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Volumn 14, Issue 2, 2008, Pages

Dyschromatosis universalis hereditaria: Two cases

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CASE REPORT; CLINICAL EXAMINATION; DYSCHROMATOSIS UNIVERSALIS HEREDITARIA; FEMALE; FOLLOW UP; GENODERMATOSIS; HISTOPATHOLOGY; HUMAN; HYPERPIGMENTATION; INCONTINENTIA PIGMENTI; INFANT; MELANOSIS; PHYSICAL EXAMINATION; PRESCHOOL CHILD; SKIN EXAMINATION; CONSANGUINITY; GENETICS; PATHOLOGY; PIGMENT DISORDER; TUNISIA;

EID: 41149100486     PISSN: None     EISSN: 10872108     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (12)

References (11)
  • 1
    • 0000486941 scopus 로고
    • A propos d'une anomalie pigmentaire inédite.
    • Ichikawa T, Higara Y. A propos d'une anomalie pigmentaire inédite. Jpn J Dermatol 1933 ; 34 : 360-4.
    • (1933) Jpn J Dermatol , vol.34 , pp. 360-364
    • Ichikawa, T.1    Higara, Y.2
  • 2
    • 0002531661 scopus 로고
    • Dyschromatosis symmetrica herediteria
    • Toyama I. Dyschromatosis symmetrica herediteria. Jpn J Dermatol 1929 ; 29 : 95-6.
    • (1929) Jpn J Dermatol , vol.29 , pp. 95-96
    • Toyama, I.1
  • 4
    • 33646033001 scopus 로고    scopus 로고
    • Dyschromatosis universalis hereditaria as an autosomal recessive disease in five members of one family
    • Bukhari IA, El-Harith EA, Stuhrmann M. Dyschromatosis universalis hereditaria as an autosomal recessive disease in five members of one family. J Eur Acad Dermatol Venereol. 2006; 20(5): 628-9.
    • (2006) J Eur Acad Dermatol Venereol , vol.20 , Issue.5 , pp. 628-629
    • Bukhari, I.A.1    El-Harith, E.A.2    Stuhrmann, M.3
  • 5
    • 0036862123 scopus 로고    scopus 로고
    • Dyschromatosis universalis hereditaria: Report of a case and review of the literature
    • Al Hawsawi K, Al Aboud K, Ramesh V, Al Aboud D. Dyschromatosis universalis hereditaria: report of a case and review of the literature. Pediatr Dermatol. 2002; 19: 523-526.
    • (2002) Pediatr Dermatol , vol.19 , pp. 523-526
    • Al Hawsawi, K.1    Al Aboud, K.2    Ramesh, V.3    Al Aboud, D.4
  • 6
    • 0035107492 scopus 로고    scopus 로고
    • Dychromatose universelle: 2 cas
    • Dhaoui MA, Doss N. Dychromatose universelle: 2 cas. Ann Dermatol Venereol. 2001; 128: 136-8.
    • (2001) Ann Dermatol Venereol , vol.128 , pp. 136-138
    • Dhaoui, M.A.1    Doss, N.2
  • 7
    • 0042888576 scopus 로고    scopus 로고
    • Mutations of the RNA-specific adenosine deaminase gene (DSRAD) are involved in dyschromatosis symmetrica hereditaria
    • Miyamura Y, Suzuki T, Kono M, Inagaki K, Ito S, Suzuki N, Tomita Y: Mutations of the RNA-specific adenosine deaminase gene (DSRAD) are involved in dyschromatosis symmetrica hereditaria. Am J Hum Genet 2003; 73:693-699.
    • (2003) Am J Hum Genet , vol.73 , pp. 693-699
    • Miyamura, Y.1    Suzuki, T.2    Kono, M.3    Inagaki, K.4    Ito, S.5    Suzuki, N.6    Tomita, Y.7
  • 8
    • 4644229966 scopus 로고    scopus 로고
    • A novel mutation of DSRAD gene in a Chinese family with dyschromatosis symmetrica hereditaria
    • Li M, Jiang YX, Liu JB, et al: A novel mutation of DSRAD gene in a Chinese family with dyschromatosis symmetrica hereditaria. Clin Exp Dermatol 2004; 29:533-535.
    • (2004) Clin Exp Dermatol , vol.29 , pp. 533-535
    • Li, M.1    Jiang, Y.X.2    Liu, J.B.3
  • 9
    • 2342476651 scopus 로고    scopus 로고
    • Novel mutations of the RNA-specific adenosine deaminase gene (DSRAD) in Chinese families with dyschromatosis symmetrica hereditaria
    • Liu Q, Liu W, Jiang L, et al: Novel mutations of the RNA-specific adenosine deaminase gene (DSRAD) in Chinese families with dyschromatosis symmetrica hereditaria. J Invest Dermatol. 2004;122:896-899.
    • (2004) J Invest Dermatol , vol.122 , pp. 896-899
    • Liu, Q.1    Liu, W.2    Jiang, L.3
  • 11
    • 1542378712 scopus 로고    scopus 로고
    • Dyschromatosis universalis hereditaria: Familial case and ultrastructural skin investigation
    • Nuber UA, Tinschert S, Mundlos S, Hauber I. Dyschromatosis universalis hereditaria: familial case and ultrastructural skin investigation. Am J Med Gen A. 2004; 125(3): 261-6.
    • (2004) Am J Med Gen A , vol.125 , Issue.3 , pp. 261-266
    • Nuber, U.A.1    Tinschert, S.2    Mundlos, S.3    Hauber, I.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.