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Epilepsia
|
April 6, 2011
The genetics of Dravet syndrome
Carla Marini, Ingrid E Scheffer, Rima Nabbout, et al.
International Journal of Molecular Sciences
|
June 24, 2022
Genomic Analysis Made It Possible to Identify Gene-Driver Alterations Covering the Time Window between Diagnosis of Neuroblastoma 4S and the Progression to Stage 4
Marzia Ognibene, Patrizia De Marco, Stefano Parodi, et al.
Journal of Child Neurology
|
August 24, 2010
Genotype-phenotype correlations in a group of 15 SCN1A-mutated Italian patients with GEFS+ spectrum (seizures plus, classical and borderline severe myoclonic epilepsy of infancy)
Francesco Nicita, Alberto Spalice, Laura Papetti, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
August 31, 2010
Familial nonkinesigenic paroxysmal dyskinesia and intracranial calcifications: a new syndrome?
Nune S Yeghiazaryan, Pasquale Striano, Patrizia Accorsi, et al.
CNS Neuroscience & Therapeutics
|
November 11, 2024
Antisense oligonucleotides as a precision therapy for developmental and epileptic encephalopathies
Paloma García Quilón, Greta Volpedo, Serena Cappato, et al.
Acta Neurologica Belgica
|
December 1, 2010
A novel de novo SCN1A missense mutation in Severe Myoclonic Epilepsy Borderland
Nicola Specchio, Marina Trivisano, Martina Balestri, et al.
Seizure
|
January 20, 2010
Galloway-Mowat syndrome: an early-onset progressive encephalopathy with intractable epilepsy associated to renal impairment. Two novel cases and review of literature
Marianna Pezzella, Nune S Yeghiazaryan, Pierangelo Veggiotti, et al.
Seizure
|
March 24, 2018
De novo 12q22.q23.3 duplication associated with temporal lobe epilepsy
Maria Stella Vari, Monica Traverso, Tommaso Bellini, et al.
Archives of Neurology
|
February 14, 2007
Periodic myoclonus due to cytomegalovirus encephalitis in a patient with good syndrome
Pasquale Striano, Fabio Tortora, Amelia Evoli, et al.
Seizure
|
April 25, 2018
Erratum to "De novo 12q22.q23.3 duplication associated with temporal lobe epilepsy" [Seizure 57 (2018) 63-65]
Maria Stella Vari, Monica Traverso, Tommaso Bellini, et al.
Page
of 40
Search research articles
Search
Showing results (81-90 of 398) with videos related to
Sort By:
Page
of 40
Epilepsia
|
April 6, 2011
The genetics of Dravet syndrome
Carla Marini, Ingrid E Scheffer, Rima Nabbout, et al.
International Journal of Molecular Sciences
|
June 24, 2022
Genomic Analysis Made It Possible to Identify Gene-Driver Alterations Covering the Time Window between Diagnosis of Neuroblastoma 4S and the Progression to Stage 4
Marzia Ognibene, Patrizia De Marco, Stefano Parodi, et al.
Journal of Child Neurology
|
August 24, 2010
Genotype-phenotype correlations in a group of 15 SCN1A-mutated Italian patients with GEFS+ spectrum (seizures plus, classical and borderline severe myoclonic epilepsy of infancy)
Francesco Nicita, Alberto Spalice, Laura Papetti, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
August 31, 2010
Familial nonkinesigenic paroxysmal dyskinesia and intracranial calcifications: a new syndrome?
Nune S Yeghiazaryan, Pasquale Striano, Patrizia Accorsi, et al.
CNS Neuroscience & Therapeutics
|
November 11, 2024
Antisense oligonucleotides as a precision therapy for developmental and epileptic encephalopathies
Paloma García Quilón, Greta Volpedo, Serena Cappato, et al.
Acta Neurologica Belgica
|
December 1, 2010
A novel de novo SCN1A missense mutation in Severe Myoclonic Epilepsy Borderland
Nicola Specchio, Marina Trivisano, Martina Balestri, et al.
Seizure
|
January 20, 2010
Galloway-Mowat syndrome: an early-onset progressive encephalopathy with intractable epilepsy associated to renal impairment. Two novel cases and review of literature
Marianna Pezzella, Nune S Yeghiazaryan, Pierangelo Veggiotti, et al.
Seizure
|
March 24, 2018
De novo 12q22.q23.3 duplication associated with temporal lobe epilepsy
Maria Stella Vari, Monica Traverso, Tommaso Bellini, et al.
Archives of Neurology
|
February 14, 2007
Periodic myoclonus due to cytomegalovirus encephalitis in a patient with good syndrome
Pasquale Striano, Fabio Tortora, Amelia Evoli, et al.
Seizure
|
April 25, 2018
Erratum to "De novo 12q22.q23.3 duplication associated with temporal lobe epilepsy" [Seizure 57 (2018) 63-65]
Maria Stella Vari, Monica Traverso, Tommaso Bellini, et al.
Page
of 40