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9,072 results

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Page 1
Autosomal dominant polycystic kidney disease.
Cornec-Le Gall E, Alam A, Perrone RD. Cornec-Le Gall E, et al. Lancet. 2019 Mar 2;393(10174):919-935. doi: 10.1016/S0140-6736(18)32782-X. Epub 2019 Feb 25. Lancet. 2019. PMID: 30819518 Review.
Autosomal dominant polycystic kidney disease (ADPKD) is the most common hereditary kidney disease and one of the most common causes of end-stage kidney disease. ...Phase 3 randomised, placebo-controlled clinical trial …
Autosomal dominant polycystic kidney disease (ADPKD) is the most common hereditary kidney disea …
Novel mutations of PKD genes in Chinese patients suffering from autosomal dominant polycystic kidney disease and seeking assisted reproduction.
He WB, Xiao WJ, Tan YQ, Zhao XM, Li W, Zhang QJ, Zhong CG, Li XR, Hu L, Lu GX, Lin G, Du J. He WB, et al. BMC Med Genet. 2018 Oct 17;19(1):186. doi: 10.1186/s12881-018-0693-7. BMC Med Genet. 2018. PMID: 30333007 Free PMC article.
BACKGROUND: Autosomal dominant polycystic kidney disease (ADPKD), the commonest inherited kidney disease, is generally caused by heterozygous mutations in PKD1, PKD2, or GANAB (PKD3). ...
BACKGROUND: Autosomal dominant polycystic kidney disease (ADPKD), the commonest inherited kidney …
Renal Lymphangiomatosis Mimicking Polycystic Kidney Disease In An Adult, A Case Report and Literature Review.
Koc NS, Yilmaz SR, Karcaaltincaba M, Yildirim T, Erdem Y. Koc NS, et al. Iran J Kidney Dis. 2021 Jan;15(1):61-63. Iran J Kidney Dis. 2021. PMID: 33492306 Review.
The differential diagnosis contains renal lymphoma, polycystic kidney disease, multicystic dysplasia and renal tumors. We report a case of renal lymphangiomatosis, previously diagnosed as autosomal dominant polycystic kidney dis …
The differential diagnosis contains renal lymphoma, polycystic kidney disease, multicystic dysplasia and renal tumors. …
Primary Histiocytic Sarcoma in Adult Polycystic Kidney Disease: Case Report and Review of Literature.
Krishnamurthy K, Delgado R, Kochiyil J, Medina AM. Krishnamurthy K, et al. Int J Surg Pathol. 2021 May;29(3):321-326. doi: 10.1177/1066896920942891. Epub 2020 Jul 17. Int J Surg Pathol. 2021. PMID: 32677548 Review.
Genetically driven tissue destruction followed by remodeling in adult polycystic kidney disease (APKD) raises the possibility of malignant transformation. ...In this article, we describe a case of primary HS occurring in a 61-year-old man with end-stag …
Genetically driven tissue destruction followed by remodeling in adult polycystic kidney disease (APKD) raises th …
[Polycystic liver disease].
Ongaro M, Bronstein FN, Goossens N, Spahr L, Bresson Hadni S. Ongaro M, et al. Rev Med Suisse. 2022 Aug 31;18(793):1599-1605. doi: 10.53738/REVMED.2022.18.793.1599. Rev Med Suisse. 2022. PMID: 36047551 French.
Polycystic liver disease (PLD) includes three entities in adults : biliary hamartomas which develop as a result of ductal plate malformation, autosomal dominant polycystic liver disease (ADPLD) and autosomal dominant poly …
Polycystic liver disease (PLD) includes three entities in adults : biliary hamartomas which develop as a result of ductal plat …
Prevalence, risk factors and disease knowledge of polycystic kidney disease in Pakistan.
Zahid R, Akram M, Rafique E. Zahid R, et al. Int J Immunopathol Pharmacol. 2020 Jan-Dec;34:2058738420966083. doi: 10.1177/2058738420966083. Int J Immunopathol Pharmacol. 2020. PMID: 33125856 Free PMC article.
Polycystic kidneys disease refers to cyst(s) formation in kidneys with severe consequences of end stage renal disease thus have higher mortality. It is a common genetic disease occurring either as autosomal dominant polycystic k …
Polycystic kidneys disease refers to cyst(s) formation in kidneys with severe consequences of end stage renal disease t …
A miRNA-Based Approach in Autosomal Dominant Polycystic Kidney Disease: Challenges and Insights from Adult to Pediatric Evidence.
Vitulano C, Forcina G, Colosimo S, Frattolillo V, Villani AV, Marzuillo P, Miraglia Del Giudice E, Di Sessa A. Vitulano C, et al. Mol Diagn Ther. 2025 Mar;29(2):183-193. doi: 10.1007/s40291-024-00761-7. Epub 2025 Jan 17. Mol Diagn Ther. 2025. PMID: 39820940 Review.
Autosomal dominant polycystic kidney disease (ADPKD) represents the most common inherited kidney disorder leading to kidney failure in a significant percentage of patients over time. Although previously considered as an adult …
Autosomal dominant polycystic kidney disease (ADPKD) represents the most common inherited kidney d …
Is autosomal dominant polycystic kidney disease an early sweet disease?
Dachy A, Decuypere JP, Vennekens R, Jouret F, Mekahli D. Dachy A, et al. Pediatr Nephrol. 2022 Sep;37(9):1945-1955. doi: 10.1007/s00467-021-05406-z. Epub 2022 Jan 5. Pediatr Nephrol. 2022. PMID: 34988697 Free article. Review.
The clinical course of autosomal dominant polycystic kidney disease (ADPKD) starts in childhood. Evidence of the beneficial impact of early nephron-protective strategies and lifestyle modifications on ADPKD prognosis is accumulating. Recent stud …
The clinical course of autosomal dominant polycystic kidney disease (ADPKD) starts in childhood. Evidence …
Modulating inflammation with interleukin 37 treatment ameliorates murine Autosomal Dominant Polycystic Kidney Disease.
Zylberberg AK, Cottle DL, Runting J, Rodrigues G, Tham MS, Jones LK, Cumming HE, Short KM, Zaph C, Smyth IM. Zylberberg AK, et al. Kidney Int. 2024 Apr;105(4):731-743. doi: 10.1016/j.kint.2023.12.006. Epub 2023 Dec 28. Kidney Int. 2024. PMID: 38158181
Autosomal Dominant Polycystic Kidney Disease (ADPKD) is a leading cause of kidney failure and is associated with substantial morbidity and mortality. ...Interestingly, transgenic IL37b expression also did not alter macrophage numbers in a …
Autosomal Dominant Polycystic Kidney Disease (ADPKD) is a leading cause of kidney failure and is a …
9,072 results