Search research articles
Contact Us
Filters
Showing results (11-20 of 19) with videos related to
Page
of 2
Sort By:
You have reached the last page of results.
This site can display upto 19 results.
Public Health Nutrition
|
October 16, 2018
Applying international guidelines for calcium supplementation to prevent pre-eclampsia: simulation of recommended dosages suggests risk of excess intake in Ethiopia
Biniyam Tesfaye, Kate Sinclair, Sara E Wuehler, et al.
Neuroimage. Clinical
|
September 29, 2015
Motor pathway degeneration in young ataxia telangiectasia patients: A diffusion tractography study
Ishani Sahama, Kate Sinclair, Simona Fiori, et al.
Bioengineering (Basel, Switzerland)
|
October 28, 2023
Mechanical Characterization of the Human Abdominal Wall Using Uniaxial Tensile Testing
Kyleigh Kriener, Raushan Lala, Ryan Anthony Peter Homes, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
October 12, 2013
Herpes simplex encephalitis relapse with chorea is associated with autoantibodies to N-Methyl-D-aspartate receptor or dopamine-2 receptor
Shekeeb S Mohammad, Kate Sinclair, Sekhar Pillai, et al.
Pediatric Neurology
|
August 5, 2019
Acute Hemorrhagic Leukoencephalopathy: Pathological Features and Cerebrospinal Fluid Cytokine Profiles
Michaela Waak, Stephen Malone, Kate Sinclair, et al.
Food and Nutrition Bulletin
|
September 13, 2023
Food Insecurity and Perceived Effects of COVID-19 on Livelihoods in Rural Sri Lanka
Nishmeet Singh, Samuel Scott, Neha Kumar, et al.
Human Molecular Genetics
|
March 12, 2013
A patient-derived olfactory stem cell disease model for ataxia-telangiectasia
Romal Stewart, Sergei Kozlov, Nicholas Matigian, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
July 3, 2017
GNAO1-related movement disorder with life-threatening exacerbations: movement phenomenology and response to DBS
Michaela Waak, Shekeeb S Mohammad, David Coman, et al.
The Journal of Biological Chemistry
|
June 16, 2012
Mutations in the GlyT2 gene (SLC6A5) are a second major cause of startle disease
Eloisa Carta, Seo-Kyung Chung, Victoria M James, et al.
Page
of 2
Search research articles
Search
Showing results (11-20 of 19) with videos related to
Sort By:
Page
of 2
You have reached the last page of results.
This site can display upto 19 results.
Public Health Nutrition
|
October 16, 2018
Applying international guidelines for calcium supplementation to prevent pre-eclampsia: simulation of recommended dosages suggests risk of excess intake in Ethiopia
Biniyam Tesfaye, Kate Sinclair, Sara E Wuehler, et al.
Neuroimage. Clinical
|
September 29, 2015
Motor pathway degeneration in young ataxia telangiectasia patients: A diffusion tractography study
Ishani Sahama, Kate Sinclair, Simona Fiori, et al.
Bioengineering (Basel, Switzerland)
|
October 28, 2023
Mechanical Characterization of the Human Abdominal Wall Using Uniaxial Tensile Testing
Kyleigh Kriener, Raushan Lala, Ryan Anthony Peter Homes, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
October 12, 2013
Herpes simplex encephalitis relapse with chorea is associated with autoantibodies to N-Methyl-D-aspartate receptor or dopamine-2 receptor
Shekeeb S Mohammad, Kate Sinclair, Sekhar Pillai, et al.
Pediatric Neurology
|
August 5, 2019
Acute Hemorrhagic Leukoencephalopathy: Pathological Features and Cerebrospinal Fluid Cytokine Profiles
Michaela Waak, Stephen Malone, Kate Sinclair, et al.
Food and Nutrition Bulletin
|
September 13, 2023
Food Insecurity and Perceived Effects of COVID-19 on Livelihoods in Rural Sri Lanka
Nishmeet Singh, Samuel Scott, Neha Kumar, et al.
Human Molecular Genetics
|
March 12, 2013
A patient-derived olfactory stem cell disease model for ataxia-telangiectasia
Romal Stewart, Sergei Kozlov, Nicholas Matigian, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
July 3, 2017
GNAO1-related movement disorder with life-threatening exacerbations: movement phenomenology and response to DBS
Michaela Waak, Shekeeb S Mohammad, David Coman, et al.
The Journal of Biological Chemistry
|
June 16, 2012
Mutations in the GlyT2 gene (SLC6A5) are a second major cause of startle disease
Eloisa Carta, Seo-Kyung Chung, Victoria M James, et al.
Page
of 2