Zobrazeno 1 - 10
of 4 439
pro vyhledávání: '"Membranoproliferative Glomerulonephritis"'
Publikováno v:
BMC Nephrology, Vol 25, Iss 1, Pp 1-4 (2024)
Abstract Background Membranoproliferative glomerulonephritis is a rare entity which can be a result from autoimmune diseases, caused by various medications and infections. Case presentation We herein present the case of a 62-year-old male patient who
Externí odkaz:
https://doaj.org/article/5e2dbc0f17e6400ea5d2f08caaeca4f1
Publikováno v:
Indian Journal of Paediatric Dermatology, Vol 25, Iss 3, Pp 237-239 (2024)
Cutis marmorata telangiectatica congenita (CMTC) is a rare capillary malformation characterized by persistent reticulated marbled erythema. A 16-year-old boy presented with reddish net-like lesion over the left side of his body which was initially no
Externí odkaz:
https://doaj.org/article/0dfaeb6c5c364a2cb0240882d5167ea9
Autor:
Simone Arnold, Manuela Nickler, Michael Dickenmann, Thomas Menter, Helmut Hopfer, Patricia Hirt-Minkowski
Publikováno v:
Case Reports in Nephrology and Dialysis, Vol 14, Iss 1, Pp 138-147 (2024)
Introduction: Nowadays, there is insufficient evidence for the recommendation of management patients with a primary membranoproliferative glomerulonephritis (MPGN). A better understanding of the pathogenesis has led to the reclassification of primary
Externí odkaz:
https://doaj.org/article/2eb0823faa304f9d9b6363921f44e9e5
Autor:
Hannah O'Keeffe, Joshua Storrar, Chethana Ramakrishna, Sara Metaoy, Constantina Chrysochou, Rajkumar Chinnadurai, Philip A. Kalra, Smeeta Sinha
Publikováno v:
Glomerular Diseases, Vol 4, Iss 1, Pp 159-166 (2024)
Introduction: Membranoproliferative glomerulonephritis (MPGN) is a pattern of injury seen on kidney biopsy, with various underlying etiologies. The component types, including complement-mediated MPGN, are relatively rare. This study presents longitud
Externí odkaz:
https://doaj.org/article/4f5e7c8d20154dc4a634ee5abea3d952
Autor:
Viktor Rydberg, Sigridur Sunna Aradottir, Ann-Charlotte Kristoffersson, Naila Svitacheva, Diana Karpman
Publikováno v:
Frontiers in Immunology, Vol 15 (2024)
Externí odkaz:
https://doaj.org/article/26a595d54f074a8eb687540ef0957a13
Autor:
Misa Hata, Takayasu Mori, Yurika Hirose, Yuriko Nishida, Shintaro Mandai, Fumiaki Ando, Koichiro Susa, Soichiro Iimori, Shotaro Naito, Eisei Sohara, Tatemitsu Rai, Towako Taguchi, Shohei Tomii, Kenichi Ohashi, Shinichi Uchida
Publikováno v:
BMC Nephrology, Vol 25, Iss 1, Pp 1-6 (2024)
Abstract Fibronectin (FN) glomerulopathy (FNG), a rare autosomal hereditary renal disease, is characterized by proteinuria resulting from the massive accumulation of FN in the glomeruli. It typically affects individuals aged 10–50 years. In this re
Externí odkaz:
https://doaj.org/article/17e22ae0bef5490582eebc7e79569bba
Autor:
Mengjun Liang, Shiyan Zhu, Shaoqin Liu, Jianquan Chen, Danni Li, Chengzhi Luo, Xiaowen Wang, Zongpei Jiang
Publikováno v:
BMC Nephrology, Vol 24, Iss 1, Pp 1-6 (2023)
Abstract Background Gaucher disease (GD) is a rare autosomal recessive inherited, lysosomal storage disoder that involves liver, spleen, lung, bone, bone marrow even central nervous. However, GD associated membranoproliferative glomerulonephritis (MP
Externí odkaz:
https://doaj.org/article/027224df7858444ab7760f0936a28c54
Autor:
Michael Cieza-Terrones, José C. De La Flor, Christian Requejo, Daniel Villa, Jacqueline Apaza, Pablo Rodríguez-Doyágüez, Rocío Zamora, Carmen Asato-Higa, David Rivera-Estrella, Antonio Carrasco-Yalán
Publikováno v:
Medicines, Vol 11, Iss 6, p 13 (2024)
Background: Idiopathic hypereosinophilic syndrome (IHES) is a disorder characterized by abnormal and persistent peripheral blood hypereosinophilia (eosinophil count ≥ 1.5 × 109/L and ≥10% eosinophils) with duration ≥ 6 months, associated organ
Externí odkaz:
https://doaj.org/article/ecc5fc55e2bb4b729039f16202860108
Autor:
Ru-Yue Chen, Xiao-Zhong LI, Qiang Lin, Han-Yun Tang, Ning-Xun Cui, Lu Jiang, Xiao-Mei Dai, Wei-Qing Chen, Fan Deng, Shao-Yan Hu, Xue-Ming Zhu
Publikováno v:
BMC Pediatrics, Vol 23, Iss 1, Pp 1-11 (2023)
Abstract Background Allogeneic hematopoietic stem cell transplantation (allo-HSCT) is a curative therapy for hematologic malignancies and non-malignant disorders, such as aplastic anemia, fanconi anemia, and certain immune deficiencies. Post-transpla
Externí odkaz:
https://doaj.org/article/ce2310a0e4664e5e88befd56f0e134a7
Autor:
Viktor Rydberg, Sigridur Sunna Aradottir, Ann-Charlotte Kristoffersson, Naila Svitacheva, Diana Karpman
Publikováno v:
Frontiers in Immunology, Vol 14 (2023)
BackgroundComplement activation in atypical hemolytic uremic syndrome (aHUS), C3 glomerulonephropathy (C3G) and immune complex-mediated membranoproliferative glomerulonephritis (IC-MPGN) may be associated with rare genetic variants. Here we describe
Externí odkaz:
https://doaj.org/article/cf5e974e7ce04cb3be958bb057b9b403