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Showing results (1231-1240 of 1,650) with videos related to
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Circulation Research
|
September 1, 1990
Functional and autoradiographic evidence for endothelin 1 receptors on human and rat cardiac myocytes. Comparison with single smooth muscle cells
C J Moody, M R Dashwood, R M Sykes, et al.
The British Journal of Surgery
|
November 1, 1982
Measurement of gastric emptying after gastric bypass surgery using radionuclides
M Horowitz, D J Cook, P J Collins, et al.
Journal of Developmental Origins of Health and Disease
|
November 20, 2020
Effects of maternal periconceptional undernutrition in sheep on offspring glucose-insulin axis function into adulthood
Mark H Oliver, Frank H Bloomfield, Amita Bansal, et al.
BMC Geriatrics
|
May 20, 2016
A meta-review of stress, coping and interventions in dementia and dementia caregiving
K J Gilhooly, M L M Gilhooly, M P Sullivan, et al.
Clinical & Experimental Optometry
|
December 2, 2017
Vision screening at two years does not reduce the prevalence of reduced vision at four and a half years of age
Lucy Goodman, Arijit Chakraborty, Nabin Paudel, et al.
Journal of Diabetes Research
|
June 2, 2017
The Effectiveness of Lifestyle Adaptation for the Prevention of Prediabetes in Adults: A Systematic Review
George Kerrison, Richard B Gillis, Shahwar I Jiwani, et al.
Ebiomedicine
|
August 29, 2020
Effect of antenatal magnesium sulphate on MRI biomarkers of white matter development at term equivalent age: The magnum study
Tanya Poppe, Benjamin Thompson, James P Boardman, et al.
The Journal of Physiology
|
October 1, 1992
Role of basal release of nitric oxide on coronary flow and mechanical performance of the isolated rat heart
M Amrani, J O'Shea, N J Allen, et al.
Neurology
|
August 1, 1997
A mitochondrial DNA tRNA(Val) point mutation associated with adult-onset Leigh syndrome
R M Chalmers, P J Lamont, I Nelson, et al.
American Journal of Human Genetics
|
January 1, 1991
Pearson syndrome and mitochondrial encephalomyopathy in a patient with a deletion of mtDNA
M A McShane, S R Hammans, M Sweeney, et al.
Page
of 165
Search research articles
Search
Showing results (1231-1240 of 1,650) with videos related to
Sort By:
Page
of 165
Circulation Research
|
September 1, 1990
Functional and autoradiographic evidence for endothelin 1 receptors on human and rat cardiac myocytes. Comparison with single smooth muscle cells
C J Moody, M R Dashwood, R M Sykes, et al.
The British Journal of Surgery
|
November 1, 1982
Measurement of gastric emptying after gastric bypass surgery using radionuclides
M Horowitz, D J Cook, P J Collins, et al.
Journal of Developmental Origins of Health and Disease
|
November 20, 2020
Effects of maternal periconceptional undernutrition in sheep on offspring glucose-insulin axis function into adulthood
Mark H Oliver, Frank H Bloomfield, Amita Bansal, et al.
BMC Geriatrics
|
May 20, 2016
A meta-review of stress, coping and interventions in dementia and dementia caregiving
K J Gilhooly, M L M Gilhooly, M P Sullivan, et al.
Clinical & Experimental Optometry
|
December 2, 2017
Vision screening at two years does not reduce the prevalence of reduced vision at four and a half years of age
Lucy Goodman, Arijit Chakraborty, Nabin Paudel, et al.
Journal of Diabetes Research
|
June 2, 2017
The Effectiveness of Lifestyle Adaptation for the Prevention of Prediabetes in Adults: A Systematic Review
George Kerrison, Richard B Gillis, Shahwar I Jiwani, et al.
Ebiomedicine
|
August 29, 2020
Effect of antenatal magnesium sulphate on MRI biomarkers of white matter development at term equivalent age: The magnum study
Tanya Poppe, Benjamin Thompson, James P Boardman, et al.
The Journal of Physiology
|
October 1, 1992
Role of basal release of nitric oxide on coronary flow and mechanical performance of the isolated rat heart
M Amrani, J O'Shea, N J Allen, et al.
Neurology
|
August 1, 1997
A mitochondrial DNA tRNA(Val) point mutation associated with adult-onset Leigh syndrome
R M Chalmers, P J Lamont, I Nelson, et al.
American Journal of Human Genetics
|
January 1, 1991
Pearson syndrome and mitochondrial encephalomyopathy in a patient with a deletion of mtDNA
M A McShane, S R Hammans, M Sweeney, et al.
Page
of 165