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

Case Report: Scurvy-a modifiable cause of psychiatric refractoriness and lithium pharmacokinetic abnormalities in autism

病例报告:坏血病——自闭症患者精神疾病难治性和锂药代动力学异常的可控病因

Geiser, Marie; Guggisberg, Nicolas; Convertini, Josephine; Crettol, Severine; Ansermot, Nicolas; Guinchat, Vincent

Case report: Case series of urinary retention in young adults with severe autism hospitalized for behavioral crisis

病例报告:重度自闭症青年因行为危机住院治疗期间发生尿潴留的病例系列

Nollace, Leslie; Panagiotis, Drolapas; Convertini, Josephine; Grilo, Nuno; Ansermot, Nicolas; Guinchat, Vincent

Pregabalin treatment in a 30-year-old patient with Bainbridge-Ropers syndrome: a case-report

普瑞巴林治疗一名30岁Bainbridge-Ropers综合征患者的病例报告

Geiser, Marie; Good, Jean-Marc; Guinchat, Vincent

Case Report: Opioid Use Disorder Associated With Low/Moderate Dose of Loperamide in an Intellectual Disability Patient With CYP3A and P-Glycoprotein Reduced Activity

病例报告:一名智力障碍患者因服用低/中剂量洛哌丁胺而出现阿片类药物使用障碍,该患者CYP3A和P-糖蛋白活性降低

Guinchat, Vincent; Ansermot, Nicolas; Ing Lorenzini, Kuntheavy; Politis, Dimitri; Daali, Youssef; Eap, Chin B; Crettol, Séverine

Compressive Garments in Individuals with Autism and Severe Proprioceptive Dysfunction: A Retrospective Exploratory Case Series

自闭症伴严重本体感觉功能障碍患者的压力服治疗:回顾性探索性病例系列研究

Guinchat, Vincent; Vlamynck, Elodie; Diaz, Lautaro; Chambon, Coralie; Pouzenc, Justine; Cravero, Cora; Baeza-Velasco, Carolina; Hamonet, Claude; Xavier, Jean; Cohen, David

Management of Severe Developmental Regression in an Autistic Child with a 1q21.3 Microdeletion and Self-Injurious Blindness

对患有1q21.3微缺失和自伤性失明的自闭症儿童的严重发育倒退进行管理

Cravero, Cora; Guinchat, Vincent; Xavier, Jean; Meunier, Camille; Diaz, Lautaro; Mignot, Cyril; Doummar, Diane; Chantot-Bastaraud, Sandra; Consoli, Angèle; Cohen, David

Genetic and functional analyses demonstrate a role for abnormal glycinergic signaling in autism

遗传和功能分析表明,异常的甘氨酸能信号传导在自闭症中发挥作用

Pilorge, M; Fassier, C; Le Corronc, H; Potey, A; Bai, J; De Gois, S; Delaby, E; Assouline, B; Guinchat, V; Devillard, F; Delorme, R; Nygren, G; Råstam, M; Meier, J C; Otani, S; Cheval, H; James, V M; Topf, M; Dear, T N; Gillberg, C; Leboyer, M; Giros, B; Gautron, S; Hazan, J; Harvey, R J; Legendre, P; Betancur, C

Paracentric inversion of chromosome 2 associated with cryptic duplication of 2q14 and deletion of 2q37 in a patient with autism

一名自闭症患者存在2号染色体臂间倒位,伴有2q14隐匿性重复和2q37缺失

Devillard, Françoise; Guinchat, Vincent; Moreno-De-Luca, Daniel; Tabet, Anne-Claude; Gruchy, Nicolas; Guillem, Pascale; Nguyen Morel, Marie-Ange; Leporrier, Nathalie; Leboyer, Marion; Jouk, Pierre-Simon; Lespinasse, James; Betancur, Catalina