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Wild-type transthyretin amyloidosis as a cause of heart failure with preserved ejection fraction

European heart journal, 2015-10, Vol.36 (38), p.2585-2594

2015

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Is funding related to higher research impact? Exploring its relationship and the mediating role of collaboration in several disciplines

Journal of informetrics, 2021-02, Vol.15 (1), p.101102, Article 101102

2021

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Funding acknowledgements in scientific publications: A literature review

Research evaluation, 2020-10, Vol.29 (4), p.469-488

2020

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Funding acknowledgments in the Web of Science: completeness and accuracy of collected data

Scientometrics, 2017-09, Vol.112 (3), p.1793-1812

2017

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How to automatically identify major research sponsors selecting keywords from the WoS Funding Agency field

Scientometrics, 2018-12, Vol.117 (3), p.1755-1770

2018

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Towards higher standardization of funding acknowledgements in scientific publications: Current status in the case of a national and a European research fellowship scheme

Research evaluation, 2024-04

2024

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Investigación interdisciplinaria e impacto social: análisis de medios sociales

Información, cultura y sociedad, 2020-06 (42), p.127-144

2020

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Who is interacting with researchers on Twitter? A survey in the field of Information Science

JLIS.it : Italian journal of library and information science, 2019-05, Vol.10 (2), p.87

2019

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What characterises funded biomedical research? Evidence from a basic and a clinical domain

Scientometrics, 2019-05, Vol.119 (2), p.805-825

2019

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Genetic basis of end-stage hypertrophic cardiomyopathy

European journal of heart failure, 2011-11, Vol.13 (11), p.1193-1201

2011

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Parkinsonism, cognitive deficit and behavioural disturbance caused by a novel mutation in the polymerase gamma gene

Journal of the neurological sciences, 2015-03, Vol.350 (1), p.93-97

2015

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Investigacion interdisciplinaria e impacto social: Analisis de medios sociales/Interdisciplinary research and societal impact: analysis of social media

Información, cultura y sociedad, 2020-06 (42), p.127-144

2020

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Defining a theoretical framework for information seeking and parenting

Journal of documentation, 2017-03, Vol.73 (2), p.186-209

2017

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Severe TK2 enzyme activity deficiency in patients with mild forms of myopathy

Neurology, 2015-06, Vol.84 (22), p.2286-2288

2015

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Mitochondrial DNA depletion syndrome due to mutations in the RRM2B gene

Neuromuscular disorders : NMD, 2008-06, Vol.18 (6), p.453-459

2008

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La comunicación entre investigadores en Twitter. Una etnografía virtual en el ámbito de las ciencias de la documentación

Revista española de documentación científica, 2016-12, Vol.39 (4), p.156-e156

2016

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Usefulness of a diagnostic algorithm hyperferritinemia: A case report of a Spanish family with hereditary hemochromatosis and mutation in SLC40A1 gene

Medicina clinica, 2015-07, Vol.145 (1), p.42

2015

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Mitochondrial haplogroups associated with end-stage heart failure and coronary allograft vasculopathy in heart transplant patients

European heart journal, 2012-02, Vol.33 (3), p.346-353

2012

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Defining a theoretical framework for information seeking and parenting: Concepts and themes from a study with mothers supportive of attachment parenting

Journal of documentation, 2017-01, Vol.73 (2), p.186-209

2017

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The pathogenicity scoring system for mitochondrial tRNA mutations revisited

Molecular genetics & genomic medicine, 2014-03, Vol.2 (2), p.107-114

2014

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Mitochondrial tRNA valine as a recurrent target for mutations involved in mitochondrial cardiomyopathies

Mitochondrion, 2012-03, Vol.12 (2), p.357-362

2012

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Co-occurrence of four nucleotide changes associated with an adult mitochondrial ataxia phenotype

BMC research notes, 2014-12, Vol.7 (1), p.883-883, Article 883

2014

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Idiopathic Restrictive Cardiomyopathy Is Primarily a Genetic Disease

Journal of the American College of Cardiology, 2016-06, Vol.67 (25), p.3021-3023

2016

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COLABORACIÓN MÁS ALLÁ DE LA COAUTORÍA: ANÁLISIS DE LAS DIFERENCIAS DE GÉNERO Y ÁREAS DE CONOCIMIENTO EN LOS GRUPOS DE INVESTIGACIÓN DE LA UNIVERSIDAD COMPLUTENSE DE MADRID

Revista EDICIC, 2023-12, Vol.3 (3), p.1-16

2023

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Wild-type transthyretin amyloidosis as a cause of heart failure with preserved ejection fraction

Is funding related to higher research impact? Exploring its relationship and the mediating role of collaboration in several disciplines

Funding acknowledgements in scientific publications: A literature review

Funding acknowledgments in the Web of Science: completeness and accuracy of collected data

How to automatically identify major research sponsors selecting keywords from the WoS Funding Agency field

Towards higher standardization of funding acknowledgements in scientific publications: Current status in the case of a national and a European research fellowship scheme

Investigación interdisciplinaria e impacto social: análisis de medios sociales

Who is interacting with researchers on Twitter? A survey in the field of Information Science

What characterises funded biomedical research? Evidence from a basic and a clinical domain

OPA1 mutations induce mitochondrial DNA instability and optic atrophy ‘plus’ phenotypes

Genetic basis of end-stage hypertrophic cardiomyopathy

Parkinsonism, cognitive deficit and behavioural disturbance caused by a novel mutation in the polymerase gamma gene

Investigacion interdisciplinaria e impacto social: Analisis de medios sociales/Interdisciplinary research and societal impact: analysis of social media

Defining a theoretical framework for information seeking and parenting

Severe TK2 enzyme activity deficiency in patients with mild forms of myopathy

Mitochondrial DNA depletion syndrome due to mutations in the RRM2B gene

La comunicación entre investigadores en Twitter. Una etnografía virtual en el ámbito de las ciencias de la documentación

Usefulness of a diagnostic algorithm hyperferritinemia: A case report of a Spanish family with hereditary hemochromatosis and mutation in SLC40A1 gene

Mitochondrial haplogroups associated with end-stage heart failure and coronary allograft vasculopathy in heart transplant patients

Defining a theoretical framework for information seeking and parenting: Concepts and themes from a study with mothers supportive of attachment parenting

The pathogenicity scoring system for mitochondrial tRNA mutations revisited

Mitochondrial tRNA valine as a recurrent target for mutations involved in mitochondrial cardiomyopathies

Co-occurrence of four nucleotide changes associated with an adult mitochondrial ataxia phenotype

Idiopathic Restrictive Cardiomyopathy Is Primarily a Genetic Disease

COLABORACIÓN MÁS ALLÁ DE LA COAUTORÍA: ANÁLISIS DE LAS DIFERENCIAS DE GÉNERO Y ÁREAS DE CONOCIMIENTO EN LOS GRUPOS DE INVESTIGACIÓN DE LA UNIVERSIDAD COMPLUTENSE DE MADRID

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