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Page 1
In-Depth Phenotyping of PIGW-Related Disease and Its Role in 17q12 Genomic Disorder.
Feresin A, Lefebvre M, Sjøstrøm E, Zanus C, Paccagnella E, Bruno I, Valencic E, Morgan A, Tommasini A, Thauvin C, Bayat A, Girotto G, Musante L. Feresin A, et al. Among authors: zanus c. Biomolecules. 2024 Dec 18;14(12):1626. doi: 10.3390/biom14121626. Biomolecules. 2024. PMID: 39766333 Free PMC article.
COVID-19 Pandemic School Disruptions and Acute Mental Health in Children and Adolescents.
Davico C, Marcotulli D, Abbracciavento G, Anfosso T, Apicella M, Averna R, Bazzoni M, Calderoni D, Cammisa L, Carta A, Carucci S, Cozzi G, Di Santo F, Fazzi E, Lux C, Narducci C, Nobili L, Onida I, Pisano T, Raucci U, Sforzi I, Siri L, Sotgiu S, Tavano S, Terrinoni A, Uccella S, Vicari S, Zanus C, Vitiello B; Italian Covid-Child and Adolescent Psychiatric Emergencies Study Group. Davico C, et al. Among authors: zanus c. JAMA Netw Open. 2024 Aug 1;7(8):e2425829. doi: 10.1001/jamanetworkopen.2024.25829. JAMA Netw Open. 2024. PMID: 39102265 Free PMC article.
Vertical Parasagittal Hemispherotomy in a Pediatric Case of Epilepsy Due to Rasmussen Encephalitis: 2-Dimensional Operative Video.
De Benedictis A, Pepi C, Herur-Raman A, Barba M, Marasi A, Rossi-Espagnet MC, Napolitano A, Rossi S, Luglietto D, Capelli S, Zanus C, Savioli A, de Palma L, Specchio N, Marras CE. De Benedictis A, et al. Among authors: zanus c. Oper Neurosurg (Hagerstown). 2025 Feb 1;28(2):283-284. doi: 10.1227/ons.0000000000001261. Epub 2024 Jul 5. Oper Neurosurg (Hagerstown). 2025. PMID: 38967453 No abstract available.
A new neurodevelopmental disorder linked to heterozygous variants in UNC79.
Bayat A, Liu Z, Luo S, Fenger CD, Højte AF, Isidor B, Cogne B, Larson A, Zanus C, Faletra F, Keren B, Musante L, Gourfinkel-An I, Perrine C, Demily C, Lesca G, Liao W, Ren D. Bayat A, et al. Among authors: zanus c. Genet Med. 2023 Sep;25(9):100894. doi: 10.1016/j.gim.2023.100894. Epub 2023 May 11. Genet Med. 2023. PMID: 37183800 Free article.
TTC5 syndrome: Clinical and molecular spectrum of a severe and recognizable condition.
Musante L, Faletra F, Meier K, Tomoum H, Najarzadeh Torbati P, Blair E, North S, Gärtner J, Diegmann S, Beiraghi Toosi M, Ashrafzadeh F, Ghayoor Karimiani E, Murphy D, Murru FM, Zanus C, Magnolato A, La Bianca M, Feresin A, Girotto G, Gasparini P, Costa P, Carrozzi M. Musante L, et al. Among authors: zanus c. Am J Med Genet A. 2022 Sep;188(9):2652-2665. doi: 10.1002/ajmg.a.62852. Epub 2022 Jun 7. Am J Med Genet A. 2022. PMID: 35670379 Free PMC article.
The Genetic Diagnosis of Ultrarare DEEs: An Ongoing Challenge.
Musante L, Costa P, Zanus C, Faletra F, Murru FM, Bianco AM, La Bianca M, Ragusa G, Athanasakis E, d'Adamo AP, Carrozzi M, Gasparini P. Musante L, et al. Among authors: zanus c. Genes (Basel). 2022 Mar 12;13(3):500. doi: 10.3390/genes13030500. Genes (Basel). 2022. PMID: 35328054 Free PMC article.
27 results