Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

David A Weinstein

Showing results (71-80 of 91) with videos related to

Pageof 10
Sort By:
Human Molecular Genetics|September 19, 2009
Chromosomal and genetic alterations in human hepatocellular adenomas associated with type Ia glycogen storage diseasePriya S Kishnani, Tzu-Po Chuang, Deeksha Bali, et al.
Molecular Genetics and Metabolism|July 25, 2018
Safety issues associated with dietary management in patients with hepatic glycogen storage diseaseThomas A H Steunenberg, Fabian Peeks, Irene J Hoogeveen, et al.
Journal of Inherited Metabolic Disease|December 17, 2020
The potential of dietary treatment in patients with glycogen storage disease type IVTerry G J Derks, Fabian Peeks, Foekje de Boer, et al.
Journal of Inherited Metabolic Disease|July 30, 2014
Evaluation of glycogen storage disease as a cause of ketotic hypoglycemia in childrenLaurie M Brown, Michelle M Corrado, Rixt M van der Ende, et al.
Journal of Inherited Metabolic Disease|September 17, 2014
In vitro digestion of starches in a dynamic gastrointestinal model: an innovative study to optimize dietary management of patients with hepatic glycogen storage diseasesTatiéle Nalin, Koen Venema, David A Weinstein, et al.
Journal of Gastroenterology|October 17, 2013
Identification of differentially expressed microRNAs in human hepatocellular adenoma associated with type I glycogen storage disease: a potential utility as biomarkersLi-Ya Chiu, Priya S Kishnani, Tzu-Po Chuang, et al.
International Journal of Molecular Sciences|January 11, 2022
Exosomal MicroRNAs as Potential Biomarkers of Hepatic Injury and Kidney Disease in Glycogen Storage Disease Type Ia PatientsRoberta Resaz, Davide Cangelosi, Daniela Segalerba, et al.
Journal of Inherited Metabolic Disease|May 21, 2015
Erratum to: In vitro digestion of starches in a dynamic gastrointestinal model: an innovative study to optimize dietary management of patients with hepatic glycogen storage diseasesTatiéle Nalin, Koen Venema, David A Weinstein, et al.
Journal of Biomedicine & Biotechnology|February 15, 2011
Glycogen storage disease type Ia in canines: a model for human metabolic and genetic liver diseaseAndrew Specht, Laurie Fiske, Kirsten Erger, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 20, 2019
Diagnosis and management of glycogen storage diseases type VI and IX: a clinical practice resource of the American College of Medical Genetics and Genomics (ACMG)Priya S Kishnani, Jennifer Goldstein, Stephanie L Austin, et al.
Pageof 10

Showing results (71-80 of 91) with videos related to

Sort By:
Pageof 10
Human Molecular Genetics|September 19, 2009
Chromosomal and genetic alterations in human hepatocellular adenomas associated with type Ia glycogen storage diseasePriya S Kishnani, Tzu-Po Chuang, Deeksha Bali, et al.
Molecular Genetics and Metabolism|July 25, 2018
Safety issues associated with dietary management in patients with hepatic glycogen storage diseaseThomas A H Steunenberg, Fabian Peeks, Irene J Hoogeveen, et al.
Journal of Inherited Metabolic Disease|December 17, 2020
The potential of dietary treatment in patients with glycogen storage disease type IVTerry G J Derks, Fabian Peeks, Foekje de Boer, et al.
Journal of Inherited Metabolic Disease|July 30, 2014
Evaluation of glycogen storage disease as a cause of ketotic hypoglycemia in childrenLaurie M Brown, Michelle M Corrado, Rixt M van der Ende, et al.
Journal of Inherited Metabolic Disease|September 17, 2014
In vitro digestion of starches in a dynamic gastrointestinal model: an innovative study to optimize dietary management of patients with hepatic glycogen storage diseasesTatiéle Nalin, Koen Venema, David A Weinstein, et al.
Journal of Gastroenterology|October 17, 2013
Identification of differentially expressed microRNAs in human hepatocellular adenoma associated with type I glycogen storage disease: a potential utility as biomarkersLi-Ya Chiu, Priya S Kishnani, Tzu-Po Chuang, et al.
International Journal of Molecular Sciences|January 11, 2022
Exosomal MicroRNAs as Potential Biomarkers of Hepatic Injury and Kidney Disease in Glycogen Storage Disease Type Ia PatientsRoberta Resaz, Davide Cangelosi, Daniela Segalerba, et al.
Journal of Inherited Metabolic Disease|May 21, 2015
Erratum to: In vitro digestion of starches in a dynamic gastrointestinal model: an innovative study to optimize dietary management of patients with hepatic glycogen storage diseasesTatiéle Nalin, Koen Venema, David A Weinstein, et al.
Journal of Biomedicine & Biotechnology|February 15, 2011
Glycogen storage disease type Ia in canines: a model for human metabolic and genetic liver diseaseAndrew Specht, Laurie Fiske, Kirsten Erger, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 20, 2019
Diagnosis and management of glycogen storage diseases type VI and IX: a clinical practice resource of the American College of Medical Genetics and Genomics (ACMG)Priya S Kishnani, Jennifer Goldstein, Stephanie L Austin, et al.
Pageof 10