Results 271 to 280 of about 952,925 (309)
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Journal of Urology, 2012
Retroperitoneal fibrosis is a rare syndrome hallmarked by a fibrosclerotic tissue in the retroperitoneum, often leading to encasement of the ureters. About two-thirds of cases of retroperitoneal fibrosis are idiopathic, while the remaining cases are secondary to a variety of different causes, including drugs, tumors and infections.
Kevin, Day +2 more
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Retroperitoneal fibrosis is a rare syndrome hallmarked by a fibrosclerotic tissue in the retroperitoneum, often leading to encasement of the ureters. About two-thirds of cases of retroperitoneal fibrosis are idiopathic, while the remaining cases are secondary to a variety of different causes, including drugs, tumors and infections.
Kevin, Day +2 more
openaire +5 more sources
Urologic Radiology, 1990
Retroperitoneal fibrosis is idiopathic in two thirds of cases and is found most commonly as an isolated fibrotic plaque centered over the lower lumbar spine and entrapping one or both ureters. It has been postulated that the fibrosis in the idiopathic cases results from a hypersensitivity reaction to antigens leaking into the retroperitoneum from ...
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Retroperitoneal fibrosis is idiopathic in two thirds of cases and is found most commonly as an isolated fibrotic plaque centered over the lower lumbar spine and entrapping one or both ureters. It has been postulated that the fibrosis in the idiopathic cases results from a hypersensitivity reaction to antigens leaking into the retroperitoneum from ...
openaire +3 more sources
Seminars in Respiratory and Critical Care Medicine, 2023
Siobhain, Mulrennan, Andrew M, Jones
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Siobhain, Mulrennan, Andrew M, Jones
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Clinics in Perinatology, 2001
Although mutation detection rates have not universally reached the 95% detection level recommended by the American Society of Human Genetics and are not likely to exceed 90% for many populations in the foreseeable future, CF carrier screening will probably be offered routinely in the near future.
L P, Shulman, S, Elias
openaire +2 more sources
Although mutation detection rates have not universally reached the 95% detection level recommended by the American Society of Human Genetics and are not likely to exceed 90% for many populations in the foreseeable future, CF carrier screening will probably be offered routinely in the near future.
L P, Shulman, S, Elias
openaire +2 more sources
Fibrosis: A General Feature in Cystic Fibrosis?
Journal of Pediatric Gastroenterology and Nutrition, 2002M, Häusler, G, Heimann, S, Biesterfeld
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