List of works - Alessandra Serio

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

scientific article published in January 2017

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

scientific article published on 5 October 2013

Atlas of the clinical genetics of human dilated cardiomyopathy

scientific article (publication date: 7 May 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).

scientific article

Cardio-Oncology: The Carney Complex Type I.

scientific article published in October 2016

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

scientific article published on 08 October 2019

Familial dilated cardiomyopathy. Clinical and genetic characteristics.

scientific article published on December 2012

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

scientific article

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

scientific article

Genetic causes of dilated cardiomyopathy

scientific article published on 15 September 2016

Left Ventricular Noncompaction: A Distinct Genetic Cardiomyopathy?

scientific article

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

scientific article published on 14 March 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.

scientific article published in October 2009

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

scientific article

List of works by 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.