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Kristin Engelstad

Showing results (31-40 of 47) with videos related to

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Journal of Child Neurology|July 13, 2013
Weakness and fatigue in diverse neuromuscular diseasesJacqueline Montes, Michelle Blumenschine, Sally Dunaway, et al.
Therapeutic Advances in Rare Disease|March 6, 2024
A United States-based patient-reported adult polyglucosan body disease registry: initial resultsJacy Sparks, Francesco Michelassi, John L P Thompson, et al.
Annals of Clinical and Translational Neurology|May 6, 2022
Visual memory failure presages conversion to MELAS phenotypeEmily B Leaffer, Darryl C De Vivo, Kristin Engelstad, et al.
The Journal of Pediatrics|January 15, 2004
Mitochondrial DNA abnormalities and autistic spectrum disordersRoser Pons, Antoni L Andreu, Nicoletta Checcarelli, et al.
Annals of Neurology|December 23, 2011
Glut1 deficiency syndrome and erythrocyte glucose uptake assayHong Yang, Dong Wang, Kristin Engelstad, et al.
Human Reproduction (Oxford, England)|March 4, 2016
Attitudes toward prevention of mtDNA-related diseases through oocyte mitochondrial replacement therapyKristin Engelstad, Miriam Sklerov, Joshua Kriger, et al.
Journal of Translational Genetics and Genomics|July 1, 2020
The North American mitochondrial disease registryXiomara Q Rosales, John L P Thompson, Richard Haas, et al.
Journal of the Neurological Sciences|April 10, 2012
Decreased hippocampal expression of calbindin D28K and cognitive impairment in MELASValentina Emmanuele, Angels Garcia-Cazorla, Hua-Bin Huang, et al.
Pediatric Neurology|June 19, 2012
Allelic variations of glut-1 deficiency syndrome: the chinese experienceYanyan Liu, Xinhua Bao, Dong Wang, et al.
Archives of Neurology|January 14, 2009
Protean phenotypic features of the A3243G mitochondrial DNA mutationPetra Kaufmann, Kristin Engelstad, Ying Wei, et al.
Pageof 5

Showing results (31-40 of 47) with videos related to

Sort By:
Pageof 5
Journal of Child Neurology|July 13, 2013
Weakness and fatigue in diverse neuromuscular diseasesJacqueline Montes, Michelle Blumenschine, Sally Dunaway, et al.
Therapeutic Advances in Rare Disease|March 6, 2024
A United States-based patient-reported adult polyglucosan body disease registry: initial resultsJacy Sparks, Francesco Michelassi, John L P Thompson, et al.
Annals of Clinical and Translational Neurology|May 6, 2022
Visual memory failure presages conversion to MELAS phenotypeEmily B Leaffer, Darryl C De Vivo, Kristin Engelstad, et al.
The Journal of Pediatrics|January 15, 2004
Mitochondrial DNA abnormalities and autistic spectrum disordersRoser Pons, Antoni L Andreu, Nicoletta Checcarelli, et al.
Annals of Neurology|December 23, 2011
Glut1 deficiency syndrome and erythrocyte glucose uptake assayHong Yang, Dong Wang, Kristin Engelstad, et al.
Human Reproduction (Oxford, England)|March 4, 2016
Attitudes toward prevention of mtDNA-related diseases through oocyte mitochondrial replacement therapyKristin Engelstad, Miriam Sklerov, Joshua Kriger, et al.
Journal of Translational Genetics and Genomics|July 1, 2020
The North American mitochondrial disease registryXiomara Q Rosales, John L P Thompson, Richard Haas, et al.
Journal of the Neurological Sciences|April 10, 2012
Decreased hippocampal expression of calbindin D28K and cognitive impairment in MELASValentina Emmanuele, Angels Garcia-Cazorla, Hua-Bin Huang, et al.
Pediatric Neurology|June 19, 2012
Allelic variations of glut-1 deficiency syndrome: the chinese experienceYanyan Liu, Xinhua Bao, Dong Wang, et al.
Archives of Neurology|January 14, 2009
Protean phenotypic features of the A3243G mitochondrial DNA mutationPetra Kaufmann, Kristin Engelstad, Ying Wei, et al.
Pageof 5