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J Cahen-Varsaux

Showing results (1-10 of 8) with videos related to

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BMJ (Clinical Research Ed.)|July 23, 1994
Integrated care for diabetesP Chedin, J Cahen-Varsaux
Annals of Internal Medicine|September 15, 1996
Non-insulin-dependent diabetes mellitus developing during interferon-alpha therapy for chronic hepatitis CP Chedin, J Cahen-Varsaux, N Boyer
Gastroenterologie Clinique Et Biologique|April 1, 1995
[Dysthyroidism and interferon-alpha: the withdrawal of interferon should not be systematic]P Chédin, J Cahen-Varsaux, S Demmane
Diabetes Research (Edinburgh, Scotland)|March 1, 1988
Creatinine clearance evaluation in routine diabetes practiceP J Guillausseau, A Fontbonne, J Cahen-Varsaux, et al.
Kidney International|October 24, 2000
Focal segmental glomerulosclerosis associated with mitochondrial cytopathyL M Doleris, G S Hill, P Chedin, 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 1

Showing results (1-10 of 8) with videos related to

Sort By:
Pageof 1
BMJ (Clinical Research Ed.)|July 23, 1994
Integrated care for diabetesP Chedin, J Cahen-Varsaux
Annals of Internal Medicine|September 15, 1996
Non-insulin-dependent diabetes mellitus developing during interferon-alpha therapy for chronic hepatitis CP Chedin, J Cahen-Varsaux, N Boyer
Gastroenterologie Clinique Et Biologique|April 1, 1995
[Dysthyroidism and interferon-alpha: the withdrawal of interferon should not be systematic]P Chédin, J Cahen-Varsaux, S Demmane
Diabetes Research (Edinburgh, Scotland)|March 1, 1988
Creatinine clearance evaluation in routine diabetes practiceP J Guillausseau, A Fontbonne, J Cahen-Varsaux, et al.
Kidney International|October 24, 2000
Focal segmental glomerulosclerosis associated with mitochondrial cytopathyL M Doleris, G S Hill, P Chedin, 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 1