Showing results (571-580 of 586) with videos related to
Sort By:
Pageof 59
American Journal of Epidemiology|October 11, 2024
From Fetus to Eight: the CHILD Cohort StudyKozeta Miliku, Myrtha E Reyna, Maria Medeleanu, et al.Neurology. Genetics|October 30, 2023
mTOR Pathway Somatic Pathogenic Variants in Focal Malformations of Cortical Development: Novel Variants, Topographic Mapping, and Clinical OutcomesEric Krochmalnek, Andrea Accogli, Judith St-Onge, et al.Cell Metabolism|June 23, 2015
A Periodic Diet that Mimics Fasting Promotes Multi-System Regeneration, Enhanced Cognitive Performance, and HealthspanSebastian Brandhorst, In Young Choi, Min Wei, et al.Epilepsia|January 12, 2011
The clinicopathologic spectrum of focal cortical dysplasias: a consensus classification proposed by an ad hoc Task Force of the ILAE Diagnostic Methods CommissionIngmar Blümcke, Maria Thom, Eleonora Aronica, et al.Epidemiology and Health|October 19, 2023
Cohort profile: investigating SARS-CoV-2 infection and the health and psychosocial impact of the COVID-19 pandemic in the Canadian CHILD CohortRilwan Azeez, Larisa Lotoski, Aimée Dubeau, et al.Human Molecular Genetics|September 5, 2001
Mutations in the X-linked filamin 1 gene cause periventricular nodular heterotopia in males as well as in femalesV L Sheen, P H Dixon, J W Fox, et al.Neurology|January 26, 2005
Filamin A mutations cause periventricular heterotopia with Ehlers-Danlos syndromeV L Sheen, A Jansen, M H Chen, et al.Genome Medicine|October 27, 2015
HOTAIR and its surrogate DNA methylation signature indicate carboplatin resistance in ovarian cancerAndrew E Teschendorff, Shih-Han Lee, Allison Jones, et al.Brain : a Journal of Neurology|October 23, 2002
Subcortical band heterotopia (SBH) in males: clinical, imaging and genetic findings in comparison with femalesMaria Daniela D'Agostino, Andrea Bernasconi, Soma Das, et al.Neuroimage|July 21, 2018
Probabilistic functional tractography of the human cortex revisitedLena Trebaul, Pierre Deman, Viateur Tuyisenge, et al.Pageof 59