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Gerhard Binder

Showing results (51-60 of 130) with videos related to

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European Journal of Medical Genetics|July 1, 2008
No evidence for isolated imprinting mutations in the PEG1/MEST locus in Silver-Russell patientsNadine Schöherr, Susanne Jäger, Michael B Ranke, et al.
Genetic Testing|March 1, 2008
Search for subtelomeric imbalances by multiplex ligation-dependent probe amplification in Silver-Russell syndromeKatja Eggermann, Nadine Schönherr, Michael B Ranke, et al.
Archives of Neurology|July 13, 2011
Serum insulinlike growth factor 1 as possible marker for risk and early diagnosis of Parkinson diseaseJana Godau, Katharina Knauel, Karin Weber, et al.
American Journal of Medical Genetics. Part A|January 27, 2010
Identification of a 21q22 duplication in a Silver-Russell syndrome patient further narrows down the Down syndrome critical regionThomas Eggermann, Nadine Schönherr, Sabrina Spengler, et al.
European Journal of Pediatrics|June 16, 2015
Changes in whole-body fat distribution, intrahepatic lipids, and insulin resistance of obese adolescents during a low-level lifestyle interventionFabian Springer, Verena Ballweg, Roland Schweizer, et al.
Pediatric Radiology|June 7, 2012
Comparison of radiogrammetrical metacarpal indices in children and reference data from the First Zurich Longitudinal StudyDavid D Martin, Conrad Heckmann, Julia Neuhof, et al.
Clinical Epigenetics|October 20, 2020
Novel mutation points to a hot spot in CDKN1C causing Silver-Russell syndromeGerhard Binder, Julian Ziegler, Roland Schweizer, et al.
Clinical Endocrinology|October 28, 2020
Adolescent boys with constitutional delay of growth and puberty grow faster than patients with organic growth hormone deficiencyGerhard Binder, Theresa J Lehrian, Elisa Hoffmann, et al.
Clinical Endocrinology|June 11, 2020
Diagnosis of severe growth hormone deficiency in the newbornGerhard Binder, Karin Weber, Nora Rieflin, et al.
Pediatric Radiology|April 1, 2009
Clinical application of automated Greulich-Pyle bone age determination in children with short statureDavid D Martin, Dorothee Deusch, Roland Schweizer, et al.
Pageof 13

Showing results (51-60 of 130) with videos related to

Sort By:
Pageof 13
European Journal of Medical Genetics|July 1, 2008
No evidence for isolated imprinting mutations in the PEG1/MEST locus in Silver-Russell patientsNadine Schöherr, Susanne Jäger, Michael B Ranke, et al.
Genetic Testing|March 1, 2008
Search for subtelomeric imbalances by multiplex ligation-dependent probe amplification in Silver-Russell syndromeKatja Eggermann, Nadine Schönherr, Michael B Ranke, et al.
Archives of Neurology|July 13, 2011
Serum insulinlike growth factor 1 as possible marker for risk and early diagnosis of Parkinson diseaseJana Godau, Katharina Knauel, Karin Weber, et al.
American Journal of Medical Genetics. Part A|January 27, 2010
Identification of a 21q22 duplication in a Silver-Russell syndrome patient further narrows down the Down syndrome critical regionThomas Eggermann, Nadine Schönherr, Sabrina Spengler, et al.
European Journal of Pediatrics|June 16, 2015
Changes in whole-body fat distribution, intrahepatic lipids, and insulin resistance of obese adolescents during a low-level lifestyle interventionFabian Springer, Verena Ballweg, Roland Schweizer, et al.
Pediatric Radiology|June 7, 2012
Comparison of radiogrammetrical metacarpal indices in children and reference data from the First Zurich Longitudinal StudyDavid D Martin, Conrad Heckmann, Julia Neuhof, et al.
Clinical Epigenetics|October 20, 2020
Novel mutation points to a hot spot in CDKN1C causing Silver-Russell syndromeGerhard Binder, Julian Ziegler, Roland Schweizer, et al.
Clinical Endocrinology|October 28, 2020
Adolescent boys with constitutional delay of growth and puberty grow faster than patients with organic growth hormone deficiencyGerhard Binder, Theresa J Lehrian, Elisa Hoffmann, et al.
Clinical Endocrinology|June 11, 2020
Diagnosis of severe growth hormone deficiency in the newbornGerhard Binder, Karin Weber, Nora Rieflin, et al.
Pediatric Radiology|April 1, 2009
Clinical application of automated Greulich-Pyle bone age determination in children with short statureDavid D Martin, Dorothee Deusch, Roland Schweizer, et al.
Pageof 13