Results 31 to 40 of about 15,419 (219)
Journal of the American Society of Nephrology, 2008 Superficially, autosomal dominant polycystic kidney disease (ADPKD) and autosomal recessive polycystic kidney disease (ARPKD) seem to be more different than alike. ADPKD is common, its cysts arise from any nephron segment, and it is slowly progressive.[1][1] Hepatic cysts are its primary ...
Jun-ya Kaimori, Gregory G. Germino
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Giant Bilateral Adrenal Myelolipoma: Case Report
Indian Journal of Endocrinology and Metabolism, 2020 Adrenal myelolipomas are nonfunctional tumors that are usually asymptomatic; however, they have been known to coexist with other endocrine disorders, such as Cushing's syndrome, congenital adrenal hyperplasia (CAH), Conn's syndrome, and pheochromocytoma.
B Rathna Roger +3 more
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Bone Reports, 2023 ADPKD is caused by pathogenic variants in PKD1 or PKD2, encoding polycystin-1 and -2 proteins. Polycystins are expressed in osteoblasts and chondrocytes in animal models, and loss of function is associated with low bone mineral density (BMD) and volume ...
Dalia Zubidat +19 more
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Cyst growth in ADPKD is prevented by pharmacological and genetic inhibition of TMEM16A in vivo
Nature Communications, 2020 In autosomal dominant polycystic kidney disease (ADPKD) multiple bilateral renal cysts gradually enlarge, leading to a decline in renal function. Transepithelial chloride secretion through cystic fibrosis transmembrane conductance regulator (CFTR) and ...
Inês Cabrita +6 more
semanticscholar +1 more source
Canadian Journal of Kidney Health and Disease, 2021 Purpose: With evolving evidence around the progression, assessment, and management of autosomal dominant polycystic kidney disease (ADPKD), care of the disease has become increasingly complex.
M. Bevilacqua +6 more
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Cardiac structural and functional findings in Persian cats with autosomal dominant polycystic kidney disease [PDF]
Ciência Rural, 2020 : Autosomal dominant polycystic kidney disease (ADPKD) has been related to left ventricular structural and functional abnormalities in human patients. The present study aimed to evaluate the cardiac structural and functional findings in Persian cats with
Juliana Mariotti Guerra +10 more
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A Hidden Culprit: Aldosteronoma as a Rare Cause of Refractory Hypertension in Autosomal‐Dominant Polycystic Kidney Disease [PDF]
Clin Case RepABSTRACT Hypertension is common in autosomal‐dominant polycystic kidney disease (ADPKD) but may occasionally reflect a secondary etiology. We report a 71‐year‐old man with ADPKD and end‐stage renal disease who developed persistent, refractory hypertension following renal transplantation despite multidrug therapy and bilateral native nephrectomy ...
Wainstein M +7 more
europepmc +2 more sources
ADPKD, Tolvaptan, and Nephrolithiasis Risk [PDF]
Clinical Journal of the American Society of Nephrology, 2020 Patients with autosomal dominant polycystic kidney disease (ADPKD) have a higher risk of nephrolithiasis ([1][1]). When using unenhanced computed tomography, calculi can be identified in up to 25% of patients with ADPKD ([2][2]).
Ewout J. Hoorn, Robert Zietse
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Patient Preference and Adherence, 2021 Holger Schirutschke, Peter Gross, Alexander Paliege, Christian Hugo University Hospital Carl Gustav Carus at the Technische, Universität Dresden, Department of Internal Medicine III, Division of Nephrology, Dresden, GermanyCorrespondence: Holger ...
Schirutschke H +3 more
doaj
Exome sequencing of Saudi Arabian patients with ADPKD
Renal Failure, 2019 Purpose: Autosomal dominant polycystic kidney disease (ADPKD) is characterized by progressive development of kidney cysts and enlargement and dysfunction of the kidneys. The Consortium of Radiologic Imaging Studies of the Polycystic Kidney Disease (CRISP)
Fahad A. Al-Muhanna +19 more
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