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

Prevalence of Asthma Symptoms and Environmental Triggers Among School-Aged Children in the Eastern Province of Saudi Arabia

沙特阿拉伯东部省份学龄儿童哮喘症状及环境诱因的患病率

Yaqoob, Masooma J; Aqroof, Hadi A; Busehail, Mohamed J; Abdali, Noor M; Alkhayat, Hasan A; Alasfoor, Yusuf H; Alawi, Sayed Mohamed E; Abdelsaid, Mark M; Abdulla, Mahmood A; Alshamlan, Noor H; Husain, Habib A

Uncovering Glucose-6-Phosphate Isomerase (GPI) Deficiency in a Five-Year-Old With Hemolytic Anemia in Bahrain

在巴林一名患有溶血性贫血的五岁儿童中发现葡萄糖-6-磷酸异构酶(GPI)缺乏症

Busehail, Maryam; Qasim, Fajer N; Alasheeri, Fatema J; Aloraibi, Ameera

Acrodermatitis Enteropathica in a Child in Bahrain: A Case Report and Literature Review

巴林一名儿童的肠病性肢端皮炎:病例报告及文献综述

Isa, Hasan M; Ali, Zainab H; Abdulla, Kawthar M; Alshaikh, Zainab J; Busehail, Maryam Y

Brooke-Spiegler Syndrome With Simultaneous Occurrence of Cylindroma, Spiradenoma, and Trichoepithelioma: A Rare Case With Malignant Progression

Brooke-Spiegler综合征同时发生圆柱瘤、螺旋腺瘤和毛发上皮瘤:一例罕见的恶性进展病例

Gorovanchi, Parastou; Busehail, Mohammed; Emami, Ehsan; Yaqoob, Masooma; Faramin Lashkarian, Mahsa; Khalili, Nima; Eftekhari, Nima; Hadimaleki, Sepideh; Mehramouz, Bahareh

Cowden Syndrome: A Rare Cause of Intestinal Polyposis

考登综合征:一种罕见的肠息肉病因

Isa, Hasan M; Mohamed, Zahra S; Isa, Zahra H; Busehail, Maryam Y; Alaradi, Zahra A

Trichohepatoenteric Syndrome: A Report of Two Children From Bahrain With a Novel Mutation and a Literature Review

毛发肝肠综合征:两例来自巴林的儿童新突变病例报告及文献综述

Isa, Hasan M; Matar, Wafa M; Ali, Ghufran J; Busehail, Maryam Y; Alsheala, Narjis A; Shajira, Eman S

A Novel Cyclin-Dependent Kinase 13 Variant and Unusual Association of Situs Inversus Partialis in a Child From Bahrain: A Case Report and Literature Review

巴林一名儿童的罕见内脏反位伴发新型细胞周期蛋白依赖性激酶13变异:病例报告及文献综述

Isa, Hasan M; Abdulla, Abdulla M; Abdulla, Kawthar M; Abdulnabi, Marwa J; Khudhair, Zainab A; Hubail, Zakariya J; Busehail, Maryam Y; Abdulrasool, Hasan A

Genetically Confirmed Wilson Disease: A Retrospective Cohort Study From Bahrain

基因确诊的威尔逊病:来自巴林的一项回顾性队列研究

Isa, Hasan M; Alahmed, Fawzeya A; Busehail, Maryam Y; Isa, Zahra H; Abdulla, Kawthar M

Alstrom's Syndrome: An Experience of Tertiary Care Center

阿尔斯特罗姆综合征:三级医疗中心的经验

Gosadi, Ghadah; Busehail, Maryam; Rahbeeni, Zuhair

A Novel PTRH2 Gene Mutation Causing Infantile-onset Multisystem Neurologic, Endocrine, and Pancreatic Disease in a Bahraini Patient

巴林一名患者罹患婴儿期发病的多系统神经、内分泌和胰腺疾病,其原因是一种新型的PTRH2基因突变。

Isa, Hasan M; Khalaf, Sara D; Janahi, Sara; Naser, Mohamed M; Al Hamad, Noor; Alhaddar, Hasan; Busehail, Maryam