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出典(authority):フリー百科事典『ウィキペディア（Wikipedia）』「2016/03/15 01:40:18」(JST)
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- 1. 後天性表皮水疱症 epidermolysis bullosa acquisita
- 2. 炎症性腸疾患の皮膚および眼症状 dermatologic and ocular manifestations of inflammatory bowel disease
- 3. 水疱性類天疱瘡および粘膜類天疱瘡の臨床的特徴および診断 clinical features and diagnosis of bullous pemphigoid and mucous membrane pemphigoid
- 4. 皮膚の水疱を有する患者に対するアプローチ approach to the patient with cutaneous blisters
- 5. 偽ポルフィリン症 pseudoporphyria
English Journal
- Anti-p200 pemphigoid.
- Goletz S1, Hashimoto T2, Zillikens D1, Schmidt E3.
- Journal of the American Academy of Dermatology.J Am Acad Dermatol.2014 Jul;71(1):185-191. doi: 10.1016/j.jaad.2014.02.036. Epub 2014 Apr 24.
- Anti-p200 pemphigoid is a rare subepidermal blistering skin disease. Patients' autoantibodies label the dermal side of 1 mol/L NaCl-split human skin by indirect immunofluorescence microscopy and recognize a 200-kd protein by immunoblotting of human dermal extract. Clinically, anti-p200 pemphigoid is
- PMID 24767733
- Esophageal involvement in epidermolysis bullosa acquisita.
- Ishii N1, Furumura M, Hamada T, Mori O, Ohzono A, Ueda A, Karashima T, Nakama T, Tsuruta D, Takedatsu H, Fujita H, Hashimoto T.
- The British journal of dermatology.Br J Dermatol.2014 Jun 28. doi: 10.1111/bjd.13224. [Epub ahead of print]
- Epidermolysis bullosa acquisita (EBA) is an acquired autoimmune bullous disease of skin and mucous membranes characterized by IgG autoantibodies to type VII collagen, major component of the anchoring fibrils in basement membrane zone (BMZ).1 Type VII collagen is also expressed on esophageal mucosa.2
- PMID 24975454
- Peristomal Epidermolysis Bullosa Acquisita in a Patient with Crohn's Disease.
- Ormaechea-Pérez N1, Tuneu-Valls A, Borja-Consigliere HA, Alcazar-Viladomiu ED, Jaka-Moreno A.
- Acta dermato-venereologica.Acta Derm Venereol.2014 Jun 24;94(4):489-490. doi: 10.2340/00015555-1769.
- Abstract is missing (Short).
- PMID 24322876
Japanese Journal
- 症例報告 免疫グロブリン大量静注療法が著効した後天性表皮水疱症が疑われた1例
- 神山 由佳,長谷川 道子,永井 弥生 [他]
- 臨床皮膚科 66(1), 35-40, 2012-01
- NAID 40019145139
- Heterogeneity of Brunsting-Perry type pemphigoid : A case showing blister formation at the lamina lucida, immune deposition beneath the lamina densa and autoantibodies against the 290-kD polypeptide along the lamina densa
- MINATO Haruka,ISHII Norito,FUKUDA Shunpei,WAKASA Tomoko,WAKASA Ken'ichi,SOGAME Ryosuke,HASHIMOTO Takashi,HORIGUCHI Yuji
- Journal of dermatology 38(9), 887-892, 2011-09-01
- NAID 10030728050
- 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
- SALEH Marwah Adly,ISHII Ken,KIM Yool-Ja,MURAKAMI Akihiro,ISHII Norito,HASHIMOTO Takashi,SCHMIDT Enno,ZILLIKENS Detlef,SHIRAKATA Yuji,HASHIMOTO Koji,KITAJIMA Yasuo,AMAGAI Masayuki
- Journal of dermatological science 62(3), 169-175, 2011-06-01
- NAID 10030891389
Related Links
- Epidermolysis Bullosa Acquisita. Epidermolysis bullosa acquisita (EBA) is a chronic autoimmune subepidermal blistering disease of the skin and mucus membranes. ... Race The race distribution of epidermolysis ...
- Race The race distribution of epidermolysis bullosa acquisita is not known. In one of the largest patient groups (24 patients) followed by the authors, 19 were white and 5 were black. This distribution is roughly proportional to the ...
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★リンクテーブル★
| リンク元 | 「EBA」「後天性表皮水疱症」「acquired epidermolysis bullosa」 |
| 関連記事 | 「acquisita」「epidermolysis」 |
「EBA」
「後天性表皮水疱症」
「acquired epidermolysis bullosa」
「acquisita」