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

J Cahen

Showing results (11-20 of 16) with videos related to

Pageof 2
Sort By:
You have reached the last page of results.This site can display upto 16 results.
Kidney International|October 24, 2000
Focal segmental glomerulosclerosis associated with mitochondrial cytopathyL M Doleris, G S Hill, P Chedin, et al.
Diabetes, Obesity & Metabolism|November 21, 2015
One-year metreleptin improves insulin secretion in patients with diabetes linked to genetic lipodystrophic syndromesC Vatier, S Fetita, P Boudou, et al.
Annals of Internal Medicine|May 1, 2001
Maternally inherited diabetes and deafness: a multicenter studyP J Guillausseau, P Massin, D Dubois-LaForgue, et al.
Diabetes & Metabolism|June 30, 2004
Heterogeneity of diabetes phenotype in patients with 3243 bp mutation of mitochondrial DNA (Maternally Inherited Diabetes and Deafness or MIDD)P J Guillausseau, D Dubois-Laforgue, P Massin, et al.
Diabetologia|June 27, 2008
Retinal and renal complications in patients with a mutation of mitochondrial DNA at position 3,243 (maternally inherited diabetes and deafness). A case-control studyP Massin, D Dubois-Laforgue, T Meas, et al.
The Journal of Clinical Endocrinology and Metabolism|May 28, 2009
The clinical variability of maternally inherited diabetes and deafness is associated with the degree of heteroplasmy in blood leukocytesM Laloi-Michelin, T Meas, C Ambonville, et al.
Pageof 2

Showing results (11-20 of 16) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 16 results.
Kidney International|October 24, 2000
Focal segmental glomerulosclerosis associated with mitochondrial cytopathyL M Doleris, G S Hill, P Chedin, et al.
Diabetes, Obesity & Metabolism|November 21, 2015
One-year metreleptin improves insulin secretion in patients with diabetes linked to genetic lipodystrophic syndromesC Vatier, S Fetita, P Boudou, et al.
Annals of Internal Medicine|May 1, 2001
Maternally inherited diabetes and deafness: a multicenter studyP J Guillausseau, P Massin, D Dubois-LaForgue, et al.
Diabetes & Metabolism|June 30, 2004
Heterogeneity of diabetes phenotype in patients with 3243 bp mutation of mitochondrial DNA (Maternally Inherited Diabetes and Deafness or MIDD)P J Guillausseau, D Dubois-Laforgue, P Massin, et al.
Diabetologia|June 27, 2008
Retinal and renal complications in patients with a mutation of mitochondrial DNA at position 3,243 (maternally inherited diabetes and deafness). A case-control studyP Massin, D Dubois-Laforgue, T Meas, et al.
The Journal of Clinical Endocrinology and Metabolism|May 28, 2009
The clinical variability of maternally inherited diabetes and deafness is associated with the degree of heteroplasmy in blood leukocytesM Laloi-Michelin, T Meas, C Ambonville, et al.
Pageof 2