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Genes
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January 21, 2023
Insights into the Cardiac Phenotype in 9p Deletion Syndrome: A Multicenter Italian Experience and Literature Review
Flaminia Pugnaloni, Roberta Onesimo, Rita Blandino, et al.
Genes
|
August 6, 2021
Cardiac Defects and Genetic Syndromes: Old Uncertainties and New Insights
Giulio Calcagni, Flaminia Pugnaloni, Maria Cristina Digilio, et al.
European Journal of Human Genetics : EJHG
|
July 12, 2012
Atrioventricular canal defect in patients with RASopathies
Maria Cristina Digilio, Francesca Romana Lepri, Maria Lisa Dentici, et al.
Calcified Tissue International
|
January 19, 2024
Is Osteogenesis Imperfecta Associated with Cardiovascular Abnormalities? A Systematic Review of the Literature
Sara J E Verdonk, Silvia Storoni, Dimitra Micha, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics
|
November 21, 2022
The heart in RASopathies
Angelica Bibiana Delogu, Giuseppe Limongelli, Paolo Versacci, et al.
American Journal of Medical Genetics. Part A
|
April 18, 2018
Congenital heart diseases and cardiovascular abnormalities in 22q11.2 deletion syndrome: From well-established knowledge to new frontiers
Marta Unolt, Paolo Versacci, Silvia Anaclerio, et al.
The American Journal of Cardiology
|
August 19, 2007
Prevalence and clinical significance of cardiovascular abnormalities in patients with the LEOPARD syndrome
Giuseppe Limongelli, Giuseppe Pacileo, Bruno Marino, et al.
Human Mutation
|
May 7, 2019
Clinical and functional characterization of a novel RASopathy-causing SHOC2 mutation associated with prenatal-onset hypertrophic cardiomyopathy
Marialetizia Motta, Antonella Giancotti, Gioia Mastromoro, et al.
The Journal of Allergy and Clinical Immunology. in Practice
|
October 24, 2022
COVID-19 Severity, Cardiological Outcome, and Immunogenicity of mRNA Vaccine on Adult Patients With 22q11.2 DS
Federica Pulvirenti, Eva Piano Mortari, Carolina Putotto, et al.
Plos One
|
April 2, 2019
Left pulmonary artery in 22q11.2 deletion syndrome. Echocardiographic evaluation in patients without cardiac defects and role of Tbx1 in mice
Gioia Mastromoro, Giulio Calcagni, Paolo Versacci, et al.
Page
of 9
Search research articles
Search
Showing results (61-70 of 84) with videos related to
Sort By:
Page
of 9
Genes
|
January 21, 2023
Insights into the Cardiac Phenotype in 9p Deletion Syndrome: A Multicenter Italian Experience and Literature Review
Flaminia Pugnaloni, Roberta Onesimo, Rita Blandino, et al.
Genes
|
August 6, 2021
Cardiac Defects and Genetic Syndromes: Old Uncertainties and New Insights
Giulio Calcagni, Flaminia Pugnaloni, Maria Cristina Digilio, et al.
European Journal of Human Genetics : EJHG
|
July 12, 2012
Atrioventricular canal defect in patients with RASopathies
Maria Cristina Digilio, Francesca Romana Lepri, Maria Lisa Dentici, et al.
Calcified Tissue International
|
January 19, 2024
Is Osteogenesis Imperfecta Associated with Cardiovascular Abnormalities? A Systematic Review of the Literature
Sara J E Verdonk, Silvia Storoni, Dimitra Micha, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics
|
November 21, 2022
The heart in RASopathies
Angelica Bibiana Delogu, Giuseppe Limongelli, Paolo Versacci, et al.
American Journal of Medical Genetics. Part A
|
April 18, 2018
Congenital heart diseases and cardiovascular abnormalities in 22q11.2 deletion syndrome: From well-established knowledge to new frontiers
Marta Unolt, Paolo Versacci, Silvia Anaclerio, et al.
The American Journal of Cardiology
|
August 19, 2007
Prevalence and clinical significance of cardiovascular abnormalities in patients with the LEOPARD syndrome
Giuseppe Limongelli, Giuseppe Pacileo, Bruno Marino, et al.
Human Mutation
|
May 7, 2019
Clinical and functional characterization of a novel RASopathy-causing SHOC2 mutation associated with prenatal-onset hypertrophic cardiomyopathy
Marialetizia Motta, Antonella Giancotti, Gioia Mastromoro, et al.
The Journal of Allergy and Clinical Immunology. in Practice
|
October 24, 2022
COVID-19 Severity, Cardiological Outcome, and Immunogenicity of mRNA Vaccine on Adult Patients With 22q11.2 DS
Federica Pulvirenti, Eva Piano Mortari, Carolina Putotto, et al.
Plos One
|
April 2, 2019
Left pulmonary artery in 22q11.2 deletion syndrome. Echocardiographic evaluation in patients without cardiac defects and role of Tbx1 in mice
Gioia Mastromoro, Giulio Calcagni, Paolo Versacci, et al.
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of 9