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 (161-170 of 582) with videos related to

Pageof 59
Sort By:
American Journal of Otolaryngology|December 15, 2016
Correlation analysis of oral lesion sizes by various standardized criteriaCarrie E Flanagan, Nelson L Rhodus, Kate A Cole, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|April 28, 2015
Protein-induced hyperinsulinaemic hypoglycaemia due to a homozygous HADH mutation in three siblings of a Saudi familyOmer Babiker, Sarah E Flanagan, Sian Ellard, et al.
Otolaryngology--Head and Neck Surgery : Official Journal of American Academy of Otolaryngology-Head and Neck Surgery|April 28, 2009
Surgical debridement and adjunctive hyperbaric oxygen in cervical necrotizing fasciitisCarrie E Flanagan, Opeyemi O Daramola, Robert H Maisel, et al.
Diabetic Medicine : a Journal of the British Diabetic Association|December 5, 2013
HNF4A mutation: switch from hyperinsulinaemic hypoglycaemia to maturity-onset diabetes of the young, and incretin responseV B Arya, S Rahman, S Senniappan, et al.
Frontiers in Pediatrics|July 17, 2020
A Novel <i>HNF4A</i> Mutation Causing Three Phenotypic Forms of Glucose Dysregulation in a FamilySuresh Chandran, Victor Samuel Rajadurai, Wai Han Hoi, et al.
Journal of Clinical Research in Pediatric Endocrinology|August 29, 2015
A Deep Intronic HADH Splicing Mutation (c.636+471G>T) in a Congenital Hyperinsulinemic Hypoglycemia Case: Long Term Clinical CourseEmine Çamtosun, Sarah E Flanagan, Sian Ellard, et al.
Journal of General Internal Medicine|April 24, 2019
The Thrill Is Gone: Burdensome Electronic Documentation Takes Its Toll on Physicians' Time and AttentionMindy E Flanagan, Laura G Militello, Nicholas A Rattray, et al.
Plos One|December 15, 2012
Non-traditional antibacterial screening approaches for the identification of novel inhibitors of the glyoxylate shunt in gram-negative pathogensKelly C Fahnoe, Mark E Flanagan, Glenn Gibson, et al.
Diabetes Research and Clinical Practice|June 23, 2016
Clinical and genetic features of Argentinian children with diabetes-onset before 12months of age: Successful transfer from insulin to oral sulfonylureaPatricia Taberner, Sarah E Flanagan, Deborah J Mackay, et al.
The Journal of Clinical Investigation|February 22, 2023
Monogenic disease analysis establishes that fetal insulin accounts for half of human fetal growthAlice E Hughes, Elisa De Franco, Rachel M Freathy, et al.
Pageof 59

Showing results (161-170 of 582) with videos related to

Sort By:
Pageof 59
American Journal of Otolaryngology|December 15, 2016
Correlation analysis of oral lesion sizes by various standardized criteriaCarrie E Flanagan, Nelson L Rhodus, Kate A Cole, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|April 28, 2015
Protein-induced hyperinsulinaemic hypoglycaemia due to a homozygous HADH mutation in three siblings of a Saudi familyOmer Babiker, Sarah E Flanagan, Sian Ellard, et al.
Otolaryngology--Head and Neck Surgery : Official Journal of American Academy of Otolaryngology-Head and Neck Surgery|April 28, 2009
Surgical debridement and adjunctive hyperbaric oxygen in cervical necrotizing fasciitisCarrie E Flanagan, Opeyemi O Daramola, Robert H Maisel, et al.
Diabetic Medicine : a Journal of the British Diabetic Association|December 5, 2013
HNF4A mutation: switch from hyperinsulinaemic hypoglycaemia to maturity-onset diabetes of the young, and incretin responseV B Arya, S Rahman, S Senniappan, et al.
Frontiers in Pediatrics|July 17, 2020
A Novel <i>HNF4A</i> Mutation Causing Three Phenotypic Forms of Glucose Dysregulation in a FamilySuresh Chandran, Victor Samuel Rajadurai, Wai Han Hoi, et al.
Journal of Clinical Research in Pediatric Endocrinology|August 29, 2015
A Deep Intronic HADH Splicing Mutation (c.636+471G>T) in a Congenital Hyperinsulinemic Hypoglycemia Case: Long Term Clinical CourseEmine Çamtosun, Sarah E Flanagan, Sian Ellard, et al.
Journal of General Internal Medicine|April 24, 2019
The Thrill Is Gone: Burdensome Electronic Documentation Takes Its Toll on Physicians' Time and AttentionMindy E Flanagan, Laura G Militello, Nicholas A Rattray, et al.
Plos One|December 15, 2012
Non-traditional antibacterial screening approaches for the identification of novel inhibitors of the glyoxylate shunt in gram-negative pathogensKelly C Fahnoe, Mark E Flanagan, Glenn Gibson, et al.
Diabetes Research and Clinical Practice|June 23, 2016
Clinical and genetic features of Argentinian children with diabetes-onset before 12months of age: Successful transfer from insulin to oral sulfonylureaPatricia Taberner, Sarah E Flanagan, Deborah J Mackay, et al.
The Journal of Clinical Investigation|February 22, 2023
Monogenic disease analysis establishes that fetal insulin accounts for half of human fetal growthAlice E Hughes, Elisa De Franco, Rachel M Freathy, et al.
Pageof 59