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

Inmaculada García Jiménez

Showing results (1-10 of 6) with videos related to

Pageof 1
Sort By:
Archivos Argentinos De Pediatria|January 19, 2017
[A regenerative anemia in infants: 2 cases of Pearson´s syndrome]José M Martínez de Zabarte Fernández, Carmen Rodríguez-Vigil Iturrate, Cristina Martínez Faci, et al.
Neuroradiology|June 6, 2022
Volumetric study of brain MRI in a cohort of patients with neurotransmitter disordersChiara Alfonsi, Christian Stephan-Otto, Elisenda Cortès-Saladelafont, et al.
Journal of Clinical Medicine|November 6, 2019
Genes and Variants Underlying Human Congenital Lactic Acidosis-From Genetics to Personalized TreatmentIrene Bravo-Alonso, Rosa Navarrete, Ana Isabel Vega, et al.
European Journal of Human Genetics : EJHG|January 11, 2019
Value of genetic analysis for confirming inborn errors of metabolism detected through the Spanish neonatal screening programRosa Navarrete, Fátima Leal, Ana I Vega, et al.
Orphanet Journal of Rare Diseases|December 1, 2014
Urea cycle disorders in Spain: an observational, cross-sectional and multicentric study of 104 casesElena Martín-Hernández, Luis Aldámiz-Echevarría, Esperanza Castejón-Ponce, et al.
Clinical Genetics|January 18, 2019
Clinical and molecular diagnosis of non-phosphomannomutase 2 N-linked congenital disorders of glycosylation in SpainCelia Medrano, Ana Vega, Rosa Navarrete, et al.
Pageof 1

Showing results (1-10 of 6) with videos related to

Sort By:
Pageof 1
Archivos Argentinos De Pediatria|January 19, 2017
[A regenerative anemia in infants: 2 cases of Pearson´s syndrome]José M Martínez de Zabarte Fernández, Carmen Rodríguez-Vigil Iturrate, Cristina Martínez Faci, et al.
Neuroradiology|June 6, 2022
Volumetric study of brain MRI in a cohort of patients with neurotransmitter disordersChiara Alfonsi, Christian Stephan-Otto, Elisenda Cortès-Saladelafont, et al.
Journal of Clinical Medicine|November 6, 2019
Genes and Variants Underlying Human Congenital Lactic Acidosis-From Genetics to Personalized TreatmentIrene Bravo-Alonso, Rosa Navarrete, Ana Isabel Vega, et al.
European Journal of Human Genetics : EJHG|January 11, 2019
Value of genetic analysis for confirming inborn errors of metabolism detected through the Spanish neonatal screening programRosa Navarrete, Fátima Leal, Ana I Vega, et al.
Orphanet Journal of Rare Diseases|December 1, 2014
Urea cycle disorders in Spain: an observational, cross-sectional and multicentric study of 104 casesElena Martín-Hernández, Luis Aldámiz-Echevarría, Esperanza Castejón-Ponce, et al.
Clinical Genetics|January 18, 2019
Clinical and molecular diagnosis of non-phosphomannomutase 2 N-linked congenital disorders of glycosylation in SpainCelia Medrano, Ana Vega, Rosa Navarrete, et al.
Pageof 1