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

R Antonini

Showing results (81-90 of 112) with videos related to

Pageof 12
Sort By:
Hormone Research in Paediatrics|June 16, 2021
Adult Height in 299 Patients with Turner Syndrome with or without Growth Hormone Therapy: Results and Literature ReviewNaiara C B Dantas, Adriana F Braz, Alexsandra Malaquias, et al.
The Journal of Clinical Endocrinology and Metabolism|January 27, 2012
The interactive effect of GHR-exon 3 and -202 A/C IGFBP3 polymorphisms on rhGH responsiveness and treatment outcomes in patients with Turner syndromeAdriana F Braz, Everlayny F Costalonga, Luciana R Montenegro, et al.
Arquivos Brasileiros De Endocrinologia E Metabologia|April 15, 2014
NR3C1 polymorphisms in Brazilians of Caucasian, African, and Asian ancestry: glucocorticoid sensitivity and genotype associationManoel Carlos L A Souza, Clarissa S Martins, Ivan M Silva-Junior, et al.
The Journal of Clinical Endocrinology and Metabolism|January 18, 2014
A novel ADIPOQ mutation (p.M40K) impairs assembly of high-molecular-weight adiponectin and is associated with early-onset obesity and metabolic syndromeAna Carolina Bueno, Kai Sun, Clarissa Silva Martins, et al.
The Journal of Clinical Endocrinology and Metabolism|June 7, 2014
Genetic predictors of long-term response to growth hormone (GH) therapy in children with GH deficiency and Turner syndrome: the influence of a SOCS2 polymorphismAdriana F Braz, Everlayny F Costalonga, Ericka B Trarbach, et al.
JAMA Network Open|May 13, 2021
Clinical and Biochemical Features of Hypopituitarism Among Brazilian Children With Zika Virus-Induced MicrocephalyLeda L Ferreira, Juan P Aguilar Ticona, Paulo S Silveira-Mattos, et al.
Neuroendocrinology|November 1, 2019
Outcomes of Patients with Central Precocious Puberty Due to Loss-of-Function Mutations in the MKRN3 Gene after Treatment with Gonadotropin-Releasing Hormone AnalogCarolina de Oliveira Ramos, Delanie B Macedo, Ana Pinheiro M Canton, et al.
Molecular and Cellular Endocrinology|September 1, 2022
Vitamin D receptor activation is a feasible therapeutic target to impair adrenocortical tumorigenesisAna Carolina Bueno, Candy Bellido More, Junier Marrero-Gutiérrez, et al.
Molecular and Cellular Endocrinology|December 18, 2020
Pde8b haploinsufficiency in mice is associated with modest adrenal defects, impaired steroidogenesis, and male infertility, unaltered by concurrent PKA or Wnt activationLeticia Ferro Leal, Eva Szarek, Annabel Berthon, et al.
The Journal of Clinical Endocrinology and Metabolism|January 9, 2025
YAP1 is a prognostic marker and its inhibition reduces tumor progression in adrenocortical tumorsCandy C B More, Ana Carolina Bueno, César A O Rojas, et al.
Pageof 12

Showing results (81-90 of 112) with videos related to

Sort By:
Pageof 12
Hormone Research in Paediatrics|June 16, 2021
Adult Height in 299 Patients with Turner Syndrome with or without Growth Hormone Therapy: Results and Literature ReviewNaiara C B Dantas, Adriana F Braz, Alexsandra Malaquias, et al.
The Journal of Clinical Endocrinology and Metabolism|January 27, 2012
The interactive effect of GHR-exon 3 and -202 A/C IGFBP3 polymorphisms on rhGH responsiveness and treatment outcomes in patients with Turner syndromeAdriana F Braz, Everlayny F Costalonga, Luciana R Montenegro, et al.
Arquivos Brasileiros De Endocrinologia E Metabologia|April 15, 2014
NR3C1 polymorphisms in Brazilians of Caucasian, African, and Asian ancestry: glucocorticoid sensitivity and genotype associationManoel Carlos L A Souza, Clarissa S Martins, Ivan M Silva-Junior, et al.
The Journal of Clinical Endocrinology and Metabolism|January 18, 2014
A novel ADIPOQ mutation (p.M40K) impairs assembly of high-molecular-weight adiponectin and is associated with early-onset obesity and metabolic syndromeAna Carolina Bueno, Kai Sun, Clarissa Silva Martins, et al.
The Journal of Clinical Endocrinology and Metabolism|June 7, 2014
Genetic predictors of long-term response to growth hormone (GH) therapy in children with GH deficiency and Turner syndrome: the influence of a SOCS2 polymorphismAdriana F Braz, Everlayny F Costalonga, Ericka B Trarbach, et al.
JAMA Network Open|May 13, 2021
Clinical and Biochemical Features of Hypopituitarism Among Brazilian Children With Zika Virus-Induced MicrocephalyLeda L Ferreira, Juan P Aguilar Ticona, Paulo S Silveira-Mattos, et al.
Neuroendocrinology|November 1, 2019
Outcomes of Patients with Central Precocious Puberty Due to Loss-of-Function Mutations in the MKRN3 Gene after Treatment with Gonadotropin-Releasing Hormone AnalogCarolina de Oliveira Ramos, Delanie B Macedo, Ana Pinheiro M Canton, et al.
Molecular and Cellular Endocrinology|September 1, 2022
Vitamin D receptor activation is a feasible therapeutic target to impair adrenocortical tumorigenesisAna Carolina Bueno, Candy Bellido More, Junier Marrero-Gutiérrez, et al.
Molecular and Cellular Endocrinology|December 18, 2020
Pde8b haploinsufficiency in mice is associated with modest adrenal defects, impaired steroidogenesis, and male infertility, unaltered by concurrent PKA or Wnt activationLeticia Ferro Leal, Eva Szarek, Annabel Berthon, et al.
The Journal of Clinical Endocrinology and Metabolism|January 9, 2025
YAP1 is a prognostic marker and its inhibition reduces tumor progression in adrenocortical tumorsCandy C B More, Ana Carolina Bueno, César A O Rojas, et al.
Pageof 12