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Y Morel

Showing results (61-70 of 138) with videos related to

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Steroids|January 1, 1997
Structure-function relationships of 3 beta-hydroxysteroid dehydrogenase: contribution made by the molecular genetics of 3 beta-hydroxysteroid dehydrogenase deficiencyY Morel, F Mébarki, E Rhéaume, et al.
Presse Medicale (Paris, France : 1983)|December 16, 1995
[Cystic fibrosis in adults]I Durieu, G Bellon, D Vital Durand, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|April 1, 1994
[Final height in 69 patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency]M David, M Sempé, M Blanc, et al.
Lancet (London, England)|July 25, 1987
RU 486 administration in a child with Cushing's syndromeB Beaufrère, L de Parscau, P Chatelain, et al.
Autoimmunity|January 1, 1992
Assessment of antibody dependent cell cytotoxicity in autoimmune thyroid disease using porcine thyroid cellsP Rodien, A M Madec, Y Morel, et al.
Medecine Tropicale : Revue Du Corps De Sante Colonial|October 6, 2004
[Late occurrence of first epileptic seizures: a 42-case series]T M Diallo, A Cisse, Y Morel, et al.
Annales D'Endocrinologie|January 15, 2010
Detection and management of late-onset 21-hydroxylase deficiency in women with hyperandrogenismJ Young, V Tardy, A-B de la Perrière, et al.
Annales D'Endocrinologie|November 5, 2003
[Fetal intersexuality: management approach]Y Morel, V Tardy, L Calemard-Michel, et al.
Diabete & Metabolisme|February 1, 1995
Cardiovascular autonomic neuropathy in diabetic patients with macular oedemaA Dosso, A Golay, Y Morel, et al.
The Journal of Clinical Endocrinology and Metabolism|July 10, 2001
Deletion hybrid genes, due to unequal crossing over between CYP11B1 (11beta-hydroxylase) and CYP11B2(aldosterone synthase) cause steroid 11beta-hydroxylase deficiency and congenital adrenal hyperplasiaS Portrat, P Mulatero, K M Curnow, et al.
Pageof 14

Showing results (61-70 of 138) with videos related to

Sort By:
Pageof 14
Steroids|January 1, 1997
Structure-function relationships of 3 beta-hydroxysteroid dehydrogenase: contribution made by the molecular genetics of 3 beta-hydroxysteroid dehydrogenase deficiencyY Morel, F Mébarki, E Rhéaume, et al.
Presse Medicale (Paris, France : 1983)|December 16, 1995
[Cystic fibrosis in adults]I Durieu, G Bellon, D Vital Durand, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|April 1, 1994
[Final height in 69 patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency]M David, M Sempé, M Blanc, et al.
Lancet (London, England)|July 25, 1987
RU 486 administration in a child with Cushing's syndromeB Beaufrère, L de Parscau, P Chatelain, et al.
Autoimmunity|January 1, 1992
Assessment of antibody dependent cell cytotoxicity in autoimmune thyroid disease using porcine thyroid cellsP Rodien, A M Madec, Y Morel, et al.
Medecine Tropicale : Revue Du Corps De Sante Colonial|October 6, 2004
[Late occurrence of first epileptic seizures: a 42-case series]T M Diallo, A Cisse, Y Morel, et al.
Annales D'Endocrinologie|January 15, 2010
Detection and management of late-onset 21-hydroxylase deficiency in women with hyperandrogenismJ Young, V Tardy, A-B de la Perrière, et al.
Annales D'Endocrinologie|November 5, 2003
[Fetal intersexuality: management approach]Y Morel, V Tardy, L Calemard-Michel, et al.
Diabete & Metabolisme|February 1, 1995
Cardiovascular autonomic neuropathy in diabetic patients with macular oedemaA Dosso, A Golay, Y Morel, et al.
The Journal of Clinical Endocrinology and Metabolism|July 10, 2001
Deletion hybrid genes, due to unequal crossing over between CYP11B1 (11beta-hydroxylase) and CYP11B2(aldosterone synthase) cause steroid 11beta-hydroxylase deficiency and congenital adrenal hyperplasiaS Portrat, P Mulatero, K M Curnow, et al.
Pageof 14