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Page 1
Psychopathological features in Noonan syndrome.
Perrino F, Licchelli S, Serra G, Piccini G, Caciolo C, Pasqualetti P, Cirillo F, Leoni C, Digilio MC, Zampino G, Tartaglia M, Alfieri P, Vicari S. Perrino F, et al. Among authors: alfieri p. Eur J Paediatr Neurol. 2018 Jan;22(1):170-177. doi: 10.1016/j.ejpn.2017.09.009. Epub 2017 Sep 28. Eur J Paediatr Neurol. 2018. PMID: 29037749
Visual function in Noonan and LEOPARD syndrome.
Alfieri P, Cesarini L, Zampino G, Pantaleoni F, Selicorni A, Salerni A, Vasta I, Cerutti M, Dickmann A, Colitto F, Staccioli S, Leoni C, Ricci D, Brogna C, Tartaglia M, Mercuri E. Alfieri P, et al. Neuropediatrics. 2008 Dec;39(6):335-40. doi: 10.1055/s-0029-1216354. Epub 2009 Jun 30. Neuropediatrics. 2008. PMID: 19568997
Visual and visuoperceptual function in children with Panayiotopoulos syndrome.
De Rose P, Perrino F, Lettori D, Alfieri P, Cesarini L, Battaglia D, Ricci D, Guzzetta F, Mercuri E. De Rose P, et al. Among authors: alfieri p. Epilepsia. 2010 Jul;51(7):1205-11. doi: 10.1111/j.1528-1167.2009.02484.x. Epub 2010 Jan 7. Epilepsia. 2010. PMID: 20067504 Free article.
Enhanced human brain associative plasticity in Costello syndrome.
Dileone M, Profice P, Pilato F, Alfieri P, Cesarini L, Mercuri E, Leoni C, Tartaglia M, Di Iorio R, Zampino G, Di Lazzaro V. Dileone M, et al. Among authors: alfieri p. J Physiol. 2010 Sep 15;588(Pt 18):3445-56. doi: 10.1113/jphysiol.2010.191072. Epub 2010 Jul 26. J Physiol. 2010. PMID: 20660566 Free PMC article.
Increased sleep spindle activity in patients with Costello syndrome (HRAS gene mutation).
Della Marca G, Leoni C, Dittoni S, Battaglia D, Losurdo A, Testani E, Colicchio S, Gnoni V, Gambardella ML, Mariotti P, Alfieri P, Tartaglia M, Zampino G. Della Marca G, et al. Among authors: alfieri p. J Clin Neurophysiol. 2011 Jun;28(3):314-8. doi: 10.1097/WNP.0b013e31821c3ad5. J Clin Neurophysiol. 2011. PMID: 21633259
Visual processing in Noonan syndrome: dorsal and ventral stream sensitivity.
Alfieri P, Cesarini L, De Rose P, Ricci D, Selicorni A, Menghini D, Guzzetta A, Baranello G, Tinelli F, Mallardi M, Zampino G, Vicari S, Atkinson J, Mercuri E. Alfieri P, et al. Am J Med Genet A. 2011 Oct;155A(10):2459-64. doi: 10.1002/ajmg.a.34229. Epub 2011 Sep 9. Am J Med Genet A. 2011. PMID: 21910245
Attention deficit hyperactivity disorder and cognitive function in Duchenne muscular dystrophy: phenotype-genotype correlation.
Pane M, Lombardo ME, Alfieri P, D'Amico A, Bianco F, Vasco G, Piccini G, Mallardi M, Romeo DM, Ricotti V, Ferlini A, Gualandi F, Vicari S, Bertini E, Berardinelli A, Mercuri E. Pane M, et al. Among authors: alfieri p. J Pediatr. 2012 Oct;161(4):705-9.e1. doi: 10.1016/j.jpeds.2012.03.020. Epub 2012 May 5. J Pediatr. 2012. PMID: 22560791
Neurobehavioral phenotype observed in KBG syndrome caused by ANKRD11 mutations.
Lo-Castro A, Brancati F, Digilio MC, Garaci FG, Bollero P, Alfieri P, Curatolo P. Lo-Castro A, et al. Among authors: alfieri p. Am J Med Genet B Neuropsychiatr Genet. 2013 Jan;162B(1):17-23. doi: 10.1002/ajmg.b.32113. Epub 2012 Nov 26. Am J Med Genet B Neuropsychiatr Genet. 2013. PMID: 23184435
98 results