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

Spontaneous Right Thalamic Hemorrhage With Intraventricular Extension in a Two-Month-Old Preterm Infant Initially Suspected of Having Cow's Milk Protein Allergy

一名两个月大的早产儿最初被怀疑患有牛奶蛋白过敏症,后确诊为自发性右丘脑出血伴脑室内扩散。

Abdulsalam, Tuqa A; Musa, Rehab; Aldirawi, Mohammed; Hamdi, Moataz; Yavuz, Lemis

Abernethy malformation type II masquerading as unexplained hypoxemia in early childhood: a case report

一例以不明原因低氧血症为表现的II型阿伯内西畸形:病例报告

Abdulaal, Hawra; Yavuz, Lemis; Musa, Rehab; Kasem, Mohamed; Anwar, Muhammad; Alteneiji, Majid

Acquired methemoglobinemia in infancy secondary to diarrhea: a case report

婴儿腹泻继发获得性高铁血红蛋白血症:病例报告

Aly, Mariam Hany; Bukhari, Hessa Mohammed; Aldirawi, Mohammed A H; Yavuz, Lemis

From multisystem inflammatory syndrome in children to secondary hemophagocytic lymphohistiocytosis a series of misfortunate events: case report and review of literature

从儿童多系统炎症综合征到继发性噬血细胞性淋巴组织细胞增生症:一系列不幸事件——病例报告及文献综述

Mansoor, Zahraa; Nugud, Ahmed; Abuhammour, Walid; Yavuz, Lemis; Belt, Ernestina; Sharif, Elsadeg

The genomic landscape of rare disorders in the Middle East

中东罕见病的基因组图谱

El Naofal, Maha; Ramaswamy, Sathishkumar; Alsarhan, Ali; Nugud, Ahmed; Sarfraz, Fatima; Janbaz, Hiba; Taylor, Alan; Jain, Ruchi; Halabi, Nour; Yaslam, Sawsan; Alfalasi, Roudha; Shenbagam, Shruti; Rabea, Fatma; Bitzan, Martin; Yavuz, Lemis; Wafadari, Deena; Abulhoul, Hamda; Shankar, Shiva; Al Maazmi, Munira; Rizk, Ruba; Alloub, Zeinab; Elbashir, Haitham; Babiker, Mohamed O E; Chencheri, Nidheesh; AlBanna, Ammar; Sultan, Meshal; El Bitar, Mohamed; Kherani, Safeena; Thalange, Nandu; Alshryda, Sattar; Di Donato, Roberto; Tzivinikos, Christos; Majid, Ibrar; Freeman, Alexandra F; Gonzalez, Corina; Khan, Arif O; Hamdan, Hisham; Abuhammour, Walid; AlAwadhi, Mohamed; AlKhayat, Abdulla; Alsheikh-Ali, Alawi; Abou Tayoun, Ahmad N

Rapid-Onset Obesity With Hypothalamic Dysfunction, Hypoventilation, Autonomic Dysregulation, and Neuroendocrine Tumor (ROHHADNET) Syndrome: A Case Report

快速起病的肥胖伴下丘脑功能障碍、通气不足、自主神经功能紊乱和神经内分泌肿瘤(ROHHADNET)综合征:病例报告

Aldirawi, Mohammed; Yavuz, Lemis; Ghoweba, Yousra; Mohamedali, Saril; Chencheri, Nidheesh; Thalange, Nandu

Rapid whole genome sequencing of critically ill pediatric patients from genetically underrepresented populations

对来自遗传代表性不足人群的危重儿科患者进行快速全基因组测序

Halabi, Nour; Ramaswamy, Sathishkumar; El Naofal, Maha; Taylor, Alan; Yaslam, Sawsan; Jain, Ruchi; Alfalasi, Roudha; Shenbagam, Shruti; Bitzan, Martin; Yavuz, Lemis; Abulhoul, Hamda; Shankar, Shiva; Janjua, Dalwinder; Jadhav, Devendrasing; Al Maazmi, Munira Mahmoud; Abuhammour, Walid; Alsheikh-Ali, Alawi; Al Awadhi, Mohamed; Al Khayat, Abdulla; Abou Tayoun, Ahmad N

Genetic and Clinical Characteristics of Patients in the Middle East With Multisystem Inflammatory Syndrome in Children

中东地区儿童多系统炎症综合征患者的遗传和临床特征

Walid Abuhammour ,Lemis Yavuz ,Ruchi Jain ,Khawla Abu Hammour ,Ghalia F Al-Hammouri ,Maha El Naofal ,Nour Halabi ,Sawsan Yaslam ,Sathishkumar Ramaswamy ,Alan Taylor ,Deena Wafadari ,Ali Alsarhan ,Hamda Khansaheb ,Zulfa Omar Deesi ,Rupa Murthy Varghese ,Mohammed Uddin ,Hanan Al Suwaidi ,Suleiman Al-Hammadi ,Abdulmajeed Alkhaja ,Laila Mohamed AlDabal ,Tom Loney ,Norbert Nowotny ,Abdulla Al Khayat ,Alawi Alsheikh-Ali ,Ahmad Abou Tayoun

Signs and Symptoms of Vitamin D Deficiency in Children: A Cross-Sectional Study in a Tertiary Pediatric Hospital in the United Arab Emirates

儿童维生素D缺乏症的体征和症状:阿联酋一家三级儿科医院的横断面研究

Alawadhi, Fatma; Yavuz, Lemis