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European Heart Journal. Cardiovascular Imaging
|
August 8, 2018
Mitral valve abnormalities in hypertrophic cardiomyopathy: a primary expression of the disease? Getting closer to the answer
Paolo Spirito, Maria Iascone, Paolo Ferrazzi
Circulation. Cardiovascular Genetics
|
December 20, 2012
Letter by Iascone et al regarding article, "Population-based variation in cardiomyopathy genes"
Maria Iascone, Maria Elena Sana, Paolo Ferrazzi
Human Genetics
|
October 21, 2010
Gene symbol: LAMP2. Disease: Danon disease
Maria Iascone, Attilio Iacovoni, Daniela Marchetti, et al.
Gene
|
July 24, 2012
A new mutational mechanism for hypertrophic cardiomyopathy
Laura Pezzoli, Maria Elena Sana, Paolo Ferrazzi, et al.
Journal of the American College of Cardiology
|
March 12, 2021
Reply: Hypertrophic Cardiomyopathy as Congenital Heart Disease
Aleksei Zyrianov, Paolo Spirito, Paolo Ferrazzi, et al.
Clinical Dysmorphology
|
October 21, 2020
A novel HIST1HE pathogenic variant in a girl with macrocephaly and intellectual disability: a new case and review of literature
Alessandra Pelle, Laura Pezzoli, Erika Apuril, et al.
Human Genetics
|
August 21, 2009
Novel human pathological mutations. Gene symbol: MYBPC3. Disease: cardiomyopathy, hypertrophic
Maria Iascone, D Marchetti, A R Lincesso, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology
|
November 7, 2025
A novel deep intronic mutation expands the genotype spectrum of MYH7-related myopathies
Andrea Barp, Luca Maria Neri, Lorenzo Maggi, et al.
Journal of Cardiovascular Electrophysiology
|
October 28, 2014
Cavotricuspid isthmus ablation and subcutaneous monitoring device implantation in a 2-year-old baby with 2 SCN5A mutations, sinus node dysfunction, atrial flutter recurrences, and drug induced long-QT syndrome: a tricky case of pediatric overlap syndrome?
Paolo De Filippo, Paola Ferrari, Maria Iascone, et al.
American Journal of Medical Genetics. Part A
|
May 28, 2016
Temporomandibular joint ankylosis as part of the clinical spectrum of Carey-Fineman-Ziter syndrome?
Martina Pasetti, Fabio Mazzoleni, Giorgio Novelli, et al.
Page
of 18
Search research articles
Search
Showing results (1-10 of 178) with videos related to
Sort By:
Page
of 18
European Heart Journal. Cardiovascular Imaging
|
August 8, 2018
Mitral valve abnormalities in hypertrophic cardiomyopathy: a primary expression of the disease? Getting closer to the answer
Paolo Spirito, Maria Iascone, Paolo Ferrazzi
Circulation. Cardiovascular Genetics
|
December 20, 2012
Letter by Iascone et al regarding article, "Population-based variation in cardiomyopathy genes"
Maria Iascone, Maria Elena Sana, Paolo Ferrazzi
Human Genetics
|
October 21, 2010
Gene symbol: LAMP2. Disease: Danon disease
Maria Iascone, Attilio Iacovoni, Daniela Marchetti, et al.
Gene
|
July 24, 2012
A new mutational mechanism for hypertrophic cardiomyopathy
Laura Pezzoli, Maria Elena Sana, Paolo Ferrazzi, et al.
Journal of the American College of Cardiology
|
March 12, 2021
Reply: Hypertrophic Cardiomyopathy as Congenital Heart Disease
Aleksei Zyrianov, Paolo Spirito, Paolo Ferrazzi, et al.
Clinical Dysmorphology
|
October 21, 2020
A novel HIST1HE pathogenic variant in a girl with macrocephaly and intellectual disability: a new case and review of literature
Alessandra Pelle, Laura Pezzoli, Erika Apuril, et al.
Human Genetics
|
August 21, 2009
Novel human pathological mutations. Gene symbol: MYBPC3. Disease: cardiomyopathy, hypertrophic
Maria Iascone, D Marchetti, A R Lincesso, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology
|
November 7, 2025
A novel deep intronic mutation expands the genotype spectrum of MYH7-related myopathies
Andrea Barp, Luca Maria Neri, Lorenzo Maggi, et al.
Journal of Cardiovascular Electrophysiology
|
October 28, 2014
Cavotricuspid isthmus ablation and subcutaneous monitoring device implantation in a 2-year-old baby with 2 SCN5A mutations, sinus node dysfunction, atrial flutter recurrences, and drug induced long-QT syndrome: a tricky case of pediatric overlap syndrome?
Paolo De Filippo, Paola Ferrari, Maria Iascone, et al.
American Journal of Medical Genetics. Part A
|
May 28, 2016
Temporomandibular joint ankylosis as part of the clinical spectrum of Carey-Fineman-Ziter syndrome?
Martina Pasetti, Fabio Mazzoleni, Giorgio Novelli, et al.
Page
of 18