List of works - Valentina Favalli

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

scientific article published in January 2017

Age-specific reference values for carotid arterial stiffness estimated by ultrasonic wall tracking

scientific article published on 21 August 2019

An International External Validation Study of the 2014 European Society of Cardiology Guideline on Sudden Cardiac Death Prevention in Hypertrophic Cardiomyopathy (Evidence from HCM).

scientific article

Anderson-Fabry disease

scientific article published on 01 February 2018

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

scientific article published on 5 October 2013

Autosomal recessive atrial dilated cardiomyopathy with standstill evolution associated with mutation of Natriuretic Peptide Precursor A.

scientific article published on 29 December 2012

Cardiac Phenotypes in Hereditary Muscle Disorders: JACC State-of-the-Art Review

scientific article published on 01 November 2018

Cardio-Oncology: The Carney Complex Type I.

scientific article published in October 2016

Common presentation of rare diseases: Aortic aneurysms & valves.

scientific article published in April 2018

Correction: Age-specific reference values for carotid arterial stiffness estimated by ultrasonic wall tracking

scientific article published on 01 March 2020

Diagnostic work-up and risk stratification in X-linked dilated cardiomyopathies caused by dystrophin defects

scientific article published in August 2011

Endomyocardial Biopsy in acute cardiogenic shock: Diagnosis of pheochromocytoma.

scientific article published on 9 October 2015

European Cardiomyopathy Pilot Registry: EURObservational Research Programme of the European Society of Cardiology

scientific article

Extracellular Volume in Dilated Cardiomyopathy: Interstitial Fibrosis and More?

scientific article published in January 2018

Familial dilated cardiomyopathy. Clinical and genetic characteristics.

scientific article published on December 2012

Functionally Incomplete Re-Endothelialization of Stents and Neoatherosclerosis.

scientific article published on 25 October 2017

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

Genetic counselling and high-penetrance susceptibility gene analysis reveal the novel CDKN2A p.D84V (c.251A>T) mutation in melanoma-prone families from Italy.

scientific article published in April 2017

Genetics and clinics: current applications, limitations, and future developments

scientific article published on 29 March 2019

LMNA Mutations Associated With Mild and Late-Onset Phenotype: The Case of the Dutch Founder Mutation p.(Arg331Gln)

scientific article published on 01 August 2017

Left Ventricular Noncompaction: A Distinct Genetic Cardiomyopathy?

scientific article

Long-Term Outcome and Risk Stratification in Dilated Cardiolaminopathies

MOGE(S) nosology in low-to-middle-income countries

scientific article

Non-contact measurement of carotid arterial stiffness by two-point heart-pulse laser detection

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

article

Radiation Therapy for Head and Neck Cancer and Angioneogenesis

scientific article published on 18 May 2016

Rationale and design of a trial evaluating the effects of losartan vs. nebivolol vs. the association of both on the progression of aortic root dilation in Marfan syndrome with FBN1 gene mutations

scientific article

Renal and brain complications in GLA p.Phe113Leu Fabry disease. Comments on "Fabry disease caused by the GLA p.Phe113Leu (p.F113L) variant: Natural history in males" by Oliveira et al. (Eur. J. Med. Genet. 2019)

scientific article published on 13 January 2020

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

scientific article

Reply: The MOGE(S) classification for a phenotype-genotype nomenclature of cardiomyopathy: more questions than answers?

scientific article published on 23 April 2014

Risk of dissection in thoracic aneurysms associated with mutations of smooth muscle alpha-actin 2 (ACTA2)

scientific article published on 06 January 2011

Structures of the lamin A/C R335W and E347K mutants: implications for dilated cardiolaminopathies

scientific article

Supporting Translational Research on Inherited Cardiomyopathies through Information Technology

scientific article published on 28 February 2013

The MOGE(S) Classification for a Phenotype-Genotype Nomenclature of Cardiomyopathy: Endorsed by the World Heart Federation

scientific article

The MOGE(S) Classification for a Phenotype–Genotype Nomenclature of Cardiomyopathy

article

The MOGE(S) classification of cardiomyopathy for clinicians

scientific article published on July 2014

The need to modify patient selection to improve the benefits of implantable cardioverter-defibrillator for primary prevention of sudden death in non-ischaemic dilated cardiomyopathy

scientific article published on 14 August 2013

The pathologic basis of recovery

scientific article published on January 2014

Transcriptomic and proteomic analysis in the cardiovascular setting: unravelling the disease?

