Results 331 to 340 of about 1,163,030 (369)
Some of the next articles are maybe not open access.
Journal of the Iowa Medical Society, 2009
Cystic fibrosis (CF) has traditionally been considered a disease for pediatricians and pediatric pulmonologists owing to the short life expectancy for patients suffering from this disease in the recent past.
John McArdle1, Laurie Whittaker2
semanticscholar +1 more source
Cystic fibrosis (CF) has traditionally been considered a disease for pediatricians and pediatric pulmonologists owing to the short life expectancy for patients suffering from this disease in the recent past.
John McArdle1, Laurie Whittaker2
semanticscholar +1 more source
Identification of the cystic fibrosis gene: Cloning and characterization of complementary DNA
Science, 1989Overlapping complementary DNA clones were isolated from epithelial cell libraries with a genomic DNA segment containing a portion of the putative cystic fibrosis (CF) locus, which is on chromosome 7.
J. Riordan
semanticscholar +2 more sources
MYOCARDIAL FIBROSIS IN CYSTIC FIBROSIS OF THE PANCREAS
Journal of Paediatrics and Child Health, 1970SYNOPSIS A series of 6 cases of cystic fibrosis of the pancreas complicated by myocardial fibrosis is presented. This complication has been reported on only 2 occasions in the English literature. In the Dunedin hospital, which serves a population of less than 250,000, 5 cases have been found at necropsy since 1948.
G L Barnes, J F Gwynne, J M Watt
openaire +4 more sources
Frontiers in Bioscience, 2003
Renal fibrosis causes significant morbidity and mortality as the primary acquired lesion leading to the need for dialysis or kidney transplantation. Fibrosis can occur in either the filtering or reabsorptive component of the nephron, the functional unit of the kidney.
H William, Schnaper, Jeffrey B, Kopp
openaire +3 more sources
Renal fibrosis causes significant morbidity and mortality as the primary acquired lesion leading to the need for dialysis or kidney transplantation. Fibrosis can occur in either the filtering or reabsorptive component of the nephron, the functional unit of the kidney.
H William, Schnaper, Jeffrey B, Kopp
openaire +3 more sources
Best Practice & Research Clinical Rheumatology, 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.
Pipitone, Nicolò +2 more
openaire +3 more sources
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.
Pipitone, Nicolò +2 more
openaire +3 more sources
Annual Review of Immunology, 2013
Fibrosis is the production of excessive amounts of connective tissue, i.e., scar formation, in the course of reactive and reparative processes. Fibrosis develops as a consequence of various underlying diseases and presents a major diagnostically and therapeutically unsolved problem.
Roswitha Sgonc +7 more
openaire +3 more sources
Fibrosis is the production of excessive amounts of connective tissue, i.e., scar formation, in the course of reactive and reparative processes. Fibrosis develops as a consequence of various underlying diseases and presents a major diagnostically and therapeutically unsolved problem.
Roswitha Sgonc +7 more
openaire +3 more sources
2010
Abstract Cystic fibrosis (CF) is a recessively inherited disease caused by mutations in the cystic fibrosis gene, located on the long arm of chromosome 7, which codes for a membrane protein—the cystic fibrosis transmembrane regulator protein—that is a chloride channel.
Andrew Bush, Caroline Elston
openaire +1 more source
Abstract Cystic fibrosis (CF) is a recessively inherited disease caused by mutations in the cystic fibrosis gene, located on the long arm of chromosome 7, which codes for a membrane protein—the cystic fibrosis transmembrane regulator protein—that is a chloride channel.
Andrew Bush, Caroline Elston
openaire +1 more source