Results 31 to 40 of about 31,827 (245)

The role of miRNAs in the development of cholangiopathies. Part 2

open access: yesZdorovʹe Rebenka, 2023
The role of miRNA in the development of cho­langiopathies is considered in the scientific review. This article discusses the role of miRNA in biliary atresia, polycystic liver disease, and cholangiocarcinoma.
A.E. Abaturov, V.L. Babуch
doaj   +2 more sources

Simultaneous liver kidney transplantation and (bilateral) nephrectomy through a midline is feasible and safe in polycystic disease. [PDF]

open access: yesPLoS ONE, 2017
In Eurotransplant, 50% of simultaneous liver kidney transplantations (SLK) are performed for polycystic disease. Classically, liver and kidney are transplanted in two steps: liver through a subcostal incision, kidney through a separate oblique incision ...
Ina Jochmans   +4 more
doaj   +1 more source

Isolated Polycystic Liver Disease: An Unusual Cause of Recurrent Variceal Bleed

open access: yesCase Reports in Gastrointestinal Medicine, 2018
Isolated polycystic liver disease is a rare disorder. Majority of the patients with isolated polycystic liver disease are asymptomatic with incidental detection of liver cysts on imaging studies done for other purposes.
Mohammad Saud Khan   +7 more
doaj   +1 more source

Supra Hepatic Inferior Vena Cava Thrombosis–Surgical Challenges [PDF]

open access: yesJournal of Clinical and Diagnostic Research, 2016
Autosomal Dominant Polycystic Kidney Disease (ADPKD) is a chronic affliction characterized by numerous liver and kidney cysts. There is a gradual but progressive renal and liver impairment which may require combined liver-kidney transplantation ...
SENTHIL MUTHURAMAN   +4 more
doaj   +1 more source

Multiple Gastric Carcinomas Associated with Potter Type III Cystic Disease

open access: yesCase Reports in Gastroenterology, 2011
We report a case of multiple gastric carcinomas associated with Potter type III cystic disease of the liver, mesenterium and kidney. A 65-year-old man with chronic renal failure due to polycystic kidneys and under hemodialysis treatment 3 times a week ...
Kenji Mimatsu   +7 more
doaj   +1 more source

Amebic liver abscess and polycystic liver disease

open access: yesMedical Journal of Dr. D.Y. Patil University, 2013
Polycystic liver disease is a rare disorder which remains asymptomatic. Infection of cyst is a major complication and is usually pyogenic. We report a rare case of amebic liver abscess in a patient with polycystic liver disease.
Karan V. S. Rana   +3 more
doaj   +1 more source

Kidney Organoids in Drug Development: Integrating Technological Advances and Standardization for Effective Implementation

open access: yesAdvanced Healthcare Materials, EarlyView.
This review examines how emerging enabling technologies enhance the physiological relevance, scalability, and reproducibility of kidney organoids, while advanced analytical approaches support model validation and deepen mechanistic insight into nephrotoxicity.
Helen Kearney   +3 more
wiley   +1 more source

Polycystic liver disease with huge infected cyst displacing the pancreas, inferior vena cava and right kidney

open access: yesSaudi Journal of Medicine and Medical Sciences, 2016
Multiple liver cysts can be an isolated disease (isolated polycystic liver disease [PLD]) or they can be part of multi-organ involvement in other diseases, such as adult autosomal dominant polycystic disease (APD), which is the most frequently inherited ...
Adil H Al-Harthi   +2 more
doaj   +1 more source

A Biomarker‐Driven Ovary–Endometrium Organ‐on‐a‐Chip Mimicking 3D Multicellular Complexity and Menstrual Cyclicity for Predicting Reproductive Toxicity

open access: yesAdvanced Science, EarlyView.
We present a dual‐organ, biomarker‐integrated ovaryendometrium organ‐on‐a‐chip that recapitulates 3D tissue complexity, menstrual cycle dynamics, and hormonal crosstalk. This platform enables real‐time, cell‐typespecific fluorescent readouts of reproductive toxicity using ANGPTL4 and SERPINB2 as early‐response reporters.
Soo‐Rim Kim   +6 more
wiley   +1 more source

Chronic brucellosis with hepatic brucelloma and AA amyloidosis in a patient with autosomal dominant polycystic kidney disease

open access: yesAutopsy and Case Reports, 2020
We describe an autopsy case of a 45-year-old male diagnosed with autosomal dominant polycystic kidney disease who presented with complaints of altered sensorium.
Arpitha Kollabathula   +6 more
doaj   +1 more source

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