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A comparative randomized multicentric study comparing the step‐up versus step‐down protocol in polycystic ovary syndrome

Human reproduction (Oxford), 2003-08, Vol.18 (8), p.1626-1631

2003

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Added value of buccal cell FISH analysis in the diagnosis and management of Turner syndrome

Human reproduction (Oxford), 2020-10, Vol.35 (10), p.2391-2398

2020

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MEN1 Disease Occurring Before 21 Years Old: A 160-Patient Cohort Study From the Groupe d'étude des Tumeurs Endocrines

The journal of clinical endocrinology and metabolism, 2015-04, Vol.100 (4), p.1568-1577

2015

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Unilateral nonhaemorrhagic adrenal infarction as a cause of abdominal pain during pregnancy

Gynecological endocrinology, 2019-11, Vol.35 (11), p.941-944

2019

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Ovarian hyperthecosis on grayscale and color Doppler ultrasound

Ultrasound in obstetrics & gynecology, 2008-10, Vol.32 (5), p.694-699

2008

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Impact on testicular function of a single ablative activity of 3.7 GBq radioactive iodine for differentiated thyroid carcinoma

Human reproduction (Oxford), 2018-08, Vol.33 (8), p.1408-1416

2018

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X chromosome gene dosage as a determinant of congenital malformations and of age-related comorbidity risk in patients with Turner syndrome, from childhood to early adulthood

European journal of endocrinology, 2019-06, Vol.180 (6), p.397-406

2019

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Significant prevalence of NR3C1 mutations in incidentally discovered bilateral adrenal hyperplasia: results of the French MUTA-GR Study

European journal of endocrinology, 2018-04, Vol.178 (4), p.411-423

2018

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Dunnigan lipodystrophy syndrome: French National Diagnosis and Care Protocol (PNDS; Protocole National de Diagnostic et de Soins)

Orphanet journal of rare diseases, 2022-04, Vol.17 (Suppl 1), p.170-170, Article 170

2022

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Deletion of CPEB1 Gene: A Rare but Recurrent Cause of Premature Ovarian Insufficiency

The journal of clinical endocrinology and metabolism, 2016-05, Vol.101 (5), p.2099-2104

2016

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Comparison of a 24-day and a 21-day pill regimen for the novel combined oral contraceptive, nomegestrol acetate and 17β-estradiol (NOMAC/E2): a double-blind, randomized study

Human reproduction (Oxford), 2011-06, Vol.26 (6), p.1338-1347

2011

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Unraveling the intrafamilial correlations and heritability of tumor types in MEN1: a Groupe d'étude des Tumeurs Endocrines study

European journal of endocrinology, 2015-12, Vol.173 (6), p.819-826

2015

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A New Clinical Condition Linked to a Novel Mutation in Lamins A and C with Generalized Lipoatrophy, Insulin-Resistant Diabetes, Disseminated Leukomelanodermic Papules, Liver Steatosis, and Cardiomyopathy

The journal of clinical endocrinology and metabolism, 2003-03, Vol.88 (3), p.1006-1013

2003

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Contre le traitement hormonal de ménopause

Annales d'endocrinologie, 2012-09, Vol.73 (4), p.249-249

Christin-Maitre, S

2012

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Pregnancy-associated hormones and fetal-maternal relations

Annales d'endocrinologie, 2015-10, Vol.76 (6 Suppl 1), p.S39

2015

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Birth after TESE–ICSI in a man with hypogonadotropic hypogonadism and congenital adrenal hypoplasia linked to a DAX-1 (NR0B1) mutation

Human reproduction (Oxford), 2011-03, Vol.26 (3), p.724-728

2011

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Hormones, grossesse et relation materno-fætale

Annales d'endocrinologie, 2015-10, Vol.76 (6), p.S39-S50

2015

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Nucleocytoplasmic shuttling of the progesterone receptor

The EMBO journal, 1991-12, Vol.10 (12), p.3851-3859

1991

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Genome-wide association study and premature ovarian failure

