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Melissa Andrew

Showing results (31-40 of 37) with videos related to

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BMJ Open|March 8, 2022
CUP study: protocol for a comparative analysis of centralised waitlist effectiveness, policies and innovations for connecting unattached patients to primary care providersEmily Gard Marshall, Mylaine Breton, Michael Green, et al.
American Journal of Human Genetics|June 4, 2016
Mutations in TKT Are the Cause of a Syndrome Including Short Stature, Developmental Delay, and Congenital Heart DefectsLia Boyle, Mirjam M C Wamelink, Gajja S Salomons, et al.
Molecular Neurobiology|March 20, 2025
Use of Drugs Affecting GABA<sub>A</sub> Receptors and the Risk of Developing Alzheimer's Disease and Dementia: a Meta-Analysis and Literature ReviewKimia Vakili, Mobina Fathi, Rasoul Ebrahimi, et al.
The Journal of Clinical Endocrinology and Metabolism|March 22, 2017
Paternally Inherited DLK1 Deletion Associated With Familial Central Precocious PubertyAndrew Dauber, Marina Cunha-Silva, Delanie B Macedo, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|July 17, 2019
The Comprehensive Assessment of Neurodegeneration and Dementia: Canadian Cohort StudyHoward Chertkow, Michael Borrie, Victor Whitehead, et al.
The Journal of Clinical Endocrinology and Metabolism|November 22, 2016
Clinical Characterization of Patients With Autosomal Dominant Short Stature due to Aggrecan MutationsAlexandra Gkourogianni, Melissa Andrew, Leah Tyzinski, et al.
BMJ Open|August 3, 2025
Canadian Adaptive Platform Trial of Treatments for COVID in Community Settings (CanTreatCOVID): protocol for a randomised controlled adaptive platform trial of treatments for acute SARS-CoV-2 infection in community settingsBanafshe Hosseini, Amanda Condon, Bruno R da Costa, et al.
Pageof 4

Showing results (31-40 of 37) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 37 results.
BMJ Open|March 8, 2022
CUP study: protocol for a comparative analysis of centralised waitlist effectiveness, policies and innovations for connecting unattached patients to primary care providersEmily Gard Marshall, Mylaine Breton, Michael Green, et al.
American Journal of Human Genetics|June 4, 2016
Mutations in TKT Are the Cause of a Syndrome Including Short Stature, Developmental Delay, and Congenital Heart DefectsLia Boyle, Mirjam M C Wamelink, Gajja S Salomons, et al.
Molecular Neurobiology|March 20, 2025
Use of Drugs Affecting GABA<sub>A</sub> Receptors and the Risk of Developing Alzheimer's Disease and Dementia: a Meta-Analysis and Literature ReviewKimia Vakili, Mobina Fathi, Rasoul Ebrahimi, et al.
The Journal of Clinical Endocrinology and Metabolism|March 22, 2017
Paternally Inherited DLK1 Deletion Associated With Familial Central Precocious PubertyAndrew Dauber, Marina Cunha-Silva, Delanie B Macedo, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|July 17, 2019
The Comprehensive Assessment of Neurodegeneration and Dementia: Canadian Cohort StudyHoward Chertkow, Michael Borrie, Victor Whitehead, et al.
The Journal of Clinical Endocrinology and Metabolism|November 22, 2016
Clinical Characterization of Patients With Autosomal Dominant Short Stature due to Aggrecan MutationsAlexandra Gkourogianni, Melissa Andrew, Leah Tyzinski, et al.
BMJ Open|August 3, 2025
Canadian Adaptive Platform Trial of Treatments for COVID in Community Settings (CanTreatCOVID): protocol for a randomised controlled adaptive platform trial of treatments for acute SARS-CoV-2 infection in community settingsBanafshe Hosseini, Amanda Condon, Bruno R da Costa, et al.
Pageof 4