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Missense mutations of CACNA1A are a frequent cause of autosomal dominant nonprogressive congenital ataxia.
Travaglini L, Nardella M, Bellacchio E, D'Amico A, Capuano A, Frusciante R, Di Capua M, Cusmai R, Barresi S, Morlino S, Fernández-Fernández JM, Trivisano M, Specchio N, Valeriani M, Vigevano F, Bertini E, Zanni G. Travaglini L, et al. Among authors: capuano a. Eur J Paediatr Neurol. 2017 May;21(3):450-456. doi: 10.1016/j.ejpn.2016.11.005. Epub 2016 Nov 30. Eur J Paediatr Neurol. 2017. PMID: 28007337
Chronic paroxysmal hemicrania in paediatric age: report of two cases.
Tarantino S, Vollono C, Capuano A, Vigevano F, Valeriani M. Tarantino S, et al. Among authors: capuano a. J Headache Pain. 2011 Apr;12(2):263-7. doi: 10.1007/s10194-011-0315-7. Epub 2011 Feb 22. J Headache Pain. 2011. PMID: 21340658 Free PMC article.
Migraine equivalents as part of migraine syndrome in childhood.
Tarantino S, Capuano A, Torriero R, Citti M, Vollono C, Gentile S, Vigevano F, Valeriani M. Tarantino S, et al. Among authors: capuano a. Pediatr Neurol. 2014 Nov;51(5):645-9. doi: 10.1016/j.pediatrneurol.2014.07.018. Epub 2014 Jul 22. Pediatr Neurol. 2014. PMID: 25155656
606 results