Annales d'endocrinologie, 2010-05, Vol.71 (3), p.218-221

2010

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Mixed ductal-pancreatic polypeptide-cell carcinoma of the pancreas

Histopathology, 2002-08, Vol.41 (2), p.122-126

2002

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Croissance staturale d’un adulte porteur d’une insuffisance antéhypophysaire congénitale traité par hormone de croissance

Annales d'endocrinologie, 2016-09, Vol.77 (4), p.479-479

2016

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Therapeutic issues concerning male fertility

Annales d'endocrinologie, 2014-10, Vol.75 Suppl 1, p.S13

2014

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Enjeux thérapeutiques en fertilité masculine

Annales d'endocrinologie, 2014-10, Vol.75, p.S13-S20

2014

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A new LH receptor splice mutation responsible for male hypogonadism with subnormal sperm production in the propositus, and infertility with regular cycles in an affected sister

Human reproduction (Oxford), 2008-08, Vol.23 (8), p.1917-1923

2008

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Deletions Involving Long-Range Conserved Nongenic Sequences Upstream and Downstream of FOXL2 as a Novel Disease-Causing Mechanism in Blepharophimosis Syndrome

American journal of human genetics, 2005-08, Vol.77 (2), p.205-218

2005

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A comparative randomized multicentric study comparing the step‐up versus step‐down protocol in polycystic ovary syndrome

Added value of buccal cell FISH analysis in the diagnosis and management of Turner syndrome

MEN1 Disease Occurring Before 21 Years Old: A 160-Patient Cohort Study From the Groupe d'étude des Tumeurs Endocrines

Unilateral nonhaemorrhagic adrenal infarction as a cause of abdominal pain during pregnancy

Ovarian hyperthecosis on grayscale and color Doppler ultrasound

Impact on testicular function of a single ablative activity of 3.7 GBq radioactive iodine for differentiated thyroid carcinoma

X chromosome gene dosage as a determinant of congenital malformations and of age-related comorbidity risk in patients with Turner syndrome, from childhood to early adulthood

Significant prevalence of NR3C1 mutations in incidentally discovered bilateral adrenal hyperplasia: results of the French MUTA-GR Study

Dunnigan lipodystrophy syndrome: French National Diagnosis and Care Protocol (PNDS; Protocole National de Diagnostic et de Soins)

Deletion of CPEB1 Gene: A Rare but Recurrent Cause of Premature Ovarian Insufficiency

Comparison of a 24-day and a 21-day pill regimen for the novel combined oral contraceptive, nomegestrol acetate and 17β-estradiol (NOMAC/E2): a double-blind, randomized study

Unraveling the intrafamilial correlations and heritability of tumor types in MEN1: a Groupe d'étude des Tumeurs Endocrines study

A New Clinical Condition Linked to a Novel Mutation in Lamins A and C with Generalized Lipoatrophy, Insulin-Resistant Diabetes, Disseminated Leukomelanodermic Papules, Liver Steatosis, and Cardiomyopathy

Contre le traitement hormonal de ménopause

Pregnancy-associated hormones and fetal-maternal relations

Birth after TESE–ICSI in a man with hypogonadotropic hypogonadism and congenital adrenal hypoplasia linked to a DAX-1 (NR0B1) mutation

Hormones, grossesse et relation materno-fætale

Nucleocytoplasmic shuttling of the progesterone receptor

Genome-wide association study and premature ovarian failure

Mixed ductal-pancreatic polypeptide-cell carcinoma of the pancreas

Croissance staturale d’un adulte porteur d’une insuffisance antéhypophysaire congénitale traité par hormone de croissance

Therapeutic issues concerning male fertility

Enjeux thérapeutiques en fertilité masculine

A new LH receptor splice mutation responsible for male hypogonadism with subnormal sperm production in the propositus, and infertility with regular cycles in an affected sister

Deletions Involving Long-Range Conserved Nongenic Sequences Upstream and Downstream of FOXL2 as a Novel Disease-Causing Mechanism in Blepharophimosis Syndrome

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