Works by Guillén‐Navarro, Encarna

Results: 48
    1

    Genotypic Findings in Noonan and Non-Noonan RASopathies and Patient Eligibility for Growth Hormone Treatment.

    Published in:
    Journal of Clinical Medicine, 2023, v. 12, n. 15, p. 5003, doi. 10.3390/jcm12155003
    By:
    • Carcavilla, Atilano;
    • Cambra, Ana;
    • Santomé, José L.;
    • Seidel, Verónica;
    • Cruz, Jaime;
    • Alonso, Milagros;
    • Pozo, Jesús;
    • Valenzuela, Irene;
    • Guillén-Navarro, Encarna;
    • Santos-Simarro, Fernando;
    • González-Casado, Isabel;
    • Rodríguez, Amparo;
    • Medrano, Constancio;
    • López-Siguero, Juan Pedro;
    • Ezquieta, Begoña
    Publication type:
    Article
    2

    EDA, EDAR, EDARADD and WNT10A allelic variants in patients with ectodermal derivative impairment in the Spanish population.

    Published in:
    2019
    By:
    • Martínez-Romero, María Carmen;
    • Ballesta-Martínez, María Juliana;
    • López-González, Vanesa;
    • Sánchez-Soler, María José;
    • Serrano-Antón, Ana Teresa;
    • Barreda-Sánchez, María;
    • Rodriguez-Peña, Lidya;
    • Martínez-Menchon, María Teresa;
    • Frías-Iniesta, José;
    • Sánchez-Pedreño, Paloma;
    • Carbonell-Meseguer, Pablo;
    • Glover-López, Guillermo;
    • Guillén-Navarro, Encarna;
    • GIEDE (Spanish multidisciplinary research group for ectodermal dysplasia);
    • Alcalá-García, Rebeca;
    • Barcia-Ramírez, Ana;
    • Cruz-Rojo, Jaime;
    • Gener-Querol, Blanca;
    • Hernández-Martín, Angela;
    • Lapunzina-Badía, Pablo
    Publication type:
    journal article
    3

    European Achondroplasia Forum Practical Considerations for Following Adults with Achondroplasia.

    Published in:
    Advances in Therapy, 2024, v. 41, n. 7, p. 2545, doi. 10.1007/s12325-024-02880-3
    By:
    • Fredwall, Svein;
    • AlSayed, Moeenaldeen;
    • Ben-Omran, Tawfeg;
    • Boero, Silvio;
    • Cormier-Daire, Valérie;
    • Fauroux, Brigitte;
    • Guillén-Navarro, Encarna;
    • Innig, Florian;
    • Kunkel, Philip;
    • Lampe, Christian;
    • Maghnie, Mohamad;
    • Mohnike, Klaus;
    • Mortier, Geert;
    • Pejin, Zagorka;
    • Sessa, Marco;
    • Sousa, Sérgio B.;
    • Irving, Melita
    Publication type:
    Article
    4

    Pharmacogenomic Study of SARS-CoV-2 Treatments: Identifying Polymorphisms Associated with Treatment Response in COVID-19 Patients.

    Published in:
    Biomedicines, 2025, v. 13, n. 3, p. 553, doi. 10.3390/biomedicines13030553
    By:
    • Serra-Llovich, Alexandre;
    • Cullell, Natalia;
    • Maroñas, Olalla;
    • José Herrero, María;
    • Cruz, Raquel;
    • Almoguera, Berta;
    • Ayuso, Carmen;
    • López-Rodríguez, Rosario;
    • Domínguez-Garrido, Elena;
    • Ortiz-Lopez, Rocio;
    • Barreda-Sánchez, María;
    • Corton, Marta;
    • Dalmau, David;
    • Calbo, Esther;
    • Boix-Palop, Lucía;
    • Dietl, Beatriz;
    • Sangil, Anna;
    • Gil-Rodriguez, Almudena;
    • Guillén-Navarro, Encarna;
    • Mancebo, Esther
    Publication type:
    Article
    5

    Androgen receptor polyQ alleles and COVID‐19 severity in men: A replication study.

