Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Nicolas Scheyer"'
Autor:
George Riley, Nicolas Scheyer, Marc Klein, Isabelle Merlot, Bruno Guerci, Elodie Jeanbert, Lea Demarquet
Publikováno v:
Frontiers in Endocrinology, Vol 14 (2024)
ObjectiveThe primary aim of this study was to identify predictive factors associated with onset of de-novo clinically significant pituitary insufficiencies following endoscopic endonasal surgery (EES) for pituitary adenomas. The secondary objective e
Externí odkaz:
https://doaj.org/article/58ce5be86b2b4d5f949a90a60d9771b0
Autor:
Marine Gérard, Meliha Mahmutovic, Aurélie Malgras, Niasha Michot, Nicolas Scheyer, Roland Jaussaud, Phi-Linh Nguyen-Thi, Didier Quilliot
Publikováno v:
Nutrients, Vol 13, Iss 11, p 3964 (2021)
Post-acute consequences of COVID-19, also termed long COVID, include signs and symptoms persisting for more than 12 weeks with prolonged multisystem involvement; most often, however, malnutrition is ignored. Method: The objective was to analyze persi
Externí odkaz:
https://doaj.org/article/f45f9361978347e592c4a8bcbe425ac1
Autor:
George Riley, Cecile Creton, Lea Demarquet, Perrine Raymond, Elodie Chevalier, Aurelien Lambert, Bruno Guerci, Marc Klein, Nicolas Scheyer
Publikováno v:
Endocrine Abstracts.
Publikováno v:
Diabetes Therapy
Introduction The COVID-19 pandemic led to an international health crisis and restrictions. While the phenotype associated with COVID-19 severity in people with diabetes has rapidly been explored, the impact of restrictive measures, including lockdown
Autor:
Lucie Coppin, Sophie Giraud, Eric Pasmant, Arnaud Lagarde, Marie-Odile North, Lauriane Le-Collen, Valérie Aubert, Grégory Mougel, Miriam Ladsous, Alyzée Louboutin, Hedia Brixi, Magalie Haissaguerre, Nicolas Scheyer, Marc Klein, Antoine Tabarin, Brigitte Delemer, Anne Barlier, Marie-Françoise Odou, Pauline Romanet
Publikováno v:
European Journal of Endocrinology
European Journal of Endocrinology, 2023, 187 (1), pp.K1-K6. ⟨10.1530/EJE-22-0171⟩
European Journal of Endocrinology, 2023, 187 (1), pp.K1-K6. ⟨10.1530/EJE-22-0171⟩
MEN1 is an autosomal dominant hereditary syndrome characterized by several endocrine tumors, in most cases affecting the parathyroid glands, pancreas, and anterior pituitary. It is the result of inactivating mutations in the tumor suppressor gene MEN
Autor:
Didier Quilliot, Niasha Michot, Roland Jaussaud, Phi-Linh Nguyen-Thi, Aurélie Malgras, Meliha Mahmutovic, Nicolas Scheyer, Marine Gérard
Publikováno v:
Nutrients
Volume 13
Issue 11
Nutrients, Vol 13, Iss 3964, p 3964 (2021)
Volume 13
Issue 11
Nutrients, Vol 13, Iss 3964, p 3964 (2021)
Post-acute consequences of COVID-19, also termed long COVID, include signs and symptoms persisting for more than 12 weeks with prolonged multisystem involvement
most often, however, malnutrition is ignored. Method: The objective was to analyze p
most often, however, malnutrition is ignored. Method: The objective was to analyze p