Quantitative evaluation of the development of the exocrine pancreas in cystic fibrosis and control infants

scientific article published on June 1, 1979

Quantitative evaluation of the development of the exocrine pancreas in cystic fibrosis and control infants is …
instance of (P31):
scholarly articleQ13442814

External links are
P953full work available at URLhttp://ajp.amjpathol.org/cgi/content/abstract/95/3/697
https://europepmc.org/articles/PMC2042306
https://europepmc.org/articles/PMC2042306?pdf=render
https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/453330/?tool=EBI
https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/453330/pdf/?tool=EBI
P932PMC publication ID2042306
P698PubMed publication ID453330

P2093author name stringJ. M. Sturgess
D. G. Fagan
J. R. Imrie
P2860cites workPathology of cystic fibrosis review of the literature and comparison with 146 autopsied casesQ34426002
Intralumenal intestinal obstructionQ40001638
A review of 164 children with meconium ileus seen at the Children's Hospital Medical Center, BostonQ40071176
The pancreas in cystic fibrosis: chemical composition and comparative morphologyQ67760192
Cystic fibrosis of the pancreas. Morphologic findings in infants with and without diagnostic pancreatic lesionsQ69558473
THE INTESTINAL LESIONS IN CYSTIC FIBROSIS OF THE PANCREASQ76555898
P433issue3
P407language of work or nameEnglishQ1860
P921main subjectpancreasQ9618
cystic fibrosisQ178194
P304page(s)697-708
P577publication date1979-06-01
P1433published inThe American Journal of PathologyQ4744259
P1476titleQuantitative evaluation of the development of the exocrine pancreas in cystic fibrosis and control infants
P478volume95

Reverse relations

cites work (P2860)
Q37624228A novel gene delivery method transduces porcine pancreatic duct epithelial cells.
Q55172112Abdominal pain in cystic fibrosis.
Q36499679Abnormal endocrine pancreas function at birth in cystic fibrosis ferrets
Q35574197An activated immune and inflammatory response targets the pancreas of newborn pigs with cystic fibrosis
Q35178642Animal models of gastrointestinal and liver diseases. Animal models of cystic fibrosis: gastrointestinal, pancreatic, and hepatobiliary disease and pathophysiology.
Q30538611Cftr controls lumen expansion and function of Kupffer's vesicle in zebrafish
Q35097413Characteristic multiorgan pathology of cystic fibrosis in a long-living cystic fibrosis transmembrane regulator knockout murine model
Q72569721Chronic alcoholism and hypertension
Q55376866Cystic Fibrosis-Related Diabetes.
Q39690281Cystic fibrosis--a gastroenterological cornucopia
Q37470271Cystic fibrosis-related diabetes: from CFTR dysfunction to oxidative stress.
Q42172793Development of a porcine model of cystic fibrosis.
Q36944556Disruption of the CFTR gene produces a model of cystic fibrosis in newborn pigs
Q33646755Evidence for a causal relationship between early exocrine pancreatic disease and cystic fibrosis-related diabetes: a Mendelian randomization study
Q52874114Gastrointestinal complications in cystic fibrosis.
Q55386161Gastrointestinal tract and nutrition in cystic fibrosis: pathophysiology.
Q35136628Glycaemic regulation and insulin secretion are abnormal in cystic fibrosis pigs despite sparing of islet cell mass.
Q91825728Gut Microbiota in Children With Cystic Fibrosis: A Taxonomic and Functional Dysbiosis
Q35595921Molecular consequences of cystic fibrosis transmembrane regulator (CFTR) gene mutations in the exocrine pancreas
Q24186571Omega-3 fatty acids for cystic fibrosis
Q40485071Ontogeny of human pancreatic exocrine function
Q36131548Pancreatic damage in fetal and newborn cystic fibrosis pigs involves the activation of inflammatory and remodeling pathways
Q36424575Pancreatic pathophysiology in cystic fibrosis
Q33703755Pathology of gastrointestinal organs in a porcine model of cystic fibrosis
Q69503720Pathophysiology of the exocrine pancreas in cystic fibrosis
Q41961145Quantitative evaluation of the development of tracheal submucosal glands in infants with cystic fibrosis and control infants
Q52878106Rationale of modern dietary recommendations in cystic fibrosis.
Q40069404Safety, pharmacokinetics, and pharmacodynamics of ivacaftor in patients aged 2-5 years with cystic fibrosis and a CFTR gating mutation (KIWI): an open-label, single-arm study.
Q47154527Structural abnormalities in islets from very young children with cystic fibrosis may contribute to cystic fibrosis-related diabetes
Q72569725Trisomy 18, cystic fibrosis, and blood immunoreactive trypsin
Q35597003Value of genetic testing in the management of pancreatitis
Q35934114Variants in Solute Carrier SLC26A9 Modify Prenatal Exocrine Pancreatic Damage in Cystic Fibrosis.

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