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

Children with autism spectrum disorder and attention deficit hyperactivity disorder have evidence of sensory nerve degeneration

患有自闭症谱系障碍和注意力缺陷多动障碍的儿童均有感觉神经退化的迹象。

Gad, Hoda; AlObaidi, Abdulla; Kamal, Madeeha; Elhag, Saba F; Aden, Marian; Khan, Adnan; Baraka, Areej; Bennabhaktula, Srividya; Joseph, Sara; Alhamadi, Aisha Yaseen; Tolefat, Mohammed A; Alhothi, Abdulla A; Malik, Rayaz A

Functional Interpretation of a Novel Homozygous METTL5 Variant Associated with ADHD and Neurodevelopmental Abnormalities: A Case Report and Literature Review

一种与注意力缺陷多动障碍和神经发育异常相关的新型纯合METTL5变异的功能解释:病例报告和文献综述

Hashem, Sheema; Elhag, Saba F; Bhat, Ajaz A; Aamer, Waleed; Al-Maraghi, Aljazi; Alhaboub, Hala; Abuthaher, Dalya; Akil, Ammira S Al-Shabeeb; Haris, Mohammad; Fakhro, Khalid; Nemer, Georges; Kamal, Madeeha

Knowledge, Attitude, and Practice of Polycystic Ovarian Syndrome Diagnosis among Health Care Providers in Addis Ababa, Ethiopia

埃塞俄比亚亚的斯亚贝巴医护人员对多囊卵巢综合征诊断的知识、态度和实践

Erku, Ephrata W; Yanni, Mariamawit M; Mohamed, Hikma M; Weldehawaria, Saba F; Asfaw, Elham M; Tibebu, Melatwork; Sisay, Abay; Negash, Mikias

Long-read sequencing identifies a novel de novo inversion in SMARCC2 in a pediatric patient with Coffin-siris syndrome 8: a case report

长读长测序在一名患有科芬-西里斯综合征8型的儿科患者中发现了SMARCC2基因的新型从头倒位:病例报告

Ibrahim, Amal Abdulsalam; Aamer, Waleed; Aliyev, Elbay; Al-Maraghi, Aljazi; Elhag, Saba F; Abdi, Mona; Syed, Najeeb; Palaniswamy, Sasirekha; Akil, Ammira S A; Kamal, Madeeha; Fakhro, Khalid A

Genomic architecture of autism spectrum disorder in Qatar: The BARAKA-Qatar Study

卡塔尔自闭症谱系障碍的基因组结构:BARAKA-Qatar 研究

Abdi, Mona; Aliyev, Elbay; Trost, Brett; Kohailan, Muhammad; Aamer, Waleed; Syed, Najeeb; Shaath, Rulan; Gandhi, Geethanjali Devadoss; Engchuan, Worrawat; Howe, Jennifer; Thiruvahindrapuram, Bhooma; Geng, Melissa; Whitney, Joe; Syed, Amira; Lakshmi, Jyothi; Hussein, Sura; Albashir, Najwa; Hussein, Amal; Poggiolini, Ilaria; Elhag, Saba F; Palaniswamy, Sasirekha; Kambouris, Marios; de Fatima Janjua, Maria; Tahir, Mohamed O El; Nazeer, Ahsan; Shahwar, Durre; Azeem, Muhammad Waqar; Mokrab, Younes; Aati, Nazim Abdel; Akil, Ammira; Scherer, Stephen W; Kamal, Madeeha; Fakhro, Khalid A

The Arabic Questionnaire for Psychotic Experiences in patients with psychotic disorders: a clinical validation

针对精神病性障碍患者精神病性体验的阿拉伯语问卷:一项临床验证

Yehya, Arij; Khaled, Salma M; Sommer, Iris E C; Elhag, Saba F; Hassan, Mohamed H M O; Woodruff, Peter; Alabdalla, Majid

Circulating Non-Coding RNAs as a Signature of Autism Spectrum Disorder Symptomatology

循环非编码 RNA 是自闭症谱系障碍症状的标志

Salam Salloum-Asfar, Ahmed K Elsayed, Saba F Elhag, Sara A Abdulla

A chromosomal microdeletion of 15q in a female patient with epilepsy, ID, and autism spectrum disorder: a case report

一例患有癫痫、智力障碍和自闭症谱系障碍的女性患者,其染色体15q存在微缺失:病例报告

Ahram, Dina F; Al-Sarraj, Yasser; Taha, Rowaida Z; Elhag, Saba F; Al-Shaban, Fouad A; El-Shanti, Hatem; Kambouris, Marios

An extremely rare case of concurrent BRAF V600E mutation driven hairy cell leukemia and melanoma: case report and review of literature

一例极其罕见的BRAF V600E突变驱动的毛细胞白血病和黑色素瘤同时发生的病例报告及文献复习

Ghorbani-Aghbolaghi, Amir; Lechpammer, Mirna; Ali, Saba F; Ku, Nam K; Dwyre, Denis M; Rashidi, Hooman H

Translocation (6;15)(q12;q15): A Novel Mutation in a Patient with Therapy-Related Myelodysplastic Syndrome

易位 (6;15)(q12;q15):治疗相关性骨髓增生异常综合征患者的一种新突变

Ali, Saba F; Sonu, Rebecca J; Dwyre, Denis M; Jonas, Brian A; Rashidi, Hooman H