Lista de obras - Taisuke Ishikawa - Dominio Público Uruguay

A novel de novo calmodulin mutation in a 6-year-old boy who experienced an aborted cardiac arrest

artículo científico publicado en 2016

A novel disease gene for Brugada syndrome: sarcolemmal membrane-associated protein gene mutations impair intracellular trafficking of hNav1.5.

artículo científico publicado en 2012

Cardiovascular effects of right ventricle-pulmonary artery valved conduit implantation in experimental pulmonic stenosis

artículo científico publicado en 2009

Clinical Manifestations and Long-Term Mortality in Lamin A/C Mutation Carriers From a Japanese Multicenter Registry

scientific article published on 04 August 2018

Clinical characteristics and risk of arrhythmia recurrences in patients with idiopathic ventricular fibrillation associated with early repolarization

artículo científico publicado en 2012

Comparative effects of amlodipine and benazepril on left atrial pressure in dogs with experimentally-induced mitral valve regurgitation.

artículo científico publicado en 2012

Daily rhythms of left atrial pressure in beagle dogs with mitral valve regurgitation

artículo científico publicado en 2009

Dilated cardiomyopathy-associated FHOD3 variant impairs the ability to induce activation of transcription factor serum response factor

artículo científico publicado en 2013

Echocardiographic estimation of left atrial pressure in beagle dogs with experimentally-induced mitral valve regurgitation.

artículo científico publicado en 2011

Electrocardiographic Characteristics and SCN5A Mutations in Idiopathic Ventricular Fibrillation Associated With Early Repolarization ⬇️

artículo científico publicado el 25 de octubre de 2011

Enhancing rare variant interpretation in inherited arrhythmias through quantitative analysis of consortium disease cohorts and population controls

artículo científico publicado en 2020

Gene-Based Risk Stratification for Cardiac Disorders in LMNA Mutation Carriers

scientific article published on 01 December 2017

Genetic defects in a His-Purkinje system transcription factor, IRX3, cause lethal cardiac arrhythmias.

artículo científico publicado en 2015

Genotype-dependent differences in age of manifestation and arrhythmia complications in short QT syndrome

artículo científico publicado en 2015

HCN4 pacemaker channels attenuate the parasympathetic response and stabilize the spontaneous firing of the sinoatrial node.

artículo científico publicado en 2018

Heart-specific small subunit of myosin light chain phosphatase activates rho-associated kinase and regulates phosphorylation of myosin phosphatase target subunit 1.

artículo científico publicado en 2010

Histological study of right ventricle-pulmonary artery valved conduit implantation (RPVC) in dogs with pulmonic stenosis

artículo científico publicado en 2009

Inherited bradyarrhythmia: A diverse genetic background

artículo científico publicado en 2016

Letter to the Editor

artículo científico publicado en 2017

Novel SCN3B mutation associated with brugada syndrome affects intracellular trafficking and function of Nav1.5.

artículo científico publicado en 2012

Novel calmodulin mutations associated with congenital arrhythmia susceptibility

artículo científico publicado en 2014

Novel mechanisms of trafficking defect caused by KCNQ1 mutations found in long QT syndrome.

artículo científico publicado en 2009

Novel mutation in the α-myosin heavy chain gene is associated with sick sinus syndrome

artículo científico publicado en 2015

Nuclear accumulation of androgen receptor in gender difference of dilated cardiomyopathy due to lamin A/C mutations.

artículo científico publicado en 2013

Postmortem genetic analysis of sudden unexpected death in infancy: neonatal genetic screening may enable the prevention of sudden infant death.

artículo científico publicado en 2017

Progressive Atrial Conduction Defects Associated With Bone Malformation Caused by a Connexin-45 Mutation.

artículo científico publicado en 2017

SCN5A Mutation Type and a Genetic Risk Score Associate Variably with Brugada Syndrome Phenotype in SCN5A Families

artículo científico publicado en 2020

Sick sinus syndrome with HCN4 mutations shows early onset and frequent association with atrial fibrillation and left ventricular noncompaction

artículo científico publicado en 2017

Sodium channelopathy underlying familial sick sinus syndrome with early onset and predominantly male characteristics.