    Published in:
    Andrology, 2023, v. 11, n. 1, p. 24, doi. 10.1111/andr.13339
    By:
    • López‐Rodríguez, Rosario;
    • Ruiz‐Hornillos, Javier;
    • Cortón, Marta;
    • Almoguera, Berta;
    • Minguez, Pablo;
    • Pérez‐Tomás, María Elena;
    • Barreda‐Sánchez, María;
    • Mancebo, Esther;
    • Ondo, Lorena;
    • Martínez‐Ramas, Andrea;
    • Fernández‐Caballero, Lidia;
    • Taracido‐Fernández, Juan Carlos;
    • Herrero‐González, Antonio;
    • Mahillo, Ignacio;
    • Paz‐Artal, Estela;
    • Guillén‐Navarro, Encarna;
    • Ayuso, Carmen
    Publication type:
    Article
    6

    Identification of copy‐number variants in patients with overgrowth disorders.

    Published in:
    Clinical Genetics, 2024, v. 106, n. 5, p. 614, doi. 10.1111/cge.14596
    By:
    • Parra, Alejandro;
    • Tenorio‐Castano, Jair;
    • Nevado, Julián;
    • Cazalla, Mario;
    • Miranda‐Alcaraz, Lucía;
    • Gallego‐Zazo, Natalia;
    • Silván, Cristina;
    • Arias, Pedro;
    • Pozo‐Román, Jesús;
    • Ballesta‐Martínez, María Juliana;
    • Guillén‐Navarro, Encarna;
    • Arroyo, Ignacio;
    • Lotersztein, Vanesa;
    • Cosentino, Viviana;
    • González‐Meneses, Antonio;
    • Galán, Enrique;
    • Rosell, Jordi;
    • Ramos, Feliciano;
    • Plasencia, Antonio;
    • Rosa, Alberto L.
    Publication type:
    Article
    7

    Expanding the mutation spectrum in 182 Spanish probands with craniosynostosis: identification and characterization of novel TCF12 variants.

    Published in:
    European Journal of Human Genetics, 2015, v. 23, n. 7, p. 907, doi. 10.1038/ejhg.2014.205
    By:
    • Paumard-Hernández, Beatriz;
    • Berges-Soria, Julia;
    • Barroso, Eva;
    • Rivera-Pedroza, Carlos I;
    • Pérez-Carrizosa, Virginia;
    • Benito-Sanz, Sara;
    • López-Messa, Eva;
    • Santos, Fernando;
    • García-Recuero, Ignacio I;
    • Romance, Ana;
    • Ballesta-Martínez, Juliana María;
    • López-González, Vanesa;
    • Campos-Barros, Ángel;
    • Cruz, Jaime;
    • Guillén-Navarro, Encarna;
    • Sánchez del Pozo, Jaime;
    • Lapunzina, Pablo;
    • García-Miñaur, Sixto;
    • Heath, Karen E
    Publication type:
    Article
    8
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    Validation of clinical exome sequencing in the diagnostic procedure of patients with intellectual disability in clinical practice.

    Published in:
    Orphanet Journal of Rare Diseases, 2023, v. 18, n. 1, p. 1, doi. 10.1186/s13023-023-02809-z
    By:
    • Ballesta-Martínez, María Juliana;
    • Pérez-Fernández, Virginia;
    • López-González, Vanesa;
    • Sánchez-Soler, María José;
    • Serrano-Antón, Ana Teresa;
    • Rodríguez-Peña, Lidia Isolina;
    • Barreda-Sánchez, Maria;
    • Armengol-Dulcet, Lluís;
    • Guillén-Navarro, Encarna
    Publication type:
    Article
    11

    Real-world evidence in achondroplasia: considerations for a standardized data set.

    Published in:
    Orphanet Journal of Rare Diseases, 2023, v. 18, n. 1, p. 1, doi. 10.1186/s13023-023-02755-w
    By:
    • Alanay, Yasemin;
    • Mohnike, Klaus;
    • Nilsson, Ola;
    • Alves, Inês;
    • AlSayed, Moeenaldeen;
    • Appelman-Dijkstra, Natasha M.;
    • Baujat, Genevieve;
    • Ben-Omran, Tawfeg;
    • Breyer, Sandra;
    • Cormier-Daire, Valerie;
    • Gregersen, Pernille Axél;
    • Guillén-Navarro, Encarna;
    • Högler, Wolfgang;
    • Maghnie, Mohamad;
    • Mukherjee, Swati;
    • Cohen, Shelda;
    • Pimenta, Jeanne;
    • Selicorni, Angelo;
    • Semler, J. Oliver;
    • Sigaudy, Sabine
    Publication type:
    Article
    12

    Clinical Heterogeneity and Different Phenotypes in Patients with SETD2 Variants: 18 New Patients and Review of the Literature.

