日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

The role of LEAP2 on cognitive impulsivity after refeeding: evidence from a preclinical study in female mice and from patients with anorexia nervosa

LEAP2 在再喂养后对认知冲动性的影响:来自雌性小鼠临床前研究和神经性厌食症患者的证据

Tezenas du Montcel, Chloé; Hamelin, Héloïse; Lebrun, Nicolas; Duriez, Philibert; Ramoz, Nicolas; Gorwood, Philip; Viltart, Odile; Tolle, Virginie

Unraveling the brain expression of bdnf in a mouse model of anorexia nervosa

揭示神经性厌食症小鼠模型中脑内bdnf的表达

Cao, Jingxian; Lebrun, Nicolas; Chen, Shiou-Ping; Tezenas du Montcel, Chloé; Gorwood, Philip; Cruciani-Guglielmacci, Céline; Tolle, Virginie; Ramoz, Nicolas; Viltart, Odile

Assessing biomarkers of remission in female patients with anorexia nervosa (REMANO): a protocol for a prospective cohort study with a nested case-control study using clinical, neurocognitive, biological, genetic, epigenetic and neuroimaging markers in a French specialised inpatient unit

评估女性神经性厌食症患者缓解期生物标志物(REMANO):一项前瞻性队列研究方案,其中包含一项嵌套病例对照研究,该研究在法国一家专科住院病房中使用了临床、神经认知、生物学、遗传学、表观遗传学和神经影像学标志物。

Duriez, Philibert; Tolle, Virginie; Ramoz, Nicolas; Kimmel, Etienne; Charron, Sylvain; Viltart, Odile; Lebrun, Nicolas; Bienvenu, Thierry; Fadigas, Marie; Oppenheim, Catherine; Gorwood, Philip

The role of dysregulated ghrelin/LEAP-2 balance in anorexia nervosa

生长素释放肽/LEAP-2 平衡失调在神经性厌食症中的作用

Chloé Tezenas du Montcel, Philibert Duriez, Jingxian Cao, Nicolas Lebrun, Nicolas Ramoz, Odile Viltart, Philip Gorwood, Virginie Tolle

[Amiodarone or COVID induced-pneumopathy: One train can hide another one!]

【胺碘酮或新冠病毒诱发性肺炎:一列火车可能掩盖另一列火车!】

Vasseur, Mélanie; Tambon, Marine; Gony, Mireille; Lebrun, Nicolas; Bagheri, Haleh

MN1 C-terminal truncation syndrome is a novel neurodevelopmental and craniofacial disorder with partial rhombencephalosynapsis

MN1 C端截断综合征是一种新型的神经发育和颅面疾病,伴有部分菱脑融合。

Mak, Christopher C Y; Doherty, Dan; Lin, Angela E; Vegas, Nancy; Cho, Megan T; Viot, Géraldine; Dimartino, Clémantine; Weisfeld-Adams, James D; Lessel, Davor; Joss, Shelagh; Li, Chumei; Gonzaga-Jauregui, Claudia; Zarate, Yuri A; Ehmke, Nadja; Horn, Denise; Troyer, Caitlin; Kant, Sarina G; Lee, Youngha; Ishak, Gisele E; Leung, Gordon; Barone Pritchard, Amanda; Yang, Sandra; Bend, Eric G; Filippini, Francesca; Roadhouse, Chelsea; Lebrun, Nicolas; Mehaffey, Michele G; Martin, Pierre-Marie; Apple, Benjamin; Millan, Francisca; Puk, Oliver; Hoffer, Mariette J V; Henderson, Lindsay B; McGowan, Ruth; Wentzensen, Ingrid M; Pei, Steven; Zahir, Farah R; Yu, Mullin; Gibson, William T; Seman, Ann; Steeves, Marcie; Murrell, Jill R; Luettgen, Sabine; Francisco, Elizabeth; Strom, Tim M; Amlie-Wolf, Louise; Kaindl, Angela M; Wilson, William G; Halbach, Sara; Basel-Salmon, Lina; Lev-El, Noa; Denecke, Jonas; Vissers, Lisenka E L M; Radtke, Kelly; Chelly, Jamel; Zackai, Elaine; Friedman, Jan M; Bamshad, Michael J; Nickerson, Deborah A; Reid, Russell R; Devriendt, Koenraad; Chae, Jong-Hee; Stolerman, Elliot; McDougall, Carey; Powis, Zöe; Bienvenu, Thierry; Tan, Tiong Y; Orenstein, Naama; Dobyns, William B; Shieh, Joseph T; Choi, Murim; Waggoner, Darrel; Gripp, Karen W; Parker, Michael J; Stoler, Joan; Lyonnet, Stanislas; Cormier-Daire, Valérie; Viskochil, David; Hoffman, Trevor L; Amiel, Jeanne; Chung, Brian H Y; Gordon, Christopher T

