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European Journal of Human Genetics : EJHG|September 27, 2025
PKD1 5'UTR variants are a rare cause of disease in ADPKD and suggest a new focus for therapeutic developmentLaura Wedd, Yvonne Hort, Chirag Patel, et al.
American Journal of Human Genetics|July 13, 2026
Landscape of parental postzygotic mutations across >11,000 rare disease triosO Isaac Garcia-Salinas, Katrina A Andrews, Rashesh Sanghvi, et al.
The Psychiatric Quarterly|June 24, 2017
Clozapine in Reducing Aggression and Violence in Forensic PopulationsKathleen Patchan, Gopal Vyas, Ann L Hackman, et al.
Journal of Traumatic Stress|October 16, 2015
Randomized Controlled Trial of Online Expressive Writing to Address Readjustment Difficulties Among U.S. Afghanistan and Iraq War VeteransNina A Sayer, Siamak Noorbaloochi, Patricia A Frazier, et al.
Gynecologic Oncology|December 31, 2002
Weekly low-dose carboplatin and paclitaxel in the treatment of recurrent ovarian and peritoneal cancerLaura J Havrilesky, Angeles A Alvarez, Robyn A Sayer, et al.
Experimental Gerontology|June 20, 2020
The feasibility of muscle mitochondrial respiratory chain phenotyping across the cognitive spectrum in Parkinson's diseaseAlison J Yarnall, Antoneta Granic, Samantha Waite, et al.
Nature Reviews. Disease Primers|September 19, 2024
SarcopeniaAvan A Sayer, Rachel Cooper, Hidenori Arai, et al.
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