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Brain : a Journal of Neurology|October 31, 2006
Mutations in progranulin explain atypical phenotypes with variants in MAPTStuart M Pickering-Brown, Matt Baker, Jenny Gass, et al.
Acta Neuropathologica|January 23, 2013
Frontotemporal dementia-amyotrophic lateral sclerosis syndrome locus on chromosome 16p12.1-q12.2: genetic, clinical and neuropathological analysisCarol Dobson-Stone, Agnes A Luty, Elizabeth M Thompson, et al.
Journal of Neural Transmission (Vienna, Austria : 1996)|August 9, 2015
Genetic markers of cholesterol transport and gray matter diffusion: a preliminary study of the CETP I405V polymorphismLauren E Salminen, Peter R Schofield, Kerrie D Pierce, et al.
Maturitas|December 3, 2019
Analysis of NR5A1 in 142 patients with premature ovarian insufficiency, diminished ovarian reserve, or unexplained infertilitySylvie Jaillard, Rajini Sreenivasan, Marion Beaumont, et al.
Biology of Reproduction|October 14, 2024
Functional characterization of human recessive DIS3 variants in premature ovarian insufficiency†Brianna L Kline, Nicole A Siddall, Fernando Wijaya, et al.
Molecular Genetics & Genomic Medicine|January 22, 2020
Analysis of variants in GATA4 and FOG2/ZFPM2 demonstrates benign contribution to 46,XY disorders of sex developmentJocelyn A van den Bergen, Gorjana Robevska, Stefanie Eggers, et al.
Translational Psychiatry|August 3, 2022
Epigenetic signatures relating to disease-associated genotypic burden in familial risk of bipolar disorderSonia Hesam-Shariati, Bronwyn J Overs, Gloria Roberts, et al.
Plos One|February 26, 2013
C9ORF72 repeat expansion in Australian and Spanish frontotemporal dementia patientsCarol Dobson-Stone, Marianne Hallupp, Clement T Loy, et al.
Behavioural Brain Research|August 31, 2015
Neuromarkers of the common angiotensinogen polymorphism in healthy older adults: A comprehensive assessment of white matter integrity and cognitionLauren E Salminen, Peter R Schofield, Kerrie D Pierce, et al.
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