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Quoted phrase not found in phrase index: "Polycystic kidney disease 6 with or without polycystic liver disease"
Page 1
Prevalence of unruptured intracranial aneurysms, with emphasis on sex, age, comorbidity, country, and time period: a systematic review and meta-analysis.
Vlak MH, Algra A, Brandenburg R, Rinkel GJ. Vlak MH, et al. Lancet Neurol. 2011 Jul;10(7):626-36. doi: 10.1016/S1474-4422(11)70109-0. Lancet Neurol. 2011. PMID: 21641282 Review.
The overall prevalence was estimated as 3.2% (95% CI 1.9-5.2) in a population without comorbidity, with a mean age of 50 years, and consisting of 50% men. Compared with populations without the comorbidity, PRs were 6.9 (95% CI 3.5-14) for autosomal dominant polycystic …
The overall prevalence was estimated as 3.2% (95% CI 1.9-5.2) in a population without comorbidity, with a mean age of 50 years, and consisti …
Neonatal multicystic dysplastic kidney with mass effect: A systematic review.
Pettit S, Chalmers D. Pettit S, et al. J Pediatr Urol. 2021 Dec;17(6):763-768. doi: 10.1016/j.jpurol.2021.09.003. Epub 2021 Sep 11. J Pediatr Urol. 2021. PMID: 34538561 Review.
INTRODUCTION: Multicystic Dysplastic Kidney (MCDK) is a common cause of palpable abdominal mass in a neonate, yet reports are few of resultant life-threatening extrinsic compression. ...Medical Subject Headings (MeSH) were used to search PubMed through June 8, 2021 as foll …
INTRODUCTION: Multicystic Dysplastic Kidney (MCDK) is a common cause of palpable abdominal mass in a neonate, yet reports are few of …
Outcomes associated with fetal hepatobiliary cysts: systematic review and meta-analysis.
Leombroni M, Buca D, Celentano C, Liberati M, Bascietto F, Gustapane S, Marrone L, Manzoli L, Rizzo G, D'Antonio F. Leombroni M, et al. Ultrasound Obstet Gynecol. 2017 Aug;50(2):167-174. doi: 10.1002/uog.17244. Epub 2017 Jul 9. Ultrasound Obstet Gynecol. 2017. PMID: 27553859 Free article. Review.
No case of hepatic cyst had associated malformations of the biliary tract at birth. Clinical symptoms occurred in 14.8% (95% CI, 6.3-26.1%) of cases and, in 5.4% (95% CI, 0.9-13.6%), they were related to the presence of bile obstruction due to compression of the cys …
No case of hepatic cyst had associated malformations of the biliary tract at birth. Clinical symptoms occurred in 14.8% (95% CI, 6.3- …
Systematic review: the pathophysiology and management of polycystic liver disease.
Temmerman F, Missiaen L, Bammens B, Laleman W, Cassiman D, Verslype C, van Pelt J, Nevens F. Temmerman F, et al. Aliment Pharmacol Ther. 2011 Oct;34(7):702-13. doi: 10.1111/j.1365-2036.2011.04783.x. Epub 2011 Jul 26. Aliment Pharmacol Ther. 2011. PMID: 21790682 Free article. Review.
METHODS: A PubMed search was undertaken to identify relevant literature using search terms including polycystic liver disease, pathophysiology, surgical and medical management. ...The role of the inhibitors of the mammalian target of rapamycin (mTOR) in the m …
METHODS: A PubMed search was undertaken to identify relevant literature using search terms including polycystic liver disea …
The safety and efficacy of tolvaptan in the treatment of patients with autosomal dominant polycystic kidney disease: A systematic review and meta-analysis.
Li X, Li W, Li Y, Dong C, Zhu P. Li X, et al. Nefrologia (Engl Ed). 2023 Nov-Dec;43(6):731-741. doi: 10.1016/j.nefroe.2023.04.002. Epub 2023 May 5. Nefrologia (Engl Ed). 2023. PMID: 37150675 Free article.
