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Physical Medicine and Rehabilitation Clinics of North America|November 26, 2019
The Expanding Role of Genetics in Cerebral PalsyLisa T Emrick, Shannon M DiCarloNeurotherapeutics : the Journal of the American Society for Experimental Neurotherapeutics|January 20, 2024
Functional genomics and small molecules in mitochondrial neurodevelopmental disordersDaniel G Calame, Lisa T EmrickMolecular Genetics and Metabolism|July 24, 2012
Citrulline and arginine utility in treating nitric oxide deficiency in mitochondrial disordersAyman W El-Hattab, Lisa T Emrick, William J Craigen, et al.Neurology. Genetics|April 30, 2024
<i>ATP1A3</i> Disease Spectrum Includes Paroxysmal Weakness and Encephalopathy Not Triggered by FeverChetan Immanneni, Daniel Calame, Song Jiao, et al.The International Journal of Biochemistry & Cell Biology|January 14, 2014
Mitochondria: role of citrulline and arginine supplementation in MELAS syndromeAyman W El-Hattab, Lisa T Emrick, Sirisak Chanprasert, et al.Meta Gene|November 21, 2014
The effect of citrulline and arginine supplementation on lactic acidemia in MELAS syndromeAyman W El-Hattab, Lisa T Emrick, Kaitlin C Williamson, et al.Neurology. Genetics|February 8, 2021
<i>EIF2AK2</i>-related Neurodevelopmental Disorder With Leukoencephalopathy, Developmental Delay, and Episodic Neurologic Regression Mimics Pelizaeus-Merzbacher DiseaseDaniel G Calame, Meagan Hainlen, Danielle Takacs, et al.American Journal of Medical Genetics. Part A|August 21, 2024
Recessive loss-of-function variants in DPH1 identified as the molecular cause in a sibling pair previously diagnosed with Fine-Lubinsky syndromeEmily R Waskow, , Lisa T Emrick, et al.Mitochondrion|August 3, 2014
Glucose metabolism derangements in adults with the MELAS m.3243A>G mutationAyman W El-Hattab, Lisa T Emrick, Jean W Hsu, et al.Molecular Genetics and Metabolism|February 14, 2012
Restoration of impaired nitric oxide production in MELAS syndrome with citrulline and arginine supplementationAyman W El-Hattab, Jean W Hsu, Lisa T Emrick, et al.Pageof 3