Lista de obras - Alessandra Serio - Dominio Público Uruguay

'Precision and personalized medicine,' a dream that comes true?

artículo científico publicado en 2017

Aortic root 3D parametric morphological model from 2D-echo images.

artículo científico publicado en 2013

Atlas of the clinical genetics of human dilated cardiomyopathy

artículo científico publicado en 2015

Autosomal recessive paediatric sick sinus syndrome associated with novel compound mutations in SCN5A

scientific article published on 28 November 2012

Baseline echocardiographic characteristics of heart failure patients enrolled in a large European multicentre trial (CArdiac REsynchronisation Heart Failure study).

artículo científico publicado en 2005

Cardio-Oncology: The Carney Complex Type I.

artículo científico publicado en 2016

Diagnostic Criteria of Left Ventricular Dysfunction in Patients With Myotonic Dystrophy Type 1

artículo científico publicado en 2019

Familial dilated cardiomyopathy. Clinical and genetic characteristics.

artículo científico publicado en 2012

Gender-specific differences in major cardiac events and mortality in lamin A/C mutation carriers.

artículo científico publicado en 2012

Genetic Screening of Anderson-Fabry Disease in Probands Referred From Multispecialty Clinics.

artículo científico publicado en 2016

Genetic causes of dilated cardiomyopathy

artículo científico publicado en 2016

Left Ventricular Noncompaction: A Distinct Genetic Cardiomyopathy?

artículo científico publicado en 2016

Long-term left ventricular reverse remodelling with cardiac resynchronization therapy: results from the CARE-HF trial

artículo científico publicado en 2009

Quantitative Expression of the Mutated Lamin A/C Gene in Patients With Cardiolaminopathy

article

Regional abnormalities of myocardial deformation in patients with hypertrophic cardiomyopathy: correlations with delayed enhancement in cardiac magnetic resonance.

artículo científico publicado en 2009

Reply: A Distinct Cardiomyopathy: HCN4 Syndrome Comprising Myocardial Noncompaction, Bradycardia, Mitral Valve Defects, and Aortic Dilation.

artículo científico publicado en 2017

Lista de obras de Alessandra Serio

'Precision and personalized medicine,' a dream that comes true?

Aortic root 3D parametric morphological model from 2D-echo images.

Atlas of the clinical genetics of human dilated cardiomyopathy

Autosomal recessive paediatric sick sinus syndrome associated with novel compound mutations in SCN5A

Baseline echocardiographic characteristics of heart failure patients enrolled in a large European multicentre trial (CArdiac REsynchronisation Heart Failure study).

Cardio-Oncology: The Carney Complex Type I.

Diagnostic Criteria of Left Ventricular Dysfunction in Patients With Myotonic Dystrophy Type 1

Familial dilated cardiomyopathy. Clinical and genetic characteristics.

Gender-specific differences in major cardiac events and mortality in lamin A/C mutation carriers.

Genetic Screening of Anderson-Fabry Disease in Probands Referred From Multispecialty Clinics.

Genetic causes of dilated cardiomyopathy

Left Ventricular Noncompaction: A Distinct Genetic Cardiomyopathy?

Long-term left ventricular reverse remodelling with cardiac resynchronization therapy: results from the CARE-HF trial

Quantitative Expression of the Mutated Lamin A/C Gene in Patients With Cardiolaminopathy

Regional abnormalities of myocardial deformation in patients with hypertrophic cardiomyopathy: correlations with delayed enhancement in cardiac magnetic resonance.

Reply: A Distinct Cardiomyopathy: HCN4 Syndrome Comprising Myocardial Noncompaction, Bradycardia, Mitral Valve Defects, and Aortic Dilation.