Short Stature due to SHOX Deficiency: Genotype, Phenotype, and Therapy von Binder, Gerhard

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Long-term Effect of Aromatase Inhibition in Aromatase Excess Syndrome von Binder, Gerhard, Nakamura, Akie, Schweizer, Roland, Ogata, Tsutomu, Fukami, Maki, Nagasaki, Keisuke

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Increase of jump performance during GH treatment in short children born SGA von Schweizer, Roland, Martin, David D, Binder, Gerhard

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CDKN1C mutations: two sides of the same coin von Eggermann, Thomas, Binder, Gerhard, Brioude, Frédéric, Maher, Eamonn R, Lapunzina, Pablo, Cubellis, Maria Vittoria, Bergadá, Ignacio, Prawitt, Dirk, Begemann, Matthias

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Diagnosis of severe growth hormone deficiency in the newborn von Binder, Gerhard, Weber, Karin, Rieflin, Nora, Steinruck, Louis, Blumenstock, Gunnar, Janzen, Nils, Franz, Axel R.

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New NR5A1 mutations and phenotypic variations of gonadal dysgenesis von Werner, Ralf, Mönig, Isabel, Lünstedt, Ralf, Wünsch, Lutz, Thorns, Christoph, Reiz, Benedikt, Krause, Alexandra, Schwab, Karl Otfried, Binder, Gerhard, Holterhus, Paul-Martin, Hiort, Olaf

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Anti-Müller-Hormon und Inhibin B – Marker der gonadalen Reifung und Prädiktoren der Fertilität? von Binder, Gerhard

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

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Corrigendum: GH responsiveness is not correlated to IGF1 P2 promoter methylation in children with Turner syndrome, GHD and SGA short stature von Apel, Anja, Iliev, Daniel I., Urban, Christina, Weber, Karin, Schweizer, Roland, Blumenstock, Gunnar, Pasche, Sarah, Nieratschker, Vanessa, Binder, Gerhard

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GH Responsiveness Is not Correlated to IGF1 P2 Promoter Methylation in Children With Turner Syndrome, GHD and SGA Short Stature von Apel, Anja, Iliev, Daniel I., Urban, Christina, Weber, Karin, Schweizer, Roland, Blumenstock, Gunnar, Pasche, Sarah, Nieratschker, Vanessa, Binder, Gerhard

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The Diagnostic Value of IGF-2 and the IGF/IGFBP-3 System in Silver-Russell Syndrome von Binder, Gerhard, Eggermann, Thomas, Weber, Karin, Ferrand, Nawfel, Schweizer, Roland

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The Use of Bone Age in Clinical Practice – Part 1 von Martin, David D., Wit, Jan M., Hochberg, Ze’ev, Sävendahl, Lars, van Rijn, Rick R., Fricke, Oliver, Cameron, Noël, Caliebe, Janina, Hertel, Thomas, Kiepe, Daniela, Albertsson-Wikland, Kerstin, Thodberg, Hans Henrik, Binder, Gerhard, Ranke, Michael B.

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Accuracy of Endocrine Tests for Detecting Hypogonadotropic Hypogonadism in Girls von Binder, Gerhard, MD, Schweizer, Roland, MD, Haber, Peter, MD, Blumenstock, Gunnar, MD, Braun, Regina, MD

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Novel mutation points to a hot spot in CDKN1C causing Silver-Russell syndrome von Binder, Gerhard, Ziegler, Julian, Schweizer, Roland, Habhab, Wisam, Haack, Tobias B, Heinrich, Tilman, Eggermann, Thomas

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Molecular characterisation of 36 multilocus imprinting disturbance (MLID) patients: a comprehensive approach von Bilo, Larissa, Ochoa, Eguzkine, Lee, Sunwoo, Dey, Daniela, Kurth, Ingo, Kraft, Florian, Rodger, Fay, Docquier, France, Toribio, Ana, Bottolo, Leonardo, Binder, Gerhard, Fekete, György, Elbracht, Miriam, Maher, Eamonn R, Begemann, Matthias, Eggermann, Thomas

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Insulin-like peptide 3 (INSL3) in congenital hypogonadotrophic hypogonadism (CHH) in boys with delayed puberty and adult men von Abbara, Ali, Koysombat, Kanyada, Phylactou, Maria, Eng, Pei Chia, Clarke, Sophie, Comninos, Alexander N, Yang, Lisa, Izzi-Engbeaya, Chioma, Hanassab, Simon, Smith, Neil, Jayasena, Channa N, Xu, Cheng, Quinton, Richard, Pitteloud, Nelly, Binder, Gerhard, Anand-Ivell, Ravinder, Ivell, Richard, Dhillo, Waljit S

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Silver–Russell syndrome von Binder, Gerhard, Ph.D, Begemann, Matthias, Ph.D, Eggermann, Thomas, Ph.D, Kannenberg, Kai, Ph.D

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Broad Clinical Spectrum in Silver-Russell Syndrome and Consequences for Genetic Testing in Growth Retardation von Eggermann, Thomas, Gonzalez, Daniela, Spengler, Sabrina, Arslan-Kirchner, Mine, Binder, Gerhard, Schonherr, Nadine

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Perinatally diagnosed congenital craniopharyngiomas in the KRANIOPHARYNGEOM trials von Beckhaus, Julia, Boekhoff, Svenja, Scheinemann, Katrin, Schilling, Freimut H, Fleischhack, Gudrun, Binder, Gerhard, Bison, Brigitte, Pietsch, Torsten, Friedrich, Carsten, Müller, Hermann L

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

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