing hormone receptor in its inactive conformation, causing familial hypogonadotropic hypogonadism.

Karges B, Karges W, Mine M, Ludwig L, Kühne R, Milgrom E, de Roux N. Karges B, et al. Among authors: karges w. J Clin Endocrinol Metab. 2003 Apr;88(4):1873-9. doi: 10.1210/jc.2002-020005. J Clin Endocrinol Metab. 2003. PMID: 12679486

6

TSH receptor mutation V509A causes familial hyperthyroidism by release of interhelical constraints between transmembrane helices TMH3 and TMH5.

Karges B, Krause G, Homoki J, Debatin KM, de Roux N, Karges W. Karges B, et al. Among authors: karges w. J Endocrinol. 2005 Aug;186(2):377-85. doi: 10.1677/joe.1.06208. J Endocrinol. 2005. PMID: 16079263

7

Levothyroxine in euthyroid autoimmune thyroiditis and type 1 diabetes: a randomized, controlled trial.

Karges B, Muche R, Knerr I, Ertelt W, Wiesel T, Hub R, Neu A, Klinghammer A, Aufschild J, Rapp A, Schirbel A, Boehm BO, Debatin KM, Heinze E, Karges W. Karges B, et al. Among authors: karges w. J Clin Endocrinol Metab. 2007 May;92(5):1647-52. doi: 10.1210/jc.2006-2493. Epub 2007 Feb 13. J Clin Endocrinol Metab. 2007. PMID: 17299067 Clinical Trial.

8

Fibroblast Growth Factor 21 and Fetuin-A in Obese Adolescents With and Without Type 2 Diabetes.

Reinehr T, Karges B, Meissner T, Wiegand S, Fritsch M, Holl RW, Woelfle J. Reinehr T, et al. Among authors: karges b. J Clin Endocrinol Metab. 2015 Aug;100(8):3004-10. doi: 10.1210/jc.2015-2192. Epub 2015 Jun 8. J Clin Endocrinol Metab. 2015. PMID: 26052728

9

Clinical and molecular genetics of the human GnRH receptor.

Karges B, Karges W, de Roux N. Karges B, et al. Among authors: karges w. Hum Reprod Update. 2003 Nov-Dec;9(6):523-30. doi: 10.1093/humupd/dmg040. Hum Reprod Update. 2003. PMID: 14714589 Review.

10

Bone maturation in 1788 children and adolescents with diabetes mellitus type 1.

Dost A, Rohrer T, Fussenegger J, Vogel C, Schenk B, Wabitsch M, Karges B, Vilser C, Holl RW; Initiative DPV-Science; German Competence Network Diabetes. Dost A, et al. Among authors: karges b. J Pediatr Endocrinol Metab. 2010 Sep;23(9):891-8. doi: 10.1515/jpem.2010.144. J Pediatr Endocrinol Metab. 2010. PMID: 21175088

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