Zobrazeno 1 - 10
of 57
pro vyhledávání: '"Christel Jublanc"'
Autor:
Pierre-François Pradat, Emilien Bernard, Philippe Corcia, Philippe Couratier, Christel Jublanc, Giorgia Querin, Capucine Morélot Panzini, François Salachas, Christophe Vial, Karim Wahbi, Peter Bede, Claude Desnuelle, on behalf of the French Kennedy’s Disease Writing Group
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 15, Iss 1, Pp 1-21 (2020)
Abstract Background Kennedy’s disease (KD), also known as spinal and bulbar muscular atrophy (SBMA), is a rare, adult-onset, X-linked recessive neuromuscular disease caused by CAG expansions in exon 1 of the androgen receptor gene (AR). The objecti
Externí odkaz:
https://doaj.org/article/53385653b6f54dc88c82f8af909bb4bc
Autor:
Angelo Paci, Ségolène Hescot, Atmane Seck, Christel Jublanc, Lionel Mercier, Delphine Vezzosi, Delphine Drui, Marcus Quinkler, Martin Fassnacht, Eric Bruckert, Marc Lombès, Sophie Leboulleux, Sophie Broutin, Eric Baudin
Publikováno v:
Endocrinology, Diabetes & Metabolism Case Reports, Pp 1-4 (2016)
Mitotane (o,p′-DDD) is the standard treatment for advanced adrenocortical carcinoma (ACC). Monitoring of plasma mitotane levels is recommended to look for a therapeutic window between 14 and 20mg/L, but its positive predictive value requires optimi
Externí odkaz:
https://doaj.org/article/fcc16fee6df7425e933211f6f87f4929
Autor:
Fanny Chasseloup, Lucie Tosca, Daniela Regazzo, Alexis Proust, Mirella Hage, Emmanuelle Kuhn, Christel Jublanc, Karima Mokhtari, Sylvie Salenave, Stephan Gaillard, Fabrice Parker, Anne-Laure Boch, Gerard Tachdjian, Philippe Chanson, Jerome Bouligand, Gianluca Occhi, Peter Kamenicky
Publikováno v:
Endocrine Abstracts.
Autor:
Lucas Bouys, Anna Vaczlavik, Anne Jouinot, Patricia Vaduva, Stéphanie Espiard, Guillaume Assié, Rossella Libé, Karine Perlemoine, Bruno Ragazzon, Laurence Guignat, Lionel Groussin, Léopoldine Bricaire, Isadora Pontes Cavalcante, Fidéline Bonnet-Serrano, Hervé Lefebvre, Marie-Laure Raffin-Sanson, Nicolas Chevalier, Philippe Touraine, Christel Jublanc, Camille Vatier, Gérald Raverot, Magalie Haissaguerre, Luigi Maione, Matthias Kroiss, Martin Fassnacht, Sophie Christin-Maitre, Eric Pasmant, Françoise Borson-Chazot, Antoine Tabarin, Marie-Christine Vantyghem, Martin Reincke, Peter Kamenicky, Marie-Odile North, Jérôme Bertherat
Publikováno v:
European Journal of Endocrinology
European Journal of Endocrinology, 2023, 187 (1), pp.123-134. ⟨10.1530/EJE-21-1032⟩
European Journal of Endocrinology, 2023, 187 (1), pp.123-134. ⟨10.1530/EJE-21-1032⟩
Objective Primary bilateral macronodular adrenal hyperplasia (PBMAH) is a heterogeneous disease characterized by adrenal macronodules and variable levels of cortisol excess, with not clearly established clinical diagnostic criteria. It can be caused
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4ab77e760f69441c1b7b0476dbc775fe
https://hal.science/hal-03982784/document
https://hal.science/hal-03982784/document
Autor:
Pauline Dodet, Camille Noiray, Smaranda Leu-Semenescu, Etienne Lefevre, Milan Nigam, Pauline Faucher, Jean-Baptiste Maranci, Christel Jublanc, Christine Poitou, Isabelle Arnulf
Publikováno v:
SLEEP. 46
Study Objectives To evaluate sleep, sleepiness, and excessive need for sleep in patients with craniopharyngioma (a suprasellar tumor which can affect sleep–wake systems). Methods A retrospective study of all adult patients living with craniopharyng
Autor:
Francesca Branzoli, Betty Salgues, Małgorzata Marjańska, Marie Laloi-Michelin, Philippe Herman, Lauriane Le Collen, Brigitte Delemer, Julien Riancho, Emmanuelle Kuhn, Christel Jublanc, Nelly Burnichon, Laurence Amar, Judith Favier, Anne-Paule Gimenez-Roqueplo, Alexandre Buffet, Charlotte Lussey-Lepoutre
Publikováno v:
Endocr Relat Cancer
