Search Results - Otto, Susanne

Twenty years of newborn screening for congenital adrenal hyperplasia and congenital primary hypothyroidism: experiences from the DGKED/AQUAPE study group for quality improvement in... by Hammersen, Johanna (Author) , Bettendorf, Markus (Author) , Bonfig, Walter (Author) , Schönau, Eckhard (Author) , Warncke, Katharina (Author) , Eckert, Alexander J. (Author) , Fricke-Otto, Susanne (Author) , Palm, Katja (Author) , Holl, Reinhard W. (Author) , Wölfle, Joachim (Author) ,

• Resolving-System, kostenfrei
• Verlag, lizenzpflichtig, Volltext

Cross-sectional seroprevalence surveys of SARS-CoV-2 antibodies in children in Germany, June 2020 to May 2021 by Sorg, Anna-Lisa (Author) , Bergfeld, Leon (Author) , Jank, Marietta (Author) , Corman, Victor (Author) , Semmler, Ilia (Author) , Görtz, Anna (Author) , Beyerlein, Andreas (Author) , Verjans, Eva (Author) , Wagner, Norbert (Author) , Von Bernuth, Horst (Author) , Lander, Fabian (Author) , Weil, Katharina (Author) , Hufnagel, Markus (Author) , Spiekerkötter, Ute (Author) , Chao, Cho-Ming (Author) , Naehrlich, Lutz (Author) , Muntau, Ania Carolina (Author) , Schulze-Sturm, Ulf (Author) , Hansen, Gesine (Author) , Wetzke, Martin (Author) , Jung, Anna-Maria (Author) , Niehues, Tim (Author) , Fricke-Otto, Susanne (Author) , Von Both, Ulrich (Author) , Huebner, Johannes (Author) , Behrends, Uta (Author) , Liese, Johannes G. (Author) , Schwerk, Christian (Author) , Drosten, Christian (Author) , Von Kries, Ruediger (Author) , Schroten, Horst (Author) ,

• Verlag, lizenzpflichtig, Volltext
• Verlag, lizenzpflichtig, Volltext

Guideline adherence and registry recruitment of congenital primary hypothyroidism: data from the German registry for congenital hypothyroidism (HypoDok) by Thomann, Julia (Author) , Tittel, Sascha R. (Author) , Voss, Egbert (Author) , Oeverink, Rudolf (Author) , Palm, Katja (Author) , Fricke-Otto, Susanne (Author) , Kapelari, Klaus (Author) , Holl, Reinhard W. (Author) , Wölfle, Joachim (Author) , Bettendorf, Markus (Author) ,

• Resolving-System, kostenfrei

Genotype/phenotype correlations in 538 congenital adrenal hyperplasia patients from Germany and Austria: discordances in milder genotypes and in screened versus prescreening patien... by Riedl, Stefan (Author) , Röhl, Friedrich-Wilhelm (Author) , Bonfig, Walter (Author) , Brämswig, Jürgen (Author) , Richter-Unruh, Annette (Author) , Fricke-Otto, Susanne (Author) , Bettendorf, Markus (Author) , Riepe, Felix Günther (Author) , Kriegshäuser, Gernot (Author) , Schönau, Eckhard (Author) , Even, Gertrud (Author) , Hauffa, Berthold (Author) , Dörr, Helmuth-Günther (Author) , Holl, Reinhard W. (Author) , Mohnike, Klaus (Author) ,

• Verlag, Volltext
• Verlag, Volltext

Quality of life of short-statured children born small for gestational age or idiopathic growth hormone deficiency within 1 year of growth hormone treatment by Quitmann, Julia (Author) , Bloemeke, Janika (Author) , Silva, Neuza (Author) , Bullinger, Monika (Author) , Witt, Stefanie (Author) , Akkurt, Ilker (Author) , Dunstheimer, Désirée Patricia Alexandra (Author) , Vogel, Christian (Author) , Böttcher, Volker (Author) , Kuhnle Krahl, Ursula (Author) , Bettendorf, Markus (Author) , Schönau, Eckhard (Author) , Fricke-Otto, Susanne (Author) , Keller, Alexdandra (Author) , Mohnike, Klaus (Author) , Dörr, Helmuth-Günther (Author) ,

• Verlag, Volltext
• Verlag, Volltext

Sodium chloride supplementation is not routinely performed in the majority of German and Austrian infants with classic salt-wasting congenital adrenal hyperplasia and has no effect... by Bonfig, Walter (Author) , Roehl, Friedhelm (Author) , Riedl, Stefan (Author) , Brämswig, Jürgen (Author) , Richter-Unruh, Annette (Author) , Fricke-Otto, Susanne (Author) , Hübner, Angela (Author) , Bettendorf, Markus (Author) , Schönau, Eckhard (Author) , Dörr, Helmuth-Günther (Author) , Holl, Reinhard W. (Author) , Mohnike, Klaus (Author) ,

• Resolving-System, Volltext

Hereditary spastic paraplegia: Clinicogenetic lessons from 608 patients by Schüle-Freyer, Rebecca (Author) , Wiethoff, Sarah (Author) , Martus, Peter (Author) , Karle, Kathrin Nora (Author) , Otto, Susanne (Author) , Klebe, Stephan (Author) , Klimpe, Sven (Author) , Gallenmüller, Constanze (Author) , Kurzwelly, Delia (Author) , Henkel, Dorothea (Author) , Rimmele, Florian D. (Author) , Stolze, Henning Wolfgang (Author) , Kohl, Zacharias (Author) , Kassubek, Jan Rainer (Author) , Klockgether, Thomas (Author) , Vielhaber, Stefan (Author) , Kamm, Christoph (Author) , Klopstock, Thomas (Author) , Bauer, Peter (Author) , Züchner, Stephan (Author) , Liepelt-Scarfone, Inga (Author) , Schöls, Ludger (Author) ,

Hereditary spastic paraplegia: Clinicogenetic lessons from 608 patients by Schüle-Freyer, Rebecca (Author) , Wiethoff, Sarah (Author) , Martus, Peter (Author) , Karle, Kathrin Nora (Author) , Otto, Susanne (Author) , Klebe, Stephan (Author) , Klimpe, Sven (Author) , Gallenmüller, Constanze (Author) , Kurzwelly, Delia (Author) , Henkel, Dorothea (Author) , Rimmele, Florian D. (Author) , Stolze, Henning Wolfgang (Author) , Kohl, Zacharias (Author) , Kassubek, Jan Rainer (Author) , Klockgether, Thomas (Author) , Vielhaber, Stefan (Author) , Kamm, Christoph (Author) , Klopstock, Thomas (Author) , Bauer, Peter (Author) , Züchner, Stephan (Author) , Liepelt-Scarfone, Inga (Author) , Schöls, Ludger (Author) ,

• Resolving-System, Volltext

A high-throughput resequencing microarray for autosomal dominant spastic paraplegia genes

Other Authors: “…Otto, Susanne…”