Results 321 to 330 of about 117,699 (379)

A Rare Diagnosis of Caroli Syndrome in a Young Patient [PDF]

Clin Case Rep
ABSTRACT Caroli syndrome is a rare but serious congenital disorder associated with portal hypertension and polycystic kidney disease. Early diagnosis via imaging, particularly MRCP, is crucial to prevent life‐threatening complications such as cholangitis and biliary cirrhosis.
Karimzadeh‐Soureshjani E, Pourhasan F, Simab P, Shojaei S, Mohammadian Y.   +4 more
europepmc   +2 more sources

Filling the holes in cystic kidney disease research.

Clin J Am Soc Nephrol, 2014
Guay-Woodford LM, Henske E, Igarashi P, Perrone RD, Reed-Gitomer B, Somlo S, Torres VE, Ketchum CJ, Star RA, Flessner MF, Rasooly RS.   +10 more
europepmc   +1 more source

A Case of Horseshoe Kidney and Autosomal Dominant Polycystic Kidney Disease with <i>PKD1</i> Gene Mutation. [PDF]

J Clin Med
Kim H, Lee SJ, Kim W.
europepmc   +1 more source

Malignant Transformation of Renal Cyst with Bosniak I Features. [PDF]

Diagnostics (Basel)
Ćulap S, Brkić F, Matković A, Svetec J, Jurjević N, Horvat Pavlov K, Vidjak V, Ferenc T.   +7 more
europepmc   +1 more source

Autosomal dominant polycystic kidney disease: an overview of recent genetic and clinical advances. [PDF]

Ren Fail
Borghol AH, Bou Antoun MT, Hanna C, Salih M, Rahbari-Oskoui FF, Chebib FT.   +5 more
europepmc   +1 more source

Abstracts

Molecular Oncology, Volume 19, Issue S1, Page 1-895, June 2025.
Abstracts submitted to the ‘EACR 2025 Congress: Innovative Cancer Science’, from 16–19 June 2025 and accepted by the Congress Organising Committee are published in this Supplement of Molecular Oncology, an affiliated journal of the European Association for Cancer Research (EACR).
wiley   +1 more source

Case Report: A rare case of mixed epithelial and stromal tumor of the kidney in an adolescent: imaging findings and literature review. [PDF]

Front Pediatr
Fu G, Xiao R, Yang X, Lu T.
europepmc   +1 more source

Hypertrophic cardiomyopathy combined with renal and adrenal aplasia in a male with Noonan syndrome from RAF1 variant

ESC Heart Failure, Volume 12, Issue 3, Page 2371-2376, June 2025.
Ying Wang, Guizhou Ma, Dianyu Cai, Jierong Yao, Bingying Huang, Chaojian Wu, Xiaoling Liu, Zhixiong Cai   +7 more
wiley   +1 more source

Acquired cystic kidney disease [PDF]

European Radiology, 2000
Acquired cystic kidney disease (ACKD), also known as acquired renal cystic disease (ARCD,) occurs in patients who are on dialysis for end-stage renal disease. It is generally accepted that ACKD develops as a consequence of sustained uremia and can first manifest even before dialysis is initiated while the patient is still in chronic renal failure.
Theodore I. Steinman, Jogiraju Tantravahi   +1 more
openaire   +5 more sources

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Cystic Disease of the Kidney

Annual Review of Pathology: Mechanisms of Disease, 2007
This review focuses on the mechanisms that underlie the development of human renal cystic diseases. A pathological, clinical, and pathophysiological overview is given. Initial analysis of the cell biology of inappropriate hyperproliferation accompanied by fluid secretion of cyst-lining epithelia has been followed by the elucidation of fundamental ...
Patricia D. Wilson, Beatrice Goilav
openaire   +3 more sources