A Novel Mutation of UMOD in a Chinese Family with IgA Nephropathy: A Case Report [0.03%]
UMOD的新突变在中国IgA肾病家系中的发现及功能研究——1例报告
Furong Li,Huan Zou,Li Liu et al.
Furong Li et al.
IgA nephropathy (IgAN) is the most prevalent primary glomerulonephritis worldwide, with varying clinical presentations. The hereditary susceptibility to IgAN is rather complex. In this report, a Chinese case of IgAN was recruited. Renal bio...
Kazunori Karasawa,Ken-Ichi Akiyama,Taro Akihisa et al.
Kazunori Karasawa et al.
The number of patients with diabetic nephropathy is increasing worldwide and it is important to understand the underlying pathological mechanisms of the disease. In early stage diabetic nephropathy, the hyperglycemic environment leads to va...
Michael R Gigax,Lee Yang,Glenn Austin et al.
Michael R Gigax et al.
Urolithiasis composed of pyrophosphate salts has only been reported in animals, in the form of potassium magnesium pyrophosphate. However, there have been no reports of pyrophosphate stones in humans. Hypophosphatasia is an inherited diseas...
Catheter-Related Bloodstream Infection in Hemodialysis Patient due to Atlantibacter hermannii [0.03%]
血透患者因Atlantibacter hermannii导致的导管相关性 bloodstream 感染
Preslava M Hristova,Alexandra S Alexandrova,Martin Lucanov et al.
Preslava M Hristova et al.
Atlantibacter hermannii, previously known as Escherichia hermannii, is a rare causative agent of human infections. Several reports testify that the most frequently infected patients are immunosuppressed, especially those undergoing hemodial...
Novel LAGE3 Pathogenic Variants Combined with TRPC6 and NUP160 Variants in Galloway-Mowat Syndrome: A Case Report [0.03%]
LAGE3、TRPC6和NUP160基因变异联合导致Galloway-Mowat综合征的病例报告
Limin Huang,Xiaojing Zhang,Yingying Zhang et al.
Limin Huang et al.
Galloway-Mowat syndrome (GAMOS) is a rare autosomal recessive disorder characterized by early-onset nephrotic syndrome and microcephaly with brain anomalies in children. Researchers studying GAMOS reported the first pathogenic variant ident...
Conversion from Intermittent Hemodialysis to Peritoneal Dialysis in Metastatic Catheter-Related Bloodstream Infection [0.03%]
间歇性血液透析转为导管相关血流感染患者的腹膜透析治疗
Mohamedanwar Ghandour,Ravi K Thimmisetty,James Sondheimer et al.
Mohamedanwar Ghandour et al.
Of all complications from central venous catheters (CVC) in end-stage renal disease (ESRD) patients, catheter-related bloodstream infection (CRBSI) is one of the most devastating consequences. The option of catheter salvage is not an effect...
A Case of Mesangial Proliferative Nephritis Caused by Slow Cryoglobulin [0.03%]
一例由冷 cryoglobulin引起的系膜增生性肾炎病例报告
Seiji Hashimoto,Nobuhiko Okamoto,Tomochika Maoka et al.
Seiji Hashimoto et al.
The patient was a woman in her 60s. She was found to have proteinuria on a health checkup. She did not have any particular subjective symptoms, and no definitive diagnosis was made, despite serological findings indicative of immune abnormal...
Venous Excess Doppler Ultrasound: A Visual Guide to Decongestion in Cardiorenal Syndrome [0.03%]
静脉多普勒超声检查：心肾综合征去充血的视觉指南
Sirisha Gudlawar,Abhilash Koratala
Sirisha Gudlawar
Promptly recognizing congestion, both clinical and hemodynamic, is paramount in the management of patients with heart failure. The pathophysiology of congestion involves a complex interplay of absolute fluid gain, volume redistribution from...
Chryseobacterium indologenes Peritonitis in a Peritoneal Dialysis Patient: A Case Report and Review of Literature [0.03%]
腹膜透析患者黄单胞菌属肠杆状菌腹膜炎一例及文献复习
Akira Miyakawa,Kentaro Fujii,Ai Kato et al.
Akira Miyakawa et al.
Peritonitis is one of the most important complications in patients with peritoneal dialysis (PD). Appropriate antibiotic treatment against PD-associated peritonitis is necessary to prevent PD catheter removal and withdrawal from PD. Chryseo...
Three Pediatric Patients with Congenital Nephrogenic Diabetes Insipidus due to AVPR2 Nonsense Mutations and Different Clinical Manifestations: A Case Report [0.03%]
由AVPR2终止密码突变引起的三例临床表现不同的先天性肾源性尿崩症患儿
Hijiri Watanabe,Hiroshi Tamura,Keishiro Furuie et al.
Hijiri Watanabe et al.
Congenital nephrogenic diabetes insipidus (CNDI), a rare hereditary disorder, is characterized by the inability of the kidneys to concentrate urine in response to the antidiuretic hormone arginine vasopressin (AVP); as a result, large volum...