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Expanding the phenotype associated with biallelic SLC20A2 variants.
D'Onofrio G, Scala M, Severino M, Roberti R, Romano F, De Marco P, Iacomino M, Baldassari S, Uva P, Pavanello M, Gustincich S, Striano P, Zara F, Capra V. D'Onofrio G, et al. Among authors: striano p. Eur J Hum Genet. 2023 Jul;31(7):725-729. doi: 10.1038/s41431-023-01349-1. Epub 2023 Mar 28. Eur J Hum Genet. 2023. PMID: 36977836 No abstract available.
Inherited neuromyotonia: a clinical and genetic study of a family.
Falace A, Striano P, Manganelli F, Coppola A, Striano S, Minetti C, Zara F. Falace A, et al. Among authors: striano p, striano s. Neuromuscul Disord. 2007 Jan;17(1):23-7. doi: 10.1016/j.nmd.2006.09.014. Epub 2006 Nov 30. Neuromuscul Disord. 2007. PMID: 17140792
No major role for the EMX2 gene in schizencephaly.
Merello E, Swanson E, De Marco P, Akhter M, Striano P, Rossi A, Cama A, Leventer RJ, Guerrini R, Capra V, Dobyns WB. Merello E, et al. Among authors: striano p. Am J Med Genet A. 2008 May 1;146A(9):1142-50. doi: 10.1002/ajmg.a.32264. Am J Med Genet A. 2008. PMID: 18409201
Familial benign nonprogressive myoclonic epilepsies.
Striano P, de Falco FA, Minetti C, Zara F. Striano P, et al. Epilepsia. 2009 May;50 Suppl 5:37-40. doi: 10.1111/j.1528-1167.2009.02118.x. Epilepsia. 2009. PMID: 19469844 Free article. Review.
Epilepsy: a 'going ape' model for SUDEP?
Striano P, Zara F. Striano P, et al. Nat Rev Neurol. 2009 Dec;5(12):639-40. doi: 10.1038/nrneurol.2009.190. Nat Rev Neurol. 2009. PMID: 19953110 No abstract available.
816 results