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Quoted phrase not found in phrase index: "Familial cystic renal disease"
Page 1
Predictors of autosomal dominant polycystic kidney disease progression.
Schrier RW, Brosnahan G, Cadnapaphornchai MA, Chonchol M, Friend K, Gitomer B, Rossetti S. Schrier RW, et al. J Am Soc Nephrol. 2014 Nov;25(11):2399-418. doi: 10.1681/ASN.2013111184. Epub 2014 Jun 12. J Am Soc Nephrol. 2014. PMID: 24925719 Free PMC article. Review.
Autosomal dominant polycystic kidney disease is a genetic disorder associated with substantial variability in its natural course within and between affected families. ...These factors include PKD1 mutation (particularly truncating mutation), men, early onset …
Autosomal dominant polycystic kidney disease is a genetic disorder associated with substantial variability in its natural cour …
The Clinical Characteristics and Gene Mutations of Maturity-Onset Diabetes of the Young Type 5 in Sixty-One Patients.
Ge S, Yang M, Cui Y, Wu J, Xu L, Dong J, Liao L. Ge S, et al. Front Endocrinol (Lausanne). 2022 Jun 30;13:911526. doi: 10.3389/fendo.2022.911526. eCollection 2022. Front Endocrinol (Lausanne). 2022. PMID: 35846334 Free PMC article.
AIMS: Maturity-onset diabetes of the young type 5 (MODY5), a rare disease, is very easy to be misdiagnosed as type 2 diabetes. To get better understanding of the disease, we analyzed the clinical characteristics and gene mutations of MODY5. ...Of the 39 patients wit …
AIMS: Maturity-onset diabetes of the young type 5 (MODY5), a rare disease, is very easy to be misdiagnosed as type 2 diabetes. To get …
Is Regular Screening for Intracranial Aneurysm Necessary in Patients with Autosomal Dominant Polycystic Kidney Disease? A Systematic Review and Meta-analysis.
Zhou Z, Xu Y, Delcourt C, Shan J, Li Q, Xu J, Hackett ML. Zhou Z, et al. Cerebrovasc Dis. 2017;44(1-2):75-82. doi: 10.1159/000476073. Epub 2017 May 13. Cerebrovasc Dis. 2017. PMID: 28502970 Free article. Review.
BACKGROUND: The prevalence of intracranial aneurysm in patients with autosomal dominant polycystic kidney disease (ADPKD) is higher than that among the general population. ...Studies from China, Japan and Europe (Germany, Poland) reported a higher prevalence of intr …
BACKGROUND: The prevalence of intracranial aneurysm in patients with autosomal dominant polycystic kidney disease (ADPKD) is h …
Range and Variability of Outcomes Reported in Randomized Trials Conducted in Patients With Polycystic Kidney Disease: A Systematic Review.
Sautenet B, Cho Y, Gutman T, Rangan G, Ong A, Chapman AB, Ahn C, Coolican H, Tze-Wah Kao J, Fowler K, Gansevoort RT, Geneste C, Perrone RD, Harris T, Torres VE, Pei Y, Craig JC, Tong A; SONG-PKD Initiative. Sautenet B, et al. Am J Kidney Dis. 2020 Aug;76(2):213-223. doi: 10.1053/j.ajkd.2019.12.003. Epub 2020 Mar 11. Am J Kidney Dis. 2020. PMID: 32171640 Free article.
RATIONALE & OBJECTIVE: Trials in autosomal dominant polycystic kidney disease (ADPKD) have increased, but their impact on decision making has been limited. ...The 3 most frequently reported domains were in the surrogate category: kidney function (54; 79% …
RATIONALE & OBJECTIVE: Trials in autosomal dominant polycystic kidney disease (ADPKD) have increased, but their impact on …
CFTR variants and renal abnormalities in males with congenital unilateral absence of the vas deferens (CUAVD): a systematic review and meta-analysis of observational studies.
Cai H, Qing X, Niringiyumukiza JD, Zhan X, Mo D, Zhou Y, Shang X. Cai H, et al. Genet Med. 2019 Apr;21(4):826-836. doi: 10.1038/s41436-018-0262-7. Epub 2018 Sep 14. Genet Med. 2019. PMID: 30214069 Free PMC article.
We performed a systematic review to elucidate the genetic link between CFTR variants, CUAVD, and the associated risk of renal abnormality (RA). METHODS: We searched relevant databases for eligible articles reporting CFTR variants in CUAVD. ...
