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Paediatric cholestatic liver disease: Diagnosis, assessment of disease progression and mechanisms of fibrogenesis. [World J Gastrointest Pathophys...]
Paediatric cholestatic liver disease: Diagnosis, assessment of disease progression and mechanisms of fibrogenesis.
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Recommendations for management of liver and biliary tract disease in cystic fibr...
Recommendations for management of liver and biliary tract disease in cystic fibrosis. Cystic Fibrosis Foundation Hepatobiliary Disease Consensus Group.
J Pediatr Gastroenterol Nutr. 1999 ;28 Suppl 1:S1-13.

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Comparative in vitro activities of meropenem, imipenem, temocillin, piperacillin...
Comparative in vitro activities of meropenem, imipenem, temocillin, piperacillin, and ceftazidime in combination with tobramycin, rifampin, or ciprofloxacin against Burkholderia cepacia isolates from patients with cystic fibrosis.
Antimicrob Agents Chemother. 1999 Feb ;43(2):213-7.

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9925508[uid] (1)
PubMed
Structure and function of the CFTR chloride channel.
Structure and function of the CFTR chloride channel.
Physiol Rev. 1999 Jan ;79(1 Suppl):S23-45.

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Clinical and genetic risk factors for cystic fibrosis-related liver disease.
Clinical and genetic risk factors for cystic fibrosis-related liver disease.
Pediatrics. 1999 Jan ;103(1):52-7.

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