Results 71 to 80 of about 5,682,559 (225)

Imaging medullary cystic kidney disease with magnetic resonance.

, 2003
Medullary cystic kidney disease is characterized by multiple renal cysts at the corticomedullary boundary area, by autosomal dominant inheritance, and by onset of chronic renal failure in the third decade of life.
Jacob, L., Mougenot, B., Ronco, P., Antignac, C., Meier, P., Farres, M.T., Le Goas, F.   +6 more
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Metabolic syndrome, the leptin gene and kidney disease in non-diabetic black South Africans [PDF]

, 2008
Includes abstract.Includes bibliographical references (leaves 226-256).Obesity is a worldwide problem and is a factor in the pathogenesis of the metabolic syndrome and kidney disease through the development of obesity-related hypertension and ...
Okpechi, Ikechi Gareth
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Zebrafish models of cystic kidney disease related ciliopathies [PDF]

, 2013
PhD ThesisCystic kidney diseases are a fascinating cluster of discrete conditions and an important, common cause of established renal failure. Both isolated and syndromic inherited cystic kidney diseases are known to be linked by their pathogenesis ...
Simms, Roslyn Jane
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Surfactant protein a in cystic fibrosis: supratrimeric structure and pulmonary outcome. [PDF]

, 2012
The state of oligomerization of surfactant associated protein-A (SP-A) monomers differs between individuals. This likely affects SP-A's functional properties and could thereby influence clinical status in patients with lung diseases.
Karl Paul, Matthias Kappler, Michael Kabesch, Stephanie Heinrich, Paul, Karl, Rietschel, Ernst, Griese, Matthias, Kappler, Matthias, Kabesch, Michael, Ratjen, Felix, Heinrich, Stephanie, Ballmann, Manfred, Matthias Griese, Felix Ratjen, Ernst Rietschel, Manfred Ballmann, Kappler Matthias, Heinrich Stephanie, Rietschel Ernst, Kabesch Michael, Paul Karl, Ballmann Manfred, Griese Matthias, Ratjen Felix   +23 more
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The First Pediatric Case of an IFT140 Heterozygous Deletion Causing Autosomal Dominant Polycystic Kidney Disease: Case Report

Case Reports in Nephrology and Dialysis
Introduction: Autosomal dominant polycystic kidney disease (ADPKD) is the most common hereditary kidney disease, which is mainly caused by pathogenic variants in two particular genes: PKD1 and PKD2.
Tomáš Seeman, Terezie Šuláková, Alice Bosáková, Jana Indráková, Dagmar Grečmalová   +4 more
doaj   +1 more source

Incidentally Detected Primary Giant Renal Cystic Enchinococcosis in a Young Patient: An Underestimated Entity? [PDF]

European Medical Journal Urology, 2015
Echinococcosis is a parasitic infestation caused by Echinococcus granulosus and is an endemic disease in many parts of world. The symptoms and signs depend on the location and size of the cyst.
Emre Urer, Ozer Ural Cakici, Abdullah Erdem Canda, Aylin Kilic Yazgan, Seda Marali, Erem Asil, Ali Fuat Atmaca   +6 more
doaj  

Sonographic assessment of the severity and progression of autosomal dominant polycystic kidney disease: The Consortium of Renal Imaging Studies in Polycystic Kidney Disease (CRISP)

, 2005
Background: The accuracy and precision of ultrasonography (US) in assessing the severity of autosomal dominant polycystic kidney disease (ADPKD) is unknown.
Grantham, Jared J., Thompson, Paul A., Guay-Woodford, Lisa M., O'Neill, W. Charles, Bae, Kyongtae T., Torres, Vicente E., King, Bernard F., Chapman, Arlene B., Robbin, Michelle L., Wetzel, Louis H., Miller, J. Philip   +10 more
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Glomerulocystic Kidney Disease and End-stage Renal Disease in a Child: A Rare Case Report and Literature Review: Glomerulocystic Kidney Disease [PDF]

Glomerulocystic kidney disease (GCKD) is characterized by cystic dilatation of theBowman’s capsule and adjacent tubules. It is a rare form of cystic kidney disease and canoccur at any age.
Sharmim, Shanjida, Begum, Afroza, Akbar, Romana, Uddin, Golam Muin, Huque, Syed Saimul, Hossain, Delwar   +5 more
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Deciphering the Impact of RAC1‐SPTAN1 in ARPKD Cystogenesis Using Multifaceted Models

Advanced Science
Autosomal recessive polycystic kidney disease (ARPKD) leads to severe renal cysts and progressive kidney dysfunction, with no approved treatments. The absence of such cystic phenotypes in Pkhd1−/− mice underscores the need for novel models that better ...
Shohei Kuraoka, Yuhei Higashi, Suguru Saito, Solmaz Pourgonabadi, Honami Honjoh, Sho Ishigaki, Peter C. Harris, Lisa M. Satlin, Michifumi Yamashita, Ryuji Morizane   +9 more
doaj   +1 more source

Ureteral atresia presenting as an abdominal cyst: A case report

Journal of Pediatric Surgery Case Reports
Background: Ureteral atresia is a rare disease that is usually associated with a non-functioning dysplastic kidney. The condition may be unilateral or bilateral, short, or long, and may involve any part of the ureter.
Amir Ibrahim, Mohamed Mansy, Mostafa Kotb, Mohamed Abokandil, Saber Waheeb   +4 more
doaj   +1 more source