Showing results (461-470 of 674) with videos related to
Sort By:
Pageof 68
HGG Advances|April 11, 2026
Heterozygous CECR2 Variants Support a Distinct Neurodevelopmental Syndrome with Features Overlapping Cat Eye SyndromeAnushree Acharya, Irma Järvelä, Andrea Hernandez, et al.Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|May 31, 2022
Late epileptic seizures following cerebral venous thrombosis: a systematic review and meta-analysisSara Gasparini, Sabrina Neri, Francesco Brigo, et al.Clinical Genetics|May 16, 2023
Novel biallelic variants expand the phenotype of NAA20-related syndromeGianluca D'Onofrio, Claudia Cuccurullo, Silje Kathrine Larsen, et al.Epilepsy Research|April 29, 2008
Autosomal dominant lateral temporal epilepsy: absence of mutations in ADAM22 and Kv1 channel genes encoding LGI1-associated proteinsErica Diani, Carlo Di Bonaventura, Oriano Mecarelli, et al.Epilepsy Research and Treatment|September 1, 2012
ADAM23, a Gene Related to LGI1, Is Not Linked to Autosomal Dominant Lateral Temporal EpilepsyLaura Rigon, Andrea Vettori, Giorgia Busolin, et al.Brain Sciences|September 28, 2021
Prominent and Regressive Brain Developmental Disorders Associated with Nance-Horan SyndromeCeleste Casto, Valeria Dipasquale, Ida Ceravolo, et al.Human Molecular Genetics|March 16, 2007
Characterization of a recurrent 15q24 microdeletion syndromeAndrew J Sharp, Rebecca R Selzer, Joris A Veltman, et al.Genome Research|June 2, 2026
Transfer learning enhances clinical utility of polygenic scores with small, phenotypically refined cohortsYuChung Lin, Christoph Patrick Beier, Zuzana Sobiskova, et al.Epilepsy & Behavior : E&B|February 12, 2021
Climate change and epilepsy: Insights from clinical and basic science studiesMedine I Gulcebi, Emanuele Bartolini, Omay Lee, et al.Neurobiology of Disease|January 25, 2020
Distal motor neuropathy associated with novel EMILIN1 mutationMichele Iacomino, Roberto Doliana, Maria Marchese, et al.Pageof 68