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Genome Medicine|April 28, 2022
SvAnna: efficient and accurate pathogenicity prediction of coding and regulatory structural variants in long-read genome sequencingDaniel Danis, Julius O B Jacobsen, Parithi Balachandran, et al.European Journal of Human Genetics : EJHG|May 25, 2021
Phenotypic homogeneity in childhood epilepsies evolves in gene-specific patterns across 3251 patient-years of clinical dataDavid Lewis-Smith, Shiva Ganesan, Peter D Galer, et al.Journal of Child Neurology|October 12, 2013
Atypical vitamin B6 deficiency: a rare cause of unexplained neonatal and infantile epilepsiesAnna Baumgart, Sarah von Spiczak, Nanda M Verhoeven-Duif, et al.JAMA Network Open|April 13, 2019
Use of a Dynamic Genetic Testing Approach for Childhood-Onset EpilepsyJorune Balciuniene, Elizabeth T DeChene, Gozde Akgumus, et al.Brain : a Journal of Neurology|March 17, 2022
Atypical development of Broca's area in a large family with inherited stutteringDaisy G Y Thompson-Lake, Thomas S Scerri, Susan Block, et al.Cell Reports|June 22, 2026
Stiffness-induced impairment of GLUT4 trafficking in adult cardiomyocytesAlexia Vite, Tony Guo, Nesrine Bouhrira, et al.Proceedings of the National Academy of Sciences of the United States of America|July 27, 2016
Mechanical signaling coordinates the embryonic heartbeatKevin K Chiou, Jason W Rocks, Christina Yingxian Chen, et al.Epilepsia|April 26, 2008
Gene expression analysis in absence epilepsy using a monozygotic twin designIngo Helbig, Nicholas A Matigian, Lata Vadlamudi, et al.The Neurohospitalist|April 13, 2022
Multicenter Study of the Impact of COVID-19 Shelter-In-Place on Tertiary Hospital-based Care for Pediatric Neurologic DiseaseMelissa L Hutchinson, Kendall B Nash, Nicholas S Abend, et al.Molecular Genetics and Metabolism|July 25, 2022
Psychometric outcome measures in beta-propeller protein-associated neurodegeneration (BPAN)Francesco Gavazzi, Samuel R Pierce, Joseph Vithayathil, et al.Pageof 33