    Published in:
    Genes, 2023, v. 14, n. 6, p. 1179, doi. 10.3390/genes14061179
    By:
    • Parra, Alejandro;
    • Rabin, Rachel;
    • Pappas, John;
    • Pascual, Patricia;
    • Cazalla, Mario;
    • Arias, Pedro;
    • Gallego-Zazo, Natalia;
    • Santana, Alfredo;
    • Arroyo, Ignacio;
    • Artigas, Mercè;
    • Pachajoa, Harry;
    • Alanay, Yasemin;
    • Akgun-Dogan, Ozlem;
    • Ruaud, Lyse;
    • Couque, Nathalie;
    • Levy, Jonathan;
    • Porras-Hurtado, Gloria Liliana;
    • Santos-Simarro, Fernando;
    • Ballesta-Martinez, Maria Juliana;
    • Guillén-Navarro, Encarna
    Publication type:
    Article
    13

    Protocol for the Phase 2 EDELIFE Trial Investigating the Efficacy and Safety of Intra-Amniotic ER004 Administration to Male Subjects with X-Linked Hypohidrotic Ectodermal Dysplasia.

    Published in:
    Genes, 2023, v. 14, n. 1, p. 153, doi. 10.3390/genes14010153
    By:
    • Schneider, Holm;
    • Hadj-Rabia, Smail;
    • Faschingbauer, Florian;
    • Bodemer, Christine;
    • Grange, Dorothy K.;
    • Norton, Mary E.;
    • Cavalli, Riccardo;
    • Tadini, Gianluca;
    • Stepan, Holger;
    • Clarke, Angus;
    • Guillén-Navarro, Encarna;
    • Maier-Wohlfart, Sigrun;
    • Bouroubi, Athmane;
    • Porte, Florence
    Publication type:
    Article
    14

    Deep Molecular Characterization of Milder Spinal Muscular Atrophy Patients Carrying the c.859G>C Variant in SMN2.

    Published in:
    International Journal of Molecular Sciences, 2022, v. 23, n. 15, p. 8289, doi. 10.3390/ijms23158289
    By:
    • Blasco-Pérez, Laura;
    • Costa-Roger, Mar;
    • Leno-Colorado, Jordi;
    • Bernal, Sara;
    • Alias, Laura;
    • Codina-Solà, Marta;
    • Martínez-Cruz, Desirée;
    • Castiglioni, Claudia;
    • Bertini, Enrico;
    • Travaglini, Lorena;
    • Millán, José M.;
    • Aller, Elena;
    • Sotoca, Javier;
    • Juntas, Raúl;
    • Hoei-Hansen, Christina Engel;
    • Moreno-Escribano, Antonio;
    • Guillén-Navarro, Encarna;
    • Costa-Comellas, Laura;
    • Munell, Francina;
    • Boronat, Susana
    Publication type:
    Article
    15

    Variability in Phelan-McDermid Syndrome in a Cohort of 210 Individuals.

    Published in:
    Frontiers in Genetics, 2022, v. 13, p. 1, doi. 10.3389/fgene.2022.652454
    By:
    • Nevado, Julián;
    • García-Miñaúr, Sixto;
    • Palomares-Bralo, María;
    • Vallespín, Elena;
    • Guillén-Navarro, Encarna;
    • Rosell, Jordi;
    • Bel-Fenellós, Cristina;
    • Ángeles Mori, María;
    • Milá, Montserrat;
    • del Campo, Miguel;
    • Barrúz, Pilar;
    • Santos-Simarro, Fernando;
    • Obregón, Gabriela;
    • Orellana, Carmen;
    • Pachajoa, Harry;
    • Antonio Tenorio, Jair;
    • Galán, Enrique;
    • Cigudosa, Juan C.;
    • Moresco, Angélica;
    • Saleme, César
    Publication type:
    Article
    16
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    GPI-anchor and GPI-anchored protein expression in PMM2-CDG patients.

