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Showing results (191-200 of 201) with videos related to

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Ophthalmology|September 15, 1999
Prevalence of macular pattern dystrophy in maternally inherited diabetes and deafness. GEDIAM GroupP Massin, M Virally-Monod, B Vialettes, et al.
Frontiers in Microbiology|February 14, 2018
Corrigendum: Characterization of Metagenomes in Urban Aquatic Compartments Reveals High Prevalence of Clinically Relevant Antibiotic Resistance Genes in WastewatersCharmaine Ng, Martin Tay, Boonfei Tan, et al.
JIMD Reports|February 23, 2013
Sight-threatening phenylketonuric encephalopathy in a young adult, reversed by dietS Rubin, A L Le Piffer, M B Rougier, et al.
Diabetes & Metabolism|August 19, 2007
Microalbuminuria and urinary albumin excretion: French clinical practice guidelinesJ-M Halimi, S Hadjadj, V Aboyans, et al.
Applied and Environmental Microbiology|November 23, 2014
Alternative fecal indicators and their empirical relationships with enteric viruses, Salmonella enterica, and Pseudomonas aeruginosa in surface waters of a tropical urban catchmentL Liang, S G Goh, G G R V Vergara, et al.
Annales De Biologie Clinique|June 19, 2008
[Microalbuminuria and urinary albumin excretion: French guidelines]J M Halimi, S Hadjadj, V Aboyans, et al.
Diabetes & Metabolism|November 18, 2006
Continuous intraperitoneal insulin infusion does not increase the risk of organ-specific autoimmune disease in type 1 diabetic patients: results of a multicentric, comparative studyL Dufaitre-Patouraux, J P Riveline, E Renard, 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 21

Showing results (191-200 of 201) with videos related to

Sort By:
Pageof 21
Ophthalmology|September 15, 1999
Prevalence of macular pattern dystrophy in maternally inherited diabetes and deafness. GEDIAM GroupP Massin, M Virally-Monod, B Vialettes, et al.
Frontiers in Microbiology|February 14, 2018
Corrigendum: Characterization of Metagenomes in Urban Aquatic Compartments Reveals High Prevalence of Clinically Relevant Antibiotic Resistance Genes in WastewatersCharmaine Ng, Martin Tay, Boonfei Tan, et al.
JIMD Reports|February 23, 2013
Sight-threatening phenylketonuric encephalopathy in a young adult, reversed by dietS Rubin, A L Le Piffer, M B Rougier, et al.
Diabetes & Metabolism|August 19, 2007
Microalbuminuria and urinary albumin excretion: French clinical practice guidelinesJ-M Halimi, S Hadjadj, V Aboyans, et al.
Applied and Environmental Microbiology|November 23, 2014
Alternative fecal indicators and their empirical relationships with enteric viruses, Salmonella enterica, and Pseudomonas aeruginosa in surface waters of a tropical urban catchmentL Liang, S G Goh, G G R V Vergara, et al.
Annales De Biologie Clinique|June 19, 2008
[Microalbuminuria and urinary albumin excretion: French guidelines]J M Halimi, S Hadjadj, V Aboyans, et al.
Diabetes & Metabolism|November 18, 2006
Continuous intraperitoneal insulin infusion does not increase the risk of organ-specific autoimmune disease in type 1 diabetic patients: results of a multicentric, comparative studyL Dufaitre-Patouraux, J P Riveline, E Renard, 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 21