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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 tolerance
Y Morel, A Golay, T Perneger, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)
|
October 28, 1998
Contrast sensitivity in obese dyslipidemic patients with insulin resistance
A 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 SRD5A2
J 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 deficiency
J Simard, E Rheaume, F Mebarki, et al.
Thorax
|
November 3, 2005
Late CF caused by homozygous IVS8-5T CFTR polymorphism
V 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 children
E 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 patients
A 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 deficiency
R Menassa, V Tardy, F Despert, et al.
Page
of 14
Search research articles
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Showing results (81-90 of 138) with videos related to
Sort By:
Page
of 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 tolerance
Y Morel, A Golay, T Perneger, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)
|
October 28, 1998
Contrast sensitivity in obese dyslipidemic patients with insulin resistance
A 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 SRD5A2
J 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 deficiency
J Simard, E Rheaume, F Mebarki, et al.
Thorax
|
November 3, 2005
Late CF caused by homozygous IVS8-5T CFTR polymorphism
V 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 children
E 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 patients
A 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 deficiency
R Menassa, V Tardy, F Despert, et al.
Page
of 14