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

Priscilla Cukier

Showing results (11-20 of 18) with videos related to

Pageof 2
Sort By:
You have reached the last page of results.This site can display upto 18 results.
Hormone Research in Paediatrics|September 21, 2013
Molecular and gene network analysis of thyroid transcription factor 1 (TTF1) and enhanced at puberty (EAP1) genes in patients with GnRH-dependent pubertal disordersPriscilla Cukier, Hollis Wright, Tomke Rulfs, et al.
Seizure|October 25, 2012
The benign spectrum of hypothalamic hamartomas: infrequent epilepsy and normal cognition in patients presenting with central precocious pubertyPriscilla Cukier, Luiz Henrique Martins Castro, Natalie Banaskiwitz, et al.
The Journal of Clinical Endocrinology and Metabolism|February 20, 2019
Acquired Lipodystrophy Associated With Nivolumab in a Patient With Advanced Renal Cell CarcinomaCamila Kruschewsky Falcao, Marina Campos Simoes Cabral, Jose Mauricio Mota, et al.
Arquivos Brasileiros De Endocrinologia E Metabologia|April 17, 2007
[Nelson's Syndrome: a case report]Priscilla Cukier, Flávia Moretti Duch, Manoel Jacobsen Teixeira, et al.
Sexual Development : Genetics, Molecular Biology, Evolution, Endocrinology, Embryology, and Pathology of Sex Determination and Differentiation|August 15, 2021
WT1 Pathogenic Variants are Associated with a Broad Spectrum of Differences in Sex Development Phenotypes and Heterogeneous Progression of Renal DiseaseMaria T M Ferrari, Andreia Watanabe, Thatiane E da Silva, et al.
Diabetology & Metabolic Syndrome|February 12, 2025
Screening and management of hospital hyperglycemia in non-critical patients: a position statement from the Brazilian Diabetes Society (SBD)Emerson Cestari Marino, Denise Momesso, Marcos Tadashi Kakitani Toyoshima, et al.
The New England Journal of Medicine|June 7, 2013
Central precocious puberty caused by mutations in the imprinted gene MKRN3Ana Paula Abreu, Andrew Dauber, Delanie B Macedo, et al.
The Journal of Clinical Endocrinology and Metabolism|March 18, 2014
Central precocious puberty that appears to be sporadic caused by paternally inherited mutations in the imprinted gene makorin ring finger 3Delanie B Macedo, Ana Paula Abreu, Ana Claudia S Reis, et al.
Pageof 2

Showing results (11-20 of 18) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 18 results.
Hormone Research in Paediatrics|September 21, 2013
Molecular and gene network analysis of thyroid transcription factor 1 (TTF1) and enhanced at puberty (EAP1) genes in patients with GnRH-dependent pubertal disordersPriscilla Cukier, Hollis Wright, Tomke Rulfs, et al.
Seizure|October 25, 2012
The benign spectrum of hypothalamic hamartomas: infrequent epilepsy and normal cognition in patients presenting with central precocious pubertyPriscilla Cukier, Luiz Henrique Martins Castro, Natalie Banaskiwitz, et al.
The Journal of Clinical Endocrinology and Metabolism|February 20, 2019
Acquired Lipodystrophy Associated With Nivolumab in a Patient With Advanced Renal Cell CarcinomaCamila Kruschewsky Falcao, Marina Campos Simoes Cabral, Jose Mauricio Mota, et al.
Arquivos Brasileiros De Endocrinologia E Metabologia|April 17, 2007
[Nelson's Syndrome: a case report]Priscilla Cukier, Flávia Moretti Duch, Manoel Jacobsen Teixeira, et al.
Sexual Development : Genetics, Molecular Biology, Evolution, Endocrinology, Embryology, and Pathology of Sex Determination and Differentiation|August 15, 2021
WT1 Pathogenic Variants are Associated with a Broad Spectrum of Differences in Sex Development Phenotypes and Heterogeneous Progression of Renal DiseaseMaria T M Ferrari, Andreia Watanabe, Thatiane E da Silva, et al.
Diabetology & Metabolic Syndrome|February 12, 2025
Screening and management of hospital hyperglycemia in non-critical patients: a position statement from the Brazilian Diabetes Society (SBD)Emerson Cestari Marino, Denise Momesso, Marcos Tadashi Kakitani Toyoshima, et al.
The New England Journal of Medicine|June 7, 2013
Central precocious puberty caused by mutations in the imprinted gene MKRN3Ana Paula Abreu, Andrew Dauber, Delanie B Macedo, et al.
The Journal of Clinical Endocrinology and Metabolism|March 18, 2014
Central precocious puberty that appears to be sporadic caused by paternally inherited mutations in the imprinted gene makorin ring finger 3Delanie B Macedo, Ana Paula Abreu, Ana Claudia S Reis, et al.
Pageof 2