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Volumn 28, Issue 2, 2010, Pages 201-210

Immunofluorescence mapping for the diagnosis of epidermolysis bullosa

Author keywords

Classification of subtypes; Epidermolysis bullosa; Immunofluorescence mapping

Indexed keywords

ALPHA6 INTEGRIN; ANTIBODY; BETA4 INTEGRIN; COLLAGEN TYPE 7; CYTOKERATIN 14; CYTOKERATIN 5; KALININ; PLECTIN; STRUCTURAL PROTEIN;

EID: 77952527039     PISSN: 07338635     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.det.2009.12.005     Document Type: Review
Times cited : (34)

References (11)
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  • 2
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    • Immunofluorescence mapping of antigenic determinants within the dermal-epidermal junction in mechanobullous diseases
    • Hintner H., Stingl G., Schuler G., et al. Immunofluorescence mapping of antigenic determinants within the dermal-epidermal junction in mechanobullous diseases. J Invest Dermatol 1981, 76:113-118.
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    • Hintner, H.1    Stingl, G.2    Schuler, G.3
  • 3
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    • The classification of inherited epidermolysis bullosa (EB): report of the third international consensus meeting on diagnosis and classification of EB
    • Fine J.D., Eady R.A., Bauer E.A., et al. The classification of inherited epidermolysis bullosa (EB): report of the third international consensus meeting on diagnosis and classification of EB. J Am Acad Dermatol 2008, 58(6):931-950.
    • (2008) J Am Acad Dermatol , vol.58 , Issue.6 , pp. 931-950
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  • 5
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    • Preservation of tissue-fixed immunoglobulins in skin biopsies of patients with lupus erythematosus and bullous diseases
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    • Michel, B.1    Milner, Y.2    David, K.3
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    • The use of Michel's transport media for immunofluorescence and immunoelectron microscopy in autoimmune bullous diseases
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    • (1995) J Cutan Pathol , vol.22 , pp. 365-370
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  • 7
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    • Clinical heterogeneity in recessive epidermolysis bullosa due to mutations in the keratin 14 gene, KRT14
    • Yiasemides E., Trisnowati N., Su J., et al. Clinical heterogeneity in recessive epidermolysis bullosa due to mutations in the keratin 14 gene, KRT14. Clin Exp Dermatol 2008, 33:689-697.
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    • A site-specific plectin mutation causes dominant epidermolysis bullosa simplex ogna: two identical de novo mutations
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.