Works by Espinós, Carmen

Results: 44

Audiological Findings in Charcot-Marie-Tooth Disease Type 4C.

Published in:

Journal of International Advanced Otology, 2017, v. 13, n. 1, p. 93, doi. 10.5152/iao.2017.3379

By:

Sivera, Rafael;
Cavalle, Laura;
Vílchez, Juan J.;
Espinós, Carmen;
Pérez-Garrigues, Herminio;
Sevilla, Teresa

Publication type:

Article

A Century of Progress on Wilson Disease and the Enduring Challenges of Genetics, Diagnosis, and Treatment.

Published in:

Biomedicines, 2023, v. 11, n. 2, p. 420, doi. 10.3390/biomedicines11020420

By:

Penning, Louis C.;
Berenguer, Marina;
Czlonkowska, Anna;
Double, Kay L.;
Dusek, Petr;
Espinós, Carmen;
Lutsenko, Svetlana;
Medici, Valentina;
Papenthin, Wiebke;
Stremmel, Wolfgang;
Willemse, Jose;
Weiskirchen, Ralf

Publication type:

Article

Wilson's Disease: Facing the Challenge of Diagnosing a Rare Disease.

Published in:

2021

By:

Sánchez-Monteagudo, Ana;
Ripollés, Edna;
Berenguer, Marina;
Espinós, Carmen

Publication type:

Case Study

Genetics of Wilson disease and Wilson‐like phenotype in a clinical series from eastern Spain.

Published in:

Clinical Genetics, 2020, v. 97, n. 5, p. 758, doi. 10.1111/cge.13719

By:

Sánchez‐Monteagudo, Ana;
Álvarez‐Sauco, María;
Sastre, Isabel;
Martínez‐Torres, Irene;
Lupo, Vincenzo;
Berenguer, Marina;
Espinós, Carmen

Publication type:

Article

The USH2A c.2299delG mutation: dating its common origin in a Southern European population.

Published in:

European Journal of Human Genetics, 2010, v. 18, n. 7, p. 788, doi. 10.1038/ejhg.2010.14

By:

Aller, Elena;
Larrieu, Lise;
Jaijo, Teresa;
Baux, David;
Espinós, Carmen;
González-Candelas, Fernando;
Nájera, Carmen;
Palau, Francesc;
Claustres, Mireille;
Roux, Anne-Françoise;
Millán, José M.

Publication type:

Article

Congenital hypomyelinating neuropathy due to a novel MPZ mutation.

Published in:

Journal of the Peripheral Nervous System, 2011, v. 16, n. 4, p. 347, doi. 10.1111/j.1529-8027.2011.00369.x

By:

Sevilla, Teresa;
Lupo, Vincenzo;
Sivera, Rafael;
Marco-Marín, Clara;
Martínez-Rubio, Dolores;
Rivas, Eloy;
Hernández, Arturo;
Palau, Francesc;
Espinós, Carmen

Publication type:

Article

Phenotypical features of the p.R120W mutation in the GDAP1 gene causing autosomal dominant Charcot-Marie-Tooth disease.

Published in:

Journal of the Peripheral Nervous System, 2010, v. 15, n. 4, p. 334, doi. 10.1111/j.1529-8027.2010.00286.x

By:

Sivera, Rafael;
Espinós, Carmen;
Vílchez, Juan J.;
Mas, Fernando;
Martínez-Rubio, Dolores;
Chumillas, María José;
Mayordomo, Fernando;
Muelas, Nuria;
Bataller, Luis;
Palau, Francesc;
Sevilla, Teresa

Publication type:

Article

NGLY1 Deficiency: A Rare Newly Described Condition with a Typical Presentation.

Published in:

Life (2075-1729), 2021, v. 11, n. 3, p. 187, doi. 10.3390/life11030187

By:

Dabaj, Ivana;
Sudrié-Arnaud, Bénédicte;
Lecoquierre, François;
Raymond, Kimiyo;
Ducatez, Franklin;
Guerrot, Anne-Marie;
Snanoudj, Sarah;
Coutant, Sophie;
Saugier-Veber, Pascale;
Marret, Stéphane;
Nicolas, Gaël;
Tebani, Abdellah;
Bekri, Soumeya;
Galindo, Carmen Espinós; Máximo Ibo;
Rodrigo, Regina

Publication type:

Article

Significant linkage and non-linkage of type 1 von Willebrand disease to the von Willebrand factor gene.

