Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Wilma Oostdijk

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

Pageof 6
Sort By:
You have reached the last page of results.This site can display upto 60 results.
American Journal of Medical Genetics. Part A|August 16, 2014
Central 22q11.2 deletionsPatrick Rump, Nicole de Leeuw, Anthonie J van Essen, et al.
The Journal of Clinical Endocrinology and Metabolism|August 21, 2012
Adult height in short children born SGA treated with growth hormone and gonadotropin releasing hormone analog: results of a randomized, dose-response GH trialAnnemieke J Lem, Danielle C M van der Kaay, Maria A J de Ridder, et al.
The Journal of Clinical Endocrinology and Metabolism|September 24, 2013
An activating mutation in the kinase homology domain of the natriuretic peptide receptor-2 causes extremely tall stature without skeletal deformitiesSabine E Hannema, Hermine A van Duyvenvoorde, Thomas Premsler, et al.
European Journal of Human Genetics : EJHG|September 26, 2013
Copy number variants in patients with short statureHermine A van Duyvenvoorde, Julian C Lui, Sarina G Kant, et al.
Hormone Research in Paediatrics|July 10, 2017
Global Application of the Assessment of Communication Skills of Paediatric Endocrinology Fellows in the Management of Differences in Sex Development Using the ESPE E-Learning.Org PortalLaura J C Kranenburg, Sam T H Reerds, Martine Cools, et al.
The Journal of Clinical Endocrinology and Metabolism|September 8, 2016
Mutations in TBL1X Are Associated With Central HypothyroidismCharlotte A Heinen, Monique Losekoot, Yu Sun, et al.
Pediatrics|April 1, 2009
Consensus statement on the use of gonadotropin-releasing hormone analogs in childrenJean-Claude Carel, Erica A Eugster, Alan Rogol, et al.
The Journal of Clinical Endocrinology and Metabolism|October 26, 2019
IGSF1 Deficiency Results in Human and Murine Somatotrope Neurosecretory HyperfunctionSjoerd D Joustra, Ferdinand Roelfsema, A S Paul van Trotsenburg, et al.
The Journal of Clinical Endocrinology and Metabolism|April 18, 2012
Beneficial effects of growth hormone treatment on cognition in children with Prader-Willi syndrome: a randomized controlled trial and longitudinal studyElbrich P C Siemensma, Roderick F A Tummers-de Lind van Wijngaarden, Dederieke A M Festen, et al.
Nature Genetics|November 13, 2012
Loss-of-function mutations in IGSF1 cause an X-linked syndrome of central hypothyroidism and testicular enlargementYu Sun, Beata Bak, Nadia Schoenmakers, et al.
Pageof 6

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

Sort By:
Pageof 6
You have reached the last page of results.This site can display upto 60 results.
American Journal of Medical Genetics. Part A|August 16, 2014
Central 22q11.2 deletionsPatrick Rump, Nicole de Leeuw, Anthonie J van Essen, et al.
The Journal of Clinical Endocrinology and Metabolism|August 21, 2012
Adult height in short children born SGA treated with growth hormone and gonadotropin releasing hormone analog: results of a randomized, dose-response GH trialAnnemieke J Lem, Danielle C M van der Kaay, Maria A J de Ridder, et al.
The Journal of Clinical Endocrinology and Metabolism|September 24, 2013
An activating mutation in the kinase homology domain of the natriuretic peptide receptor-2 causes extremely tall stature without skeletal deformitiesSabine E Hannema, Hermine A van Duyvenvoorde, Thomas Premsler, et al.
European Journal of Human Genetics : EJHG|September 26, 2013
Copy number variants in patients with short statureHermine A van Duyvenvoorde, Julian C Lui, Sarina G Kant, et al.
Hormone Research in Paediatrics|July 10, 2017
Global Application of the Assessment of Communication Skills of Paediatric Endocrinology Fellows in the Management of Differences in Sex Development Using the ESPE E-Learning.Org PortalLaura J C Kranenburg, Sam T H Reerds, Martine Cools, et al.
The Journal of Clinical Endocrinology and Metabolism|September 8, 2016
Mutations in TBL1X Are Associated With Central HypothyroidismCharlotte A Heinen, Monique Losekoot, Yu Sun, et al.
Pediatrics|April 1, 2009
Consensus statement on the use of gonadotropin-releasing hormone analogs in childrenJean-Claude Carel, Erica A Eugster, Alan Rogol, et al.
The Journal of Clinical Endocrinology and Metabolism|October 26, 2019
IGSF1 Deficiency Results in Human and Murine Somatotrope Neurosecretory HyperfunctionSjoerd D Joustra, Ferdinand Roelfsema, A S Paul van Trotsenburg, et al.
The Journal of Clinical Endocrinology and Metabolism|April 18, 2012
Beneficial effects of growth hormone treatment on cognition in children with Prader-Willi syndrome: a randomized controlled trial and longitudinal studyElbrich P C Siemensma, Roderick F A Tummers-de Lind van Wijngaarden, Dederieke A M Festen, et al.
Nature Genetics|November 13, 2012
Loss-of-function mutations in IGSF1 cause an X-linked syndrome of central hypothyroidism and testicular enlargementYu Sun, Beata Bak, Nadia Schoenmakers, et al.
Pageof 6