Patients with Classic Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency Can Achieve Their Target Height: The Leipzig Experience

Autor: Antje Kaufhold, Eberhard Keller, Helmut Willgerodt, Wolfgang Hoepffner

Publikováno v: Hormone Research in Paediatrics. 70:42-50

Background: Despite treatment, the mean final height (FH) of patients with classic congenital adrenal hyperplasia (CAH) is below the mean height of a normal population. Aims:To show that CAH patients can achieve their target height (TH), 39 adult sub

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::193b49a361f835195d07a78dda26937d
https://doi.org/10.1159/000129677

Re-assessment of growth hormone secretion in young adult patients with childhood-onset growth hormone deficiency

Autor: Juliane Donaubauer, Wieland Kiess, Jürgen Kratzsch, Tanja Nowak, Heinz Steinkamp, Helmut Willgerodt, Eberhard Keller, Study Group

Publikováno v: Clinical Endocrinology. 58:456-463

Summary objective Patients with childhood-onset GH deficiency (coGHD) need retesting in late adolescence or young adulthood to verify whether they need to continue GH treatment. For this purpose the Growth Hormone Research Society (GRS) recommends th

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::606a7b7b23e2295625190b68d8ab4d92
https://doi.org/10.1046/j.1365-2265.2003.01739.x

Identification of a New Thyrotropin Receptor Germline Mutation (Leu629Phe) in a Family with Neonatal Onset of Autosomal Dominant Nonautoimmune Hyperthyroidism

Autor: Dagmar Führer, Peter Wonerow, Helmut Willgerodt, Ralf Paschke, Dagmar Führer-Sakel

Publikováno v: The Journal of Clinical Endocrinology & Metabolism. 82:4234-4238

Constitutively activating germline mutations in the TSH receptor (TSHR) gene have been identified as a cause of autosomal dominant nonautoimmune hyperthyroidism and sporadic congenital hyperthyroidism. We report a 10-yr-old boy and his 31-yr-old moth

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e6ea64f538eca69d3e7a501cc2ba35ad
https://doi.org/10.1210/jcem.82.12.4405

Autorinnen und Autoren

Autor: Michael Beck, Frank Berthold, Ralf Bialek, Uta Bierbach, Michael Borte, Ulrich Brandl, Reiner Buchhorn, Guido Bürk, Stefan Burdach, Martin Burdelski, Marcus Dahlheim, Uta Dirksen, Jörg Dötsch, Walter Dorsch, Stefan Eber, Andreas Eicken, Lars Fischer, Jürgen Föll, Reiner Frank, Franz Joseph, Hans Peter, Ulrich Göbel, Norbert Graf, Bodo Grimbacher, Andreas Groll, Ulrich Hagenah, Ulrich Heininger, Alexander Hemprich, Barbara Hero, Beate Herpertz-Dahlmann, Egbert Herting, Gabriele Hessling, Olaf Hiort, Ulrich Hofmann, Hans-Iko Huppertz, Heribert Jürgens, Thomas Michael Kapellen, Matthias Kappler, Thomas Klingebiel, Gerhard Kluger, Ina Knerr, Dieter Körholz, Ewa Koscielniak, Christof Kramm, Martina Krauss-Haas, Joachim Kreuder, Anne Krümpel, Manfred Kudernatsch, Christiane Lex, Hermann Lindemann, Ulrike Lükewille, Esther M. Maier, Karl Mantel, Christine Mauz-Körholz, Otto Mehls, Andreas Merkenschlager, Ulrich Merz, Ania Carolina Muntau, Heidrun Müller, Thomas Müller, Wolfgang Müller-Felber, Erika von Mutius, Petra Nickel, Thomas Nicolai, Tim Niehues, Gerhard Niemann, Charlotte M. Niemeyer, Michele Noterdaeme, Ulrike Nowak-Göttl, Christina Ortmann, Karl P. Paul, Thomas Paul, Roland Pfäffle, Christian Plank, Christian F. Poets, Raymund Pothmann, Torsten Prietzel, Klemens Raile, Vera Raile, Wolfgang Rascher, Paul Reinhold, Ellen Renner, Annette Richter-Unruh, Joachim Roesler, Holger Römpler, Bernhard Roth, Andreas Schaper, Dieter Schlamp, Achim A. Schmaltz, Heinrich Schmidt, Eckhard Schönau, Torsten Schöneberg, Martin Schöning, Dietmar Schranz, Ingram Schulze-Neick, Volker Schuster, Dietrich von Schweinitz, Nicolaus Schwerk, Konrad Seller, Oliver Semler, Werner Siekmeyer, Thorsten Simon, Stephan Springer, Ina Sterker, Michael Sticherling, Rainer Strotmann, Anke Süß, Edelhard Thoms, Holm Uhlig, Kurt Ullrich, Hans Versmold, Katharina Vezyroglou, Isolde Wachter, Bettina Westhoff, Regina Wieland, Alexander Wild, Helmut Willgerodt, Magdalena Wojan, Johannes Wolff, Elke Wühl

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::908b4dd5569f2f90379c8584a435040e
https://doi.org/10.1016/b978-343723200-8.50002-0

Blood pressure in patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency

Autor: Helmut Willgerodt, Alexander Herrmann, Eberhard Keller, Hoepffner W

Publikováno v: Journal of pediatric endocrinologymetabolism : JPEM. 19(5)

Background In patients with congenital adrenal hyperplasia (CAH) recording of blood pressure (BP) must be included in monitoring treatment to detect hypertension. Aim To investigate the BP patterns in patients with CAH. Methods Twenty-three children

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::737a684c3ab17690d52c56372af22c2f
https://pubmed.ncbi.nlm.nih.gov/16789637