A Novel Ultrapressure Liquid Chromatography Tandem Mass Spectrometry Method for the Simultaneous Determination of Androstenedione, Testosterone, and Dihydrotestosterone in Pediatri... von Kulle, A. E., Riepe, F. G., Melchior, D., Hiort, O., Holterhus, P. M.

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Clinical and Molecular Features of Type 1 Pseudohypoaldosteronism von Riepe, Felix G.

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Androgen receptor function links human sexual dimorphism to DNA methylation von Ammerpohl, Ole, Bens, Susanne, Appari, Mahesh, Werner, Ralf, Korn, Bernhard, Drop, Stenvert L S, Verheijen, Frans, van der Zwan, Yvonne, Bunch, Trevor, Hughes, Ieuan, Cools, Martine, Riepe, Felix G, Hiort, Olaf, Siebert, Reiner, Holterhus, Paul-Martin

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Gonadotropin- and Adrenocorticotropic Hormone-Independent Precocious Puberty of Gonadal Origin in a Patient with Adrenal Hypoplasia Congenita Due to DAX1 Gene Mutation – A Case Rep... von Nagel, Stella A., Hartmann, Michaela F., Riepe, Felix G., Wudy, Stefan A., Wabitsch, Martin

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In vivo investigations of the effect of short- and long-term recombinant growth hormone treatment on DNA-methylation in humans von Kolarova, Julia, Ammerpohl, Ole, Gutwein, Jana, Welzel, Maik, Baus, Inka, Riepe, Felix G, Eggermann, Thomas, Caliebe, Almuth, Holterhus, Paul-Martin, Siebert, Reiner, Bens, Susanne

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Human and mouse TPIT gene mutations cause early onset pituitary ACTH deficiency von Pulichino, Anne-Marie, Vallette-Kasic, Sophie, Couture, Catherine, Gauthier, Yves, Brue, Thierry, David, Michel, Malpuech, Georges, Deal, Cheri, Van Vliet, Guy, De Vroede, Monique, Riepe, Felix G, Partsch, Carl-Joachim, Sippell, Wolfgang G, Berberoglu, Merih, Atasay, Begüm, Drouin, Jacques

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Recent advances in diagnosis, treatment, and outcome of congenital adrenal hyperplasia due to 21-hydroxylase deficiency von Riepe, Felix G, Sippell, Wolfgang G

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Duplication of The SOX3 Gene in an Sry-negative 46,XX Male with Associated Congenital Anomalies of Kidneys and the Urinary Tract: Case Report and Review of the Literature von Tasic, V, Mitrotti, A, Riepe, F G, Kulle, A E, Laban, N, Polenakovic, M, Plaseska-Karanfilska, D, Sanna-Cherchi, S, Kostovski, M, Gucev, Z

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Frequency and characterization of DNA methylation defects in children born SGA von Bens, Susanne, Haake, Andrea, Richter, Julia, Leohold, Judith, Kolarova, Julia, Vater, Inga, Riepe, Felix G, Buiting, Karin, Eggermann, Thomas, Gillessen-Kaesbach, Gabriele, Platzer, Konrad, Prawitt, Dirk, Caliebe, Almuth, Siebert, Reiner

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CYP17A1 intron mutation causing cryptic splicing in 17α-hydroxylase deficiency von Hwang, Daw-Yang, Hung, Chi-Chih, Riepe, Felix G, Auchus, Richard J, Kulle, Alexandra E, Holterhus, Paul-Martin, Chao, Mei-Chyn, Kuo, Mei-Chuan, Hwang, Shang-Jyh, Chen, Hung-Chun

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Classification of Wounds at Risk and Their Antimicrobial Treatment with Polihexanide: A Practice-Oriented Expert Recommendation von Dissemond, J., Assadian, O., Gerber, V., Kingsley, A., Kramer, A., Leaper, D.J., Mosti, G., Piatkowski de Grzymala, A., Riepe, G., Risse, A., Romanelli, M., Strohal, R., Traber, J., Vasel-Biergans, A., Wild, T., Eberlein, T.

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Implementation of a Liquid Chromatography Tandem Mass Spectrometry Assay for Eight Adrenal C-21 Steroids and Pediatric Reference Data von Kulle, Alexandra E., Welzel, Maik, Holterhus, Paul-Martin, Riepe, Felix G.

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What can we Learn from Explanted Endovascular Devices? von Riepe, G., Heintz, C., Kaiser, E., Chakfé, N., Morlock, M., Delling, M., Imig, H.

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No Correlation between Androgen Receptor CAG and GGN Repeat Length and the Degree of Genital Virilization in Females with 21-Hydroxylase Deficiency von Welzel, M., Schwarz, H.-P., Hedderich, J., Dörr, H. G., Binder, G., Brämswig, J. H., Krude, H., Richter-Unruh, A., Niedziela, M., Gromoll, J., Krone, N., Riepe, F. G., Holterhus, P.-M.

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Corroded Nitinol Wires in Explanted Aortic Endografts: An Important Mechanism of Failure? von Heintz, Carsten, Riepe, Gunnar, Birken, Lars, Kaiser, Edelgard, Chakfé, Nabil, Morlock, Michael, Delling, Günter, Imig, Herbert

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Homozygous Disruption of P450 Side-Chain Cleavage (CYP11A1) Is Associated with Prematurity, Complete 46,XY Sex Reversal, and Severe Adrenal Failure von Hiort, Olaf, Holterhus, Paul-Martin, Werner, Ralf, Marschke, Christine, Hoppe, Ute, Partsch, Carl-Joachim, Riepe, Felix G., Achermann, John C., Struve, Dagmar

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Congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency: functional consequences of four CYP11B1 mutations von Menabò, Soara, Polat, Seher, Baldazzi, Lilia, Kulle, Alexandra E, Holterhus, Paul-Martin, Grötzinger, Joachim, Fanelli, Flaminia, Balsamo, Antonio, Riepe, Felix G

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Correction: Congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency: functional consequences of four CYP11B1 mutations von Menabò, Soara, Polat, Seher, Baldazzi, Lilia, Kulle, Alexandra E, Holterhus, Paul-Martin, Grötzinger, Joachim, Fanelli, Flaminia, Balsamo, Antonio, Riepe, Felix G

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LC–MS/MS based determination of basal- and ACTH-stimulated plasma concentrations of 11 steroid hormones: implications for detecting heterozygote CYP21A2 mutation carriers von Kulle, A E, Riepe, F G, Hedderich, J, Sippell, W G, Schmitz, J, Niermeyer, L, Holterhus, P M

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Four Novel Missense Mutations in the CYP21A2 Gene Detected in Russian Patients Suffering from the Classical Form of Congenital Adrenal Hyperplasia: Identification, Functional Chara... von Grischuk, Yulia, Rubtsov, Petr, Riepe, Felix G., Grötzinger, Joachim, Beljelarskaia, Svetlana, Prassolov, Vladimir, Kalintchenko, Natalya, Semitcheva, Tatyana, Peterkova, Valentina, Tiulpakov, Anatoly, Sippell, Wolfgang G., Krone, Nils

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