Chitosan may decrease serum valproate and increase the risk of seizure reappearanceSTRIANO, Pasquale; ZARA, Federico; MINETTI, Carlo et al.BMJ. British medical journal (International ed.). 2009, Vol 339, Num 7725, issn 0959-8146, p. 862Article

The impact of genetics on the classification of epilepsy syndromesZARA, Federico; BIANCHI, Amedeo.Epilepsia (Copenhagen). 2009, Vol 50, pp 11-14, issn 0013-9580, 4 p., SUP5Article

Epileptic seizures can follow high doses of oral vardenafilSTRIANO, Pasquale; ZARA, Federico; MINETTI, Carlo et al.BMJ. British medical journal (International ed.). 2006, Vol 333, Num 7572, pp 785-785, issn 0959-8146, 1 p.Article

Electroclinical and genetic findings in a family with cortical tremor, myoclonus, and epilepsySTRIANO, Pasquale; MADIA, Francesca; MINETTI, Carlo et al.Epilepsia (Copenhagen). 2005, Vol 46, Num 12, pp 1993-1995, issn 0013-9580, 3 p.Article

Addition of verapamil in the treatment of severe myoclonic epilepsy in infancyIANNETTI, Paola; PARISI, Pasquale; SPALICE, Alberto et al.Epilepsy research. 2009, Vol 85, Num 1, pp 89-95, issn 0920-1211, 7 p.Article

Topiramate-associated worsening symptoms in a patient with familial hemiplegic migraineSTRIANO, Pasquale; ZARA, Federico; SANTORELLI, Filippo Maria et al.Journal of the neurological sciences. 2008, Vol 272, Num 1-2, pp 194-195, issn 0022-510X, 2 p.Article

^IH-MR spectroscopy indicates prominent cerebellar dysfunction in benign adult familial myoclonic epilepsySTRIANO, Pasquale; CARANCI, Ferdinando; DI BENEDETTO, Raffaella et al.Epilepsia (Copenhagen). 2009, Vol 50, Num 6, pp 1491-1497, issn 0013-9580, 7 p.Article

Familial benign nonprogressive myoclonic epilepsiesSTRIANO, Pasquale; DE FALCO, Fabrizio A; MINETTI, Carlo et al.Epilepsia (Copenhagen). 2009, Vol 50, pp 37-40, issn 0013-9580, 4 p., SUP5Article

Epileptic myoclonus as ciprofloxacin-associated adverse effectSTRIANO, Pasquale; ZARA, Federico; COPPOLA, Antonietta et al.Movement disorders. 2007, Vol 22, Num 11, pp 1675-1676, issn 0885-3185, 2 p.Article

Late-onset and slow-progressing lafora disease in four siblings with EPM2B mutationBAYKAN, Betul; STRIANO, Pasquale; GIANOTTI, Stefania et al.Epilepsia (Copenhagen). 2005, Vol 46, Num 10, pp 1695-1697, issn 0013-9580, 3 p.Article

Familial infantile myoclonic epilepsy: Clinical features in a large kindred with autosomal recessive inheritanceDE FALCO, Fabrizio A; MAJELLO, Luigi; SANTANGELO, Roberto et al.Epilepsia (Copenhagen). 2001, Vol 42, Num 12, pp 1541-1548, issn 0013-9580Article

TBC1 D24, an ARF6-Interacting Protein, Is Mutated in Familial Infantile Myoclonic EpilepsyFALACE, Antonio; FILIPELLO, Fabia; BENFENATI, Fabio et al.American journal of human genetics. 2010, Vol 87, Num 3, pp 365-370, issn 0002-9297, 6 p.Article

Clinical phenotype and molecular characterization of 6q terminal deletion syndrome : Five new casesSTRIANO, Pasquale; MALACARNE, Michela; GAGGERO, Roberto et al.American journal of medical genetics. Part A. 2006, Vol 140, Num 18, pp 1944-1949, issn 1552-4825, 6 p.Article

