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1 . Academic Journal
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
저자
by
Martinerie, Laetitia
;
Bouligand, Jérôme
;
North, Marie-Odile
;
Bertherat, Jérôme
;
Assié, Guillaume
, et al.
소스
In
Annales d'Endocrinologie
July 2024 85(4):284-293
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7 . Academic Journal
Meiotic studies of infertile men in case of non-obstructive azoospermia with normal karyotype and no microdeleted Y-chromosome precise the clinical couple management
저자
by
North, Marie-Odile
;
Lellei, Ilona
;
Erdei, Edit
;
Barbet, Jacques Patrick
;
Tritto, Joseph
.
소스
In
Annales de genetique
2004 47(2):113-123
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Scopus
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7 . Academic Journal
Multiple endocrine neoplasia type 1 caused by mosaic mutation: clinical follow-up and genetic counseling?
저자
by
Coppin, Lucie
;
Giraud, Sophie
;
Pasmant, Eric
;
Lagarde, Arnaud
;
North, Marie-Odile
, et al.
소스
European Journal of Endocrinology
. Jul2022, Vol. 187 Issue 1, pK1-K16. 6p.
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7 . Academic Journal
Transcriptome in paraffin samples for the diagnosis and prognosis of adrenocortical carcinoma.
저자
by
Jouinot, Anne
;
Lippert, Juliane
;
Sibony, Mathilde
;
Violon, Florian
;
Jeanpierre, Lindsay
, et al.
소스
European Journal of Endocrinology
. Jun2022, Vol. 186 Issue 6, p607-617. 11p.
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7 . Academic Journal
Value of Somatostatin Receptor PET/CT in Patients With MEN1 at Various Stages of Their Disease.
저자
by
Mennetrey, Clément
;
Bras, Maëlle Le
;
Bando-Delaunay, Aurélie
;
Al-Mansour, Laure
;
Haissaguerre, Magalie
, et al.
소스
Journal of Clinical Endocrinology & Metabolism; May2022, Vol. 107 Issue 5, pe2056-e2064, 9p
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7 . Academic Journal
Noninvasive Prenatal Diagnosis of a Paternally Inherited MEN1 Pathogenic Splicing Variant.
저자
by
Huby, Thomas
;
Guillou, Edouard Le
;
des Roziers, Cyril Burin
;
Pacot, Laurence
;
Briand-Suleau, Audrey
, et al.
소스
Journal of Clinical Endocrinology & Metabolism; Apr2022, Vol. 107 Issue 4, p1367-1373, 7p
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7 . Periodical
Noninvasive Prenatal Diagnosis of a Paternally Inherited MEN1Pathogenic Splicing Variant
저자
by
Huby, Thomas
;
Le Guillou, Edouard
;
Burin des Roziers, Cyril
;
Pacot, Laurence
;
Briand-Suleau, Audrey
, et al.
소스
The Journal of Clinical Endocrinology & Metabolism; April 2022, Vol. 107 Issue: 4 pe1367-e1373, 7p
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7 . Periodical
KDM1Ainactivation causes hereditary food-dependent Cushing syndrome
저자
by
Vaczlavik, Anna
;
Bouys, Lucas
;
Violon, Florian
;
Giannone, Gaetan
;
Jouinot, Anne
, et al.
소스
Genetics in Medicine; February 2022, Vol. 24 Issue: 2 p374-383, 10p
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7 . Academic Journal
18
F-fluorocholine PET/CT in MEN1 Patients with Primary Hyperparathyroidism.
저자
by
Gauthé, Mathieu
;
Dierick-Gallet, Anne
;
Delbot, Thierry
;
Bricaire, Léopoldine
;
Bertherat, Jérôme
, et al.
소스
World Journal of Surgery
. Nov2020, Vol. 44 Issue 11, p3761-3769. 9p.
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7 . Academic Journal
Should the GCM2 gene be tested when screening for familial primary hyperparathyroidism?
저자
by
Coppin, Lucie
;
Dufosse, Margaux
;
Romanet, Pauline
;
Giraud, Sophie
;
North, Marie-Odile
, et al.
소스
European Journal of Endocrinology
. Jan2020, Vol. 182 Issue 1, p57-65. 9p.
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