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B B Mendonca

Showing results (51-60 of 82) with videos related to

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Journal of Molecular Endocrinology|February 5, 2000
Phenotypic variability and origins of mutations in the gene encoding 3beta-hydroxysteroid dehydrogenase type IIS McCartin, A J Russell, R A Fisher, et al.
Clinical Genetics|October 19, 2017
Identification of the first homozygous 1-bp deletion in GDF9 gene leading to primary ovarian insufficiency by using targeted massively parallel sequencingM M França, M F A Funari, M Y Nishi, et al.
Brazilian Journal of Medical and Biological Research = Revista Brasileira De Pesquisas Medicas E Biologicas|August 12, 1998
Clinical and molecular characterization of Brazilian patients with growth hormone gene deletionsI J Arnhold, M G Osorio, S B Oliveira, et al.
The Journal of Clinical Investigation|September 1, 1992
Molecular genetics of steroid 5 alpha-reductase 2 deficiencyA E Thigpen, D L Davis, A Milatovich, et al.
Hormone and Metabolic Research = Hormon- Und Stoffwechselforschung = Hormones Et Metabolisme|February 1, 1993
Long-term treatment of central precocious puberty with a long-acting analogue of luteinizing hormone release hormone (D-Tryp6-GnRH) in monthly injections. Its possible use in normal pubertyJ A Marcondes, A C Abujamra, S L Minanni, et al.
Clinical Endocrinology|October 23, 2002
Glucocorticoid receptor gene polymorphisms in ACTH-secreting pituitary tumoursS R R Antonini, A C Latronico, L L K Elias, et al.
The Journal of Clinical Endocrinology and Metabolism|March 17, 2000
Origin of an ovarian steroid cell tumor causing isosexual pseudoprecocious puberty demonstrated by the expression of adrenal steroidogenic enzymes and adrenocorticotropin receptorC J Lin, A A Jorge, A C Latronico, et al.
The Journal of Clinical Endocrinology and Metabolism|September 24, 1998
The PROP1 2-base pair deletion is a common cause of combined pituitary hormone deficiencyJ D Cogan, W Wu, J A Phillips, et al.
The Journal of Clinical Endocrinology and Metabolism|July 14, 1998
A unique constitutively activating mutation in third transmembrane helix of luteinizing hormone receptor causes sporadic male gonadotropin-independent precocious pubertyA C Latronico, A N Abell, I J Arnhold, et al.
The Journal of Urology|December 1, 1995
Clinical, hormonal and pathological findings in a comparative study of adrenocortical neoplasms in childhood and adulthoodB B Mendonca, A M Lucon, C A Menezes, et al.
Pageof 9

Showing results (51-60 of 82) with videos related to

Sort By:
Pageof 9
Journal of Molecular Endocrinology|February 5, 2000
Phenotypic variability and origins of mutations in the gene encoding 3beta-hydroxysteroid dehydrogenase type IIS McCartin, A J Russell, R A Fisher, et al.
Clinical Genetics|October 19, 2017
Identification of the first homozygous 1-bp deletion in GDF9 gene leading to primary ovarian insufficiency by using targeted massively parallel sequencingM M França, M F A Funari, M Y Nishi, et al.
Brazilian Journal of Medical and Biological Research = Revista Brasileira De Pesquisas Medicas E Biologicas|August 12, 1998
Clinical and molecular characterization of Brazilian patients with growth hormone gene deletionsI J Arnhold, M G Osorio, S B Oliveira, et al.
The Journal of Clinical Investigation|September 1, 1992
Molecular genetics of steroid 5 alpha-reductase 2 deficiencyA E Thigpen, D L Davis, A Milatovich, et al.
Hormone and Metabolic Research = Hormon- Und Stoffwechselforschung = Hormones Et Metabolisme|February 1, 1993
Long-term treatment of central precocious puberty with a long-acting analogue of luteinizing hormone release hormone (D-Tryp6-GnRH) in monthly injections. Its possible use in normal pubertyJ A Marcondes, A C Abujamra, S L Minanni, et al.
Clinical Endocrinology|October 23, 2002
Glucocorticoid receptor gene polymorphisms in ACTH-secreting pituitary tumoursS R R Antonini, A C Latronico, L L K Elias, et al.
The Journal of Clinical Endocrinology and Metabolism|March 17, 2000
Origin of an ovarian steroid cell tumor causing isosexual pseudoprecocious puberty demonstrated by the expression of adrenal steroidogenic enzymes and adrenocorticotropin receptorC J Lin, A A Jorge, A C Latronico, et al.
The Journal of Clinical Endocrinology and Metabolism|September 24, 1998
The PROP1 2-base pair deletion is a common cause of combined pituitary hormone deficiencyJ D Cogan, W Wu, J A Phillips, et al.
The Journal of Clinical Endocrinology and Metabolism|July 14, 1998
A unique constitutively activating mutation in third transmembrane helix of luteinizing hormone receptor causes sporadic male gonadotropin-independent precocious pubertyA C Latronico, A N Abell, I J Arnhold, et al.
The Journal of Urology|December 1, 1995
Clinical, hormonal and pathological findings in a comparative study of adrenocortical neoplasms in childhood and adulthoodB B Mendonca, A M Lucon, C A Menezes, et al.
Pageof 9