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Grace Yoon

Showing results (11-20 of 177) with videos related to

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European Journal of Medical Genetics|March 8, 2011
Cockayne syndrome caused by paternally inherited 5 Mb deletion of 10q11.2 and a frameshift mutation of ERCC6Shailly Jain Ghai, Mary Shago, Manohar Shroff, et al.
Paediatrics & Child Health|September 3, 2010
A case report of prenatal exposure to rosuvastatin and telmisartanYannis Trakadis, Susan Blaser, Cecil D Hahn, et al.
Pediatric Neurology|April 20, 2010
Intermediate-dose idebenone and quality of life in Friedreich ataxiaJohn F Brandsema, Derek Stephens, Jessica Hartley, et al.
Journal of Child Neurology|March 4, 2010
Childhood-onset CADASIL: clinical, imaging, and neurocognitive featuresJessica Hartley, Robyn Westmacott, Jochen Decker, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|January 25, 2011
Mitochondrial mimicry of multiple system atrophy of the cerebellar subtypeArpan R Mehta, Susan H Fox, Mark Tarnopolsky, et al.
Pediatric Neurology|October 23, 2008
Stepwise developmental regression associated with novel CACNA1A mutationAndrea A Guerin, Annette Feigenbaum, Elizabeth J Donner, et al.
Developmental Medicine and Child Neurology|October 15, 2013
Prospective study of activities of daily living outcomes in children with cerebellar atrophyAlmundher Al-Maawali, Susan Blaser, Xiu Y Zhao, et al.
Neuroimaging Clinics of North America|July 18, 2016
The Pediatric Cerebellum in Inherited Neurodegenerative Disorders: A Pattern-recognition ApproachSusan I Blaser, Maja Steinlin, Almundher Al-Maawali, et al.
Plos One|October 2, 2015
Further Insights into the Allan-Herndon-Dudley Syndrome: Clinical and Functional Characterization of a Novel MCT8 MutationChristine M Armour, Simone Kersseboom, Grace Yoon, et al.
The International Journal of Biostatistics|June 14, 2019
Simple Quasi-Bayes Approach for Modeling Mean Medical CostsGrace Yoon, Wenxin Jiang, Lei Liu, et al.
Pageof 18

Showing results (11-20 of 177) with videos related to

Sort By:
Pageof 18
European Journal of Medical Genetics|March 8, 2011
Cockayne syndrome caused by paternally inherited 5 Mb deletion of 10q11.2 and a frameshift mutation of ERCC6Shailly Jain Ghai, Mary Shago, Manohar Shroff, et al.
Paediatrics & Child Health|September 3, 2010
A case report of prenatal exposure to rosuvastatin and telmisartanYannis Trakadis, Susan Blaser, Cecil D Hahn, et al.
Pediatric Neurology|April 20, 2010
Intermediate-dose idebenone and quality of life in Friedreich ataxiaJohn F Brandsema, Derek Stephens, Jessica Hartley, et al.
Journal of Child Neurology|March 4, 2010
Childhood-onset CADASIL: clinical, imaging, and neurocognitive featuresJessica Hartley, Robyn Westmacott, Jochen Decker, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|January 25, 2011
Mitochondrial mimicry of multiple system atrophy of the cerebellar subtypeArpan R Mehta, Susan H Fox, Mark Tarnopolsky, et al.
Pediatric Neurology|October 23, 2008
Stepwise developmental regression associated with novel CACNA1A mutationAndrea A Guerin, Annette Feigenbaum, Elizabeth J Donner, et al.
Developmental Medicine and Child Neurology|October 15, 2013
Prospective study of activities of daily living outcomes in children with cerebellar atrophyAlmundher Al-Maawali, Susan Blaser, Xiu Y Zhao, et al.
Neuroimaging Clinics of North America|July 18, 2016
The Pediatric Cerebellum in Inherited Neurodegenerative Disorders: A Pattern-recognition ApproachSusan I Blaser, Maja Steinlin, Almundher Al-Maawali, et al.
Plos One|October 2, 2015
Further Insights into the Allan-Herndon-Dudley Syndrome: Clinical and Functional Characterization of a Novel MCT8 MutationChristine M Armour, Simone Kersseboom, Grace Yoon, et al.
The International Journal of Biostatistics|June 14, 2019
Simple Quasi-Bayes Approach for Modeling Mean Medical CostsGrace Yoon, Wenxin Jiang, Lei Liu, et al.
Pageof 18