Germline mutations in genes encoding succinate dehydrogenase (SDH) are frequently involved in pheochromocytoma/paraganglioma (PPGL) development and were implicated in patients with the ‘3PAs’ syndrome (associating pituitary adenoma (PA) and PPGL)
Autor:
Séverine Trabado, Pierre G. Carlier, Benjamin Marty, Jacques Young, Christel Jublanc, Peter Kamenický, Hélène Agostini, Bruno Fève, Philippe Chanson, Céline Droumaguet, Nadjia Kachenoura, Anne-Lise Lecoq, Alban Redheuil, Mikaël Prigent, Sylvie Salenave, Khaoula Bouazizi, Christiane Ajzenberg, Celine Piedvache, Anne Blanchard, Peter Wolf, Emmanuelle Kuhn
Publikováno v:
Journal of Clinical Endocrinology and Metabolism
Journal of Clinical Endocrinology and Metabolism, 2021, 185 (2), pp.299-311. ⟨10.1210/clinem/dgab556⟩
Journal of Clinical Endocrinology and Metabolism, Endocrine Society, 2021, ⟨10.1210/clinem/dgab556⟩
Journal of Clinical Endocrinology and Metabolism, 2021, 185 (2), pp.299-311. ⟨10.1210/clinem/dgab556⟩
Journal of Clinical Endocrinology and Metabolism, Endocrine Society, 2021, ⟨10.1210/clinem/dgab556⟩
Context Cardiovascular disease is the leading cause of death in patients with Cushing syndrome. Cortisol excess and adverse metabolic profile could increase cardiac fat, which can subsequently impair cardiac structure and function. Objective We aimed
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5dd58bc56a1427f5fce2d2b351546c12
https://hal.science/hal-04021022
https://hal.science/hal-04021022
Autor:
Natacha Driessens, Caroline Storey, Frédéric Illouz, Laurence Amar, Hervé Lefebvre, Marie-Christine Vantyghem, Jérôme Bertherat, Laurent Brunaud, Eric Baudin, Peggy Renoult-Pierre, Isabelle Raingeard, Delphine Vezzosi, Emmanuelle Vidal-Petiot, Nicolas Chevalier, Marie-Laure Raffin-Sanson, Antoine-Guy Lopez, Bénédicte Decoudier, Michel Peuchmaur, Christel Jublanc, Delphine Drui, Pierre Goudet, Sophie Christin-Maitre, Antoine Tabarin, Aurelien Morini, Christiane Ajzenberg, Elisa Deflorenne, O. Gilly, Charlotte Lussey
Publikováno v:
European journal of endocrinology. 185(4)
Objective Adrenal ganglioneuromas are rare, differentiated, neuroblastic tumors that originate from the peripheral sympathetic nervous system. Because of their rarity, information is limited, derived from small cases series. Our objective was to char
Autor:
Emmanuelle Kuhn, Sylvie Salenave, Khaoula Bouazizi, Benjamin Marty, Christel Jublanc, Hélène Agostini, Peter Kamenický, Nadjia Kachenoura, Peter Wolf, Pierre G. Carlier, Alban Redheuil, Bruno Fève, Jacques Young, Celine Piedvache, Mikaël Prigent, Philippe Chanson, Anne Blanchard, Christiane Ajzenberg, Céline Droumaguet, Séverine Trabado, Anne-Lise Lecoq
Publikováno v:
The Journal of Clinical Endocrinology & Metabolism. 107:e443-e444
Autor:
Capucine Morélot Panzini, Philippe Corcia, Claude Desnuelle, Karim Wahbi, Emilien Bernard, Giorgia Querin, François Salachas, Peter Bede, Christophe Vial, Pierre-François Pradat, Christel Jublanc, Philippe Couratier
Publikováno v:
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases, BioMed Central, 2020, 15 (1), pp.90. ⟨10.1186/s13023-020-01366-z⟩
Orphanet Journal of Rare Diseases, 2020, 15 (1), pp.90. ⟨10.1186/s13023-020-01366-z⟩
Orphanet Journal of Rare Diseases, Vol 15, Iss 1, Pp 1-21 (2020)
Orphanet Journal of Rare Diseases, BioMed Central, 2020, 15 (1), pp.90. ⟨10.1186/s13023-020-01366-z⟩
Orphanet Journal of Rare Diseases, 2020, 15 (1), pp.90. ⟨10.1186/s13023-020-01366-z⟩
Orphanet Journal of Rare Diseases, Vol 15, Iss 1, Pp 1-21 (2020)
Background Kennedy’s disease (KD), also known as spinal and bulbar muscular atrophy (SBMA), is a rare, adult-onset, X-linked recessive neuromuscular disease caused by CAG expansions in exon 1 of the androgen receptor gene (AR). The objective of the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e3b5d0d6bd05f5af6caec13490e8a2e0
https://hal-unilim.archives-ouvertes.fr/hal-02868801
https://hal-unilim.archives-ouvertes.fr/hal-02868801