Hasil Pencarian - Mònica Coll

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  1. 1
    Valvulopathies and Genetics: Where are We?

    Valvulopathies and Genetics: Where are We? oleh Mònica Coll, Anna Fernández-Falgueras, Anna Iglesias, Ramon Brugada

    Diterbitkan 2024-01-01
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  2. 2
    Update on the Genetic Basis of Sudden Unexpected Death in Epilepsy

    Update on the Genetic Basis of Sudden Unexpected Death in Epilepsy oleh Monica Coll, Antonio Oliva, Simone Grassi, Ramon Brugada, Oscar Campuzano

    Diterbitkan 2019-04-01
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  3. 3
    The brain–heart interaction in epilepsy: implications for diagnosis, therapy, and SUDEP prevention

    The brain–heart interaction in epilepsy: implications for diagnosis, therapy, and SUDEP prevention oleh Giorgio Costagliola, Alessandro Orsini, Monica Coll, Ramon Brugada, Pasquale Parisi, Pasquale Striano

    Diterbitkan 2021-07-01
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  4. 4
    The importance of variant reinterpretation in inherited cardiovascular diseases: Establishing the optimal timeframe.

    The importance of variant reinterpretation in inherited cardiovascular diseases: Establishing the optimal timeframe. oleh Anna Fernandez-Falgueras, Monica Coll, Anna Iglesias, Coloma Tiron, Oscar Campuzano, Ramon Brugada

    Diterbitkan 2024-01-01
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  5. 5
    Update on the Diagnostic Pitfalls of Autopsy and Post-Mortem Genetic Testing in Cardiomyopathies

    Update on the Diagnostic Pitfalls of Autopsy and Post-Mortem Genetic Testing in Cardiomyopathies oleh Simone Grassi, Oscar Campuzano, Mònica Coll, Francesca Cazzato, Georgia Sarquella-Brugada, Riccardo Rossi, Vincenzo Arena, Josep Brugada, Ramon Brugada, Antonio Oliva

    Diterbitkan 2021-04-01
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  6. 6
    Understanding the socio-institutional context to support adaptation for future water security in forest landscapes

    Understanding the socio-institutional context to support adaptation for future water security in forest landscapes oleh Tahia Devisscher, Raffaele Vignola, Monica Coll Besa, Romy Cronenbold, Nelson Pacheco, Ralf Schillinger, Virginia Canedi, Claudio Sandoval, Diego Gonzalez, Grégoire Leclerc

    Diterbitkan 2016-12-01
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  7. 7
    Sudden Death without a Clear Cause after Comprehensive Investigation: An Example of Forensic Approach to Atypical/Uncertain Findings

    Sudden Death without a Clear Cause after Comprehensive Investigation: An Example of Forensic Approach to Atypical/Uncertain Findings oleh Simone Grassi, Mònica Coll Vidal, Oscar Campuzano, Vincenzo Arena, Alessandro Alfonsetti, Sabina Strano Rossi, Francesca Scarnicci, Anna Iglesias, Ramon Brugada, Antonio Oliva

    Diterbitkan 2021-05-01
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  8. 8
    Genetic Analysis of Arrhythmogenic Diseases in the Era of NGS: The Complexity of Clinical Decision-Making in Brugada Syndrome.

    Genetic Analysis of Arrhythmogenic Diseases in the Era of NGS: The Complexity of Clinical Decision-Making in Brugada Syndrome. oleh Catarina Allegue, Mònica Coll, Jesus Mates, Oscar Campuzano, Anna Iglesias, Beatriz Sobrino, Maria Brion, Jorge Amigo, Angel Carracedo, Pedro Brugada, Josep Brugada, Ramon Brugada

    Diterbitkan 2015-01-01
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  9. 9
    Incomplete Penetrance and Variable Expressivity: Hallmarks in Channelopathies Associated with Sudden Cardiac Death

