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Page 1
Bilateral perysilvian polymicrogyria in Chiari I malformation.
Spalice A, Parisi P, Mastrangelo M, De Luca F, Verrotti A, Iannetti P. Spalice A, et al. Among authors: mastrangelo m. Childs Nerv Syst. 2006 Dec;22(12):1635-7. doi: 10.1007/s00381-006-0180-x. Epub 2006 Oct 13. Childs Nerv Syst. 2006. PMID: 17058087
Early-onset hereditary neuropathy with liability to pressure palsy.
Antonini G, Luchetti A, Mastrangelo M, Ciambra GL, Di Netta S, Taioli F, Fabrizi GM, Iannetti P. Antonini G, et al. Among authors: mastrangelo m. Neuropediatrics. 2007 Feb;38(1):50-4. doi: 10.1055/s-2007-981451. Neuropediatrics. 2007. PMID: 17607607 Review.
New trends in neuronal migration disorders.
Verrotti A, Spalice A, Ursitti F, Papetti L, Mariani R, Castronovo A, Mastrangelo M, Iannetti P. Verrotti A, et al. Among authors: mastrangelo m. Eur J Paediatr Neurol. 2010 Jan;14(1):1-12. doi: 10.1016/j.ejpn.2009.01.005. Epub 2009 Mar 4. Eur J Paediatr Neurol. 2010. PMID: 19264520 Review.
Eponym : Rasmussen syndrome.
Mastrangelo M, Mariani R, Menichella A. Mastrangelo M, et al. Eur J Pediatr. 2010 Aug;169(8):919-24. doi: 10.1007/s00431-010-1148-0. Epub 2010 Feb 23. Eur J Pediatr. 2010. PMID: 20177700 Review.
Report of two never treated adult sisters with aromatic L-amino Acid decarboxylase deficiency: a portrait of the natural history of the disease or an expanding phenotype?
Leuzzi V, Mastrangelo M, Polizzi A, Artiola C, van Kuilenburg AB, Carducci C, Ruggieri M, Barone R, Tavazzi B, Abeling NG, Zoetekouw L, Sofia V, Zappia M, Carducci C. Leuzzi V, et al. Among authors: mastrangelo m. JIMD Rep. 2015;15:39-45. doi: 10.1007/8904_2014_295. Epub 2014 May 1. JIMD Rep. 2015. PMID: 24788355 Free PMC article.
470 results