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Quoted phrase not found in phrase index: "Polycystic liver disease 3 with or without kidney cysts"
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. Multiple clinical manifestations, such as enlarged kidneys filled with growing cysts …
Autosomal dominant polycystic kidney disease (ADPKD) is the most common hereditary kidney disease and one of the most common c …
Structural and Functional Changes in Human Kidneys with Healthy Aging.
Hommos MS, Glassock RJ, Rule AD. Hommos MS, et al. J Am Soc Nephrol. 2017 Oct;28(10):2838-2844. doi: 10.1681/ASN.2017040421. Epub 2017 Aug 8. J Am Soc Nephrol. 2017. PMID: 28790143 Free PMC article. Review.
Aging is associated with significant changes in structure and function of the kidney, even in the absence of age-related comorbidities. On the macrostructural level, kidney cortical volume decreases, surface roughness increases, and the number and size of simple ren …
Aging is associated with significant changes in structure and function of the kidney, even in the absence of age-related comorbiditie …
Genetic Complexity of Autosomal Dominant Polycystic Kidney and Liver Diseases.
Cornec-Le Gall E, Torres VE, Harris PC. Cornec-Le Gall E, et al. J Am Soc Nephrol. 2018 Jan;29(1):13-23. doi: 10.1681/ASN.2017050483. Epub 2017 Oct 16. J Am Soc Nephrol. 2018. PMID: 29038287 Free PMC article. Review.
Data indicate significant phenotypic and genotypic overlap, plus a common pathogenesis, between two groups of inherited disorders, autosomal dominant polycystic kidney diseases (ADPKD), a significant cause of ESRD, and autosomal dominant polycystic liver diseases (ADPLD), …
Data indicate significant phenotypic and genotypic overlap, plus a common pathogenesis, between two groups of inherited disorders, autosomal …
Genetics, pathobiology and therapeutic opportunities of polycystic liver disease.
Olaizola P, Rodrigues PM, Caballero-Camino FJ, Izquierdo-Sanchez L, Aspichueta P, Bujanda L, Larusso NF, Drenth JPH, Perugorria MJ, Banales JM. Olaizola P, et al. Nat Rev Gastroenterol Hepatol. 2022 Sep;19(9):585-604. doi: 10.1038/s41575-022-00617-7. Epub 2022 May 13. Nat Rev Gastroenterol Hepatol. 2022. PMID: 35562534 Review.
Liver cysts arise in patients with autosomal dominant PLD (ADPLD) or in co-occurrence with renal cysts in patients with autosomal dominant or autosomal recessive polycystic kidney disease (ADPKD and ARPKD, respectively). Hepatic cystogenesis is a heterogeneou …
Liver cysts arise in patients with autosomal dominant PLD (ADPLD) or in co-occurrence with renal cysts in patients with autoso …
Polycystic Liver Disease: Advances in Understanding and Treatment.
Masyuk TV, Masyuk AI, LaRusso NF. Masyuk TV, et al. Annu Rev Pathol. 2022 Jan 24;17:251-269. doi: 10.1146/annurev-pathol-042320-121247. Epub 2021 Nov 1. Annu Rev Pathol. 2022. PMID: 34724412 Free PMC article. Review.
Polycystic liver disease (PLD) is a group of genetic disorders characterized by progressive development of cholangiocyte-derived fluid-filled hepatic cysts. PLD is the most common manifestation of autosomal dominant and autosomal recessive polycystic …
Polycystic liver disease (PLD) is a group of genetic disorders characterized by progressive development of cholangiocyt …
Dysplastic kidneys.
Winyard P, Chitty LS. Winyard P, et al. Semin Fetal Neonatal Med. 2008 Jun;13(3):142-51. doi: 10.1016/j.siny.2007.10.009. Epub 2007 Dec 11. Semin Fetal Neonatal Med. 2008. PMID: 18065301 Review.
Dysplastic kidneys are common malformations affecting up to 1 in 1000 of the general population. ...Excluding syndromic cases with defects in other organ systems, features linked to worse prognosis at presentation are: (1) bilateral disease; (2) decreased functional renal …
Dysplastic kidneys are common malformations affecting up to 1 in 1000 of the general population. ...Excluding syndromic cases with de …
Genetics of polycystic liver diseases.
Lee-Law PY, van de Laarschot LFM, Banales JM, Drenth JPH. Lee-Law PY, et al. Curr Opin Gastroenterol. 2019 Mar;35(2):65-72. doi: 10.1097/MOG.0000000000000514. Curr Opin Gastroenterol. 2019. PMID: 30652979 Review.
PURPOSE OF REVIEW: This review provides an outline of the most recent insights and significant discoveries regarding the genetic mechanisms involved in polycystic liver disease. RECENT FINDINGS: Polycystic liver disease includes a heterog …
PURPOSE OF REVIEW: This review provides an outline of the most recent insights and significant discoveries regarding the genetic mechanisms …
Therapeutic Targets in Polycystic Liver Disease.
Masyuk TV, Masyuk AI, LaRusso NF. Masyuk TV, et al. Curr Drug Targets. 2017;18(8):950-957. doi: 10.2174/1389450116666150427161743. Curr Drug Targets. 2017. PMID: 25915482 Free PMC article. Review.
Polycystic liver diseases (PLD) are a group of genetic disorders initiated by mutations in several PLD-related genes and characterized by the presence of multiple cholangiocyte-derived hepatic cysts that progressively replace liver tissue. PLD co-exists with Autosomal Domi …
Polycystic liver diseases (PLD) are a group of genetic disorders initiated by mutations in several PLD-related genes and characterized by th …
Cystic Kidney Diseases in Children and Adults: Differences and Gaps in Clinical Management.
Hanna C, Iliuta IA, Besse W, Mekahli D, Chebib FT. Hanna C, et al. Semin Nephrol. 2023 Jul;43(4):151434. doi: 10.1016/j.semnephrol.2023.151434. Epub 2023 Nov 22. Semin Nephrol. 2023. PMID: 37996359 Review.
Cystic kidney diseases, when broadly defined, have a wide differential diagnosis extending from recessive diseases with a prenatal or pediatric diagnosis, to the most common autosomal-dominant polycystic kidney disease primarily affecting adults, and several other g …
Cystic kidney diseases, when broadly defined, have a wide differential diagnosis extending from recessive diseases with a prenatal or …
Polycystic renal disease.
Anderson GA, Degroot D, Lawson RK. Anderson GA, et al. Urology. 1993 Oct;42(4):358-64. doi: 10.1016/0090-4295(93)90358-h. Urology. 1993. PMID: 8212435 Review.
Renal cystic disease is a relatively common disorder whose development and progression currently appear to be due to an interaction between an abnormal basement membrane matrix, a potentially immature, hyperproliferative epithelium, and an abnormal epithelial secretory apparatus. …
Renal cystic disease is a relatively common disorder whose development and progression currently appear to be due to an interaction between …
1,978 results