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Daisy Castiñeiras

Showing results (1-10 of 8) with videos related to

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Revista Espanola De Salud Publica|January 26, 2021
[Neonatal screening for congenital hypothyroidism.]Rosa Mª López Galera, Daisy Castiñeiras Ramos, Hugo Rocha
Molecular Genetics and Metabolism|April 17, 2015
Corrigendum to "A glimpse into past, present, and future DNA sequencing" [Mol. Genet. Metab. 110 (2013) 3-24]Marcos Morey, Ana Fernández-Marmiesse, Daisy Castiñeiras, et al.
Molecular Genetics and Metabolism|June 8, 2013
A glimpse into past, present, and future DNA sequencingMarcos Morey, Ana Fernández-Marmiesse, Daisy Castiñeiras, et al.
Advances in Laboratory Medicine|June 26, 2023
Identification of a new mutation in the human xanthine dehydrogenase responsible for xanthinuria type ICristina Collazo Abal, Susana Romero Santos, Carmen González Mao, et al.
JIMD Reports|July 12, 2014
Birth Prevalence of Fatty Acid β-Oxidation Disorders in IberiaHugo Rocha, Daisy Castiñeiras, Carmen Delgado, et al.
Medicina Clinica|July 15, 2011
[Clinical and genetic findings in patients with biotinidase deficiency detected through newborn screening or selective screening for hearing loss or inherited metabolic disease]María Luz Couce, Celia Pérez-Cerdá, María Teresa García Silva, et al.
Orphanet Journal of Rare Diseases|April 29, 2014
Assessment of a targeted resequencing assay as a support tool in the diagnosis of lysosomal storage disordersAna Fernández-Marmiesse, Marcos Morey, Merce Pineda, et al.
Revista Espanola De Salud Publica|February 23, 2021
[Beginnings, evolution and current situation of the Newborn Screening Programs in Spain.]José Luis Marín Soria, José Manuel González de Aledo Castillo, Ana Argudo Ramírez, et al.
Pageof 1

Showing results (1-10 of 8) with videos related to

Sort By:
Pageof 1
Revista Espanola De Salud Publica|January 26, 2021
[Neonatal screening for congenital hypothyroidism.]Rosa Mª López Galera, Daisy Castiñeiras Ramos, Hugo Rocha
Molecular Genetics and Metabolism|April 17, 2015
Corrigendum to "A glimpse into past, present, and future DNA sequencing" [Mol. Genet. Metab. 110 (2013) 3-24]Marcos Morey, Ana Fernández-Marmiesse, Daisy Castiñeiras, et al.
Molecular Genetics and Metabolism|June 8, 2013
A glimpse into past, present, and future DNA sequencingMarcos Morey, Ana Fernández-Marmiesse, Daisy Castiñeiras, et al.
Advances in Laboratory Medicine|June 26, 2023
Identification of a new mutation in the human xanthine dehydrogenase responsible for xanthinuria type ICristina Collazo Abal, Susana Romero Santos, Carmen González Mao, et al.
JIMD Reports|July 12, 2014
Birth Prevalence of Fatty Acid β-Oxidation Disorders in IberiaHugo Rocha, Daisy Castiñeiras, Carmen Delgado, et al.
Medicina Clinica|July 15, 2011
[Clinical and genetic findings in patients with biotinidase deficiency detected through newborn screening or selective screening for hearing loss or inherited metabolic disease]María Luz Couce, Celia Pérez-Cerdá, María Teresa García Silva, et al.
Orphanet Journal of Rare Diseases|April 29, 2014
Assessment of a targeted resequencing assay as a support tool in the diagnosis of lysosomal storage disordersAna Fernández-Marmiesse, Marcos Morey, Merce Pineda, et al.
Revista Espanola De Salud Publica|February 23, 2021
[Beginnings, evolution and current situation of the Newborn Screening Programs in Spain.]José Luis Marín Soria, José Manuel González de Aledo Castillo, Ana Argudo Ramírez, et al.
Pageof 1