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Neurology
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April 23, 2003
Benign adult familial myoclonic epilepsy: genetic heterogeneity and allelism with ADCME
F A de Falco, P Striano, A de Falco, et al.
Seizure
|
November 29, 2019
De novo Absence Status Epilepticus in a pediatric cohort: Electroclinical pattern in a multicenter Italian patients cohort
C Pepi, E Cesaroni, P Striano, et al.
Eye (London, England)
|
November 4, 2008
Is retinal assessment useful in epileptic patients with hyperhomocysteinemia?
V Belcastro, P Striano, C Ciampa, et al.
Minerva Pediatrica
|
November 13, 2013
Glioneuronal tumors and epilepsy in children: seizure outcome related to lesionectomy
A Consales, P Striano, P Nozza, et al.
Neurology
|
March 30, 2011
Familial temporal lobe epilepsy with psychic auras associated with a novel LGI1 mutation
P Striano, G Busolin, L Santulli, et al.
Seizure
|
December 6, 2019
A validation study of the clinical diagnosis of Dup15q syndrome: Which symptoms matter most?
E Beghi, G Giussani, E Bianchi, et al.
Neurology
|
October 13, 2006
Cryptic chromosome deletions involving SCN1A in severe myoclonic epilepsy of infancy
F Madia, P Striano, E Gennaro, et al.
AJNR. American Journal of Neuroradiology
|
February 9, 2023
Neuroimaging Features of Biotinidase Deficiency
A Biswas, C McNamara, V K Gowda, et al.
Neuropediatrics
|
July 4, 2007
Revelation of a novel CLN5 mutation in early juvenile neuronal ceroid lipofuscinosis
N Cannelli, N Nardocci, D Cassandrini, et al.
Frontiers in Pediatrics
|
December 11, 2023
Neuroinflammation and status epilepticus: a narrative review unraveling a complex interplay
T Foiadelli, A Santangelo, G Costagliola, et al.
Page
of 6
Search research articles
Search
Showing results (31-40 of 57) with videos related to
Sort By:
Page
of 6
Neurology
|
April 23, 2003
Benign adult familial myoclonic epilepsy: genetic heterogeneity and allelism with ADCME
F A de Falco, P Striano, A de Falco, et al.
Seizure
|
November 29, 2019
De novo Absence Status Epilepticus in a pediatric cohort: Electroclinical pattern in a multicenter Italian patients cohort
C Pepi, E Cesaroni, P Striano, et al.
Eye (London, England)
|
November 4, 2008
Is retinal assessment useful in epileptic patients with hyperhomocysteinemia?
V Belcastro, P Striano, C Ciampa, et al.
Minerva Pediatrica
|
November 13, 2013
Glioneuronal tumors and epilepsy in children: seizure outcome related to lesionectomy
A Consales, P Striano, P Nozza, et al.
Neurology
|
March 30, 2011
Familial temporal lobe epilepsy with psychic auras associated with a novel LGI1 mutation
P Striano, G Busolin, L Santulli, et al.
Seizure
|
December 6, 2019
A validation study of the clinical diagnosis of Dup15q syndrome: Which symptoms matter most?
E Beghi, G Giussani, E Bianchi, et al.
Neurology
|
October 13, 2006
Cryptic chromosome deletions involving SCN1A in severe myoclonic epilepsy of infancy
F Madia, P Striano, E Gennaro, et al.
AJNR. American Journal of Neuroradiology
|
February 9, 2023
Neuroimaging Features of Biotinidase Deficiency
A Biswas, C McNamara, V K Gowda, et al.
Neuropediatrics
|
July 4, 2007
Revelation of a novel CLN5 mutation in early juvenile neuronal ceroid lipofuscinosis
N Cannelli, N Nardocci, D Cassandrini, et al.
Frontiers in Pediatrics
|
December 11, 2023
Neuroinflammation and status epilepticus: a narrative review unraveling a complex interplay
T Foiadelli, A Santangelo, G Costagliola, et al.
Page
of 6