PubRank

Biagio Didona

Author PubWeight™ 11.36‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 Recurrent mutations in kindlin-1, a novel keratinocyte focal contact protein, in the autosomal recessive skin fragility and photosensitivity disorder, Kindler syndrome. J Invest Dermatol 2004 1.95
2 Pemphigus autoantibodies generated through somatic mutations target the desmoglein-3 cis-interface. J Clin Invest 2012 1.25
3 Treatment of severe pemphigus with rituximab: report of 12 cases and a review of the literature. Arch Dermatol 2007 1.21
4 Molecular basis of Kindler syndrome in Italy: novel and recurrent Alu/Alu recombination, splice site, nonsense, and frameshift mutations in the KIND1 gene. J Invest Dermatol 2006 1.10
5 Quality-of-life assessment in patients with pemphigus using a minimum set of evaluation tools. J Am Acad Dermatol 2008 0.96
6 Toxic epidermal necrolysis successfully treated with etanercept. J Dermatol 2009 0.95
7 Connexin 26 (GJB2) mutations as a cause of the KID syndrome with hearing loss. Biochem Biophys Res Commun 2010 0.91
8 Connexin 26 (GJB2) mutations, causing KID Syndrome, are associated with cell death due to calcium gating deregulation. Biochem Biophys Res Commun 2010 0.91
9 Persistent subcutaneous Scedosporium apiospermum infection. Eur J Dermatol 2004 0.81
10 Toxic epidermal necrolysis-like acute cutaneous lupus erythematosus successfully treated with a single dose of etanercept: report of three cases. J Am Acad Dermatol 2013 0.77
11 Pemphigus foliaceus treated with etanercept. J Am Acad Dermatol 2006 0.76
12 Association of dermoscopic profiles of telangiectases with nailfold videocapillaroscopic patterns in patients with systemic sclerosis. J Rheumatol 2013 0.75
13 Resolution of a case of pediatric pemphigus vulgaris treated with rituximab. Acta Dermatovenerol Croat 2014 0.75
14 Association of segmental neurofibromatosis 1 and oculo-auriculo-vertebral spectrum in a 24-year-old female. Eur J Dermatol 2007 0.75