Results 21 to 30 of about 2,817,125 (290)

Renal Neoplasms in Patients With Renal Cystic Diseases [PDF]

open access: yesThe Journal of Urology, 1998
With advances in diagnostic imaging, small renal masses are being detected earlier and with increased frequency. The differential diagnosis of a small renal mass is extensive and includes a cyst, infarction, focal infection, angiomyolipoma, lymphoma, metastatic neoplasm, oncocytoma, renal cell carcinoma, and pseudotumor [1]. Differentiation is based on
Roubidoux, Marilyn A.   +2 more
openaire   +3 more sources

Cystic Renal Disease in Children: A Broad Spectrum from Simple Cyst to End Stage Renal Failure

open access: yesTurkish Journal of Nephrology, 2019
Objective: Renal cystic diseases consist of a broad spectrum of hereditary or acquired conditions that may lead to end stage renal disease. We aimed to evaluate our patients diagnosed as renal cystic disease in terms of their diagnosis, demographic ...
Neslihan Çiçek   +4 more
doaj   +1 more source

Unilateral renal cystic disease

open access: yesIndian Journal of Nephrology, 2010
Unilateral renal cystic disease of kidney is a non-familial and non-progressive disorder, characterized by replacement of the renal parenchyma by a cluster of multiple cysts with a normal contralateral kidney. This rare condition is not related to autosomal dominant polycystic kidney disease; as such, hepatic and pancreatic cysts are not seen.
Choh, N. A., Rashid, M.
openaire   +2 more sources

Fetal polycystic kidney disease: Pathological overview

open access: yesJournal of the Scientific Society, 2013
Polycystic kidney disease is a rare developmental anomaly inherited as autosomal dominant or autosomal recessive. It is characterized by cystic dilatation of the collecting ducts frequently associated with hepatic involvement and progression to renal ...
Sunita B Patil   +3 more
doaj   +1 more source

Using bacterial biomarkers to identify early indicators of cystic fibrosis pulmonary exacerbation onset [PDF]

open access: yes, 2011
Acute periods of pulmonary exacerbation are the single most important cause of morbidity in cystic fibrosis patients, and may be associated with a loss of lung function.
Matt W Johnson   +19 more
core   +1 more source

Development of lymphangioleiomyomatosis in a female patient with Sjö gren's disease: a review of literature and a case report

open access: yesСовременная ревматология, 2019
Cystic and bullous lung transformation occurs in diseases of various origins: neoplastic, genetically determined, rheumatic, lymphoproliferative, and infectious diseases. The paper presents a review of the literature and a clinical case of a young female
Yu. I. Khvan   +2 more
doaj   +1 more source

Renal impairment in a rural African antiretroviral programme [PDF]

open access: yes, 2009
Background: There is little knowledge regarding the prevalence and nature of renal impairment in African populations initiating antiretroviral treatment, nor evidence to inform the most cost effective methods of screening for renal impairment.
Till Barnighausen   +31 more
core   +2 more sources

Evaluating the effectiveness of the simple renal cysts treatment using minimally invasive techniques based on the analysis of cyst recurrences

open access: yesPatologìâ, 2015
Relevance of the work is due the lack of a single uniform opinion concerning the choice of the optimal method of minimally invasive treatment of simple renal cysts.
M. V. Varvashenia
doaj   +1 more source

Renal cystic diseases in children: New concepts

open access: yes, 2010
This review highlights the changes that have occurred in the general approach to cystic renal diseases in children. For instance, genetic mutations at the level of the primary cilia are considered as the origin of many renal cystic diseases. Furthermore,
Avni, Efraim, Hall, Michelle
core   +1 more source

Surfactant protein a in cystic fibrosis: supratrimeric structure and pulmonary outcome. [PDF]

open access: yes, 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   +15 more
core   +1 more source

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