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Elizabeth McCormick

Showing results (1-10 of 13) with videos related to

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The Mount Sinai Journal of Medicine, New York|September 15, 2012
Integrating palliative care into primary careElizabeth McCormick, Emily Chai, Diane E Meier
Neurotherapeutics : the Journal of the American Society for Experimental Neurotherapeutics|December 28, 2012
Molecular genetic testing for mitochondrial disease: from one generation to the nextElizabeth McCormick, Emily Place, Marni J Falk
Physiotherapy Theory and Practice|October 13, 2023
Perceptions and experiences of burnout: A survey of physical therapists across practice settings and patient populationsJennifer Elinich, Kimberly D Wynarczuk, Elizabeth McCormick
Case Reports in Genetics|April 13, 2016
Early Infantile Epileptic Encephalopathy in an STXBP1 Patient with Lactic Acidemia and Normal Mitochondrial Respiratory Chain FunctionDong Li, Elizabeth Bhoj, Elizabeth McCormick, et al.
RNA Biology|March 8, 2016
A novel HSD17B10 mutation impairing the activities of the mitochondrial RNase P complex causes X-linked intractable epilepsy and neurodevelopmental regressionMarni J Falk, Xiaowu Gai, Megumi Shigematsu, et al.
Plos One|July 30, 2013
Primary respiratory chain disease causes tissue-specific dysregulation of the global transcriptome and nutrient-sensing signaling networkZhe Zhang, Mai Tsukikawa, Min Peng, et al.
Neurotherapeutics : the Journal of the American Society for Experimental Neurotherapeutics|September 18, 2023
Optimized Nutrition in Mitochondrial Disease Correlates to Improved Muscle Fatigue, Strength, and Quality of LifeDonna DiVito, Amanda Wellik, Jessica Burfield, et al.
JIMD Reports|February 12, 2014
AGC1 Deficiency Causes Infantile Epilepsy, Abnormal Myelination, and Reduced N-AcetylaspartateMarni J Falk, Dong Li, Xiaowu Gai, et al.
JIMD Reports|June 30, 2014
Erratum to: AGC1 Deficiency Causes Infantile Epilepsy, Abnormal Myelination, and Reduced N-AcetylaspartateMarni J Falk, Dong Li, Xiaowu Gai, et al.
JCI Insight|November 5, 2016
Muscle oxidative phosphorylation quantitation using creatine chemical exchange saturation transfer (CrCEST) MRI in mitochondrial disordersCatherine DeBrosse, Ravi Prakash Reddy Nanga, Neil Wilson, et al.
Pageof 2

Showing results (1-10 of 13) with videos related to

Sort By:
Pageof 2
The Mount Sinai Journal of Medicine, New York|September 15, 2012
Integrating palliative care into primary careElizabeth McCormick, Emily Chai, Diane E Meier
Neurotherapeutics : the Journal of the American Society for Experimental Neurotherapeutics|December 28, 2012
Molecular genetic testing for mitochondrial disease: from one generation to the nextElizabeth McCormick, Emily Place, Marni J Falk
Physiotherapy Theory and Practice|October 13, 2023
Perceptions and experiences of burnout: A survey of physical therapists across practice settings and patient populationsJennifer Elinich, Kimberly D Wynarczuk, Elizabeth McCormick
Case Reports in Genetics|April 13, 2016
Early Infantile Epileptic Encephalopathy in an STXBP1 Patient with Lactic Acidemia and Normal Mitochondrial Respiratory Chain FunctionDong Li, Elizabeth Bhoj, Elizabeth McCormick, et al.
RNA Biology|March 8, 2016
A novel HSD17B10 mutation impairing the activities of the mitochondrial RNase P complex causes X-linked intractable epilepsy and neurodevelopmental regressionMarni J Falk, Xiaowu Gai, Megumi Shigematsu, et al.
Plos One|July 30, 2013
Primary respiratory chain disease causes tissue-specific dysregulation of the global transcriptome and nutrient-sensing signaling networkZhe Zhang, Mai Tsukikawa, Min Peng, et al.
Neurotherapeutics : the Journal of the American Society for Experimental Neurotherapeutics|September 18, 2023
Optimized Nutrition in Mitochondrial Disease Correlates to Improved Muscle Fatigue, Strength, and Quality of LifeDonna DiVito, Amanda Wellik, Jessica Burfield, et al.
JIMD Reports|February 12, 2014
AGC1 Deficiency Causes Infantile Epilepsy, Abnormal Myelination, and Reduced N-AcetylaspartateMarni J Falk, Dong Li, Xiaowu Gai, et al.
JIMD Reports|June 30, 2014
Erratum to: AGC1 Deficiency Causes Infantile Epilepsy, Abnormal Myelination, and Reduced N-AcetylaspartateMarni J Falk, Dong Li, Xiaowu Gai, et al.
JCI Insight|November 5, 2016
Muscle oxidative phosphorylation quantitation using creatine chemical exchange saturation transfer (CrCEST) MRI in mitochondrial disordersCatherine DeBrosse, Ravi Prakash Reddy Nanga, Neil Wilson, et al.
Pageof 2