ZANUS, CATERINA
ZANUS, CATERINA
Dipartimento Universitario Clinico di Scienze mediche, chirurgiche e della salute
Dottorandi
Case report: A relevant misdiagnosis: Photosensitive epilepsy mimicking a blinking tic
2022-01-01 Burlo, Francesca; Barbi, Egidio; Carrozzi, Marco; Zanus, Caterina
Does a standard triage tool adequately detect the needs of children and adolescents admitted for mental health problem?
2022-01-01 Zanchi, Chiara; Skabar, Aldo; Zanus, Caterina; Tolomei, Greta; Ghirardo, Sergio; Giorgi, Rita; Velkoski, Angelika; Barbi, Egidio; Cozzi, Giorgio
Haploinsufficiency as a Foreground Pathomechanism of Poirer-Bienvenu Syndrome and Novel Insights Underlying the Phenotypic Continuum of CSNK2B-Associated Disorders
2023-01-01 Di Stazio, Mariateresa; Zanus, Caterina; Faletra, Flavio; Pesaresi, Alessia; Ziccardi, Ilaria; Morgan, Anna; Girotto, Giorgia; Costa, Paola; Carrozzi, Marco; D’Adamo, Adamo P.; Musante, Luciana
Paroxysmal awakenings and seizures in congenital hyperinsulinism: a late diagnosis
2016-01-01 Zanus, Caterina; Costa, Paola; Tornese, Gianluca; Faleschini, Elena; Carrozzi, Marco
Sleep Spindle-Related EEG Connectivity in Children with Attention-Deficit/Hyperactivity Disorder: An Exploratory Study
2023-01-01 Zanus, Caterina; Miladinović, Aleksandar; De Dea, Federica; Skabar, Aldo; Stecca, Matteo; Ajcevic, Miloš; Accardo, Agostino; Carrozzi, Marco
SPEN haploinsufficiency causes a neurodevelopmental disorder overlapping proximal 1p36 deletion syndrome with an episignature of X chromosomes in females
2021-01-01 Radio, F. C.; Pang, K.; Ciolfi, A.; Levy, M. A.; Hernandez-Garcia, A.; Pedace, L.; Pantaleoni, F.; Liu, Z.; de Boer, E.; Jackson, A.; Bruselles, A.; Mcconkey, H.; Stellacci, E.; Lo Cicero, S.; Motta, M.; Carrozzo, R.; Dentici, M. L.; Mcwalter, K.; Desai, M.; Monaghan, K. G.; Telegrafi, A.; Philippe, C.; Vitobello, A.; Au, M.; Grand, K.; Sanchez-Lara, P. A.; Baez, J.; Lindstrom, K.; Kulch, P.; Sebastian, J.; Madan-Khetarpal, S.; Roadhouse, C.; Mackenzie, J. J.; Monteleone, B.; Saunders, C. J.; Jean Cuevas, J. K.; Cross, L.; Zhou, D.; Hartley, T.; Sawyer, S. L.; Monteiro, F. P.; Secches, T. V.; Kok, F.; Schultz-Rogers, L. E.; Macke, E. L.; Morava, E.; Klee, E. W.; Kemppainen, J.; Iascone, M.; Selicorni, A.; Tenconi, R.; Amor, D. J.; Pais, L.; Gallacher, L.; Turnpenny, P. D.; Stals, K.; Ellard, S.; Cabet, S.; Lesca, G.; Pascal, J.; Steindl, K.; Ravid, S.; Weiss, K.; Castle, A. M. R.; Carter, M. T.; Kalsner, L.; de Vries, B. B. A.; van Bon, B. W.; Wevers, M. R.; Pfundt, R.; Stegmann, A. P. A.; Kerr, B.; Kingston, H. M.; Chandler, K. E.; Sheehan, W.; Elias, A. F.; Shinde, D. N.; Towne, M. C.; Robin, N. H.; Goodloe, D.; Vanderver, A.; Sherbini, O.; Bluske, K.; Hagelstrom, R. T.; Zanus, C.; Faletra, F.; Musante, L.; Kurtz-Nelson, E. C.; Earl, R. K.; Anderlid, B. -M.; Morin, G.; van Slegtenhorst, M.; Diderich, K. E. M.; Brooks, A. S.; Gribnau, J.; Boers, R. G.; Finestra, T. R.; Carter, L. B.; Rauch, A.; Gasparini, P.; Boycott, K. M.; Barakat, T. S.; Graham, J. M.; Faivre, L.; Banka, S.; Wang, T.; Eichler, E. E.; Priolo, M.; Dallapiccola, B.; Vissers, L. E. L. M.; Sadikovic, B.; Scott, D. A.; Holder, J. L.; Tartaglia, M.
The Genetic Diagnosis of Ultrarare DEEs: An Ongoing Challenge
2022-01-01 Musante, Luciana; Costa, Paola; Zanus, Caterina; Faletra, Flavio; Murru, Flora M.; Bianco, Anna M.; La Bianca, Martina; Ragusa, Giulia; Athanasakis, Emmanouil; D’Adamo, Adamo P.; Carrozzi, Marco; Gasparini, Paolo
TTC5 syndrome: Clinical and molecular spectrum of a severe and recognizable condition
2022-01-01 Musante, Luciana; Faletra, Flavio; Meier, Kolja; Tomoum, Hoda; Najarzadeh Torbati, Paria; Blair, Edward; North, Sally; Gärtner, Jutta; Diegmann, Susann; Beiraghi Toosi, Mehran; Ashrafzadeh, Farah; Ghayoor Karimiani, Ehsan; Murphy, David; Murru, Flora Maria; Zanus, Caterina; Magnolato, Andrea; La Bianca, Martina; Feresin, Agnese; Girotto, Giorgia; Gasparini, Paolo; Costa, Paola; Carrozzi, Marco