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Pediatrics International
Volumn 47, Issue 5, 2005, Pages 586-588
Two infantile cases of congenital myotonic dystrophy with cholelithiasis/cholestasis
Author keywords

Cholelithiasis; Cholestasis; Congenital; Myotonic dystrophy
Indexed keywords

MYOTONIC DYSTROPHY PROTEIN KINASE;
EID: 29144515781     PISSN: 13288067     EISSN: None     Source Type: Journal    
DOI: 10.1111/j.1442-200x.2005.02104.x     Document Type: Article
Times cited : (4)
References (9)
  • 1
    • 0027246344 scopus 로고
    • Decreased expression of myotonin-protein kinase messenger RNA and protein in adult form of myotonic dystrophy
    • Fu YH, Friedman DL, Richards S et al. Decreased expression of myotonin-protein kinase messenger RNA and protein in adult form of myotonic dystrophy. Science 1993; 260: 235-8.
    • (1993) Science , vol.260 , pp. 235-238
    • Fu, Y.H.1    Friedman, D.L.2    Richards, S.3
  • 2
    • 0028334933 scopus 로고
    • Myotonic dystrophy with no trinucleotide reperat expansion
    • Thoronton CA, Griggs RC, Moxley RT. Myotonic dystrophy with no trinucleotide reperat expansion. Ann. Neurol. 1994; 35: 269-72.
    • (1994) Ann. Neurol. , vol.35 , pp. 269-272
    • Thoronton, C.A.1    Griggs, R.C.2    Moxley, R.T.3
  • 3
    • 0035800434 scopus 로고    scopus 로고
    • Myotonic dystrophy type 2 caused by a CCTG expansion in intron 1 of ZNF9
    • Liquori CL, Ricker K, Moseley ML et al. Myotonic dystrophy type 2 caused by a CCTG expansion in intron 1 of ZNF9. Science 2001; 293: 864-7.
    • (2001) Science , vol.293 , pp. 864-867
    • Liquori, C.L.1    Ricker, K.2    Moseley, M.L.3
  • 4
    • 0026566108 scopus 로고
    • Molecular basis of myotonic dystrophy: Expansion of trinucleotide (CTG) repeats at the 3-prime end of a transcript encoding a protein kinase family member
    • Brook JD, McCurrach ME, Harley HG et al. Molecular basis of myotonic dystrophy: expansion of trinucleotide (CTG) repeats at the 3-prime end of a transcript encoding a protein kinase family member. Cell 1992; 68: 799-808.
    • (1992) Cell , vol.68 , pp. 799-808
    • Brook, J.D.1    McCurrach, M.E.2    Harley, H.G.3
  • 5
    • 0026879229 scopus 로고
    • Correlation between CTG trinucleotide repeats length and frequency of severe congenital myotonic dystrophy
    • Tshlfidis C, MacKenzie AE, Mettler G, Barcelo J, Korneluk RG. Correlation between CTG trinucleotide repeats length and frequency of severe congenital myotonic dystrophy. Nat. Genet. 1992; 1: 192-5.
    • (1992) Nat. Genet. , vol.1 , pp. 192-195
    • Tshlfidis, C.1    MacKenzie, A.E.2    Mettler, G.3    Barcelo, J.4    Korneluk, R.G.5
  • 6
    • 0016813740 scopus 로고
    • Congenital myotonic dystrophy in Britain. 1. Clinical aspects
    • Herper PS. Congenital myotonic dystrophy in Britain. 1. Clinical aspects. Arch. Dis. Child. 1975; 50: 505-13.
    • (1975) Arch. Dis. Child. , vol.50 , pp. 505-513
    • Herper, P.S.1
  • 7
    • 0014643025 scopus 로고
    • Cholelithiasis and associated complication of myotonia dystrophica
    • Schwindt WD, Bernhardt LC, Peters HA. Cholelithiasis and associated complication of myotonia dystrophica. Postgrad. Med. 1969; 46: 80-3.
    • (1969) Postgrad. Med. , vol.46 , pp. 80-83
    • Schwindt, W.D.1    Bernhardt, L.C.2    Peters, H.A.3
  • 8
    • 0017327486 scopus 로고    scopus 로고
    • Smooth muscle involvement in congenital myotonic dystrophy
    • Lenard HG, Goebel HH, Weigel W. Smooth muscle involvement in congenital myotonic dystrophy. Neuropadiatrie 1997; 8: 42-52.
    • (1997) Neuropadiatrie , vol.8 , pp. 42-52
    • Lenard, H.G.1    Goebel, H.H.2    Weigel, W.3
  • 9
    • 0031777112 scopus 로고    scopus 로고
    • Abnormal liver test results in myotonic dystrophy
    • Achiron A, Barak Y, Magal N et al. Abnormal liver test results in myotonic dystrophy. J. Clin. Gastroenterol. 1998; 26: 292-5.
    • (1998) J. Clin. Gastroenterol. , vol.26 , pp. 292-295
    • Achiron, A.1    Barak, Y.2    Magal, N.3

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.