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KCNH2 p.Gly262AlafsTer98: A New Threatening Variant Associated with Long QT Syndrome in a Spanish Cohort

Life (Basel, Switzerland), 2022-04, Vol.12 (4), p.556

2022

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Low voltage with high suspicion in athlete's heart

Europace (London, England), 2022-10, Vol.24 (9), p.1538-1538

2022

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Characterization of Left Ventricular Non-Compaction Cardiomyopathy

Journal of clinical medicine, 2020-08, Vol.9 (8), p.2524

2020

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Clinical Implications and Gender Differences of KCNQ1 p.Gly168Arg Pathogenic Variant in Long QT Syndrome

Journal of clinical medicine, 2020-11, Vol.9 (12), p.3846

2020

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Prevalence of positive ECG criteria in young competitive athletes: a single region experience

European heart journal, 2008-03, Vol.29 (5), p.680-681

2008

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Familial Hypercholesterolemia in Premature Acute Coronary Syndrome. Insights from CholeSTEMI Registry

Journal of clinical medicine, 2020-10, Vol.9 (11), p.3489

2020

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Different Phenotypes in Monozygotic Twins, Carriers of the Same Pathogenic Variant for Hypertrophic Cardiomyopathy

Life (Basel, Switzerland), 2022-08, Vol.12 (9), p.1346

2022

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Expresividad variable de una mutación fundadora en el gen EIF2AK4 en pacientes con enfermedad venooclusiva pulmonar hereditaria. Impacto en la supervivencia

Revista española de cardiologia, 2018-02, Vol.71 (2), p.86-94

2018

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Variable Expressivity of a Founder Mutation in the EIF2AK4 Gene in Hereditary Pulmonary Veno-occlusive Disease and Its Impact on Survival

Revista española de cardiología (English ed.), 2018-02, Vol.71 (2), p.86-94

2018

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Comments on the 2015 ESC/ERS Guidelines for the Diagnosis and Treatment of Pulmonary Hypertension

Revista española de cardiología (English ed.), 2016-02, Vol.69 (2), p.102-108

Subias, P Escribano

2016

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Comments on the 2014 ESC Guidelines on the Diagnosis and Management of Hypertrophic Cardiomyopathy. A Critical View From the Perspective of Spanish Cardiology

Revista española de cardiología (English ed.), 2015-01, Vol.68 (1), p.4-9

2015

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Pre-participation screening and athlete's heart: A long way to run

International journal of cardiology, 2015-07, Vol.191, p.81-81

2015

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Pregnancy in Aortopathies: Foresight and Anticipation

International journal of cardiology, 2016-11, Vol.222, p.792-792

2016

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Founder mutation C.3344C>t(p.Pro1115Leu) in the EIF2KA4 gene in iberian romani patients with pulmonary veno-occlusive disease: A warning for our daily practice

Archivos de bronconeumología (English ed.), 2016-08, Vol.52 (8), p.444-445

2016

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Thoracic Aneurysms and Dissections: Towards a Further and Better Knowledge

Journal of cardiovascular translational research, 2017-08, Vol.10 (4), p.433-434

2017

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Founder Mutation C.3344C>t(p.Pro1115Leu) in the EIF2KA4 Gene in Iberian Romani Patients With Pulmonary Veno-Occlusive Disease: A Warning for our Daily Practice

Archivos de bronconeumología (English ed.), 2016-08, Vol.52 (8), p.444-445

2016

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Hallazgo de la mutación fundadora C.3344C>t(p.Pro1115Leu) en el gen EIF2KA4 en pacientes ibéricos de etnia gitana con enfermedad veno-oclusiva pulmonar: una llamada de atención a nuestra práctica diaria

Archivos de bronconeumología, 2016-08, Vol.52 (8), p.444-445

2016

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Pregnancy in aortopathies: Foresight and anticipation

International journal of cardiology, 2016, Vol.222, p.792-792

2016

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La lipoproteína (a) es predictora de severidad angiográfica en varones menores de 50 años con inicio clínico de enfermedad coronaria

Revista española de cardiologia, 2000, Vol.53 (8), p.1047-1051

2000

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Hypertrophic cardiomyopathy and athlete's heart: a tale of two entities