    Published in:
    Orphanet Journal of Rare Diseases, 2013, v. 8, n. 1, p. 1, doi. 10.1186/1750-1172-8-170
    By:
    • Morena-Barrio, Maria E de la;
    • Hernández-Caselles, Trinidad;
    • Corral, Javier;
    • García-López, Roberto;
    • Martínez-Martínez, Irene;
    • Pérez-Dueñas, Belen;
    • Altisent, Carmen;
    • Sevivas, Teresa;
    • Kristensen, Soren R.;
    • Guillén-Navarro, Encarna;
    • Miñano, Antonia;
    • Vicente, Vicente;
    • Jaeken, Jaak;
    • Lozano, Maria L.
    Publication type:
    Article
    19
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    GPI-anchor and GPI-anchored protein expression in PMM2-CDG patients.

    Published in:
    2013
    By:
    • de la Morena-Barrio, Maria E;
    • Hernández-Caselles, Trinidad;
    • Corral, Javier;
    • García-López, Roberto;
    • Martínez-Martínez, Irene;
    • Pérez-Dueñas, Belen;
    • Altisent, Carmen;
    • Sevivas, Teresa;
    • Kristensen, Soren R;
    • Guillén-Navarro, Encarna;
    • Miñano, Antonia;
    • Vicente, Vicente;
    • Jaeken, Jaak;
    • Lozano, Maria L
    Publication type:
    journal article
    22
    23

    Mucopolysaccharidosis type II: European recommendations for the diagnosis and multidisciplinary management of a rare disease.

    Published in:
    2011
    By:
    • Scarpa, Maurizio;
    • Almássy, Zsuzsanna;
    • Beck, Michael;
    • Bodamer, Olaf;
    • Bruce, Iain A;
    • De Meirleir, Linda;
    • Guffon, Nathalie;
    • Guillén-Navarro, Encarna;
    • Hensman, Pauline;
    • Jones, Simon;
    • Kamin, Wolfgang;
    • Kampmann, Christoph;
    • Lampe, Christina;
    • Lavery, Christine A;
    • Leao Teles, Elisa;
    • Link, Bianca;
    • Lund, Allan M;
    • Malm, Gunilla;
    • Pitz, Susanne;
    • Rothera, Michael
    Publication type:
    journal article
    24
    25

    Comprehensive long‐term efficacy and safety of recombinant human alpha‐mannosidase (velmanase alfa) treatment in patients with alpha‐mannosidosis.

    Published in:
    Journal of Inherited Metabolic Disease, 2018, v. 41, n. 6, p. 1225, doi. 10.1007/s10545-018-0175-2
    By:
    • Lund, Allan M.;
    • Borgwardt, Line;
    • Cattaneo, Federica;
    • Ardigò, Diego;
    • Geraci, Silvia;
    • Gil‐Campos, Mercedes;
    • De Meirleir, Linda;
    • Laroche, Cécile;
    • Dolhem, Philippe;
    • Cole, Duncan;
    • Tylki‐Szymanska, Anna;
    • Lopez‐Rodriguez, Monica;
    • Guillén‐Navarro, Encarna;
    • Dali, Christine I.;
    • Héron, Bénédicte;
    • Fogh, Jens;
    • Muschol, Nicole;
    • Phillips, Dawn;
    • Van den Hout, J. M. Hannerieke;
    • Jones, Simon A.
    Publication type:
    Article
    26

    Comprehensive long-term efficacy and safety of recombinant human alpha-mannosidase (velmanase alfa) treatment in patients with alpha-mannosidosis.

    Published in:
    Journal of Inherited Metabolic Disease, 2018, v. 41, n. 6, p. 1225, doi. 10.1007/s10545-018-0175-2
    By:
    • Lund, Allan M.;
    • Borgwardt, Line;
    • Cattaneo, Federica;
    • Ardigò, Diego;
    • Geraci, Silvia;
    • Gil-Campos, Mercedes;
    • De Meirleir, Linda;
    • Laroche, Cécile;
    • Dolhem, Philippe;
    • Cole, Duncan;
    • Tylki-Szymanska, Anna;
    • Lopez-Rodriguez, Monica;
    • Guillén-Navarro, Encarna;
    • Dali, Christine I.;
    • Héron, Bénédicte;
    • Fogh, Jens;
    • Muschol, Nicole;
    • Phillips, Dawn;
    • Van den Hout, J. M. Hannerieke;
    • Jones, Simon A.
    Publication type:
    Article
    27
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    Exome sequencing unravels unexpected differential diagnoses in individuals with the tentative diagnosis of Coffin-Siris and Nicolaides-Baraitser syndromes.

