Belen Bornstein
Majadahonda, MD, Spain
Last Updated: 09/26/2026
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Found 15 publications
Titin Missense Variants as a Cause of Familial Dilated Cardiomyopathy.
Journal: Circulation
Published: May 30, 2023
Clinical profile and outcome of cardiac amyloidosis in a Spanish referral center.
Journal: Revista espanola de cardiologia (English ed.)
Published: May 08, 2019
Idiopathic Restrictive Cardiomyopathy Is Primarily a Genetic Disease.
Journal: Journal of the American College of Cardiology
Published: July 22, 2015
Wild-type transthyretin amyloidosis as a cause of heart failure with preserved ejection fraction.
Journal: European heart journal
Published: February 08, 2015
Severe TK2 enzyme activity deficiency in patients with mild forms of myopathy.
Journal: Neurology
Published: November 04, 2014
Parkinsonism, cognitive deficit and behavioural disturbance caused by a novel mutation in the polymerase gamma gene.
Journal: Journal of the neurological sciences
Published: September 29, 2014
Mitochondrial cardiomyopathies associated with the m.3243A>G mutation in the MT-TL1 gene: two sides of the same coin.
Journal: Revista espanola de cardiologia (English ed.)
Published: August 03, 2014
Usefulness of a diagnostic algorithm hyperferritinemia: A case report of a Spanish family with hereditary hemochromatosis and mutation in SLC40A1 gene
Journal: Medicina clinica
Published: June 29, 2014
Co-occurrence of four nucleotide changes associated with an adult mitochondrial ataxia phenotype.
Journal: BMC research notes
Published: April 28, 2014
Cardiac dysfunction in mitochondrial disease. Clinical and molecular features.
Journal: Circulation journal : official journal of the Japanese Circulation Society
Published: August 23, 2013
Last Updated: 09/26/2026