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V Tardy

Showing results (11-20 of 22) with videos related to

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Annales D'Endocrinologie|November 5, 2003
[Fetal intersexuality: management approach]Y Morel, V Tardy, L Calemard-Michel, 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.
Annales D'Endocrinologie|November 28, 2009
Adrenocortical incidentaloma with uncertain prognosis associated with an inadequately treated congenital adrenal hyperplasiaN Chevalier, P Carrier, M Piche, et al.
The Journal of Clinical Endocrinology and Metabolism|March 7, 2001
Phenotype-genotype correlation in 56 women with nonclassical congenital adrenal hyperplasia due to 21-hydroxylase deficiencyC Deneux, V Tardy, A Dib, et al.
Endocrine Research|February 24, 2001
A new insight into the molecular basis of 3beta-hydroxysteroid dehydrogenase deficiencyJ Simard, M L Ricketts, A M Moisan, et al.
The Journal of Clinical Endocrinology and Metabolism|January 19, 2010
Phenotype-genotype correlations of 13 rare CYP21A2 mutations detected in 46 patients affected with 21-hydroxylase deficiency and in one carrierV Tardy, R Menassa, V Sulmont, et al.
Clinical Genetics|November 22, 2008
Pseudoexon activation in the PKHD1 gene: a French founder intronic mutation IVS46+653A>G causing severe autosomal recessive polycystic kidney diseaseL Michel-Calemard, F Dijoud, M Till, et al.
The Journal of Clinical Endocrinology and Metabolism|June 6, 2003
Follow-up of 68 children with congenital adrenal hyperplasia due to 21-hydroxylase deficiency: relevance of genotype for managementG Pinto, V Tardy, C Trivin, et al.
Hormone Research|September 6, 2000
Mutational analysis in Lebanese patients with congenital adrenal hyperplasia due to a deficit in 21-hydroxylaseV Delague, N Souraty, E Khallouf, et al.
Journal of Environmental Management|December 12, 2018
A field-pilot for passive bioremediation of As-rich acid mine drainageL Fernandez-Rojo, C Casiot, E Laroche, et al.
Pageof 3

Showing results (11-20 of 22) with videos related to

Sort By:
Pageof 3
Annales D'Endocrinologie|November 5, 2003
[Fetal intersexuality: management approach]Y Morel, V Tardy, L Calemard-Michel, 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.
Annales D'Endocrinologie|November 28, 2009
Adrenocortical incidentaloma with uncertain prognosis associated with an inadequately treated congenital adrenal hyperplasiaN Chevalier, P Carrier, M Piche, et al.
The Journal of Clinical Endocrinology and Metabolism|March 7, 2001
Phenotype-genotype correlation in 56 women with nonclassical congenital adrenal hyperplasia due to 21-hydroxylase deficiencyC Deneux, V Tardy, A Dib, et al.
Endocrine Research|February 24, 2001
A new insight into the molecular basis of 3beta-hydroxysteroid dehydrogenase deficiencyJ Simard, M L Ricketts, A M Moisan, et al.
The Journal of Clinical Endocrinology and Metabolism|January 19, 2010
Phenotype-genotype correlations of 13 rare CYP21A2 mutations detected in 46 patients affected with 21-hydroxylase deficiency and in one carrierV Tardy, R Menassa, V Sulmont, et al.
Clinical Genetics|November 22, 2008
Pseudoexon activation in the PKHD1 gene: a French founder intronic mutation IVS46+653A>G causing severe autosomal recessive polycystic kidney diseaseL Michel-Calemard, F Dijoud, M Till, et al.
The Journal of Clinical Endocrinology and Metabolism|June 6, 2003
Follow-up of 68 children with congenital adrenal hyperplasia due to 21-hydroxylase deficiency: relevance of genotype for managementG Pinto, V Tardy, C Trivin, et al.
Hormone Research|September 6, 2000
Mutational analysis in Lebanese patients with congenital adrenal hyperplasia due to a deficit in 21-hydroxylaseV Delague, N Souraty, E Khallouf, et al.
Journal of Environmental Management|December 12, 2018
A field-pilot for passive bioremediation of As-rich acid mine drainageL Fernandez-Rojo, C Casiot, E Laroche, et al.
Pageof 3