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Page 1
Setleis syndrome: genetic and clinical findings in a new case with epilepsy.
Giordano L, Desnick RJ, Molinaro A, Uliana V, Forzano F, Edelmann L, Nazarenko I, Pinelli L, Accorsi P, Faravelli F. Giordano L, et al. Among authors: molinaro a. Pediatr Neurol. 2014 Apr;50(4):389-91. doi: 10.1016/j.pediatrneurol.2013.12.009. Epub 2013 Dec 14. Pediatr Neurol. 2014. PMID: 24486222
Non-epileptic myoclonic attacks in infancy: three cases.
Vignoli A, Giordano L, Guerra D, La Briola F, Accorsi P, Savini MN, Iodice A, Molinaro A, Canevini MP. Vignoli A, et al. Among authors: molinaro a. Epileptic Disord. 2014 Dec;16(4):433-8. doi: 10.1684/epd.2014.0713. Epileptic Disord. 2014. PMID: 25498312 Free article.
The hyperkinetic movement disorder of FOXG1-related epileptic-dyskinetic encephalopathy.
Cellini E, Vignoli A, Pisano T, Falchi M, Molinaro A, Accorsi P, Bontacchio A, Pinelli L, Giordano L, Guerrini R; FOXG1 Syndrome Study Group. Cellini E, et al. Among authors: molinaro a. Dev Med Child Neurol. 2016 Jan;58(1):93-7. doi: 10.1111/dmcn.12894. Epub 2015 Sep 6. Dev Med Child Neurol. 2016. PMID: 26344814 Free article.
Neurovisual Assessment in Children with Ataxia Telangiectasia.
Iodice A, Galli J, Molinaro A, Franzoni A, Micheli R, Pinelli L, Plebani A, Soresina A, Fazzi E. Iodice A, et al. Among authors: molinaro a. Neuropediatrics. 2018 Feb;49(1):26-34. doi: 10.1055/s-0037-1607216. Epub 2017 Oct 9. Neuropediatrics. 2018. PMID: 28992644
Neurodevelopmental Profile in Children Affected by Ocular Albinism.
Galli J, Loi E, Morandi A, Scaglioni V, Rossi A, Molinaro A, Pasini N, Semeraro F, Ruberto G, Fazzi E. Galli J, et al. Among authors: molinaro a. Neuropediatrics. 2022 Feb;53(1):7-14. doi: 10.1055/s-0041-1732430. Epub 2021 Jul 29. Neuropediatrics. 2022. PMID: 34327695
691 results