WISC-IV intellectual profiles in Italian children with self-limited epilepsy with centrotemporal spikes.

Autor: Zanaboni MP; Department of Child Neurology and Psychiatry, IRCCS Mondino Foundation, Pavia, Italy., Pasca L; Department of Child Neurology and Psychiatry, IRCCS Mondino Foundation, Pavia, Italy.; Department of Brain and Behavioral Sciences, University of Pavia, Pavia, Italy., Bova SM; Vittore Buzzi Children's Hospital, Pediatric Neurology Unit, Milan, Italy., Chiappedi MA; Child Neuropsychiatry Unit, U.O.N.P.I.A., ASST-Vigevano, Italy., Filippini M; Piccolo Principe Cooperativa Sociale, Ferrara, Italy., Giordano L; Child Neurology and Psychiatry Unit, ASST Spedali Civili of Brescia, Brescia, Italy., Grumi S; Department of Child Neurology and Psychiatry, IRCCS Mondino Foundation, Pavia, Italy., Micheletti S; Child Neurology and Psychiatry Unit, ASST Spedali Civili of Brescia, Brescia, Italy., Operto FF; Child and Adolescent Neuropsychiatry Unit, Department of Medicine, Surgery and Dentistry, University of Salerno, Salerno, Italy., Pruna D; Department of Pediatric Neurology and Epileptology, Pediatric ARNAS Brotzu, Cagliari, Italy., Ragona F; Department of Paediatric Neuroscience, Fondazione IRCCS Istituto Neurologico Carlo Besta, Milan, Italy., Raviglione F; Child Neuropsychiatry Unit, U.O.N.P.I.A. ASST-Rhodense, Rho, Milan, Italy., Totaro M; Department of Child Neurology and Psychiatry, IRCCS Mondino Foundation, Pavia, Italy.; Department of Brain and Behavioral Sciences, University of Pavia, Pavia, Italy., Varesio C; Department of Child Neurology and Psychiatry, IRCCS Mondino Foundation, Pavia, Italy.; Department of Brain and Behavioral Sciences, University of Pavia, Pavia, Italy., Vignoli A; Child Neuropsychiatry Unit, Department of Health Sciences, ASST Grande Ospedale Metropolitano Niguarda, Milan, Italy., De Giorgis V; Department of Child Neurology and Psychiatry, IRCCS Mondino Foundation, Pavia, Italy.; Department of Brain and Behavioral Sciences, University of Pavia, Pavia, Italy.

Publikováno v: Epileptic disorders : international epilepsy journal with videotape [Epileptic Disord] 2023 Apr; Vol. 25 (2), pp. 160-172. Date of Electronic Publication: 2023 May 04.

Overall cognitive profiles in patients with GLUT1 Deficiency Syndrome.

Autor: De Giorgis V; Department of Child Neurology and Psychiatry, IRCCS Mondino Foundation, Pavia, Italy., Masnada S; Department of Child Neurology and Psychiatry, IRCCS Mondino Foundation, Pavia, Italy.; Department of Brain and Behavioral Sciences, University of Pavia, Pavia, Italy., Varesio C; Department of Child Neurology and Psychiatry, IRCCS Mondino Foundation, Pavia, Italy.; Brain and Behavior Department, University of Pavia, Pavia, Italy., Chiappedi MA; Department of Child Neurology and Psychiatry, IRCCS Mondino Foundation, Pavia, Italy., Zanaboni M; Department of Child Neurology and Psychiatry, IRCCS Mondino Foundation, Pavia, Italy., Pasca L; Department of Child Neurology and Psychiatry, IRCCS Mondino Foundation, Pavia, Italy.; Brain and Behavior Department, University of Pavia, Pavia, Italy., Filippini M; Child Neurology Unit, IRCCS Istituto delle Scienze Neurologiche, Bologna, Italy., Macasaet JA; Department of Neurosciences, Makati Medical Center, Manila, Philippines., Valente M; Genomic and post-Genomic Center, IRCCS ''C. Mondino'' National Neurological Institute, Pavia, Italy., Ferraris C; Human Nutrition and Eating Disorder Research Center, Department of Public Health, Experimental and Forensic Medicine University of Pavia, Pavia, Italy., Tagliabue A; Human Nutrition and Eating Disorder Research Center, Department of Public Health, Experimental and Forensic Medicine University of Pavia, Pavia, Italy., Veggiotti P; Pediatric Neurology Unit, 'V. Buzzi' Hospital, Milan, Italy.; Biomedical and Clinical Sciences Department, L Sacco, University of Milan, Milan, Italy.

Publikováno v: Brain and behavior [Brain Behav] 2019 Mar; Vol. 9 (3), pp. e01224. Date of Electronic Publication: 2019 Feb 04.

