메뉴 건너뛰기




Volumn 65, Issue 2, 1996, Pages 167-170

Congenital alopecia and nail dystrophy associated with severe functional T-cell immunodeficiency in two sibs

Author keywords

alopecia; immunodeficiency; nail dystrophy

Indexed keywords

ADENOSINE DEAMINASE; CELL MARKER; PURINE NUCLEOSIDE PHOSPHORYLASE;

EID: 0029959773     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1096-8628(19961016)65:2<167::AID-AJMG17>3.0.CO;2-O     Document Type: Article
Times cited : (104)

References (24)
  • 2
    • 0027216789 scopus 로고
    • Dyskeratosis congenita: Three additional families show linkage to a locus in Xq28
    • Arngrimsson R, Dokal I, Luzzatto L, Connor JM (1993): Dyskeratosis congenita: Three additional families show linkage to a locus in Xq28. J Med Genet 30:618-619.
    • (1993) J Med Genet , vol.30 , pp. 618-619
    • Arngrimsson, R.1    Dokal, I.2    Luzzatto, L.3    Connor, J.M.4
  • 3
    • 0025233576 scopus 로고
    • Genetic and mutational analysis of the T-cell antigen receptor
    • Ashwell JD, Klausner RD (1990): Genetic and mutational analysis of the T-cell antigen receptor. Annu Rev Immunol 8:139-167.
    • (1990) Annu Rev Immunol , vol.8 , pp. 139-167
    • Ashwell, J.D.1    Klausner, R.D.2
  • 4
    • 0026598252 scopus 로고
    • Molecular associations between the T-lymphocyte antigen receptor complex and the surface antigens CD2, CD4, or CDS and CDS
    • Beyers AD, Spruyt LL, Williams AF (1992): Molecular associations between the T-lymphocyte antigen receptor complex and the surface antigens CD2, CD4, or CDS and CDS. Proc Natl Acad Sci USA 89: 2945-2949.
    • (1992) Proc Natl Acad Sci USA , vol.89 , pp. 2945-2949
    • Beyers, A.D.1    Spruyt, L.L.2    Williams, A.F.3
  • 6
    • 0026691858 scopus 로고
    • Molecular approaches to analysis of X-linked immunodeficiencies
    • Conley ME (1992): Molecular approaches to analysis of X-linked immunodeficiencies. Annu Rev Immunol 10:215-238.
    • (1992) Annu Rev Immunol , vol.10 , pp. 215-238
    • Conley, M.E.1
  • 8
    • 2742543634 scopus 로고
    • Primary immunodeficiency diseases: Severe combined immunodeficiency diseases (SCIDs)
    • Paul WE (ed): New York: Raven Press
    • Cooper MD, Butler JL (1989): Primary immunodeficiency diseases: Severe combined immunodeficiency diseases (SCIDs). In Paul WE (ed): "Fundamental Immunology." New York: Raven Press, pp 1034-1039.
    • (1989) Fundamental Immunology , pp. 1034-1039
    • Cooper, M.D.1    Butler, J.L.2
  • 11
    • 0021926097 scopus 로고
    • Dyskeratosis congenita with hypoplastic anemia and stem cell defect
    • Friedland M, Lutton JD, Spitzer R, Leverk RD (1985): Dyskeratosis congenita with hypoplastic anemia and stem cell defect. Am J Hematol 20:85-87.
    • (1985) Am J Hematol , vol.20 , pp. 85-87
    • Friedland, M.1    Lutton, J.D.2    Spitzer, R.3    Leverk, R.D.4
  • 12
    • 0027506211 scopus 로고
    • Transmembrane signaling and T-cell immunodeficiency
    • Gelfand EW (1993): Transmembrane signaling and T-cell immunodeficiency. Pediatr Res 33:16-19.
    • (1993) Pediatr Res , vol.33 , pp. 16-19
    • Gelfand, E.W.1
  • 13
    • 0021068521 scopus 로고
    • Diagnosis and Classification of Severe Combined Immunodeficiency Disease
    • New York: Alan R. Liss, Inc., for the National Foundation-March of Dimes
    • Gelfand EW, Dosch HM (1983): Diagnosis and Classification of Severe Combined Immunodeficiency Disease. New York: Alan R. Liss, Inc., for the National Foundation-March of Dimes. BD:OAS XIX(3):65-72.
    • (1983) BD:OAS , vol.19 , Issue.3 , pp. 65-72
    • Gelfand, E.W.1    Dosch, H.M.2
  • 15
    • 0024469727 scopus 로고
    • Associations of the skeletal and immune system
    • Hong R (1989): Associations of the skeletal and immune system. Am J Med Genet 34:55-59.
    • (1989) Am J Med Genet , vol.34 , pp. 55-59
    • Hong, R.1
  • 16
    • 0025971630 scopus 로고
    • T cell antigen receptor activation pathways: The tyrosine kinase connection
    • Klausner RD, Samelson LE (1991): T cell antigen receptor activation pathways: The tyrosine kinase connection. Cell 64:875-878.
    • (1991) Cell , vol.64 , pp. 875-878
    • Klausner, R.D.1    Samelson, L.E.2
  • 18
    • 0021972279 scopus 로고
    • The gene encoding the human interleukin-2 receptor is located on chromosome 10
    • Leonard WJ, Donlon TA, Lebo RB, Greene WC (1985): The gene encoding the human interleukin-2 receptor is located on chromosome 10. Science 228:1547-1549.
    • (1985) Science , vol.228 , pp. 1547-1549
    • Leonard, W.J.1    Donlon, T.A.2    Lebo, R.B.3    Greene, W.C.4
  • 21
    • 0015427342 scopus 로고
    • Congenital dyskeratosis: Zinner-Engman-Cole syndrome with thymic dysplasia and aplastic anemia
    • Ortega JA, Swanson VL, Landig BH, Hammond GD (1972): Congenital dyskeratosis: Zinner-Engman-Cole syndrome with thymic dysplasia and aplastic anemia. Am J Dis Child 124:701-704.
    • (1972) Am J Dis Child , vol.124 , pp. 701-704
    • Ortega, J.A.1    Swanson, V.L.2    Landig, B.H.3    Hammond, G.D.4
  • 22
    • 0024492985 scopus 로고
    • Etiologic heterogeneity in dyskeratosis congenita
    • Pai GS, Morgan S, Whetsell C (1989): Etiologic heterogeneity in dyskeratosis congenita. Am J Med Genet 32:63-66.
    • (1989) Am J Med Genet , vol.32 , pp. 63-66
    • Pai, G.S.1    Morgan, S.2    Whetsell, C.3
  • 23
    • 18744436873 scopus 로고
    • New and old immunodeficiencies
    • Stiehm ER (1993): New and old immunodeficiencies. Pediatr Res 33: 2-8.
    • (1993) Pediatr Res , vol.33 , pp. 2-8
    • Stiehm, E.R.1
  • 24
    • 0020084060 scopus 로고
    • Dyskeratosis congenita: An autosomal dominant disorder
    • Tchou PK, Kohn T (1982): Dyskeratosis congenita: An autosomal dominant disorder. J Am Acad Dermatol 6:1034-1039.
    • (1982) J Am Acad Dermatol , vol.6 , pp. 1034-1039
    • Tchou, P.K.1    Kohn, T.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.