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The Pathophysiology of Inherited Renal Cystic Diseases. [PDF]
Genes (Basel)Renal cystic diseases (RCDs) can arise from utero to early adulthood and present with a variety of symptoms including renal, hepatic, and cardiovascular manifestations.
Satariano M, Ghose S, Raina R.
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The process of adhering to aerosol therapy in adolescents with cystic fibrosis: patient and parent perspectives [PDF]
, 2012 Advances in medicine and healthcare have resulted in significant improvements for those children and adolescents living with a chronic health condition. However, the treatments prescribed will only work if they are taken.
O'Toole, Daniel Patrick Harry
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Fighting time: A qualitative analysis on the impact of lung transplantation in adults with Cystic Fibrosis [PDF]
, 2001 During the last decade lung transplantation has become an option for those with end-stage respiratory disease, including Cystic Fibrosis. However, there appears to have been very little written about the experiences of those who are on the lung ...
McCarthy, Janet Mary
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A novel mutation causing nephronophthisis in the Lewis polycystic kidney rat localises to a conserved RCC1 domain in Nek8 [PDF]
, 2012 Background Nephronophthisis (NPHP) as a cause of cystic kidney disease is the most common genetic cause of progressive renal failure in children and young adults.
Morahan, G. +23 more
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Bicaudal C mutation causes myc and TOR pathway up-regulation and polycystic kidney disease-like phenotypes in Drosophila. [PDF]
PLoS Genetics, 2017 Progressive cystic kidney degeneration underlies diverse renal diseases, including the most common cause of kidney failure, autosomal dominant Polycystic Kidney Disease (PKD).
Chiara Gamberi +3 more
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Brazilian Journal of Nephrology, 2021 Wunderlich syndrome, or spontaneous renal hemorrhage (SRH), is a rare condition encountered in patients undergoing chronic hemodialysis (HD) usually attributed to acquired cystic kidney disease (ACKD) among other causes. In the literature, colonoscopy is
Antoine Jean Zgheib +2 more
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Medeniyet Medical Journal, 2021 Mutations in hepatocyte nuclear factor-1 beta (HNF1B) are the most commonly identified genetic cause of renal malformations. Heterozygous mutations are associated with renal cysts and diabetes syndrome.
Nilüfer Göknar +5 more
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Unilateral renal cystic disease [PDF]
Kidney International, 2012 A 26-year-old Asian female initially presented to the emergency department with transient abdominal pain following a motor vehicle accident. Further evaluation by computed tomography of the abdomen incidentally revealed multiple cysts in the left kidney resembling autosomal dominant polycystic kidney disease (Figures 1 and 2).
Baradhi, Krishna M., Abuelo, Gary J.
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Nephronophthisis and medullary cystic kidney disease complex [PDF]
Vojnosanitetski Pregled, 2005 Background. Nephronophthisis and medullary cystic kidney disease complex refers to the genetic heterogeneous group of inherited tubulointerstital nephritis. Nephronophthisis comprises at last 3 clinical manifestations, has the autosomal recessive pattern
Stanišić Marijana +3 more
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The critical role of the Hippo signaling pathway in kidney diseases
Frontiers in Pharmacology, 2022 The Hippo signaling pathway is involved in cell growth, proliferation, and apoptosis, and it plays a key role in regulating organ size, tissue regeneration, and tumor development.
Yuting Sun +9 more
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