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Paula Fernández-Alvarez

Showing results (1-10 of 11) with videos related to

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Journal of Hazardous Materials|September 5, 2008
Removal and destruction of endocrine disrupting contaminants by adsorption with molecularly imprinted polymers followed by simultaneous extraction and phototreatmentPaula Fernández-Alvarez, Mathieu Le Noir, Benoit Guieysse
Journal of Clinical Research in Pediatric Endocrinology|October 25, 2021
Prolyl Endopeptidase-like Deficiency Associated with Growth Hormone DeficiencyLaura Sayol-Torres, Maria Irene Valenzuela, Rosangela Tomasini, et al.
Frontiers in Endocrinology|July 15, 2022
A New <i>MAMLD1</i> Variant in an Infant With Microphallus and Hypospadias With Hormonal Pattern Suggesting Partial Hypogonadotropic Hypogonadism-Case ReportDiego Yeste, Cristina Aguilar-Riera, Gennaro Canestrino, et al.
Human Genome Variation|June 19, 2020
Unusual context of <i>CENPJ</i> variants and primary microcephaly: compound heterozygosity and nonconsanguinity in an Argentinian patientAnna M Cueto-González, Mónica Fernández-Cancio, Paula Fernández-Alvarez, et al.
European Journal of Medical Genetics|March 28, 2017
Arthrogryposis as neonatal presentation of Loeys-Dietz syndrome due to a novel TGFBR2 mutationIrene Valenzuela, Paula Fernández-Alvarez, Francina Munell, et al.
European Journal of Medical Genetics|July 15, 2018
Further delineation of the phenotype caused by loss of function mutations in PRMT7Irene Valenzuela, Maria Segura-Puimedon, Benjamín Rodríguez-Santiago, et al.
European Journal of Medical Genetics|January 9, 2018
Further delineation of the SOX18-related Hypotrichosis, Lymphedema, Telangiectasia syndrome (HTLS)Irene Valenzuela, Paula Fernández-Alvarez, Alberto Plaja, et al.
Viruses|June 28, 2023
Dynamic Changes in Non-Invasive Markers of Liver Fibrosis Are Predictors of Liver Events after SVR in HCV PatientsPaula Fernández-Alvarez, María Fernanda Guerra-Veloz, Angel Vilches-Arenas, et al.
American Journal of Medical Genetics. Part A|November 1, 2024
New Insights Into the Spectrum of RASopathies: Clinical and Genetic Data in a Cohort of 121 Spanish PatientsAna Isabel Sánchez Barbero, Irene Valenzuela, Paula Fernández-Alvarez, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|December 25, 2024
Spectrum disorder of RFC1 expansions/CANVAS: Clinical and electrophysiological characterization of a group of 31 patientsElena Lainez, Daniel Sánchez-Tejerina, Paula Fernández Alvarez, et al.
Pageof 2

Showing results (1-10 of 11) with videos related to

Sort By:
Pageof 2
Journal of Hazardous Materials|September 5, 2008
Removal and destruction of endocrine disrupting contaminants by adsorption with molecularly imprinted polymers followed by simultaneous extraction and phototreatmentPaula Fernández-Alvarez, Mathieu Le Noir, Benoit Guieysse
Journal of Clinical Research in Pediatric Endocrinology|October 25, 2021
Prolyl Endopeptidase-like Deficiency Associated with Growth Hormone DeficiencyLaura Sayol-Torres, Maria Irene Valenzuela, Rosangela Tomasini, et al.
Frontiers in Endocrinology|July 15, 2022
A New <i>MAMLD1</i> Variant in an Infant With Microphallus and Hypospadias With Hormonal Pattern Suggesting Partial Hypogonadotropic Hypogonadism-Case ReportDiego Yeste, Cristina Aguilar-Riera, Gennaro Canestrino, et al.
Human Genome Variation|June 19, 2020
Unusual context of <i>CENPJ</i> variants and primary microcephaly: compound heterozygosity and nonconsanguinity in an Argentinian patientAnna M Cueto-González, Mónica Fernández-Cancio, Paula Fernández-Alvarez, et al.
European Journal of Medical Genetics|March 28, 2017
Arthrogryposis as neonatal presentation of Loeys-Dietz syndrome due to a novel TGFBR2 mutationIrene Valenzuela, Paula Fernández-Alvarez, Francina Munell, et al.
European Journal of Medical Genetics|July 15, 2018
Further delineation of the phenotype caused by loss of function mutations in PRMT7Irene Valenzuela, Maria Segura-Puimedon, Benjamín Rodríguez-Santiago, et al.
European Journal of Medical Genetics|January 9, 2018
Further delineation of the SOX18-related Hypotrichosis, Lymphedema, Telangiectasia syndrome (HTLS)Irene Valenzuela, Paula Fernández-Alvarez, Alberto Plaja, et al.
Viruses|June 28, 2023
Dynamic Changes in Non-Invasive Markers of Liver Fibrosis Are Predictors of Liver Events after SVR in HCV PatientsPaula Fernández-Alvarez, María Fernanda Guerra-Veloz, Angel Vilches-Arenas, et al.
American Journal of Medical Genetics. Part A|November 1, 2024
New Insights Into the Spectrum of RASopathies: Clinical and Genetic Data in a Cohort of 121 Spanish PatientsAna Isabel Sánchez Barbero, Irene Valenzuela, Paula Fernández-Alvarez, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|December 25, 2024
Spectrum disorder of RFC1 expansions/CANVAS: Clinical and electrophysiological characterization of a group of 31 patientsElena Lainez, Daniel Sánchez-Tejerina, Paula Fernández Alvarez, et al.
Pageof 2