Zobrazeno 1 - 10
of 18 461
pro vyhledávání: '"Microangiopathy"'
Publikováno v:
Guoji Yanke Zazhi, Vol 24, Iss 9, Pp 1426-1431 (2024)
Diabetic retinopathy(DR)is one of the major complications of diabetes mellitus, characterized by neurodegeneration and microangiopathy. Currently, the treatment of DR is mainly focused on the management of late complications and has not achieved the
Externí odkaz:
https://doaj.org/article/3ed328bf99da4711a0b3994dda84882b
Publikováno v:
BMC Nephrology, Vol 25, Iss 1, Pp 1-6 (2024)
Abstract Background Sunitinib, a multi-targeted tyrosine kinase inhibitor, is used as a second-line therapy for gastrointestinal stromal tumors (GIST) resistant to imatinib. However, its impact on the vascular endothelial growth factor (VEGF) pathway
Externí odkaz:
https://doaj.org/article/b320103d1eee4cb8acfbf8c0e0944dca
Autor:
Xiaoyu Zhou, Yishan Ye, Aiyun Jin, Zhengwen Pan, Zhe Xu, Shuyi Ding, Jiali Yan, Yin Cheng, Yixuan Huang, Kai Cao, Wei Xie, Jianli Zhang, Liwei Xu, Weiwei Zhou, Lihua Huang
Publikováno v:
BMC Nursing, Vol 23, Iss 1, Pp 1-8 (2024)
Abstract Objective The early identification and diagnosis of transplant-associated thrombotic microangiopathy (TA-TMA) are essential yet difficult in patients underwent hematopoietic stem cell transplantation (HSCT). To develop an evidence-based, nur
Externí odkaz:
https://doaj.org/article/89cb91f2ad1e4cf7b1492445850f68e7
Autor:
Yoshitaka Tatematsu, Takahiro Imaizumi, Nobuaki Michihata, Noritoshi Kato, Ryosuke Kumazawa, Hiroki Matsui, Kiyohide Fushimi, Hideo Yasunaga, Shoichi Maruyama
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-9 (2024)
Abstract Atypical haemolytic uremic syndrome (aHUS) is a rare disorder characterised by complement-mediated thrombotic microangiopathy (TMA). Despite clinical guidelines, the diagnosis and treatment of aHUS in its early stages remains challenging. Th
Externí odkaz:
https://doaj.org/article/87308da8e3544269b6ee9fd6e8912eae
Autor:
Antonio Alessandro Biancardino, MD, Salvatore Marrone, MD, Federica Paolini, MD, Evier Andrea Giovannini, MD, Giovanni Cinquemani, MD, Rita Lipani, MD, Luca Ruggeri, MD, Jaime Mandelli, MD, Antonio Crea, MD, Giuseppe Vaccaro, MD, Domenico Gerardo Iacopino, MD, PhD, Luigi Basile, MD
Publikováno v:
Radiology Case Reports, Vol 19, Iss 8, Pp 2937-2942 (2024)
Bony hemangiomas are benign vascular lesions with an expansive growth; usually they tend to obliterate the entire bony cavity. They are typical lesion of the spinal bones, but they can rarely arise within other bones of the neurocranium. Diabetic mic
Externí odkaz:
https://doaj.org/article/cadd4d9a79094d4390bac3f29889c4e6
Autor:
Kasumi Satoh, Takeshi Wada, Akihito Tampo, Gaku Takahashi, Kota Hoshino, Hironori Matsumoto, Takayuki Taira, Satoshi Kazuma, Takamitsu Masuda, Takashi Tagami, Hiroyasu Ishikura, J-STAD (JAPAN Sepsis Treatment and Diagnosis) Study Group
Publikováno v:
Thrombosis Journal, Vol 22, Iss 1, Pp 1-16 (2024)
Abstract Thrombocytopenia frequently occurs in patients with sepsis. Disseminated intravascular coagulation (DIC) may be a possible cause of thrombocytopenia owing to its high prevalence and association with poor outcomes; however, it is important to
Externí odkaz:
https://doaj.org/article/2bd6b6e8f7d146a68ddb1ddf1c17b6b7
Autor:
Shigekazu Kurihara, Akinori Yamaguchi, Kosuke Sonoda, Yosuke Yamada, Makoto Harada, Koji Hashimoto, Hisashi Shimojo, Yoichiro Ikeda, Yuji Kamijo
Publikováno v:
BMC Nephrology, Vol 25, Iss 1, Pp 1-10 (2024)
Abstract Background No reports have shown histological changes before and after anti-C5 monoclonal antibody treatment in patients with atypical hemolytic uremic syndrome (aHUS). Here, we report a rare case of complement-mediated aHUS with a complemen
Externí odkaz:
https://doaj.org/article/b011f8b76e914462afcb34a0f76927ad
Publikováno v:
Journal of Medical Case Reports, Vol 18, Iss 1, Pp 1-7 (2024)
Abstract Background Thrombotic microangiopathy is characterized by microangiopathic hemolytic anemia, thrombocytopenia, and organ injury. The pathological features include vascular damage that is manifested by arteriolar and capillary thrombosis with
Externí odkaz:
https://doaj.org/article/5a0a47a0dfb8408a988dea9961889671
Autor:
Kinan Kafa, Jessica I. Hoell
Publikováno v:
Frontiers in Oncology, Vol 14 (2024)
BackgroundTransplant-associated thrombotic microangiopathy (TA-TMA) is a critical complication of hematopoietic stem cell transplantation. Awareness about TA-TMA has increased in recent years, resulting in the implementation of TA-TMA screening in mo
Externí odkaz:
https://doaj.org/article/ee8499b9b55c4152ab7e2dc00d42c0d5
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 18, Iss 07, Pp 01-03 (2024)
Atypical Haemolytic Uraemic Syndrome (aHUS) is a rare type of thrombotic microangiopathy that occurs without Shiga toxin producing bacteria. It is a condition related to complement regulation, which may be genetic or acquired. The complement system
Externí odkaz:
https://doaj.org/article/ae71406025ac4b609a7cbc6987d8c5d3