Results 121 to 130 of about 25,511 (203)

Autophagy and Autosomal Dominant Polycystic Kidney Disease

Turkish Journal of Nephrology, 2023
Özgür Akın Oto, Charles L. Edelstein
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CLINICAL CASE OF AUTOSOMAL DOMINANT POLYCYSTOSIS OF THE KIDNEY IN A CHILD WITH CONNECTIVE TISSUE DYPLASIA

Мать и дитя в Кузбассе, 2022
The relevance of the problem of autosomal dominant polycystic kidney disease in childhood is due to age-related features of the formation of renal cysts and clinical manifestations, the frequent development of arterial hypertension syndrome and ...
Андрей Васильевич Налетов, Любовь Феликсовна Чалая, Оксана Николаевна Москалюк, Мария Александровна Мацынина   +3 more
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Echocardiographic characteristics of autosomal dominant polycystic kidney disease

Scientific Reports
Cardiovascular complications in patients with autosomal dominant polycystic kidney disease (ADPKD) are frequently investigated extrarenal manifestations with contradictory outcomes.
Agata Koska-Ścigała, Hanna Jankowska, Magdalena Jankowska, Maria Dudziak, Marcin Hellmann, Alicja Dębska-Ślizień   +5 more
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Autosomal-dominante polyzystische Nierenerkrankung: Neue therapeutische Ansätze [PDF]

, 2018
Zusammenfassung: Die autosomal-dominante polyzystische Nierenerkrankung ("autosomal dominant polycystic kidney disease", ADPKD) ist die häufigste genetische Nierenerkrankung, sie betrifft weltweit etwa 6Mio. Menschen.
Poster, D., Serra, A.L., Wüthrich, R.P.
core  

Polycystic kidney disease in a Persian cat [PDF]

, 2015
A 6-year-old intact Persian cat was presented for the primary complaint of inappetence and weight loss. Irregular surface of kidneys was palpated during physical examination. Abdominal radiograph findings were indicative of renomegaly.
Khor, Kuan Hua, Lau, Seng Fong, Phoon, Melissa Hoi Ee, Saw, Ming Hooi   +3 more
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Autosomal dominant polycystic kidney disease [PDF]

Journal of Medical Genetics, 1996
openaire   +2 more sources

Unusual familial cystic kidney disease: combining fine radiologic and genetic evaluation to solve the case

BMC Nephrology
Background Autosomal dominant polycystic kidney disease (ADPKD) is the most prevalent hereditary kidney disease, characterized by enlarged kidneys with numerous cysts, high blood pressure, and a variety of extrarenal complications.
Sylvain Bodard, Rim Nabbout, Olivier Hélénon, Bertrand Knebelmann   +3 more
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Tolvaptan in Autosomal Dominant Polycystic Kidney Disease [PDF]

New England Journal of Medicine, 2013
Ron T. Gansevoort, Vicente E. Torres, Frank S. Czerwiec   +2 more
openaire   +9 more sources

Insights into autosomal dominant polycystic kidney disease by quantitative mass spectrometry-based proteomics [PDF]

, 2018
Autosomal dominant polycystic kidney disease (ADPKD) is a common monogenetic disorder that is caused by mutations in the genes PKD1 and PKD2 encoding polycystin-1 and polycystin-2, respectively.
Dengjel, Jörn, Diedrich, Britta
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New Therapies Targeting Cystogenesis in Autosomal Polycystic Kidney Disease

European Medical Journal Nephrology, 2017
Autosomal dominant polycystic kidney disease is the most common inherited kidney disease and results from mutations in the polycystin 1 gene (PKD1) or the polycystin 2 gene (PKD2).
Maurizio Salvadori, Aris Tsalouchos
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