Published in:

British Journal of Haematology, 2001, v. 115, n. 3, p. 692, doi. 10.1046/j.1365-2141.2001.03132.x

By:

Casaña, Pilar;
Martínez, Francisco;
Haya, Saturnino;
Espinós, Carmen;
Aznar, José A.

Publication type:

Article

Genetic Heterogeneity Underlying Phenotypes with Early-Onset Cerebellar Atrophy.

Published in:

International Journal of Molecular Sciences, 2023, v. 24, n. 22, p. 16400, doi. 10.3390/ijms242216400

By:

Martínez-Rubio, Dolores;
Hinarejos, Isabel;
Argente-Escrig, Herminia;
Marco-Marín, Clara;
Lozano, María Ana;
Gorría-Redondo, Nerea;
Lupo, Vincenzo;
Martí-Carrera, Itxaso;
Miranda, Concepción;
Vázquez-López, María;
García-Pérez, Asunción;
Marco-Hernández, Ana Victoria;
Tomás-Vila, Miguel;
Aguilera-Albesa, Sergio;
Espinós, Carmen

Publication type:

Article

Expanding the β-III Spectrin-Associated Phenotypes toward Non-Progressive Congenital Ataxias with Neurodegeneration.

Published in:

International Journal of Molecular Sciences, 2021, v. 22, n. 5, p. 2505, doi. 10.3390/ijms22052505

By:

Sancho, Paula;
Andrés-Bordería, Amparo;
Gorría-Redondo, Nerea;
Llano, Katia;
Martínez-Rubio, Dolores;
Yoldi-Petri, María Eugenia;
Blumkin, Luba;
Rodríguez de la Fuente, Pablo;
Gil-Ortiz, Fernando;
Fernández-Murga, Leonor;
Sánchez-Monteagudo, Ana;
Lupo, Vincenzo;
Pérez-Dueñas, Belén;
Espinós, Carmen;
Aguilera-Albesa, Sergio;
Lazzarino, Giuseppe

Publication type:

Article

Distal hereditary motor neuronopathy as a new phenotype associated with variants in BAG3.

Published in:

Journal of Neurology, 2024, v. 271, n. 2, p. 986, doi. 10.1007/s00415-023-12039-9

By:

de Fuenmayor-Fernández de la Hoz, Carlos Pablo;
Lupo, Vincenzo;
Bermejo-Guerrero, Laura;
Martín-Jiménez, Paloma;
Hernández-Laín, Aurelio;
Olivé, Montse;
Gallardo, Eduard;
Esteban-Pérez, Jesús;
Espinós, Carmen;
Domínguez-González, Cristina

Publication type:

Article

Sh3tc2 deficiency affects neuregulin-1/ErbB signaling.

Published in:

Glia (0894-1491), 2013, v. 61, n. 7, p. 1041, doi. 10.1002/glia.22493

By:

Gouttenoire, Estelle Arnaud;
Lupo, Vincenzo;
Calpena, Eduardo;
Bartesaghi, Luca;
Schüpfer, Fanny;
Médard, Jean‐Jacques;
Maurer, Fabienne;
Beckmann, Jacques S.;
Senderek, Jan;
Palau, Francesc;
Espinós, Carmen;
Chrast, Roman

Publication type:

Article

Prevalence of 2314delG mutation in Spanish patients with Ushersyndrome type II (USH2).

Published in:

Ophthalmic Genetics, 2000, v. 21, n. 2, p. 123, doi. 10.1076/1381-6810(200006)21:2;1-8;FT123

By:

Beneyto, Magdalena;
Cuevas, José M.;
Millán, José M.;
Espinós, Carmen;
Mateu, Emilia;
González-Cabo, Pilar;
Baiget, Montserrat;
Doménech, Montserrat;
Bernal, Sara;
Ayuso, Carmen;
García-Sandoval, Blanca;
Trujillo, Ma José;
Borrego, Salud;
Antiñolo, Guillermo;
Carballo, Miguel;
Nájera, Carmen

Publication type:

Article

Ancient origin of the CTH alelle carrying the c.200C>T (p.T67I) variant in patients with cystathioninuria Espinós et al.

