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期刊名:Cen case reports

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ISSN:2192-4449

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IF/分区:1.0/Q4

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共收录本刊相关文章索引1127
Clinical Trial Case Reports Meta-Analysis RCT Review Systematic Review
Classical Article Case Reports Clinical Study Clinical Trial Clinical Trial Protocol Comment Comparative Study Editorial Guideline Letter Meta-Analysis Multicenter Study Observational Study Randomized Controlled Trial Review Systematic Review
Takahiko Hoshino,Takahiro Uchida,Minami Koizumi et al. Takahiko Hoshino et al.
A Japanese man in his 60 s with end-stage kidney disease due to diabetic nephropathy, who initially underwent peritoneal dialysis (PD) and was transferred to combined PD and hemodialysis (HD) therapy 4 years prior, was admitted to our hospi...
Mitsuru Tomizawa,Shunta Hori,Kuniaki Inoue et al. Mitsuru Tomizawa et al.
Drug-induced hypersensitivity syndrome/drug reaction with eosinophilia and systemic symptoms (DIHS/DRESS) is a severe cutaneous adverse reaction (SCAR) with a reported mortality rate of approximately 2-10%. DIHS/DRESS typically develops 2-8...
Perry Martel Sy,Minato Baba,Kaori Fujiwara et al. Perry Martel Sy et al.
Nephronophthisis is an autosomal recessive ciliopathy and a major genetic cause of end-stage kidney disease in children and young adults. Although next-generation sequencing panels have improved diagnostic yield, some patients remain geneti...
Akira Mima,Masasuke Kumagai,Shizuka Fukumoto et al. Akira Mima et al.
Lupus nephritis (LN) is characterized by immune system attacks on self-tissues, triggered by the production of pathological autoantibodies, leading to damage in multiple organs and tissues throughout the body. The second-generation calcineu...
Yosuke Nakagawa,Masahiro Koizumi,Norisuke Shimamura et al. Yosuke Nakagawa et al.
Patients who undergo hematopoietic stem cell transplantation (HSCT) face a high risk of acute kidney injury (AKI), which significantly increases the likelihood of developing chronic kidney disease (CKD). Proteinuria is also frequently obser...
Takuya Yamazaki,Shokichi Naito,Shun Sakurabayashi et al. Takuya Yamazaki et al.
Familial lecithin-cholesterol acyltransferase deficiency (FLD) is a rare hereditary disorder. In FLD, a clinical triad of corneal opacity, anemia, and proteinuria typically precedes progressive renal dysfunction. Although early renal involv...
Yasser Isaac Arana-Escandón,Paula Eliana Ramírez-Arboleda,Lina María Gaviria-Jaramillo et al. Yasser Isaac Arana-Escandón et al.
Disseminated adenovirus infection is a rare but often fatal complication of hematopoietic stem cell transplantation (HSCT), particularly uncommon in the autologous setting. We report the case of a 59-year-old man with stage IVB diffuse larg...
Saki Takeda,Haruki Chiba,Takeru Yamazaki et al. Saki Takeda et al.
Hemodialysis is an effective treatment option for acute caffeine intoxication. However, the efficacy of continuous renal replacement therapy remains a subject of debate. We encountered a case of acute caffeine intoxication that was managed ...
Yuto Matsui,Kan Katayama,Yuka Mitamura et al. Yuto Matsui et al.
This case report describes a rare instance of minimal change disease (MCD) associated with Mycobacterium marinum infection. MCD is typically idiopathic but can occasionally occur secondary to infections. The patient was a 61-year-old fisher...
Sachio Iwanari,Mari Tanaka,Toshihisa Akimune et al. Sachio Iwanari et al.
Dialysis-related amyloidosis (DRA) is a clinically significant complication of long-term hemodialysis, primarily affecting the bones and joints. Involvement of oral cavity is uncommon, and almost all reported cases are localized to the tong...