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Neurology
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March 26, 2017
Paroxysmal eye-head movements in Glut1 deficiency syndrome
Toni S Pearson, Roser Pons, Kristin Engelstad, et al.
Annals of Neurology
|
August 6, 2010
Glut1 deficiency: inheritance pattern determined by haploinsufficiency
Michael Rotstein, Kristin Engelstad, Hong Yang, et al.
Annals of Neurology
|
December 29, 2004
Glut-1 deficiency syndrome: clinical, genetic, and therapeutic aspects
Dong Wang, Juan M Pascual, Hong Yang, et al.
Annals of Clinical and Translational Neurology
|
August 7, 2019
Exploring mTOR inhibition as treatment for mitochondrial disease
Abigail Sage-Schwaede, Kristin Engelstad, Rachel Salazar, et al.
Pediatric Research
|
July 11, 2008
Functional studies of the T295M mutation causing Glut1 deficiency: glucose efflux preferentially affected by T295M
Dong Wang, Hong Yang, Lei Shi, et al.
Archives of Neurology
|
May 10, 2006
Nerve conduction abnormalities in patients with MELAS and the A3243G mutation
Petra Kaufmann, Juan M Pascual, Yaacov Anziska, et al.
Annals of Neurology
|
February 27, 2010
Acute hyperglycemia produces transient improvement in glucose transporter type 1 deficiency
Cigdem I Akman, Kristin Engelstad, Veronica J Hinton, et al.
Molecular Genetics and Metabolism
|
April 13, 2010
Uncovering microdeletions in patients with severe Glut-1 deficiency syndrome using SNP oligonucleotide microarray analysis
Brynn Levy, Dong Wang, Paivi M Ullner, et al.
Archives of Neurology
|
February 14, 2007
Brain glucose supply and the syndrome of infantile neuroglycopenia
Juan M Pascual, Dong Wang, Veronica Hinton, et al.
Journal of Child Neurology
|
May 3, 2014
Long-term clinical course of Glut1 deficiency syndrome
Aliza S Alter, Kristin Engelstad, Veronica J Hinton, et al.
Page
of 5
Search research articles
Search
Showing results (11-20 of 47) with videos related to
Sort By:
Page
of 5
Neurology
|
March 26, 2017
Paroxysmal eye-head movements in Glut1 deficiency syndrome
Toni S Pearson, Roser Pons, Kristin Engelstad, et al.
Annals of Neurology
|
August 6, 2010
Glut1 deficiency: inheritance pattern determined by haploinsufficiency
Michael Rotstein, Kristin Engelstad, Hong Yang, et al.
Annals of Neurology
|
December 29, 2004
Glut-1 deficiency syndrome: clinical, genetic, and therapeutic aspects
Dong Wang, Juan M Pascual, Hong Yang, et al.
Annals of Clinical and Translational Neurology
|
August 7, 2019
Exploring mTOR inhibition as treatment for mitochondrial disease
Abigail Sage-Schwaede, Kristin Engelstad, Rachel Salazar, et al.
Pediatric Research
|
July 11, 2008
Functional studies of the T295M mutation causing Glut1 deficiency: glucose efflux preferentially affected by T295M
Dong Wang, Hong Yang, Lei Shi, et al.
Archives of Neurology
|
May 10, 2006
Nerve conduction abnormalities in patients with MELAS and the A3243G mutation
Petra Kaufmann, Juan M Pascual, Yaacov Anziska, et al.
Annals of Neurology
|
February 27, 2010
Acute hyperglycemia produces transient improvement in glucose transporter type 1 deficiency
Cigdem I Akman, Kristin Engelstad, Veronica J Hinton, et al.
Molecular Genetics and Metabolism
|
April 13, 2010
Uncovering microdeletions in patients with severe Glut-1 deficiency syndrome using SNP oligonucleotide microarray analysis
Brynn Levy, Dong Wang, Paivi M Ullner, et al.
Archives of Neurology
|
February 14, 2007
Brain glucose supply and the syndrome of infantile neuroglycopenia
Juan M Pascual, Dong Wang, Veronica Hinton, et al.
Journal of Child Neurology
|
May 3, 2014
Long-term clinical course of Glut1 deficiency syndrome
Aliza S Alter, Kristin Engelstad, Veronica J Hinton, et al.
Page
of 5