    Incomplete Penetrance and Variable Expressivity: Hallmarks in Channelopathies Associated with Sudden Cardiac Death oleh Monica Coll, Alexandra Pérez-Serra, Jesus Mates, Bernat del Olmo, Marta Puigmulé, Anna Fernandez-Falgueras, Anna Iglesias, Ferran Picó, Laura Lopez, Ramon Brugada, Oscar Campuzano

    Diterbitkan 2017-12-01
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  10. 10
    Rare Titin (TTN) Variants in Diseases Associated with Sudden Cardiac Death

    Rare Titin (TTN) Variants in Diseases Associated with Sudden Cardiac Death oleh Oscar Campuzano, Olallo Sanchez-Molero, Irene Mademont-Soler, Helena Riuró, Catarina Allegue, Monica Coll, Alexandra Pérez-Serra, Jesus Mates, Ferran Picó, Anna Iglesias, Ramon Brugada

    Diterbitkan 2015-10-01
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  11. 11
    Identification of Genetic Alterations, as Causative Genetic Defects in Long QT Syndrome, Using Next Generation Sequencing Technology.

    Identification of Genetic Alterations, as Causative Genetic Defects in Long QT Syndrome, Using Next Generation Sequencing Technology. oleh Oscar Campuzano, Georgia Sarquella-Brugada, Irene Mademont-Soler, Catarina Allegue, Sergi Cesar, Carles Ferrer-Costa, Monica Coll, Jesus Mates, Anna Iglesias, Josep Brugada, Ramon Brugada

    Diterbitkan 2014-01-01
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  12. 12
    Eosinophilic Infiltration of the Sino-Atrial Node in Sudden Cardiac Death Caused by Long QT Syndrome

    Eosinophilic Infiltration of the Sino-Atrial Node in Sudden Cardiac Death Caused by Long QT Syndrome oleh Simone Grassi, Oscar Campuzano, Mònica Coll, Francesca Cazzato, Anna Iglesias, Francesco Ausania, Francesca Scarnicci, Georgia Sarquella-Brugada, Josep Brugada, Vincenzo Arena, Antonio Oliva, Ramon Brugada

    Diterbitkan 2022-10-01
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  13. 13
    Targeted next-generation sequencing provides novel clues for associated epilepsy and cardiac conduction disorder/SUDEP.

    Targeted next-generation sequencing provides novel clues for associated epilepsy and cardiac conduction disorder/SUDEP. oleh Monica Coll, Pasquale Striano, Carles Ferrer-Costa, Oscar Campuzano, Jesús Matés, Bernat Del Olmo, Anna Iglesias, Alexandra Pérez-Serra, Irene Mademont, Ferran Picó, Antonio Oliva, Ramon Brugada

    Diterbitkan 2017-01-01
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  14. 14
    Role of genetic and electrolyte abnormalities in prolonged QTc interval and sudden cardiac death in end-stage renal disease patients.

    Role of genetic and electrolyte abnormalities in prolonged QTc interval and sudden cardiac death in end-stage renal disease patients. oleh Monica Coll, Carles Ferrer-Costa, Sara Pich, Catarina Allegue, Emilio Rodrigo, Gema Fernández-Fresnedo, Paloma Barreda, Jesus Mates, Angel Luis Martinez de Francisco, Israel Ortega, Anna Iglesias, Oscar Campuzano, Eduardo Salas, Manuel Arias, Ramon Brugada

    Diterbitkan 2018-01-01
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  15. 15
    Reanalysis and reclassification of rare genetic variants associated with inherited arrhythmogenic syndromes

    Reanalysis and reclassification of rare genetic variants associated with inherited arrhythmogenic syndromes oleh Oscar Campuzano, Georgia Sarquella-Brugada, Anna Fernandez-Falgueras, Mónica Coll, Anna Iglesias, Carles Ferrer-Costa, Sergi Cesar, Elena Arbelo, Ana García-Álvarez, Paloma Jordà, Rocío Toro, Coloma Tiron de Llano, Simone Grassi, Antonio Oliva, Josep Brugada, Ramon Brugada

    Diterbitkan 2020-04-01
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  16. 16
    Unpredicted Aberrant Splicing Products Identified in Postmortem Sudden Cardiac Death Samples

