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BMJ (Clinical Research Ed.)
|
July 23, 1994
Integrated care for diabetes
P Chedin, J Cahen-Varsaux
Annals of Internal Medicine
|
September 15, 1996
Non-insulin-dependent diabetes mellitus developing during interferon-alpha therapy for chronic hepatitis C
P 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 practice
P J Guillausseau, A Fontbonne, J Cahen-Varsaux, et al.
Kidney International
|
October 24, 2000
Focal segmental glomerulosclerosis associated with mitochondrial cytopathy
L 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 study
P 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 leukocytes
M Laloi-Michelin, T Meas, C Ambonville, et al.
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of 1
Search research articles
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Showing results (1-10 of 8) with videos related to
Sort By:
Page
of 1
BMJ (Clinical Research Ed.)
|
July 23, 1994
Integrated care for diabetes
P Chedin, J Cahen-Varsaux
Annals of Internal Medicine
|
September 15, 1996
Non-insulin-dependent diabetes mellitus developing during interferon-alpha therapy for chronic hepatitis C
P 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 practice
P J Guillausseau, A Fontbonne, J Cahen-Varsaux, et al.
Kidney International
|
October 24, 2000
Focal segmental glomerulosclerosis associated with mitochondrial cytopathy
L 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 study
P 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 leukocytes
M Laloi-Michelin, T Meas, C Ambonville, et al.
Page
of 1