Marie-odile O. North

Paris, France

Last Updated: 09/26/2026

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Found 15 publications

Consensus statement by the French Society of Endocrinology (SFE) and French Society of Pediatric Endocrinology & Diabetology (SFEDP) for the diagnosis of Cushing's syndrome: Genetics of Cushing's syndrome.

Consensus statement by the French Society of Endocrinology (SFE) and French Society of Pediatric Endocrinology & Diabetology (SFEDP) for the diagnosis of Cushing's syndrome: Genetics of Cushing's syndrome.

Journal: Annales d'endocrinologie

Published: December 20, 2023

Multiple endocrine neoplasia type 1 caused by mosaic mutation: clinical follow-up and genetic counseling?

Multiple endocrine neoplasia type 1 caused by mosaic mutation: clinical follow-up and genetic counseling?

Journal: European journal of endocrinology

Published: February 24, 2022

Transcriptome in paraffin samples for the diagnosis and prognosis of adrenocortical carcinoma.

Transcriptome in paraffin samples for the diagnosis and prognosis of adrenocortical carcinoma.

Journal: European journal of endocrinology

Published: December 09, 2021

Identification of predictive criteria for pathogenic variants of primary bilateral macronodular adrenal hyperplasia (PBMAH) gene ARMC5 in 352 unselected patients.

Identification of predictive criteria for pathogenic variants of primary bilateral macronodular adrenal hyperplasia (PBMAH) gene ARMC5 in 352 unselected patients.

Journal: European journal of endocrinology

Published: October 06, 2021

Value of Somatostatin Receptor PET/CT in Patients With MEN1 at Various Stages of Their Disease.

Value of Somatostatin Receptor PET/CT in Patients With MEN1 at Various Stages of Their Disease.

Journal: The Journal of clinical endocrinology and metabolism

Published: September 20, 2021

Noninvasive Prenatal Diagnosis of a Paternally Inherited MEN1 Pathogenic Splicing Variant.

Noninvasive Prenatal Diagnosis of a Paternally Inherited MEN1 Pathogenic Splicing Variant.

Journal: The Journal of clinical endocrinology and metabolism

Published: August 11, 2021

KDM1A inactivation causes hereditary food-dependent Cushing syndrome.

KDM1A inactivation causes hereditary food-dependent Cushing syndrome.

Journal: Genetics in medicine : official journal of the American College of Medical Genetics

Published: April 06, 2021

18F-fluorocholine PET/CT in MEN1 Patients with Primary Hyperparathyroidism.

18F-fluorocholine PET/CT in MEN1 Patients with Primary Hyperparathyroidism.

Journal: World journal of surgery

Published: July 05, 2020

Should the GCM2 gene be tested when screening for familial primary hyperparathyroidism?

Should the GCM2 gene be tested when screening for familial primary hyperparathyroidism?

Journal: European journal of endocrinology

Published: August 16, 2019

Acromegaly in Carney complex.

Acromegaly in Carney complex.

Journal: Pituitary

Published: July 03, 2019

Proposition of adjustments to the ACMG-AMP framework for the interpretation of MEN1 missense variants.

Proposition of adjustments to the ACMG-AMP framework for the interpretation of MEN1 missense variants.

Journal: Human mutation

Published: June 15, 2018

UMD-MEN1 Database: An Overview of the 370 MEN1 Variants Present in 1676 Patients From the French Population.

UMD-MEN1 Database: An Overview of the 370 MEN1 Variants Present in 1676 Patients From the French Population.

Journal: The Journal of clinical endocrinology and metabolism

Published: May 29, 2018

Showing 1-12 of 15

Last Updated: 09/26/2026