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

Molecular Genetics of 1α-Hydroxylase Deficiency in the Saudi Population

沙特阿拉伯人群中1α-羟化酶缺乏症的分子遗传学

Bin-Abbas, Bassam; Alsagheir, Afaf; Alghamdi, Balgees; Benito, Allianah; Shi, Yufei; Alzelaye, Somaya Khader; Ahmad, Noman; Al Juraibah, Fahad; Alali, Amer Omar; Al Shaikh, Adnan; Attia, Najya; Albunyan, Abdulhameed Abdulmohsen; Alshahrany, Abdullah Saad; Nahari, Ahmed Ali; Sulaimani, Nabilah; Alrubaya, Khloud M; Alzahrani, Ali S

Burden of Illness of Type 2 Diabetes Mellitus in the Kingdom of Saudi Arabia: A Five-Year Longitudinal Study

沙特阿拉伯王国2型糖尿病疾病负担:一项为期五年的纵向研究

AlHarbi, Mohammed; Othman, Abdullah; Nahari, Ahmed Ali; Al-Jedai, Ahmed Hamdan; Cuadras, Daniel; Almalky, Faisal; AlAzmi, Fayez; Almudaiheem, Hajer Yousef; AlShubrumi, Hamad; AlSwat, Hameed; AlSahafi, Homaid; Sindi, Kamelia; Basaikh, Khadija; AlQahtani, Majed; Lamotte, Mark; Yahia, Moataz; Hassan, Mohamed El-Khedr; AlMutlaq, Mohammed; AlRoaly, Mohammed; AlZelaye, Somaya; AlGhamdi, Zein

Analysis of disease characteristics of a large patient cohort with congenital generalized lipodystrophy from the Middle East and North Africa

对来自中东和北非的大量先天性全身性脂肪营养不良患者队列的疾病特征进行分析

Al Yaarubi, Saif; Alsagheir, Afaf; Al Shidhani, Azza; Alzelaye, Somaya; Alghazir, Nadia; Brema, Imad; Alsaffar, Hussain; Al Dubayee, Mohammed; Alshahrani, Awad; Abdelmeguid, Yasmine; Omar, Omneya M; Attia, Najya; Al Amiri, Elham; Al Jubeh, Jamal; Algethami, Albandari; Alkhayyat, Haya; Haleem, Azad; Al Yahyaei, Mouza; Khochtali, Ines; Babli, Saleha; Nugud, Ahmed; Thalange, Nandu; Albalushi, Sarah; Hergli, Nadia; Deeb, Asma; Alfadhel, Majid

Familial Screening for the Prevention of Rare Diseases: A Focus on Lipodystrophy in Southern Saudi Arabia

针对罕见病的家族筛查:聚焦沙特阿拉伯南部地区的脂肪营养不良症

Abuzenadah, Adel; Alganmi, Nofe; AlQurashi, Raghad; Hawsa, Esraa; AlOtibi, Abdullah; Hummadi, Abdulrahman; Nahari, Ahmed Ali; AlZelaye, Somaya; Aljuhani, Nasser R; Al-Attas, Manal; Abusamra, Heba; Turkistany, Shereen; Karim, Sajjad; Mirza, Zeenat; Al-Qahtani, Mohammed; Chaudhary, Adeel; Al Eissa, Mariam M

A homozygous mutation in the insulin gene (INS) causing autosomal recessive neonatal diabetes in Saudi families

沙特阿拉伯家族中,胰岛素基因(INS)的纯合突变导致常染色体隐性遗传性新生儿糖尿病。

Shaikh, Adnan Al; Shirah, Bader; Alzelaye, Somaya