Guía práctica del español actual : diccionario breve de dudas y dificultades /

Por Seco, Manuel., Hernández, Elena.
Publicado em 1999

Brave New World: How to connect with college students of the Internet generation

Por Hernández, Elena, Kang, Allison, Miller, Lori, Peterson, Lisa
Publicado em 2009

Brain Training in Children and Adolescents: Is It Scientifically Valid?

Por Rossignoli-Palomeque, Teresa, Perez-Hernandez, Elena, González-Marqués, Javier
Publicado no Front Psychol (2018)

Manganese and its Role in Parkinson’s Disease: From Transport to Neuropathology

Por Aschner, Michael, Erikson, Keith M., Hernández, Elena Herrero, Tjalkens, Ronald
Publicado no Neuromolecular Med (2009)

Role of manganese in neurodegenerative diseases

Por Bowman, Aaron B., Kwakye, Gunnar F., Hernández, Elena Herrero, Aschner, Michael
Publicado em 2011

Möbius Syndrome: Surgical Treatment for Eyelid Dysfunction

Por Lopez-Valverde, Gloria, Jarrin-Hernandez, Elena, Cruz-Gonzalez, Fernando, Mateos-Sanchez, Encarnacion
Publicado em 2013

Augmented Reality for the Assessment of Children's Spatial Memory in Real Settings

Por Juan, M.-Carmen, Mendez-Lopez, Magdalena, Perez-Hernandez, Elena, Albiol-Perez, Sergio
Publicado no PLoS One (2014)

Bottlenecks in the Efficient Use of Advanced Therapy Medicinal Products Based on Mesenchymal Stromal Cells

Por Escacena, Natalia, Quesada-Hernández, Elena, Capilla-Gonzalez, Vivian, Soria, Bernat, Hmadcha, Abdelkrim
Publicado no Stem Cells Int (2015)

A Virtual Object-Location Task for Children: Gender and Videogame Experience Influence Navigation; Age Impacts Memory and Completion Time

Por Rodriguez-Andres, David, Mendez-Lopez, Magdalena, Juan, M.-Carmen, Perez-Hernandez, Elena
Publicado no Front Psychol (2018)

The use of artificial neural networks in electrostatic force microscopy

Por Castellano-Hernández, Elena, Rodríguez, Francisco B, Serrano, Eduardo, Varona, Pablo, Sacha, Gomez Monivas
Publicado em 2012

No Role for Melanoma Treatment in the Association between Melanoma and Amyotrophic Lateral Sclerosis or Parkinson's Disease

Por Baade, Peter D., Herrero Hernández, Elena, Freedman, D. Michal, Smithers, B. Mark, Fritschi, Lin
Publicado em 2010

MnemoCity Task: Assessment of Childrens Spatial Memory Using Stereoscopy and Virtual Environments

Por Rodríguez-Andrés, David, Juan, M.-Carmen, Méndez-López, Magdalena, Pérez-Hernández, Elena, Lluch, Javier
Publicado no PLoS One (2016)

AC electrified jets in a flow-focusing device: Jet length scaling

Por Castro-Hernández, Elena, García-Sánchez, Pablo, Alzaga-Gimeno, Javier, Tan, Say Hwa, Baret, Jean-Christophe, Ramos, Antonio
Publicado no Biomicrofluidics (2016)

Defects in the mitochondrial-tRNA modification enzymes MTO1 and GTPBP3 promote different metabolic reprogramming through a HIF-PPARγ-UCP2-AMPK axis

Por Boutoual, Rachid, Meseguer, Salvador, Villarroya, Magda, Martín-Hernández, Elena, Errami, Mohammed, Martín, Miguel A., Casado, Marta, Armengod, M.-Eugenia
Publicado no Sci Rep (2018)

Carnitine-Acylcarnitine Translocase Deficiency: Experience with Four Cases in Spain and Review of the Literature

Por Vitoria, Isidro, Martín-Hernández, Elena, Peña-Quintana, Luis, Bueno, María, Quijada-Fraile, Pilar, Dalmau, Jaime, Molina-Marrero, Sofia, Pérez, Belén, Merinero, Begoña
Publicado no JIMD Rep (2015)

