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

Bi-allelic variants in NRDC cause a neurodevelopmental disorder characterized by neonatal lethality, microcephaly, and brain abnormalities

NRDC基因的双等位基因变异会导致一种神经发育障碍,其特征是新生儿死亡、小头畸形和脑部异常。

Pehlivan, Davut; Sandoval, Abigail; Maroofian, Reza; Lecoquierre, François; Al Shamsi, Aisha M; Lee, Gyu S; Yesilbas, Osman; Taylor, Preston; McDougal, Matthew B; Bahrambeigi, Vahid; Aryani, Omid; Ramirez, Juan Felipe; Salih, Khalid Hama; Al Alam, Chadi; Morsy, Heba; Hussien, Haytham; Omar, Tarek; Abdelrazek, Ibrahim M; Brehin, Anne Claire; Marafi, Dana; Kalayci, Tugba; Rahma, Jubran Abu; Talbeya, Jawabreh Kassem; Dabbah, Husein; Verspyck, Eric; Moosavian, Toktam; Fatih, Jawid M; Mitani, Tadahiro; Akay, Gulsen; Calame, Daniel G; Guerrot, Anne-Marie; Chung, Wendy K; Houlden, Henry; Lupski, James R; Shalata, Adel; Yoon, Wan Hee

Vancomycin Resistance Streptococcus pneumoniae, a Case Report

万古霉素耐药性肺炎链球菌病例报告

Najmadden, Zana Baqi; Salih, Khalid Hama; Hama, Jihad Ibrahim; Kakamad, Fahmi Hussein; Khurshid, Bakhtyar Qadr Hama

Genetic Insights from Consanguineous Cardiomyopathy Families

近亲结婚心肌病家族的遗传学启示

Maurer, Constance; Boleti, Olga; Najarzadeh Torbati, Paria; Norouzi, Farzaneh; Fowler, Anna Nicole Rebekah; Minaee, Shima; Salih, Khalid Hama; Taherpour, Mehdi; Birjandi, Hassan; Alizadeh, Behzad; Salih, Aso Faeq; Bijari, Moniba; Houlden, Henry; Pittman, Alan Michael; Maroofian, Reza; Almashham, Yahya H; Karimiani, Ehsan Ghayoor; Kaski, Juan Pablo; Faqeih, Eissa Ali; Vakilian, Farveh; Jamshidi, Yalda

A Syrian Refugee in Iraq Diagnosed as a Case of IL12RB1 Deficiency in Japan Using Dried Blood Spots

一名在伊拉克的叙利亚难民在日本通过干血斑检测被诊断为IL12RB1缺乏症

Al-Kzayer, Lika'a Fasih Y; Yassin, Ahmed K; Salih, Khalid Hama; Shigemura, Tomonari; Sano, Kenji; Al-Simaani, Ruwaid Behnam Y; Tanaka, Miyuki; Nakazawa, Yozo; Okuno, Yusuke