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Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology
|
December 14, 2007
EEG spectral power and sleepiness during 24 h of sustained wakefulness in patients with obstructive sleep apnea syndrome
J Grenèche, J Krieger, C Erhardt, et al.
Nutrition, Metabolism, and Cardiovascular Diseases : NMCD
|
May 24, 2016
Interaction between GPR120 p.R270H loss-of-function variant and dietary fat intake on incident type 2 diabetes risk in the D.E.S.I.R. study
A Lamri, A Bonnefond, D Meyre, et al.
Accident; Analysis and Prevention
|
July 9, 2008
Are OSAS patients impaired in their driving ability on a circuit with medium traffic density?
P Tassi, J Grenèche, T Pebayle, et al.
La Presse Medicale
|
August 1, 1971
[Presence of serum alpha 1-fetoprotein in 4 cases of primary digestive neoplasms other than hepatoma]
P Bernades, M Smadja, B Rueff, et al.
La Revue De Medecine Interne
|
June 1, 1985
[Maintenance therapy of ulcer disease. Comparative multicenter study of sucralfate, cimetidine and a placebo]
F Jean, A Bonnefond, J Gislon, et al.
La Presse Medicale
|
August 4, 1971
[Presence of serum alpha fetoprotein in 4 cases of primary digestive cancers other than hepatomas]
P Bernades, M Smadja, B Rueff, et al.
International Journal of Obesity (2005)
|
June 4, 2014
A nonsense loss-of-function mutation in PCSK1 contributes to dominantly inherited human obesity
J Philippe, P Stijnen, D Meyre, et al.
Diabetologia
|
February 25, 2009
Mutations in G6PC2 do not contribute to monogenic forms of early infancy diabetes and beta cell dysfunction
A Bonnefond, N Bouatia-Naji, A Simon, et al.
International Journal of Obesity (2005)
|
October 24, 2012
Contribution of 24 obesity-associated genetic variants to insulin resistance, pancreatic beta-cell function and type 2 diabetes risk in the French population
S Robiou-du-Pont, A Bonnefond, L Yengo, et al.
Diabetes & Metabolism
|
April 9, 2013
Transcription factor gene MNX1 is a novel cause of permanent neonatal diabetes in a consanguineous family
A Bonnefond, E Vaillant, J Philippe, et al.
Page
of 4
Search research articles
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Showing results (21-30 of 35) with videos related to
Sort By:
Page
of 4
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology
|
December 14, 2007
EEG spectral power and sleepiness during 24 h of sustained wakefulness in patients with obstructive sleep apnea syndrome
J Grenèche, J Krieger, C Erhardt, et al.
Nutrition, Metabolism, and Cardiovascular Diseases : NMCD
|
May 24, 2016
Interaction between GPR120 p.R270H loss-of-function variant and dietary fat intake on incident type 2 diabetes risk in the D.E.S.I.R. study
A Lamri, A Bonnefond, D Meyre, et al.
Accident; Analysis and Prevention
|
July 9, 2008
Are OSAS patients impaired in their driving ability on a circuit with medium traffic density?
P Tassi, J Grenèche, T Pebayle, et al.
La Presse Medicale
|
August 1, 1971
[Presence of serum alpha 1-fetoprotein in 4 cases of primary digestive neoplasms other than hepatoma]
P Bernades, M Smadja, B Rueff, et al.
La Revue De Medecine Interne
|
June 1, 1985
[Maintenance therapy of ulcer disease. Comparative multicenter study of sucralfate, cimetidine and a placebo]
F Jean, A Bonnefond, J Gislon, et al.
La Presse Medicale
|
August 4, 1971
[Presence of serum alpha fetoprotein in 4 cases of primary digestive cancers other than hepatomas]
P Bernades, M Smadja, B Rueff, et al.
International Journal of Obesity (2005)
|
June 4, 2014
A nonsense loss-of-function mutation in PCSK1 contributes to dominantly inherited human obesity
J Philippe, P Stijnen, D Meyre, et al.
Diabetologia
|
February 25, 2009
Mutations in G6PC2 do not contribute to monogenic forms of early infancy diabetes and beta cell dysfunction
A Bonnefond, N Bouatia-Naji, A Simon, et al.
International Journal of Obesity (2005)
|
October 24, 2012
Contribution of 24 obesity-associated genetic variants to insulin resistance, pancreatic beta-cell function and type 2 diabetes risk in the French population
S Robiou-du-Pont, A Bonnefond, L Yengo, et al.
Diabetes & Metabolism
|
April 9, 2013
Transcription factor gene MNX1 is a novel cause of permanent neonatal diabetes in a consanguineous family
A Bonnefond, E Vaillant, J Philippe, et al.
Page
of 4