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Gerhard Binder

Showing results (81-90 of 130) with videos related to

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Frontiers in Endocrinology|October 14, 2022
Corrigendum: GH responsiveness is not correlated to <i>IGF1</i> P2 promoter methylation in children with Turner syndrome, GHD and SGA short statureAnja Apel, Daniel I Iliev, Christina Urban, et al.
Hormone Research in Paediatrics|August 18, 2015
Levothyroxine Treatment of Euthyroid Children with Autoimmune Hashimoto Thyroiditis: Results of a Multicenter, Randomized, Controlled TrialHelmuth G Dörr, Markus Bettendorf, Gerhard Binder, et al.
Frontiers in Endocrinology|June 30, 2022
GH Responsiveness Is not Correlated to <i>IGF1</i> P2 Promoter Methylation in Children With Turner Syndrome, GHD and SGA Short StatureAnja Apel, Daniel I Iliev, Christina Urban, et al.
Journal of the American Chemical Society|March 28, 2022
Noncovalent Liquid Phase Functionalization of 2H-WS<sub>2</sub> with PDI: An Energy Conversion Platform with Long-Lived Charge SeparationTobias Scharl, Gerhard Binder, Xin Chen, et al.
Hormone Research|February 4, 2009
Height gains in response to growth hormone treatment to final height are similar in patients with SHOX deficiency and Turner syndromeWerner F Blum, Dachuang Cao, Volker Hesse, et al.
Trends in Molecular Medicine|September 29, 2014
CDKN1C mutations: two sides of the same coinThomas Eggermann, Gerhard Binder, Frédéric Brioude, et al.
European Journal of Human Genetics : EJHG|December 27, 2007
IGF2/H19 hypomethylation in Silver-Russell syndrome and isolated hemihypoplasiaMichael Zeschnigk, Beate Albrecht, Karin Buiting, et al.
The Journal of Clinical Endocrinology and Metabolism|January 31, 2008
The endocrine phenotype in silver-russell syndrome is defined by the underlying epigenetic alterationGerhard Binder, Ann-Kathrin Seidel, David D Martin, et al.
The Journal of Pediatrics|April 13, 2012
Health and quality of life in adults with Noonan syndromeGerhard Binder, Sabrina Grathwol, Karoline von Loeper, et al.
The New England Journal of Medicine|July 9, 2015
Paternally Inherited IGF2 Mutation and Growth RestrictionMatthias Begemann, Birgit Zirn, Gijs Santen, et al.
Pageof 13

Showing results (81-90 of 130) with videos related to

Sort By:
Pageof 13
Frontiers in Endocrinology|October 14, 2022
Corrigendum: GH responsiveness is not correlated to <i>IGF1</i> P2 promoter methylation in children with Turner syndrome, GHD and SGA short statureAnja Apel, Daniel I Iliev, Christina Urban, et al.
Hormone Research in Paediatrics|August 18, 2015
Levothyroxine Treatment of Euthyroid Children with Autoimmune Hashimoto Thyroiditis: Results of a Multicenter, Randomized, Controlled TrialHelmuth G Dörr, Markus Bettendorf, Gerhard Binder, et al.
Frontiers in Endocrinology|June 30, 2022
GH Responsiveness Is not Correlated to <i>IGF1</i> P2 Promoter Methylation in Children With Turner Syndrome, GHD and SGA Short StatureAnja Apel, Daniel I Iliev, Christina Urban, et al.
Journal of the American Chemical Society|March 28, 2022
Noncovalent Liquid Phase Functionalization of 2H-WS<sub>2</sub> with PDI: An Energy Conversion Platform with Long-Lived Charge SeparationTobias Scharl, Gerhard Binder, Xin Chen, et al.
Hormone Research|February 4, 2009
Height gains in response to growth hormone treatment to final height are similar in patients with SHOX deficiency and Turner syndromeWerner F Blum, Dachuang Cao, Volker Hesse, et al.
Trends in Molecular Medicine|September 29, 2014
CDKN1C mutations: two sides of the same coinThomas Eggermann, Gerhard Binder, Frédéric Brioude, et al.
European Journal of Human Genetics : EJHG|December 27, 2007
IGF2/H19 hypomethylation in Silver-Russell syndrome and isolated hemihypoplasiaMichael Zeschnigk, Beate Albrecht, Karin Buiting, et al.
The Journal of Clinical Endocrinology and Metabolism|January 31, 2008
The endocrine phenotype in silver-russell syndrome is defined by the underlying epigenetic alterationGerhard Binder, Ann-Kathrin Seidel, David D Martin, et al.
The Journal of Pediatrics|April 13, 2012
Health and quality of life in adults with Noonan syndromeGerhard Binder, Sabrina Grathwol, Karoline von Loeper, et al.
The New England Journal of Medicine|July 9, 2015
Paternally Inherited IGF2 Mutation and Growth RestrictionMatthias Begemann, Birgit Zirn, Gijs Santen, et al.
Pageof 13