Search Results - Elliott, Perry M.
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Genetic basis of right and left ventricular heart shape
Article | by Burns, Richard; Young, William J.; Aung, Nay; Lopes, Luis R.; Elliott, Perry M.; Syrris, Petros; Barriales-Villa, Roberto; Sohrabi, Catrin; Petersen, Steffen E.; Ramírez, Julia; Young, Alistair; Munroe, Patricia B. | Published 2024 | -
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Deletions of specific exons of FHOD3 detected by next‐generation sequencing are associated with hypertrophic cardiomyopathy
Article | by Ochoa, Juan P.; Lopes, Luis R.; Perez Barbeito, Marlene; Cazón Varela, Laura; Torre Carpente, Maria M. de la; Sonicheva‐Paterson, Natalia; Uña Iglesias, David de; Quinn, Ellen; Kuzmina‐Krutetskaya, Svetlana; Garrote Adrados, José Antonio; Elliott, Perry M.; Monserrat, Lorenzo | Published 2020 | -
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The effect of enzyme replacement therapy on clinical outcomes in female patients with Fabry disease: A systematic literature review by a European panel of experts
Article | by Germain, Dominique P.; Arad, Michael; Burlina, Alessandro; Elliott, Perry M.; Falissard, Bruno; Feldt-Rasmussen, Ulla; Hilz, Max J.; Hughes, Derralynn A.; Ortiz Arduán, Alberto; Wanner, Christoph; Weidemann, Frank; Spada, Marco | Published 2018 | -
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Alpha-protein kinase 3 (ALPK3) truncating variants are a cause of autosomal dominant hypertrophic cardiomyopathy.
Article | by Lopes, Luis R; Garcia-Hernández, Soledad; Lorenzini, Massimiliano; Futema, Marta; Chumakova, Olga; Zateyshchikov, Dmitry; Isidoro-Garcia, Maria; Villacorta, Eduardo; Escobar-Lopez, Luis; Garcia-Pavia, Pablo; Bilbao, Raquel; Dobarro, David; Sandin-Fuentes, Maria; Catalli, Claudio; Gener Querol, Blanca; Mezcua, Ainhoa; Garcia Pinilla, Jose; Bloch Rasmussen, Torsten; Ferreira-Aguar, Ana; Revilla-Martí, Pablo; Basurte Elorz, Maria Teresa; Bautista Paves, Alicia; Ramon Gimeno, Juan; Figueroa, Ana Virginia; Franco-Gutierrez, Raul; Fuentes-Cañamero, Maria Eugenia; Martinez Moreno, Marina; Ortiz-Genga, Martin; Piqueras-Flores, Jesus; Analia Ramos, Karina; Rudzitis, Ainars; Ruiz-Guerrero, Luis; Stein, Ricardo; Triguero-Bocharán, Mayte; de la Higuera, Luis; Ochoa, Juan Pablo; Abu-Bonsrah, Dad; Kwok, Cecilia Y T; Smith, Jacob B; Porrello, Enzo R; Akhtar, Mohammed M; Jager, Joanna; Ashworth, Michael; Syrris, Petros; Elliott, David A; Monserrat, Lorenzo; Elliott, Perry M | Published 2021 | -
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Mutations in TRIM63 cause an autosomal-recessive form of hypertrophic cardiomyopathy
Article | by Salazar Mendiguchía, Joel; Ochoa, Juan Pablo; Palomino Doza, Julián; Domínguez, Fernando; Díez López, Carles; Akhtar, Mohammed; Ramiro León, Soraya; Clemente, María M.; Pérez Cejas, Antonia; Robledo, María; Gómez Díaz, Iria; Peña Peña, María Luisa; Climent, Vicente; Salmerón Martínez, Francisco; Hernández, Celestino; García Granja, Pablo Elpidio; Mogollón, M. Victoria; Cárdenas Reyes, Ivonne; Cicerchia, Marcos; García Giustiniani, Diego; Lamounier Jr., Arsonval; Gil Fournier, Belén; Díaz Flores, Felícitas; Salguero, Rafael; Santomé, Luis; Syrris, Petros; Olivé i Plana, Montserrat; Garcia Pavia, Pablo; Ortiz Genga, Martín; Elliott, Perry M.; Monserrat, Lorenzo; Genescopic Research Group | Published 2020 | -
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Mutations in TRIM63 cause an autosomal-recessive form of hypertrophic cardiomyopathy.
