Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Caterina Morassutto"'
Autor:
Serena Xodo, Giulia Trombetta, Caterina Morassutto, Giovanni Baccarini, Lisa Celante, Lorenza Driul, Ambrogio P Londero
Publikováno v:
Ultrasonography, Vol 43, Iss 1, Pp 47-56 (2024)
Purpose This study was conducted to evaluate the prevalence of perineal trauma during childbirth and to assess the correlations of the pelvic floor dimensions and fetal head station with obstetric trauma in a prospectively recruited cohort of women.
Externí odkaz:
https://doaj.org/article/34434634c73440928ed37439d9b48354
Publikováno v:
PLoS ONE, Vol 11, Iss 4, p e0154227 (2016)
Despite being quite frequent and having serious implications in terms of symptomatology and fertility, data on incidence and prevalence of endometriosis and adenomyosis following gold standard definitions are dramatically lacking. The average time fr
Externí odkaz:
https://doaj.org/article/c4cf68224ab24574bc2795f9e6ce6926
Autor:
Carla Spazzolini, Thomas Meitinger, Althea Goosen, Marshall Heradien, Gianfranco Parati, Peter J. Schwartz, Caterina Morassutto, Paul A. Brink, Elisa Mastantuono, Heikki Swan, Annukka M. Lahtinen, Peter Lichtner, Kimmo Kontula, Mari Cristina A Monti, Lia Crotti
We welcome the opportunity to respond to the expected comments by Amin et al regarding our article on the modifying role of 3′ untranslated region (3′UTR) single-nucleotide polymorphisms (SNPs) in type 1 long-QT syndrome patients.1 In the origina
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1adc902dc4611b98cc694af022a8b575
http://hdl.handle.net/10281/148488
http://hdl.handle.net/10281/148488
Autor:
Lia Crotti, Althea Goosen, Heikki Swan, Paul A. Brink, Marshall Heradien, Kimmo Kontula, Elisa Mastantuono, Peter J. Schwartz, Caterina Morassutto, Gianfranco Parati, Annukka M. Lahtinen, Thomas Meitinger, Maria Cristina Monti, Peter Lichtner, Carla Spazzolini
Background— Long-QT syndrome is an inherited cardiac channelopathy characterized by delayed repolarization, risk of life-threatening arrhythmia, and significant clinical variability even within families. Three single-nucleotide polymorphisms (SNPs)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7a6427bb92b381e9ed78386590987a32
http://hdl.handle.net/10281/131754
http://hdl.handle.net/10281/131754