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Y Morel

Showing results (41-50 of 138) with videos related to

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Journal of Cardiovascular Pharmacology|August 1, 1995
Insulin sensitivity in obese hypertensive dyslipidemic patients treated with enalapril or atenololY Morel, A Gadient, U Keller, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 1, 1989
Transcript encoded on the opposite strand of the human steroid 21-hydroxylase/complement component C4 gene locusY Morel, J Bristow, S E Gitelman, et al.
Gastroenterologie Clinique Et Biologique|January 1, 1994
[Mucoviscidosis in adult age in 1994]I Durieu, L Calemar, G Bellon, et al.
Annales D'Endocrinologie|July 1, 2005
21-Hydroxylase deficiency: an exemplary model of the contribution of molecular biology in the understanding and management of the diseaseM G Forest, V Tardy, M Nicolino, et al.
Archives Francaises De Pediatrie|February 1, 1990
[Incomplete androgen insensitivity syndrome. Difficulties of diagnosis and management]M G Forest, P Mollard, M David, et al.
Endocrine Research|February 24, 2001
Two novel mutations in splice donor sites of CYP11B1 in congenital adrenal hyperplasia due to 11beta-hydroxylase deficiencyO Chabre, S Portrat-Doyen, J Vivier, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|December 5, 2000
Clinical report of three patients with hereditary hemochromatosis and movement disordersG Demarquay, A Setiey, Y Morel, et al.
Endocrine Research|November 1, 1996
Nonclassical adrenal hyperplasia due to 21-hydroxylase-deficiency: does genotyping predict the clinical manifestation?D l'Allemand, E Keller, W Hoeppner, et al.
The Journal of Clinical Endocrinology and Metabolism|January 3, 2001
How a patient homozygous for a 30-kb deletion of the C4-CYP 21 genomic region can have a nonclassic form of 21-hydroxylase deficiencyD L'Allemand, V Tardy, A Grüters, et al.
Praxis|December 3, 1996
[Diet treatment of obesity--weight-loss stage and weight-maintenance stage]Y Morel, A F Allaz, N de Tonnac, et al.
Pageof 14

Showing results (41-50 of 138) with videos related to

Sort By:
Pageof 14
Journal of Cardiovascular Pharmacology|August 1, 1995
Insulin sensitivity in obese hypertensive dyslipidemic patients treated with enalapril or atenololY Morel, A Gadient, U Keller, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 1, 1989
Transcript encoded on the opposite strand of the human steroid 21-hydroxylase/complement component C4 gene locusY Morel, J Bristow, S E Gitelman, et al.
Gastroenterologie Clinique Et Biologique|January 1, 1994
[Mucoviscidosis in adult age in 1994]I Durieu, L Calemar, G Bellon, et al.
Annales D'Endocrinologie|July 1, 2005
21-Hydroxylase deficiency: an exemplary model of the contribution of molecular biology in the understanding and management of the diseaseM G Forest, V Tardy, M Nicolino, et al.
Archives Francaises De Pediatrie|February 1, 1990
[Incomplete androgen insensitivity syndrome. Difficulties of diagnosis and management]M G Forest, P Mollard, M David, et al.
Endocrine Research|February 24, 2001
Two novel mutations in splice donor sites of CYP11B1 in congenital adrenal hyperplasia due to 11beta-hydroxylase deficiencyO Chabre, S Portrat-Doyen, J Vivier, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|December 5, 2000
Clinical report of three patients with hereditary hemochromatosis and movement disordersG Demarquay, A Setiey, Y Morel, et al.
Endocrine Research|November 1, 1996
Nonclassical adrenal hyperplasia due to 21-hydroxylase-deficiency: does genotyping predict the clinical manifestation?D l'Allemand, E Keller, W Hoeppner, et al.
The Journal of Clinical Endocrinology and Metabolism|January 3, 2001
How a patient homozygous for a 30-kb deletion of the C4-CYP 21 genomic region can have a nonclassic form of 21-hydroxylase deficiencyD L'Allemand, V Tardy, A Grüters, et al.
Praxis|December 3, 1996
[Diet treatment of obesity--weight-loss stage and weight-maintenance stage]Y Morel, A F Allaz, N de Tonnac, et al.
Pageof 14