Showing results (381-390 of 510) with videos related to
Sort By:
Pageof 51
Neurology|May 9, 2007
ATP13A2 missense mutations in juvenile parkinsonism and young onset Parkinson diseaseA Di Fonzo, H F Chien, M Socal, et al.Annals of Neurology|January 10, 2002
PARK6-linked parkinsonism occurs in several European familiesEnza Maria Valente, Francesco Brancati, Alessandro Ferraris, et al.Human Genetics|October 17, 2007
A new syndrome with noncompaction cardiomyopathy, bradycardia, pulmonary stenosis, atrial septal defect and heterotaxy with suggestive linkage to chromosome 6pMarja W Wessels, Bianca M De Graaf, Titia E Cohen-Overbeek, et al.Cell|May 15, 2012
Species-dependent posttranscriptional regulation of NOS1 by FMRP in the developing cerebral cortexKenneth Y Kwan, Mandy M S Lam, Matthew B Johnson, et al.Journal of Medical Genetics|November 8, 2011
Linkage and association analyses of glaucoma related traits in a large pedigree from a Dutch genetically isolated populationTatiana Axenovich, Irina Zorkoltseva, Nadezhda Belonogova, et al.Ophthalmology|August 30, 2011
Clinical implications of old and new genes for open-angle glaucomaWishal D Ramdas, Leonieke M E van Koolwijk, Angela J Cree, et al.Molecular Psychiatry|June 23, 2010
Genetic risk profiles for depression and anxiety in adult and elderly cohortsA Demirkan, B W J H Penninx, K Hek, et al.Neurogenetics|October 9, 2014
An exome study of Parkinson's disease in Sardinia, a Mediterranean genetic isolateMarialuisa Quadri, Xu Yang, Giovanni Cossu, et al.Plos Genetics|June 16, 2010
A genome-wide association study of optic disc parametersWishal D Ramdas, Leonieke M E van Koolwijk, M Kamran Ikram, et al.Parkinsonism & Related Disorders|June 2, 2009
GIGYF2 mutations are not a frequent cause of familial Parkinson's diseaseAlessio Di Fonzo, Edito Fabrizio, Astrid Thomas, et al.Pageof 51