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Electroclinical phenotype in Rubinstein-Taybi syndrome.
Giacobbe A, Ajmone PF, Milani D, Avignone S, Triulzi F, Gervasini C, Menni F, Monti F, Biffi D, Canavesi K, Costantino MA. Giacobbe A, et al. Among authors: ajmone pf. Brain Dev. 2016 Jun;38(6):563-70. doi: 10.1016/j.braindev.2015.12.003. Epub 2016 Feb 8. Brain Dev. 2016. PMID: 26867510
Sleep disorders in Cornelia de Lange syndrome.
Zambrelli E, Fossati C, Turner K, Taiana M, Vignoli A, Gervasini C, Russo S, Furia F, Masciadri M, Ajmone P, Kullman G, Canevini MP, Selicorni A. Zambrelli E, et al. Am J Med Genet C Semin Med Genet. 2016 Jun;172(2):214-21. doi: 10.1002/ajmg.c.31497. Epub 2016 May 2. Am J Med Genet C Semin Med Genet. 2016. PMID: 27133889
Daily life changes and adaptations investigated in 154 families with a child suffering from a rare disability at a public centre for rare diseases in Northern Italy.
Silibello G, Vizziello P, Gallucci M, Selicorni A, Milani D, Ajmone PF, Rigamonti C, De Stefano S, Bedeschi MF, Lalatta F. Silibello G, et al. Among authors: ajmone pf. Ital J Pediatr. 2016 Aug 31;42(1):76. doi: 10.1186/s13052-016-0285-0. Ital J Pediatr. 2016. PMID: 27576488 Free PMC article.
36 results