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Human Genetics|April 29, 2022
Genetic genealogy uncovers a founder deletion mutation in the cerebral cavernous malformations 2 geneCarol J Gallione, Matthew R Detter, Adrienne Sheline, et al.The Journal of Clinical Investigation|July 12, 2016
Natural allelic variation of the IL-21 receptor modulates ischemic stroke infarct volumeHan Kyu Lee, Sehoon Keum, Huaxin Sheng, et al.Pediatric Neurology|December 3, 2014
Stimulant use in patients with sturge-weber syndrome: safety and efficacyEboni I Lance, Kira E Lanier, T Andrew Zabel, et al.Annals of the Child Neurology Society|August 7, 2026
Development and Retrospective Application of Novel Outcome Measure: Sturge-Weber Syndrome Acute Crisis (SWAC) IndexKieran D McKenney, Luther G Kalb, Adrienne M Hammill, et al.Journal of Neurodevelopmental Disorders|August 24, 2025
Biomarker development in Sturge-Weber syndromeSiddharth S Gupta, Katharine E Joslyn, Kieran D McKenney, et al.American Journal of Physical Medicine & Rehabilitation|January 14, 2010
Physiatric findings in individuals with Sturge-Weber syndromeStacy J Suskauer, Melissa K Trovato, T Andrew Zabel, et al.Journal of Child Neurology|October 18, 2005
Comorbidity of epilepsy and headache in patients with Sturge-Weber syndromeEric H Kossoff, Laura A Hatfield, Karen L Ball, et al.Pediatric Neurology|April 30, 2017
Cannabidiol Treatment for Refractory Seizures in Sturge-Weber SyndromeEmma H Kaplan, Elizabeth A Offermann, Jacqueline W Sievers, et al.Plos One|November 28, 2012
Unexpected relationships and inbreeding in HapMap phase III populationsEric L Stevens, Joseph D Baugher, Matthew D Shirley, et al.Mammalian Genome : Official Journal of the International Mammalian Genome Society|August 3, 2005
QTL mapping in a mouse model of cardiomyopathy reveals an ancestral modifier allele affecting heart function and survivalFerrin C Wheeler, Liliana Fernandez, Kerri M Carlson, et al.Pageof 27