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Volumn 19, Issue 7, 2003, Pages 358-360

Alström syndrome with acute pancreatitis: A case report

Author keywords

Acute pancreatitis; Alstr m syndrome

Indexed keywords

GEMFIBROZIL; GLIBENCLAMIDE;

EID: 0042528835     PISSN: 02575655     EISSN: None     Source Type: Journal    
DOI: 10.1016/s1607-551x(09)70438-3     Document Type: Article
Times cited : (10)

References (8)
  • 1
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    • The Alström syndrome. Report of three cases with further delineation of the clinical, pathophysiological, and genetic aspects of the disorder
    • Goldstein JL, Fialkow PJ. The Alström syndrome. Report of three cases with further delineation of the clinical, pathophysiological, and genetic aspects of the disorder. Medicine (Baltimore) 1973;52:53-71.
    • (1973) Medicine (Baltimore) , vol.52 , pp. 53-71
    • Goldstein, J.L.1    Fialkow, P.J.2
  • 2
    • 0030732665 scopus 로고    scopus 로고
    • Genealogy, natural history, and phenotype of Alström syndrome in a large Acadian kindred and three additional families
    • Marshall JD, Ludman MD, Shea SE, et al. Genealogy, natural history, and phenotype of Alström syndrome in a large Acadian kindred and three additional families. Am J Med Genet 1997;73:150-61.
    • (1997) Am J Med Genet , vol.73 , pp. 150-161
    • Marshall, J.D.1    Ludman, M.D.2    Shea, S.E.3
  • 4
    • 0036578890 scopus 로고    scopus 로고
    • Mutations in ALMS1 cause obesity, type 2 diabetes and neurosensory degeneration in Alström syndrome
    • Collin GB, Marshall JD, Ikeda A, et al. Mutations in ALMS1 cause obesity, type 2 diabetes and neurosensory degeneration in Alström syndrome. Nat Genet 2002;31:74-8.
    • (2002) Nat Genet , vol.31 , pp. 74-78
    • Collin, G.B.1    Marshall, J.D.2    Ikeda, A.3
  • 5
    • 18544391142 scopus 로고    scopus 로고
    • Mutation of ALMS1, a large gene with a tandem repeat encoding 47 amino acids, causes Alström syndrome
    • Hearn T, Renforth GL, Spalluto C, et al. Mutation of ALMS1, a large gene with a tandem repeat encoding 47 amino acids, causes Alström syndrome. Nat Genet 2002;31:79-83.
    • (2002) Nat Genet , vol.31 , pp. 79-83
    • Hearn, T.1    Renforth, G.L.2    Spalluto, C.3
  • 6
    • 0034111554 scopus 로고    scopus 로고
    • The continuing failure to recognise Alström syndrome and further evidence of genetic homogeneity
    • Letter
    • Deeble VJ, Roberts E, Jackson A, et al. The continuing failure to recognise Alström syndrome and further evidence of genetic homogeneity. J Med Genet 2000;37:219. (Letter)
    • (2000) J Med Genet , vol.37 , pp. 219
    • Deeble, V.J.1    Roberts, E.2    Jackson, A.3
  • 7
    • 0031046702 scopus 로고    scopus 로고
    • Hepatic dysfunction in two sibs with Alström syndrome: Case report and review of the literature
    • Awazu M, Tanaka T, Sato S, et al. Hepatic dysfunction in two sibs with Alström syndrome: case report and review of the literature. Am J Med Genet 1997;69:13-6.
    • (1997) Am J Med Genet , vol.69 , pp. 13-16
    • Awazu, M.1    Tanaka, T.2    Sato, S.3
  • 8
    • 0035370870 scopus 로고    scopus 로고
    • Early-onset liver disease complicated with acute liver failure in Alström syndrome
    • Quiros-Tejeira RE, Vargas J, Ament ME. Early-onset liver disease complicated with acute liver failure in Alström syndrome. Am J Med Genet 2001;101:9-11.
    • (2001) Am J Med Genet , vol.101 , pp. 9-11
    • Quiros-Tejeira, R.E.1    Vargas, J.2    Ament, M.E.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.