Lista de obras - Francesca Girolami - Dominio Público Uruguay

A molecular screening strategy based on beta-myosin heavy chain, cardiac myosin binding protein C and troponin T genes in Italian patients with hypertrophic cardiomyopathy

artículo científico publicado en 2006

A rare case of pediatric cardiomyopathy: Alström syndrome identified by gene panel analysis

artículo científico publicado en 2020

An Investigation of the Molecular Mechanism of Double cMyBP-C Mutation in a Patient with End-Stage Hypertrophic Cardiomyopathy

artículo científico publicado en 2015

Bioinformatics for next generation sequencing data

artículo científico publicado en 2010

Care in Specialized Centers and Data Sharing Increase Agreement in Hypertrophic Cardiomyopathy Genetic Test Interpretation

artículo científico publicado en 2017

Clinical Features and Outcome of Hypertrophic Cardiomyopathy Associated With Triple Sarcomere Protein Gene Mutations

article

Clinical Spectrum, Therapeutic Options, and Outcome of Advanced Heart Failure in Hypertrophic Cardiomyopathy

artículo científico publicado en 2015

Clinical phenotype and outcome of hypertrophic cardiomyopathy associated with thin-filament gene mutations

artículo científico publicado en 2014

Contemporary Insights Into the Genetics of Hypertrophic Cardiomyopathy: Toward a New Era in Clinical Testing?

scientific article published on 18 April 2020

Contemporary genetic testing in inherited cardiac disease: tools, ethical issues, and clinical applications

artículo científico publicado en 2017

Genetic advances in sarcomeric cardiomyopathies: state of the art.

artículo científico publicado en 2015

Genetic profile of hypertrophic cardiomyopathy in Tunisia: Is it different?

artículo científico publicado en 2015

Genotype and Lifetime Burden of Disease in Hypertrophic Cardiomyopathy: Insights from the Sarcomeric Human Cardiomyopathy Registry (SHaRe)

scientific article published on 23 August 2018

Identification of seven novel mutations of F8C by DHPLC.

artículo científico publicado en 2002

Impact of Genotype on the Occurrence of Atrial Fibrillation in Patients With Hypertrophic Cardiomyopathy

artículo científico publicado en 2016

Incident Atrial Fibrillation Is Associated With MYH7 Sarcomeric Gene Variation in Hypertrophic Cardiomyopathy

article

Looking for hypertrophic cardiomyopathy in the community: why is it important?

artículo científico publicado en 2009

Microsatellite analysis of chromosome 3p region in sporadic renal cell carcinomas

artículo científico publicado en 2002

Microvascular Function Is Selectively Impaired in Patients With Hypertrophic Cardiomyopathy and Sarcomere Myofilament Gene Mutations

article

Molecular genetics made simple

artículo científico publicado en 2012

Myofilament protein gene mutation screening and outcome of patients with hypertrophic cardiomyopathy

artículo científico publicado en 2008

Novel α-actinin 2 variant associated with familial hypertrophic cardiomyopathy and juvenile atrial arrhythmias: a massively parallel sequencing study.

artículo científico publicado en 2014

Phospholamban Cardiomyopathy: Unveiling a Distinct Phenotype Through Heart Failure Stages Progression

artículo científico publicado en 2022

Prevalence and clinical profile of troponin T mutations among patients with hypertrophic cardiomyopathy in tuscany

artículo científico publicado en 2003

Prevalence of cardiac amyloidosis among adult patients referred to tertiary centres with an initial diagnosis of hypertrophic cardiomyopathy

artículo científico publicado en 2019

Prognostic value of N-terminal pro-brain natriuretic Peptide in outpatients with hypertrophic cardiomyopathy

artículo científico publicado en 2013

Relevance of coronary microvascular flow impairment to long-term remodeling and systolic dysfunction in hypertrophic cardiomyopathy

artículo científico publicado en 2006

Significance of sarcomere gene mutations analysis in the end-stage phase of hypertrophic cardiomyopathy

article

The familial hypertrophic cardiomyopathy-associated myosin mutation R403Q accelerates tension generation and relaxation of human cardiac myofibrils

The many faces of hypertrophic cardiomyopathy: from developmental biology to clinical practice

artículo científico publicado en 2009

[A new type of "tracing" for cardiologists?]

