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Volumn 16, Issue 4, 2012, Pages 561-563

Pulmonary non-tuberculous mycobacterial infection in congenital contractural arachnodactyly

Author keywords

Atypical mycobacterial; Fibrillin; Human fibrillin 2 (congenital contractural arachnodactyly) protein; Mycobacterium avium complex

Indexed keywords

CHLORIDE; CLARITHROMYCIN; ETHAMBUTOL; FIBRILLIN 2; GAMMA INTERFERON RECEPTOR; GENOMIC DNA; RIFABUTIN;

EID: 84858665577     PISSN: 10273719     EISSN: None     Source Type: Journal    
DOI: 10.5588/ijtld.11.0301     Document Type: Article
Times cited : (17)

References (10)
  • 1
    • 0021284636 scopus 로고
    • Cardiovascular findings in congenital contraction arachnodactyly: Report of an affected kindred
    • Anderson R A, Koch S, Camerini-Otero R D. Cardiovascular findings in congenital contractural arachnodactyly: report of an affected kindred. Am J Med Genet 1984; 18: 265-271. (Pubitemid 14124901)
    • (1984) American Journal of Medical Genetics , vol.18 , Issue.2 , pp. 265-271
    • Anderson, R.A.1    Koch, S.2    Camerini-Otero, R.D.3
  • 2
    • 61649103114 scopus 로고    scopus 로고
    • Comprehensive clinical and molecular assessment of 32 probands with congenital contractural arachnodactyly: Report of 14 novel mutations and review of the literature
    • Callewaert B L, Loeys B L, Ficcadenti A, et al. Comprehensive clinical and molecular assessment of 32 probands with congenital contractural arachnodactyly: report of 14 novel mutations and review of the literature. Hum Mutat 2009; 30: 334-341.
    • (2009) Hum Mutat , vol.30 , pp. 334-341
    • Callewaert, B.L.1    Loeys, B.L.2    Ficcadenti, A.3
  • 3
    • 59749088792 scopus 로고    scopus 로고
    • The FBN2 gene: New mutations, locus-specific database (Universal Mutation Database FBN2), and genotype-phenotype correlations
    • Frédéric M Y, Monino C, Marschall C, et al. The FBN2 gene: new mutations, locus-specific database (Universal Mutation Database FBN2), and genotype-phenotype correlations. Hum Mutat 2009; 30: 181-190.
    • (2009) Hum Mutat , vol.30 , pp. 181-190
    • Frédéric, M.Y.1    Monino, C.2    Marschall, C.3
  • 5
    • 0029023792 scopus 로고
    • Developmental expression of fibrillin genes suggests heterogeneity of extracellular microfibrils
    • Zhang H, Hu W, Ramirez F. Developmental expression of fibrillin genes suggests heterogeneity of extracellular microfibrils. J Cell Biol 1995; 129: 1165-1176.
    • (1995) J Cell Biol , vol.129 , pp. 1165-1176
    • Zhang, H.1    Hu, W.2    Ramirez, F.3
  • 8
    • 0021181422 scopus 로고
    • Pulmonary disease in patients with Marfan syndrome
    • Wood J R, Bellamy D, Child A H, Citron K M. Pulmonary disease in patients with Marfan syndrome. Thorax 1984; 39: 780-784. (Pubitemid 14038832)
    • (1984) Thorax , vol.39 , Issue.10 , pp. 780-784
    • Wood, J.R.1    Bellamy, D.2    Child, A.H.3    Citron, K.M.4
  • 9
    • 57349187991 scopus 로고    scopus 로고
    • Pulmonary non-tuberculous mycobacterial disease: Prospective study of morphotype, laboratory and genetic features of a distinct syndrome
    • Kim R D, Greenberg D E, Ehrmantraut M E, et al. Pulmonary non-tuberculous mycobacterial disease: prospective study of morphotype, laboratory and genetic features of a distinct syndrome. Am J Respir Crit Care Med 2008; 178: 1066-1074.
    • (2008) Am J Respir Crit Care Med , vol.178 , pp. 1066-1074
    • Kim, R.D.1    Greenberg, D.E.2    Ehrmantraut, M.E.3
  • 10
    • 77949506650 scopus 로고    scopus 로고
    • Familial clustering of pulmonary non-tuberculous mycobacterial disease
    • Colombo R E, Hill S C, Claypool R J, Holland S M, Olivier K N. Familial clustering of pulmonary non-tuberculous mycobacterial disease. Chest 2010; 137: 629-634.
    • (2010) Chest , vol.137 , pp. 629-634
    • Colombo, R.E.1    Hill, S.C.2    Claypool, R.J.3    Holland, S.M.4    Olivier, K.N.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.