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Annals of Internal Medicine
|
May 1, 2001
Maternally inherited diabetes and deafness: a multicenter study
P 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.
Diabetes & Metabolism
|
November 28, 2017
Practical implementation, education and interpretation guidelines for continuous glucose monitoring: A French position statement
S Borot, P Y Benhamou, C Atlan, 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 study
P Massin, D Dubois-Laforgue, T Meas, et al.
Diabetes & Metabolism
|
November 5, 2020
Practical implementation of automated closed-loop insulin delivery: A French position statement
N Tubiana-Rufi, P Schaepelynck, S Franc, et al.
Diabetes & Metabolism
|
March 12, 2025
Practical implementation of automated insulin delivery systems in 2025: A French position statement update
E Bismuth, M Joubert, E Renard, 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 leukocytes
M Laloi-Michelin, T Meas, C Ambonville, et al.
Diabetologia
|
November 20, 2012
Exome sequencing-driven discovery of coding polymorphisms associated with common metabolic phenotypes
A Albrechtsen, N Grarup, Y Li, et al.
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of 11
Search research articles
Search
Showing results (101-110 of 108) with videos related to
Sort By:
Page
of 11
You have reached the last page of results.
This site can display upto 108 results.
Annals of Internal Medicine
|
May 1, 2001
Maternally inherited diabetes and deafness: a multicenter study
P 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.
Diabetes & Metabolism
|
November 28, 2017
Practical implementation, education and interpretation guidelines for continuous glucose monitoring: A French position statement
S Borot, P Y Benhamou, C Atlan, 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 study
P Massin, D Dubois-Laforgue, T Meas, et al.
Diabetes & Metabolism
|
November 5, 2020
Practical implementation of automated closed-loop insulin delivery: A French position statement
N Tubiana-Rufi, P Schaepelynck, S Franc, et al.
Diabetes & Metabolism
|
March 12, 2025
Practical implementation of automated insulin delivery systems in 2025: A French position statement update
E Bismuth, M Joubert, E Renard, 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 leukocytes
M Laloi-Michelin, T Meas, C Ambonville, et al.
Diabetologia
|
November 20, 2012
Exome sequencing-driven discovery of coding polymorphisms associated with common metabolic phenotypes
A Albrechtsen, N Grarup, Y Li, et al.
Page
of 11