scientific article published on 01 April 2009

[Clinical and genetic features of left ventricular noncompaction: a continuum in cardiomyopathies]

artículo científico publicado en 2010

[Clinical relevance of genetic testing in hypertrophic cardiomyopathy]

artículo científico publicado en 2011

[Disease progression and systolic dysfunction in patients with hypertrophic cardiomyopathy: genetic basis, pathophysiology and clinical presentation]

artículo científico publicado en 2011

[Management of refractory symptoms in hypertrophic cardiomyopathy with restrictive pathophysiology: novel perspectives for ranolazine]

artículo científico publicado en 2012

Lista de obras de Francesca Girolami

A molecular screening strategy based on beta-myosin heavy chain, cardiac myosin binding protein C and troponin T genes in Italian patients with hypertrophic cardiomyopathy

A rare case of pediatric cardiomyopathy: Alström syndrome identified by gene panel analysis

An Investigation of the Molecular Mechanism of Double cMyBP-C Mutation in a Patient with End-Stage Hypertrophic Cardiomyopathy

Bioinformatics for next generation sequencing data

Care in Specialized Centers and Data Sharing Increase Agreement in Hypertrophic Cardiomyopathy Genetic Test Interpretation

Clinical Features and Outcome of Hypertrophic Cardiomyopathy Associated With Triple Sarcomere Protein Gene Mutations

Clinical Spectrum, Therapeutic Options, and Outcome of Advanced Heart Failure in Hypertrophic Cardiomyopathy

Clinical phenotype and outcome of hypertrophic cardiomyopathy associated with thin-filament gene mutations

Contemporary Insights Into the Genetics of Hypertrophic Cardiomyopathy: Toward a New Era in Clinical Testing?

Contemporary genetic testing in inherited cardiac disease: tools, ethical issues, and clinical applications

Genetic advances in sarcomeric cardiomyopathies: state of the art.

Genetic profile of hypertrophic cardiomyopathy in Tunisia: Is it different?

Genotype and Lifetime Burden of Disease in Hypertrophic Cardiomyopathy: Insights from the Sarcomeric Human Cardiomyopathy Registry (SHaRe)

Identification of seven novel mutations of F8C by DHPLC.

Impact of Genotype on the Occurrence of Atrial Fibrillation in Patients With Hypertrophic Cardiomyopathy

Incident Atrial Fibrillation Is Associated With MYH7 Sarcomeric Gene Variation in Hypertrophic Cardiomyopathy

Looking for hypertrophic cardiomyopathy in the community: why is it important?

Microsatellite analysis of chromosome 3p region in sporadic renal cell carcinomas

Microvascular Function Is Selectively Impaired in Patients With Hypertrophic Cardiomyopathy and Sarcomere Myofilament Gene Mutations

Molecular genetics made simple

Myofilament protein gene mutation screening and outcome of patients with hypertrophic cardiomyopathy

Novel α-actinin 2 variant associated with familial hypertrophic cardiomyopathy and juvenile atrial arrhythmias: a massively parallel sequencing study.

Phospholamban Cardiomyopathy: Unveiling a Distinct Phenotype Through Heart Failure Stages Progression

Prevalence and clinical profile of troponin T mutations among patients with hypertrophic cardiomyopathy in tuscany

Prevalence of cardiac amyloidosis among adult patients referred to tertiary centres with an initial diagnosis of hypertrophic cardiomyopathy

Prognostic value of N-terminal pro-brain natriuretic Peptide in outpatients with hypertrophic cardiomyopathy

Relevance of coronary microvascular flow impairment to long-term remodeling and systolic dysfunction in hypertrophic cardiomyopathy

Significance of sarcomere gene mutations analysis in the end-stage phase of hypertrophic cardiomyopathy

The familial hypertrophic cardiomyopathy-associated myosin mutation R403Q accelerates tension generation and relaxation of human cardiac myofibrils

The many faces of hypertrophic cardiomyopathy: from developmental biology to clinical practice

[A new type of "tracing" for cardiologists?]

[Clinical and genetic features of left ventricular noncompaction: a continuum in cardiomyopathies]

[Clinical relevance of genetic testing in hypertrophic cardiomyopathy]

[Disease progression and systolic dysfunction in patients with hypertrophic cardiomyopathy: genetic basis, pathophysiology and clinical presentation]

[Management of refractory symptoms in hypertrophic cardiomyopathy with restrictive pathophysiology: novel perspectives for ranolazine]