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Annals of Surgery|October 26, 2012
Barrett's esophagus and adenocarcinoma risk: the experience of the North-Eastern Italian Registry (EBRA)Massimo Rugge, Giovanni Zaninotto, Paola Parente, et al.
BJS Open|March 4, 2025
Inter-rater variability for the American Society of Anesthesiologists classification in patients undergoing hepato-pancreato-biliary surgery (MILESTONE-2): international survey among surgeons and anaesthesiologistsSimone Augustinus, Jasper P Sijberden, Matthanja Bieze, et al.
Nature Genetics|November 18, 2014
A recurrent de novo mutation in KCNC1 causes progressive myoclonus epilepsyMikko Muona, Samuel F Berkovic, Leanne M Dibbens, et al.
Legal Medicine (Tokyo, Japan)|September 25, 2025
Towards a standard of scientific evidence in on-site inspection: compilation of the ECLM on-site inspection form in a broad case historyJessika Camatti, Anna Laura Santunione, Monica Bolognini, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|January 4, 2019
GEN-O-MA project: an Italian network studying clinical course and pathogenic pathways of moyamoya disease-study protocol and preliminary resultsAnna Bersano, Gloria Bedini, Sara Nava, et al.
Legal Medicine (Tokyo, Japan)|September 10, 2025
A nationwide forensic case-series of femicides in Italy - Part 1: Clues to the motives of the murderRossana Cecchi, Anna Laura Santunione, Jessika Camatti, et al.
Brain : a Journal of Neurology|October 24, 2018
HCN1 mutation spectrum: from neonatal epileptic encephalopathy to benign generalized epilepsy and beyondCarla Marini, Alessandro Porro, Agnès Rastetter, et al.
Legal Medicine (Tokyo, Japan)|September 18, 2025
A nationwide forensic case-series of femicides in Italy - Part 2: Clues to its epidemiology, prediction and preventionRossana Cecchi, Jessika Camatti, Anna Laura Santunione, et al.
Nature Communications|October 31, 2019
Intronic ATTTC repeat expansions in STARD7 in familial adult myoclonic epilepsy linked to chromosome 2Mark A Corbett, Thessa Kroes, Liana Veneziano, et al.
The Lancet. Neurology|July 24, 2018
Rare coding variants in genes encoding GABA<sub>A</sub> receptors in genetic generalised epilepsies: an exome-based case-control studyPatrick May, Simon Girard, Merle Harrer, et al.
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