Author:
Pascual-Castroviejo Ignacio,Restivo Domenico A.,Milone Pietro
Reference19 articles.
1. Anderson PJ, Molony D, Haan E, David DJ (2005) Familial Parry-Romberg disease. Int J Pediatr Otorhonolaryngol 69: 705–708.
2. Asher SW, Berg BO (1982) Progressive facial hemiatrophy: report of three cases, including one observed over 43 years, and computed tomography findings. Arch Neurol 39: 44–46.
3. de Crecchio G, Forte R, Strianese D, Rinaldi M, D’Aponte A (2008) Clinical evolution of neuroretinitis in Parry-Romberg syndrome. J Pediatr Ophthalmol Strabismus 45: 125–126.
4. Dupont S, Catala M, Hasdboun D, Semah F, Baulac M (1997) Progressive facial hemiatrophy and epilepsy: a common underlying dysgenetic mechanism. Neurology 48: 1013–1018.
5. Fry JA, Alvarellos A, Fink CW, Blaw ME, Roach ES (1992) Intracranial findings in progressive facial hemiatrophy. J Rheumatol 19: 956–958.