Zobrazeno 1 - 10
of 196
pro vyhledávání: '"infusion related reactions"'
Publikováno v:
Diagnostic Pathology, Vol 19, Iss 1, Pp 1-9 (2024)
Abstract Background Waldenström’s macroglobulinemia (WM) is defined as a lymphoplasmacytic lymphoma (LPL) involving the bone marrow (BM) with presence of IgM monoclonal protein, and comprises > 95% of all LPL cases. Rituximab-based regimens have b
Externí odkaz:
https://doaj.org/article/ee1e7a3fc90c49d9b4b6e4f16100db86
Autor:
Xi‐xi Yin, Yueyun Hu, Yusi Yang, Xinglan Zhang, Li Liu, Xi Cao, Jianwen Chen, Zhongjun Xia, Ye Wang
Publikováno v:
Cancer Medicine, Vol 13, Iss 11, Pp n/a-n/a (2024)
Abstract Background With the increasing use of daratumumab (DARA)‐containing regimens for multiple myeloma (MM) patients in China, the standard infusion time of DARA is long, with the potential for infusion‐related reactions (IRRs) and increased
Externí odkaz:
https://doaj.org/article/868e14b1ee2a491a844bffe30f8b8049
Publikováno v:
Clinical Case Reports, Vol 12, Iss 5, Pp n/a-n/a (2024)
Key Clinical Message This report documents the treatment of a 41‐year‐old male with sickle cell disease (SCD) and repeated stuttering priapism using crizanlizumab, which alleviated the priapism but induced a significant vaso‐occlusive crisis du
Externí odkaz:
https://doaj.org/article/e0b4af9978ef4f7383392d490e7ce4f1
Autor:
Line Gutte Borgwardt, Ferdinando Ceravolo, Giulia Zardi, Andrea Ballabeni, Allan Meldgaard Lund
Publikováno v:
JIMD Reports, Vol 64, Iss 2, Pp 187-198 (2023)
Abstract Alpha‐mannosidosis (AM), an autosomal recessive disorder caused by pathogenic biallelic variants in the MAN2B1 gene, leads to lysosomal alpha‐mannosidase deficiency and accumulation of mannose‐rich oligosaccharides. Velmanase alfa (VA)
Externí odkaz:
https://doaj.org/article/70f1d07fdc024aabb477b895d1046324
Publikováno v:
Frontiers in Oncology, Vol 13 (2023)
Monoclonal antibodies, such as PD-1 inhibitors, are increasingly used in various cancers. Acute low back pain as infusion-related reaction (IRR) to monoclonal antibodies is poorly described. We report a bicentric series of 10 cases of acute low back
Externí odkaz:
https://doaj.org/article/bc9be32746094726bca763ff1eccc7bb
Akademický článek
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Autor:
Julia G. Levina, Nato D. Vashakmadze, Leyla S. Namazova-Baranova, Elena A. Vishneva, Natalia V. Zhurkova, Kamilla E. Efendieva, Anna A. Alekseeva, Vera G. Kalugina
Publikováno v:
Вопросы современной педиатрии, Vol 20, Iss 6s, Pp 624-629 (2021)
Mucopolysaccharidosis type II (MPS II; Hunter syndrome) is rare hereditary disease caused by changes in the IDS gene and associated deficiency of lysosomal enzyme iduronate-2-sulfatase (I2S). The main treatment scheme for children with MPS II is enzy
Externí odkaz:
https://doaj.org/article/43b99bf093e444f8a3b9a08a8d576030
Autor:
Awni Alshurafa, Mohamed A. Yassin
Publikováno v:
Frontiers in Medicine, Vol 9 (2022)
Sickle cell disease is an autosomal recessive disorder characterized by the presence of sickle hemoglobin that leads to chronic hemolysis and vaso-occlusive crisis. After decades of limited therapy options, crizanlizumab is a humanized monoclonal ant
Externí odkaz:
https://doaj.org/article/02308d2e9fe446a7b21fdf3bbc79cd9c
Akademický článek
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Publikováno v:
Current Oncology, Vol 28, Iss 5, Pp 4118-4128 (2021)
The most common adverse reactions to rituximab are infusion-related reactions (IRR). We evaluated the efficacy of split dosing the first rituximab infusion over two days to reduce IRR incidence in patients with hematological cancer and a high lymphoc
Externí odkaz:
https://doaj.org/article/133b16f81ece44638a284f7851393b87