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

The safety and efficacy of umbilical cord blood mononuclear cells in individuals with spastic cerebral palsy: a randomized double-blind sham-controlled clinical trial

脐带血单核细胞治疗痉挛型脑瘫患者的安全性和有效性:一项随机、双盲、假手术对照临床试验

Zarrabi, Morteza; Akbari, Masood Ghahvechi; Amanat, Man; Majmaa, Anahita; Moaiedi, Ali Reza; Montazerlotfelahi, Hadi; Nouri, Masoumeh; Hamidieh, Amir Ali; Badv, Reza Shervin; Karimi, Hossein; Rabbani, Ali; Mohebbi, Ali; Rahimi-Dehgolan, Shahram; Rahimi, Rosa; Dehghan, Ensieh; Vosough, Massoud; Abroun, Saeed; Shamsabadi, Farhad Mahvelati; Tavasoli, Ali Reza; Alizadeh, Houman; Pak, Neda; Zamani, Gholam Reza; Mohammadi, Mahmoud; Javadzadeh, Mohsen; Ghofrani, Mohammad; Hassanpour, Seyed Hossein; Heidari, Morteza; Taghdiri, Mohammad Mehdi; Mohseni, Mohamad Javad; Noparast, Zahra; Masoomi, Safdar; Goudarzi, Mehrdad; Mohamadpour, Masood; Shodjaee, Razieh; Samimi, Solaleh; Mohammad, Monireh; Gholami, Mona; Vafaei, Nahid; Koochakzadeh, Leyli; Valizadeh, Amir; Malamiri, Reza Azizi; Ashrafi, Mahmoud Reza

The preventive Effectiveness of Rituximab in Pediatric Autoimmune and Inflammatory CNS Diseases Relapse: an Iranian Experience

利妥昔单抗预防儿童自身免疫性和炎症性中枢神经系统疾病复发的疗效:伊朗的经验

Nasehi, Mohammad Mahdi; Ghofrani, Mohammad; Tabrizi, Aydin; Abdollah Gorji, Fatemeh; Khosravi, Bakhtyar

Epidemiology of Guillain-Barré Syndrome in Iranian Children Aged 0-15 Years (2008-2013)

伊朗0-15岁儿童格林-巴利综合征的流行病学研究(2008-2013年)

Tonekaboni, Seyed Hassan; Mahmoudi, Sussan; Abdollah Gorji, Fatemeh; Nejad Biglari, Habibe; Taghdiri, Mohammad Mahdi; Etemadi, Koroush; Ghofrani, Mohammad; Karimi, Abdollah; Rezaei Zadeh, Mohammad

Risk Factors of Pediatric Arterial Ischemic Stroke; A Regional Survey

儿童动脉缺血性卒中的危险因素:一项区域性调查

Ghofrani, Mohammad; Tonekaboni, Hassan; Karimzadeh, Parvaneh; Nasiri, Jafar; Pirzadeh, Zahra; Ghazzavi, Mohamadreza; Yghini, Omid

Homozygosity Mapping and Targeted Sanger Sequencing Identifies Three Novel CRB1 (Crumbs homologue 1) Mutations in Iranian Retinal Degeneration Families.

纯合性作图和靶向 Sanger 测序在伊朗视网膜变性家族中发现了三个新的 CRB1(Crumbs 同源物 1)突变

Ghofrani Mohammad, Yahyaei Mahin, Brunner Han G, Cremers Frans PM, Movasat Morteza, Imran Khan Muhammad, Keramatipour Mohammad

Whole Exome Sequencing Reveals a BSCL2 Mutation Causing Progressive Encephalopathy with Lipodystrophy (PELD) in an Iranian Pediatric Patient

全外显子组测序揭示伊朗一名儿科患者患有进行性脑病伴脂肪营养不良(PELD)的BSCL2基因突变

Alaei, Mohammad Reza; Talebi, Saeed; Ghofrani, Mohammad; Taghizadeh, Mohsen; Keramatipour, Mohammad