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Elena Gennaro

Showing results (31-40 of 37) with videos related to

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Epilepsia|March 27, 2007
Brain MRI findings in severe myoclonic epilepsy in infancy and genotype-phenotype correlationsPasquale Striano, Maria Margherita Mancardi, Roberta Biancheri, et al.
Epilepsia|January 31, 2013
Genetic testing in benign familial epilepsies of the first year of life: clinical and diagnostic significanceFederico Zara, Nicola Specchio, Pasquale Striano, et al.
Epilepsia|February 13, 2003
Exploration of a putative susceptibility locus for idiopathic generalized epilepsy on chromosome 8p12Thomas Sander, Christine Windemuth, Herbert Schulz, et al.
Journal of the Neurological Sciences|March 27, 2021
Italian cohort of Lafora disease: Clinical features, disease evolution, and genotype-phenotype correlationsAntonella Riva, Alessandro Orsini, Marcello Scala, et al.
Neurology. Genetics|March 4, 2021
Genotype-phenotype correlations in patients with de novo <i>KCNQ2</i> pathogenic variantsFederica Malerba, Giulio Alberini, Ganna Balagura, et al.
Neurology. Genetics|June 3, 2022
Epilepsy Course and Developmental Trajectories in <i>STXBP1</i>-DEEGanna Balagura, Julie Xian, Antonella Riva, et al.
Molecular Genetics & Genomic Medicine|July 29, 2016
Pitfalls in genetic testing: the story of missed SCN1A mutationsTania Djémié, Sarah Weckhuysen, Sarah von Spiczak, et al.
Pageof 4

Showing results (31-40 of 37) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 37 results.
Epilepsia|March 27, 2007
Brain MRI findings in severe myoclonic epilepsy in infancy and genotype-phenotype correlationsPasquale Striano, Maria Margherita Mancardi, Roberta Biancheri, et al.
Epilepsia|January 31, 2013
Genetic testing in benign familial epilepsies of the first year of life: clinical and diagnostic significanceFederico Zara, Nicola Specchio, Pasquale Striano, et al.
Epilepsia|February 13, 2003
Exploration of a putative susceptibility locus for idiopathic generalized epilepsy on chromosome 8p12Thomas Sander, Christine Windemuth, Herbert Schulz, et al.
Journal of the Neurological Sciences|March 27, 2021
Italian cohort of Lafora disease: Clinical features, disease evolution, and genotype-phenotype correlationsAntonella Riva, Alessandro Orsini, Marcello Scala, et al.
Neurology. Genetics|March 4, 2021
Genotype-phenotype correlations in patients with de novo <i>KCNQ2</i> pathogenic variantsFederica Malerba, Giulio Alberini, Ganna Balagura, et al.
Neurology. Genetics|June 3, 2022
Epilepsy Course and Developmental Trajectories in <i>STXBP1</i>-DEEGanna Balagura, Julie Xian, Antonella Riva, et al.
Molecular Genetics & Genomic Medicine|July 29, 2016
Pitfalls in genetic testing: the story of missed SCN1A mutationsTania Djémié, Sarah Weckhuysen, Sarah von Spiczak, et al.
Pageof 4