    Published in:
    Human Genetics, 2015, v. 134, n. 6, p. 553, doi. 10.1007/s00439-015-1535-8
    By:
    • Bramswig, Nuria;
    • Lüdecke, Hermann-Josef;
    • Alanay, Yasemin;
    • Albrecht, Beate;
    • Barthelmie, Alexander;
    • Boduroglu, Koray;
    • Braunholz, Diana;
    • Caliebe, Almuth;
    • Chrzanowska, Krystyna;
    • Czeschik, Johanna;
    • Endele, Sabine;
    • Graf, Elisabeth;
    • Guillén-Navarro, Encarna;
    • Kiper, Pelin;
    • López-González, Vanesa;
    • Parenti, Ilaria;
    • Pozojevic, Jelena;
    • Utine, Gulen;
    • Wieland, Thomas;
    • Kaiser, Frank
    Publication type:
    Article
    30

    Clinical Spectrum and Tumour Risk Analysis in Patients with Beckwith-Wiedemann Syndrome Due to CDKN1C Pathogenic Variants.

    Published in:
    Cancers, 2022, v. 14, n. 15, p. 3807, doi. 10.3390/cancers14153807
    By:
    • Cardoso, Leila Cabral de Almeida;
    • Parra, Alejandro;
    • Gil, Cristina Ríos;
    • Arias, Pedro;
    • Gallego, Natalia;
    • Romanelli, Valeria;
    • Kantaputra, Piranit Nik;
    • Lima, Leonardo;
    • Llerena Júnior, Juan Clinton;
    • Arberas, Claudia;
    • Guillén-Navarro, Encarna;
    • Nevado, Julián;
    • Tenorio-Castano, Jair;
    • Lapunzina, Pablo
    Publication type:
    Article
    31

    Two Novel POC1A Mutations in the Primordial Dwarfism, SOFT Syndrome: Clinical Homogeneity but Also Unreported Malformations.

    Published in:
    American Journal of Medical Genetics. Part A, 2016, v. 170A, n. 1, p. 210, doi. 10.1002/ajmg.a.37393
    By:
    • Barraza‐García, Jimena;
    • Iván Rivera‐Pedroza, Carlos;
    • Salamanca, Luis;
    • Belinchón, Alberta;
    • López‐González, Vanesa;
    • Sentchordi‐Montané, Lucía;
    • del Pozo, Ángela;
    • Santos‐Simarro, Fernando;
    • Campos‐Barros, Ángel;
    • Lapunzina, Pablo;
    • Guillén‐Navarro, Encarna;
    • González‐Casado, Isabel;
    • García‐Miñaur, Sixto;
    • Heath, Karen E.
    Publication type:
    Article
    32
    33

    Two mutations in IFITM5 causing distinct forms of osteogenesis imperfecta.

    Published in:
    American Journal of Medical Genetics. Part A, 2014, v. 164A, n. 5, p. 1136, doi. 10.1002/ajmg.a.36409
    By:
    • Guillén‐Navarro, Encarna;
    • Ballesta‐Martínez, María Juliana;
    • Valencia, María;
    • Bueno, Ana María;
    • Martinez‐Glez, Victor;
    • López‐González, Vanesa;
    • Burnyte, Birute;
    • Utkus, Algirdas;
    • Lapunzina, Pablo;
    • Ruiz‐Perez, Victor L.
    Publication type:
    Article
    34

    Pre- and postnatal findings in a patient with a novel rec(8)dup(8q)inv(8)(p23.2q22.3) associated with san luis valley syndrome.

    Published in:
    American Journal of Medical Genetics. Part A, 2013, v. 161A, n. 9, p. 2369, doi. 10.1002/ajmg.a.36103
    By:
    • Vera ‐ Carbonell, AscENsión;
    • López ‐ González, Vanesa;
    • Bafalliu, Juan Antonio;
    • Piñero ‐ Fernández, Juan;
    • Susmozas, Joaquín;
    • Sorli, Moisés;
    • López ‐ Pérez, Rocío;
    • Fernández, Asunción;
    • Guillén ‐ Navarro, Encarna;
    • López ‐ Expósito, Isabel
    Publication type:
    Article
    35

    Mutations in WNT10A are frequently involved in oligodontia associated with minor signs of ectodermal dysplasia.

