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

Rare STAT1 variants in Moroccan tuberculosis patients: insights into host genetic susceptibility

摩洛哥结核病患者中罕见的STAT1变异:对宿主遗传易感性的启示

Zaidi, Sanae; Rafik, Aniss; Skhoun, Hanaa; Elkarhat, Zouhair; Guennoun, Aya; Tabehout, Fatima; Errami, Abderrahmane; Abid, Ahmed; Abderrhamani Ghorfi, Ismail; El Ouazzani, Hanane; Souhi, Hicham; Zegmout, Adil; El Hassani, Amal; Ailal, Fatima; Abilkassem, Rachid; Ouzzif, Zohra; Benhsaien, Ibtihal; Bousfiha, Ahmed Aziz; El Baghdadi, Jamila

Fatal Hemorrhagic Rupture of a Cystic Hepatic Hemangioma in a 27-Week Preterm Neonate

27周早产新生儿肝囊性血管瘤出血性破裂致死

El Athmani, Omayma; Saghir, Salah; Azzakhmam, Mustapha; Ayad, Anas; Abilkassem, Rachid

Type 3 Von Willebrand disease: two clinical cases of a rare disorder

型血管性血友病:两例罕见疾病的临床病例

Belcadi Abassi, Khadija; Larbi Ouassou, Karima; Radi, Abdelilah; Laaraje, Azzdine; Babour, Sara; Ait Hmadouch, Soukaina; Hassani, Amale; Khorassani, Mohammed E L; Abilkassem, Rachid

Novel ANKRD11 Mutation in KBG Syndrome: A diagnostic triad of hearing loss, radiological macrodontia and artificial intelligence-assisted facial phenotyping

KBG综合征中ANKRD11基因的新型突变:听力丧失、放射学巨牙症和人工智能辅助面部表型分析的诊断三联征

Laaraje, Azzeddine; Belcadi Abassi, Khadija; Lemaamer, Mouna; Radi, Abdelilah; Hassani, Amale; Abilkassem, Rachid

Thymic Hyperplasia Mimicking Lymphoma in a Pediatric Patient: A Case Report

儿童患者胸腺增生酷似淋巴瘤:病例报告

Belcadi Abassi, Khadija; Laaraje, Azzeddine; Abdelilah, Radi; Abilkassem, Rachid Sr

Griscelli Syndrome Type 2 Revealed by Macrophage Activation Syndrome: Two Cases From the Same Family

巨噬细胞活化综合征揭示格里塞利综合征2型:同一家族的两例病例

Halimy, Boutayna; Radi, Abdelilah; Laaraje, Azzeddine; Amale, Hassani; Abilkassem, Rachid

The Pena-Shokeir Syndrome in a Twin Pregnancy: A Rare Case Report

双胎妊娠中的佩纳-肖凯尔综合征:一例罕见病例报告

El Gazzane, Souhaila; Saghir, Salahiddine; Bahous, Mehdi; Sellouti, Mohamed; Ayad, Anass; Abilkassem, Rachid

First case of infective endocarditis due to NDM-type carbapenemase-producing Serratia marcescens in a preterm infant: a case report

首例由产NDM型碳青霉烯酶的粘质沙雷氏菌引起的早产儿感染性心内膜炎病例报告

Malihy, Zakaria; El Abdallaoui, Ikram; Abassor, Tilila; Sghir, Salah; Ben Lahlou, Yassine; Abilkassem, Rachid; Benaissa, Elmostafa; Chadli, Mariama

Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay with Early-Onset Epilepsy and Novel Clinical Features: A rare entity from Morocco in the Middle East and North Africa region

伴有早发性癫痫和新型临床特征的沙勒沃伊-萨格奈常染色体隐性痉挛性共济失调:一种来自中东和北非地区摩洛哥的罕见疾病

Laaraje, Azzeddine; Alaoui, Basma; Radi, Abdelilah; Hasani, Amal; Agadr, Aomar; Abilkassem, Rachid

Complicated meconium ileus in a male neonate with cystic fibrosis: Case report

囊性纤维化男婴并发复杂性胎粪性肠梗阻:病例报告

Sellouti, Mohamed; Agadr, Aomar; Abilkassem, Rachid