THALASSEMIA

作品数:84被引量:128H指数:6
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相关领域:医药卫生更多>>
相关作者:李承军黄有文王荣新邱长春陈朝更多>>
相关机构:中国人民解放军中国医学科学院北京协和医学院中国中医研究院海南医学院附属医院更多>>
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相关基金:国家自然科学基金泰国研究基金国家电网公司科技项目更多>>
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Clinical course and management of hypertriglyceridemia thalassemia syndrome:A case-based systematic review
《World Journal of Clinical Pediatrics》2025年第2期117-125,共9页Chane Choed-Amphai Pattranan Kusontammarat Supapitch Chanthong Nattawan Arkarattanakul Poonyapon Rodchaprom Lalita Sathitsamitphong Rungrote Natesirinilkul Pimlak Charoenkwan 
BACKGROUND Hypertriglyceridemia thalassemia syndrome is a rare condition that occurs in patients with thalassemia.It typically presents with a combination of profound anemia and milky serum.Although previous case seri...
关键词:THALASSEMIA HYPERTRIGLYCERIDEMIA DYSLIPIDEMIA CHILDREN TRANSFUSION 
Combinatorial approach to treat iron overload cardiomyopathy in pediatric patients with thalassemia-major: A systematic review and meta-analysis
《World Journal of Cardiology》2025年第2期93-102,共10页Moaz Safwan Mariam Safwan Bourgleh Aseel Alsudays Khawaja Husnain Haider 
BACKGROUND Iron overload cardiomyopathy is a significant cause of morbidity and mortality in transfusion-dependent thalassemia patients.Standard iron chelation therapy is less efficient in alleviating iron accumulatio...
关键词:AMLODIPINE CARDIOMYOPATHY Iron overload Randomized controlled trials THALASSEMIA 
Assessing the auditory effects of oral chelation therapy drug Deferasirox in individuals withβ-thalassemia major
《World Journal of Otorhinolaryngology-Head and Neck Surgery》2024年第4期309-314,共6页Balwinder S.Tiwana Ankita Aggarwal Sanjeev Bhagat Harjinder Singh Dimple Sahni Vishav Yadav 
Objective:Our study aimed to investigate the ototoxicity associated with the iron chelator deferasirox in patients withβ-thalassemia major,who were receiving regular transfusion therapy,along with evaluating the data...
关键词:AUDITORY DEFERASIROX distortion product otoacoustic emissions ORAL CHELATING agent pure tone AUDIOMETRY THALASSEMIA 
Global, Regional, and National Epidemiology of Thalassemia in Childhood from 1990 to 2021
《Journal of Biosciences and Medicines》2024年第12期361-379,共19页Yongle Li Wanshuo Wei Yuan Gan Xiaomei Xie Pengtao Qin Liangsen Teng Lihe Jiang 
Objective: To analyze trends in prevalence, mortality, and disability-adjusted life years (DALYs) of childhood thalassemia from 1990 to 2021. Methods: Using the 2021 Global Burden of Disease (GBD) database, we conduct...
关键词:THALASSEMIA CHILDHOOD Cross-Sectional Study 
Comparative Study of Neurosurgical Complications of Thalassemia and Sickle Cell Disease
《Open Journal of Modern Neurosurgery》2024年第3期190-202,共13页Léon Boukassa Didace Massamba Miabaou Hugues Brieux Ekouélé Mbaki Sinclair Brice Kinata Bambino Olivier Brice Ngackosso Rel Boukaka Kala Gédéon Colin Thouassa Ruth Ibara Wamé 
Introduction: Sickle cell disease and thalassemia are the most frequent hemoglobinopathies. During their evolution, they present certain complications, among which are two neurosurgical emergencies, namely spontaneous...
关键词:HEMOGLOBINOPATHY Sickle Cell Disease THALASSEMIA Spontaneous Epidural Hematoma Extra Marrow Hematopoiesis Slow Marrow Compression 
Clinical Insights:Prevalence of β-Thalassemia Mutations(IVSI-5,FSC8/9,and CD41/42)in the Swat District
《Journal of Bio-X Research》2024年第1期1-7,共7页Sumaia Saif Shah Lila Gulalai Ghani Murad Ali Rahat Akhtar Rasool Muhammad Israr 
Background:Thalassemia is a prevalent condition characterized by decreased production or absence of hemoglobin globin chains.There are 2 types of thalassemia,alpha thalassemia and beta thalassemia(β-thalassemia),clas...
关键词:THALASSEMIA annually Pakistan 
An Application of Machine Learning to Thalassemia Diagnosis
《Journal of Computer and Communications》2024年第2期211-230,共20页Sitan Liu 
Mediterranean anemia is a genetic disease that currently relies heavily on expert clinical experience to determine whether patients are affected. This method is overly reliant on expert experience and is not precise e...
关键词:MULTICOLLINEARITY Statistical Analysis Models Data Mining PCA-LR PLS 
Therapeutic genome editing of an aberrant splice site inβ-thalassemia by CRISPR/Cas9 with multiple sgRNAs被引量:1
《Genes & Diseases》2024年第1期15-18,共4页Fei Yang Shuqian Xu Chao Huang Zhiqiang Shao Yuefen Hu Yang Yang Yongrong Lai Qing Ke Dan Liang Yuxuan Wu 
supported by the National Key R&D Program ofChina(No.2019YFA0109900,2019YFA0109901,2019YFA0802800,2019YFA0110803,2021YFC2700901);the Shanghai Municipal Commission for Science and Technology(No.19PJ1403500);the National Natural Science Foundation of China(No.82101802,81300383);the Scientific Research of BSKY(No.XJ2020025)from Anhui Medical University,and the Non-profit Central Research Institute Fund of Chinese Academy of Medical Sciences(No.2019PT310002);Young Taishan Scholar Foundation of Shandong Province,China(No.tsqn202103167);Clinical Research Center of Shandong University(China)(No.2020SDUCRCC015).
Genetic mutations cause aberrant splicing,one of the important molecular mechanisms in human diseases.Ivs2-654,a mutation causing aberrant splicing ofβ-globin premRNA and contributing toβ-globin deficiency,is one of...
关键词:CRISPR/Cas9 China THALASSEMIA 
Measuring the Awareness of Thalassemia in Saudi Arabia
《Advances in Bioscience and Biotechnology》2023年第9期399-408,共10页Noorah Saleh Al-Sowayan Abrar Mohammed Al-Fadhel Tahiyat Al Othaim 
Introduction: Thalassemia disorder is a genetic disease that causes the blood to have less hemoglobin than normal, the main requirement to control thalassemia’s propagation is to educate the entire society. Methodolo...
关键词:THALASSEMIA Genetic Disorder Thalassemia Syndrome AWARENESS SURVEY Saudi Arabia 
Secondary Iron Overload and the Liver:A Comprehensive Review被引量:5
《Journal of Clinical and Translational Hepatology》2023年第4期932-941,共10页Kanokwan Pinyopornpanish Adisak Tantiworawit Apinya Leerapun Atiwat Soontornpun Satawat Thongsawat 
Iron overload is a condition involving excessive iron deposit in various organs,the liver being the main target organ for iron deposition and overload which are associated with significant liver morbidity and mortalit...
关键词:Iron overload HEMOCHROMATOSIS CIRRHOSIS Hepatocellular carcinoma THALASSEMIA 
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