    Published in:
    American Journal of Medical Genetics. Part A, 2013, v. 161A, n. 4, p. 671, doi. 10.1002/ajmg.a.35747
    By:
    • Plaisancié, Julie;
    • Bailleul‐Forestier, Isabelle;
    • Gaston, Véronique;
    • Vaysse, Fréderic;
    • Lacombe, Didier;
    • Holder‐Espinasse, Muriel;
    • Abramowicz, Marc;
    • Coubes, Christine;
    • Plessis, Ghislaine;
    • Faivre, Laurence;
    • Demeer, Bénédicte;
    • Vincent‐Delorme, Catherine;
    • Dollfus, Hélène;
    • Sigaudy, Sabine;
    • Guillén‐Navarro, Encarna;
    • Verloes, Alain;
    • Jonveaux, Philippe;
    • Martin‐Coignard, Dominique;
    • Colin, Estelle;
    • Bieth, Eric
    Publication type:
    Article
    36
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    39

    Whole Blood Transcriptome Analysis in Congenital Anemia Patients.

    Published in:
    International Journal of Molecular Sciences, 2024, v. 25, n. 21, p. 11706, doi. 10.3390/ijms252111706
    By:
    • Sanchez-Villalobos, Maria;
    • Campos Baños, Eulalia;
    • Martínez-Balsalobre, Elena;
    • Navarro-Ramirez, Veronica;
    • Videla, María Asunción Beltrán;
    • Pinilla, Miriam;
    • Guillén-Navarro, Encarna;
    • Salido-Fierrez, Eduardo;
    • Pérez-Oliva, Ana Belén
    Publication type:
    Article
    40
    41
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    High penetrance of acute intermittent porphyria in a Spanish founder mutation population and CYP2D6 genotype as a susceptibility factor.

    Published in:
    2019
    By:
    • Barreda-Sánchez, María;
    • Buendía-Martínez, Juan;
    • Glover-López, Guillermo;
    • Carazo-Díaz, Carmen;
    • Ballesta-Martínez, María Juliana;
    • López-González, Vanesa;
    • Sánchez-Soler, María José;
    • Rodriguez-Peña, Lidya;
    • Serrano-Antón, Ana Teresa;
    • Gil-Ferrer, Remedios;
    • Martínez-Romero, Maria del Carmen;
    • Carbonell-Meseguer, Pablo;
    • Guillén-Navarro, Encarna
    Publication type:
    journal article
    43

    Heterozygous pathogenic variants in GLI1 are a common finding in isolated postaxial polydactyly A/B.

    Published in:
    Human Mutation, 2020, v. 41, n. 1, p. 265, doi. 10.1002/humu.23921
    By:
    • Palencia‐Campos, Adrián;
    • Martínez‐Fernández, María‐Luisa;
    • Altunoglu, Umut;
    • Soto‐Bielicka, Patricia;
    • Torres, Antonio;
    • Marín, Purificación;
    • Aller, Elena;
    • Şentürk, Leyli;
    • Berköz, Ömer;
    • Yıldıran, Mehmet;
    • Kayserili, Hülya;
    • Gil‐Camarero, Elena;
    • Colli‐Lista, Gloria;
    • Sanchís‐Calvo, Amparo;
    • Carretero, Alba;
    • Guillén‐Navarro, Encarna;
    • López‐González, Vanesa;
    • Ballesta‐Martínez, María;
    • Rosell, Jordi;
    • Aglan, Mona S.
    Publication type:
    Article
    44

    A New Overgrowth Syndrome is due to Mutations in RNF125.

    Published in:
    Human Mutation, 2014, v. 35, n. 12, p. 1436, doi. 10.1002/humu.22689
    By:
    • Tenorio, Jair;
    • Mansilla, Alicia;
    • Valencia, María;
    • Martínez‐Glez, Víctor;
    • Romanelli, Valeria;
    • Arias, Pedro;
    • Castrejón, Nerea;
    • Poletta, Fernando;
    • Guillén‐Navarro, Encarna;
    • Gordo, Gema;
    • Mansilla, Elena;
    • García‐Santiago, Fé;
    • González‐Casado, Isabel;
    • Vallespín, Elena;
    • Palomares, María;
    • Mori, María A.;
    • Santos‐Simarro, Fernando;
    • García‐Miñaur, Sixto;
    • Fernández, Luis;
    • Mena, Rocío
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    45

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    46
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    48

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