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

Fabio R Faucz

Showing results (31-40 of 115) with videos related to

Pageof 12
Sort By:
Endocrine|May 18, 2022
USP13 genetics and expression in a family with thyroid cancerAndrea G Maria, Bruna Azevedo, Nikolaos Settas, et al.
Hormones (Athens, Greece)|July 19, 2015
McCune Albright syndrome and bilateral adrenal hyperplasia: the GNAS mutation may only be present in adrenal tissueAnna Angelousi, Filip Fencl, Fabio R Faucz, et al.
Journal of the Endocrine Society|April 18, 2024
Spatial Transcriptomic Analysis of Pituitary Corticotroph TumorsJeremie Oliver Piña, Fabio R Faucz, Cameron Padilla, et al.
Medrxiv : the Preprint Server for Health Sciences|September 4, 2023
Spatial Transcriptomic Analysis of Pituitary Corticotroph Tumors Unveils Intratumor HeterogeneityJeremie Oliver Piña, Fabio R Faucz, Cameron Padilla, et al.
The Journal of Pediatrics|December 26, 2015
Kidney Stones as an Underrecognized Clinical Sign in Pediatric Cushing DiseaseSara H Rahman, Georgios Z Papadakis, Margaret F Keil, et al.
Pediatric Research|April 5, 2020
Steroid hormone analysis of adolescents and young women with polycystic ovarian syndrome and adrenocortical dysfunction using UPC<sup>2</sup>-MS/MSAmanda C Swart, Therina du Toit, Evgenia Gourgari, et al.
Hormones (Athens, Greece)|March 9, 2018
Medullary thyroid cancer, leukemia, mesothelioma and meningioma associated with germline APC and RASAL1 variants: a new syndrome?Anna Angelousi, Nikolaos Settas, Fabio R Faucz, et al.
The Journal of Clinical Endocrinology and Metabolism|December 6, 2018
SGPL1 Deficiency: A Rare Cause of Primary Adrenal InsufficiencyNikolaos Settas, Rebecca Persky, Fabio R Faucz, et al.
Endokrynologia Polska|October 30, 2020
Is there a common cause for paediatric Cushing's disease?Katarzyna Pasternak-Pietrzak, Fabio R Faucz, Constantine A Stratakis, et al.
Journal of the Endocrine Society|July 10, 2019
Somatic <i>PRKAR1A</i> Gene Mutation in a Nonsyndromic Metastatic Large Cell Calcifying Sertoli Cell TumorChristina Tatsi, Fabio R Faucz, Emmanouil Blavakis, et al.
Pageof 12

Showing results (31-40 of 115) with videos related to

Sort By:
Pageof 12
Endocrine|May 18, 2022
USP13 genetics and expression in a family with thyroid cancerAndrea G Maria, Bruna Azevedo, Nikolaos Settas, et al.
Hormones (Athens, Greece)|July 19, 2015
McCune Albright syndrome and bilateral adrenal hyperplasia: the GNAS mutation may only be present in adrenal tissueAnna Angelousi, Filip Fencl, Fabio R Faucz, et al.
Journal of the Endocrine Society|April 18, 2024
Spatial Transcriptomic Analysis of Pituitary Corticotroph TumorsJeremie Oliver Piña, Fabio R Faucz, Cameron Padilla, et al.
Medrxiv : the Preprint Server for Health Sciences|September 4, 2023
Spatial Transcriptomic Analysis of Pituitary Corticotroph Tumors Unveils Intratumor HeterogeneityJeremie Oliver Piña, Fabio R Faucz, Cameron Padilla, et al.
The Journal of Pediatrics|December 26, 2015
Kidney Stones as an Underrecognized Clinical Sign in Pediatric Cushing DiseaseSara H Rahman, Georgios Z Papadakis, Margaret F Keil, et al.
Pediatric Research|April 5, 2020
Steroid hormone analysis of adolescents and young women with polycystic ovarian syndrome and adrenocortical dysfunction using UPC<sup>2</sup>-MS/MSAmanda C Swart, Therina du Toit, Evgenia Gourgari, et al.
Hormones (Athens, Greece)|March 9, 2018
Medullary thyroid cancer, leukemia, mesothelioma and meningioma associated with germline APC and RASAL1 variants: a new syndrome?Anna Angelousi, Nikolaos Settas, Fabio R Faucz, et al.
The Journal of Clinical Endocrinology and Metabolism|December 6, 2018
SGPL1 Deficiency: A Rare Cause of Primary Adrenal InsufficiencyNikolaos Settas, Rebecca Persky, Fabio R Faucz, et al.
Endokrynologia Polska|October 30, 2020
Is there a common cause for paediatric Cushing's disease?Katarzyna Pasternak-Pietrzak, Fabio R Faucz, Constantine A Stratakis, et al.
Journal of the Endocrine Society|July 10, 2019
Somatic <i>PRKAR1A</i> Gene Mutation in a Nonsyndromic Metastatic Large Cell Calcifying Sertoli Cell TumorChristina Tatsi, Fabio R Faucz, Emmanouil Blavakis, et al.
Pageof 12