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C Latronico

Showing results (11-20 of 68) with videos related to

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The Journal of Clinical Endocrinology and Metabolism|July 1, 1995
A novel mutation of the adrenocorticotropin receptor (ACTH-R) gene in a family with the syndrome of isolated glucocorticoid deficiency, but no ACTH-R abnormalities in two families with the triple A syndromeC Tsigos, K Arai, A C Latronico, et al.
Clinical Endocrinology|December 7, 2000
The effect of distinct activating mutations of the luteinizing hormone receptor gene on the pituitary-gonadal axis in both sexesA C Latronico, T S Lins, V N Brito, et al.
Clinical Endocrinology|January 5, 2000
Clinical features of women with resistance to luteinizing hormoneI J Arnhold, A C Latronico, M C Batista, et al.
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.
Pageof 7

Showing results (11-20 of 68) with videos related to

Sort By:
Pageof 7
The Journal of Clinical Endocrinology and Metabolism|July 1, 1995
A novel mutation of the adrenocorticotropin receptor (ACTH-R) gene in a family with the syndrome of isolated glucocorticoid deficiency, but no ACTH-R abnormalities in two families with the triple A syndromeC Tsigos, K Arai, A C Latronico, et al.
Clinical Endocrinology|December 7, 2000
The effect of distinct activating mutations of the luteinizing hormone receptor gene on the pituitary-gonadal axis in both sexesA C Latronico, T S Lins, V N Brito, et al.
Clinical Endocrinology|January 5, 2000
Clinical features of women with resistance to luteinizing hormoneI J Arnhold, A C Latronico, M C Batista, et al.
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.
Pageof 7