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1979 1
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33 results

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Page 1
[Four cases of nephrotic syndrome with TRPC6 gene variations and literature review].
Sun LW, Sun L, Wang P, Kang YL, Wu Y, Zhu GH, Huang WY. Sun LW, et al. Zhonghua Er Ke Za Zhi. 2021 Mar 2;59(3):223-227. doi: 10.3760/cma.j.cn112140-20200824-00822. Zhonghua Er Ke Za Zhi. 2021. PMID: 33657698 Review. Chinese.
Objective: To investigate the clinical characteristics, treatment and prognosis of TRPC6 variation induced children with steroid-resistant nephrotic syndrome (SRNS). Methods: Clinical data of four patients with nephrotic syndrome carrying TRPC6 variati …
Objective: To investigate the clinical characteristics, treatment and prognosis of TRPC6 variation induced children with steroid-resistant …
Rituximab in children with steroid-dependent nephrotic syndrome: experience of a tertiary center and review of the literature.
Van Horebeek I, Knops N, Van Dyck M, Levtchenko E, Mekahli D. Van Horebeek I, et al. Acta Clin Belg. 2017 Jun;72(3):147-155. doi: 10.1080/17843286.2016.1208955. Epub 2016 Jul 13. Acta Clin Belg. 2017. PMID: 27409338 Review.
OBJECTIVES: Rituximab (RTX) is a new treatment option in children with difficult-to-treat steroid-dependent nephrotic syndrome (SDNS). We evaluated the experience of our tertiary center and reviewed the current literature. ...RESULTS: Nine children with a median age …
OBJECTIVES: Rituximab (RTX) is a new treatment option in children with difficult-to-treat steroid-dependent nephrotic syndrome …
What is circulating factor disease and how is it currently explained?
Hayward S, Parmesar K, Saleem MA. Hayward S, et al. Pediatr Nephrol. 2023 Nov;38(11):3513-3518. doi: 10.1007/s00467-023-05928-8. Epub 2023 Mar 23. Pediatr Nephrol. 2023. PMID: 36952039 Free PMC article. Review.
Nephrotic syndrome (NS) consists of the clinical triad of hypoalbuminaemia, high levels of proteinuria and oedema, and describes a heterogeneous group of disease processes with different underlying drivers. ...Several circulating factors have been proposed and studi …
Nephrotic syndrome (NS) consists of the clinical triad of hypoalbuminaemia, high levels of proteinuria and oedema, and describ …
Sphingosine phosphate lyase insufficiency syndrome: a systematic review.
Pournasiri Z, Madani A, Nazarpack F, Sayer JA, Chavoshzadeh Z, Nili F, Tran P, Saba JD, Jamee M. Pournasiri Z, et al. World J Pediatr. 2023 May;19(5):425-437. doi: 10.1007/s12519-022-00615-4. Epub 2022 Nov 12. World J Pediatr. 2023. PMID: 36371483 Review.
BACKGROUND: Sphingosine-1-phosphate lyase insufficiency syndrome (SPLIS) or nephrotic syndrome type-14 is caused by biallelic mutations in SGPL1. ...Kidney disorders (42, 80.8%) were mainly in the form of steroid-resistant nephrotic syndrome …
BACKGROUND: Sphingosine-1-phosphate lyase insufficiency syndrome (SPLIS) or nephrotic syndrome type-14 is caused …
Genetics of the nephrotic syndrome.
Salomon R, Gubler MC, Niaudet P. Salomon R, et al. Curr Opin Pediatr. 2000 Apr;12(2):129-34. doi: 10.1097/00008480-200004000-00008. Curr Opin Pediatr. 2000. PMID: 10763762 Review.
There are a large number of glomerular diseases that may be responsible for a nephrotic syndrome, the most frequent in childhood being minimal change disease. In the past few years, the molecular genetic basis of several conditions that may cause a nephrotic …
There are a large number of glomerular diseases that may be responsible for a nephrotic syndrome, the most frequent in childho …
Advances in antigens associated with Idiopathic Membranous Nephropathy.
