The evolution of liver disease in cystic fibrosis.

scientific article

The evolution of liver disease in cystic fibrosis. is …
instance of (P31):
scholarly articleQ13442814

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P356DOI10.1136/ADC.81.2.129
P8608Fatcat IDrelease_75e3d3ngxzdtreb24oimjeuldy
P932PMC publication ID1718033
P698PubMed publication ID10490519
P5875ResearchGate publication ID12808742

P50authorSimon C LingQ38642068
P2093author name stringJ D Wilkinson
J McColl
J Y Paton
A S Hollman
T J Evans
P2860cites workIndications, methods, and outcomes of percutaneous liver biopsy in England and Wales: an audit by the British Society of Gastroenterology and the Royal College of Physicians of LondonQ24541328
Liver cirrhosis in cystic fibrosis--therapeutic implications and long term follow up.Q33623427
Effects of ursodeoxycholic acid treatment on nutrition and liver function in patients with cystic fibrosis and longstanding cholestasisQ34392767
Liver disease and common-bile-duct stenosis in cystic fibrosisQ39533300
The relationship between chest radiographic scores and respiratory function tests in children with cystic fibrosisQ40468887
Effects of ursodeoxycholic acid on liver function in patients with cystic fibrosis and chronic cholestasisQ43551362
Localization of the cystic fibrosis transmembrane conductance regulator in human bile duct epithelial cellsQ45866124
Effect of a Medium Dose of Ursodeoxycholic Acid with or without Taurine Supplementation on the Nutritional Status of Patients with Cystic FibrosisQ60199019
A comparison of survival, growth, and pulmonary function in patients with cystic fibrosis in Boston and TorontoQ68095095
Liver cirrhosis: changes of Doppler waveform of hepatic veinsQ68182543
Ultrasonography in the diagnosis of portal hypertension: diminished response of portal vessels to respirationQ70264571
The changing epidemiology of cystic fibrosisQ70528025
Ursodeoxycholic acid for liver disease associated with cystic fibrosis: a double-blind multicenter trial. The Italian Group for the Study of Ursodeoxycholic Acid in Cystic FibrosisQ71173367
Liver disease in cystic fibrosisQ71695013
An ultrasound scoring system for the diagnosis of liver disease in cystic fibrosisQ71997598
Analysis of risk factors for the development of liver disease associated with cystic fibrosisQ72274632
Can the histologic changes of cystic fibrosis-associated hepatobiliary disease be predicted by clinical criteria?Q73517330
Recommendations for management of liver and biliary tract disease in cystic fibrosis. Cystic Fibrosis Foundation Hepatobiliary Disease Consensus GroupQ77958537
P433issue2
P407language of work or nameEnglishQ1860
P921main subjectcystic fibrosisQ178194
liver diseaseQ929737
P304page(s)129-132
P577publication date1999-08-01
P1433published inArchives of Disease in ChildhoodQ4787296
P1476titleThe evolution of liver disease in cystic fibrosis
P478volume81

Reverse relations

cites work (P2860)
Q44927735Endogenous ursodeoxycholic acid and cholic acid in liver disease due to cystic fibrosis.
Q33431380Features of Severe Liver Disease With Portal Hypertension in Patients With Cystic Fibrosis
Q37850707Intestinal obstruction syndromes in cystic fibrosis: meconium ileus, distal intestinal obstruction syndrome, and constipation
Q79325382Liver involvement in cystic fibrosis
Q44980713Mechanistic similarities between cultured cell models of cystic fibrosis and niemann-pick type C.
Q35099096Metabolic liver disease in the young adult
Q84800550Outcome in Cystic Fibrosis Liver Disease
Q34992341Paediatric cholestatic liver disease: Diagnosis, assessment of disease progression and mechanisms of fibrogenesis.
Q64077819The emerging burden of liver disease in cystic fibrosis patients: A UK nationwide study
Q36085123The gallbladder and biliary tract in cystic fibrosis
Q80386847The role of abdominal ultrasound in the diagnosis, staging and management of cystic fibrosis liver disease
Q51141266Transient elastography in patients with cystic fibrosis.
Q46121018Vaccine induced Hepatitis A and B protection in children at risk for cystic fibrosis associated liver disease.
Q84341387[Vaccination of cystic fibrosis patients]

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