Zobrazeno 1 - 10
of 316
pro vyhledávání: '"SRNS"'
Autor:
Youmna Ahmed Hassan Elbeltagi, Mahmoud Mohi El Din El Kersh, Hanan Mohammad Fathy, Nancy Abdel-Salam Kamel
Publikováno v:
Egyptian Pediatric Association Gazette, Vol 72, Iss 1, Pp 1-9 (2024)
Abstract Background Nephrotic syndrome (NS) is a disease with favorable outcomes in most cases. Failure to respond to steroids is one of the most important predictors of clinical outcome. We performed a retrospective study on 51 primary idiopathic SR
Externí odkaz:
https://doaj.org/article/31916a90ae624432b453d5b43e329fdb
Autor:
Dmytro Ivanov, Lutz T. Weber, Elena Levtchenko, Liudmyla Vakulenko, Mariia Ivanova, Iryna Zavalna, Yelizaveta Lagodych, Ninel Boiko
Publikováno v:
Biomedicines, Vol 12, Iss 11, p 2600 (2024)
Background: Steroid-sensitive nephrotic syndrome (SSNS) and steroid-resistant nephrotic syndrome (SRNS) significantly affect children’s quality of life. There are frequent relapses in SSNS and progression in SRNS. IPNA guidelines suggest that monoc
Externí odkaz:
https://doaj.org/article/d1b9c272fff24fb09d4beb9de1238a1f
Autor:
Li Lin, Yuhong Ye, Haidong Fu, Weizhong Gu, Manli Zhao, Jingmiao Sun, Zhongkai Cao, Guoping Huang, Yi Xie, Fei Liu, Lu Li, Qiuyu Li, Jianhua Mao, Lidan Hu
Publikováno v:
Cell Communication and Signaling, Vol 21, Iss 1, Pp 1-15 (2023)
Abstract Background Steroid-resistant nephrotic syndrome (SRNS) is characterized by unrelieved proteinuria after an initial 4–8 weeks of glucocorticoid therapy. Genes in podocytes play an important role in causing SRNS. Objective This study aimed t
Externí odkaz:
https://doaj.org/article/084c9fdc16784bd9997de7973a0d265a
Autor:
Mst. Shanjida Sharmim, Golam Muin Uddin, Afroza Begum, Habibur Rahman, Ranjit Ranjan Roy, Tahmina Shirin, Mohammad Rashidul Alam, AKM Muraduzzaman, Syed Saimul Huque, Tahmina Jesmin, Abdullah Al Mamun
Publikováno v:
Bangabandhu Sheikh Mujib Medical University Journal, Vol 16, Iss 4 (2023)
Background: Many children with idiopathic steroid resistant nephrotic syndrome have been reported worldwide due to mutation of NPHS1, NPHS2, WT1 and LAMB2 genes. This study aimed to determine the frequency of mutation of NPHS1, NPHS2, WT1, LAMB2, COL
Externí odkaz:
https://doaj.org/article/90533c22693e4de59707b1d6e5e1ab61
Autor:
Rachel K. Cason, Eileen Chambers, Tiffany Tu, Megan Chryst-Stangl, Kinsie Huggins, Brandon M. Lane, Alejandro Ochoa, Annette M. Jackson, Rasheed A. Gbadegesin
Publikováno v:
Frontiers in Pediatrics, Vol 11 (2023)
IntroductionThe etiology of most cases of nephrotic syndrome (NS) remains unknown, therefore patients are phenotypically categorized based on response to corticosteroid therapy as steroid sensitive NS (SSNS), or steroid resistant NS (SRNS). Genetic r
Externí odkaz:
https://doaj.org/article/e887ae7d61aa455c9f142c84468fad29
Publikováno v:
Egyptian Journal of Medical Human Genetics, Vol 23, Iss 1, Pp 1-18 (2022)
Abstract Background Steroid-resistant nephrotic syndrome (SRNS) is characterized by unresponsiveness of nephrotic range proteinuria to standard steroid therapy, and is the main cause of childhood renal failure. The identification of more than 53 mono
Externí odkaz:
https://doaj.org/article/6d449fb15255411088cca8d0e240e656
Akademický článek
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Akademický článek
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Publikováno v:
Egyptian Pediatric Association Gazette, Vol 70, Iss 1, Pp 1-6 (2022)
Abstract Background Nephrotic syndrome is characterized by proteinuria, hyperlipidemia, and edema. The annual incidence of nephrotic syndrome is 2–7 cases/100,000 children. Methods and results The present study included 32 control, 32 steroid-sensi
Externí odkaz:
https://doaj.org/article/edf03991b6cd41e5b06bb8df58538f10
Autor:
Adriel Roa-Bautista, Mahreen Sohail, Emma Wakeling, Kimberly C. Gilmour, Mark Davis, Anthony Gait, Giovanna Lucchini, David Cox, Reem Elfeky, Maaike Kusters
Publikováno v:
Frontiers in Immunology, Vol 14 (2023)
BackgroundSphingosine phosphate lyase insufficiency syndrome (SPLIS) is associated with biallelic variants in SGPL1, comprising a multisystemic disease characterized by steroid resistant nephrotic syndrome, primary adrenal insufficiency, neurological
Externí odkaz:
https://doaj.org/article/64535b3c0be948c49117b737d3543dc5