Export 9 results:
Autore Titolo Tipo [ Anno(Desc)]
Filtri: Autore è Pensiero, Stefano  [Clear All Filters]
2010
Accardo A, Pensiero S, Ciana G, Parentin F, Bembi B. Eye movement impairment recovery in a Gaucher patient treated with miglustat. Neurol Res Int 2010;2010:358534.
2011
Pensiero S, Cecchini P, Michieletto P, Pelizzo G, Madonia M, Parentin F. Congenital aplasia of the optic chiasm and esophageal atresia: a case report. J Med Case Rep 2011;5:335.
De Silva S, Parentin F, Michieletto P, Pensiero S. Corneal curvature and thickness development in premature infants. J Pediatr Ophthalmol Strabismus 2011;48(1):25-9.
Abu-Amero KK, Faletra F, Gasparini P, Parentin F, Pensiero S, Alorainy IA, Hellani AM, Catalano D, Bosley TM. Horizontal gaze palsy and progressive scoliosis without ROBO3 mutations. Ophthalmic Genet 2011;32(4):212-6.
Parentin F, Lepore L, Rabach I, Pensiero S. Paediatric Behçet's disease presenting with recurrent papillitis and episcleritis: a case report. J Med Case Rep 2011;5:81.
Parentin F, Ventura G, Pastore S, Kiren V, Bibalo C, Pensiero S, Lepore L. A singular case of congenital self-healing histiocytosis with skin, liver and atypical eye involvement. Ocul Immunol Inflamm 2011;19(5):337-9.
2013
Faletra F, d'Adamo APio, Pensiero S, Athanasakis E, Catalano D, Bruno I, Gasparini P. A novel CRYBB2 missense mutation causing congenital autosomal dominant cataract in an Italian family. Ophthalmic Genet 2013;34(1-2):115-7.
2015
Parentin F, Matarazzo L, Lepore L, Pensiero S, Ventura A. Early onset bilateral anterior uveitis preceding a late manifestation of juvenile idiopathic arthritis: a case report. Ocul Immunol Inflamm 2015;23(1):102-5.
Girotto G, Scheffer DI, Morgan A, Vozzi D, Rubinato E, Di Stazio M, Muzzi E, Pensiero S, Giersch AB, Corey DP, Gasparini P. PSIP1/LEDGF: a new gene likely involved in sensorineural progressive hearing loss. Sci Rep 2015;5:18568.

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