Zobrazeno 1 - 10
of 23
pro vyhledávání: '"M L, Biondi"'
Autor:
M Lippi, M Chiesa, C Ascione, M Pedrazzini, S Mushtaq, D Rovina, D Riggio, A Di Blasio, M L Biondi, G Pompilio, G I Colombo, V Novelli, M Casella, E Sommariva
Publikováno v:
European Heart Journal. 43
Background Arrhythmogenic cardiomyopathy (ACM) is a rare inherited cardiac disorder, whose genetic cause is elusive in about 50% of cases. ACM pathogenic mutations mainly involve desmosomal genes (PKP2, JUP, DSP, DSG2, DSC2). ACM presents a variable
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::35387af2c666713c0af0c6fbbb191436
https://doi.org/10.1093/eurheartj/ehac544.362
https://doi.org/10.1093/eurheartj/ehac544.362
Autor:
V Novelli, M Manzoni, E Sommariva, G Colombo, M L Biondi, S Mushtaq, S Farina, M Roberto, F Pizzamiglio, M Casella, G Pompilio
Publikováno v:
European Heart Journal. 43
Introduction In the last years, genetic testing for inherited cardiac conditions (ICCs) is expanded and evolved at an incredible rate. This tool may inform treatment options and lifestyle choices to avoid arrhythmia triggers. Furthermore, identifying
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9f5a8daa558c7e5d072928725452a730
https://doi.org/10.1093/eurheartj/ehac544.363
https://doi.org/10.1093/eurheartj/ehac544.363
Autor:
Francesco Blasi, F. Casanova, Pierachille Santus, Stefano Centanni, F. Di Marco, M. L. Biondi
Publikováno v:
Monaldi Archives for Chest Disease, Vol 71, Iss 1 (2016)
Background. Chronic obstructive lung disease (COPD) is characterised by partially reversible usually progressive airflow limitation caused by inflammation and remodelling. Stromelysin-1 (MMP-3) has regulatory activity on other matrix-metalloproteinas
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::70c98859dd1f91daa8cc627470930d03
https://doi.org/10.4081/monaldi.2009.371
https://doi.org/10.4081/monaldi.2009.371
Autor:
Alejandro G. Schijman, J. García, José Burgos, M. L. Biondi, Marisa M. Fernández, D. Nicita, Marcelo Corti, V. Latini, Susana Alicia Besuschio
Publikováno v:
International Journal of Infectious Diseases. 73:322
Fil: Fernandez, Marisa. Gobierno de la Ciudad de Buenos Aires. Hospital de Infecciosas "Dr. Francisco Javier Muniz"; Argentina
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b121ffe14a8adeb305945593ca8d6da4
https://doi.org/10.1016/j.ijid.2018.04.4147
https://doi.org/10.1016/j.ijid.2018.04.4147
Autor:
E. Riva, M L Biondi, Elvira Verduci, Silvia Scaglioni, Ana Sousa Manso, Carlo Agostoni, Marcello Giovannini, Giovanni Radaelli
Publikováno v:
Pediatric research. 66(3)
This study examined the association of insulin resistance with single-nucleotide polymorphism (SNP) 276GT at adiponectin gene and the plasma long-chain polyunsaturated fatty acids (LCPUFAs) profile in obese children. One hundred thirty-one normolipid
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c901898ccddc89ed2357fb6298100204
https://pubmed.ncbi.nlm.nih.gov/19542908
https://pubmed.ncbi.nlm.nih.gov/19542908
Publikováno v:
The Journal of cardiovascular surgery. 45(2)
Genetic factors appear to be important in the pathogenesis of cardiovascular and cerebrovascular disease. Adhesion molecules like the members of the selectin family participate in the interaction between leukocytes and the endothelium. They are also
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::4f75e3d58476b5f79f4a3969fba0a500
https://pubmed.ncbi.nlm.nih.gov/15179350
https://pubmed.ncbi.nlm.nih.gov/15179350
Autor:
E, Verduci, E, Riva, C, Agostoni, S, Leviti, L, Fiori, A M, Lammardo, M L, Biondi, M, Giovannini
Publikováno v:
Acta paediatrica (Oslo, Norway : 1992). 91(7)
The aim of this study was to determine whether any relationship exists between the severity of mutation of the phenylalanine hydroxylase (PAH) gene and the plasma concentrations of phenylalanine (Phe) and tyrosine (Tyr) under fasting and semifasting
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::423079d67110dbd3f0cefa1fbc487b2b
https://pubmed.ncbi.nlm.nih.gov/12200907
https://pubmed.ncbi.nlm.nih.gov/12200907
Publikováno v:
Clinical cancer research : an official journal of the American Association for Cancer Research. 7(8)
Matrix metalloproteinase-1 (MMP-1) is likely to be involved in invasion and metastasis of several tumors by degrading the extracellular matrix. A single guanine insertion polymorphism (2G) in the MMP-1 promoter region creates an Ets binding site caus
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::29ba1ce5f83ae6a7c1a64d56ebf2b477
https://pubmed.ncbi.nlm.nih.gov/11489811
https://pubmed.ncbi.nlm.nih.gov/11489811
Autor:
B, Marasini, S, Casari, A, Bestetti, C, Maioli, M, Cugno, S, Zeni, O, Turri, E, Guagnellini, M L, Biondi
Publikováno v:
The Journal of rheumatology. 27(11)
To investigate whether patients with systemic sclerosis (SSc) have raised homocysteine (Hcy) plasma levels, thought to be an independent risk factor for vascular disease, and to study the relationship between Hcy and endothelial damage, and between H
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::bfa6e3449e533fb08f8cfe0e5ad3d5f1
https://pubmed.ncbi.nlm.nih.gov/11093443
https://pubmed.ncbi.nlm.nih.gov/11093443