VEGGIOTTI, PIERANGELO

VEGGIOTTI, PIERANGELO  

Dipartimento di Scienze Biomediche e Cliniche  

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Titolo Data di pubblicazione Autori Tipo File Abstract
Genetic Epilepsies and Developmental Epileptic Encephalopathies with Early Onset: A Multicenter Study 2024 Cavirani, BenedettaPeron, AngelaVignoli, AglaiaCanevini, Maria PaolaVeggiotti, Pierangelo + Article (author) -
Thyroid dysfunction in children and adolescents affected by undernourished and overnourished eating disorders 2023 Magenes, Vittoria CarlottaSiccardo, FrancescaHruby, ChiaraBasso, MartinaFabiano, ValentinaVeggiotti, PierangeloZuccotti, Gianvincenzo + Article (author) -
Newborn screening for X-linked adrenoleukodystrophy in Italy: Diagnostic algorithm and disease monitoring 2023 Di Profio, ElisabettaFiore, GiuliaMameli, ChiaraSangiorgio, AriannaZuccotti, Gian VincenzoVeggiotti, PierangeloVerduci, ElviraTonduti, Davide + Article (author) -
GLUT1-DS Italian registry: past, present, and future: a useful tool for rare disorders 2023 Veggiotti, PierangeloPrevitali, Roberto + Article (author) -
FDXR-associated disease: a challenging differential diagnosis with inflammatory peripheral neuropathy 2023 Previtali, RobertoVeggiotti, PierangeloTonduti, Davide + Article (author) -
Long-term follow-up of nutritional status in children with GLUT1 Deficiency Syndrome treated with classic ketogenic diet: a 5-year prospective study 2023 De Amicis, RamonaLeone, AlessandroPellizzari, MartaFoppiani, AndreaBattezzati, AlbertoLessa, ChiaraDe Giorgis, ValentinaPrevitali, RobertoVeggiotti, PierangeloBertoli, Simona + Article (author) -
Extended Glasgow Outcome Scale to Evaluate the Functional Impairment of Patients With Subcortical Band Heterotopia: A Multicentric Cross-sectional Study 2023 Chiesa, ValentinaVeggiotti, Pierangelo + Article (author) -
Menkes disease complicated by concurrent ACY1 deficiency: A case report 2023 Mauri, AlessiaVeggiotti, Pierangelo + Article (author) -
Seizures may be an early sign of acute COVID-19, and the Omicron variant could present a more epileptogenic profile 2022 Serafini, LudovicaSerati, IlariaFiori, LauraVeggiotti, Pierangelo + Article (author) -
Sex-dependent association between variability in infants’ OXTR methylation at birth and negative affectivity at 3 months 2022 Villa, MarcoVeggiotti, Pierangelo + Article (author) -
EEG at onset and MRI predict long-term clinical outcome in Aicardi syndrome 2022 Previtali, RobertoArrigoni, FilippoDe Giorgis, ValentinaLa Briola, FrancescaVeggiotti, Pierangelo + Article (author) -
A complex epileptic and dysmorphic phenotype associated with a novel frameshift KDM5B variant and deletion of SCN gene cluster 2022 Veggiotti P. + Article (author) -
Genotype-phenotype correlations in SCN8A-related disorders reveal prognostic and therapeutic implications 2022 Veggiotti, PierangeloSartori, Stefano + Article (author) -
Successful use of perampanel in GABRA1-related myoclonic epilepsy with photosensitivity 2022 Freddi, AnnaLavatelli, RossellaBasso, EleonoraLeidi, AlessiaVeggiotti, Pierangelo + Article (author) -
Molecular Genetics of GLUT1DS Italian Pediatric Cohort: 10 Novel Disease-Related Variants and Structural Analysis 2022 Alessia MauriAlessandra DuseRoberto PrevitaliSara BenedettiPierangelo Veggiotti + Article (author) -
Glut1 deficiency syndrome throughout life: clinical phenotypes, intelligence, life achievements and quality of life in familial cases 2022 Alessandra DuseElia BiganzoliAlberto MilaneseSimona BertoliRoberto PrevitaliPierangelo Veggiotti + Article (author) -
Functional correlates of clinical phenotype and severity in recurrent SCN2A variants 2022 Veggiotti, Pierangelo + Article (author) -
Cognitive, Behavioral and Socioemotional Development in a Cohort of Preterm Infants at School Age: A Cross-Sectional Study 2022 Veggiotti, Pierangelo + Article (author) -
Long-term therapeutic effect of eslicarbazepine acetate in children: An open-label extension of a cognition study in children aged 6–16 years 2022 Veggiotti P. + Article (author) -
Progressive clinical and neuroradiological findings in a child with BCL11B missense mutation : expanding the phenotypic spectrum of related disorder 2022 Veggiotti, PierangeloDoneda, Chiara + Article (author) -