Search research articles
Contact Us
Filters
Showing results (1-10 of 15) with videos related to
Page
of 2
Sort By:
International Journal of Pediatric Endocrinology
|
February 3, 2017
Deferring surgical treatment of ambiguous genitalia into adolescence in girls with 21-hydroxylase deficiency: a feasibility study
Pierre Bougnères, Claire Bouvattier, Maryse Cartigny, et al.
American Journal of Medical Genetics
|
September 5, 2002
Familial reciprocal translocation t(7;16) associated with maternal uniparental disomy 7 in a Silver-Russell patient
Jean-Michel Dupont, Laurence Cuisset, Maryse Cartigny, et al.
European Journal of Human Genetics : EJHG
|
June 8, 2017
Cerebellar hypoplasia with endosteal sclerosis is a POLR3-related disorder
Jamal Ghoumid, Florence Petit, Odile Boute-Benejean, et al.
Reproductive Biomedicine Online
|
December 14, 2019
In cases of familial primary ovarian insufficiency and disorders of gonadal development, consider NR5A1/SF-1 sequence variants
Juliette Bertrand-Delepine, Sylvie Manouvrier-Hanu, Maryse Cartigny, et al.
Pediatric Radiology
|
May 25, 2019
Plea for a standardized imaging approach to disorders of sex development in neonates: consensus proposal from European Society of Paediatric Radiology task force
Fred E Avni, Heloise Lerisson, Maria-Luisa Lobo, et al.
Pediatric Radiology
|
June 23, 2019
Correction to: Plea for a standardized imaging approach to disorders of sex development in neonates: Consensus proposal from European Society of Paediatric Radiology task force
Fred E Avni, Heloise Lerisson, Maria-Luisa Lobo, et al.
Hormone Research in Paediatrics
|
April 8, 2026
MKRN3 variants in central precocious puberty as an example of the complexity to classify missense variants in imprinted genes as pathogenic
Clémence Delcour, Carole Harbulot, Leila Drira, et al.
Endocrine Connections
|
December 4, 2025
Splenic structural and functional abnormalities in individuals with NR5A1/SF-1 variants
Khadidja Fouatih, Camille Roussel, Maryse Cartigny, et al.
The Journal of Clinical Endocrinology and Metabolism
|
April 9, 2022
Defining Reference Ranges for Serum Anti-Müllerian Hormone on a Large Cohort of Normozoospermic Adult Men Highlights New Potential Physiological Functions of AMH on FSH Secretion and Sperm Motility
Hamza Benderradji, Anne-Laure Barbotin, Maryse Leroy-Billiard, et al.
Diabetes, Obesity & Metabolism
|
April 21, 2022
Therapeutic indications and metabolic effects of metreleptin in patients with lipodystrophy syndromes: Real-life experience from a national reference network
Héléna Mosbah, Marie-Christine Vantyghem, Estelle Nobécourt, et al.
Page
of 2
Search research articles
Search
Showing results (1-10 of 15) with videos related to
Sort By:
Page
of 2
International Journal of Pediatric Endocrinology
|
February 3, 2017
Deferring surgical treatment of ambiguous genitalia into adolescence in girls with 21-hydroxylase deficiency: a feasibility study
Pierre Bougnères, Claire Bouvattier, Maryse Cartigny, et al.
American Journal of Medical Genetics
|
September 5, 2002
Familial reciprocal translocation t(7;16) associated with maternal uniparental disomy 7 in a Silver-Russell patient
Jean-Michel Dupont, Laurence Cuisset, Maryse Cartigny, et al.
European Journal of Human Genetics : EJHG
|
June 8, 2017
Cerebellar hypoplasia with endosteal sclerosis is a POLR3-related disorder
Jamal Ghoumid, Florence Petit, Odile Boute-Benejean, et al.
Reproductive Biomedicine Online
|
December 14, 2019
In cases of familial primary ovarian insufficiency and disorders of gonadal development, consider NR5A1/SF-1 sequence variants
Juliette Bertrand-Delepine, Sylvie Manouvrier-Hanu, Maryse Cartigny, et al.
Pediatric Radiology
|
May 25, 2019
Plea for a standardized imaging approach to disorders of sex development in neonates: consensus proposal from European Society of Paediatric Radiology task force
Fred E Avni, Heloise Lerisson, Maria-Luisa Lobo, et al.
Pediatric Radiology
|
June 23, 2019
Correction to: Plea for a standardized imaging approach to disorders of sex development in neonates: Consensus proposal from European Society of Paediatric Radiology task force
Fred E Avni, Heloise Lerisson, Maria-Luisa Lobo, et al.
Hormone Research in Paediatrics
|
April 8, 2026
MKRN3 variants in central precocious puberty as an example of the complexity to classify missense variants in imprinted genes as pathogenic
Clémence Delcour, Carole Harbulot, Leila Drira, et al.
Endocrine Connections
|
December 4, 2025
Splenic structural and functional abnormalities in individuals with NR5A1/SF-1 variants
Khadidja Fouatih, Camille Roussel, Maryse Cartigny, et al.
The Journal of Clinical Endocrinology and Metabolism
|
April 9, 2022
Defining Reference Ranges for Serum Anti-Müllerian Hormone on a Large Cohort of Normozoospermic Adult Men Highlights New Potential Physiological Functions of AMH on FSH Secretion and Sperm Motility
Hamza Benderradji, Anne-Laure Barbotin, Maryse Leroy-Billiard, et al.
Diabetes, Obesity & Metabolism
|
April 21, 2022
Therapeutic indications and metabolic effects of metreleptin in patients with lipodystrophy syndromes: Real-life experience from a national reference network
Héléna Mosbah, Marie-Christine Vantyghem, Estelle Nobécourt, et al.
Page
of 2