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Diabetes & Metabolism
|
February 15, 2001
[Considerations on delocalized HbA1c assays]
M Bordas-Fonfrède, J Sélam, J Goudable, et al.
European Journal of Clinical Nutrition
|
May 21, 2010
Specific adipocytokines profiles in patients with hyperactive and/or binge/purge form of anorexia nervosa
J-P Nogueira, M Maraninchi, A-M Lorec, et al.
The Journal of Clinical Endocrinology and Metabolism
|
January 27, 1999
Influence of obesity and body fat distribution on postprandial lipemia and triglyceride-rich lipoproteins in adult women
N Mekki, M A Christofilis, M Charbonnier, et al.
Diabetologia
|
July 1, 1990
Autoantibodies to the insulin receptor are infrequent findings in type 1 (insulin-dependent) diabetes mellitus of recent onset
N Rochet, J L Sadoul, B Ferrua, et al.
American Journal of Medical Genetics. Part A
|
June 15, 2007
Identification of novel mutations in WFS1 and genotype-phenotype correlation in Wolfram syndrome
A Cano, C Rouzier, S Monnot, et al.
Diabetes & Metabolism
|
September 28, 1999
HBA1c: clinical and biological agreement for standardization of assay methods. Report by the experts of ALFEDIAM (Association de Langue Française pour lEtude du Diabète et des Maladies Métabolique) and SFBC (Société Française de Biologie Clinique)
P Gillery, M Bordas-Fonfrède, J P Chapelle, et al.
Ophthalmology
|
September 15, 1999
Prevalence of macular pattern dystrophy in maternally inherited diabetes and deafness. GEDIAM Group
P Massin, M Virally-Monod, B Vialettes, et al.
Diabetes Care
|
July 1, 1995
Extra-pancreatic manifestations in diabetes secondary to mitochondrial DNA point mutation within the tRNALeu(UUR) gene
B Vialettes, V Paquis-Fluckinger, P Silvestre-Aillaud, et al.
Annales De Biologie Clinique
|
August 10, 2000
[Hemoglobin A1C determination and hemoglobinopathies: problems and strategies]
P Gillery, G Hue, M Bordas-Fonfrède, et al.
Biochimica Et Biophysica Acta
|
October 24, 2002
Molecular and functional effects of the T14709C point mutation in the mitochondrial DNA of a patient with maternally inherited diabetes and deafness
D Perucca-Lostanlen, R W Taylor, H Narbonne, et al.
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Search research articles
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Showing results (161-170 of 178) with videos related to
Sort By:
Page
of 18
Diabetes & Metabolism
|
February 15, 2001
[Considerations on delocalized HbA1c assays]
M Bordas-Fonfrède, J Sélam, J Goudable, et al.
European Journal of Clinical Nutrition
|
May 21, 2010
Specific adipocytokines profiles in patients with hyperactive and/or binge/purge form of anorexia nervosa
J-P Nogueira, M Maraninchi, A-M Lorec, et al.
The Journal of Clinical Endocrinology and Metabolism
|
January 27, 1999
Influence of obesity and body fat distribution on postprandial lipemia and triglyceride-rich lipoproteins in adult women
N Mekki, M A Christofilis, M Charbonnier, et al.
Diabetologia
|
July 1, 1990
Autoantibodies to the insulin receptor are infrequent findings in type 1 (insulin-dependent) diabetes mellitus of recent onset
N Rochet, J L Sadoul, B Ferrua, et al.
American Journal of Medical Genetics. Part A
|
June 15, 2007
Identification of novel mutations in WFS1 and genotype-phenotype correlation in Wolfram syndrome
A Cano, C Rouzier, S Monnot, et al.
Diabetes & Metabolism
|
September 28, 1999
HBA1c: clinical and biological agreement for standardization of assay methods. Report by the experts of ALFEDIAM (Association de Langue Française pour lEtude du Diabète et des Maladies Métabolique) and SFBC (Société Française de Biologie Clinique)
P Gillery, M Bordas-Fonfrède, J P Chapelle, et al.
Ophthalmology
|
September 15, 1999
Prevalence of macular pattern dystrophy in maternally inherited diabetes and deafness. GEDIAM Group
P Massin, M Virally-Monod, B Vialettes, et al.
Diabetes Care
|
July 1, 1995
Extra-pancreatic manifestations in diabetes secondary to mitochondrial DNA point mutation within the tRNALeu(UUR) gene
B Vialettes, V Paquis-Fluckinger, P Silvestre-Aillaud, et al.
Annales De Biologie Clinique
|
August 10, 2000
[Hemoglobin A1C determination and hemoglobinopathies: problems and strategies]
P Gillery, G Hue, M Bordas-Fonfrède, et al.
Biochimica Et Biophysica Acta
|
October 24, 2002
Molecular and functional effects of the T14709C point mutation in the mitochondrial DNA of a patient with maternally inherited diabetes and deafness
D Perucca-Lostanlen, R W Taylor, H Narbonne, et al.
Page
of 18