artículo científico publicado en 2014

The effect of angiotensin-converting enzyme inhibitors of left atrial pressure in dogs with mitral valve regurgitation.

artículo científico publicado en 2010

The effect of furosemide on left atrial pressure in dogs with mitral valve regurgitation

artículo científico publicado en 2011

The effect of pimobendan on left atrial pressure in dogs with mitral valve regurgitation

scientific article published on 21 September 2011

Lista de obras de Taisuke Ishikawa

A novel de novo calmodulin mutation in a 6-year-old boy who experienced an aborted cardiac arrest

A novel disease gene for Brugada syndrome: sarcolemmal membrane-associated protein gene mutations impair intracellular trafficking of hNav1.5.

Cardiovascular effects of right ventricle-pulmonary artery valved conduit implantation in experimental pulmonic stenosis

Clinical Manifestations and Long-Term Mortality in Lamin A/C Mutation Carriers From a Japanese Multicenter Registry

Clinical characteristics and risk of arrhythmia recurrences in patients with idiopathic ventricular fibrillation associated with early repolarization

Comparative effects of amlodipine and benazepril on left atrial pressure in dogs with experimentally-induced mitral valve regurgitation.

Daily rhythms of left atrial pressure in beagle dogs with mitral valve regurgitation

Dilated cardiomyopathy-associated FHOD3 variant impairs the ability to induce activation of transcription factor serum response factor

Echocardiographic estimation of left atrial pressure in beagle dogs with experimentally-induced mitral valve regurgitation.

Electrocardiographic Characteristics and SCN5A Mutations in Idiopathic Ventricular Fibrillation Associated With Early Repolarization ⬇️

Enhancing rare variant interpretation in inherited arrhythmias through quantitative analysis of consortium disease cohorts and population controls

Gene-Based Risk Stratification for Cardiac Disorders in LMNA Mutation Carriers

Genetic defects in a His-Purkinje system transcription factor, IRX3, cause lethal cardiac arrhythmias.

Genotype-dependent differences in age of manifestation and arrhythmia complications in short QT syndrome

HCN4 pacemaker channels attenuate the parasympathetic response and stabilize the spontaneous firing of the sinoatrial node.

Heart-specific small subunit of myosin light chain phosphatase activates rho-associated kinase and regulates phosphorylation of myosin phosphatase target subunit 1.

Histological study of right ventricle-pulmonary artery valved conduit implantation (RPVC) in dogs with pulmonic stenosis

Inherited bradyarrhythmia: A diverse genetic background

Letter to the Editor

Novel SCN3B mutation associated with brugada syndrome affects intracellular trafficking and function of Nav1.5.

Novel calmodulin mutations associated with congenital arrhythmia susceptibility

Novel mechanisms of trafficking defect caused by KCNQ1 mutations found in long QT syndrome.

Novel mutation in the α-myosin heavy chain gene is associated with sick sinus syndrome

Nuclear accumulation of androgen receptor in gender difference of dilated cardiomyopathy due to lamin A/C mutations.

Postmortem genetic analysis of sudden unexpected death in infancy: neonatal genetic screening may enable the prevention of sudden infant death.

Progressive Atrial Conduction Defects Associated With Bone Malformation Caused by a Connexin-45 Mutation.

SCN5A Mutation Type and a Genetic Risk Score Associate Variably with Brugada Syndrome Phenotype in SCN5A Families

Sick sinus syndrome with HCN4 mutations shows early onset and frequent association with atrial fibrillation and left ventricular noncompaction

Sodium channelopathy underlying familial sick sinus syndrome with early onset and predominantly male characteristics.

The effect of angiotensin-converting enzyme inhibitors of left atrial pressure in dogs with mitral valve regurgitation.

The effect of furosemide on left atrial pressure in dogs with mitral valve regurgitation

The effect of pimobendan on left atrial pressure in dogs with mitral valve regurgitation