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

Maria Susana Mallea-Gil

Showing results (1-10 of 7) with videos related to

Pageof 1
Sort By:
Case Reports in Endocrinology|March 16, 2016
Pegvisomant-Induced Cholestatic Hepatitis in an Acromegalic Patient with UGT1A1 (⁎) 28 MutationMaria Susana Mallea-Gil, Ignacio Bernabeu, Adriana Spiraquis, et al.
Endocrine Practice : Official Journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists|March 20, 2015
CONDITIONING FACTORS FOR HIGH CARDIOVASCULAR RISK IN PATIENTS WITH CUSHING SYNDROMELaura Boero, Marcos Manavela, Eliana Botta, et al.
Pituitary|August 10, 2012
Primary empty sella (PES): a review of 175 casesM Guitelman, Natalia Garcia Basavilbaso, M Vitale, et al.
Pituitary|October 1, 2011
Comparison of two immunoassays in the determination of IGF-I levels and its correlation with oral glucose tolerance test (OGTT) and with clinical symptoms in acromegalic patientsLaura Boero, Marcos Manavela, Karina Danilowicz, et al.
Archives of Endocrinology and Metabolism|February 25, 2016
Prolactinomas: evolution after menopauseMaria Susana Mallea-Gil, Marcos Manavela, Analia Alfieri, et al.
Archives of Endocrinology and Metabolism|August 29, 2019
Pegvisomant in acromegaly: a multicenter real-life study in ArgentinaNatalia Ximena Garcia Basavilbaso, Maria Carolina Ballarino, Darío Bruera, et al.
The Journal of Clinical Endocrinology and Metabolism|May 8, 2024
Exome Sequencing Has a High Diagnostic Rate in Sporadic Congenital Hypopituitarism and Reveals Novel Candidate GenesJulian Martinez-Mayer, Sebastian Vishnopolska, Catalina Perticarari, et al.
Pageof 1

Showing results (1-10 of 7) with videos related to

Sort By:
Pageof 1
Case Reports in Endocrinology|March 16, 2016
Pegvisomant-Induced Cholestatic Hepatitis in an Acromegalic Patient with UGT1A1 (⁎) 28 MutationMaria Susana Mallea-Gil, Ignacio Bernabeu, Adriana Spiraquis, et al.
Endocrine Practice : Official Journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists|March 20, 2015
CONDITIONING FACTORS FOR HIGH CARDIOVASCULAR RISK IN PATIENTS WITH CUSHING SYNDROMELaura Boero, Marcos Manavela, Eliana Botta, et al.
Pituitary|August 10, 2012
Primary empty sella (PES): a review of 175 casesM Guitelman, Natalia Garcia Basavilbaso, M Vitale, et al.
Pituitary|October 1, 2011
Comparison of two immunoassays in the determination of IGF-I levels and its correlation with oral glucose tolerance test (OGTT) and with clinical symptoms in acromegalic patientsLaura Boero, Marcos Manavela, Karina Danilowicz, et al.
Archives of Endocrinology and Metabolism|February 25, 2016
Prolactinomas: evolution after menopauseMaria Susana Mallea-Gil, Marcos Manavela, Analia Alfieri, et al.
Archives of Endocrinology and Metabolism|August 29, 2019
Pegvisomant in acromegaly: a multicenter real-life study in ArgentinaNatalia Ximena Garcia Basavilbaso, Maria Carolina Ballarino, Darío Bruera, et al.
The Journal of Clinical Endocrinology and Metabolism|May 8, 2024
Exome Sequencing Has a High Diagnostic Rate in Sporadic Congenital Hypopituitarism and Reveals Novel Candidate GenesJulian Martinez-Mayer, Sebastian Vishnopolska, Catalina Perticarari, et al.
Pageof 1