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

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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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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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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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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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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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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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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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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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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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Congenital Adrenal Hyperplasia due to 11-Hydroxylase Deficiency – Insights from Two Novel CYP11B1 Mutations (p.M92X, p.R453Q) von Krone, Nils, Grötzinger, Joachim, Holterhus, Paul-Martin, Sippell, Wolfgang G., Schwarz, Hans-Peter, Riepe, Felix G.

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Hashimoto Encephalopathy in a 15-Year-Old-Girl: EEG Findings and Follow-Up von Muhle, Hiltrud, MD, van Baalen, Andreas, MD, Riepe, Felix G., MD, Rohr, Axel, MD, Stephani, Ulrich, MD

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Age and skin site related differences in steroid metabolism in male skin point to a key role of sebocytes in cutaneous hormone metabolism von Haag, Markus, Hamann, Tina, Kulle, Alexandra E., Riepe, Felix G., Blatt, Thomas, Wenck, Horst, Holterhus, Paul-Martin, Peirano, Reto Ivo

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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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Pseudohypoaldosteronism von Riepe, Felix G.

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Steroid 17α-Hydroxylase Deficiency: Functional Characterization of Four Mutations (A174E, V178D, R440C, L465P) in the CYP17A1 Gene von Dhir, Vivek, Reisch, Nicole, Bleicken, Caroline M., Lebl, Jan, Kamrath, Clemens, Schwarz, Hans-Peter, Grötzinger, Joachim, Sippell, Wolfgang G., Riepe, Felix G., Arlt, Wiebke, Krone, Nils

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Neonatal Screening: Identification of Children with 11β-Hydroxylase Deficiency by Second-Tier Testing von Janzen, Nils, Riepe, Felix G., Peter, Michael, Sander, Stefanie, Steuerwald, Ulrike, Korsch, Eckhard, Krull, Friedrich, Müller, Hermann L., Heger, Sabine, Brack, Christoph, Sander, Johannes

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Management of Congenital Adrenal Hyperplasia: Results of the ESPE Questionnaire von Riepe, Felix G., Krone, Nils, Viemann, Matthias, Partsch, Carl-Joachim, Sippell, Wolfgang G.

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Two novel CYP11B1 mutations in congenital adrenal hyperplasia due to steroid 11β hydroxylase deficiency in a Tunisian family von Ben Charfeddine, Ilhem, Riepe, Felix G, Kahloul, Najoua, Kulle, Alexandra E, Adala, Labiba, Mamaï, Ons, Amara, Abdelbasset, Mili, Amira, Amri, Fathi, Saad, Ali, Holterhus, Paul-Martin, Gribaa, Moez

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