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Plos One
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September 26, 2023
The impacts of social restrictions during the COVID-19 pandemic on the physical activity levels of over 50-year olds: The CHARIOT COVID-19 Rapid Response (CCRR) cohort study
Conall Green, Thomas Beaney, David Salman, et al.
Annals of the New York Academy of Sciences
|
July 21, 1998
Congenital myasthenic syndrome. (CMS) type Ia. Clinical and genetic diversity
L T Middleton, K Christodoulou, F Deymeer, et al.
Annals of Biomedical Engineering
|
May 15, 2024
Human and Porcine Lumbar Endplate Injury Risk in Repeated Flexion-Compression
Concetta F Morino, Allison L Schmidt, Elizabeth Dimbath, et al.
Genomics
|
August 1, 1993
Localization of a gene (CMT2A) for autosomal dominant Charcot-Marie-Tooth disease type 2 to chromosome 1p and evidence of genetic heterogeneity
K Ben Othmane, L T Middleton, L J Loprest, et al.
The Journal of Physician Assistant Education : the Official Journal of the Physician Assistant Education Association
|
December 10, 2025
Dermoscopy Education: Association With Skin Lesion Evaluation Confidence Among Physician Associate/Assistant Students
Hayden T Middleton, Peter A Young, Sean Kolhoff, et al.
International Journal of Cardiology
|
September 21, 2022
Atrial flutter and fibrillation in patients with pulmonary arterial hypertension or chronic thromboembolic pulmonary hypertension in the ASPIRE registry: Comparison of rate versus rhythm control approaches
Mark Anthony Sammut, Robin Condliffe, Charlie Elliot, et al.
Annals of the New York Academy of Sciences
|
December 10, 1999
Distal hereditary motor neuronopathy of the Jerash type
L T Middleton, K Christodoulou, A Mubaidin, et al.
Journal of the American Chemical Society
|
September 16, 2011
2DIR spectroscopy of human amylin fibrils reflects stable β-sheet structure
Lu Wang, Chris T Middleton, Sadanand Singh, et al.
Annals of the New York Academy of Sciences
|
November 1, 2017
Distal Hereditary Motor Neuronopathy of the Jerash Type
L T Middleton, K Christodoulou, A Mubaidin, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
April 30, 2020
Mitochondrial Complex 1, Sigma 1, and Synaptic Vesicle 2A in Early Drug-Naive Parkinson's Disease
Heather Wilson, Gennaro Pagano, Edoardo Rosario de Natale, et al.
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of 19
Search research articles
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Showing results (121-130 of 181) with videos related to
Sort By:
Page
of 19
Plos One
|
September 26, 2023
The impacts of social restrictions during the COVID-19 pandemic on the physical activity levels of over 50-year olds: The CHARIOT COVID-19 Rapid Response (CCRR) cohort study
Conall Green, Thomas Beaney, David Salman, et al.
Annals of the New York Academy of Sciences
|
July 21, 1998
Congenital myasthenic syndrome. (CMS) type Ia. Clinical and genetic diversity
L T Middleton, K Christodoulou, F Deymeer, et al.
Annals of Biomedical Engineering
|
May 15, 2024
Human and Porcine Lumbar Endplate Injury Risk in Repeated Flexion-Compression
Concetta F Morino, Allison L Schmidt, Elizabeth Dimbath, et al.
Genomics
|
August 1, 1993
Localization of a gene (CMT2A) for autosomal dominant Charcot-Marie-Tooth disease type 2 to chromosome 1p and evidence of genetic heterogeneity
K Ben Othmane, L T Middleton, L J Loprest, et al.
The Journal of Physician Assistant Education : the Official Journal of the Physician Assistant Education Association
|
December 10, 2025
Dermoscopy Education: Association With Skin Lesion Evaluation Confidence Among Physician Associate/Assistant Students
Hayden T Middleton, Peter A Young, Sean Kolhoff, et al.
International Journal of Cardiology
|
September 21, 2022
Atrial flutter and fibrillation in patients with pulmonary arterial hypertension or chronic thromboembolic pulmonary hypertension in the ASPIRE registry: Comparison of rate versus rhythm control approaches
Mark Anthony Sammut, Robin Condliffe, Charlie Elliot, et al.
Annals of the New York Academy of Sciences
|
December 10, 1999
Distal hereditary motor neuronopathy of the Jerash type
L T Middleton, K Christodoulou, A Mubaidin, et al.
Journal of the American Chemical Society
|
September 16, 2011
2DIR spectroscopy of human amylin fibrils reflects stable β-sheet structure
Lu Wang, Chris T Middleton, Sadanand Singh, et al.
Annals of the New York Academy of Sciences
|
November 1, 2017
Distal Hereditary Motor Neuronopathy of the Jerash Type
L T Middleton, K Christodoulou, A Mubaidin, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
April 30, 2020
Mitochondrial Complex 1, Sigma 1, and Synaptic Vesicle 2A in Early Drug-Naive Parkinson's Disease
Heather Wilson, Gennaro Pagano, Edoardo Rosario de Natale, et al.
Page
of 19