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Archives of Neurology|January 1, 1977
Mannosidosis. New clinical presentation, enzyme studied, and carbohydrate analysisJ P Kistler, I T Lott, E H Kolodny, et al.Journal of Medical Internet Research|October 31, 2024
How Do Scholars Conceptualize and Conduct Health and Digital Health Literacy Research? Survey of Federally Funded ScholarsMayank Sakhuja, Brooks Yelton, Simone Kavarana, et al.Alimentary Pharmacology & Therapeutics|February 19, 2025
Clinical Trial: The Effects of Emulsifiers in the Food Supply on Disease Activity in Crohn's Disease: An Exploratory Double-Blinded Randomised Feeding TrialJessica A Fitzpatrick, Peter R Gibson, Kirstin M Taylor, et al.International Journal of Aging & Human Development|January 29, 2013
Beliefs about promoting cognitive health among Filipino Americans who care for persons with dementiaSarah B Laditka, Winston Tseng, Anna E Price, et al.Clinical Pharmacology and Therapeutics|July 1, 1994
Pharmacokinetics and pharmacodynamics of multiple oral doses of MK-0591, a 5-lipoxygenase-activating protein inhibitorM Depré, B Friedman, A Van Hecken, et al.Investigational New Drugs|October 12, 2012
The novel antiangiogenic VJ115 inhibits the NADH oxidase ENOX1 and cytoskeleton-remodeling proteinsAmudhan Venkateswaran, David B Friedman, Alexandra J Walsh, et al.JMIR Formative Research|July 3, 2023
Assessment and Documentation of Social Determinants of Health Among Health Care Providers: Qualitative StudyBrooks Yelton, Jancham Rachel Rumthao, Mayank Sakhuja, et al.Nature Communications|September 1, 2025
Single-molecule fluorescence microscopy reveals regulatory mechanisms of MYO7A-driven cargo transport in stereocilia of live inner ear hair cellsTakushi Miyoshi, Harshad D Vishwasrao, Inna A Belyantseva, et al.Journal of Medical Genetics|August 3, 2004
Mutations of ESPN cause autosomal recessive deafness and vestibular dysfunctionS Naz, A J Griffith, S Riazuddin, et al.Human Genetics|August 23, 2008
Gene structure and mutant alleles of PCDH15: nonsyndromic deafness DFNB23 and type 1 Usher syndromeZubair M Ahmed, Saima Riazuddin, Sandar Aye, et al.Pageof 97