M. Vanni

发表

Relationship between café-au-lait spots as the only symptom and peripheral neurofibromatosis (NF1): A follow-up study

P. Balestri, A. Fois, G. Bartalini, 1993, European Journal of Pediatrics.

Familial Axenfeld-Rieger anomaly, cardiac malformations, and sensorineural hearing loss: a provisionally unique genetic syndrome?

G. Morgese, P. Balestri, M. Farnetani, 2002, American journal of medical genetics.

Evolving aspects of solitary granuloma of the sphenoid bone after radiation and cortisone therapy observed with computed tomography

A. Leccisotti, E. Polito, G. Filosomi, 1992 .

Optic atrophy in Marinesco-Sjögren syndrome: an additional ocular feature. Report of three cases in two families.

G. Guazzi, A. Malandrini, A. Federico, 1993, Ophthalmic paediatrics and genetics.

Propranolol 0.2% Eye Micro-Drops for Retinopathy of Prematurity: A Prospective Phase IIB Study

G. Buonocore, P. Fortunato, F. Mosca, 2019, Front. Pediatr..

Study protocol: safety and efficacy of propranolol 0.2% eye drops in newborns with a precocious stage of retinopathy of prematurity (DROP-ROP-0.2%): a multicenter, open-label, single arm, phase II trial

G. Buonocore, P. Fortunato, F. Mosca, 2017, BMC Pediatrics.

Eye involvement in sarcoidosis: survey of 197 patients.

C. Traversi, A. Bardelli, L. Barberi, 1993, Sarcoidosis.

Propranolol 0.1% eye micro-drops in newborns with retinopathy of prematurity: a pilot clinical trial

P. Fortunato, F. Mosca, M. Fumagalli, 2017, Pediatric Research.

Ocular manifestations in Kniest syndrome, Smith-Lemli-Opitz syndrome, Hallermann-Streiff-François syndrome, Rubinstein-Taybi syndrome and median cleft face syndrome.

A. Bardelli, L. Barberi, G. Lasorella, 1985, Ophthalmic paediatrics and genetics.

Congenital and developmental cataracts and multimalformation syndromes.

A. Bardelli, G. Lasorella, M. Vanni, 1989, Ophthalmic paediatrics and genetics.