We performed a systematic review to elucidate the genetic link between CFTR variants, CUAVD, and the associated risk of renal abnorma …
Characteristics of intracranial aneurysms and subarachnoid haemorrhage in patients with polycystic kidney disease.
Gieteling EW, Rinkel GJ. Gieteling EW, et al. J Neurol. 2003 Apr;250(4):418-23. doi: 10.1007/s00415-003-0997-0. J Neurol. 2003. PMID: 12700905 Review.
BACKGROUND AND PURPOSE: Subarachnoid haemorrhage is a common cause of death in patients with autosomal dominant polycystic kidney disease (ADPKD), but little is known about specific characteristics of subarachnoid haemorrhage and intracranial aneurysms in this group …
BACKGROUND AND PURPOSE: Subarachnoid haemorrhage is a common cause of death in patients with autosomal dominant polycystic kidney …
Umbrella systematic review finds limited evidence that school absence explains the association between chronic health conditions and lower academic attainment.
Jay MA, Sanders-Ellis D, Blackburn R, Deighton J, Gilbert R. Jay MA, et al. Front Public Health. 2023 Jun 9;11:1122769. doi: 10.3389/fpubh.2023.1122769. eCollection 2023. Front Public Health. 2023. PMID: 37361156 Free PMC article.
Whereas reviews found an association between a range of CHCs (CHCs generally, cystic fibrosis, hemophilia A, end-stage renal disease (pre-transplant), end-stage kidney disease (pre-transplant), spina bifida, congenital heart disease, orof …
Whereas reviews found an association between a range of CHCs (CHCs generally, cystic fibrosis, hemophilia A, end-stage renal …
Hereditary Hypophosphatemic Rickets with Hypercalciuria Presenting with Enthesopathy, Renal Cysts, and High Serum c-Terminal FGF23: Single-Center Experience and Systematic Review.
Dodamani MH, Memon SS, Karlekar M, Lila AR, Khan M, Sarathi V, Arya S, Jamale T, Thakare S, Patil VA, Shah NS, Bergwitz C, Bandgar TR. Dodamani MH, et al. Calcif Tissue Int. 2024 Feb;114(2):137-146. doi: 10.1007/s00223-023-01156-2. Epub 2023 Nov 19. Calcif Tissue Int. 2024. PMID: 37981601
On systematic review of 58 probands (with biallelic SLC34A3 mutations; 35 males), early-onset HHRH and renal calcification were present in ~ 70% and late-onset HHRH in 10%. c.575C > T p....Renal calcifications correlated with age but were similar across truncatin …
On systematic review of 58 probands (with biallelic SLC34A3 mutations; 35 males), early-onset HHRH and renal calcification were prese …
Chronic jejuno-colonic fistula and intestinal malabsorption due to multiple magnet ingestions: A case report and systematic review.
Özcan R, Hakalmaz AE, Kalyoncu Uçar A, Beser O, Emre S. Özcan R, et al. Ulus Travma Acil Cerrahi Derg. 2024 May;30(5):361-369. doi: 10.14744/tjtes.2024.50845. Ulus Travma Acil Cerrahi Derg. 2024. PMID: 38738679 Free article. Review. English.
A six-year-old girl was admitted to the Pediatric Gastroenterology Department pre-senting with intermittent abdominal pain, vomiting, and diarrhea persisting for two years. Initial differential diagnoses included celiac disease, cystic fibrosis, inflammatory bowel …
A six-year-old girl was admitted to the Pediatric Gastroenterology Department pre-senting with intermittent abdominal pain, vomiting, and di …
Prevalence and risk of rupture of intracranial aneurysms: a systematic review.
Rinkel GJ, Djibuti M, Algra A, van Gijn J. Rinkel GJ, et al. Stroke. 1998 Jan;29(1):251-6. doi: 10.1161/01.str.29.1.251. Stroke. 1998. PMID: 9445359
The prevalence was higher in patients with autosomal dominant polycystic kidney disease (relative risk [RR], 4.4 [2.7 to 7.2]), a familial predisposition (RR, 4.0 [2.7 to 6.0]), or atherosclerosis (RR, 2.3 [1.7 to 3.1]). ...
The prevalence was higher in patients with autosomal dominant polycystic kidney disease (relative risk [RR], 4.4 [2.7 to 7.2]) …