Li SS, Tang DE, Dai Y. Li SS, et al. J Formos Med Assoc. 2021 Nov;120(11):1941-1948. doi: 10.1016/j.jfma.2021.06.014. Epub 2021 Jul 7. J Formos Med Assoc. 2021. PMID: 34244038 Free article. Review.
Membranous nephropathy (MN) is a common cause of nephrotic syndrome in adults. Idiopathic MN (IMN), one of the forms of MN, usually has an unknown etiology. IMN is described as an autoimmune disease, and its pathogenesis is quite complex. The discovery of the M-t …
Membranous nephropathy (MN) is a common cause of nephrotic syndrome in adults. Idiopathic MN (IMN), one of the forms of MN, us …
Deriving and understanding the risk of post-transplant recurrence of nephrotic syndrome in the light of current molecular and genetic advances.
Bierzynska A, Saleem MA. Bierzynska A, et al. Pediatr Nephrol. 2018 Nov;33(11):2027-2035. doi: 10.1007/s00467-017-3793-2. Epub 2017 Oct 11. Pediatr Nephrol. 2018. PMID: 29022104 Free PMC article. Review.
The most dramatic manifestation of this phenomenon is in patients with nephrotic syndrome (NS). NS is a descriptive term describing a clinical picture centred on proteinuria arising from damage to the glomerular filtration barrier (GFB). ...This review is aimed at o …
The most dramatic manifestation of this phenomenon is in patients with nephrotic syndrome (NS). NS is a descriptive term descr …
Disease recurrence in paediatric renal transplantation.
Cochat P, Fargue S, Mestrallet G, Jungraithmayr T, Koch-Nogueira P, Ranchin B, Zimmerhackl LB. Cochat P, et al. Pediatr Nephrol. 2009 Nov;24(11):2097-108. doi: 10.1007/s00467-009-1137-6. Epub 2009 Feb 27. Pediatr Nephrol. 2009. PMID: 19247694 Free PMC article. Review.
The more typical presentation is a recurrence of the full disease, either with a high risk of GL (focal and segmental glomerulosclerosis 14-50% DR, 40-60% GL; atypical haemolytic uraemic syndrome 20-80% DR, 10-83% GL; membranoproliferative glomerulonephritis 30-100% DR, 17 …
The more typical presentation is a recurrence of the full disease, either with a high risk of GL (focal and segmental glomerulosclerosis 14- …
Kidney Lipidomics by Mass Spectrometry Imaging: A Focus on the Glomerulus.
Abbas I, Noun M, Touboul D, Sahali D, Brunelle A, Ollero M. Abbas I, et al. Int J Mol Sci. 2019 Apr 1;20(7):1623. doi: 10.3390/ijms20071623. Int J Mol Sci. 2019. PMID: 30939806 Free PMC article. Review.
Lipid disorders have been associated with glomerulopathies, a distinct type of renal pathologies, such as nephrotic syndrome. Global analyses targeting kidney lipids in this pathophysiologic context have been extensively performed, but most often regardless o …
Lipid disorders have been associated with glomerulopathies, a distinct type of renal pathologies, such as nephrotic syndrom …
Molecular basis of proteinuria.
Akhtar M, Al Mana H. Akhtar M, et al. Adv Anat Pathol. 2004 Nov;11(6):304-9. doi: 10.1097/01.pap.0000146219.03058.ea. Adv Anat Pathol. 2004. PMID: 15505531 Review.
Mutations in the gene-encoding nephrin are known to result in the Finnish type of nephrotic syndrome. The exact mechanism by which nephrin controls permselectivity is not yet clear, but it is known to interact with several podocyte proteins including CD2AP, p …
Mutations in the gene-encoding nephrin are known to result in the Finnish type of nephrotic syndrome. The exact mechani …
33 results