Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Francesca, Lepri"'
Autor:
Francesca Lepri, Fabrizio Balducci, Giacomo Chetoni, Lorenzo Raugei, Danilo Bondi, Virginia Lanzini
Publikováno v:
The Journal of Sports Medicine and Physical Fitness. 61
Background The current study represents the preliminary report of an Italian regional project aimed to monitor the status of young athletes in modern times and linking it to the monitoring started in the nineties. Methods After the preparatory stage,
Autor:
M. Cristina Digilio, Paolo Versacci, Francesca Lepri, Anwar Baban, Bruno Dallapiccola, Bruno Marino
Publikováno v:
Cardiogenetics, Vol 1, Iss 1, Pp e7-e7 (2011)
Atrioventricular canal defect (AVCD) is a common congenital heart defect (CHD), representing 7.4% of all cardiac malformations, considered secondary to an extracellular matrix anomaly. The AVCD is associated with extracardiac defects in about 75% of
Externí odkaz:
https://doaj.org/article/8766ced296f34471a22c798b84a177a6
Autor:
Aldo Caporossi, Patrizia Pichierri, Claudio Traversi, Gianluca Martone, Fabrizio Casprini, Francesca Lepri
Publikováno v:
Clinical & Experimental Ophthalmology. 35:582-585
Pseudoexfoliation (PEX) syndrome is a common ocular disease that also affects the cornea. A case of clinical PEX syndrome, studied by in vivo corneal confocal microscopy is reported. The morphological analysis of the confocal images demonstrated hype
Autor:
Luca Pannone, Gianfranco Bocchinfuso, Elisabetta Flex, Cesare Rossi, Giuseppina Baldassarre, Christina Lissewski, Francesca Pantaleoni, Federica Consoli, Francesca Lepri, Monia Magliozzi, Massimiliano Anselmi, Silvia Delle Vigne, Giovanni Sorge, Kadri Karaer, Goran Cuturilo, Alessandro Sartorio, Sigrid Tinschert, Maria Accadia, Maria C. Digilio, Giuseppe Zampino, Alessandro De Luca, Hélène Cavé, Martin Zenker, Bruce D. Gelb, Bruno Dallapiccola, Lorenzo Stella, Giovanni B. Ferrero, Simone Martinelli, Marco Tartaglia
Publikováno v:
Human Mutation. 38:i-i
Autor:
Maria Cristina Digilio, Luca, Ad, Alessandro De Luca, Francesca, Lepri, Valentina, Guida, Rosangela, Ferese, Maria Lisa Dentici, Adriano, Angioni, MARINO TAUSSIG DE BODONIA, Bruno, DALLA PICCOLA, Bruno, Bruno, Marino, Bruno, Dallapiccola
Publikováno v:
American journal of medical genetics. Part A. (12)
Deletion 22q11.2 (del22q11.2) syndrome, also known as DiGeorge/Velo-cardio-facial syndrome (DG/VCFS), and Alagille syndrome are genetic disorders characteristically associated with congenital heart defects (CHDs). We report on a patient with tetralog
Autor:
Valentina, Guida, Francesca, Lepri, Raymon, Vijzelaar, Andrea, De Zorzi, Versacci, Paolo, Maria, Cristina Digilio, MARINO TAUSSIG DE BODONIA, Bruno, Alessandro, De Luca, Bruno, Dallapiccola
Publikováno v:
Disease markers
Disease Markers, Vol 28, Iss 5, Pp 287-292 (2010)
Disease Markers, Vol 28, Iss 5, Pp 287-292 (2010)
GATA4mutations are found in patients with different isolated congenital heart defects (CHDs), mostly cardiac septal defects and tetralogy of Fallot. In addition,GATA4is supposed to be the responsible gene for the CHDs in the chromosomal 8p23 deletion
Autor:
Francesca Lepri, Gian Marco Tosi, Aldo Caporossi, Tomaso Caporossi, Alex Malandrini, Marco Lazzarotto, Angelo Balestrazzi, Fabrizio Casprini, Gianluca Martone
Publikováno v:
Europe PubMed Central
Scopus-Elsevier
Scopus-Elsevier
PURPOSETo evaluate aberrometric outcomes in eyes with posterior capsule opacification after 2.5-mm Nd:YAG laser capsulotomy compared to pseudophakic eyes without posterior capsule opacification. METHODSPhotographic image analysis of posterior capsule