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Volumn 2, Issue , 2008, Pages

Cystic fibrosis presenting as recurrent pancreatitis in a young child with a normal sweat test and pancreas divisum: A case report

Author keywords

[No Author keywords available]

Indexed keywords

AMILORIDE; AMYLASE; CHLORIDE; ISOPRENALINE; PANCREAS ENZYME; TRANSMEMBRANE CONDUCTANCE REGULATOR; TRIACYLGLYCEROL LIPASE;

EID: 46349101160     PISSN: 17521947     EISSN: 17521947     Source Type: Journal    
DOI: 10.1186/1752-1947-2-176     Document Type: Article
Times cited : (12)

References (14)
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    • Sharer, N.1    Schwarz, M.2    Malone, G.3    Howarth, A.4    Painter, J.5    Super, M.6    Braganza, J.7
  • 5
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    • High frequency of cystic fibrosis transmembrane regulator mutation L997F in patients with recurrent idiopathic pancreatitis and in newborns with hypertypsinemia
    • 10.1086/302928 10801389 1378065
    • Gomez Lira M Benetazzo MG Marzari MG Bombieri C Belpinati F Castellani C Cavallini GC Mastella G Pignatti PF High frequency of cystic fibrosis transmembrane regulator mutation L997F in patients with recurrent idiopathic pancreatitis and in newborns with hypertypsinemia Am J Hum Genet 2000, 66(6):2013-2014. 10.1086/302928 10801389 1378065
    • (2000) Am J Hum Genet , vol.66 , Issue.6 , pp. 2013-2014
    • Gomez Lira, M.1    Benetazzo, M.G.2    Marzari, M.G.3    Bombieri, C.4    Belpinati, F.5    Castellani, C.6    Cavallini, G.C.7    Mastella, G.8    Pignatti, P.F.9
  • 7
    • 0031900652 scopus 로고    scopus 로고
    • The diagnosis of cystic fibrosis: A consensus statement
    • 10.1016/S0022-3476(98)70344-0
    • Rosenstein BJ Cutting GR The diagnosis of cystic fibrosis: A consensus statement J Peds 1998, 132:589-95. 10.1016/S0022-3476(98)70344-0
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    • Rosenstein, B.J.1    Cutting, G.R.2
  • 8
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    • Homozygosity for L997F in a child with normal clinical and chloride secretory phenotype provides evidence that this Cystic Fibrosis Transmembrane Conductance Regulator mutation does not cause cystic fibrosis
    • 10.1111/j.1399-0004.2005.00437.x 15857421
    • Derichs N Schuster A Grund I Ernsting A Stolpe C Körtge-Jung S Gallati S Stuhrmann M Kozlowski P Ballmann M Homozygosity for L997F in a child with normal clinical and chloride secretory phenotype provides evidence that this Cystic Fibrosis Transmembrane Conductance Regulator mutation does not cause cystic fibrosis Clin Genet 2005, 67:529-531. 10.1111/j.1399-0004.2005.00437.x 15857421
    • (2005) Clin Genet , vol.67 , pp. 529-531
    • Derichs, N.1    Schuster, A.2    Grund, I.3    Ernsting, A.4    Stolpe, C.5    Körtge-Jung, S.6    Gallati, S.7    Stuhrmann, M.8    Kozlowski, P.9    Ballmann, M.10
  • 9
    • 0034679893 scopus 로고    scopus 로고
    • Is the spectrum of mutations in Indian patients with cystic fibrosis different?
    • 10.1002/1096-8628(20000717)93:2<161::AID-AJMG15>3.0.CO;2-L 10869121
    • Kabra M Kabra SK Ghosh M Khanna A Arora S Menon PS Verma IC Wallace A Is the spectrum of mutations in Indian patients with cystic fibrosis different? Am J Med Genet 2000, 93:161-163. 10.1002/ 1096-8628(20000717)93:2<161::AID-AJMG15>3.0.CO;2-L 10869121
    • (2000) Am J Med Genet , vol.93 , pp. 161-163
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.