SAT-279 Crooke’s Cell Adenoma- an Aggressive Form of Cushing’s Disease

SAT-279 克鲁克细胞腺瘤——一种侵袭性库欣病

Hassouna, Rim; Fernandez, Gimena; Lebrun, Nicolas; Fiquet, Oriane; Roelfsema, Ferdinand; Labarthe, Alexandra; Zizzari, Philippe; Tomasetto, Catherine; Epelbaum, Jacques; Viltart, Odile; Chauveau, Christophe; Perello, Mario; Tolle, Virginie; Patel, Goonja S; Prater, Janna; Seki, Yasufumi; Morimoto, Satoshi; Bokuda, Kanako; Watanabe, Daisuke; Watanabe, Satoshi; Yamashita, Kaoru; Takano, Noriyoshi; Ichihara, Atsuhiro; Magar, Maria; Radovanovic, Natasa; Alexa, Yuen; Tabatabaie, Vafa

Mosaic parental germline mutations causing recurrent forms of malformations of cortical development

亲代生殖细胞嵌合突变导致皮质发育畸形的复发性表现

Zillhardt, Julia Lauer; Poirier, Karine; Broix, Loïc; Lebrun, Nicolas; Elmorjani, Adrienne; Martinovic, Jelena; Saillour, Yoann; Muraca, Giuseppe; Nectoux, Juliette; Bessieres, Bettina; Fallet-Bianco, Catherine; Lyonnet, Stanislas; Dulac, Olivier; Odent, Sylvie; Rejeb, Imen; Ben Jemaa, Lamia; Rivier, Francois; Pinson, Lucile; Geneviève, David; Musizzano, Yuri; Bigi, Nicole; Leboucq, Nicolas; Giuliano, Fabienne; Philip, Nicole; Vilain, Catheline; Van Bogaert, Patrick; Maurey, Hélène; Beldjord, Cherif; Artiguenave, François; Boland, Anne; Olaso, Robert; Masson, Cécile; Nitschké, Patrick; Deleuze, Jean-François; Bahi-Buisson, Nadia; Chelly, Jamel

Variants in CUL4B are associated with cerebral malformations.

CUL4B基因变异与脑畸形有关

Vulto-van Silfhout Anneke T, Nakagawa Tadashi, Bahi-Buisson Nadia, Haas Stefan A, Hu Hao, Bienek Melanie, Vissers Lisenka E L M, Gilissen Christian, Tzschach Andreas, Busche Andreas, Müsebeck Jörg, Rump Patrick, Mathijssen Inge B, Avela Kristiina, Somer Mirja, Doagu Fatma, Philips Anju K, Rauch Anita, Baumer Alessandra, Voesenek Krysta, Poirier Karine, Vigneron Jacqueline, Amram Daniel, Odent Sylvie, Nawara Magdalena, Obersztyn Ewa, Lenart Jacek, Charzewska Agnieszka, Lebrun Nicolas, Fischer Ute, Nillesen Willy M, Yntema Helger G, Järvelä Irma, Ropers Hans-Hilger, de Vries Bert B A, Brunner Han G, van Bokhoven Hans, Raymond F Lucy, Willemsen Michèl A A P, Chelly Jamel, Xiong Yue, Barkovich A James, Kalscheuer Vera M, Kleefstra Tjitske, de Brouwer Arjan P M

Novel IL1RAPL1 mutations associated with intellectual disability impair synaptogenesis

与智力障碍相关的IL1RAPL1新突变会损害突触发生

Ramos-Brossier, Mariana; Montani, Caterina; Lebrun, Nicolas; Gritti, Laura; Martin, Christelle; Seminatore-Nole, Christine; Toussaint, Aurelie; Moreno, Sarah; Poirier, Karine; Dorseuil, Olivier; Chelly, Jamel; Hackett, Anna; Gecz, Jozef; Bieth, Eric; Faudet, Anne; Heron, Delphine; Frank Kooy, R; Loeys, Bart; Humeau, Yann; Sala, Carlo; Billuart, Pierre