2q24–q31 Deletion: Report of a case and review of the literature
Pescucci, C, Caselli, R, Grosso, S, Mencarelli, M.A, Mari, F, Farnetani, M.A, Piccini, B, Artuso, R, Bruttini, M, Priolo, M, Zuffardi, O, Gimelli, S, Balestri, P, Renieri, A
Published in European journal of medical genetics (01.01.2007)
Published in European journal of medical genetics (01.01.2007)
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Intractable reflex audiogenic seizures in Aicardi syndrome
Grosso, S., Farnetani, M.A., Bernardoni, E., Morgese, G., Balestri, P.
Published in Brain & development (Tokyo. 1979) (01.05.2007)
Published in Brain & development (Tokyo. 1979) (01.05.2007)
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Epilepsy, progressive cerebral calcifications, and coeliac disease
Fois, A., Vascotto, M., Di Bartolo, R.M., Balestri, P., Farnetani, M.A., Di Marco, V.
Published in The Lancet (British edition) (31.10.1992)
Published in The Lancet (British edition) (31.10.1992)
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Efficacy and safety of topiramate in infants according to epilepsy syndromes
Grosso, S., Galimberti, D., Farnetani, M.A., Cioni, M., Mostardini, R., Vivarelli, R., Di Bartolo, R.M., Bernardoni, E., Berardi, R., Morgese, G., Balestri, P.
Published in Seizure (London, England) (01.04.2005)
Published in Seizure (London, England) (01.04.2005)
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Chromosome 18 aberrations and epilepsy: A review
Grosso, S., Pucci, L., Di Bartolo, R.M., Gobbi, G., Bartalini, G., Anichini, C., Scarinci, R., Balestri, M., Farnetani, M.A., Cioni, M., Morgese, G., Balestri, P.
Published in American journal of medical genetics. Part A (01.04.2005)
Published in American journal of medical genetics. Part A (01.04.2005)
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Facial hemangioma and malformation of the cortical development: A broadening of the PHACE spectrum or a new entity?
Grosso, S., de Cosmo, L., Bonifazi, E., Galluzzi, P., Farnetani, M.A., Loffredo, P., Anichini, C., Berardi, R., Morgese, G., Balestri, Paolo
Published in American journal of medical genetics. Part A (15.01.2004)
Published in American journal of medical genetics. Part A (15.01.2004)
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Familial Axenfeld-Rieger anomaly, cardiac malformations, and sensorineural hearing loss: a provisionally unique genetic syndrome?
Grosso, S, Farnetani, M A, Berardi, R, Vivarelli, R, Vanni, M, Morgese, G, Balestri, P
Published in American journal of medical genetics (01.08.2002)
Published in American journal of medical genetics (01.08.2002)
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Chromosome 18 aberrations and epilepsy: A review
Grosso, S., Pucci, L., Di Bartolo, R.M., Gobbi, G., Bartalini, G., Anichini, C., Scarinci, R., Balestri, M., Farnetani, M.A., Cioni, M., Morgese, G., Balestri, P.
Published in American Journal of Medical Genetics Part A (01.04.2005)
Published in American Journal of Medical Genetics Part A (01.04.2005)
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Report
Facial hemangioma and malformation of the cortical development: A broadening of the PHACE spectrum or a new entity?
Grosso, S., de Cosmo, L., Bonifazi, E., Galluzzi, P., Farnetani, M.A., Loffredo, P., Anichini, C., Berardi, R., Morgese, G., Balestri, Paolo
Published in American Journal of Medical Genetics Part A (15.01.2004)
Published in American Journal of Medical Genetics Part A (15.01.2004)
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Interictal Qualitative Positron Emission Tomography with Fluoro-Desoxyglucose (PET-FDG) May Contribute to the Diagnostic Accuracy of Epileptic Foci in Drug-Resistant Patients
Marchetti, S, Salvadori, P A., Giovacchini, G, Iudice, A, Ferrari, E, Pisani, P, Sorace, O, Farnetani, M A., Fois, A, Pietrini, P, Guazzelli, M
Published in Clinical positron imaging (01.11.1999)
Published in Clinical positron imaging (01.11.1999)
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Familial Tyrosinaemia with Eye and Skin Lesions
Bardelli, A.M., Borgogni, P., Farnetani, M.A., Fois, A., Frezzotti, R., Mattei, R., Molinelli, M., Sargentini, L.
Published in Ophthalmologica (Basel) (01.01.1977)
Published in Ophthalmologica (Basel) (01.01.1977)
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