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Familial Cancer|December 11, 2012
A novel missense mutation (N78D) in a family with von Hippel-Lindau disease with central nervous system haemangioblastomas, pancreatic and renal cystsS Cingoz, R B van der Luijt, E Kurt, et al.Pediatric Endocrinology Reviews : PER|January 24, 2006
Progeria: a new kind of Laminopathy-- report of the First European Symposium on Progeria and creation of EURO-Progeria, a European Consortium on Progeria and related disordersThomas Brune, Gisele Bonne, Jonas Denecke, et al.Journal of Autism and Developmental Disorders|May 18, 2010
Morphological features in children with autism spectrum disorders: a matched case-control studyHeval Ozgen, Gerhard S Hellemann, Rebecca K Stellato, et al.Frontiers in Neurology|July 23, 2020
Chronic Neurology in COVID-19 Era: Clinical Considerations and Recommendations From the REPROGRAM ConsortiumSonu Bhaskar, Sian Bradley, Simon Israeli-Korn, et al.Pageof 1