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Neurophysiologie Clinique = Clinical Neurophysiology|December 20, 2002
Eyelid myoclonia with absences: an overlooked epileptic syndrome?Salvatore Striano, Pasquale Striano, Cristofaro Nocerino, et al.
Neuromuscular Disorders : NMD|December 5, 2006
Inherited neuromyotonia: a clinical and genetic study of a familyAntonio Falace, Pasquale Striano, Fiore Manganelli, et al.
Epilepsia|March 30, 2023
Familial adult myoclonus epilepsy: Clinical findings, disease course, and comorbiditiesBeatriz G Giraldez, José M Serratosa, Salvatore Striano, et al.
Epilepsia|March 24, 2011
Natural history and long-term evolution in families with autosomal dominant cortical tremor, myoclonus, and epilepsyAntonietta Coppola, Lia Santulli, Luigi Del Gaudio, et al.
Journal of Neurology|May 10, 2006
Levetiracetam for cerebellar tremor in multiple sclerosis: an open-label pilot tolerability and efficacy studyPasquale Striano, Antonietta Coppola, Giovanni Vacca, et al.
Medical Science Monitor : International Medical Journal of Experimental and Clinical Research|November 1, 2005
Clinical spectrum and critical care management of Posterior Reversible Encephalopathy Syndrome (PRES)Pasquale Striano, Salvatore Striano, Fabio Tortora, et al.
European Journal of Medical Genetics|October 1, 2013
Neurological features and long-term follow-up in 15q11.2-13.1 duplicationAntonietta Coppola, Patrizia Ruosi, Lia Santulli, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape|June 22, 2019
Clinical evolution and epilepsy outcome in three patients with CDKL5-related developmental encephalopathyPia Bernardo, Alessandro Ferretti, Gaetano Terrone, et al.
Journal of Neuroimmunology|May 12, 2009
Autoantibodies to glutamic acid decarboxylase (GAD) in focal and generalized epilepsy: A study on 233 patientsLuca Errichiello, Giuseppe Perruolo, Angelo Pascarella, et al.
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