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Journal of Child Neurology|June 27, 2000
The syndrome of inv dup (15): clinical, electroencephalographic, and imaging findingsS Buoni, L Sorrentino, M A Farnetani, et al.Brain & Development|November 7, 2006
Intractable reflex audiogenic seizures in Aicardi syndromeS Grosso, M A Farnetani, E Bernardoni, et al.Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery|December 1, 1992
Biochemical diagnosis of Canavan diseaseG Bartalini, M Margollicci, P Balestri, et al.American Journal of Medical Genetics|September 5, 2002
Familial Axenfeld-Rieger anomaly, cardiac malformations, and sensorineural hearing loss: a provisionally unique genetic syndrome?S Grosso, M A Farnetani, R Berardi, et al.Journal of Child Neurology|October 24, 2001
Multiple neuroendocrine disorder in Salla diseaseS Grosso, R Berardi, M A Farnetani, et al.Brain & Development|January 1, 1993
Progressive cerebral calcifications, epilepsy, and celiac diseaseA Fois, P Balestri, M Vascotto, et al.Ophthalmologica. Journal International D'Ophtalmologie. International Journal of Ophthalmology. Zeitschrift Fur Augenheilkunde|January 1, 1977
Familial tyrosinaemia with eye and skin lesions. Presentation of two casesA M Bardelli, P Borgogni, M A Farnetani, et al.British Journal of Haematology|September 1, 1985
Human erythrocyte hexokinase deficiency: a new variant with abnormal kinetic propertiesM Magnani, V Stocchi, F Canestrari, et al.Neurology|December 25, 2003
Malformations of cortical development in neurofibromatosis type 1P Balestri, R Vivarelli, S Grosso, et al.European Journal of Pediatrics|September 1, 1985
Giant axonal neuropathy. Endocrinological and histological studiesA Fois, P Balestri, M A Farnetani, et al.Pageof 2