Published in:

Clinical Genetics, 2010, v. 78, n. 6, p. 554, doi. 10.1111/j.1399-0004.2010.01431.x

By:

Espinós, Carmen;
García-Cazorla, A.;
Martínez-Rubio, D.;
Martínez-Martínez, E.;
Vilaseca, M. A.;
Pérez-Dueñas, B.;
Kožich, V.;
Palau, F.;
Artuch, R.

Publication type:

Article

Charcot–Marie–Tooth disease due to MORC2 mutations in Spain.

Published in:

European Journal of Neurology, 2021, v. 28, n. 9, p. 3001, doi. 10.1111/ene.15001

By:

Sivera, Rafael;
Lupo, Vincenzo;
Frasquet, Marina;
Argente‐Escrig, Herminia;
Alonso‐Pérez, Jorge;
Díaz‐Manera, Jordi;
Querol, Luis;
del Mar García‐Romero, María;
Ignacio Pascual, Samuel;
García‐Sobrino, Tania;
Paradas, Carmen;
Francisco Vázquez‐Costa, Juan;
Muelas, Nuria;
Millet, Elvira;
Jesús Vílchez, Juan;
Espinós, Carmen;
Sevilla, Teresa

Publication type:

Article

Distal hereditary motor neuropathies: Mutation spectrum and genotype–phenotype correlation.

Published in:

European Journal of Neurology, 2021, v. 28, n. 4, p. 1334, doi. 10.1111/ene.14700

By:

Frasquet, Marina;
Rojas‐García, Ricard;
Argente‐Escrig, Herminia;
Vázquez‐Costa, Juan Francisco;
Muelas, Nuria;
Vílchez, Juan Jesús;
Sivera, Rafael;
Millet, Elvira;
Barreiro, Marisa;
Díaz‐Manera, Jordi;
Turon‐Sans, Janina;
Cortés‐Vicente, Elena;
Querol, Luis;
Ramírez‐Jiménez, Laura;
Martínez‐Rubio, Dolores;
Sánchez‐Monteagudo, Ana;
Espinós, Carmen;
Sevilla, Teresa;
Lupo, Vincenzo

Publication type:

Article

Q1311X: a novel nonsense mutation of putative ancient origin in the von Willebrand factor gene.

Published in:

British Journal of Haematology, 2000, v. 111, n. 2, p. 552, doi. 10.1046/j.1365-2141.2000.02410.x

By:

Casaña, Pilar;
Martínez, Francisco;
Haya, Saturnino;
Lorenzo, J. Ignacio;
Espinós, Carmen;
Aznar, José A.

Publication type:

Article

A newly distal hereditary motor neuropathy caused by a rare AIFM1 mutation.

Published in:

Neurogenetics, 2017, v. 18, n. 4, p. 245, doi. 10.1007/s10048-017-0524-6

By:

Sancho, Paula;
Sánchez-Monteagudo, Ana;
Collado, Antonio;
Marco-Marín, Clara;
Domínguez-González, Cristina;
Camacho, Ana;
Knecht, Erwin;
Espinós, Carmen;
Lupo, Vincenzo

Publication type:

Article

A novel TRMT5 mutation causes a complex inherited neuropathy syndrome: The role of nerve pathology in defining a demyelinating neuropathy.

Published in:

Neuropathology & Applied Neurobiology, 2022, v. 48, n. 5, p. 1, doi. 10.1111/nan.12817

By:

Argente‐Escrig, Herminia;
Vílchez, Juan J.;
Frasquet, Marina;
Muelas, Nuria;
Azorín, Inmaculada;
Vílchez, Roger;
Millet‐Sancho, Elvira;
Pitarch, Inmaculada;
Tomás‐Vila, Miguel;
Vázquez‐Costa, Juan F.;
Mas‐Estellés, Fernando;
Marco‐Marín, Clara;
Espinós, Carmen;
Serrano‐Lorenzo, Pablo;
Martin, Miguel A.;
Lupo, Vincenzo;
Sevilla, Teresa

Publication type:

Article

New insights into the genetics of 5-oxoprolinase deficiency and further evidence that it is a benign biochemical condition.

Published in:

European Journal of Pediatrics, 2015, v. 174, n. 3, p. 407, doi. 10.1007/s00431-014-2397-0

By:

Calpena, Eduardo;
Deshpande, Anup;
Yap, Sufin;
Kumar, Akhilesh;
Manning, Nigel;
Bachhawat, Anand;
Espinós, Carmen

Publication type:

Article

Autosomal recessive cerebellar ataxias.

