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

Get full text

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 by Tasic, V, Mitrotti, A, Riepe, F G, Kulle, A E, Laban, N, Polenakovic, M, Plaseska-Karanfilska, D, Sanna-Cherchi, S, Kostovski, M, Gucev, Z

Get full text

No Correlation between Androgen Receptor CAG and GGN Repeat Length and the Degree of Genital Virilization in Females with 21-Hydroxylase Deficiency by 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.

Get full text

Principles and clinical applications of liquid chromatography — tandem mass spectrometry for the determination of adrenal and gonadal steroid hormones by Kulle, A. E., Welzel, M., Holterhus, P.-M., Riepe, F. G.

Get full text

Automated chromatographic system for the simultaneous measurement of plasma pregnenolone and 17-hydroxypregnenolone by radioimmunoassay by RIEPE, F. G, WONKA, S, PARTSCH, C.-J, SIPPELL, W. G

Get full text

Human and mouse TPIT gene mutations cause early onset pituitary ACTH deficiency by 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

Get full text

Chromatographic system for the simultaneous measurement of plasma 18-hydroxy-11-deoxycorticosterone and 18-hydroxycorticosterone by radioimmunoassay: reference data for neonates an... by Riepe, F.G, Krone, N, Peter, M, Sippell, W.G, Partsch, C.-J

Get full text

Aldosterone synthase deficiency type II with hypospadias by Gucev, Z, Tasic, V, Pop-Jordanova, N, Riepe, F G

Get full text

Longitudinal imaging reveals pituitary enlargement preceding hypoplasia in two brothers with combined pituitary hormone deficiency attributable to PROP1 mutation by RIEPE, Felix G, PARTSCH, Carl-Joachim, BLANKENSTEIN, Oliver, MÖNIG, Heiner, PFÄFFLE, Roland W, SIPPELL, Wolfgang G

Get full text

Serum cortisol and cortisone levels in newborns with congenital adrenal hyperplasia before the start of therapy by Dötsch, J, Hohenberger, I, Riepe, F G, Sippell, W G, Dörr, H G

Get full text

The Increased Lysis of Fetal Cells in the Mother after Pregnancies Complicated by Pre-eclampsia or HELLP Syndrome is not the Result of a Specific Anti-fetal Cytotoxicity of the Mot... by Brune, Thomas, Hornung, Tanja, Koch, Hans-Georg, G. Riepe, Felix, Louwen, Frank

Get full text

Differentiation of single populations in a bidirectional mixed lymphocyte culture using X and Y chromosome-specific FiSH markers by Brune, Thomas, Riepe, Felix G, Beier, Kirsten, Exeler, Rita, Louwen, Frank, Garritsen, Henk

Get full text

The Cellular Immune Response of Children is Specifically Decreased Against their Parents but not Vice versa, Independent of Pregnancy, age, or HLA or HY Antigens by Brune, Thomas, Riepe, Felix G., Garritsen, Henk, Exeler, Rita, Louwen, Frank, Harms, Erik

Get full text

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

Get full text

Congenital Adrenal Hyperplasia Due to 11-Hydroxylase Deficiency: Functional Characterization of Two Novel Point Mutations and a Three-Base Pair Deletion in the CYP11B1 Gene by Krone, Nils, Riepe, Felix G., Götze, Dorothea, Korsch, Eckhard, Rister, Manfred, Commentz, Jens, Partsch, Carl-Joachim, Grötzinger, Joachim, Peter, Michael, Sippell, Wolfgang G.

Get full text

Functional Characterization of Two Novel Point Mutations in the CYP21 Gene Causing Simple Virilizing Forms of Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency by Krone, Nils, Riepe, Felix G., Grötzinger, Joachim, Partsch, Carl-Joachim, Sippell, Wolfgang G.

Get full text

Congenital adrenal hyperplasia: the molecular basis of 21-hydroxylase deficiency in H-2(aw18) mice by Riepe, Felix G, Tatzel, Stephan, Sippell, Wolfgang G, Pleiss, Jürgen, Krone, Nils

Get full text

Serum Cortisol and cortisone levels in newborns with congenital adrenal hyperplasia before the start of therapy by Dötsch, J., Hohenberger, I., Riepe, F. G., Sippell, W. G., Dörr, H. G.

Get full text

Autosomal-Dominant Pseudohypoaldosteronism Type 1 in a Turkish Family Is Associated with a Novel Nonsense Mutation in the Human Mineralocorticoid Receptor Gene by Riepe, Felix G., Krone, Nils, Morlot, Michel, Peter, Michael, Sippell, Wolfgang G., Partsch, Carl-Joachim

Get full text

Identification of a Novel Mutation in the Human Mineralocorticoid Receptor Gene in a German Family with Autosomal-Dominant Pseudohypoaldosteronism Type 1: Further Evidence for Mark... by Riepe, Felix G., Krone, Nils, Morlot, Michel, Ludwig, Michael, Sippell, Wolfgang G., Partsch, Carl-Joachim

Get full text