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Showing results (171-180 of 178) with videos related to

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Clinical Genetics|June 4, 2014
Mutation update and uncommon phenotypes in a French cohort of 96 patients with WFS1-related disordersA Chaussenot, C Rouzier, M Quere, et al.
Nature Genetics|June 1, 1997
Multilocus linkage of familial hyperkalaemia and hypertension, pseudohypoaldosteronism type II, to chromosomes 1q31-42 and 17p11-q21T A Mansfield, D B Simon, Z Farfel, et al.
Diabetes & Metabolism|June 17, 2008
Aggressive multimodal therapy of sporadic malignant insulinoma can improve survival: a retrospective 35-year study of 12 patientsA Bégu-Le Corroller, R Valéro, V Moutardier, et al.
Diabetes Research and Clinical Practice|June 7, 2005
Glucose evaluation trial for remission (GETREM) in type 1 diabetes: a European multicentre studyP Pozzilli, S Manfrini, R Buzzetti, 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 18

Showing results (171-180 of 178) with videos related to

Sort By:
Pageof 18
You have reached the last page of results.This site can display upto 178 results.
Clinical Genetics|June 4, 2014
Mutation update and uncommon phenotypes in a French cohort of 96 patients with WFS1-related disordersA Chaussenot, C Rouzier, M Quere, et al.
Nature Genetics|June 1, 1997
Multilocus linkage of familial hyperkalaemia and hypertension, pseudohypoaldosteronism type II, to chromosomes 1q31-42 and 17p11-q21T A Mansfield, D B Simon, Z Farfel, et al.
Diabetes & Metabolism|June 17, 2008
Aggressive multimodal therapy of sporadic malignant insulinoma can improve survival: a retrospective 35-year study of 12 patientsA Bégu-Le Corroller, R Valéro, V Moutardier, et al.
Diabetes Research and Clinical Practice|June 7, 2005
Glucose evaluation trial for remission (GETREM) in type 1 diabetes: a European multicentre studyP Pozzilli, S Manfrini, R Buzzetti, 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 18