Zobrazeno 1 - 10
of 100
pro vyhledávání: '"Ingrid, Plotton"'
Autor:
Estelle Bonnet, Mathias Winter, Delphine Mallet, Ingrid Plotton, Claire Bouvattier, Maryse Cartigny, Laetiti Martinerie, Michel Polak, Anne Bachelot, Frédéric Huet, Sabine Baron, Muriel Houang, Sylvie Soskin, Anne Lienhardt, Jérôme Bertherat, Cyril Amouroux, Aurore Bouty, Lise Duranteau, Rémi Besson, Alaa El Ghoneimi, Dinane Samara-Boustani, François Becmeur, Nicolas Kalfa, Françoise Paris, François Medjkane, Aude Brac de la Perrière, Patricia Bretones, Hervé Lejeune, Marc Nicolino, Pierre Mouriquand, Daniela-Brindusa Gorduza, Claire-Lise Gay
Publikováno v:
Endocrine Connections, Vol 12, Iss 3, Pp 1-16 (2023)
Objectives: To examine the changes in diagnostic practices and clinical management of patients with 5α-reductase type 2 (SRD5A2) or 17β-hydroxysteroid dehydrogenase type 3 (HSD17B3) deficiency since molecular diagnoses became available. Methods: C
Externí odkaz:
https://doaj.org/article/077e01f7ec9b4ad58a9537aefd1f10ce
Autor:
Jordan Teoli, Delphine Mallet, Lucie Renault, Claire-Lise Gay, Elsa Labrune, Patricia Bretones, Sandrine Giscard D’Estaing, Béatrice Cuzin, Frédérique Dijoud, Florence Roucher-Boulez, Ingrid Plotton
Publikováno v:
Frontiers in Endocrinology, Vol 14 (2023)
BackgroundSteroidogenic factor 1 (SF-1), encoded by the nuclear receptor subfamily 5 group A member 1 (NR5A1) gene, is a transcriptional factor crucial for adrenal and gonadal organogenesis. Pathogenic variants of NR5A1 are responsible for a wide spe
Externí odkaz:
https://doaj.org/article/bd8247ec449a4b639cda5b0679321f0f
Autor:
Alice Bongrani, Ingrid Plotton, Namya Mellouk, Christelle Ramé, Fabrice Guerif, Pascal Froment, Joëlle Dupont
Publikováno v:
Reproductive Biology and Endocrinology, Vol 20, Iss 1, Pp 1-16 (2022)
Abstract Background According to current definitions of Polycystic Ovary Syndrome (PCOS), hyperandrogenism is considered as a key element in the pathogenesis of this common endocrinopathy. However, until now, studies about ovarian androgen profile in
Externí odkaz:
https://doaj.org/article/169af290c44d485bab57c1598120df46
Autor:
Cécily Lucas, Kay-Sara Sauter, Michael Steigert, Delphine Mallet, James Wilmouth, Julie Olabe, Ingrid Plotton, Yves Morel, Daniel Aeberli, Franca Wagner, Hans Clevers, Amit V. Pandey, Pierre Val, Florence Roucher-Boulez, Christa E. Flück
Publikováno v:
The Journal of Clinical Investigation, Vol 133, Iss 4 (2023)
Disorders of isolated mineralocorticoid deficiency, which cause potentially life-threatening salt-wasting crisis early in life, have been associated with gene variants of aldosterone biosynthesis or resistance; however, in some patients no such varia
Externí odkaz:
https://doaj.org/article/7c038c7fdaca42ca83fa509abb64c789
Publikováno v:
Basic and Clinical Andrology, Vol 31, Iss 1, Pp 1-13 (2021)
Résumé Contexte Les androgènes sont bien connus pour être nécessaires à la spermatogenèse. Le but de l’étude était de déterminer l’évolution de la réactivité des cellules de Sertoli aux androgènes en fonction de l’âge depuis la p
Externí odkaz:
https://doaj.org/article/5840a908e84b4547a976846e798dc0a0
Autor:
Laurie Denis-Laroque, Youenn Drouet, Ingrid Plotton, Nicolas Chopin, Valérie Bonadona, Jacqueline Lornage, Bruno Salle, Christine Lasset, Christine Rousset-Jablonski
Publikováno v:
Breast, Vol 59, Iss , Pp 239-247 (2021)
Background: Some studies suggested a decreased ovarian reserve among BRCA1/2 pathogenic variant carriers, with conflicting results. Methods: We conducted a retrospective single-center observational study of ovarian reserve and spontaneous fertility c
Externí odkaz:
https://doaj.org/article/c3ed57a5c7f4439994f4518dca9d8351
Autor:
Asmahane Ladjouze, Malcolm Donaldson, Ingrid Plotton, Nacima Djenane, Kahina Mohammedi, Véronique Tardy-Guidollet, Delphine Mallet, Kamélia Boulesnane, Zair Bouzerar, Yves Morel, Florence Roucher-Boulez
Publikováno v:
Frontiers in Endocrinology, Vol 13 (2022)
Background3β-hydroxysteroid dehydrogenase 2 (3βHSD2) deficiency is a rare form of congenital adrenal hyperplasia (CAH), with fewer than 200 cases reported in the world literature and few data on outcomes.Patients and MethodsWe report a mixed longit
Externí odkaz:
https://doaj.org/article/f02b49e95a504f2db237a481c5202d46
Autor:
Jordan Teoli, Vincent Mezzarobba, Lucie Renault, Delphine Mallet, Hervé Lejeune, Pierre Chatelain, Frédérique Tixier, Marc Nicolino, Noël Peretti, Sandrine Giscard D’estaing, Béatrice Cuzin, Frédérique Dijoud, Florence Roucher-Boulez, Ingrid Plotton
Publikováno v:
Frontiers in Endocrinology, Vol 13 (2022)
BackgroundNR0B1 pathogenic variants can cause congenital adrenal hypoplasia or primary adrenal insufficiency in early childhood usually associated with hypogonadotropic hypogonadism. NR0B1 is necessary for organogenesis of the adrenal cortex and to m
Externí odkaz:
https://doaj.org/article/ef86f28659bf4fe2a50c23e556146cd3
Autor:
Guillaume Bourdon, Anthony Estienne, Claire Chevaleyre, Christelle Ramé, Fabrice Guérif, Jean-Sébastien Brun, Claudine Vasseur, Gaelle Fromont, Ingrid Plotton, Diane Dufour-Rainfray, Erika Caldas-Silveira, Joëlle Dupont, Pascal Froment, Pierre-Henri Ducluzeau
Publikováno v:
Frontiers in Endocrinology, Vol 13 (2022)
Lifestyle, environment and excess body weight are not only associated with an increased risk of metabolic disorders, such as type 2 diabetes, but also to other pathological processes, such as infertility. A hormone produced mainly by the liver called
Externí odkaz:
https://doaj.org/article/1121dad6512449618274ff10916d7f85
Autor:
Clément Janot, Pauline Perrin, Patricia Bretones, Ingrid Plotton, Florence Roucher-Boulez, Vincent des Portes, Véronique Raverot
Publikováno v:
Journal of Pediatric Endocrinology and Metabolism. 36:478-483
Objectives Elevated free T3 (FT3) is an important feature for the early diagnosis of several diseases among which Grave’s disease or Allan-Hernon-Dudley syndrome. However, there is a lack of age-adapted reference intervals for plasma thyroid hormon
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1ca282ef19a390871ef387199f92f964
https://doi.org/10.1515/jpem-2022-0330
https://doi.org/10.1515/jpem-2022-0330