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Minerva Pediatrica|June 10, 2011
[Epilepsy genetics and genetic epilepsies]P Striano, A Bianchi, F Zara, et al.Acta Neurologica Scandinavica|March 3, 2005
Autosomal dominant cortical tremor, myoclonus and epilepsy: many syndromes, one phenotypeP Striano, F Zara, S StrianoNeurology|October 13, 2006
Cryptic chromosome deletions involving SCN1A in severe myoclonic epilepsy of infancyF Madia, P Striano, E Gennaro, et al.Clinical Neurology and Neurosurgery|December 4, 2003
Bioptically demonstrated Lafora disease without EPM2A mutation: a clinical and neurophysiological study of two sistersP Boccella, P Striano, F Zara, et al.AJNR. American Journal of Neuroradiology|November 3, 2007
Hypomyelination and congenital cataract: neuroimaging features of a novel inherited white matter disorderA Rossi, R Biancheri, F Zara, et al.Neurology|April 23, 2003
Benign adult familial myoclonic epilepsy: genetic heterogeneity and allelism with ADCMEF A de Falco, P Striano, A de Falco, et al.Clinical Genetics|March 18, 2008
Inclusion body myopathy, Paget's disease of the bone and frontotemporal dementia: recurrence of the VCP R155H mutation in an Italian family and implications for genetic counsellingV Viassolo, S C Previtali, E Schiatti, et al.Human Molecular Genetics|July 1, 1995
Mapping of genes predisposing to idiopathic generalized epilepsyF Zara, A Bianchi, G Avanzini, et al.Applied Optics|November 19, 2010
Reduction in correlation-filter sensitivity to background clutter by the automatic spatial frequency selection algorithmC Minetti, F DuboisCurrent Opinion in Genetics & Development|June 23, 1999
Muscular dystrophies: alterations in a limited number of cellular pathways?D Toniolo, C MinettiPageof 97