BACKGROUND: The irreversible progression of autosomal dominant polycystic kidney disease (ADPKD) to end-stage renal disease (ESRD) is delayed by tolvaptan. ...Both of the decline of estimated glomerular filtration rate (eGFR) [MD=1.89, 95% CI (0.74, 3. …
BACKGROUND: The irreversible progression of autosomal dominant polycystic kidney disease (ADPKD) to end-stage renal …
Cardiovascular implications of hypertensive autosomal dominant polycystic kidney disease: a systematic review and meta-analysis.
Raina R, Shah R, Hong G, Bhatt GC, Abboud B, Jain R, Chanchlani R, Sethi SK. Raina R, et al. Pediatr Nephrol. 2023 Sep;38(9):2957-2972. doi: 10.1007/s00467-023-05893-2. Epub 2023 Feb 22. Pediatr Nephrol. 2023. PMID: 36811694 Review.
BACKGROUND: Autosomal dominant polycystic kidney disease (ADPKD) is among the most common inherited kidney diseases. ...Further research, particularly in younger patients, is necessary to further elucidate the relationship between hypertension i …
BACKGROUND: Autosomal dominant polycystic kidney disease (ADPKD) is among the most common inherited kidney di …
Laparoscopic Nephrectomy versus Open Nephrectomy for Patients with Autosomal Dominant Polycystic Kidney Disease: A Systematic Review and Meta-Analysis.
Guo P, Xu W, Li H, Ren T, Ni S, Ren M. Guo P, et al. PLoS One. 2015 Jun 8;10(6):e0129317. doi: 10.1371/journal.pone.0129317. eCollection 2015. PLoS One. 2015. PMID: 26053633 Free PMC article. Review.
OBJECTIVE: To compare efficacy and safety of laparoscopicnephrectomy (LN) versus open nephrectomy (ON) in the management of autosomal dominant polycystic kidney disease (ADPKD), we conducted a systematic review and meta-analysis. ...
OBJECTIVE: To compare efficacy and safety of laparoscopicnephrectomy (LN) versus open nephrectomy (ON) in the management of autosomal domina …
A systematic review to determine the most effective interventions to increase water intake.
Chua TX, Prasad NS, Rangan GK, Allman-Farinelli M, Rangan AM. Chua TX, et al. Nephrology (Carlton). 2016 Oct;21(10):860-9. doi: 10.1111/nep.12675. Nephrology (Carlton). 2016. PMID: 26599520 Review.
BACKGROUND: Maintaining adequate fluid intake has been hypothesized to be beneficial for the progression of chronic kidney disease (CKD). The aim of this study was to undertake a systematic review to determine the most effective interventions to increase water intak …
BACKGROUND: Maintaining adequate fluid intake has been hypothesized to be beneficial for the progression of chronic kidney disease …
Interventions for preventing the progression of autosomal dominant polycystic kidney disease.
Bolignano D, Palmer SC, Ruospo M, Zoccali C, Craig JC, Strippoli GF. Bolignano D, et al. Cochrane Database Syst Rev. 2015 Jul 14;2015(7):CD010294. doi: 10.1002/14651858.CD010294.pub2. Cochrane Database Syst Rev. 2015. PMID: 26171904 Free PMC article. Review.
BACKGROUND: Autosomal dominant polycystic kidney disease (ADPKD) is the most common inherited disorder causing kidney disease. ...In recent years, improved understanding of molecular and cellular mechanisms involved in kidney cyst growth …
BACKGROUND: Autosomal dominant polycystic kidney disease (ADPKD) is the most common inherited disorder causing kidne …
Outcomes of patients with autosomal-dominant polycystic kidney disease on peritoneal dialysis: A meta-analysis.
Boonpheng B, Thongprayoon C, Wijarnpreecha K, Medaura J, Chebib FT, Cheungpasitporn W. Boonpheng B, et al. Nephrology (Carlton). 2019 Jun;24(6):638-646. doi: 10.1111/nep.13431. Epub 2019 Apr 23. Nephrology (Carlton). 2019. PMID: 29952039
BACKGROUND: Complications related to peritoneal dialysis (PD) in patients with autosomal-dominant polycystic kidney disease (ADPKD), including intraperitoneal rupture of renal cyst, hernia, membrane failure and peritonitis, have been reported. ...
BACKGROUND: Complications related to peritoneal dialysis (PD) in patients with autosomal-dominant polycystic kidney disease …
33 results