Increase of jump performance during GH treatment in short children born SGA

por Schweizer, Roland, Martin, David D., Binder, Gerhard
Publicado 2023

Silver-Russell syndrome: genetic basis and molecular genetic testing

por Eggermann, Thomas, Begemann, Matthias, Binder, Gerhard, Spengler, Sabrina
Publicado 2010

Decreased expression of cell proliferation-related genes in clonally derived skin fibroblasts from children with Silver-Russell syndrome is independent of the degree of 11p15 ICR1...

por Heckmann, Doreen, Urban, Christina, Weber, Karin, Kannenberg, Kai, Binder, Gerhard
Publicado 2015

Auditory habituation to simple tones: reduced evidence for habituation in children compared to adults

por Muenssinger, Jana, Stingl, Krunoslav T., Matuz, Tamara, Binder, Gerhard, Ehehalt, Stefan, Preissl, Hubert
Publicado 2013

Long-Term Effect of Aromatase Inhibition in Aromatase Excess Syndrome

por Binder, Gerhard, Nakamura, Akie, Schweizer, Roland, Ogata, Tsutomu, Fukami, Maki, Nagasaki, Keisuke
Publicado 2021

IGF2/H19 hypomethylation is tissue, cell, and CpG site dependent and not correlated with body asymmetry in adolescents with Silver-Russell syndrome

por Kannenberg, Kai, Weber, Karin, Binder, Cathrin, Urban, Christina, Kirschner, Hans-Joachim, Binder, Gerhard
Publicado 2012

OR10-02 Diagnosis of Severe GH Deficiency in Newborns: New Reference Range for the Preterm and Confirmation of the GH Cut-Off

por Binder, Gerhard, Weber, Karin, degree, no, Rieflin, Nora, degree, no, Steinruck, Louis, degree, no, Franz, Axel
Publicado 2020

Comparison of radiogrammetrical metacarpal indices in children and reference data from the First Zurich Longitudinal Study

por Martin, David D., Heckmann, Conrad, Neuhof, Julia, Jenni, Oskar G., Ranke, Michael B., Binder, Gerhard
Publicado 2012

Novel mutation points to a hot spot in CDKN1C causing Silver–Russell syndrome

por Binder, Gerhard, Ziegler, Julian, Schweizer, Roland, Habhab, Wisam, Haack, Tobias B., Heinrich, Tilman, Eggermann, Thomas
Publicado 2020

Eating Disorder Pathology in Adolescents Participating in a Lifestyle Intervention for Obesity: Associations with Weight Change, General Psychopathology and Health-Related Quality...

por Giel, Katrin E., Zipfel, Stephan, Schweizer, Roland, Braun, Regina, Ranke, Michael B., Binder, Gerhard, Ehehalt, Stefan
Publicado 2013

Evolving pituitary hormone deficits in primarily isolated GHD: a review and experts’ consensus

por Binder, Gerhard, Schnabel, Dirk, Reinehr, Thomas, Pfäffle, Roland, Dörr, Helmuth-Günther, Bettendorf, Markus, Hauffa, Berthold, Woelfle, Joachim
Publicado 2020

GH Responsiveness Is not Correlated to IGF1 P2 Promoter Methylation in Children With Turner Syndrome, GHD and SGA Short Stature

por Apel, Anja, Iliev, Daniel I., Urban, Christina, Weber, Karin, Schweizer, Roland, Blumenstock, Gunnar, Pasche, Sarah, Nieratschker, Vanessa, Binder, Gerhard
Publicado 2022

Corrigendum: GH responsiveness is not correlated to IGF1 P2 promoter methylation in children with Turner syndrome, GHD and SGA short stature

por Apel, Anja, Iliev, Daniel I., Urban, Christina, Weber, Karin, Schweizer, Roland, Blumenstock, Gunnar, Pasche, Sarah, Nieratschker, Vanessa, Binder, Gerhard
Publicado 2022

Noncovalent Liquid Phase Functionalization of 2H-WS(2) with PDI: An Energy Conversion Platform with Long-Lived Charge Separation

por Scharl, Tobias, Binder, Gerhard, Chen, Xin, Yokosawa, Tadahiro, Cadranel, Alejandro, Knirsch, Kathrin C., Spiecker, Erdmann, Hirsch, Andreas, Guldi, Dirk M.
Publicado 2022

Perinatally diagnosed congenital craniopharyngiomas in the KRANIOPHARYNGEOM trials

por Beckhaus, Julia, Boekhoff, Svenja, Scheinemann, Katrin, Schilling, Freimut H, Fleischhack, Gudrun, Binder, Gerhard, Bison, Brigitte, Pietsch, Torsten, Friedrich, Carsten, Müller, Hermann L
Publicado 2023

New NR5A1 mutations and phenotypic variations of gonadal dysgenesis

por Werner, Ralf, Mönig, Isabel, Lünstedt, Ralf, Wünsch, Lutz, Thorns, Christoph, Reiz, Benedikt, Krause, Alexandra, Schwab, Karl Otfried, Binder, Gerhard, Holterhus, Paul-Martin, Hiort, Olaf
Publicado 2017

Very High Dehydroepiandrosterone Sulfate (DHEAS) in Serum of an Overweight Female Adolescent Without a Tumor

por Iliev, Daniel I., Braun, Regina, Sánchez-Guijo, Alberto, Hartmann, Michaela, Wudy, Stefan A., Heckmann, Doreen, Bruchelt, Gernot, Rösner, Anika, Grosser, Gary, Geyer, Joachim, Binder, Gerhard
Publicado 2020

Retinoic acid catabolizing enzyme CYP26C1 is a genetic modifier in SHOX deficiency

por Montalbano, Antonino, Juergensen, Lonny, Roeth, Ralph, Weiss, Birgit, Fukami, Maki, Fricke‐Otto, Susanne, Binder, Gerhard, Ogata, Tsutomu, Decker, Eva, Nuernberg, Gudrun, Hassel, David, Rappold, Gudrun A
Publicado 2016

Comprehensive genetic testing approaches as the basis for personalized management of growth disturbances: current status and perspectives

por van der Kaay, Danielle Christine Maria, Rochtus, Anne, Binder, Gerhard, Kurth, Ingo, Prawitt, Dirk, Netchine, Irène, Johannsson, Gudmundur, Hokken-Koelega, Anita C S, Elbracht, Miriam, Eggermann, Thomas
Publicado 2022

Insulin-Like Growth Factor 1 (IGF-1) in Parkinson's Disease: Potential as Trait-, Progression- and Prediction Marker and Confounding Factors

por Bernhard, Felix P., Heinzel, Sebastian, Binder, Gerhard, Weber, Karin, Apel, Anja, Roeben, Benjamin, Deuschle, Christian, Maechtel, Mirjam, Heger, Tanja, Nussbaum, Susanne, Gasser, Thomas, Maetzler, Walter, Berg, Daniela
Publicado 2016