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Diabetic Medicine : a Journal of the British Diabetic Association
|
December 1, 1995
Symptoms, hormones, and glucose fluxes during a gradual hypoglycaemia induced by intraperitoneal vs venous insulin infusion in Type I diabetes
J L Selam, R Medlej, J M'bemba, et al.
Annales D'Endocrinologie
|
January 1, 1991
[Physiopathology of androgen insensitivity syndromes. Contribution of molecular biology]
C Sultan, J M Lobaccaro, R Defay, et al.
The Journal of Clinical Endocrinology and Metabolism
|
April 9, 2004
Diabetes mellitus and optic atrophy: a study of Wolfram syndrome in the Lebanese population
R Medlej, J Wasson, P Baz, et al.
The Journal of Clinical Endocrinology and Metabolism
|
January 1, 1997
Heterogeneity in clinical manifestation of autosomal dominant neurohypophyseal diabetes insipidus caused by a mutation encoding Ala-1-->Val in the signal peptide of the arginine vasopressin/neurophysin II/copeptin precursor
D R Repaske, R Medlej, E K Gültekin, et al.
Journal of Endocrinological Investigation
|
May 5, 2009
Predictors of intra-operative parathyroid hormone decline in subjects operated for primary hyperparathyroidism by minimally invasive parathyroidectomy
M-H Gannagé-Yared, B Abboud, M Amm-Azar, et al.
Journal of Community Genetics
|
March 7, 2012
Genetics of autoimmune thyroid disease in the Lebanese population
C Farra, J Awwad, A Fadlallah, et al.
The Journal of Clinical Endocrinology and Metabolism
|
November 1, 1992
Screening for Y-derived sex determining gene SRY in 40 patients with Turner syndrome
R Medlej, J M Lobaccaro, P Berta, et al.
International Journal of Clinical Practice
|
September 5, 2013
The effect of vildagliptin relative to sulphonylureas in Muslim patients with type 2 diabetes fasting during Ramadan: the VIRTUE study
M Al-Arouj, A A K Hassoun, R Medlej, et al.
Clinical Endocrinology
|
February 1, 1993
PCR analysis and sequencing of the SRY sex determining gene in four patients with bilateral congenital anorchia
J M Lobaccaro, R Medlej, P Berta, et al.
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of 2
Search research articles
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Showing results (11-20 of 19) with videos related to
Sort By:
Page
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You have reached the last page of results.
This site can display upto 19 results.
Diabetic Medicine : a Journal of the British Diabetic Association
|
December 1, 1995
Symptoms, hormones, and glucose fluxes during a gradual hypoglycaemia induced by intraperitoneal vs venous insulin infusion in Type I diabetes
J L Selam, R Medlej, J M'bemba, et al.
Annales D'Endocrinologie
|
January 1, 1991
[Physiopathology of androgen insensitivity syndromes. Contribution of molecular biology]
C Sultan, J M Lobaccaro, R Defay, et al.
The Journal of Clinical Endocrinology and Metabolism
|
April 9, 2004
Diabetes mellitus and optic atrophy: a study of Wolfram syndrome in the Lebanese population
R Medlej, J Wasson, P Baz, et al.
The Journal of Clinical Endocrinology and Metabolism
|
January 1, 1997
Heterogeneity in clinical manifestation of autosomal dominant neurohypophyseal diabetes insipidus caused by a mutation encoding Ala-1-->Val in the signal peptide of the arginine vasopressin/neurophysin II/copeptin precursor
D R Repaske, R Medlej, E K Gültekin, et al.
Journal of Endocrinological Investigation
|
May 5, 2009
Predictors of intra-operative parathyroid hormone decline in subjects operated for primary hyperparathyroidism by minimally invasive parathyroidectomy
M-H Gannagé-Yared, B Abboud, M Amm-Azar, et al.
Journal of Community Genetics
|
March 7, 2012
Genetics of autoimmune thyroid disease in the Lebanese population
C Farra, J Awwad, A Fadlallah, et al.
The Journal of Clinical Endocrinology and Metabolism
|
November 1, 1992
Screening for Y-derived sex determining gene SRY in 40 patients with Turner syndrome
R Medlej, J M Lobaccaro, P Berta, et al.
International Journal of Clinical Practice
|
September 5, 2013
The effect of vildagliptin relative to sulphonylureas in Muslim patients with type 2 diabetes fasting during Ramadan: the VIRTUE study
M Al-Arouj, A A K Hassoun, R Medlej, et al.
Clinical Endocrinology
|
February 1, 1993
PCR analysis and sequencing of the SRY sex determining gene in four patients with bilateral congenital anorchia
J M Lobaccaro, R Medlej, P Berta, et al.
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of 2