Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Valentina Lodato"'
Autor:
Filippo Camerota, Rachele Mariani, Giulia Cordiano, Michela Di Trani, Valentina Lodato, Alessandro Ferraris, Massimo Pasquini, Claudia Celletti
Publikováno v:
Brain Sciences, Vol 13, Iss 7, p 1042 (2023)
Ehlers–Danlos syndromes are a heterogeneous group of Heritable Connective Tissue Disorders characterized by joint hypermobility, skin hyperextensibility, and tissue fragility. Among the different types, the hypermobile Ehlers–Danlos syndrome is t
Externí odkaz:
https://doaj.org/article/735c3fe76d88444a9050e9074d2a09dc
Autor:
Anwar Baban, Viola Alesi, Monia Magliozzi, Giovanni Parlapiano, Silvia Genovese, Marianna Cicenia, Sara Loddo, Valentina Lodato, Luca Di Chiara, Fabiana Fattori, Adele D’Amico, Paola Francalanci, Antonio Amodeo, Antonio Novelli, Fabrizio Drago
Publikováno v:
Journal of Cardiovascular Development and Disease, Vol 9, Iss 10, p 332 (2022)
Filamin C is a protein specifically expressed in myocytes and cardiomyocytes and is involved in several biological functions, including sarcomere contractile activity, signaling, cellular adhesion, and repair. FLNC variants are associated with differ
Externí odkaz:
https://doaj.org/article/ef7faa1979664ab1b7f888d2edb197ac
Autor:
Valentina Lodato, Giovanni Parlapiano, Federica Calì, Massimo Stefano Silvetti, Rachele Adorisio, Michela Armando, May El Hachem, Antonino Romanzo, Carlo Dionisi-Vici, Maria Cristina Digilio, Antonio Novelli, Fabrizio Drago, Massimiliano Raponi, Anwar Baban
Publikováno v:
Journal of Cardiovascular Development and Disease, Vol 9, Iss 2, p 47 (2022)
Cardiomyopathy (CMP) is a rare disease in the pediatric population, with a high risk of morbidity and mortality. The genetic etiology of CMPs in children is extremely heterogenous. These two factors play a major role in the difficulties of establishi
Externí odkaz:
https://doaj.org/article/1938c87682ec40158430281cf5e0d2cb
Autor:
Valentina Lodato, Valeria Orlando, Viola Alesi, Silvia Di Tommaso, Mario Bengala, Giovanni Parlapiano, Elisa Agnolucci, Marianna Cicenia, Federica Calì, Maria Cristina Digilio, Fabrizio Drago, Antonio Novelli, Anwar Baban
Publikováno v:
Journal of Cardiovascular Development and Disease, Vol 8, Iss 11, p 159 (2021)
Background: Monosomy 1p36 syndrome is now considered the most common terminal deletion syndrome, with an estimated incidence of 1 in 5000. Cardiac involvement is well described in the literature mainly in terms of congenital heart defects (CHDs) and
Externí odkaz:
https://doaj.org/article/e66cb9230e3c4788851e8444807e9dd6
Autor:
Anwar Baban, Valentina Lodato, Giovanni Parlapiano, Corrado di Mambro, Rachele Adorisio, Enrico Silvio Bertini, Carlo Dionisi-Vici, Fabrizio Drago, Diego Martinelli
Publikováno v:
Biomolecules, Vol 11, Iss 11, p 1578 (2021)
Neuromuscular disorders (NMDs) are highly heterogenous from both an etiological and clinical point of view. Their signs and symptoms are often multisystemic, with frequent cardiac involvement. In fact, childhood onset forms can predispose a person to
Externí odkaz:
https://doaj.org/article/987ea053af7342c4b76cb0fd5785834d
Autor:
Celletti, Filippo Camerota, Rachele Mariani, Giulia Cordiano, Michela Di Trani, Valentina Lodato, Alessandro Ferraris, Massimo Pasquini, Claudia
Publikováno v:
Brain Sciences; Volume 13; Issue 7; Pages: 1042
Ehlers–Danlos syndromes are a heterogeneous group of Heritable Connective Tissue Disorders characterized by joint hypermobility, skin hyperextensibility, and tissue fragility. Among the different types, the hypermobile Ehlers–Danlos syndrome is t
Publikováno v:
Heart Failure Clinics. 18:139-153
The genetic background of congenital heart diseases (CHDs) is extremely complex, heterogenous, and still majorly to be determined. CHDs can be sporadic or familial. In this article we discuss in detail the phenotypic spectrum of selected genes includ
Autor:
Viola Alesi, Silvia Di Tommaso, Mario Bengala, Maria Cristina Digilio, Valentina Lodato, Federica Calì, Antonio Novelli, Valeria Orlando, Fabrizio Drago, Anwar Baban, Giovanni Parlapiano, Marianna Cicenia, Elisa Agnolucci
Publikováno v:
Journal of Cardiovascular Development and Disease
Volume 8
Issue 11
Journal of Cardiovascular Development and Disease, Vol 8, Iss 159, p 159 (2021)
Volume 8
Issue 11
Journal of Cardiovascular Development and Disease, Vol 8, Iss 159, p 159 (2021)
Background: Monosomy 1p36 syndrome is now considered the most common terminal deletion syndrome, with an estimated incidence of 1 in 5000. Cardiac involvement is well described in the literature mainly in terms of congenital heart defects (CHDs) and
Publikováno v:
Heart failure clinics. 18(1)
The genetic background of congenital heart diseases (CHDs) is extremely complex, heterogenous, and still majorly to be determined. CHDs can be sporadic or familial. In this article we discuss in detail the phenotypic spectrum of selected genes includ
Autor:
Fabrizio Drago, Carlo Dionisi-Vici, Corrado Di Mambro, Valentina Lodato, Enrico Bertini, Giovanni Parlapiano, Rachele Adorisio, Diego Martinelli, Anwar Baban
Publikováno v:
Biomolecules, Vol 11, Iss 1578, p 1578 (2021)
Biomolecules
Biomolecules
Neuromuscular disorders (NMDs) are highly heterogenous from both an etiological and clinical point of view. Their signs and symptoms are often multisystemic, with frequent cardiac involvement. In fact, childhood onset forms can predispose a person to