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

The Burden of Congenital Hypothyroidism Without Newborn Screening: Clinical and Cognitive Findings from a Multicenter Study in Algeria

未进行新生儿筛查的先天性甲状腺功能减退症的负担：阿尔及利亚一项多中心研究的临床和认知发现

期刊:International Journal of Neonatal Screening
影响因子:4
doi:10.3390/ijns11030078
Djermane, Adel; Ouarezki, Yasmine; Boulesnane, Kamelia; Kherra, Sakina; Bouferoua, Fadila; Bessahraoui, Mimouna; Selim, Nihad; Djahlat, Larbi; Mohammedi, Kahina; Bouziane Nedjadi, Karim; Abes, Hakima; Bensalah, Meriem; Lograb, Dyaeddine; Abdelaziz, Foued; Douiri, Dalila; Djebari, Soumia; Demdoum, Mohamed Seghir; Rouabeh, Nadira; Oussalah, Meriem; Van Vliet, Guy; Ladjouze, Asmahane
甲状腺功能减退
神经科学
免疫/内分泌
发表日期：2025
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Genotype, Mortality, Morbidity, and Outcomes of 3β-Hydroxysteroid Dehydrogenase Deficiency in Algeria

阿尔及利亚3β-羟类固醇脱氢酶缺乏症的基因型、死亡率、发病率和预后

期刊:Frontiers in Endocrinology
影响因子:4.6
doi:10.3389/fendo.2022.867073
Ladjouze, Asmahane; Donaldson, Malcolm; Plotton, Ingrid; Djenane, Nacima; Mohammedi, Kahina; Tardy-Guidollet, Véronique; Mallet, Delphine; Boulesnane, Kamélia; Bouzerar, Zair; Morel, Yves; Roucher-Boulez, Florence
发表日期：2022
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Novel Genomic Variants, Atypical Phenotypes and Evidence of a Digenic/Oligogenic Contribution to Disorders/Differences of Sex Development in a Large North African Cohort

北非大型队列研究中发现的新型基因组变异、非典型表型以及双基因/寡基因对性发育障碍/差异的贡献证据

期刊:Frontiers in Genetics
影响因子:2.8
doi:10.3389/fgene.2022.900574
Zidoune, Housna; Ladjouze, Asmahane; Chellat-Rezgoune, Djalila; Boukri, Asma; Dib, Scheher Aman; Nouri, Nassim; Tebibel, Meryem; Sifi, Karima; Abadi, Noureddine; Satta, Dalila; Benelmadani, Yasmina; Bignon-Topalovic, Joelle; El-Zaiat-Munsch, Maeva; Bashamboo, Anu; McElreavey, Ken
发育与干细胞
发表日期：2022
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Access to fludrocortisone and to hydrocortisone in children with congenital adrenal hyperplasia in the WHO Eastern Mediterranean Region: it takes a village…

世界卫生组织东地中海区域先天性肾上腺皮质增生症患儿获得氟氢可的松和氢化可的松的途径：这需要整个社区的共同努力……

期刊:Bmj Global Health
影响因子:6.1
doi:10.1136/bmjgh-2021-007195
Rowlands, Amanda; Deeb, Asma; Ladjouze, Asmahane; Hamza, Rasha T; Musa, Salwa A; Raza, Jamal; Jennane, Farida; Abu-Libdeh, Abdulsalam; Chanoine, Jean-Pierre
免疫/内分泌
发表日期：2021
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Ankylosing spondylitis: analysis of gene-gene interactions between IL-12β, JAK2, and STAT3 in Han Chinese and Algerian cohorts

强直性脊柱炎：汉族和阿尔及利亚人群中IL-12β、JAK2和STAT3基因间相互作用的分析

期刊:Central European Journal of Immunology
影响因子:1.6
doi:10.5114/ceji.2019.84019
Saadi, Ahlem; Dang, Jie; Shan, Shan; Ladjouze-Rezig, Aicha; Lefkir-Tafiani, Salima; Gong, Yaoqin; Liu, Qiji; Benhassine, Traki
JAK/STAT
JAK2
STAT3
强直性脊柱炎
免疫/内分泌
发表日期：2019
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The Prevalence of Non-radiographic Axial Spondyloarthritis Among Patients with Inflammatory Back Pain from Northwest and South Africa: Data from a Noninterventional, Cross-Sectional Study

西北非洲和南非炎症性背痛患者中非放射性中轴型脊柱关节炎的患病率：一项非干预性横断面研究的数据

期刊:Rheumatology and Therapy
影响因子:2.9
doi:10.1007/s40744-018-0122-6
Shirazy, Khalid; Hajjaj-Hassouni, Najia; Hammond, Constance; Jones, Heather; Ladjouze Rezig, Aicha; Pedersen, Ron; Vlahos, Bonnie
炎症/感染
关节炎
炎症
发表日期：2018
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Familial Multiplicity of Estrogen Insensitivity Associated With a Loss-of-Function ESR1 Mutation

与 ESR1 功能丧失突变相关的家族性多发性雌激素不敏感症

期刊:Journal of Clinical Endocrinology & Metabolism
影响因子:5.1
doi:10.1210/jc.2016-2749
Bernard, Valérie; Kherra, Sakina; Francou, Bruno; Fagart, Jérôme; Viengchareun, Say; Guéchot, Jérôme; Ladjouze, Asmahane; Guiochon-Mantel, Anne; Korach, Kenneth S; Binart, Nadine; Lombès, Marc; Christin-Maitre, Sophie
免疫/内分泌
发表日期：2017
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Successful treatment of Acrodermatitis continua of Hallopeau associated with psoriatic arthritis with adalimumab

阿达木单抗成功治疗与银屑病关节炎相关的哈洛波肢端皮炎

期刊:European Journal of Rheumatology
影响因子:1.8
doi:10.5152/eurjrheum.2015.0072
Lefkir, Salima; Slimani, Samy; Brahimi, Nadjia; Ladjouze-Rezig, Aicha
关节炎
银屑病
发表日期：2015
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