Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Canchan Cui"'
Autor:
Hua Jiang, Lu Li, Meiyu Guo, Meizhang Li, Hao Wu, Xiaomei Chen, Mingzhao Gao, Qianqian Xu, Jia Mi, Canchan Cui, Weijun Fu
Publikováno v:
Hematology, Vol 29, Iss 1 (2024)
Background Renal insufficiency (RI) is a key factor affecting the prognosis of multiple myeloma (MM) patients. Because the benefit of daratumumab for treating MM patients with RI remains unclear, our objective was to evaluate the efficacy of daratumu
Externí odkaz:
https://doaj.org/article/302e5dbd9ad74865a01f97feb11fa76a
Autor:
Gang An, Zheng Ge, Hongmei Jing, Jing Liu, Guoping Yang, Ru Feng, Zhongyuan Xu, Ming Qi, Jianping Wang, Juanjuan Song, Wei Zhou, Binbin Sun, Dian Zhu, Xi Chen, Canchan Cui, Lugui Qiu
Publikováno v:
Blood Science, Vol 6, Iss 3, p e00193 (2024)
Despite recent progress in multiple myeloma (MM) treatments, most patients will relapse and require additional treatment. Intravenous daratumumab, a human IgGκ monoclonal antibody targeting CD38, has shown good efficacy in the treatment of MM. A sub
Externí odkaz:
https://doaj.org/article/2ec97b8f16874c84a24dcc58cf904ec0
Autor:
Xuelin Dou, Yang Liu, Aijun Liao, Yuping Zhong, Rong Fu, Lihong Liu, Canchan Cui, Xiaohong Wang, Jin Lu
Publikováno v:
JMIR Formative Research, Vol 7, p e44420 (2023)
BackgroundSystemic light chain (AL) amyloidosis is a rare and multisystem disease associated with increased morbidity and a poor prognosis. Delayed diagnoses are common due to the heterogeneity of the symptoms. However, real-world insights from Chine
Externí odkaz:
https://doaj.org/article/75a616f6a3814de8ba164af5af2816e9
BACKGROUND Systemic light chain (AL) amyloidosis is a rare and multi-system disease. Delayed diagnoses were common in AL amyloidosis, resulting in poor prognosis. OBJECTIVE To better understand the current situation and patient journey of AL amyloido
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::47e5ed8c218862b6f4464068cffc385d
https://doi.org/10.2196/preprints.44420
https://doi.org/10.2196/preprints.44420