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Y Morel

Showing results (81-90 of 138) with videos related to

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Diabetic Medicine : a Journal of the British Diabetic Association|September 7, 1999
Metformin treatment leads to an increase in basal, but not insulin-stimulated, glucose disposal in obese patients with impaired glucose toleranceY Morel, A Golay, T Perneger, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|October 28, 1998
Contrast sensitivity in obese dyslipidemic patients with insulin resistanceA A Dosso, F Yenice-Ustun, J Sommerhalder, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|October 16, 2012
[Four cases of aldosterone synthase deficiency in childhood]E Collinet, P Pelissier, O Richard, et al.
Annales D'Endocrinologie|August 13, 2011
REMOVAL: Pelvic MRI in a 17-year-old XY girl with 5-alpha reductase deficiency and a homozygous Gly115Asp mutation in SRD5A2J Sarfati, S Trabado, L Rocher, et al.
The Journal of Steroid Biochemistry and Molecular Biology|June 1, 1995
Molecular basis of human 3 beta-hydroxysteroid dehydrogenase deficiencyJ Simard, E Rheaume, F Mebarki, et al.
Thorax|November 3, 2005
Late CF caused by homozygous IVS8-5T CFTR polymorphismV Cottin, Y Thibout, F Bey-Omar, et al.
La Revue De Medecine Interne|January 1, 1993
[Is male infertility caused by congenital bilateral atrophy of the vas deferens a clinical form of mucoviscidosis?]I Durieu, F B Omar, J Rollet, et al.
Acta Endocrinologica. Supplementum|January 1, 1986
Usefulness of plasma pregnenolone sulfate in testing pituitary-adrenal function in childrenE de Peretti, M G Forest, B Loras, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|May 1, 1996
Risk factors associated with contrast sensitivity loss in diabetic patientsA A Dosso, E R Bonvin, Y Morel, et al.
The Journal of Clinical Endocrinology and Metabolism|March 6, 2008
p.H62L, a rare mutation of the CYP21 gene identified in two forms of 21-hydroxylase deficiencyR Menassa, V Tardy, F Despert, et al.
Pageof 14

Showing results (81-90 of 138) with videos related to

Sort By:
Pageof 14
Diabetic Medicine : a Journal of the British Diabetic Association|September 7, 1999
Metformin treatment leads to an increase in basal, but not insulin-stimulated, glucose disposal in obese patients with impaired glucose toleranceY Morel, A Golay, T Perneger, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|October 28, 1998
Contrast sensitivity in obese dyslipidemic patients with insulin resistanceA A Dosso, F Yenice-Ustun, J Sommerhalder, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|October 16, 2012
[Four cases of aldosterone synthase deficiency in childhood]E Collinet, P Pelissier, O Richard, et al.
Annales D'Endocrinologie|August 13, 2011
REMOVAL: Pelvic MRI in a 17-year-old XY girl with 5-alpha reductase deficiency and a homozygous Gly115Asp mutation in SRD5A2J Sarfati, S Trabado, L Rocher, et al.
The Journal of Steroid Biochemistry and Molecular Biology|June 1, 1995
Molecular basis of human 3 beta-hydroxysteroid dehydrogenase deficiencyJ Simard, E Rheaume, F Mebarki, et al.
Thorax|November 3, 2005
Late CF caused by homozygous IVS8-5T CFTR polymorphismV Cottin, Y Thibout, F Bey-Omar, et al.
La Revue De Medecine Interne|January 1, 1993
[Is male infertility caused by congenital bilateral atrophy of the vas deferens a clinical form of mucoviscidosis?]I Durieu, F B Omar, J Rollet, et al.
Acta Endocrinologica. Supplementum|January 1, 1986
Usefulness of plasma pregnenolone sulfate in testing pituitary-adrenal function in childrenE de Peretti, M G Forest, B Loras, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|May 1, 1996
Risk factors associated with contrast sensitivity loss in diabetic patientsA A Dosso, E R Bonvin, Y Morel, et al.
The Journal of Clinical Endocrinology and Metabolism|March 6, 2008
p.H62L, a rare mutation of the CYP21 gene identified in two forms of 21-hydroxylase deficiencyR Menassa, V Tardy, F Despert, et al.
Pageof 14