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

A C Latronico

Showing results (11-20 of 50) with videos related to

Pageof 5
Sort By:
Cancer Genetics and Cytogenetics|January 1, 1995
Selection of adrenal tumor cells in culture demonstrated by interphase cytogeneticsC Rosenberg, V A Della-Rosa, A C Latronico, et al.
Molecular Endocrinology (Baltimore, Md.)|March 26, 1998
A homozygous microdeletion in helix 7 of the luteinizing hormone receptor associated with familial testicular and ovarian resistance is due to both decreased cell surface expression and impaired effector activation by the cell surface receptorA C Latronico, Y Chai, I J Arnhold, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|December 24, 1997
Long-acting gonadotropin-releasing hormone agonists in the differential diagnosis of male precocious pubertyM C Albano, A C Latronico, I J Arnhold, et al.
The Journal of Clinical Endocrinology and Metabolism|August 18, 2000
Combined pituitary hormone deficiency caused by a novel mutation of a highly conserved residue (F88S) in the homeodomain of PROP-1M G Osorio, P Kopp, S Marui, et al.
The Journal of Clinical Endocrinology and Metabolism|September 11, 2001
Adrenocorticotropin-dependent precocious puberty of testicular origin in a boy with X-linked adrenal hypoplasia congenita due to a novel mutation in the DAX1 geneS Domenice, A C Latronico, V N Brito, et al.
The Journal of Clinical Endocrinology and Metabolism|November 14, 1997
A novel nonsense mutation in the first zinc finger of the vitamin D receptor causing hereditary 1,25-dihydroxyvitamin D3-resistant ricketsJ B Mechica, M O Leite, B B Mendonca, et al.
Human Mutation|March 1, 2000
A novel homozygous nonsense mutations E135* in the type II 3beta-hydroxysteroid dehydrogenase gene in a girl with salt-losing congenital adrenal hyperplasia. Mutations in brief no. 168. OnlineS Marui, I M Torrealba, A J Russell, et al.
The Journal of Clinical Endocrinology and Metabolism|March 20, 1999
Longitudinal hormonal and pituitary imaging changes in two females with combined pituitary hormone deficiency due to deletion of A301,G302 in the PROP1 geneB B Mendonca, M G Osorio, A C Latronico, et al.
Fertility and Sterility|November 1, 2000
No evidence of somatic activating mutations on gonadotropin receptor genes in sex cord stromal tumorsL R Giacaglia, F Kohek MB da, F M Carvalho, et al.
The Journal of Clinical Endocrinology and Metabolism|June 9, 2001
Two novel mutations in the gonadotropin-releasing hormone receptor gene in Brazilian patients with hypogonadotropic hypogonadism and normal olfactionE M Costa, G Y Bedecarrats, B B Mendonca, et al.
Pageof 5

Showing results (11-20 of 50) with videos related to

Sort By:
Pageof 5
Cancer Genetics and Cytogenetics|January 1, 1995
Selection of adrenal tumor cells in culture demonstrated by interphase cytogeneticsC Rosenberg, V A Della-Rosa, A C Latronico, et al.
Molecular Endocrinology (Baltimore, Md.)|March 26, 1998
A homozygous microdeletion in helix 7 of the luteinizing hormone receptor associated with familial testicular and ovarian resistance is due to both decreased cell surface expression and impaired effector activation by the cell surface receptorA C Latronico, Y Chai, I J Arnhold, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|December 24, 1997
Long-acting gonadotropin-releasing hormone agonists in the differential diagnosis of male precocious pubertyM C Albano, A C Latronico, I J Arnhold, et al.
The Journal of Clinical Endocrinology and Metabolism|August 18, 2000
Combined pituitary hormone deficiency caused by a novel mutation of a highly conserved residue (F88S) in the homeodomain of PROP-1M G Osorio, P Kopp, S Marui, et al.
The Journal of Clinical Endocrinology and Metabolism|September 11, 2001
Adrenocorticotropin-dependent precocious puberty of testicular origin in a boy with X-linked adrenal hypoplasia congenita due to a novel mutation in the DAX1 geneS Domenice, A C Latronico, V N Brito, et al.
The Journal of Clinical Endocrinology and Metabolism|November 14, 1997
A novel nonsense mutation in the first zinc finger of the vitamin D receptor causing hereditary 1,25-dihydroxyvitamin D3-resistant ricketsJ B Mechica, M O Leite, B B Mendonca, et al.
Human Mutation|March 1, 2000
A novel homozygous nonsense mutations E135* in the type II 3beta-hydroxysteroid dehydrogenase gene in a girl with salt-losing congenital adrenal hyperplasia. Mutations in brief no. 168. OnlineS Marui, I M Torrealba, A J Russell, et al.
The Journal of Clinical Endocrinology and Metabolism|March 20, 1999
Longitudinal hormonal and pituitary imaging changes in two females with combined pituitary hormone deficiency due to deletion of A301,G302 in the PROP1 geneB B Mendonca, M G Osorio, A C Latronico, et al.
Fertility and Sterility|November 1, 2000
No evidence of somatic activating mutations on gonadotropin receptor genes in sex cord stromal tumorsL R Giacaglia, F Kohek MB da, F M Carvalho, et al.
The Journal of Clinical Endocrinology and Metabolism|June 9, 2001
Two novel mutations in the gonadotropin-releasing hormone receptor gene in Brazilian patients with hypogonadotropic hypogonadism and normal olfactionE M Costa, G Y Bedecarrats, B B Mendonca, et al.
Pageof 5