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Journal of Child Neurology|December 3, 2003
Clinical variability in Rett syndromeSakkuBai Naidu, Genila Bibat, Lisa Kratz, et al.Genes & Development|November 3, 2004
Mitochondrial fission proteins regulate programmed cell death in yeastYihru Fannjiang, Wen-Chih Cheng, Sarah J Lee, et al.Vascular Medicine (London, England)|May 31, 2013
Urine vascular biomarkers in Sturge-Weber syndromeAditya K Sreenivasan, Catherine D Bachur, Kira E Lanier, et al.Pediatric Neurology|August 1, 2017
Reliability and Clinical Correlation of Transcranial Doppler Ultrasound in Sturge-Weber SyndromeElizabeth A Offermann, Aditya Sreenivasan, M Robert DeJong, et al.Neurosurgery|January 28, 2004
Gene microarray analysis of human brain arteriovenous malformationsTomoki Hashimoto, Michael T Lawton, Gen Wen, et al.Lancet (London, England)|March 20, 2004
A combined syndrome of juvenile polyposis and hereditary haemorrhagic telangiectasia associated with mutations in MADH4 (SMAD4)Carol J Gallione, Gabriela M Repetto, Eric Legius, et al.Journal of Stroke and Cerebrovascular Diseases : the Official Journal of National Stroke Association|March 29, 2024
Pathologic features of brain hemorrhage after radiation treatment: case series with somatic mutation analysisRoberto J Alcazar-Felix, Abhinav Srinath, Stephanie Hage, et al.Human Molecular Genetics|February 21, 2007
FXYD1 is an MeCP2 target gene overexpressed in the brains of Rett syndrome patients and Mecp2-null miceVivianne Deng, Valerie Matagne, Fatima Banine, et al.Neuroscience Research|September 26, 2022
Dysfunction of mitochondria and GABAergic interneurons in the anterior cingulate cortex of individuals with schizophreniaMari A Kondo, Alexis L Norris, Kun Yang, et al.Human Mutation|December 6, 2005
Low frequency of PDCD10 mutations in a panel of CCM3 probands: potential for a fourth CCM locusChristina L Liquori, Michel J Berg, Ferdinando Squitieri, et al.Pageof 27