Published in:

Orphanet Journal of Rare Diseases, 2006, v. 1, p. 47, doi. 10.1186/1750-1172-1-47

By:

Palau, Francesc;
Espinós, Carmen

Publication type:

Article

Characterization of CoQ biosynthesis in fibroblasts of patients with primary and secondary CoQ deficiency.

Published in:

Journal of Inherited Metabolic Disease, 2014, v. 37, n. 1, p. 53, doi. 10.1007/s10545-013-9620-4

By:

Buján, Nuria;
Arias, Angela;
Montero, Raquel;
García-Villoria, Judit;
Lissens, Willy;
Seneca, Sara;
Espinós, Carmen;
Navas, Plácido;
Meirleir, Linda;
Artuch, Rafael;
Briones, Paz;
Ribes, Antonia

Publication type:

Article

Ancient origin of the CAG expansion causing Huntington disease in a Spanish population.

Published in:

Human Mutation, 2005, v. 25, n. 5, p. 453, doi. 10.1002/humu.20167

By:

García-Planells, Javier;
Burguera, Juan A.;
Solís, Pilar;
Millán, José M.;
Ginestar, Damián;
Palau, Francesc;
Espinós, Carmen

Publication type:

Article

Profile of plasma microRNAs as a potential biomarker of Wilson's disease.

Published in:

Journal of Gastroenterology, 2024, v. 59, n. 10, p. 921, doi. 10.1007/s00535-024-02135-6

By:

Sánchez-Monteagudo, Ana;
Ripollés, Edna;
Murillo, Oihana;
Domènech, Sofia;
Álvarez-Sauco, María;
Girona, Eva;
Sastre-Bataller, Isabel;
Bono, Ariadna;
García-Villarreal, Luis;
Tugores, Antonio;
García-García, Francisco;
González-Aseguinolaza, Gloria;
Berenguer, Marina;
Espinós, Carmen

Publication type:

Article

Wilson disease: revision of diagnostic criteria in a clinical series with great genetic homogeneity.

Published in:

Journal of Gastroenterology, 2021, v. 56, n. 1, p. 78, doi. 10.1007/s00535-020-01745-0

By:

García-Villarreal, Luis;
Hernández-Ortega, Andrea;
Sánchez-Monteagudo, Ana;
Peña-Quintana, Luis;
Ramírez-Lorenzo, Teresa;
Riaño, Marta;
Moreno-Pérez, Raquel;
Monescillo, Alberto;
González-Santana, Daniel;
Quiñones, Ildefonso;
Sánchez-Villegas, Almudena;
Olmo-Quintana, Vicente;
Garay-Sánchez, Paloma;
Espinós, Carmen;
González, Jesús M.;
Tugores, Antonio

Publication type:

Article

Novel human pathological mutations.

Published in:

2009

By:

Martínez-Rubio, Dolores;
Millán, José;
Palau, Francesc;
Espinós, Carmen

Publication type:

Correction Notice

Sensory Tricks in Pantothenate Kinase‐Associated Neurodegeneration: Video‐Analysis of 43 Patients.

Published in:

Movement Disorders Clinical Practice, 2019, v. 6, n. 8, p. 704, doi. 10.1002/mdc3.12842

By:

Martins, Joana;
Darling, Alejandra;
Garrido, Cristina;
Espinós, Carmen;
Martí, María José;
Dueñas, Belen Pérez;
Temudo, Teresa

Publication type:

Article

Mitochondrial Dysfunction, Oxidative Stress and Neuroinflammation in Neurodegeneration with Brain Iron Accumulation (NBIA).

Published in:

Antioxidants, 2020, v. 9, n. 10, p. 1020, doi. 10.3390/antiox9101020

By:

Hinarejos, Isabel;
Machuca, Candela;
Sancho, Paula;
Espinós, Carmen

Publication type:

Article

Mitochondrial Dysfunction, Oxidative Stress and Neuroinflammation in Neurodegeneration with Brain Iron Accumulation (NBIA).

Published in:

Antioxidants, 2020, v. 9, n. 10, p. 1020, doi. 10.3390/antiox9101020

By:

Hinarejos, Isabel;
Machuca, Candela;
Sancho, Paula;
Espinós, Carmen

Publication type:

Article

Oxidative Stress, a Crossroad between Rare Diseases and Neurodegeneration.

Published in:

Antioxidants, 2020, v. 9, n. 4, p. 313, doi. 10.3390/antiox9040313

By:

Espinós, Carmen;
Galindo, Máximo Ibo;
García-Gimeno, María Adelaida;
Ibáñez-Cabellos, José Santiago;
Martínez-Rubio, Dolores;
Millán, José María;
Rodrigo, Regina;
Sanz, Pascual;
Seco-Cervera, Marta;
Sevilla, Teresa;
Tapia, Andrea;
Pallardó, Federico V.

Publication type:

Article

Mutations in the MORC2 gene cause axonal Charcot-Marie-Tooth disease.

Published in:

2016

By:

Sevilla, Teresa;
Lupo, Vincenzo;
Martínez-Rubio, Dolores;
Sancho, Paula;
Sivera, Rafael;
Chumillas, María J.;
García-Romero, Mar;
Pascual-Pascual, Samuel I.;
Muelas, Nuria;
Dopazo, Joaquín;
Vílchez, Juan J.;
Palau, Francesc;
Espinós, Carmen

Publication type:

journal article

Vocal cord paresis and diaphragmatic dysfunction are severe and frequent symptoms of GDAP1-associated neuropathy.

Published in:

Brain: A Journal of Neurology, 2008, v. 131, n. 11, p. 3051, doi. 10.1093/brain/awn228

By:

Teresa Sevilla;
Teresa Jaijo;
Dolores Nauffal;
Diego Collado;
María José Chumillas;
Juan J. Vilchez;
Nuria Muelas;
Luis Bataller;
Rosalía Domenech;
Carmen Espinós;
Francesc Palau

Publication type:

Article

Pediatric inherited peripheral neuropathy: a prospective study at a Spanish referral center.

Published in:

Annals of Clinical & Translational Neurology, 2021, v. 8, n. 9, p. 1809, doi. 10.1002/acn3.51432

By:

Argente‐Escrig, Herminia;
Frasquet, Marina;
Vázquez‐Costa, Juan Francisco;
Millet‐Sancho, Elvira;
Pitarch, Inmaculada;
Tomás‐Vila, Miguel;
Espinós, Carmen;
Lupo, Vincenzo;
Sevilla, Teresa

Publication type:

Article

Impaired proteasome activity and neurodegeneration with brain iron accumulation in FBXO7 defect.

Published in:

Annals of Clinical & Translational Neurology, 2020, v. 7, n. 8, p. 1436, doi. 10.1002/acn3.51095

By:

Correa‐Vela, Marta;
Lupo, Vincenzo;
Montpeyó, Marta;
Sancho, Paula;
Marcé‐Grau, Anna;
Hernández‐Vara, Jorge;
Darling, Alejandra;
Jenkins, Alison;
Fernández‐Rodríguez, Sandra;
Tello, Cristina;
Ramírez‐Jiménez, Laura;
Pérez, Belén;
Sánchez‐Montáñez, Ángel;
Macaya, Alfons;
Sobrido, María J.;
Martinez‐Vicente, Marta;
Pérez‐Dueñas, Belén;
Espinós, Carmen

Publication type:

Article

Evolutionary History of the Smyd Gene Family in Metazoans: A Framework to Identify the Orthologs of Human Smyd Genes in Drosophila and Other Animal Species.

Published in:

PLoS ONE, 2015, v. 10, n. 7, p. 1, doi. 10.1371/journal.pone.0134106

By:

Calpena, Eduardo;
Palau, Francesc;
Espinós, Carmen;
Galindo, Máximo Ibo

Publication type:

Article

Search for mutations in a segment of the exon 28 of the human von Willebrand factor gene: New mutations, R1315C and R1341W, associated with type 2M and 2B variants.

Published in:

American Journal of Hematology, 1998, v. 59, n. 1, p. 57, doi. 10.1002/(SICI)1096-8652(199809)59:1<57::AID-AJH11>3.0.CO;2-Z

By:

Casaña, Pilar;
Martínez, Francisco;
Espinós, Carmen;
Haya, Saturnino;
Lorenzo, José I.;
Aznar, José A.

Publication type:

Article

Complexity of the Hereditary Motor and Sensory Neuropathies.

Published in:

Journal of Child Neurology, 2015, v. 30, n. 11, p. 1544, doi. 10.1177/0883073815571049

By:

Lupo, Vincenzo;
Pascual-Pascual, Samuel I.;
Sancho, Paula;
Calpena, Eduardo;
Gutiérrez-Molina, Manuel;
Mateo-Martínez, Gonzalo;
Espinós, Carmen;
Arriola-Pereda, Gema

Publication type:

Article

Cover Image, Volume 39, Issue 3.

Published in:

Human Mutation, 2018, v. 39, n. 3, p. i, doi. 10.1002/humu.23405

By:

Abbott, Jamie A.;
Meyer‐Schuman, Rebecca;
Lupo, Vincenzo;
Feely, Shawna;
Mademan, Inès;
Oprescu, Stephanie N.;
Griffin, Laurie B.;
Alberti, M. Antonia;
Casasnovas, Carlos;
Aharoni, Sharon;
Basel‐Vanagaite, Lina;
Züchner, Stephan;
De Jonghe, Peter;
Baets, Jonathan;
Shy, Michael E.;
Espinós, Carmen;
Demeler, Borries;
Antonellis, Anthony;
Francklyn, Christopher

Publication type:

Article

Substrate interaction defects in histidyl‐tRNA synthetase linked to dominant axonal peripheral neuropathy.

Published in:

Human Mutation, 2018, v. 39, n. 3, p. 415, doi. 10.1002/humu.23380

By:

Abbott, Jamie A.;
Meyer‐Schuman, Rebecca;
Lupo, Vincenzo;
Feely, Shawna;
Mademan, Inès;
Oprescu, Stephanie N.;
Griffin, Laurie B.;
Alberti, M. Antonia;
Casasnovas, Carlos;
Aharoni, Sharon;
Basel‐Vanagaite, Lina;
Züchner, Stephan;
De Jonghe, Peter;
Baets, Jonathan;
Shy, Michael E.;
Espinós, Carmen;
Demeler, Borries;
Antonellis, Anthony;
Francklyn, Christopher

Publication type:

Article

Characterization of molecular mechanisms underlying the axonal Charcot–Marie–Tooth neuropathy caused by MORC2 mutations.

Published in:

Human Molecular Genetics, 2019, v. 28, n. 10, p. 1629, doi. 10.1093/hmg/ddz006

By:

Sancho, Paula;
Bartesaghi, Luca;
Miossec, Olivia;
García-García, Francisco;
Ramírez-Jiménez, Laura;
Siddell, Anna;
Åkesson, Elisabet;
Hedlund, Eva;
Laššuthová, Petra;
Pascual-Pascual, Samuel I;
Sevilla, Teresa;
Kennerson, Marina;
Lupo, Vincenzo;
Chrast, Roman;
Espinós, Carmen

Publication type:

Article

Junctophilin-1 is a modifier gene of GDAP1-related Charcot–Marie–Tooth disease.

Published in:

Human Molecular Genetics, 2015, v. 24, n. 1, p. 213, doi. 10.1093/hmg/ddu440

By:

Pla-Martín, David;
Calpena, Eduardo;
Lupo, Vincenzo;
Márquez, Celedonio;
Rivas, Eloy;
Sivera, Rafael;
Sevilla, Teresa;
Palau, Francesc;
Espinós, Carmen

Publication type:

Article

Missense mutations in the SH3TC2 protein causing Charcot-Marie-Tooth disease type 4C affect its localization in the plasma membrane and endocytic pathway.

Published in:

Human Molecular Genetics, 2009, v. 18, n. 23, p. 4603, doi. 10.1093/hmg/ddp427

By:

Lupo, Vincenzo;
Galindo, Máximo I.;
Martínez-Rubio, Dolores;
Sevilla, Teresa;
Vílchez, Juan J.;
Palau, Francesc;
Espinós, Carmen

Publication type:

Article

Molecular diagnosis of coenzyme Q<sub>10</sub> deficiency.

Published in:

Expert Review of Molecular Diagnostics, 2015, v. 15, n. 8, p. 1049, doi. 10.1586/14737159.2015.1062727

By:

Yubero, Delia;
Montero, Raquel;
Armstrong, Judith;
Espinós, Carmen;
Palau, Francesc;
Santos-Ocaña, Carlos;
Salviati, Leonardo;
Navas, Placido;
Artuch, Rafael

Publication type:

Article