Filters
Sharp liver excision under hepatic vascular exclusion in case of liver transplant for large polycystic disease. Case report of a new surgical technique
INTRODUCTION: Polycystic liver disease is observed in 75-90% of patients with autosomal dominant polycystic kidney disease (ADPKD). ADPKD has a high prevalence of 1 bleeding during the polycystic ...
Transplantation
- 2018 •
- Jimp •
- Link
Rok uplatnění
Jimp - Článek v periodiku v databázi Web of Science
Výsledek na webu
Fibropolycystic Liver Disease
Fibropolycystic liver disease is an entity comprising several rare diseases having a common origin in the abnormal embryonic development of the hepatobiliary system. The most common of these is polycystic liver...
Gastroenterology and hepatology
- 2022 •
- C
Rok uplatnění
C - Kapitola v odborné knize
Autosomal recessive and dominant polycystic kidney disease
The incidence of the autosomal recessive polycystic kidney disease is ca 1:10.000 birth. There are 2 main forms of ARPKD, one with an early onset, the second on starting later, both combined with liver fibrosis......
FG - Pediatrie
- 1999 •
- Jx
Rok uplatnění
Jx - Nezařazeno - Článek v odborném periodiku (Jimp, Jsc a Jost)
Non-alcoholic fatty liver disease, women's health and the role of the environment
Non-alcoholic fatty liver disease (NAFLD) is a major cause of chronic liver disorders and is currently one of the leading indications for liver transplantation. To date, prevention is the only effective management,...
Obstetrics and gynaecology
- 2024 •
- Jimp •
- Link
Rok uplatnění
Jimp - Článek v periodiku v databázi Web of Science
Výsledek na webu
Infection of hepatae cysts in patient with autosomal dominant polycystic kidney disease
Infection of hepatal cysts in patients with autosomal dominant polycystic kidney disease is quite rare but severe complication. This case report describes a case of patient with ADPKO, history of kidney transplantation with chronic ...
FE - Ostatní obory vnitřního lékařství
- 2014 •
- Jx
Rok uplatnění
Jx - Nezařazeno - Článek v odborném periodiku (Jimp, Jsc a Jost)
Severity in polycystic liver disease is associated with aetiology and female gender: Results of the International PLD Registry
Background & Aims: Polycystic liver disease (PLD) occurs in two genetic disorders, autosomal-dominant polycystic kidney disease (ADPKD) and autosomal-dominant polycystic liver dis...
Gastroenterology and hepatology
- 2019 •
- Jimp •
- Link
Rok uplatnění
Jimp - Článek v periodiku v databázi Web of Science
Výsledek na webu
Simultaneous liver kidney transplantation and (bilateral) nephrectomy through a midline is feasible and safe in polycystic disease
) are performed for polycystic disease. Classically, liver and kidney are transplanted in two of the voluminous polycystic liver and native nephrectomy whilst offering access to iliac fossae for kidney tra...
Transplantation
- 2017 •
- Jimp •
- Link
Rok uplatnění
Jimp - Článek v periodiku v databázi Web of Science
Výsledek na webu
Gastrointestinal tract involvement in hereditary kidney diseases
are an important component of autosomal dominant polycystic kidney disease. Even mild symptomsHereditary kidney diseases are an important and specific group of kidney diseases having often systemic and multiorgan ...
Gastroenterology and hepatology
- 2018 •
- JSC •
- Link
Rok uplatnění
JSC - Článek v periodiku v databázi SCOPUS
Výsledek na webu
Polycystic ovary disease - multisystem endoorinopathy
Polycystic ovary disease - multisystem endoorinopathy. A review the recent progress in the diagnostic, pathophysiology, and treatment of polycystic ovary disease....
FB - Endokrinologie, diabetologie, metabolismus, výživa
- 2000 •
- Jx
Rok uplatnění
Jx - Nezařazeno - Článek v odborném periodiku (Jimp, Jsc a Jost)
Kidney Versus Combined Kidney and Liver Transplantation in Young People With Autosomal Recessive Polycystic Kidney Disease: Data From the European Society for Pediatric Nephrology/European Renal
Background: The choice for either kidney or combined liver-kidney transplantation in young people with kidney failure and liver fibrosis due to autosomal recessive polycystic kidney disease(ARPKD) can be challengin...
FG - Pediatrie
- 2016 •
- Jx •
- Link
Rok uplatnění
Jx - Nezařazeno - Článek v odborném periodiku (Jimp, Jsc a Jost)
Výsledek na webu
- 1 - 10 out of 54 533