Jacob O. Day
Exeter, ENG, United Kingdom
Last Updated: 09/26/2026
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Found 11 publications
Bi-allelic UGGT1 variants cause a congenital disorder of glycosylation.
Journal: American journal of human genetics
Published: November 19, 2024
Acute monocular visual loss: time to call the stroke team?
Journal: Practical neurology
Published: April 23, 2024
Challenges of Incorporating Digital Health Technology Outcomes in a Clinical Trial: Experiences from PD STAT.
Journal: Journal of Parkinson's disease
Published: April 25, 2022
Biallelic variants in TRAPPC10 cause a microcephalic TRAPPopathy disorder in humans and mice.
Journal: PLoS genetics
Published: September 26, 2021
Long-Term Effects of Hatha Yoga on Heart Rate Variability In Healthy Practitioners: Potential Benefits For Cardiovascular Risk Reduction.
Journal: Alternative therapies in health and medicine
Published: August 28, 2021
TMEM63C mutations cause mitochondrial morphology defects and underlie hereditary spastic paraplegia.
TMEM63C mutations cause mitochondrial morphology defects and underlie hereditary spastic paraplegia.
Journal: Brain : a journal of neurology
Published: July 07, 2021
The Genetics of Parkinson's Disease and Implications for Clinical Practice.
Journal: Genes
Published: May 31, 2021
Cognitive, Neurological, and Behavioral Features in Adults With KCNJ11 Neonatal Diabetes.
Journal: Diabetes care
Published: May 15, 2018
A man with paraesthesia, headache, and vertigo.
Journal: BMJ (Clinical research ed.)
Published: November 25, 2017
The dopamine D2/D3 receptor agonist quinpirole increases checking-like behaviour in an operant observing response task with uncertain reinforcement: a novel possible model of OCD.
Journal: Behavioural brain research
Published: August 02, 2013
Showing 1-11 of 11
Last Updated: 09/26/2026