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Journal Abstract Search

238 related items for PubMed ID: 2664729

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  • 3. Xeroderma pigmentosum complementation group E: a case report.
    Kawada A, Satoh Y, Fujiwara Y.
    Photodermatol; 1986 Aug; 3(4):233-8. PubMed ID: 3774595
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  • 4. Report of three sisters with XP-E, a rare xeroderma pigmentosum complementation group.
    Fischer E, Schnyder UW, Jung EG.
    Photodermatol; 1984 Oct; 1(5):232-6. PubMed ID: 6531300
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  • 6. Clinical symptoms and DNA repair characteristics of xeroderma pigmentosum patients from Germany.
    Thielmann HW, Popanda O, Edler L, Jung EG.
    Cancer Res; 1991 Jul 01; 51(13):3456-70. PubMed ID: 2054785
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  • 8. No apparent neurologic defect in a patient with xeroderma pigmentosum complementation group D.
    Ichihashi M, Yamamura K, Hiramoto T, Fujiwara Y.
    Arch Dermatol; 1988 Feb 01; 124(2):256-60. PubMed ID: 3341805
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  • 12. [A whole family affected by xeroderma pigmentosum: clinical and genetic particularities].
    Zghal M, Fazaa B, Zghal A, Mokhtar I, Sarasin A, Kamoun MR, Gharbi MR.
    Ann Dermatol Venereol; 2003 Jan 01; 130(1 Pt 1):31-6. PubMed ID: 12605154
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  • 13. Xeroderma pigmentosum group D patient bearing lentigo maligna without neurological symptoms.
    Fukuro S, Yamaguchi J, Mamada A, Kondo S, Satoh Y.
    Dermatologica; 1990 Jan 01; 181(2):129-33. PubMed ID: 2242781
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  • 18. Clinical and photobiological characteristics of Japanese xeroderma pigmentosum variant.
    Ichihashi M, Fujiwara Y.
    Br J Dermatol; 1981 Jul 01; 105(1):1-12. PubMed ID: 7259973
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  • 20. Different sensitivities to ultraviolet light-induced cytotoxicity and sister chromatid exchanges in xeroderma pigmentosum and Bloom's syndrome fibroblasts.
    Mamada A, Kondo S, Satoh Y.
    Photodermatol; 1989 Jun 01; 6(3):124-30. PubMed ID: 2762203
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