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European Journal of Anaesthesiology
|
January 23, 2008
Posterior reversible encephalopathy syndrome and spinal epidural haematoma in a hypertensive patient
P Striano, S Striano, G Servillo, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
|
January 13, 2004
Epileptic seizures in multiple sclerosis: clinical and EEG correlations
P Striano, G Orefice, V Brescia Morra, et al.
Neuromolecular Medicine
|
June 23, 2005
Screening for C677T and A1298C MTHFR polymorphisms in patients with epilepsy and risk of hyperhomocysteinemia
D Caccamo, S Condello, G Gorgone, et al.
Clinical Neurology and Neurosurgery
|
December 4, 2003
Bioptically demonstrated Lafora disease without EPM2A mutation: a clinical and neurophysiological study of two sisters
P Boccella, P Striano, F Zara, et al.
Neurology
|
June 15, 2007
A de novo LGI1 mutation causing idiopathic partial epilepsy with telephone-induced seizures
R Michelucci, O Mecarelli, G Bovo, et al.
Seizure
|
May 8, 2018
Generalized epilepsy and mild intellectual disability associated with 13q34 deletion: A potential role for SOX1 and ARHGEF7
A Orsini, A Bonuccelli, P Striano, et al.
Epilepsy & Behavior : E&B
|
May 31, 2011
Low long-term efficacy and tolerability of add-on rufinamide in patients with Dravet syndrome
A Mueller, R Boor, G Coppola, et al.
Epilepsy & Behavior Reports
|
March 7, 2020
Efficacy and tolerability of mycophenolate mofetil in a pediatric Rasmussen syndrome
A Orsini, G Costagliola, D Perna, et al.
Seizure
|
August 10, 2020
Rasmussen's encephalitis: From immune pathogenesis towards targeted-therapy
A Orsini, T Foiadelli, N Carli, et al.
Gene
|
June 13, 2020
Lamotrigine induced Brugada-pattern in a patient with genetic epilepsy associated with a novel variant in SCN9A
P Banfi, M Coll, A Oliva, et al.
Page
of 6
Search research articles
Search
Showing results (21-30 of 57) with videos related to
Sort By:
Page
of 6
European Journal of Anaesthesiology
|
January 23, 2008
Posterior reversible encephalopathy syndrome and spinal epidural haematoma in a hypertensive patient
P Striano, S Striano, G Servillo, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
|
January 13, 2004
Epileptic seizures in multiple sclerosis: clinical and EEG correlations
P Striano, G Orefice, V Brescia Morra, et al.
Neuromolecular Medicine
|
June 23, 2005
Screening for C677T and A1298C MTHFR polymorphisms in patients with epilepsy and risk of hyperhomocysteinemia
D Caccamo, S Condello, G Gorgone, et al.
Clinical Neurology and Neurosurgery
|
December 4, 2003
Bioptically demonstrated Lafora disease without EPM2A mutation: a clinical and neurophysiological study of two sisters
P Boccella, P Striano, F Zara, et al.
Neurology
|
June 15, 2007
A de novo LGI1 mutation causing idiopathic partial epilepsy with telephone-induced seizures
R Michelucci, O Mecarelli, G Bovo, et al.
Seizure
|
May 8, 2018
Generalized epilepsy and mild intellectual disability associated with 13q34 deletion: A potential role for SOX1 and ARHGEF7
A Orsini, A Bonuccelli, P Striano, et al.
Epilepsy & Behavior : E&B
|
May 31, 2011
Low long-term efficacy and tolerability of add-on rufinamide in patients with Dravet syndrome
A Mueller, R Boor, G Coppola, et al.
Epilepsy & Behavior Reports
|
March 7, 2020
Efficacy and tolerability of mycophenolate mofetil in a pediatric Rasmussen syndrome
A Orsini, G Costagliola, D Perna, et al.
Seizure
|
August 10, 2020
Rasmussen's encephalitis: From immune pathogenesis towards targeted-therapy
A Orsini, T Foiadelli, N Carli, et al.
Gene
|
June 13, 2020
Lamotrigine induced Brugada-pattern in a patient with genetic epilepsy associated with a novel variant in SCN9A
P Banfi, M Coll, A Oliva, et al.
Page
of 6