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Jacob O Day

Showing results (1-10 of 5) with videos related to

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BMJ (Clinical Research Ed.)|November 25, 2017
A man with paraesthesia, headache, and vertigoJacob O Day, Pragnesh Bhatt
Journal of Parkinson'S Disease|April 25, 2022
Challenges of Incorporating Digital Health Technology Outcomes in a Clinical Trial: Experiences from PD STATJacob O Day, Stephen Smith, Alastair J Noyce, et al.
Behavioural Brain Research|January 11, 2014
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 OCDDawn M Eagle, Cristie Noschang, Laure-Sophie Camilla d'Angelo, et al.
Plos Genetics|March 17, 2022
Biallelic variants in TRAPPC10 cause a microcephalic TRAPPopathy disorder in humans and miceLettie E Rawlins, Hashem Almousa, Shazia Khan, et al.
Brain : a Journal of Neurology|June 19, 2022
TMEM63C mutations cause mitochondrial morphology defects and underlie hereditary spastic paraplegiaLuis Carlos Tábara, Fatema Al-Salmi, Reza Maroofian, et al.
Pageof 1

Showing results (1-10 of 5) with videos related to

Sort By:
Pageof 1
BMJ (Clinical Research Ed.)|November 25, 2017
A man with paraesthesia, headache, and vertigoJacob O Day, Pragnesh Bhatt
Journal of Parkinson'S Disease|April 25, 2022
Challenges of Incorporating Digital Health Technology Outcomes in a Clinical Trial: Experiences from PD STATJacob O Day, Stephen Smith, Alastair J Noyce, et al.
Behavioural Brain Research|January 11, 2014
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 OCDDawn M Eagle, Cristie Noschang, Laure-Sophie Camilla d'Angelo, et al.
Plos Genetics|March 17, 2022
Biallelic variants in TRAPPC10 cause a microcephalic TRAPPopathy disorder in humans and miceLettie E Rawlins, Hashem Almousa, Shazia Khan, et al.
Brain : a Journal of Neurology|June 19, 2022
TMEM63C mutations cause mitochondrial morphology defects and underlie hereditary spastic paraplegiaLuis Carlos Tábara, Fatema Al-Salmi, Reza Maroofian, et al.
Pageof 1