Benign familial infantile convulsions : Mapping of a novel locus on chromosome 2q24 and evidence for genetic heterogeneityMALACARNE, Michela; GENNARO, Elena; GAMBARDELLA, Antonio et al.American journal of human genetics. 2001, Vol 68, Num 6, pp 1521-1526, issn 0002-9297Article

A Proof-of-Concept Trial of the Whey Protein Alfa-Lactalbumin in Chronic Cortical MyoclonusERRICHIELLO, Luca; PEZZELLA, Marianna; SANTULLI, Lia et al.Movement disorders. 2011, Vol 26, Num 14, pp 2573-2575, issn 0885-3185, 3 p.Article

SCNIA duplications and deletions detected in Dravet syndrome: Implications for molecular diagnosisMARINI, Carla; SCHEFFER, Ingrid E; CILIO, Maria Roberta et al.Epilepsia (Copenhagen). 2009, Vol 50, Num 7, pp 1670-1678, issn 0013-9580, 9 p.Article

Periodic myoclonus due to cytomegalovirus encephalitis in a patient with good syndromeSTRIANO, Pasquale; TORTORA, Fabio; EVOLI, Amelia et al.Archives of neurology (Chicago). 2007, Vol 64, Num 2, pp 277-279, issn 0003-9942, 3 p.Article

Phenotypic characterization of hypomyelination and congenital cataractBIANCHERI, Roberta; ZARA, Federico; UZIEL, Graziella et al.Annals of neurology. 2007, Vol 62, Num 2, pp 121-127, issn 0364-5134, 7 p.Article

6q terminal deletion syndrome associated with a distinctive EEG and clinical pattern : A report of five casesELIA, Maurizio; STRIANO, Pasquale; ROMANO, Corrado et al.Epilepsia (Copenhagen). 2006, Vol 47, Num 5, pp 830-838, issn 0013-9580, 9 p.Article

Benign familial neonatal-infantile seizures: Characterization of a new sodium channelopathyBERKOVIC, Samuel F; HERON, Sarah E; BORDO, Laura et al.Annals of neurology. 2004, Vol 55, Num 4, pp 550-557, issn 0364-5134, 8 p.Article

Therapeutic Potential of Proteasome Inhibition in Duchenne and Becker Muscular DystrophiesGAZZERRO, Elisabetta; ASSERETO, Stefania; LISANTI, Michael P et al.The American journal of pathology. 2010, Vol 176, Num 4, pp 1863-1877, issn 0002-9440, 15 p.Article

A pilot trial of levetiracetam in eyelid myoclonia with absences (Jeavons syndrome)STRIANO, Pasquale; SOFIA, Vito; ROMEO, Antonino et al.Epilepsia (Copenhagen). 2008, Vol 49, Num 3, pp 425-430, issn 0013-9580, 6 p.Article

Benign adult familial myoclonic epilepsy (BAFME) : evidence of an extended founder haplotype on chromosome 2p11.1-q12.2 in five Italian familiesMADIA, Francesca; STRIANO, Pasquale; DI BONAVENTURA, Carlo et al.Neurogenetics (Oxford. Print). 2008, Vol 9, Num 2, pp 139-142, issn 1364-6745, 4 p.Article

Severe epilepsy in X-linked creatine transporter defect (CRTR-D)MARGHERITA MANCARDI, Maria; CARUSO, Ubaldo; GAGGERO, Roberto et al.Epilepsia (Copenhagen). 2007, Vol 48, Num 6, pp 1211-1213, issn 0013-9580, 3 p.Article

Deficiency of hyccin, a newly identified membrane protein, causes hypomyelination and congenital cataractZARA, Federico; BIANCHERI, Roberta; PEDEMONTE, Marina et al.Nature genetics. 2006, Vol 38, Num 10, pp 1111-1113, issn 1061-4036, 3 p.Article