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Bilateral Adrenal Hyperplasia as a Possible Mechanism for Hyperandrogenism in Women With Polycystic Ovary Syndrome

The journal of clinical endocrinology and metabolism, 2016-09, Vol.101 (9), p.3353-3360

2016

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Association of a COL1A1 polymorphism with lumbar disc disease in young military recruits

Journal of medical genetics, 2005-07, Vol.42 (7), p.e44-e44

2005

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Armc5 : un régulateur potentiel de l’acétylation dans les cellules corticosurrénaliennes grâce à Sirt1

Annales d'endocrinologie, 2022-10, Vol.83 (5), p.321

2022

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Expression des récepteurs de l’œstradiol dans la dysplasie micronodulaire pigmentée des surrénales : rôle dans le contrôle de la sécrétion de cortisol

Annales d'endocrinologie, 2023-10, Vol.84 (5), p.553-553

2023

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Diurnal Plasma Cortisol Measurements Utility in Differentiating Various Etiologies of Endogenous Cushing Syndrome

Hormone and metabolic research, 2016-09, Vol.48 (10), p.677-681

2016

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Use of 3-Dimensional Volumetric Modeling of Adrenal Gland Size in Patients with Primary Pigmented Nodular Adrenocortical Disease

Hormone and metabolic research, 2016-04, Vol.48 (4), p.242-246

2016

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Attention Deficit Hyperactivity Disorder in Pediatric Patients with Pheochromocytoma and Paraganglioma

Hormone and metabolic research, 2016-08, Vol.48 (8), p.509-513

2016

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Les altérations génétiques guident le phénotype des patients avec PBMAH : étude de 354 cas index

Annales d'endocrinologie, 2024-10, Vol.85 (5), p.374-374

2024

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Vers une explication développementale de l’origine des lésions cutanées dans le complexe de Carney

Annales d'endocrinologie, 2021-10, Vol.82 (5), p.272-272

2021

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Variations in maternal adenylate cyclase genes are associated with congenital Zika syndrome in a cohort from Northeast, Brazil

Journal of internal medicine, 2019-02, Vol.285 (2), p.215-222

2019

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Threat bias in mice with inactivating mutations of Prkar1a

Neuroscience, 2013-06, Vol.241, p.206-214

2013

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The lentiginoses: cutaneous markers of systemic disease and a window to new aspects of tumourigenesis

Journal of Medical Genetics, 2005-11, Vol.42 (11), p.801-810

2005

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Developmental focus on disorders of sex development: special issue overview

Hormone and metabolic research, 2015-05, Vol.47 (5), p.309-311

2015

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Dependence of the Excitability of Pituitary Cells on Cyclic Nucleotides

Journal of neuroendocrinology, 2012-09, Vol.24 (9), p.1183-1200

2012

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Multiple endocrine neoplasias: advances and challenges for the future

Journal of internal medicine, 2009-07, Vol.266 (1), p.1-4

2009

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Comparison of the effects of PRKAR1A and PRKAR2B depletion on signaling pathways, cell growth, and cell cycle control of adrenocortical cells

Hormone and metabolic research, 2014-11, Vol.46 (12), p.883-888

2014

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Systematic screening for PRKAR1A gene rearrangement in Carney complex: identification and functional characterization of a new in-frame deletion

European journal of endocrinology, 2014-01, Vol.170 (1), p.151-160

2014

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A novel genetic locus for low renin hypertension: familial hyperaldosteronism type II maps to chromosome 7 (7p22)

Journal of medical genetics, 2000-11, Vol.37 (11), p.831-835

2000

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Not all glucocorticoid-induced obesity is the same: differences in adiposity among various diagnostic groups of Cushing syndrome

Hormone and metabolic research, 2014-11, Vol.46 (12), p.897-903

2014

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Chromosome 2 (2p16) abnormalities in Carney complex tumours

Journal of medical genetics, 2003-04, Vol.40 (4), p.268-277

2003

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Mutations of the gene encoding the protein kinase A type I-α regulatory subunit in patients with the Carney complex

Nature genetics, 2000-09, Vol.26 (1), p.89-92

2000

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Prkar1a in the regulation of insulin secretion

Hormone and metabolic research, 2012-09, Vol.44 (10), p.759-765

2012

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Les mutations d’ARMC5 et KDM1A sont associées à des profils différentiels d’expression de récepteurs illégitimes dans l’hyperplasie macronodulaire bilatérale des surrénales

Annales d'endocrinologie, 2022-10, Vol.83 (5), p.321-322

2022

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A transgenic mouse bearing an antisense construct of regulatory subunit type 1A of protein kinase A develops endocrine and other tumours: comparison with Carney complex and other PRKAR1A induced lesions

Journal of medical genetics, 2004-12, Vol.41 (12), p.923-931

2004

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Bilateral Adrenal Hyperplasia as a Possible Mechanism for Hyperandrogenism in Women With Polycystic Ovary Syndrome

Le Gigantisme : les résultats d’une étude clinique et génétique internationale

Association of a COL1A1 polymorphism with lumbar disc disease in young military recruits

Armc5 : un régulateur potentiel de l’acétylation dans les cellules corticosurrénaliennes grâce à Sirt1

Expression des récepteurs de l’œstradiol dans la dysplasie micronodulaire pigmentée des surrénales : rôle dans le contrôle de la sécrétion de cortisol

Diurnal Plasma Cortisol Measurements Utility in Differentiating Various Etiologies of Endogenous Cushing Syndrome

Use of 3-Dimensional Volumetric Modeling of Adrenal Gland Size in Patients with Primary Pigmented Nodular Adrenocortical Disease

Attention Deficit Hyperactivity Disorder in Pediatric Patients with Pheochromocytoma and Paraganglioma

Les altérations génétiques guident le phénotype des patients avec PBMAH : étude de 354 cas index

Vers une explication développementale de l’origine des lésions cutanées dans le complexe de Carney

Variations in maternal adenylate cyclase genes are associated with congenital Zika syndrome in a cohort from Northeast, Brazil

Threat bias in mice with inactivating mutations of Prkar1a

The lentiginoses: cutaneous markers of systemic disease and a window to new aspects of tumourigenesis

Developmental focus on disorders of sex development: special issue overview

Dependence of the Excitability of Pituitary Cells on Cyclic Nucleotides

Multiple endocrine neoplasias: advances and challenges for the future

Comparison of the effects of PRKAR1A and PRKAR2B depletion on signaling pathways, cell growth, and cell cycle control of adrenocortical cells

Systematic screening for PRKAR1A gene rearrangement in Carney complex: identification and functional characterization of a new in-frame deletion

A novel genetic locus for low renin hypertension: familial hyperaldosteronism type II maps to chromosome 7 (7p22)

Not all glucocorticoid-induced obesity is the same: differences in adiposity among various diagnostic groups of Cushing syndrome

Chromosome 2 (2p16) abnormalities in Carney complex tumours

Mutations of the gene encoding the protein kinase A type I-α regulatory subunit in patients with the Carney complex

Prkar1a in the regulation of insulin secretion

Les mutations d’ARMC5 et KDM1A sont associées à des profils différentiels d’expression de récepteurs illégitimes dans l’hyperplasie macronodulaire bilatérale des surrénales

A transgenic mouse bearing an antisense construct of regulatory subunit type 1A of protein kinase A develops endocrine and other tumours: comparison with Carney complex and other PRKAR1A induced lesions

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