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P Massin

Showing results (211-220 of 221) with videos related to

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Diabetes & Metabolism|June 1, 1996
[Detection, monitoring and treatment of diabetic retinopathy. Recommendations of ALFEDIAM. Committee of above-mentioned experts and validated by the board of directors and scientific board of ALFEDIAM]P Massin, K Angioi-Duprez, F Bacin, et al.
Journal Francais D'Ophtalmologie|March 10, 2001
[Central serous chorioretinopathy and systemic steroid therapy]G Chaine, M Haouat, C Menard-Molcard, et al.
Diabetes & Metabolism|June 17, 2005
Evaluation of a screening program for diabetic retinopathy in a primary care setting Dodia (Dépistage ophtalmologique du diabète) studyP Massin, J P Aubert, E Eschwege, et al.
Diabetes & Metabolism|January 27, 2005
Screening for diabetic retinopathy: the first telemedical approach in a primary care setting in FranceP Massin, J-P Aubert, A Erginay, et al.
Neurology|January 15, 2003
Hereditary infantile hemiparesis, retinal arteriolar tortuosity, and leukoencephalopathyK Vahedi, P Massin, J-P Guichard, et al.
Diabetes & Metabolism|April 8, 2009
Benefits of Ophdiat, a telemedical network to screen for diabetic retinopathy: a retrospective study in five reference hospital centresA Chabouis, M Berdugo, T Meas, et al.
Infection, Genetics and Evolution : Journal of Molecular Epidemiology and Evolutionary Genetics in Infectious Diseases|April 13, 2018
Emergence and multiple reassortments of French 2015-2016 highly pathogenic H5 avian influenza virusesF X Briand, E Niqueux, A Schmitz, 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.
Pageof 23

Showing results (211-220 of 221) with videos related to

Sort By:
Pageof 23
Diabetes & Metabolism|June 1, 1996
[Detection, monitoring and treatment of diabetic retinopathy. Recommendations of ALFEDIAM. Committee of above-mentioned experts and validated by the board of directors and scientific board of ALFEDIAM]P Massin, K Angioi-Duprez, F Bacin, et al.
Journal Francais D'Ophtalmologie|March 10, 2001
[Central serous chorioretinopathy and systemic steroid therapy]G Chaine, M Haouat, C Menard-Molcard, et al.
Diabetes & Metabolism|June 17, 2005
Evaluation of a screening program for diabetic retinopathy in a primary care setting Dodia (Dépistage ophtalmologique du diabète) studyP Massin, J P Aubert, E Eschwege, et al.
Diabetes & Metabolism|January 27, 2005
Screening for diabetic retinopathy: the first telemedical approach in a primary care setting in FranceP Massin, J-P Aubert, A Erginay, et al.
Neurology|January 15, 2003
Hereditary infantile hemiparesis, retinal arteriolar tortuosity, and leukoencephalopathyK Vahedi, P Massin, J-P Guichard, et al.
Diabetes & Metabolism|April 8, 2009
Benefits of Ophdiat, a telemedical network to screen for diabetic retinopathy: a retrospective study in five reference hospital centresA Chabouis, M Berdugo, T Meas, et al.
Infection, Genetics and Evolution : Journal of Molecular Epidemiology and Evolutionary Genetics in Infectious Diseases|April 13, 2018
Emergence and multiple reassortments of French 2015-2016 highly pathogenic H5 avian influenza virusesF X Briand, E Niqueux, A Schmitz, 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.
Pageof 23