    Unpredicted Aberrant Splicing Products Identified in Postmortem Sudden Cardiac Death Samples oleh Monica Coll, Anna Fernandez-Falgueras, Anna Iglesias, Bernat del Olmo, Laia Nogue-Navarro, Adria Simon, Alexandra Perez Serra, Marta Puigmule, Laura Lopez, Ferran Pico, Monica Corona, Marta Vallverdu-Prats, Coloma Tiron, Oscar Campuzano, Josep Castella, Ramon Brugada, Mireia Alcalde

    Diterbitkan 2022-10-01
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  17. 17
    Molecular autopsy: Twenty years of post-mortem diagnosis in sudden cardiac death

    Molecular autopsy: Twenty years of post-mortem diagnosis in sudden cardiac death oleh Estefanía Martínez-Barrios, Estefanía Martínez-Barrios, Estefanía Martínez-Barrios, Simone Grassi, María Brión, María Brión, María Brión, María Brión, Rocío Toro, Sergi Cesar, Sergi Cesar, Sergi Cesar, José Cruzalegui, José Cruzalegui, José Cruzalegui, Mònica Coll, Mònica Coll, Mireia Alcalde, Mireia Alcalde, Ramon Brugada, Ramon Brugada, Ramon Brugada, Ramon Brugada, Andrea Greco, Andrea Greco, María Luisa Ortega-Sánchez, María Luisa Ortega-Sánchez, Eneko Barberia, Eneko Barberia, Antonio Oliva, Georgia Sarquella-Brugada, Georgia Sarquella-Brugada, Georgia Sarquella-Brugada, Georgia Sarquella-Brugada, Oscar Campuzano, Oscar Campuzano, Oscar Campuzano

    Diterbitkan 2023-02-01
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  18. 18
    Unexpected complexity in the molecular diagnosis of spastic paraplegia 11

    Unexpected complexity in the molecular diagnosis of spastic paraplegia 11 oleh Irene Mademont‐Soler, Susanna Esteba‐Castillo, Aida Jiménez‐Xifra, Berta Alemany, Núria Ribas‐Vidal, Maria Cutillas, Mònica Coll, Mel·lina Pinsach, Sara Pagans, Mireia Alcalde, Marina Viñas‐Jornet, Mercedes Montero‐Vale, Marta deCastro‐Miró, Jairo Rodríguez, Lluís Armengol, Xavier Queralt, María Obón

    Diterbitkan 2024-06-01
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  19. 19
    Implementing a New Algorithm for Reinterpretation of Ambiguous Variants in Genetic Dilated Cardiomyopathy

    Implementing a New Algorithm for Reinterpretation of Ambiguous Variants in Genetic Dilated Cardiomyopathy oleh Alexandra Pérez-Serra, Rocío Toro, Estefanía Martinez-Barrios, Anna Iglesias, Anna Fernandez-Falgueras, Mireia Alcalde, Mónica Coll, Marta Puigmulé, Bernat del Olmo, Ferran Picó, Laura Lopez, Elena Arbelo, Sergi Cesar, Coloma Tiron de Llano, Alipio Mangas, Josep Brugada, Georgia Sarquella-Brugada, Ramon Brugada, Oscar Campuzano

    Diterbitkan 2024-03-01
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  20. 20
    Comprehensive Genetic Characterization of a Spanish Brugada Syndrome Cohort.

    Comprehensive Genetic Characterization of a Spanish Brugada Syndrome Cohort. oleh Elisabet Selga, Oscar Campuzano, Mel Lina Pinsach-Abuin, Alexandra Pérez-Serra, Irene Mademont-Soler, Helena Riuró, Ferran Picó, Mònica Coll, Anna Iglesias, Sara Pagans, Georgia Sarquella-Brugada, Paola Berne, Begoña Benito, Josep Brugada, José M Porres, Matilde López Zea, Víctor Castro-Urda, Ignacio Fernández-Lozano, Ramon Brugada

    Diterbitkan 2015-01-01
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