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1.
Certain heterozygous variants in the kinase domain of the serine/threonine kinase NEK8 can cause an autosomal dominant form of polycystic kidney disease.
Kidney Int
; 104(5): 995-1007, 2023 Nov.
Article
in English
| MEDLINE | ID: mdl-37598857
2.
Clinical course and management of children with IgA vasculitis with nephritis.
Pediatr Nephrol
; 38(11): 3721-3733, 2023 11.
Article
in English
| MEDLINE | ID: mdl-37316676
3.
Primary hyperoxaluria diagnosed after kidney transplant: A review of the literature and case report of aggressive renal replacement therapy and lumasiran to prevent allograft loss.
Am J Transplant
; 21(12): 4061-4067, 2021 12.
Article
in English
| MEDLINE | ID: mdl-34254430
4.
External Validation of a Urinary Biomarker Risk Score for the Prediction of Steroid Responsiveness in Adults With Nephrotic Syndrome.
Kidney Int Rep
; 8(11): 2458-2468, 2023 Nov.
Article
in English
| MEDLINE | ID: mdl-38025209
5.
Frontotemporal degeneration genetic risk loci and transcription regulation as a possible mechanistic link to disease risk.
Medicine (Baltimore)
; 101(41): e31078, 2022 Oct 14.
Article
in English
| MEDLINE | ID: mdl-36253972
6.
Comprehensive Review of Steroid-Sensitive Nephrotic Syndrome Genetic Risk Loci and Transcriptional Regulation as a Possible Mechanistic Link to Disease Risk.
Kidney Int Rep
; 6(1): 187-195, 2021 Jan.
Article
in English
| MEDLINE | ID: mdl-33426398
7.
Bleeding Complications after Pediatric Kidney Biopsy: A Systematic Review and Meta-Analysis.
Clin J Am Soc Nephrol
; 14(1): 57-65, 2019 01 07.
Article
in English
| MEDLINE | ID: mdl-30522995
8.
Disarranged Sphingolipid Metabolism From Sphingosine-1-Phosphate Lyase Deficiency Leads to Congenital Nephrotic Syndrome.
Kidney Int Rep
; 4(12): 1763-1769, 2019 Dec.
Article
in English
| MEDLINE | ID: mdl-31844815
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