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Martina Caiazza

Showing results (11-20 of 98) with videos related to

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Genes|January 23, 2024
A Novel Homozygous Loss-of-Function Variant in <i>SPRED2</i> Causes Autosomal Recessive Noonan-like SyndromeMaria Elena Onore, Martina Caiazza, Antonella Farina, et al.
Molecular Genetics & Genomic Medicine|May 13, 2020
Genetic analysis resolves differential diagnosis of a familial syndromic dilated cardiomyopathy: A new case of Alström syndromeBarbara Lombardo, Valeria D'Argenio, Emanuele Monda, et al.
The American Journal of Cardiology|February 12, 2026
Prevalence of Desmoplakin Variants in Patients with Recurrent MyocarditisEmanuele Monda, Sabrina Montuoro, Martina Caiazza, et al.
American Journal of Medical Genetics. Part A|September 15, 2023
An atypical Aymé-Gripp phenotype detected by exome sequencingMartina Caiazza, Alberto Budillon, Emanuele Monda, et al.
Genes|July 29, 2023
A Novel Homozygous <i>GPAA1</i> Variant in a Patient with a Glycosylphosphatidylinositol Biosynthesis DefectPaolo Fontana, Alberto Budillon, Domenico Simeone, et al.
Frontiers in Physiology|December 19, 2022
Heart rate reduction as a marker to optimize carvedilol treatment and enhance myocardial recovery in pediatric dilated cardiomyopathyRachele Adorisio, Giuseppe Pontrelli, Nicoletta Cantarutti, et al.
American Journal of Hematology|November 28, 2017
Hereditary hypochromic microcytic anemia associated with loss-of-function DMT1 gene mutations and absence of liver iron overloadMaddalena Casale, Adriana Borriello, Saverio Scianguetta, et al.
European Journal of Heart Failure|September 20, 2024
Aetiology and clinical manifestations of patients with non-dilated left ventricular cardiomyopathyEmanuele Monda, Anna Murredda, Marta Rubino, et al.
Cardiac Failure Review|August 21, 2023
Cardiovascular Involvement in Fabry's Disease: New Advances in Diagnostic Strategies, Outcome Prediction and ManagementEmanuele Monda, Luigi Falco, Giuseppe Palmiero, et al.
Circulation. Genomic and Precision Medicine|April 14, 2026
Yield of Postmortem Genetic Testing in Sudden Arrhythmic Death Syndrome: A Systematic Review and Meta-AnalysisEmanuele Monda, Sabrina Montuoro, Lia Crotti, et al.
Pageof 10

Showing results (11-20 of 98) with videos related to

Sort By:
Pageof 10
Genes|January 23, 2024
A Novel Homozygous Loss-of-Function Variant in <i>SPRED2</i> Causes Autosomal Recessive Noonan-like SyndromeMaria Elena Onore, Martina Caiazza, Antonella Farina, et al.
Molecular Genetics & Genomic Medicine|May 13, 2020
Genetic analysis resolves differential diagnosis of a familial syndromic dilated cardiomyopathy: A new case of Alström syndromeBarbara Lombardo, Valeria D'Argenio, Emanuele Monda, et al.
The American Journal of Cardiology|February 12, 2026
Prevalence of Desmoplakin Variants in Patients with Recurrent MyocarditisEmanuele Monda, Sabrina Montuoro, Martina Caiazza, et al.
American Journal of Medical Genetics. Part A|September 15, 2023
An atypical Aymé-Gripp phenotype detected by exome sequencingMartina Caiazza, Alberto Budillon, Emanuele Monda, et al.
Genes|July 29, 2023
A Novel Homozygous <i>GPAA1</i> Variant in a Patient with a Glycosylphosphatidylinositol Biosynthesis DefectPaolo Fontana, Alberto Budillon, Domenico Simeone, et al.
Frontiers in Physiology|December 19, 2022
Heart rate reduction as a marker to optimize carvedilol treatment and enhance myocardial recovery in pediatric dilated cardiomyopathyRachele Adorisio, Giuseppe Pontrelli, Nicoletta Cantarutti, et al.
American Journal of Hematology|November 28, 2017
Hereditary hypochromic microcytic anemia associated with loss-of-function DMT1 gene mutations and absence of liver iron overloadMaddalena Casale, Adriana Borriello, Saverio Scianguetta, et al.
European Journal of Heart Failure|September 20, 2024
Aetiology and clinical manifestations of patients with non-dilated left ventricular cardiomyopathyEmanuele Monda, Anna Murredda, Marta Rubino, et al.
Cardiac Failure Review|August 21, 2023
Cardiovascular Involvement in Fabry's Disease: New Advances in Diagnostic Strategies, Outcome Prediction and ManagementEmanuele Monda, Luigi Falco, Giuseppe Palmiero, et al.
Circulation. Genomic and Precision Medicine|April 14, 2026
Yield of Postmortem Genetic Testing in Sudden Arrhythmic Death Syndrome: A Systematic Review and Meta-AnalysisEmanuele Monda, Sabrina Montuoro, Lia Crotti, et al.
Pageof 10