GLUT1-DS Italian registry: past, present, and future: a useful tool for rare disorders.

Autor: Varesio, Costanza^1,2 (AUTHOR), De Giorgis, Valentina^1,2 (AUTHOR) Valentina.degiorgis@mondino.it, Veggiotti, Pierangelo^3,4 (AUTHOR), Nardocci, Nardo⁵ (AUTHOR), Granata, Tiziana⁵ (AUTHOR), Ragona, Francesca⁵ (AUTHOR), Pasca, Ludovica^1,2 (AUTHOR), Mensi, Martina Maria¹ (AUTHOR), Borgatti, Renato^1,2 (AUTHOR), Olivotto, Sara³ (AUTHOR), Previtali, Roberto⁴ (AUTHOR), Riva, Antonella^6,7 (AUTHOR), Mancardi, Maria Margherita⁸ (AUTHOR), Striano, Pasquale^6,7 (AUTHOR), Cavallin, Mara⁹ (AUTHOR), Guerrini, Renzo⁹ (AUTHOR), Operto, Francesca Felicia¹⁰ (AUTHOR), Pizzolato, Alice¹¹ (AUTHOR), Di Maulo, Ruggero¹¹ (AUTHOR), Martino, Fabiola¹² (AUTHOR)

Publikováno v: Orphanet Journal of Rare Diseases. 3/21/2023, Vol. 18 Issue 1, p1-9. 9p.

Exploring ketogenic diet resistance in glucose transporter type 1 deficiency syndrome: A comprehensive review and critical appraisal.

Autor: Falsaperla R; Neonatal Intensive Care Unit and Neonatal Accompaniment Unit, Azienda Ospedaliero-Universitaria Policlinico 'Rodolico-San Marco,' San Marco Hospital, University of Catania, Catania, Italy.; Unit of Pediatrics and Pediatric Emergency, Azienda Ospedaliero-Universitaria Policlinico 'Rodolico-San Marco,' San Marco Hospital, University of Catania, Catania, Italy.; Department of Medical Sciences-Pediatric Section, University of Ferrara, Ferrara, Italy., Sortino V; Unit of Pediatrics and Pediatric Emergency, Azienda Ospedaliero-Universitaria Policlinico 'Rodolico-San Marco,' San Marco Hospital, University of Catania, Catania, Italy., Kluger GJ; Epilepsy Center for Children and Adolescents, Schön Clinic Vogtareuth, Vogtareuth, Germany., Herberhold T; Clinic for Neuropediatrics and Neurorehabilitation, Epilepsy Center for Children and Adolescents, Schön Klinik Vogtareuth, Vogtareuth, Germany., Rüegger A; Department of Neuropediatrics, University Children's Hospital Zurich, Zurich, Switzerland., Striano P; Pediatric Neurology and Muscular Diseases Unit, IRCCS Istituto Giannina Gaslini', Full Member of ERN-Epicare, Genova, Italy.; Department of Neurosciences, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health, University of Genova, Genova, Italy., Ruggieri M; Unit of Rare Diseases of the Nervous System in Childhood, Department of Clinical and Experimental Medicine, Section of Pediatrics and Child Neuropsychiatry, University of Catania, Catania, Italy., Klepper J; Klinikum Aschaffenburg-Alzenau, Aschaffenburg, Germany., Ramantani G; Department of Neuropediatrics, University Children's Hospital Zurich, Zurich, Switzerland.; University of Zurich, Zurich, Switzerland.

Publikováno v: Epilepsia open [Epilepsia Open] 2024 Dec 06. Date of Electronic Publication: 2024 Dec 06.

Glucose transporter 1 deficiency syndrome: nutritional and growth pattern phenotypes at diagnosis.

Autor: Bertoli, Simona^1,2 (AUTHOR) simona.bertoli@unimi.it, Masnada, Silvia³ (AUTHOR), De Amicis, Ramona¹ (AUTHOR), Sangiorgio, Arianna⁴ (AUTHOR), Leone, Alessandro¹ (AUTHOR), Gambino, Mirko³ (AUTHOR), Lessa, Chiara¹ (AUTHOR), Tagliabue, Anna⁵ (AUTHOR), Ferraris, Cinzia⁵ (AUTHOR), De Giorgis, Valentina^2,6 (AUTHOR), Battezzati, Alberto¹ (AUTHOR), Zuccotti, Gian Vincenzo⁴ (AUTHOR), Veggiotti, Pierangelo^7,8 (AUTHOR), Mameli, Chiara⁴ (AUTHOR)

Publikováno v: European Journal of Clinical Nutrition. Sep2020, Vol. 74 Issue 9, p1290-1298. 9p.