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1
von Andrea Santangelo ; Alessandra Sardi ; Luca Bergonzini ; et al.
Frontiers in Neurology, Vol 17 (2026)
Schlagworte: ADHD; autism spectrum disorder; cognitive assessment; neurodevelopment; neurofibromatosis type 1; NF1; Neurology. Diseases of the nervous system; RC346-429
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2
von Alessia Cafaro ; Antonella Riva ; Federica Pigliasco ; et al.
Epilepsia Open, Vol 10, Iss 5, Pp 1699-1704 (2025)
Schlagworte: cannabidiol; cannabis; children; epilepsy; safety; Neurology. Diseases of the nervous system; RC346-429
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3
von Daiana Mariano ; Valentina Petrone ; Francesca Madia ; et al.
Children, Vol 13, Iss 5, p 599 (2026)
Schlagworte: ASXL3 gene; ASXL3-related syndrome; Bainbridge–Ropers syndrome; BRPS; neurodevelopmental disorder; Pediatrics; RJ1-570
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4
von Antonella Riva ; Roberta Roberti ; Gianluca D'Onofrio ; et al.
Epilepsia Open, Vol 8, Iss 3, Pp 1142-1150 (2023)
Schlagworte: antiseizure medications; epilepsy; pharmacogenomics; precision medicine; Neurology. Diseases of the nervous system; RC346-429
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5
von Santagostino Barbone, Alessandro ; Giacomini, Thea ; Casabona, Silvia ; et al.
In Multiple Sclerosis and Related Disorders April 2026 108
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6
Genotype–phenotype correlations and disease mechanisms in PEX13-related Zellweger spectrum disorders
von Paola Borgia ; Simona Baldassari ; Nicoletta Pedemonte ; et al.
Orphanet Journal of Rare Diseases, Vol 17, Iss 1, Pp 1-18 (2022)
Schlagworte: Peroxisome biogenesis disorders; Zellweger spectrum disorder; PEX13; mitochondrial dysfunction; Medicine
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7
von Antonella Riva ; Elisabetta Amadori ; Maria Stella Vari ; et al.
Italian Journal of Pediatrics, Vol 48, Iss 1, Pp 1-6 (2022)
Schlagworte: Drooling; Neurological disorders; Pediatrics; Cerebral palsy; Delphi; RJ1-570
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8
von Antonella Riva ; Gianluca Piccolo ; Federica Balletti ; et al.
Frontiers in Pediatrics, Vol 10 (2022)
Schlagworte: acute; COVID-19; children; neurological symptoms; SARS-CoV-2; Pediatrics; RJ1-570
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9
von Elisabetta Amadori ; Marcello Scala ; Giulia Sofia Cereda ; et al.
Italian Journal of Pediatrics, Vol 46, Iss 1, Pp 1-9 (2020)
Schlagworte: CLN2; TPP1; Targeted re-sequencing; Next generation sequencing (NGS); Early diagnosis; Epilepsy; Pediatrics; RJ1-570
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10
von Antonella Riva ; Alice Golda ; Ganna Balagura ; et al.
Frontiers in Neurology, Vol 12 (2021)
Schlagworte: anti-seizure medications; epilepsy; genetics; inflammation; precision medicine; Neurology. Diseases of the nervous system; RC346-429
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11
von Chen, Siwei ; Abou-Khalil, Bassel W. ; Afawi, Zaid ; et al.
Nature Neuroscience. 27(10):1864-1879
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13
von Alessandro Santagostino Barbone ; Thea Giacomini ; Silvia Casabona ; et al.
Schlagworte: Acquired demyelinating syndrome (ADS); Acute demyelinating encephalomyelitis (ADEM); Clinically isolated syndrome (CIS); Multiple Sclerosis (MS); Myelin-oligodendrocyte glycoprotein antibody-associated disease (MOGAD); Optic neuritis (ON)
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14
von Feng, Yen-Chen Anne ; Howrigan, Daniel P ; Abbott, Liam E ; et al.
In eBioMedicine October 2021 72
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15
von Ronzano, Nadia ; Scala, Marcello ; Abiusi, Emanuela ; et al.
In Seizure: European Journal of Epilepsy August 2022 100:82-86
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16
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17
von Gerarda Cappuccio ; Michele Pinelli ; Marianna Alagia ; et al.
PLoS ONE, Vol 12, Iss 9, p e0184022 (2017)
Schlagworte: Medicine; Science
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18
von Motelow, Joshua E. ; Povysil, Gundula ; Dhindsa, Ryan S. ; et al.
In The American Journal of Human Genetics 3 June 2021 108(6):965-982
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19
von Raviglione, Federico ; Douzgou, Sofia ; Scala, Marcello ; et al.
In Seizure: European Journal of Epilepsy May 2021 88:60-72
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20
von Balagura, Ganna ; Riva, Antonella ; Marchese, Francesca ; et al.
In European Journal of Paediatric Neurology September 2020 28:193-197
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21
von Ganna Balagura ; Julie Xian ; Antonella Riva ; et al.
Schlagworte: ASM = antiseizure medication; DEE = developmental and epileptic encephalopathy; FCD = focal cortical dysplasia; ID = intellectual disability.
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22
von Pasquale Striano ; Maria Stella Vari
Pediatric Neurology Briefs, Vol 29, Iss 7 (2015)
Schlagworte: post-ictal paresis; rolandic epilepsy; migraine; Pediatrics; RJ1-570; Neurology. Diseases of the nervous system; RC346-429
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23
Ultra-Rare Genetic Variation in the Epilepsies: A Whole-Exome Sequencing Study of 17,606 Individuals
von Feng, Yen-Chen Anne ; Howrigan, Daniel P. ; Abbott, Liam E. ; et al.
In The American Journal of Human Genetics 1 August 2019 105(2):267-282
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24
von Alessandro Orsini ; Andrea Santangelo ; Francesca Bravin ; et al.
Genes ; Volume 13 ; Issue 2 ; Pages: 276
Schlagworte: Pobinds; neurodevelopment; epilepsy; seizure; CSNK2B
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25
von Mari E. K. Niemi ; Juha Karjalainen ; Rachel G. Liao ; et al.
Schlagworte: Genetics; Genome-wide association studies; SARS-CoV-2; Viral infection
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