A new mutation in the gene encoding mitochondrial seryl-tRNA synthetase as a cause of HUPRA syndrome

Por Rivera, Henry, Martín-Hernández, Elena, Delmiro, Aitor, García-Silva, María Teresa, Quijada-Fraile, Pilar, Muley, Rafael, Arenas, Joaquín, Martín, Miguel A, Martínez-Azorín, Francisco
Publicado em 2013

Follow-up of folinic acid supplementation for patients with cerebral folate deficiency and Kearns-Sayre syndrome

Por Quijada-Fraile, Pilar, O’Callaghan, Mar, Martín-Hernández, Elena, Montero, Raquel, Garcia-Cazorla, Àngels, de Aragón, Ana Martínez, Muchart, Jordi, Málaga, Ignacio, Pardo, Rafael, García-Gonzalez, Pedro, Jou, Cristina, Montoya, Julio, Emperador, Sonia, Ruiz-Pesini, Eduardo, Arenas, Joaquín, Martin, Miguel Angel, Ormazabal, Aida, Pineda, Mercè, García-Silva, María T, Artuch, Rafael
Publicado no Orphanet J Rare Dis (2014)

Improving the diagnosis of cobalamin and related defects by genomic analysis, plus functional and structural assessment of novel variants

Por Brasil, Sandra, Leal, Fátima, Vega, Ana, Navarrete, Rosa, Ecay, María Jesús, Desviat, Lourdes R., Riera, Casandra, Padilla, Natàlia, de la Cruz, Xavier, Couce, Mari Luz, Martin-Hernández, Elena, Morais, Ana, Pedrón, Consuelo, Peña-Quintana, Luis, Rigoldi, Miriam, Specola, Norma, de Almeida, Isabel Tavares, Vives, Inmaculada, Yahyaoui, Raquel, Rodríguez-Pombo, Pilar, Ugarte, Magdalena, Pérez-Cerda, Celia, Merinero, Begoña, Pérez, Belén
Publicado no Orphanet J Rare Dis (2018)

Diagnosis features of pediatric Gaucher disease patients in the era of enzymatic therapy, a national-base study from the Spanish Registry of Gaucher Disease

Por Andrade-Campos, Marcio, Alfonso, Pilar, Irun, Pilar, Armstrong, Judith, Calvo, Carmen, Dalmau, Jaime, Domingo, Maria-Rosario, Barbera, Jose-Luis, Cano, Horacio, Fernandez-Galán, Maria-Angeles, Franco, Rafael, Gracia, Inmaculada, Gracia-Antequera, Miguel, Ibañez, Angela, Lendinez, Francisco, Madruga, Marcos, Martin-Hernández, Elena, O’Callaghan, Maria del Mar, del Soto, Alberto Pérez, del Prado, Yolanda Ruiz, Sancho-Val, Ignacio, Sanjurjo, Pablo, Pocovi, Miguel, Giraldo, Pilar
Publicado no Orphanet J Rare Dis (2017)

Recessive mutations in ATP8A2 cause severe hypotonia, cognitive impairment, hyperkinetic movement disorders and progressive optic atrophy

Por McMillan, Hugh J., Telegrafi, Aida, Singleton, Amanda, Cho, Megan T., Lelli, Daniel, Lynn, Francis C., Griffin, Julie, Asamoah, Alexander, Rinne, Tuula, Erasmus, Corrie E., Koolen, David A., Haaxma, Charlotte A., Keren, Boris, Doummar, Diane, Mignot, Cyril, Thompson, Islay, Velsher, Lea, Dehghani, Mohammadreza, Vahidi Mehrjardi, Mohammad Yahya, Maroofian, Reza, Tchan, Michel, Simons, Cas, Christodoulou, John, Martín-Hernández, Elena, Guillen Sacoto, Maria J., Henderson, Lindsay B., McLaughlin, Heather, Molday, Laurie L., Molday, Robert S., Yoon, Grace
Publicado no Orphanet J Rare Dis (2018)