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Archives of Neurology
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January 13, 2006
Double trouble in hereditary neuropathy: concomitant mutations in the PMP-22 gene and another gene produce novel phenotypes
Julie A Hodapp, Gregory T Carter, Hillary P Lipe, et al.
Molecular & General Genetics : MGG
|
March 26, 1997
PRS1 is a key member of the gene family encoding phosphoribosylpyrophosphate synthetase in Saccharomyces cerevisiae
A T Carter, F Beiche, B Hove-Jensen, et al.
Muscle & Nerve
|
August 22, 2000
Magnetic resonance imaging of denervated muscle: comparison to electromyography
C M McDonald, G T Carter, R C Fritz, et al.
Archives of Physical Medicine and Rehabilitation
|
December 9, 2008
Pain in myotonic muscular dystrophy, type 1
Gregory T Carter, Mark P Jensen, Amy J Hoffman, et al.
Muscle & Nerve
|
February 12, 2009
Homozygous contiguous gene deletion of 13q12 causing LGMD2C and ARSACS in the same patient
Hugh J McMillan, Melissa T Carter, Pierre J Jacob, et al.
The American Journal of Hospice & Palliative Care
|
April 15, 2014
Life Support After Brain Death
Steven J Baumrucker, Laura Hutchinson, Matt Stolick, et al.
The Journal of Applied Psychology
|
November 6, 2013
Uncovering curvilinear relationships between conscientiousness and job performance: how theoretically appropriate measurement makes an empirical difference
Nathan T Carter, Dev K Dalal, Anthony S Boyce, et al.
Open Forum Infectious Diseases
|
April 10, 2023
Increased Myocardial Infarction Risk Following Herpes Zoster Infection
Ganapathi I Parameswaran, Alexandra F Drye, Bethany A Wattengel, et al.
Aggressive Behavior
|
May 6, 2023
Development of a measure of aggressive behavior expectancies in adults: The Aggression Expectancy Questionnaire
Courtland S Hyatt, Donald R Lynam, Samuel J West, et al.
The American Journal of Hospice & Palliative Care
|
August 4, 2021
Ethics Roundtable: The Case of the Surrogate Versus the Living Will
Steven J Baumrucker, Keelin F Roche, Matt Stolick, et al.
Page
of 89
Search research articles
Search
Showing results (581-590 of 884) with videos related to
Sort By:
Page
of 89
Archives of Neurology
|
January 13, 2006
Double trouble in hereditary neuropathy: concomitant mutations in the PMP-22 gene and another gene produce novel phenotypes
Julie A Hodapp, Gregory T Carter, Hillary P Lipe, et al.
Molecular & General Genetics : MGG
|
March 26, 1997
PRS1 is a key member of the gene family encoding phosphoribosylpyrophosphate synthetase in Saccharomyces cerevisiae
A T Carter, F Beiche, B Hove-Jensen, et al.
Muscle & Nerve
|
August 22, 2000
Magnetic resonance imaging of denervated muscle: comparison to electromyography
C M McDonald, G T Carter, R C Fritz, et al.
Archives of Physical Medicine and Rehabilitation
|
December 9, 2008
Pain in myotonic muscular dystrophy, type 1
Gregory T Carter, Mark P Jensen, Amy J Hoffman, et al.
Muscle & Nerve
|
February 12, 2009
Homozygous contiguous gene deletion of 13q12 causing LGMD2C and ARSACS in the same patient
Hugh J McMillan, Melissa T Carter, Pierre J Jacob, et al.
The American Journal of Hospice & Palliative Care
|
April 15, 2014
Life Support After Brain Death
Steven J Baumrucker, Laura Hutchinson, Matt Stolick, et al.
The Journal of Applied Psychology
|
November 6, 2013
Uncovering curvilinear relationships between conscientiousness and job performance: how theoretically appropriate measurement makes an empirical difference
Nathan T Carter, Dev K Dalal, Anthony S Boyce, et al.
Open Forum Infectious Diseases
|
April 10, 2023
Increased Myocardial Infarction Risk Following Herpes Zoster Infection
Ganapathi I Parameswaran, Alexandra F Drye, Bethany A Wattengel, et al.
Aggressive Behavior
|
May 6, 2023
Development of a measure of aggressive behavior expectancies in adults: The Aggression Expectancy Questionnaire
Courtland S Hyatt, Donald R Lynam, Samuel J West, et al.
The American Journal of Hospice & Palliative Care
|
August 4, 2021
Ethics Roundtable: The Case of the Surrogate Versus the Living Will
Steven J Baumrucker, Keelin F Roche, Matt Stolick, et al.
Page
of 89