Malformations of cortical development in neurofibromatosis type 1
Balestri, P, Vivarelli, R, Grosso, S, Santori, L, Farnetani, M A, Galluzzi, P, Vatti, G P, Calabrese, F, Morgese, G
Published in Neurology (23.12.2003)
Published in Neurology (23.12.2003)
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Journal Article
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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Journal Article
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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Journal Article
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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Journal Article
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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Journal Article
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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Journal Article
Operative Results without Invasive Monitoring in Patients with Frontal Lobe Epileptogenic Lesions
Mariottini, A., Lombroso, C. T., DeGirolami, U., Fois, A., Buoni, S., DiTroia, A. M., Farnetani, M. A., Palma, L., Zalaffi, A., Black, P. McL
Published in Epilepsia (Copenhagen) (01.10.2001)
Published in Epilepsia (Copenhagen) (01.10.2001)
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Journal Article
Conference Proceeding
Dexfenfluramine effective in drug-resistant temporal lobe epilepsy
Grosso, S, Farnetani, M A, Berardi, R, Di Bartolo, R, Magi, L, Morgese, G, Balestri, P
Published in Neurology (25.09.2001)
Published in Neurology (25.09.2001)
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Journal Article
Celiac disease with cerebral calcium and silica deposits: x-ray spectroscopic findings, an autopsy study
Toti, P, Balestri, P, Cano, M, Galluzzi, P, Megha, T, Farnetani, M A, Palmeri, M L, Vascotto, M, Venturi, C, Fois, A
Published in Neurology (01.04.1996)
Published in Neurology (01.04.1996)
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Journal Article
EEG, PET, SPET and MRI in intractable childhood epilepsies: possible surgical correlations
Fois, A, Farnetani, M A, Balestri, P, Buoni, S, Di Cosmo, G, Vattimo, A, Guazzelli, M, Guzzardi, R, Salvadori, P A
Published in Child's nervous system (01.12.1995)
Published in Child's nervous system (01.12.1995)
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Journal Article
Multiple neuroendocrine disorder in Salla disease
Grosso, S, Berardi, R, Farnetani, M A, Margollicci, M, Mancini, M G, Morgese, G, Balestri, P
Published in Journal of child neurology (01.10.2001)
Published in Journal of child neurology (01.10.2001)
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Journal Article
Biochemical diagnosis of Canavan disease
Bartalini, G, Margollicci, M, Balestri, P, Farnetani, M A, Cioni, M, Fois, A
Published in Child's nervous system (01.12.1992)
Published in Child's nervous system (01.12.1992)
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Journal Article
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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Journal Article
Human erythrocyte hexokinase deficiency: a new variant with abnormal kinetic properties
Magnani, M, Stocchi, V, Canestrari, F, Dachà, M, Balestri, P, Farnetani, M A, Giorgi, D, Fois, A, Fornaini, G
Published in British journal of haematology (01.09.1985)
Published in British journal of haematology (01.09.1985)
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Journal Article
Free sialic acid storage disease. A new Italian case
Fois, A, Balestri, P, Farnetani, M A, Mancini, G M, Borgogni, P, Margollicci, M A, Molinelli, M, Alessandrini, C, Gerli, R
Published in European journal of pediatrics (01.03.1987)
Published in European journal of pediatrics (01.03.1987)
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Journal Article
Giant axonal neuropathy. Endocrinological and histological studies
Fois, A, Balestri, P, Farnetani, M A, Berardi, R, Mattei, R, Laurenzi, E, Alessandrini, C, Gerli, R, Ribuffo, A, Calvieri, S
Published in European journal of pediatrics (01.09.1985)
Published in European journal of pediatrics (01.09.1985)
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Journal Article
The Syndrome of Inv Dup (15): Clinical, Electroencephalographic, and Imaging Findings
Buoni, Sabrina, Sorrentino, Livio, Farnetani, Maria Angela, Pucci, Lucia, Fois, Alberto
Published in Journal of child neurology (01.06.2000)
Published in Journal of child neurology (01.06.2000)
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Journal Article
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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