Zucchini, Cinzia; Serpe, Carmela; De Sanctis, Paola; Ghezzo, Alessandro; Visconti, Paola; Posar, Annio; Facchin, Federica; Marini, Marina; Abruzzo, Provvidenza Maria, TLDc Domain-Containing Genes in Autism Spectrum Disorder: New Players in the Oxidative Stress Response, «INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES», 2023, 24, Article number: 15802 , pp. 1 - 13 [Scientific article]Open Access
Provvidenza Maria Abruzzo, Marina Marini, Alessandro Ghezzo, Paola Visconti, Annio Posar, Paola de Sanctis, Carmela Serpe, Luca Pampanella, Cinzia Zucchini, TLDC PROTEINS: NEW PLAYERS IN THE OXIDATIVE STRESS RESPONSE IN AUTISM SPECTRUM DISORDER, in: Abstract Book AIBG 2023, 2023, pp. 58 - 58 (atti di: XXI CONGRESSO NAZIONALE A.I.B.G., Bari, 21-23 Settembre 2023) [Abstract]
Viggiano, Marta; D'Andrea, Tiziano; Cameli, Cinzia; Posar, Annio; Visconti, Paola; Scaduto, Maria Cristina; Colucci, Roberta; Rochat, Magali J.; Ceroni, Fabiola; Milazzo, Giorgio; Fucile, Sergio; Maestrini, Elena; Bacchelli, Elena, Contribution of CACNA1H Variants in Autism Spectrum Disorder Susceptibility, «FRONTIERS IN PSYCHIATRY», 2022, 13, Article number: 858238 , pp. 1 - 13 [Scientific article]Open Access
Viggiano, Marta; D’Andrea, Tiziano; Cameli, Cinzia; Posar, Annio; Visconti, Paola; Scaduto, MARIA CRISTINA; Colucci, Roberta; Ceroni, Fabiola; Milazzo, Giorgio; Fucile, Sergio; Maestrini, Elena; Bacchelli, Elena, Contribution of CACNA1H variants in Autism Spectrum Disorder
Susceptibility, in: Poster abstract book, 2022, pp. 1 - 1 (atti di: Neurodevelopmental disorders: from molecular mechanisms to social inclusion, Bordeaux, France, Dal 18 al 20 maggio 2022) [Abstract]
Viggiano, Marta; Cameli, Cinzia; Posar, Annio; Scaduto, Maria C.; Rochat, Magalì; Visconti, Paola; Bacchelli, Elena; Maestrini, Elena, Contribution of compound heterozygous CACNA1H mutations in autism spectrum disorder susceptibility, «EUROPEAN JOURNAL OF HUMAN GENETICS», 2022, 30, pp. 266 - 267 [Abstract]Open Access
Posar, A.; Visconti, P.; Magini, P.; Ambrosini, E.; Severi, G.; Seri, M., Deletion of 4q13.2q21.1 chromosome and autism spectrum disorder, «JOURNAL OF PEDIATRIC NEUROSCIENCES», 2022, 17, pp. 131 - 134 [Scientific article]Open Access
Caporali, Leonardo; Fiorini, Claudio; Palombo, Flavia; Romagnoli, Martina; Baccari, Flavia; Zenesini, Corrado; Visconti, Paola; Posar, Annio; Scaduto, Maria Cristina; Ormanbekova, Danara; Battaglia, Agatino; Tancredi, Raffaella; Cameli, Cinzia; Viggiano, Marta; Olivieri, Anna; Torroni, Antonio; Maestrini, Elena; Rochat, Magali Jane; Bacchelli, Elena; Carelli, Valerio; Maresca, Alessandra, Dissecting the multifaceted contribution of the mitochondrial genome to autism spectrum disorder, «FRONTIERS IN GENETICS», 2022, 13, pp. 01 - 15 [Scientific article]Open Access
Posar, Annio; Visconti, Paola, Early Motor Signs in Autism Spectrum Disorder., «CHILDREN», 2022, 9, pp. 1 - 18 [Scientific article]Open Access
Caporali, Leonardo; Fiorini, Claudio; Palombo, Flavia; Baccari, Flavia; Romagnoli, Martina; Visconti, Paola; Posar, Annio; Scaduto, MARIA CRISTINA; Maestrini, Elena; Cameli, Cinzia; Viggiano, Marta; Olivieri, Anna; Torroni, Antonio; Bacchelli, Elena; Rochat, Magali; Carelli, Valerio; Maresca, Alessandra, Mitochondrial DNA influences the susceptibility to
Autism Spectrum Disorders and the severity of the clinical
phenotype, «EUROPEAN JOURNAL OF HUMAN GENETICS», 2022, 30, Supplement 1, pp. 267 - 267 [Abstract]
Posar Annio; Visconti Paola, Some Reflections about Electrical Status Epilepticus During Slow-Wave Sleep, «GLOBAL PEDIATRIC HEALTH», 2022, 9, pp. 1 - 2 [Comment or similar]Open Access
Posar A; Visconti P., Update about "minimally verbal" children with autism spectrum disorder., «REVISTA PAULISTA DE PEDIATRIA», 2022, 40, Article number: e2022402020158 , pp. 1 - 9 [Scientific article]Open Access
Posar A; Visconti P, What Underlies Autism Spectrum Disorder?, «TURK PEDIATRI ARSIVI», 2022, 57, pp. 467 - 468 [Scientific article]Open Access
Graziano C, Despang P, Palombo F, Severi G, Posar A, Cassio A, Pippucci T, Isidori F, Matthes J, Bonora E., A new homozygous CACNB2 mutation has functional relevance and supports a role for calcium channels in autism spectrum disorder., «JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS», 2021, 51, pp. 377 - 381 [Scientific article]Open Access
Cameli C, Viggiano M, Rochat MJ, Maresca A, Caporali L, Fiorini C, Palombo F, Magini P, Duardo RC, Ceroni F, Scaduto MC, Posar A, Seri M, Carelli V, Visconti P, Bacchelli E, Maestrini E., An increased burden of rare exonic variants in NRXN1 microdeletion carriers is likely to enhance the penetrance for autism spectrum disorder., «JOURNAL OF CELLULAR AND MOLECULAR MEDICINE», 2021, 25, pp. 2459 - 2470 [Scientific article]Open Access
Filardi M.; Blunda V.; Vandi S.; Musetti A.; Posar A.; Visconti P.; Pizza F.; Plazzi G.; Franceschini C., Case Report: Burden of Illness in Narcolepsy Type 1: Hikikomori in a Teenage Girl, «FRONTIERS IN PSYCHOLOGY», 2021, 12, Article number: 634941 , pp. 634941 - 634941 [Scientific article]Open Access
