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

M de Vroede

Showing results (21-30 of 27) with videos related to

Pageof 3
Sort By:
You have reached the last page of results.This site can display upto 27 results.
Nederlands Tijdschrift Voor Geneeskunde|September 19, 2000
[Children with craniopharyngioma, a 'benign' brain tumor with a high morbidity]M J Taphoorn, C van Es, R H Gooskens, et al.
Advances in Experimental Medicine and Biology|January 1, 1986
Cortisol resistance in manM B Lipsett, M Tomita, D D Brandon, et al.
European Journal of Pediatrics|March 30, 2001
Short stature as the only presenting feature in a patient with an isodicentric (Y)(q11.23) and gonadoblastoma. A clinical and molecular cytogenetic studyJ C Giltay, M G Ausems, I van Seumeren, et al.
Tijdschrift Voor Psychiatrie|May 12, 2010
[Antipsychotics and metabolic abnormalities in children and adolescents: a review of the literature and some recommendations]W A Overbeek, M A M de Vroede, B E Lahuis, et al.
European Journal of Human Genetics : EJHG|July 20, 2007
Unmasking of a hemizygous WFS1 gene mutation by a chromosome 4p deletion of 8.3 Mb in a patient with Wolf-Hirschhorn syndromeKlara Flipsen-ten Berg, Peter M van Hasselt, Marc J Eleveld, et al.
Hormone Research in Paediatrics|November 28, 2013
Splice site mutations in GH1 detected in previously (Genetically) undiagnosed families with congenital isolated growth hormone deficiency type IIM J E Kempers, S N van der Crabben, M de Vroede, et al.
Endocrine Research|January 26, 2005
A neonatal form of isolated ACTH deficiency frequently associated with Tpit gene mutationsS Vallette-Kasic, A M Pulichino, M Gueydan, et al.
Pageof 3

Showing results (21-30 of 27) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 27 results.
Nederlands Tijdschrift Voor Geneeskunde|September 19, 2000
[Children with craniopharyngioma, a 'benign' brain tumor with a high morbidity]M J Taphoorn, C van Es, R H Gooskens, et al.
Advances in Experimental Medicine and Biology|January 1, 1986
Cortisol resistance in manM B Lipsett, M Tomita, D D Brandon, et al.
European Journal of Pediatrics|March 30, 2001
Short stature as the only presenting feature in a patient with an isodicentric (Y)(q11.23) and gonadoblastoma. A clinical and molecular cytogenetic studyJ C Giltay, M G Ausems, I van Seumeren, et al.
Tijdschrift Voor Psychiatrie|May 12, 2010
[Antipsychotics and metabolic abnormalities in children and adolescents: a review of the literature and some recommendations]W A Overbeek, M A M de Vroede, B E Lahuis, et al.
European Journal of Human Genetics : EJHG|July 20, 2007
Unmasking of a hemizygous WFS1 gene mutation by a chromosome 4p deletion of 8.3 Mb in a patient with Wolf-Hirschhorn syndromeKlara Flipsen-ten Berg, Peter M van Hasselt, Marc J Eleveld, et al.
Hormone Research in Paediatrics|November 28, 2013
Splice site mutations in GH1 detected in previously (Genetically) undiagnosed families with congenital isolated growth hormone deficiency type IIM J E Kempers, S N van der Crabben, M de Vroede, et al.
Endocrine Research|January 26, 2005
A neonatal form of isolated ACTH deficiency frequently associated with Tpit gene mutationsS Vallette-Kasic, A M Pulichino, M Gueydan, et al.
Pageof 3