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Page 1
Leptin Is Not Essential for Obesity-Associated Hypertension.
von Schnurbein J, Manzoor J, Brandt S, Denzer F, Kohlsdorf K, Fischer-Posovszky P, Weißenberger M, Frank-Podlech S, Mahmood S, Wabitsch M. von Schnurbein J, et al. Among authors: denzer f. Obes Facts. 2019;12(4):460-475. doi: 10.1159/000501319. Epub 2019 Jul 29. Obes Facts. 2019. PMID: 31357197 Free PMC article.
Sleep and glycemic control in adolescents with type 1 diabetes.
von Schnurbein J, Boettcher C, Brandt S, Karges B, Dunstheimer D, Galler A, Denzer C, Denzer F, Vollbach H, Wabitsch M, Roenneberg T, Vetter C. von Schnurbein J, et al. Among authors: denzer f. Pediatr Diabetes. 2018 Feb;19(1):143-149. doi: 10.1111/pedi.12538. Epub 2017 Jun 14. Pediatr Diabetes. 2018. PMID: 28880049
A case of phace syndrome and acquired hypopituitarism?
Denzer F, Denzer C, Lennerz BS, Bode H, Wabitsch M. Denzer F, et al. Int J Pediatr Endocrinol. 2012 Jun 30;2012(1):20. doi: 10.1186/1687-9856-2012-20. Int J Pediatr Endocrinol. 2012. PMID: 22747526 Free PMC article.
A Recurrent Germline Mutation in the 5'UTR of the Androgen Receptor Causes Complete Androgen Insensitivity by Activating Aberrant uORF Translation.
Hornig NC, de Beaufort C, Denzer F, Cools M, Wabitsch M, Ukat M, Kulle AE, Schweikert HU, Werner R, Hiort O, Audi L, Siebert R, Ammerpohl O, Holterhus PM. Hornig NC, et al. Among authors: denzer f. PLoS One. 2016 Apr 25;11(4):e0154158. doi: 10.1371/journal.pone.0154158. eCollection 2016. PLoS One. 2016. PMID: 27110943 Free PMC article.
Severe Early-Onset Obesity Due to Bioinactive Leptin Caused by a p.N103K Mutation in the Leptin Gene.
Wabitsch M, Funcke JB, von Schnurbein J, Denzer F, Lahr G, Mazen I, El-Gammal M, Denzer C, Moss A, Debatin KM, Gierschik P, Mistry V, Keogh JM, Farooqi IS, Moepps B, Fischer-Posovszky P. Wabitsch M, et al. Among authors: denzer f. J Clin Endocrinol Metab. 2015 Sep;100(9):3227-30. doi: 10.1210/jc.2015-2263. Epub 2015 Jul 17. J Clin Endocrinol Metab. 2015. PMID: 26186301 Free PMC article.
Copy number variation of two separate regulatory regions upstream of SOX9 causes isolated 46,XY or 46,XX disorder of sex development.
Kim GJ, Sock E, Buchberger A, Just W, Denzer F, Hoepffner W, German J, Cole T, Mann J, Seguin JH, Zipf W, Costigan C, Schmiady H, Rostásy M, Kramer M, Kaltenbach S, Rösler B, Georg I, Troppmann E, Teichmann AC, Salfelder A, Widholz SA, Wieacker P, Hiort O, Camerino G, Radi O, Wegner M, Arnold HH, Scherer G. Kim GJ, et al. Among authors: denzer f. J Med Genet. 2015 Apr;52(4):240-7. doi: 10.1136/jmedgenet-2014-102864. Epub 2015 Jan 20. J Med Genet. 2015. PMID: 25604083