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Volumn 23, Issue 6, 2006, Pages 586-588

What syndrome is this?

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; BLISTER; CASE REPORT; DIFFERENTIAL DIAGNOSIS; GENODERMATOSIS; HUMAN; HYPERPIGMENTATION; KINDLER SYNDROME; MALE; PHOTOSENSITIVITY; PRIORITY JOURNAL; SCHOOL CHILD; SKIN ATROPHY; SKIN DISEASE; SKIN PIGMENTATION; SYNDROME DELINEATION; CHILD; INFANT; KERATOSIS PALMOPLANTARIS; NEWBORN; PATHOLOGY; PHOTOSENSITIVITY DISORDER; PRESCHOOL CHILD; SYNDROME;

EID: 33751267921     PISSN: 07368046     EISSN: 15251470     Source Type: Journal    
DOI: 10.1111/j.1525-1470.2006.00315.x     Document Type: Article
Times cited : (7)

References (17)
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  • 2
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  • 3
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    • Immunohistochemical, ultrastructural, and molecular features of Kindler syndrome distinguish it from dystrophic epidermolysis bullosa
    • Shimizu H, Sato M, Ban M et al. Immunohistochemical, ultrastructural, and molecular features of Kindler syndrome distinguish it from dystrophic epidermolysis bullosa. Arch Dermatol 1997;133:1111-1117.
    • (1997) Arch Dermatol , vol.133 , pp. 1111-1117
    • Shimizu, H.1    Sato, M.2    Ban, M.3
  • 4
    • 0021946090 scopus 로고
    • Kindler syndrome in two related Kurdish families
    • Hacham-Zadeh S, Garfunkel AA. Kindler syndrome in two related Kurdish families. Am J Med Genet 1985;20:43-48.
    • (1985) Am J Med Genet , vol.20 , pp. 43-48
    • Hacham-Zadeh, S.1    Garfunkel, A.A.2
  • 7
    • 0030461569 scopus 로고    scopus 로고
    • Kindler syndrome: Clinical and ultrastructural findings
    • Haber RM, Hanna WM. Kindler syndrome: Clinical and ultrastructural findings. Arch Dermatol 1996;132:1487-1490.
    • (1996) Arch Dermatol , vol.132 , pp. 1487-1490
    • Haber, R.M.1    Hanna, W.M.2
  • 8
    • 0029793189 scopus 로고    scopus 로고
    • Kindler syndrome: Report of a case with ultrastructural study and review of the literature
    • Patrizi A, Pauluzzi P, Neri I et al. Kindler syndrome: report of a case with ultrastructural study and review of the literature. Pediatr Dermatol 1996;13:397-402.
    • (1996) Pediatr Dermatol , vol.13 , pp. 397-402
    • Patrizi, A.1    Pauluzzi, P.2    Neri, I.3
  • 9
    • 0034061647 scopus 로고    scopus 로고
    • A Japanese case of Kindler syndrome
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    • (2000) Int J Dermatol , vol.39 , pp. 284-286
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  • 12
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    • Clinical and microbiologic study of periodontitis associated with Kindler syndrome
    • Wiebe CB, Penagos H, Luong N et al. Clinical and microbiologic study of periodontitis associated with Kindler syndrome. J Periodontol 2003;74:25-31.
    • (2003) J Periodontol , vol.74 , pp. 25-31
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  • 14
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    • Kindler syndrome
    • Ashton GH. Kindler syndrome. Clin Exp Dermatol 2004;29:116-121.
    • (2004) Clin Exp Dermatol , vol.29 , pp. 116-121
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  • 15
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    • Loss of kindlin-1, a human homolog of the Caenorhabditis elegans actin-extracellular-matrix linker protein UNC-112, causes Kindler syndrome
    • Siegel DH, Ashton GH, Penagos HG et al. Loss of kindlin-1, a human homolog of the Caenorhabditis elegans actin-extracellular-matrix linker protein UNC-112, causes Kindler syndrome. Am J Hum Genet 2003;73:174-187.
    • (2003) Am J Hum Genet , vol.73 , pp. 174-187
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  • 16
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    • Identification of mutations in a new gene encoding a FERM family protein with a pleckstrin homology domain in Kindler syndrome
    • Jobard F, Bouadjar B, Caux F et al. Identification of mutations in a new gene encoding a FERM family protein with a pleckstrin homology domain in Kindler syndrome. Hum Mol Genet 2003;12:925-935.
    • (2003) Hum Mol Genet , vol.12 , pp. 925-935
    • Jobard, F.1    Bouadjar, B.2    Caux, F.3
  • 17
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    • Recurrent mutations in kindlin-1, a novel keratinocyte focal contact protein, in the autosomal recessive skin fragility and photosensitivity disorder, Kindler syndrome
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    • Ashton, G.H.1    McLean, W.H.2    South, A.P.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.