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Journal of Clinical and Translational Science
|
February 16, 2026
A point-based system to determine authorship eligibility in a large clinical trial: Insights from the ISCHEMIA trial's authorship nomination system
Shari Esquenazi-Karonika, Judith S Hochman, June Lyo, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society
|
April 1, 1995
Genetic mapping near the myd locus on mouse chromosome 8
K A Mills, K D Mathews, T Scherpbier-Heddema, et al.
Neuromuscular Disorders : NMD
|
May 21, 2022
Selected clinical and demographic factors and all-cause mortality among individuals with Duchenne muscular dystrophy in the Muscular Dystrophy Surveillance, Tracking, and Research Network
Pangaja Paramsothy, Yinding Wang, Bo Cai, et al.
Muscle & Nerve
|
March 21, 2022
Time to diagnosis of Duchenne muscular dystrophy remains unchanged: Findings from the Muscular Dystrophy Surveillance, Tracking, and Research Network, 2000-2015
Shiny Thomas, Kristin M Conway, Olushola Fapo, et al.
Journal of the American Society of Echocardiography : Official Publication of the American Society of Echocardiography
|
July 22, 2010
Exercise-induced left ventricular systolic dysfunction in women heterozygous for dystrophinopathy
Robert M Weiss, Richard E Kerber, Jane K Jones, et al.
BMC Health Services Research
|
July 3, 2025
Quality improvement of a community-engaged authorship system: lessons learned from the RECOVER initiative
Shari Esquenazi-Karonika, Patenne D Mathews, Marion J Wood, et al.
Frontiers in Genetics
|
May 20, 2020
Analysis of the <i>F2LR3</i> (PAR4) Single Nucleotide Polymorphism (<i>rs773902</i>) in an Indigenous Australian Population
Dian Ningtyas, Russell J Thomson, Volga Tarlac, et al.
AJNR. American Journal of Neuroradiology
|
June 1, 1996
Calcium 45 autoradiography and dual-isotope single-photon emission CT in a canine model of cerebral ischemia and middle cerebral artery occlusion
P D Purdy, M B Horowitz, D Mathews, et al.
Journal of Child Neurology
|
September 7, 2010
Muscular Dystrophy Surveillance Tracking and Research Network (MD STARnet): case definition in surveillance for childhood-onset Duchenne/Becker muscular dystrophy
Katherine D Mathews, Chris Cunniff, Jiji R Kantamneni, et al.
Annals of Thoracic Surgery Short Reports
|
December 22, 2025
Assessing the Safety of Sequential Radial Artery Grafting in Coronary Revascularization
AlleaBelle Bradshaw, Ifeanyi Chinedozi, Jace C Bradshaw, et al.
Page
of 45
Search research articles
Search
Showing results (361-370 of 450) with videos related to
Sort By:
Page
of 45
Journal of Clinical and Translational Science
|
February 16, 2026
A point-based system to determine authorship eligibility in a large clinical trial: Insights from the ISCHEMIA trial's authorship nomination system
Shari Esquenazi-Karonika, Judith S Hochman, June Lyo, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society
|
April 1, 1995
Genetic mapping near the myd locus on mouse chromosome 8
K A Mills, K D Mathews, T Scherpbier-Heddema, et al.
Neuromuscular Disorders : NMD
|
May 21, 2022
Selected clinical and demographic factors and all-cause mortality among individuals with Duchenne muscular dystrophy in the Muscular Dystrophy Surveillance, Tracking, and Research Network
Pangaja Paramsothy, Yinding Wang, Bo Cai, et al.
Muscle & Nerve
|
March 21, 2022
Time to diagnosis of Duchenne muscular dystrophy remains unchanged: Findings from the Muscular Dystrophy Surveillance, Tracking, and Research Network, 2000-2015
Shiny Thomas, Kristin M Conway, Olushola Fapo, et al.
Journal of the American Society of Echocardiography : Official Publication of the American Society of Echocardiography
|
July 22, 2010
Exercise-induced left ventricular systolic dysfunction in women heterozygous for dystrophinopathy
Robert M Weiss, Richard E Kerber, Jane K Jones, et al.
BMC Health Services Research
|
July 3, 2025
Quality improvement of a community-engaged authorship system: lessons learned from the RECOVER initiative
Shari Esquenazi-Karonika, Patenne D Mathews, Marion J Wood, et al.
Frontiers in Genetics
|
May 20, 2020
Analysis of the <i>F2LR3</i> (PAR4) Single Nucleotide Polymorphism (<i>rs773902</i>) in an Indigenous Australian Population
Dian Ningtyas, Russell J Thomson, Volga Tarlac, et al.
AJNR. American Journal of Neuroradiology
|
June 1, 1996
Calcium 45 autoradiography and dual-isotope single-photon emission CT in a canine model of cerebral ischemia and middle cerebral artery occlusion
P D Purdy, M B Horowitz, D Mathews, et al.
Journal of Child Neurology
|
September 7, 2010
Muscular Dystrophy Surveillance Tracking and Research Network (MD STARnet): case definition in surveillance for childhood-onset Duchenne/Becker muscular dystrophy
Katherine D Mathews, Chris Cunniff, Jiji R Kantamneni, et al.
Annals of Thoracic Surgery Short Reports
|
December 22, 2025
Assessing the Safety of Sequential Radial Artery Grafting in Coronary Revascularization
AlleaBelle Bradshaw, Ifeanyi Chinedozi, Jace C Bradshaw, et al.
Page
of 45