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

Monique Van Helvoirt

Showing results (1-10 of 4) with videos related to

Pageof 1
Sort By:
Endocrine Connections|October 22, 2019
Is vitamin D deficiency in obese youth a risk factor for less weight loss during a weight loss program?Karolien Van De Maele, Jean De Schepper, Jesse Vanbesien, et al.
The Journal of Clinical Endocrinology and Metabolism|September 18, 2008
Compound heterozygous mutations in the GNAS gene of a boy with morbid obesity, thyroid-stimulating hormone resistance, pseudohypoparathyroidism, and a prothrombotic stateKathleen Freson, Benedetta Izzi, Jaak Jaeken, et al.
Human Molecular Genetics|April 30, 2003
Functional polymorphisms in the paternally expressed XLalphas and its cofactor ALEX decrease their mutual interaction and enhance receptor-mediated cAMP formationKathleen Freson, Jaak Jaeken, Monique Van Helvoirt, et al.
The Journal of Clinical Endocrinology and Metabolism|September 25, 2008
GNAS defects identified by stimulatory G protein alpha-subunit signalling studies in plateletsKathleen Freson, Benedetta Izzi, Veerle Labarque, et al.
Pageof 1

Showing results (1-10 of 4) with videos related to

Sort By:
Pageof 1
Endocrine Connections|October 22, 2019
Is vitamin D deficiency in obese youth a risk factor for less weight loss during a weight loss program?Karolien Van De Maele, Jean De Schepper, Jesse Vanbesien, et al.
The Journal of Clinical Endocrinology and Metabolism|September 18, 2008
Compound heterozygous mutations in the GNAS gene of a boy with morbid obesity, thyroid-stimulating hormone resistance, pseudohypoparathyroidism, and a prothrombotic stateKathleen Freson, Benedetta Izzi, Jaak Jaeken, et al.
Human Molecular Genetics|April 30, 2003
Functional polymorphisms in the paternally expressed XLalphas and its cofactor ALEX decrease their mutual interaction and enhance receptor-mediated cAMP formationKathleen Freson, Jaak Jaeken, Monique Van Helvoirt, et al.
The Journal of Clinical Endocrinology and Metabolism|September 25, 2008
GNAS defects identified by stimulatory G protein alpha-subunit signalling studies in plateletsKathleen Freson, Benedetta Izzi, Veerle Labarque, et al.
Pageof 1