Publications by authors named "Maria Orera"

Claim this Profile
B
Boosted Genomic Literacy in Nursing Students via Standardized-Patient Clinical Simulation: A Mixed-Methods Study.
Daniel Garcia-Gutiérrez, Estel la Ramírez-Baraldes, Maria Orera, Verónica Seidel, Carmen Martínez

Nurs Rep· August 2025

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
R
Response to anakinra in new-onset refractory status epilepticus: A clinical case.
Michael Palacios-Mendoza, Ana Gómez, Julio Prieto, Juan Camilo Barrios, María Orera

Seizure· January 2022

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
A collection of three integration-free iPSCs derived from old male and female healthy subjects.
Eva Rodríguez-Traver, Eva Díaz-Guerra, César Rodríguez, Fabián Arenas, María Orera

Stem Cell Res· January 2020

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
An integration-free iPSC line, ICCSICi007-A, derived from a female Alzheimer's disease patient with the APOE-ε4/ε4 alleles.
Eva Díaz-Guerra, Eva Rodríguez-Traver, Elena P Moreno-Jiménez, Itziar de Rojas, César Rodríguez, María Orera

Stem Cell Res· December 2019

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
G
Generation of an integration-free iPSC line, ICCSICi005-A, derived from a Parkinson's disease patient carrying the L444P mutation in the GBA1 gene.
Eva Rodríguez-Traver, César Rodríguez, Eva Díaz-Guerra, Fabián Arenas, Marcos Araúzo-Bravo, María Orera

Stem Cell Res· October 2019

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
G
Generation of an integration-free iPSC line, ICCSICi006-A, derived from a male Alzheimer's disease patient carrying the PSEN1-G206D mutation.
Eva Díaz-Guerra, Manuel A Oria-Muriel, Elena P Moreno-Jiménez, Itziar de Rojasb, César Rodríguez, María Orera

Stem Cell Res· October 2019

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
A collection of four integration-free iPSC lines derived from diagnosed sporadic Alzheimer's disease patients with different APOE alleles.
Eva Díaz-Guerra, Elena P Moreno-Jiménez, Itziar de Rojas, César Rodríguez, Eva Rodríguez-Traver, María Orera

Stem Cell Res· August 2019

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
A collection of integration-free iPSCs derived from Parkinson's disease patients carrying mutations in the GBA1 gene.
Eva Rodríguez-Traver, Eva Díaz-Guerra, César Rodríguez, Pablo Fernández, Fabián Arenas, María Orera

Stem Cell Res· July 2019

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
P
PIAS4 is associated with macro/microcephaly in the novel interstitial 19p13.3 microdeletion/microduplication syndrome.
Julián Nevado, Jill A Rosenfeld, Rocío Mena, María Palomares-Bralo, Elena Vallespín, María Orera

Eur J Hum Genet· December 2015

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
C
Characterization of patients' requests and pharmacists' professional practice in oropharyngeal condition in Spain.
Antonio Hernández, Pilar Garcia-Delgado, Victoria Garcia-Cardenas, Ana Ocaña, Elena Labrador, Maria Luisa Orera

Int J Clin Pharm· April 2015

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
Q
Quantitative abnormalities of peripheral blood distinct T, B, and natural killer cell subsets and clinical findings in obstetric antiphospholipid syndrome.
Javier Carbone, Antonio Gallego, Nallibe Lanio, Joaquin Navarro, Maria Orera

J Rheumatol· June 2009

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
An excess of chromosome 1 breakpoints in male infertility.
Iben Bache, Elvire Van Assche, Sultan Cingoz, Merete Bugge, Zeynep Tümer, Maria Orera

Eur J Hum Genet· December 2004

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
A case of ring chromosome 22 with deletion of the 22q13.3 region associated with agenesis of the corpus callosum, fornix and septum pellucidum.
José Delcán, María Orera, Rafael Linares, Dolores Saavedra, Angustias Palomar

Prenat Diagn· August 2004

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
[
[Antiphospholipid syndrome updating].
Juan Antonio Orts, Angel Zúñiga, María Orera

Med Clin (Barc)· October 2003

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis