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Arrieta y Corera, Emilio [Author]; Camprodón, Francisco [Author] ; Bayo, Maria [Performer]; Kraus, Alfredo [Performer]; Pons, Juan [Performer]; Baquerizo, Enrique [Performer]; Rodríiguez, Juan Jesús [Performer]; Santana, Encarna [Performer]; Pérez, Víctor Pablo [Performer] Coro de Cámara de Tenerife Santa Cruz de Tenerife, Conservatorio Superior de Música de Tenerife Santa Cruz de Tenerife Coro, Rondalla de Tenerife Santa Cruz de Tenerife, Orquesta Sinfónica de Tenerife

Marina : Ópera en tres actos. Versión integral sin diálogos (2 CD)

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[S.l.]: Auvidis, P 1999

Published in: Valois Auvidis
Ezquieta, Begoña; Santomé, José L.; Carcavilla, Atilano; Guillén-Navarro, Encarna; Pérez-Aytés, Antonio; Sánchez del Pozo, Jaime; García-Miñaur, Sixto; Castillo, Emilia; Alonso, Milagros; Vendrell, Teresa; Santana, Alfredo; Maroto, Enrique; Galbis, Liliana

Alteraciones de los genes de la vía RAS-MAPK en 200 pacientes españoles con síndrome de Noonan y otros síndromes neurocardiofaciocutáneos. Genotipo y cardiopatía

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Elsevier BV, 2012

Published in: Revista Española de Cardiología
Ezquieta, Begoña; Santomé, José L.; Carcavilla, Atilano; Guillén-Navarro, Encarna; Pérez-Aytés, Antonio; Sánchez del Pozo, Jaime; García-Miñaur, Sixto; Castillo, Emilia; Alonso, Milagros; Vendrell, Teresa; Santana, Alfredo; Maroto, Enrique; Galbis, Liliana

Alterations in RAS-MAPK Genes in 200 Spanish Patients With Noonan and Other Neuro-Cardio-Facio-Cutaneous Syndromes. Genotype and Cardiopathy

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Elsevier BV, 2012

Published in: Revista Española de Cardiología (English Edition)
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; Muñoz-Hernández, Hugo; Nevado, Julián; Tenorio-Castano, Jair; Lapunzina, Pablo

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

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MDPI AG, 2023

Published in: Genes
Perea-Romero, Irene; Gordo, Gema; Iancu, Ionut F.; Del Pozo-Valero, Marta; Almoguera, Berta; Blanco-Kelly, Fiona; Carreño, Ester; Jimenez-Rolando, Belen; Lopez-Rodriguez, Rosario; Lorda-Sanchez, Isabel; Martin-Merida, Inmaculada; Pérez de Ayala, Lucia; Riveiro-Alvarez, Rosa; Rodriguez-Pinilla, Elvira; Tahsin-Swafiri, Saoud; Trujillo-Tiebas, Maria J.; Bustamante-Aragones, Ana; Cardero-Merlo, Rocio; Fernandez-Sanchez, Ruth; Gallego-Merlo, Jesus; Garcia-Vara, Ines; Gimenez-Pardo, Ascension; Horcajada-Burgos, Laura; Infantes-Barbero, Fernando; [...]

Author Correction: Genetic landscape of 6089 inherited retinal dystrophies affected cases in Spain and their therapeutic and extended epidemiological implications

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Springer Science and Business Media LLC, 2021

Published in: Scientific Reports
Perea-Romero, Irene; Gordo, Gema; Iancu, Ionut F.; Del Pozo-Valero, Marta; Almoguera, Berta; Blanco-Kelly, Fiona; Carreño, Ester; Jimenez-Rolando, Belen; Lopez-Rodriguez, Rosario; Lorda-Sanchez, Isabel; Martin-Merida, Inmaculada; Pérez de Ayala, Lucia; Riveiro-Alvarez, Rosa; Rodriguez-Pinilla, Elvira; Tahsin-Swafiri, Saoud; Trujillo-Tiebas, Maria J.; Bustamante-Aragones, Ana; Cardero-Merlo, Rocio; Fernandez-Sanchez, Ruth; Gallego-Merlo, Jesus; Garcia-Vara, Ines; Gimenez-Pardo, Ascension; Horcajada-Burgos, Laura; Infantes-Barbero, Fernando; [...]

Genetic landscape of 6089 inherited retinal dystrophies affected cases in Spain and their therapeutic and extended epidemiological implications

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Springer Science and Business Media LLC, 2021

Published in: Scientific Reports
Stolarova, Lenka; Kleiblova, Petra; Zemankova, Petra; Stastna, Barbora; Janatova, Marketa; Soukupova, Jana; Achatz, Maria Isabel; Ambrosone, Christine; Apostolou, Paraskevi; Arun, Banu K.; Auer, Paul; Barnard, Mollie; Bertelsen, Birgitte; Matsuda, Koichi; Kamatani, Yoichiro; Morisaki, Takayuki; Nagai, Akiko; Muto, Kaori; Murakami, Yoshinori; Furukawa, Yoichi; Yamanashi, Yuji; Nakamura, Yusuke; Mushiroda, Taisei; Momozawa, Yukihide; [...]

ENIGMACHEK2gether Project: A Comprehensive Study Identifies Functionally ImpairedCHEK2Germline Missense Variants Associated with Increased Breast Cancer Risk

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American Association for Cancer Research (AACR), 2023

Published in: Clinical Cancer Research
Tenorio, Jair; Alarcón, Pablo; Arias, Pedro; Dapía, Irene; García-Miñaur, Sixto; Palomares Bralo, María; Campistol, Jaume; Climent, Salvador; Valenzuela, Irene; Ramos, Sergio; Monseny, Antonio Martínez; Grondona, Fermina López; Botet, Javier; Serrano, Mercedes; Solís, Mario; Santos-Simarro, Fernando; Álvarez, Sara; Teixidó-Tura, Gisela; Fernández Jaén, Alberto; Gordo, Gema; Bardón Rivera, María Belén; Nevado, Julián; Hernández, Alicia; Cigudosa, Juan C.; [...]

Further delineation of neuropsychiatric findings in Tatton-Brown-Rahman syndrome due to disease-causing variants in DNMT3A: seven new patients

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Springer Science and Business Media LLC, 2020

Published in: European Journal of Human Genetics

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Marina : Ópera en tres actos. Versión integral sin diálogos (2 CD)

Bookmarks

Alteraciones de los genes de la vía RAS-MAPK en 200 pacientes españoles con síndrome de Noonan y otros síndromes neurocardiofaciocutáneos. Genotipo y cardiopatía

Access

Bookmarks

Alterations in RAS-MAPK Genes in 200 Spanish Patients With Noonan and Other Neuro-Cardio-Facio-Cutaneous Syndromes. Genotype and Cardiopathy

Access

Bookmarks

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

Access

Bookmarks

Author Correction: Genetic landscape of 6089 inherited retinal dystrophies affected cases in Spain and their therapeutic and extended epidemiological implications

Access

Bookmarks

Genetic landscape of 6089 inherited retinal dystrophies affected cases in Spain and their therapeutic and extended epidemiological implications

Access

Bookmarks

ENIGMACHEK2gether Project: A Comprehensive Study Identifies Functionally ImpairedCHEK2Germline Missense Variants Associated with Increased Breast Cancer Risk

Access

Bookmarks

Further delineation of neuropsychiatric findings in Tatton-Brown-Rahman syndrome due to disease-causing variants in DNMT3A: seven new patients

Access

Bookmarks

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