scientific article published in May 2009

List of works by Valentina Favalli

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

Age-specific reference values for carotid arterial stiffness estimated by ultrasonic wall tracking

An International External Validation Study of the 2014 European Society of Cardiology Guideline on Sudden Cardiac Death Prevention in Hypertrophic Cardiomyopathy (Evidence from HCM).

Anderson-Fabry disease

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

Autosomal recessive atrial dilated cardiomyopathy with standstill evolution associated with mutation of Natriuretic Peptide Precursor A.

Cardiac Phenotypes in Hereditary Muscle Disorders: JACC State-of-the-Art Review

Cardio-Oncology: The Carney Complex Type I.

Common presentation of rare diseases: Aortic aneurysms & valves.

Correction: Age-specific reference values for carotid arterial stiffness estimated by ultrasonic wall tracking

Diagnostic work-up and risk stratification in X-linked dilated cardiomyopathies caused by dystrophin defects

Endomyocardial Biopsy in acute cardiogenic shock: Diagnosis of pheochromocytoma.

European Cardiomyopathy Pilot Registry: EURObservational Research Programme of the European Society of Cardiology

Extracellular Volume in Dilated Cardiomyopathy: Interstitial Fibrosis and More?

Familial dilated cardiomyopathy. Clinical and genetic characteristics.

Functionally Incomplete Re-Endothelialization of Stents and Neoatherosclerosis.

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

Genetic causes of dilated cardiomyopathy

Genetic counselling and high-penetrance susceptibility gene analysis reveal the novel CDKN2A p.D84V (c.251A>T) mutation in melanoma-prone families from Italy.

Genetics and clinics: current applications, limitations, and future developments

LMNA Mutations Associated With Mild and Late-Onset Phenotype: The Case of the Dutch Founder Mutation p.(Arg331Gln)

Left Ventricular Noncompaction: A Distinct Genetic Cardiomyopathy?

Long-Term Outcome and Risk Stratification in Dilated Cardiolaminopathies

MOGE(S) nosology in low-to-middle-income countries

Non-contact measurement of carotid arterial stiffness by two-point heart-pulse laser detection

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

Radiation Therapy for Head and Neck Cancer and Angioneogenesis

Rationale and design of a trial evaluating the effects of losartan vs. nebivolol vs. the association of both on the progression of aortic root dilation in Marfan syndrome with FBN1 gene mutations

Renal and brain complications in GLA p.Phe113Leu Fabry disease. Comments on "Fabry disease caused by the GLA p.Phe113Leu (p.F113L) variant: Natural history in males" by Oliveira et al. (Eur. J. Med. Genet. 2019)

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

Reply: The MOGE(S) classification for a phenotype-genotype nomenclature of cardiomyopathy: more questions than answers?

Risk of dissection in thoracic aneurysms associated with mutations of smooth muscle alpha-actin 2 (ACTA2)

Structures of the lamin A/C R335W and E347K mutants: implications for dilated cardiolaminopathies

Supporting Translational Research on Inherited Cardiomyopathies through Information Technology

The MOGE(S) Classification for a Phenotype-Genotype Nomenclature of Cardiomyopathy: Endorsed by the World Heart Federation

The MOGE(S) Classification for a Phenotype–Genotype Nomenclature of Cardiomyopathy

The MOGE(S) classification of cardiomyopathy for clinicians

The need to modify patient selection to improve the benefits of implantable cardioverter-defibrillator for primary prevention of sudden death in non-ischaemic dilated cardiomyopathy

The pathologic basis of recovery

Transcriptomic and proteomic analysis in the cardiovascular setting: unravelling the disease?

Translational Bioinformatics: Challenges and Opportunities for Case-Based Reasoning and Decision Support