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

T Brue

Showing results (81-90 of 99) with videos related to

Pageof 10
Sort By:
Pituitary|July 3, 2019
Acromegaly in Carney complexT Cuny, T T Mac, P Romanet, et al.
European Journal of Endocrinology|January 29, 2011
Pituitary stalk interruption syndrome in 83 patients: novel HESX1 mutation and severe hormonal prognosis in malformative formsR Reynaud, F Albarel, A Saveanu, et al.
Pituitary|March 24, 2024
Changes in multi-modality management of acromegaly in a tertiary centre over 2 decadesV Amodru, N Sahakian, C Piazzola, et al.
Molecular Endocrinology (Baltimore, Md.)|October 4, 2011
PITX2 AND PITX1 regulate thyrotroph function and response to hypothyroidismF Castinetti, M L Brinkmeier, D F Gordon, et al.
The Journal of Clinical Endocrinology and Metabolism|December 16, 2011
Phenotypic homogeneity and genotypic variability in a large series of congenital isolated ACTH-deficiency patients with TPIT gene mutationsC Couture, A Saveanu, A Barlier, et al.
The Journal of Clinical Endocrinology and Metabolism|September 11, 2001
PROP1 gene screening in patients with multiple pituitary hormone deficiency reveals two sites of hypermutability and a high incidence of corticotroph deficiencyS Vallette-Kasic, A Barlier, C Teinturier, et al.
QJM : Monthly Journal of the Association of Physicians|July 4, 2012
Hypothalamo-pituitary sarcoidosis: a multicenter study of 24 patientsC Langrand, H Bihan, G Raverot, et al.
Hormone and Metabolic Research = Hormon- Und Stoffwechselforschung = Hormones Et Metabolisme|January 23, 2016
GPR101 Mutations are not a Frequent Cause of Congenital Isolated Growth Hormone DeficiencyF Castinetti, A F Daly, C A Stratakis, et al.
The Journal of Clinical Endocrinology and Metabolism|May 1, 2008
A novel dysfunctional LHX4 mutation with high phenotypical variability in patients with hypopituitarismF Castinetti, A Saveanu, R Reynaud, et al.
Neuro-Chirurgie|May 14, 2021
Meningiomas in patients with long-term exposition to progestins: Characteristics and outcomeT Graillon, S Boissonneau, R Appay, et al.
Pageof 10

Showing results (81-90 of 99) with videos related to

Sort By:
Pageof 10
Pituitary|July 3, 2019
Acromegaly in Carney complexT Cuny, T T Mac, P Romanet, et al.
European Journal of Endocrinology|January 29, 2011
Pituitary stalk interruption syndrome in 83 patients: novel HESX1 mutation and severe hormonal prognosis in malformative formsR Reynaud, F Albarel, A Saveanu, et al.
Pituitary|March 24, 2024
Changes in multi-modality management of acromegaly in a tertiary centre over 2 decadesV Amodru, N Sahakian, C Piazzola, et al.
Molecular Endocrinology (Baltimore, Md.)|October 4, 2011
PITX2 AND PITX1 regulate thyrotroph function and response to hypothyroidismF Castinetti, M L Brinkmeier, D F Gordon, et al.
The Journal of Clinical Endocrinology and Metabolism|December 16, 2011
Phenotypic homogeneity and genotypic variability in a large series of congenital isolated ACTH-deficiency patients with TPIT gene mutationsC Couture, A Saveanu, A Barlier, et al.
The Journal of Clinical Endocrinology and Metabolism|September 11, 2001
PROP1 gene screening in patients with multiple pituitary hormone deficiency reveals two sites of hypermutability and a high incidence of corticotroph deficiencyS Vallette-Kasic, A Barlier, C Teinturier, et al.
QJM : Monthly Journal of the Association of Physicians|July 4, 2012
Hypothalamo-pituitary sarcoidosis: a multicenter study of 24 patientsC Langrand, H Bihan, G Raverot, et al.
Hormone and Metabolic Research = Hormon- Und Stoffwechselforschung = Hormones Et Metabolisme|January 23, 2016
GPR101 Mutations are not a Frequent Cause of Congenital Isolated Growth Hormone DeficiencyF Castinetti, A F Daly, C A Stratakis, et al.
The Journal of Clinical Endocrinology and Metabolism|May 1, 2008
A novel dysfunctional LHX4 mutation with high phenotypical variability in patients with hypopituitarismF Castinetti, A Saveanu, R Reynaud, et al.
Neuro-Chirurgie|May 14, 2021
Meningiomas in patients with long-term exposition to progestins: Characteristics and outcomeT Graillon, S Boissonneau, R Appay, et al.
Pageof 10