European journal of echocardiography, 2009-01, Vol.10 (1), p.151-153

2009

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Genetic Screening of a Large Panel of Genes Associated with Cardiac Disease in a Spanish Heart Transplanted Cohort

Cardiogenetics, 2022-06, Vol.12 (2), p.198-205

2022

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Resequencing the Whole MYH7 Gene (Including the Intronic, Promoter, and 3′ UTR Sequences) in Hypertrophic Cardiomyopathy

The Journal of molecular diagnostics : JMD, 2012-09, Vol.14 (5), p.518-524

2012

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Surveillance after Cardiac Arrest in patients with Brugada Syndrome without an implantable defibrillator: An alarm effect of the previous Syncope

International journal of cardiology, 2016-09, Vol.218, p.69-74

2016

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Congenital long QT syndrome: Should citric fruits be avoided? A case report of a cLQTS type 1 with unusual QTc prolongation with citric juices

Journal of cardiology cases, 2020-09, Vol.22 (3), p.125-127

2020

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Lesiones auriculares inducidas por cloroquina: estudio histopatológico

Revista española de patología, 2013-04, Vol.46 (2), p.117-121

2013

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KCNH2 p.Gly262AlafsTer98: A New Threatening Variant Associated with Long QT Syndrome in a Spanish Cohort

Low voltage with high suspicion in athlete's heart

Characterization of Left Ventricular Non-Compaction Cardiomyopathy

Clinical Implications and Gender Differences of KCNQ1 p.Gly168Arg Pathogenic Variant in Long QT Syndrome

Prevalence of positive ECG criteria in young competitive athletes: a single region experience

Familial Hypercholesterolemia in Premature Acute Coronary Syndrome. Insights from CholeSTEMI Registry

Different Phenotypes in Monozygotic Twins, Carriers of the Same Pathogenic Variant for Hypertrophic Cardiomyopathy

Expresividad variable de una mutación fundadora en el gen EIF2AK4 en pacientes con enfermedad venooclusiva pulmonar hereditaria. Impacto en la supervivencia

Variable Expressivity of a Founder Mutation in the EIF2AK4 Gene in Hereditary Pulmonary Veno-occlusive Disease and Its Impact on Survival

Comments on the 2015 ESC/ERS Guidelines for the Diagnosis and Treatment of Pulmonary Hypertension

Comments on the 2014 ESC Guidelines on the Diagnosis and Management of Hypertrophic Cardiomyopathy. A Critical View From the Perspective of Spanish Cardiology

Pre-participation screening and athlete's heart: A long way to run

Pregnancy in Aortopathies: Foresight and Anticipation

Founder mutation C.3344C>t(p.Pro1115Leu) in the EIF2KA4 gene in iberian romani patients with pulmonary veno-occlusive disease: A warning for our daily practice

Thoracic Aneurysms and Dissections: Towards a Further and Better Knowledge

Founder Mutation C.3344C>t(p.Pro1115Leu) in the EIF2KA4 Gene in Iberian Romani Patients With Pulmonary Veno-Occlusive Disease: A Warning for our Daily Practice

Hallazgo de la mutación fundadora C.3344C>t(p.Pro1115Leu) en el gen EIF2KA4 en pacientes ibéricos de etnia gitana con enfermedad veno-oclusiva pulmonar: una llamada de atención a nuestra práctica diaria

Pregnancy in aortopathies: Foresight and anticipation

La lipoproteína (a) es predictora de severidad angiográfica en varones menores de 50 años con inicio clínico de enfermedad coronaria

Hypertrophic cardiomyopathy and athlete's heart: a tale of two entities

Genetic Screening of a Large Panel of Genes Associated with Cardiac Disease in a Spanish Heart Transplanted Cohort

Resequencing the Whole MYH7 Gene (Including the Intronic, Promoter, and 3′ UTR Sequences) in Hypertrophic Cardiomyopathy

Surveillance after Cardiac Arrest in patients with Brugada Syndrome without an implantable defibrillator: An alarm effect of the previous Syncope

Congenital long QT syndrome: Should citric fruits be avoided? A case report of a cLQTS type 1 with unusual QTc prolongation with citric juices

Lesiones auriculares inducidas por cloroquina: estudio histopatológico

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