Search Results - Gerhard Binder
- Showing 1 - 8 results of 8
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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 by Anja Apel, Daniel I. Iliev, Christina Urban, Karin Weber, Roland Schweizer, Gunnar Blumenstock, Sarah Pasche, Vanessa Nieratschker, Gerhard Binder
Published in Frontiers in Endocrinology (2022-09-01)Get full text
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Perinatally diagnosed congenital craniopharyngiomas in the KRANIOPHARYNGEOM trials by Julia Beckhaus, Svenja Boekhoff, Katrin Scheinemann, Freimut H Schilling, Gudrun Fleischhack, Gerhard Binder, Brigitte Bison, Torsten Pietsch, Carsten Friedrich, Hermann L Müller
Published in Endocrine Connections (2023-01-01)Get full text
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New NR5A1 mutations and phenotypic variations of gonadal dysgenesis. by Ralf Werner, Isabel Mönig, Ralf Lünstedt, Lutz Wünsch, Christoph Thorns, Benedikt Reiz, Alexandra Krause, Karl Otfried Schwab, Gerhard Binder, Paul-Martin Holterhus, Olaf Hiort
Published in PLoS ONE (2017-01-01)Get full text
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Comprehensive genetic testing approaches as the basis for personalized management of growth disturbances: current status and perspectives by Danielle Christine Maria van der Kaay, Anne Rochtus, Gerhard Binder, Ingo Kurth, Dirk Prawitt, Irène Netchine, Gudmundur Johannsson, Anita C S Hokken-Koelega, Miriam Elbracht, Thomas Eggermann
Published in Endocrine Connections (2022-10-01)Get full text
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Retinoic acid catabolizing enzyme CYP26C1 is a genetic modifier in SHOX deficiency by Antonino Montalbano, Lonny Juergensen, Ralph Roeth, Birgit Weiss, Maki Fukami, Susanne Fricke‐Otto, Gerhard Binder, Tsutomu Ogata, Eva Decker, Gudrun Nuernberg, David Hassel, Gudrun A Rappold
Published in EMBO Molecular Medicine (2016-11-01)Get full text
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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. by Felix P Bernhard, Sebastian Heinzel, Gerhard Binder, Karin Weber, Anja Apel, Benjamin Roeben, Christian Deuschle, Mirjam Maechtel, Tanja Heger, Susanne Nussbaum, Thomas Gasser, Walter Maetzler, Daniela Berg
Published in PLoS ONE (2016-01-01)Get full text
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Molecular characterisation of 36 multilocus imprinting disturbance (MLID) patients: a comprehensive approach by Larissa Bilo, Eguzkine Ochoa, Sunwoo Lee, Daniela Dey, Ingo Kurth, Florian Kraft, Fay Rodger, France Docquier, Ana Toribio, Leonardo Bottolo, Gerhard Binder, György Fekete, Miriam Elbracht, Eamonn R. Maher, Matthias Begemann, Thomas Eggermann
Published in Clinical Epigenetics (2023-03-01)Get full text
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