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Neurology|May 11, 2016
Distinct molecular mechanisms of HTRA1 mutants in manifesting heterozygotes with CARASILHiroaki Nozaki, Taisuke Kato, Megumi Nihonmatsu, et al.The New England Journal of Medicine|April 24, 2009
Association of HTRA1 mutations and familial ischemic cerebral small-vessel diseaseKenju Hara, Atsushi Shiga, Toshio Fukutake, et al.Annals of Clinical and Translational Neurology|April 25, 2015
Variants associated with Gaucher disease in multiple system atrophyJun Mitsui, Takashi Matsukawa, Hidenao Sasaki, et al.Medrxiv : the Preprint Server for Health Sciences|July 10, 2023
Genome-wide association study identifies a new susceptibility locus in PLA2G4C for Multiple System AtrophyYasuo Nakahara, Jun Mitsui, Hidetoshi Date, et al.Pageof 4