Article | by Salazar-Mendiguchía, Joel; Pablo Ochoa, Juan; Palomino-Doza, Julián; Domínguez, Fernando; Díez-López, Carles; Akhtar, Mohammed; Ramiro-León, Soraya; Clemente, María M.; Pérez-Cejas, Antonia; Robledo, María; Gómez-Díaz, Iria; Peña-Peña, María Luisa; Climent, Vicente; Salmerón-Martínez, Francisco; Hernández, Celestino; García-Granja, Pablo E.; Mogollón, M. Victoria; Cárdenas-Reyes, Ivonne; Cicerchia, Marcos; García-Giustiniani, Diego; Lamounier, Arsonval Jr.; Gil-Fournier, Belén; Díaz-Flores, Felícitas; Salguero, Rafael; Santomé, Luis; Syrris, Petros; Olivé, Montse; García Pavía, Pablo; Ortiz-Genga, Martín; Elliott, Perry M.; Monserrat, Lorenzo | Published 2020 | -
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Mutations in TRIM63 cause an autosomal-recessive form of hypertrophic cardiomyopathy
Article | by Salazar Mendiguchía, Joel; Ochoa, Juan Pablo; Palomino Doza, Julián; Domínguez, Fernando; Díez López, Carles; Akhtar, Mohammed; Ramiro León, Soraya; Clemente, María M.; Pérez Cejas, Antonia; Robledo, María; Gómez Díaz, Iria; Peña Peña, María Luisa; Climent, Vicente; Salmerón Martínez, Francisco; Hernández, Celestino; García Granja, Pablo Elpidio; Mogollón, M. Victoria; Cárdenas Reyes, Ivonne; Cicerchia, Marcos; García Giustiniani, Diego; Lamounier Jr., Arsonval; Gil Fournier, Belén; Díaz Flores, Felícitas; Salguero, Rafael; Santomé, Luis; Syrris, Petros; Olivé i Plana, Montserrat; Garcia Pavia, Pablo; Ortiz Genga, Martín; Elliott, Perry M.; Monserrat, Lorenzo; Genescopic Research Group | Published 2020 | -
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ESC EORP Cardiomyopathy Registry: real-life practice of genetic counselling and testing in adult cardiomyopathy patients
Article | by Helio, Tiina M.; Elliott, Perry M.; Koskenvuo, Juha W.; Gimeno, Juan R.; Tavazzi, Luigi; Tendera, Michal; Kaski, Juan Pablo; Mansencal, Nicolas; Bilinska, Zofia; Carr-White, Gerry; Damy, Thibaud; Frustaci, Andrea; Kindermann, Ingrid; Ripoll, Tomás; Čelutkienė, Jelena; Axelsson, Anna; Lorenzini, Massimiliano; Saad, Aly; Maggioni, Aldo P.; Laroche, Cecile; Caforio, Alida L. P.; Charron, Philippe; EORP Cardiomyopathy Registry Inves | Published 2020 | -
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ESC EORP Cardiomyopathy Registry: real-life practice of genetic counselling and testing in adult cardiomyopathy patients
Article | by Helio, Tiina M; Elliott, Perry M; Koskenvuo, Juha W; Gimeno, Juan R; Tavazzi, Luigi; Tendera, Michal; Kaski, Juan Pablo; Mansencal, Nicolas; Bilinska, Zofia; Carr-White, Gerry; Damy, Thibaud; Frustaci, Andrea; Kindermann, Ingrid; Ripoll-Vera, Tomás; Celutkiene, Jelena; Axelsson, Anna; Lorenzini, Massimiliano; Saad, Aly; Maggioni, Aldo P; Laroche, Cecile; Caforio, Alida LP; Charron, Philippe; EORP Cardiomyopathy Registry Inves | Published 2020 |
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Humans
Femenino
genetics
hypertrophic cardiomyopathy
Cardiomiopatía Hipertrófica
Cardiomyopathy, Hypertrophic
FHOD3
Factores de Riesgo
Female
Genotype
Hypertrophic cardiomyopathy
Mutation
Risk Factors
cardiomyopathies
formins
Adulto Joven
Anciano
Cardiomyopathies
Cardiomyopathy
Estudios de Seguimiento
Genetics
Masculino
Persona de Mediana Edad
Ventricular arrhythmia
sudden death
Adolescente
Adult
Adulto
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