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

Identifying Therapeutic Targets for Amyotrophic Lateral Sclerosis Through Modeling of Multi-Omics Data

通过多组学数据建模识别肌萎缩侧索硬化症的治疗靶点

Blaudin de Thé, François Xavier; Klemann, Cornelius J H M; De Witte, Ward; Widomska, Joanna; Delagrange, Philippe; Mannoury La Cour, Clotilde; Fouesnard, Mélanie; Elouej, Sahar; Mayl, Keith; Lévy, Nicolas; Krupp, Johannes; Jeggo, Ross; Moingeon, Philippe; Poelmans, Geert

AB040. Subclinical myasthenia gravis after thymectomy: a 20-year retrospective cohort study

AB040. 胸腺切除术后亚临床重症肌无力:一项20年回顾性队列研究

Balasubramanian, Meena; Dingemans, Alexander J M; Albaba, Shadi; Richardson, Ruth; Yates, Thabo M; Cox, Helen; Douzgou, Sofia; Armstrong, Ruth; Sansbury, Francis H; Burke, Katherine B; Fry, Andrew E; Ragge, Nicola; Sharif, Saba; Foster, Alison; De Sandre-Giovannoli, Annachiara; Elouej, Sahar; Vasudevan, Pradeep; Mansour, Sahar; Wilson, Kate; Stewart, Helen; Heide, Solveig; Nava, Caroline; Keren, Boris; Demirdas, Serwet; Brooks, Alice S; Vincent, Marie; Isidor, Bertrand; Küry, Sebastien; Schouten, Meyke; Leenders, Erika; Chung, Wendy K; Haeringen, Arie van; Scheffner, Thomas; Debray, Francois-Guillaume; White, Susan M; Palafoll, Maria Irene Valenzuela; Pfundt, Rolph; Newbury-Ecob, Ruth; Kleefstra, Tjitske; Marcuse, Florit; Hoeijmakers, Janneke; Abdul Hamid, Myrurgia; Romeo, Jamie; Maessen, Jos; Peeters, Stephanie; Damoiseaux, Jan; Martinez, Pilar; Hochstenbag, Monique; De Baets, Marc

Antibody-mediated neutralization of galectin-3 as a strategy for the treatment of systemic sclerosis

抗体介导的半乳糖凝集素-3中和作用作为治疗系统性硬化症的一种策略

Céline Ortega-Ferreira # ,Perrine Soret # ,Gautier Robin ,Silvia Speca ,Sandra Hubert ,Marianne Le Gall ,Emiko Desvaux ,Manel Jendoubi ,Julie Saint-Paul ,Loubna Chadli ,Agnès Chomel ,Sylvie Berger ,Emmanuel Nony ,Béatrice Neau ,Benjamin Fould ,Anne Licznar ,Franck Levasseur ,Thomas Guerrier ,Sahar Elouej ,Sophie Courtade-Gaïani ,Nicolas Provost ,The Quyen Nguyen ,Julien Verdier ,David Launay ,Frédéric De Ceuninck

Association of HNF1A gene variants and haplotypes with metabolic syndrome: a case-control study in the Tunisian population and a meta-analysis

HNF1A基因变异和单倍型与代谢综合征的关联:一项突尼斯人群病例对照研究和荟萃分析

Dallali, Hamza; Hechmi, Meriem; Morjane, Imane; Elouej, Sahar; Jmel, Haifa; Ben Halima, Yosra; Abid, Abdelmajid; Bahlous, Afef; Barakat, Abdelhamid; Jamoussi, Henda; Abdelhak, Sonia; Kefi, Rym

A Rare MSH2 Variant as a Candidate Marker for Lynch Syndrome II Screening in Tunisia: A Case of Diffuse Gastric Carcinoma

突尼斯一种罕见的 MSH2 变异体作为林奇综合征 II 筛查的候选标记:一例弥漫性胃癌

Maria Kabbage, Jihenne Ben Aissa-Haj, Houcemeddine Othman, Amira Jaballah-Gabteni, Sarra Laarayedh, Sahar Elouej, Mouna Medhioub, Haifa Tounsi Kettiti, Amal Khsiba, Moufida Mahmoudi, Houda BelFekih, Afifa Maaloul, Hassen Touinsi, Lamine Hamzaoui, Emna Chelbi, Sonia Abdelhak, Mohamed Samir Boubaker, 

The Potential of Induced Pluripotent Stem Cells to Test Gene Therapy Approaches for Neuromuscular and Motor Neuron Disorders

诱导多能干细胞在神经肌肉和运动神经元疾病基因治疗方法测试中的应用潜力

Cappella, Marisa; Elouej, Sahar; Biferi, Maria Grazia

Case Report: Identification of Novel Variants in ERCC4 and DDB2 Genes in Two Tunisian Patients With Atypical Xeroderma Pigmentosum Phenotype

病例报告:在两名突尼斯非典型着色性干皮病患者中鉴定出ERCC4和DDB2基因的新变异

Nabouli, Imen; Chikhaoui, Asma; Othman, Houcemeddine; Elouej, Sahar; Jones, Meriem; Lagarde, Arnaud; Rekaya, Meriem Ben; Messaoud, Olfa; Zghal, Mohamed; Delague, Valerie; Levy, Nicolas; De Sandre-Giovannoli, Annachiara; Abdelhak, Sonia; Yacoub-Youssef, Houda

Oligogenic Inheritance Underlying Incomplete Penetrance of PROKR2 Mutations in Hypogonadotropic Hypogonadism

低促性腺激素性性腺功能减退症中PROKR2突变不完全外显的寡基因遗传基础

Mkaouar, Rahma; Abdallah, Lamia Cherif Ben; Naouali, Chokri; Lahbib, Saida; Turki, Zinet; Elouej, Sahar; Bouyacoub, Yosra; Somai, Maali; Mcelreavey, Kenneth; Bashamboo, Anu; Abdelhak, Sonia; Messaoud, Olfa

Author Correction: Loss of MTX2 causes mandibuloacral dysplasia and links mitochondrial dysfunction to altered nuclear morphology

作者更正:MTX2 缺失导致下颌肢端发育不良,并将线粒体功能障碍与核形态改变联系起来

Elouej, Sahar; Harhouri, Karim; Mao, Morgane Le; Baujat, Genevieve; Nampoothiri, Sheela; Kayserili, Hϋlya; Menabawy, Nihal Al; Selim, Laila; Paneque, Arianne Llamos; Kubisch, Christian; Lessel, Davor; Rubinsztajn, Robert; Charar, Chayki; Bartoli, Catherine; Airault, Coraline; Deleuze, Jean-François; Rötig, Agnes; Bauer, Peter; Pereira, Catarina; Loh, Abigail; Escande-Beillard, Nathalie; Muchir, Antoine; Martino, Lisa; Gruenbaum, Yosef; Lee, Song-Hua; Manivet, Philippe; Lenaers, Guy; Reversade, Bruno; Lévy, Nicolas; De Sandre-Giovannoli, Annachiara

Loss of MTX2 causes mandibuloacral dysplasia and links mitochondrial dysfunction to altered nuclear morphology

MTX2 缺失导致下颌骨发育不良,并将线粒体功能障碍与核形态改变联系起来

Sahar Elouej #, Karim Harhouri #, Morgane Le Mao, Genevieve Baujat, Sheela Nampoothiri, Hϋlya Kayserili, Nihal Al Menabawy, Laila Selim, Arianne Llamos Paneque, Christian Kubisch, Davor Lessel, Robert Rubinsztajn, Chayki Charar, Catherine Bartoli, Coraline Airault, Jean-François Deleuze, Agnes Rötig