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

S Ellard

Showing results (91-100 of 144) with videos related to

Pageof 15
Sort By:
Diabetic Medicine : a Journal of the British Diabetic Association|June 16, 2010
Novel monogenic diabetes mutations in the P2 promoter of the HNF4A gene are associated with impaired function in vitroA Wirsing, K A Johnstone, L W Harries, et al.
Human Mutation|October 1, 2003
Identification of 21 novel glucokinase (GCK) mutations in UK and European Caucasians with maturity-onset diabetes of the young (MODY)K L Thomson, A L Gloyn, K Colclough, et al.
Diabetic Medicine : a Journal of the British Diabetic Association|October 20, 2015
Successful maintenance on sulphonylurea therapy and low diabetes complication rates in a HNF1A-MODY cohortS Bacon, M P Kyithar, S R Rizvi, et al.
Annals of Oncology : Official Journal of the European Society for Medical Oncology|November 17, 2007
Survival outcome and cost-effectiveness with docetaxel and paclitaxel in patients with metastatic breast cancer: a population-based evaluationT Vu, S Ellard, C H Speers, et al.
Diabetologia|April 11, 2002
Complete glucokinase deficiency is not a common cause of permanent neonatal diabetesA L Gloyn, S Ellard, J P Shield, et al.
Neurology|July 27, 2007
A novel mutation causing DEND syndrome: a treatable channelopathy of pancreas and brainK Shimomura, F Hörster, H de Wet, et al.
Endocrinology, Diabetes & Metabolism Case Reports|March 12, 2014
Paternally inherited ABCC8 mutation causing diffuse congenital hyperinsulinismSuresh Chandran, Fabian Yap Kok Peng, Victor Samuel Rajadurai, et al.
Diabetic Medicine : a Journal of the British Diabetic Association|July 27, 2001
Predictive genetic testing in maturity-onset diabetes of the young (MODY)M Shepherd, I Ellis, A M Ahmad, et al.
Gynecologic Oncology|May 16, 2013
Phase II study of temsirolimus (CCI-779) in women with recurrent, unresectable, locally advanced or metastatic carcinoma of the cervix. A trial of the NCIC Clinical Trials Group (NCIC CTG IND 199)A V Tinker, S Ellard, S Welch, et al.
Diabetologia|March 13, 2008
A Kir6.2 mutation causing severe functional effects in vitro produces neonatal diabetes without the expected neurological complicationsP Tammaro, S E Flanagan, B Zadek, et al.
Pageof 15

Showing results (91-100 of 144) with videos related to

Sort By:
Pageof 15
Diabetic Medicine : a Journal of the British Diabetic Association|June 16, 2010
Novel monogenic diabetes mutations in the P2 promoter of the HNF4A gene are associated with impaired function in vitroA Wirsing, K A Johnstone, L W Harries, et al.
Human Mutation|October 1, 2003
Identification of 21 novel glucokinase (GCK) mutations in UK and European Caucasians with maturity-onset diabetes of the young (MODY)K L Thomson, A L Gloyn, K Colclough, et al.
Diabetic Medicine : a Journal of the British Diabetic Association|October 20, 2015
Successful maintenance on sulphonylurea therapy and low diabetes complication rates in a HNF1A-MODY cohortS Bacon, M P Kyithar, S R Rizvi, et al.
Annals of Oncology : Official Journal of the European Society for Medical Oncology|November 17, 2007
Survival outcome and cost-effectiveness with docetaxel and paclitaxel in patients with metastatic breast cancer: a population-based evaluationT Vu, S Ellard, C H Speers, et al.
Diabetologia|April 11, 2002
Complete glucokinase deficiency is not a common cause of permanent neonatal diabetesA L Gloyn, S Ellard, J P Shield, et al.
Neurology|July 27, 2007
A novel mutation causing DEND syndrome: a treatable channelopathy of pancreas and brainK Shimomura, F Hörster, H de Wet, et al.
Endocrinology, Diabetes & Metabolism Case Reports|March 12, 2014
Paternally inherited ABCC8 mutation causing diffuse congenital hyperinsulinismSuresh Chandran, Fabian Yap Kok Peng, Victor Samuel Rajadurai, et al.
Diabetic Medicine : a Journal of the British Diabetic Association|July 27, 2001
Predictive genetic testing in maturity-onset diabetes of the young (MODY)M Shepherd, I Ellis, A M Ahmad, et al.
Gynecologic Oncology|May 16, 2013
Phase II study of temsirolimus (CCI-779) in women with recurrent, unresectable, locally advanced or metastatic carcinoma of the cervix. A trial of the NCIC Clinical Trials Group (NCIC CTG IND 199)A V Tinker, S Ellard, S Welch, et al.
Diabetologia|March 13, 2008
A Kir6.2 mutation causing severe functional effects in vitro produces neonatal diabetes without the expected neurological complicationsP Tammaro, S E Flanagan, B Zadek, et al.
Pageof 15