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Reena Jethva

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

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Seminars in Pediatric Neurology|December 17, 2013
Mitochondrial dysfunction in autismAgustín Legido, Reena Jethva, Michael J Goldenthal
Molecular Genetics and Metabolism|November 4, 2008
Short-chain acyl-coenzyme A dehydrogenase deficiencyReena Jethva, Michael J Bennett, Jerry Vockley
Cytotherapy|February 5, 2009
Cell therapy for disorders of boneReena Jethva, Satoru Otsuru, Massimo Dominici, et al.
American Journal of Medical Genetics. Part A|April 25, 2012
Noonan syndrome due to a SHOC2 mutation presenting with fetal distress and fatal hypertrophic cardiomyopathy in a premature infantRebecca Hoban, Amy E Roberts, Laurie Demmer, et al.
Cytotherapy|May 1, 2010
A strategy for single nucleotide polymorphism analysis of chimerism for somatic cell therapyXiaohua Chen, Ted J Hofmann, Satoru Otsuru, et al.
Seminars in Pediatric Neurology|August 24, 2014
Fraternal twins with autism, severe cognitive deficit, and epilepsy: diagnostic role of chromosomal microarray analysisJaime Imitola, Diana Walleigh, Carol E Anderson, et al.
Clinical Case Reports|March 8, 2017
22q11.2 microduplication syndrome with associated esophageal atresia/tracheo-esophageal fistula and vascular ringLinda T Nguyen, Rachel Fleishman, Emilee Flynn, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|November 14, 2013
Tetrasomy 13q32.2qter due to an apparent inverted duplicated neocentric marker chromosome in an infant with hemangiomas, failure to thrive, laryngomalacia, and tethered cordJinglan Liu, Reena Jethva, Michael T Del Vecchio, et al.
Biomarkers in Medicine|October 7, 2015
Mitochondrial enzyme dysfunction in autism spectrum disorders; a novel biomarker revealed from buccal swab analysisMichael J Goldenthal, Shirish Damle, Sudip Sheth, et al.
JIMD Reports|June 5, 2013
Metabolic profiling of total homocysteine and related compounds in hyperhomocysteinemia: utility and limitations in diagnosing the cause of puzzling thrombophilia in a familySally P Stabler, Mark Korson, Reena Jethva, et al.
Pageof 2

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

Sort By:
Pageof 2
Seminars in Pediatric Neurology|December 17, 2013
Mitochondrial dysfunction in autismAgustín Legido, Reena Jethva, Michael J Goldenthal
Molecular Genetics and Metabolism|November 4, 2008
Short-chain acyl-coenzyme A dehydrogenase deficiencyReena Jethva, Michael J Bennett, Jerry Vockley
Cytotherapy|February 5, 2009
Cell therapy for disorders of boneReena Jethva, Satoru Otsuru, Massimo Dominici, et al.
American Journal of Medical Genetics. Part A|April 25, 2012
Noonan syndrome due to a SHOC2 mutation presenting with fetal distress and fatal hypertrophic cardiomyopathy in a premature infantRebecca Hoban, Amy E Roberts, Laurie Demmer, et al.
Cytotherapy|May 1, 2010
A strategy for single nucleotide polymorphism analysis of chimerism for somatic cell therapyXiaohua Chen, Ted J Hofmann, Satoru Otsuru, et al.
Seminars in Pediatric Neurology|August 24, 2014
Fraternal twins with autism, severe cognitive deficit, and epilepsy: diagnostic role of chromosomal microarray analysisJaime Imitola, Diana Walleigh, Carol E Anderson, et al.
Clinical Case Reports|March 8, 2017
22q11.2 microduplication syndrome with associated esophageal atresia/tracheo-esophageal fistula and vascular ringLinda T Nguyen, Rachel Fleishman, Emilee Flynn, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|November 14, 2013
Tetrasomy 13q32.2qter due to an apparent inverted duplicated neocentric marker chromosome in an infant with hemangiomas, failure to thrive, laryngomalacia, and tethered cordJinglan Liu, Reena Jethva, Michael T Del Vecchio, et al.
Biomarkers in Medicine|October 7, 2015
Mitochondrial enzyme dysfunction in autism spectrum disorders; a novel biomarker revealed from buccal swab analysisMichael J Goldenthal, Shirish Damle, Sudip Sheth, et al.
JIMD Reports|June 5, 2013
Metabolic profiling of total homocysteine and related compounds in hyperhomocysteinemia: utility and limitations in diagnosing the cause of puzzling thrombophilia in a familySally P Stabler, Mark Korson, Reena Jethva, et al.
Pageof 2