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Laura Audí

Showing results (31-40 of 40) with videos related to

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Clinical Endocrinology|January 17, 2007
Human growth hormone (GH1) gene polymorphism map in a normal-statured adult populationCristina Esteban, Laura Audí, Antonio Carrascosa, et al.
Clinical Endocrinology|June 29, 2012
Familial short stature and intrauterine growth retardation associated with a novel mutation in the IGF-I receptor (IGF1R) geneJosé I Labarta, Eva Barrio, Laura Audí, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|October 23, 2009
Longitudinal pubertal growth according to age at pubertal growth spurt onset: data from a Spanish study including 458 children (223 boys and 235 girls)Angel Ferrández, Antonio Carrascosa, Laura Audí, et al.
The Journal of Clinical Endocrinology and Metabolism|February 16, 2020
Molecular Basis of CYP19A1 Deficiency in a 46,XX Patient With R550W Mutation in POR: Expanding the PORD PhenotypeShaheena Parween, Mónica Fernández-Cancio, Sara Benito-Sanz, et al.
Plos One|November 19, 2015
Human MAMLD1 Gene Variations Seem Not Sufficient to Explain a 46,XY DSD PhenotypeNúria Camats, Mónica Fernández-Cancio, Laura Audí, et al.
Journal of Immunology (Baltimore, Md. : 1950)|October 6, 2010
Gender-associated differences of perforin polymorphisms in the susceptibility to multiple sclerosisMontse Camiña-Tato, Carlos Morcillo-Suárez, Marta F Bustamante, et al.
American Journal of Epidemiology|April 13, 2012
Growth hormone receptor polymorphism and growth hormone therapy response in children: a Bayesian meta-analysisAndrew G Renehan, Mattea Solomon, Marcel Zwahlen, et al.
Sexual Development : Genetics, Molecular Biology, Evolution, Endocrinology, Embryology, and Pathology of Sex Determination and Differentiation|April 5, 2017
Discordant Genotypic Sex and Phenotype Variations in Two Spanish Siblings with 17α-Hydroxylase/17,20-Lyase Deficiency Carrying the Most Prevalent Mutated CYP17A1 Alleles of Brazilian PatientsMónica Fernández-Cancio, Emilio García-García, Carmen González-Cejudo, et al.
Endocrinologia, Diabetes Y Nutricion|November 11, 2022
Consensus guide on prophylactic gonadectomy in different sex developmentJulio Guerrero-Fernández, Pilar González-Peramato, AmaiaRodríguez Rodríguez Estévez, et al.
Anales De Pediatria|July 24, 2018
[Management guidelines for disorders / different sex development (DSD)]Julio Guerrero-Fernández, Cristina Azcona San Julián, Jesús Barreiro Conde, et al.
Pageof 4

Showing results (31-40 of 40) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 40 results.
Clinical Endocrinology|January 17, 2007
Human growth hormone (GH1) gene polymorphism map in a normal-statured adult populationCristina Esteban, Laura Audí, Antonio Carrascosa, et al.
Clinical Endocrinology|June 29, 2012
Familial short stature and intrauterine growth retardation associated with a novel mutation in the IGF-I receptor (IGF1R) geneJosé I Labarta, Eva Barrio, Laura Audí, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|October 23, 2009
Longitudinal pubertal growth according to age at pubertal growth spurt onset: data from a Spanish study including 458 children (223 boys and 235 girls)Angel Ferrández, Antonio Carrascosa, Laura Audí, et al.
The Journal of Clinical Endocrinology and Metabolism|February 16, 2020
Molecular Basis of CYP19A1 Deficiency in a 46,XX Patient With R550W Mutation in POR: Expanding the PORD PhenotypeShaheena Parween, Mónica Fernández-Cancio, Sara Benito-Sanz, et al.
Plos One|November 19, 2015
Human MAMLD1 Gene Variations Seem Not Sufficient to Explain a 46,XY DSD PhenotypeNúria Camats, Mónica Fernández-Cancio, Laura Audí, et al.
Journal of Immunology (Baltimore, Md. : 1950)|October 6, 2010
Gender-associated differences of perforin polymorphisms in the susceptibility to multiple sclerosisMontse Camiña-Tato, Carlos Morcillo-Suárez, Marta F Bustamante, et al.
American Journal of Epidemiology|April 13, 2012
Growth hormone receptor polymorphism and growth hormone therapy response in children: a Bayesian meta-analysisAndrew G Renehan, Mattea Solomon, Marcel Zwahlen, et al.
Sexual Development : Genetics, Molecular Biology, Evolution, Endocrinology, Embryology, and Pathology of Sex Determination and Differentiation|April 5, 2017
Discordant Genotypic Sex and Phenotype Variations in Two Spanish Siblings with 17α-Hydroxylase/17,20-Lyase Deficiency Carrying the Most Prevalent Mutated CYP17A1 Alleles of Brazilian PatientsMónica Fernández-Cancio, Emilio García-García, Carmen González-Cejudo, et al.
Endocrinologia, Diabetes Y Nutricion|November 11, 2022
Consensus guide on prophylactic gonadectomy in different sex developmentJulio Guerrero-Fernández, Pilar González-Peramato, AmaiaRodríguez Rodríguez Estévez, et al.
Anales De Pediatria|July 24, 2018
[Management guidelines for disorders / different sex development (DSD)]Julio Guerrero-Fernández, Cristina Azcona San Julián, Jesús Barreiro Conde, et al.
Pageof 4