Hashimoto Takashi | Department Of Dermatology Kurume University Of Medicine

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著作論文

A Japanese family with dominant pretibial dystrophic epidermolysis bullosa : Identification of a new glycine substitution in the triple-helical collagenous domain of type VII collagen
Genotype-phenotype correlation in non-Hallopeau-Siemens recessive dystrophic epidermolysis bullosa : The splice site mutation c.6216+5G>T in the COL7A1 gene results in aberrant and normal splicings
Enzyme-linked immunosorbent assay using bacterial recombinant proteins of human BP230 as a diagnostic tool for bullous pemphigoid
BP180 ELISA using bacterial recombinant NC16a protein as a diagnostic and monitoring tool for bullous pemphigoid
Analysis of antigens recognized by autoantibodies in herpes gestationis. Usefulness of immunoblotting using a fusion protein representing an extracellular domain of the 180kD bullous pemphigoid antigen
Pemphigus : from immunofluorescence to molecular biology
Lesional Th17 cells in pemphigus vulgaris and pemphigus foliaceus
Molecular and clinical characterization in Japanese and Korean patients with Hailey-Hailey disease : Six new mutations in the ATP2C1 gene
Efficacy of interferon-γ in patients with refractory bullous pemphigoid
Subepidermal blistering disease with autoantibodies against a novel dermal 200-kDa antigen
Analysis of antigens targeted by circulating IgG and IgA autoantibodies in 50 patients with cicatricial pemphigoid
Studies of autoantigens recognized by IgA anti-keratinocyte cell surface antibodies
Two Cases of Atypical Bullous Disease Showing Linear IgG and IgA Deposition in the Basement Membrane Zone
Plectin deficient epidermolysis bullosa simplex with 27-year-history of muscular dystrophy
From anti-p200 pemphigoid to anti-laminin γ1 pemphigoid
Linear immunoglobulin A bullous dermatosis possibly induced by mefenamic acid
Epidermolysis bullosa acquisita : What's new?
The Common KRT9 Gene Mutation in a Japanese Patient with Epidermolytic Palmoplantar Keratoderma and Knuckle Pad-Like Keratoses
Mucous membrane pemphigoid with immunoglobulin G autoantibodies against full-length and 120-kDa ectodomain of BP180
The compound heterozygote for new/recurrent COL7A1 mutations in a Japanese patient with bullous dermolysis of the newborn
Development of NC1 and NC2 domains of Type VII collagen ELISA for the diagnosis and analysis of the time course of epidermolysis bullosa acquisita patients

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