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A novel clinical risk prediction model for sudden cardiac death in hypertrophic cardiomyopathy (HCM risk-SCD)

European heart journal, 2014-08, Vol.35 (30), p.2010-2020

2014

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Genetics of myocarditis in arrhythmogenic right ventricular dysplasia

Heart rhythm, 2015-04, Vol.12 (4), p.766-773

2015

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Polymorphisms in ACE, ACE2, AGTR1 genes and severity of COVID-19 disease

PloS one, 2022-02, Vol.17 (2), p.e0263140-e0263140

2022

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2023 ESC Guidelines for the management of cardiomyopathies

European heart journal, 2023-10, Vol.44 (37), p.3503-3626

2023

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An expert consensus document on the management of cardiovascular manifestations of Fabry disease

European journal of heart failure, 2020-07, Vol.22 (7), p.1076-1096

2020

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The torso integration hypothesis revisited in Homo sapiens: Contributions to the understanding of hominin body shape evolution

American journal of physical anthropology, 2018-12, Vol.167 (4), p.777-790

2018

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3D geometric morphometric analysis of variation in the human lumbar spine

American journal of physical anthropology, 2019-11, Vol.170 (3), p.361-372

2019

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Krapina atlases suggest a high prevalence of anatomical variations in the first cervical vertebra of Neanderthals

Journal of anatomy, 2020-09, Vol.237 (3), p.579-586

2020

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Male‐to‐Female Genital Reassignment Surgery: A Retrospective Review of Surgical Technique and Complications in 60 Patients

Journal of sexual medicine, 2015-08, Vol.12 (8), p.1837-1845

2015

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Diagnostic Approach to Unexplained Cardiac Arrest (from the FIVI-Gen Study)

The American journal of cardiology, 2015-09, Vol.116 (6), p.894-899

2015

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Filamin C variants are associated with a distinctive clinical and immunohistochemical arrhythmogenic cardiomyopathy phenotype

International journal of cardiology, 2020-05, Vol.307, p.101-108

2020

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Possible Further Evidence of Low Genetic Diversity in the El Sidrón (Asturias, Spain) Neandertal Group: Congenital Clefts of the Atlas

PloS one, 2015-09, Vol.10 (9), p.e0136550-e0136550

2015

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Accuracy of the angiography-based quantitative flow ratio in intermediate left main coronary artery lesions and comparison with visual estimation

International journal of cardiology, 2023-07, Vol.383, p.8-14

2023

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Prevalence of anatomic variations of the atlas vertebra

The spine journal, 2018-11, Vol.18 (11), p.2102-2111

2018

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The Spanish Fabry women study: a retrospective observational study describing the phenotype of females with GLA variants

Orphanet journal of rare diseases, 2023-01, Vol.18 (1), p.8-8, Article 8

2023

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Clinical Phenotypes and Prognosis of Dilated Cardiomyopathy Caused by Truncating Variants in the TTN Gene

Circulation. Heart failure, 2020-10, Vol.13 (10), p.e006832-e006832

2020

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Can the transverse foramen/vertebral artery ratio of double transverse foramen subjects be a risk for vertebrobasilar transient ischemic attacks?

Journal of anatomy, 2018-09, Vol.233 (3), p.341-346

2018

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Reply: Revisiting Genome Sequencing Data in Light of Novel Disease Gene Associations

Journal of the American College of Cardiology, 2019-03, Vol.73 (11), p.1366-1367

2019

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The EP300/TP53 pathway, a suppressor of the Hippo and canonical WNT pathways, is activated in human hearts with arrhythmogenic cardiomyopathy in the absence of overt heart failure

Cardiovascular research, 2022-05, Vol.118 (6), p.1466-1478

2022

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Assessing thoraco‐pelvic covariation in Homo sapiens and Pan troglodytes: A 3D geometric morphometric approach

American journal of physical anthropology, 2020-11, Vol.173 (3), p.514-534

2020

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Genetics of feline hypertrophic cardiomyopathy

Clinical genetics, 2020-09, Vol.98 (3), p.203-214

2020

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A novel clinical risk prediction model for sudden cardiac death in hypertrophic cardiomyopathy (HCM risk-SCD)

Genetics of myocarditis in arrhythmogenic right ventricular dysplasia

Polymorphisms in ACE, ACE2, AGTR1 genes and severity of COVID-19 disease

The Cardiomyopathy Registry of the EURObservational Research Programme of the European Society of Cardiology: baseline data and contemporary management of adult patients with cardiomyopathies

2023 ESC Guidelines for the management of cardiomyopathies

Proposal for a revised definition of dilated cardiomyopathy, hypokinetic non-dilated cardiomyopathy, and its implications for clinical practice: a position statement of the ESC working group on myocardial and pericardial diseases

An expert consensus document on the management of cardiovascular manifestations of Fabry disease

The torso integration hypothesis revisited in Homo sapiens: Contributions to the understanding of hominin body shape evolution

Effectiveness of the 2014 European Society of Cardiology guideline on sudden cardiac death in hypertrophic cardiomyopathy: a systematic review and meta-analysis

3D geometric morphometric analysis of variation in the human lumbar spine

Krapina atlases suggest a high prevalence of anatomical variations in the first cervical vertebra of Neanderthals

Male‐to‐Female Genital Reassignment Surgery: A Retrospective Review of Surgical Technique and Complications in 60 Patients

Diagnostic Approach to Unexplained Cardiac Arrest (from the FIVI-Gen Study)

Filamin C variants are associated with a distinctive clinical and immunohistochemical arrhythmogenic cardiomyopathy phenotype

Possible Further Evidence of Low Genetic Diversity in the El Sidrón (Asturias, Spain) Neandertal Group: Congenital Clefts of the Atlas

Accuracy of the angiography-based quantitative flow ratio in intermediate left main coronary artery lesions and comparison with visual estimation

Prevalence of anatomic variations of the atlas vertebra

The Spanish Fabry women study: a retrospective observational study describing the phenotype of females with GLA variants

Clinical Phenotypes and Prognosis of Dilated Cardiomyopathy Caused by Truncating Variants in the TTN Gene

Can the transverse foramen/vertebral artery ratio of double transverse foramen subjects be a risk for vertebrobasilar transient ischemic attacks?

Reply: Revisiting Genome Sequencing Data in Light of Novel Disease Gene Associations

The EP300/TP53 pathway, a suppressor of the Hippo and canonical WNT pathways, is activated in human hearts with arrhythmogenic cardiomyopathy in the absence of overt heart failure

Mutations in the NOTCH pathway regulator MIB1 cause left ventricular noncompaction cardiomyopathy

Assessing thoraco‐pelvic covariation in Homo sapiens and Pan troglodytes: A 3D geometric morphometric approach

Genetics of feline hypertrophic cardiomyopathy

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