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The Journal of Clinical Endocrinology and Metabolism
|
January 30, 2014
New management strategy of pregnancies at risk of congenital adrenal hyperplasia using fetal sex determination in maternal serum: French cohort of 258 cases (2002-2011)
Véronique Tardy-Guidollet, Rita Menassa, Jean-Marc Costa, et al.
The Journal of Clinical Endocrinology and Metabolism
|
November 6, 2008
CBP/p300-interacting transactivator, with Glu/Asp-rich C-terminal domain, 2, and pre-B-cell leukemia transcription factor 1 in human adrenal development and disease
Bruno Ferraz-de-Souza, Franziska Martin, Delphine Mallet, et al.
Annales D'Endocrinologie
|
November 8, 2012
Adrenal rest tissue in gonads of patients with classical congenital adrenal hyperplasia: multicenter study of 45 French male patients
Peggy Pierre, François Despert, François Tranquart, et al.
Journal of Pediatric Urology
|
April 1, 2014
Late prenatal dexamethasone and phenotype variations in 46,XX CAH: concerns about current protocols and benefits for surgical procedures
Daniela Gorduza, Véronique Tardy-Guidollet, Elsa Robert, et al.
Hormone Research in Paediatrics
|
May 27, 2020
Hypopituitarism in Patients with Blepharophimosis and FOXL2 Mutations
Sarah Castets, Florence Roucher-Boulez, Alexandru Saveanu, et al.
Mechanisms of Ageing and Development
|
November 16, 2004
Partial androgen insensitivity with phenotypic variation caused by androgen receptor mutations that disrupt activation function 2 and the NH(2)- and carboxyl-terminal interaction
Charmian A Quigley, Jiann-an Tan, Bin He, et al.
The Journal of Clinical Endocrinology and Metabolism
|
January 19, 2010
Fertility in women with nonclassical congenital adrenal hyperplasia due to 21-hydroxylase deficiency
Maud Bidet, Christine Bellanné-Chantelot, Marie-Béatrice Galand-Portier, et al.
Molecular Genetics & Genomic Medicine
|
January 29, 2019
Is interstitial 8p23 microdeletion responsible of 46,XY gonadal dysgenesis? One case report from birth to puberty
Kathy Wagner-Mahler, Jean-Yves Kurzenne, Frederique Gastaud, et al.
Mathematical Biosciences and Engineering : MBE
|
March 11, 2023
Influence of COVID-19 vaccination on the dynamics of new infected cases in the world
Mustafa Kamal, Mintodê Nicodème Atchadé, Yves Morel Sokadjo, et al.
European Journal of Pediatrics
|
January 26, 2002
Aetiological diagnosis of male sex ambiguity: a collaborative study
Yves Morel, Rodolfo Rey, Cécile Teinturier, et al.
Page
of 9
Search research articles
Search
Showing results (61-70 of 83) with videos related to
Sort By:
Page
of 9
The Journal of Clinical Endocrinology and Metabolism
|
January 30, 2014
New management strategy of pregnancies at risk of congenital adrenal hyperplasia using fetal sex determination in maternal serum: French cohort of 258 cases (2002-2011)
Véronique Tardy-Guidollet, Rita Menassa, Jean-Marc Costa, et al.
The Journal of Clinical Endocrinology and Metabolism
|
November 6, 2008
CBP/p300-interacting transactivator, with Glu/Asp-rich C-terminal domain, 2, and pre-B-cell leukemia transcription factor 1 in human adrenal development and disease
Bruno Ferraz-de-Souza, Franziska Martin, Delphine Mallet, et al.
Annales D'Endocrinologie
|
November 8, 2012
Adrenal rest tissue in gonads of patients with classical congenital adrenal hyperplasia: multicenter study of 45 French male patients
Peggy Pierre, François Despert, François Tranquart, et al.
Journal of Pediatric Urology
|
April 1, 2014
Late prenatal dexamethasone and phenotype variations in 46,XX CAH: concerns about current protocols and benefits for surgical procedures
Daniela Gorduza, Véronique Tardy-Guidollet, Elsa Robert, et al.
Hormone Research in Paediatrics
|
May 27, 2020
Hypopituitarism in Patients with Blepharophimosis and FOXL2 Mutations
Sarah Castets, Florence Roucher-Boulez, Alexandru Saveanu, et al.
Mechanisms of Ageing and Development
|
November 16, 2004
Partial androgen insensitivity with phenotypic variation caused by androgen receptor mutations that disrupt activation function 2 and the NH(2)- and carboxyl-terminal interaction
Charmian A Quigley, Jiann-an Tan, Bin He, et al.
The Journal of Clinical Endocrinology and Metabolism
|
January 19, 2010
Fertility in women with nonclassical congenital adrenal hyperplasia due to 21-hydroxylase deficiency
Maud Bidet, Christine Bellanné-Chantelot, Marie-Béatrice Galand-Portier, et al.
Molecular Genetics & Genomic Medicine
|
January 29, 2019
Is interstitial 8p23 microdeletion responsible of 46,XY gonadal dysgenesis? One case report from birth to puberty
Kathy Wagner-Mahler, Jean-Yves Kurzenne, Frederique Gastaud, et al.
Mathematical Biosciences and Engineering : MBE
|
March 11, 2023
Influence of COVID-19 vaccination on the dynamics of new infected cases in the world
Mustafa Kamal, Mintodê Nicodème Atchadé, Yves Morel Sokadjo, et al.
European Journal of Pediatrics
|
January 26, 2002
Aetiological diagnosis of male sex ambiguity: a collaborative study
Yves Morel, Rodolfo Rey, Cécile Teinturier, et al.
Page
of 9