Results 191 to 200 of about 34,123 (218)
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Endothelin in Polycystic Kidney Disease

2011
Autosomal dominant polycystic kidney disease (ADPKD) is the most common genetic kidney disease in man and is caused by germline mutations in PKD1 or PKD2. Affected patients develop progressively enlarged kidneys due to the growth of multiple renal epithelial cysts. Several studies have demonstrated marked intrafamilial phenotypic variability in PKD1 or
Ming-Yang, Chang, Albert C M, Ong
openaire   +2 more sources

Polycystic kidney disease

Seminars in Roentgenology, 1975
M A, Bosniak, M A, Ambos
openaire   +2 more sources

Genetic Spectrum of Polycystic Kidney and Liver Diseases and the Resulting Phenotypes

Advances in Kidney Disease and Health, 2023
Peter Harris   +2 more
exaly  

[Diagnosis in Polycystic Kidney Disease].

Giornale italiano di nefrologia : organo ufficiale della Societa italiana di nefrologia, 2016
The diagnosis of ADPKD should be based on a thorough assessment of the family history, radiological study and when indicated, genetic study. The anamnestic definition of 'negative family history' should be accepted only after a full clinical-instrumental assessment of close relatives of the subject .
openaire   +2 more sources

Cystic Kidney Diseases That Require a Differential Diagnosis from Autosomal Dominant Polycystic Kidney Disease (ADPKD)

Journal of Clinical Medicine, 2022
Kan Katayama   +2 more
exaly  

POLYCYSTIC DISEASE OF THE KIDNEYS

Medical Journal of Australia, 1951
openaire   +2 more sources

Polycystic Liver and Kidney Disease

Clinical Gastroenterology and Hepatology, 2022
Kwabena Oware, Adu-Gyamfi   +2 more
openaire   +2 more sources

Polycystic Kidney Disease

Southern Medical Journal, 1979
A C, Chester, W P, Argy
openaire   +2 more sources

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