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

E Flanagan

Showing results (181-190 of 582) with videos related to

Pageof 59
Sort By:
Journal of Pediatric Endocrinology & Metabolism : JPEM|September 12, 2014
Three cases of Wolfram syndrome with different clinical aspectsEmine Çamtosun, Zeynep Şıklar, Pınar Kocaay, et al.
Journal of the American Medical Informatics Association : JAMIA|March 16, 2013
Paper- and computer-based workarounds to electronic health record use at three benchmark institutionsMindy E Flanagan, Jason J Saleem, Laura G Millitello, et al.
Journal of Clinical Research in Pediatric Endocrinology|June 11, 2013
Transient neonatal diabetes mellitus in a Turkish patient with three novel homozygous variants in the ZFP57 geneMehmet Boyraz, Korkut Ulucan, Necati Taşkın, et al.
Applied Ergonomics|August 13, 2018
Comparative usability evaluation of consultation order templates in a simulated primary care environmentApril Savoy, Himalaya Patel, Mindy E Flanagan, et al.
Human Mutation|July 7, 2017
Analysis of large-scale sequencing cohorts does not support the role of variants in UCP2 as a cause of hyperinsulinaemic hypoglycaemiaThomas W Laver, Michael N Weedon, Richard Caswell, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|March 23, 2017
Clinical presentation and treatment response to diazoxide in two siblings with congenital hyperinsulinism as a result of a novel compound heterozygous ABCC8 missense mutationSonya Galcheva, Violeta Iotova, Sian Ellard, et al.
BMJ Quality & Safety|July 29, 2015
"Anybody on this list that you're more worried about?" Qualitative analysis exploring the functions of questions during end of shift handoffsColleen M O'Brien, Mindy E Flanagan, Alicia A Bergman, et al.
Clinical Genetics|November 27, 2024
The p.(Gly111Arg) ABCC8 Variant: A Founder Mutation Causing Congenital Hyperinsulinism in the Indian Agarwal CommunityVandana Jain, Venkatesan Radha, Viswanathan Mohan, et al.
European Journal of Endocrinology|March 23, 2011
Characterization of ABCC8 and KCNJ11 gene mutations and phenotypes in Korean patients with congenital hyperinsulinismSo Eun Park, Sarah E Flanagan, Khalid Hussain, et al.
Diabetes Care|March 6, 2007
Sulfonylurea treatment in young children with neonatal diabetes: dealing with hyperglycemia, hypoglycemia, and sick daysEthel Codner, Sarah E Flanagan, Francisca Ugarte, et al.
Pageof 59

Showing results (181-190 of 582) with videos related to

Sort By:
Pageof 59
Journal of Pediatric Endocrinology & Metabolism : JPEM|September 12, 2014
Three cases of Wolfram syndrome with different clinical aspectsEmine Çamtosun, Zeynep Şıklar, Pınar Kocaay, et al.
Journal of the American Medical Informatics Association : JAMIA|March 16, 2013
Paper- and computer-based workarounds to electronic health record use at three benchmark institutionsMindy E Flanagan, Jason J Saleem, Laura G Millitello, et al.
Journal of Clinical Research in Pediatric Endocrinology|June 11, 2013
Transient neonatal diabetes mellitus in a Turkish patient with three novel homozygous variants in the ZFP57 geneMehmet Boyraz, Korkut Ulucan, Necati Taşkın, et al.
Applied Ergonomics|August 13, 2018
Comparative usability evaluation of consultation order templates in a simulated primary care environmentApril Savoy, Himalaya Patel, Mindy E Flanagan, et al.
Human Mutation|July 7, 2017
Analysis of large-scale sequencing cohorts does not support the role of variants in UCP2 as a cause of hyperinsulinaemic hypoglycaemiaThomas W Laver, Michael N Weedon, Richard Caswell, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|March 23, 2017
Clinical presentation and treatment response to diazoxide in two siblings with congenital hyperinsulinism as a result of a novel compound heterozygous ABCC8 missense mutationSonya Galcheva, Violeta Iotova, Sian Ellard, et al.
BMJ Quality & Safety|July 29, 2015
"Anybody on this list that you're more worried about?" Qualitative analysis exploring the functions of questions during end of shift handoffsColleen M O'Brien, Mindy E Flanagan, Alicia A Bergman, et al.
Clinical Genetics|November 27, 2024
The p.(Gly111Arg) ABCC8 Variant: A Founder Mutation Causing Congenital Hyperinsulinism in the Indian Agarwal CommunityVandana Jain, Venkatesan Radha, Viswanathan Mohan, et al.
European Journal of Endocrinology|March 23, 2011
Characterization of ABCC8 and KCNJ11 gene mutations and phenotypes in Korean patients with congenital hyperinsulinismSo Eun Park, Sarah E Flanagan, Khalid Hussain, et al.
Diabetes Care|March 6, 2007
Sulfonylurea treatment in young children with neonatal diabetes: dealing with hyperglycemia, hypoglycemia, and sick daysEthel Codner, Sarah E Flanagan, Francisca Ugarte, et al.
Pageof 59