Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Jacopo Proietti"'
Autor:
Sean R. Mathieson, Carol Nanyunja, Samantha Sadoo, Sherinah Nakalembe, Eleanor Duckworth, Stella Muryasingura, Natalia Niombi, Jacopo Proietti, Mariam Busingye, Annettee Nakimuli, Vicki Livingstone, Emily L. Webb, Ivan Mambule, Geraldine B. Boylan, Cally J. Tann
Publikováno v:
EClinicalMedicine, Vol 78, Iss , Pp 102937- (2024)
Summary: Background: Intrapartum-related neonatal encephalopathy (NE) is a leading cause of childhood mortality and morbidity. Continuous electroencephalography (EEG) is gold standard for neonatal brain monitoring; however, low-income country data is
Externí odkaz:
https://doaj.org/article/3adecdb590f84ae581a70778ec4275de
Autor:
Jacopo Proietti, Elena Fiorini, Gaetano Cantalupo, Elena Fontana, Tommaso Lo Barco, Cecilia Bonin, Bernardo Dalla Bernardina, Francesca Darra
Publikováno v:
Heliyon, Vol 10, Iss 2, Pp e24747- (2024)
In epilepsy with myoclonic-atonic seizures (EMA), status epilepticus (SE) may occur during the onset phase, uncommonly in post-puberal patients. We report a post-puberal patient with EMA who presented SE with insidious onset and catamenial recurrence
Externí odkaz:
https://doaj.org/article/69b8e5bca7bb443296be3c410923e63c
Autor:
Tommaso Lo Barco, Francesca Offredi, Eva Castino, Jacopo Proietti, Alberto Cossu, Elena Fiorini, Elena Fontana, Gaetano Cantalupo, Bernardo Dalla Bernardina, Francesca Darra
Publikováno v:
Developmental Medicine & Child Neurology. 65:838-846
To explore the feasibility of using an adaptive behaviour profile (ABP) assessment generated from a well-known measure-the Vineland Adaptive Behavior Scales, Second Edition (VABS-II)-as an instrument for outcome measures in adolescents and adults wit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d4e2ab9cc883d1acba0e12190f5f957b
https://doi.org/10.1111/dmcn.15448
https://doi.org/10.1111/dmcn.15448
Autor:
Jacopo, Proietti, Elena, Fiorini, Lisa, Meneghello, Gaetano, Cantalupo, Elena, Fontana, Tommaso, Lo Barco, Bernardo Dalla, Bernardina, Francesca, Darra
Publikováno v:
Epileptic Disorders. 24:387-396
Febrile status epilepticus evolves from a febrile seizure (FS) in 5% of cases. Its prompt recognition is challenging, especially when motor manifestations are absent or subtle. We describe the ictal electroclinical features of non-convulsive febrile
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::515e6db7a9df250704a055fac0d93b8e
https://doi.org/10.1684/epd.2021.1402
https://doi.org/10.1684/epd.2021.1402
Autor:
Andreea M, Pavel, John M, O'Toole, Jacopo, Proietti, Vicki, Livingstone, Subhabrata, Mitra, William P, Marnane, Mikael, Finder, Eugene M, Dempsey, Deirdre M, Murray, Geraldine B, Boylan, Olga, Kapellou
Publikováno v:
Epilepsia.
To assess if early clinical and electroencephalographic(EEG) features predict later seizure development in infants with hypoxic-ischaemic encephalopathy(HIE).Clinical and EEG parameters12 hours of birth from infants with HIE across eight European Neo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c813cebbe64ea3ed60ee84b04a20c1c1
https://pubmed.ncbi.nlm.nih.gov/36398397
https://pubmed.ncbi.nlm.nih.gov/36398397
Autor:
Emilia Ricci, Francesca Darra, Jens Erik Klint Nielsen, Gaetano Cantalupo, Elena Fiorini, Elena Fontana, Elisabetta Amadori, Francesco Pisani, Bernardo Dalla Bernardina, Pasquale Striano, Tommaso Lo Barco, Robertino Dilena, Cristina Bana, Duccio Maria Cordelli, Elena Gardella, Jacopo Proietti
Objective. Coffin-Siris syndrome (CSS) is a rare congenital malformation syndrome, caused by mutations in the ARID1B gene in over half of the cases. While the clinical characteristics of the syndrome have been increasingly described, a detailed evalu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::57c5df09b8f9cad9f0a520d4f41ed4a5
http://hdl.handle.net/11585/857165
http://hdl.handle.net/11585/857165
Autor:
Gaetano Cantalupo, Giulia Galati, Jacopo Proietti, Anna Ludovica Ghobert, Tommaso Lo Barco, Francesca Lucca
Publikováno v:
The Lancet. 398:156
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::df7ca9f8744595b549ba9eb44c80d5af
https://doi.org/10.1016/s0140-6736(21)01048-5
https://doi.org/10.1016/s0140-6736(21)01048-5
Autor:
Tommaso Lo Barco, Luciana De Gaetano, Elisabetta Santangelo, Tonino Bravi, Jacopo Proietti, Gaetano Cantalupo, Isabella Brambilla, Francesca Darra
Publikováno v:
Epilepsy & Behavior. 127:108500
SYNGAP1-developmental and epileptic encephalopathy (SYNGAP1-DEE) has been recently featured as a distinct genetic disease characterized by global psychomotor delay mainly involving language, moderate-to-severe cognitive impairment, autism spectrum di
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a4327dc91dab875db87dcb7e027058b4
Autor:
Abramsky R, Acun C, Alt J, Aly H, Arad N, Baak LM, Bakalar D, Balasingham T, Bammler T, Benders MJNL, Benitez D, Boni E, Boylan G, Campbell E, Castri P, Chandrashekar P, Chavez-Valdez R, Chen M, Chiodin E, Comstock B, Damien J, Damien J, de Vries LS, de Vries L, Dickman J, Doucette L, Duckworth E, Duckworth E, Echeverria-Palacio C, El Jalbout R, El-Dib M, Elshibiny H, Flock D, Gallagher A, Gasperoni E, Glass H, Harteman JC, Harvey-Jones K, Hazan I, Heagerty P, Inder T, Jantzie L, Juul S, Karnati S, Kute N, Lacaille H, Lange F, Lemmers PMA, Liu W, Llaguno N, Magalhães M, Mambule I, Marandyuk B, Marks K, Martin LJ, Massaro A, Mathieson S, Mathieson S, McCaul MC, Meehan C, Meledin I, Menna E, Menzato F, Mintoft A, Mitra S, Nakimuli A, Nanyunya C, Norris G, Northington FJ, Numis A, O'Reilly JJ, Ortiz S, Padiyar S, Paquette N, Parmeggiani L, Patrizi S, Pavlidis E, Pellegrin S, Penn AA, Petitpas L, Pinchefsky E, Ponta A, Puthuraya JPS, Rais R, Robertson NJ, Rodrigues D, Salandin M, Salzbank J, Sánchez L, Schalij N, Serrano-Tabares C, Shany E, Staffler A, Steggerda S, Tachtsidis I, Tann C, Tataranno ML, Trabatti C, Tremblay J, Tromp S, Tucker K, Turnbill V, Vacher CM, van Bel F, van der Aa NE, Van Meurs K, Van Steenis A, van Wyk L, Vannasing P, Variane G, Verma V, Voldal E, Wagenaar N, Wu Y, Wustoff C
Publikováno v:
Journal of neonatal-perinatal medicine [J Neonatal Perinatal Med] 2023; Vol. 16 (s1), pp. S33-S62.