WordNet
- the state of being joined together (同)conjunction, conjugation, colligation
- an act of joining or adjoining things (同)adjunction
- something that joins or connects (同)conjunction
- the place where two or more things come together
PrepTutorEJDIC
- 〈U〉〈C〉連結すること(された状態),『結合』,連合,合体 / 〈C〉『結合点』,連結(接合,合流)点 / 〈C〉(鉄道の)『連絡駅』,接続駅
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出典(authority):フリー百科事典『ウィキペディア（Wikipedia）』「2012/10/04 07:34:31」(JST)
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- 1. 表皮水疱症の疫学、病因、分類、および臨床的特徴 epidemiology pathogenesis classification and clinical features of epidermolysis bullosa
- 2. 表皮水疱症のマネージメントの概要 overview of the management of epidermolysis bullosa
- 3. 表皮水疱症の診断 diagnosis of epidermolysis bullosa
- 4. 歯の発達障害 developmental defects of the teeth
- 5. Kindler syndrome
English Journal
- Inherited epidermolysis bullosa: new diagnostic criteria and classification.
- Intong LR, Murrell DF.SourceDepartment of Dermatology, St. George Hospital and The University of New South Wales, Australia.
- Clinics in dermatology.Clin Dermatol.2012 Jan;30(1):70-7. doi: 10.1016/j.clindermatol.2011.03.012.
- Epidermolysis bullosa (EB) is a group of inherited, mechanobullous disorders caused by mutations in various structural proteins in the skin. There have been several advances in the classification of EB since it was first introduced in the late 19th century. We now recognize four major types of EB, d
- PMID 22137229
- Herlitz junctional epidermolysis bullosa: diagnostic features, mutational profile, incidence and population carrier frequency in the Netherlands.
- Yuen WY, Lemmink HH, van Dijk-Bos KK, Sinke RJ, Jonkman MF.SourceDepartment of Dermatology, Centre for Blistering Diseases, University Medical Centre Groningen, University of Groningen, 9700 RB Groningen, the Netherlands. w.y.yuen@derm.umcg.nl
- The British journal of dermatology.Br J Dermatol.2011 Dec;165(6):1314-22. doi: 10.1111/j.1365-2133.2011.10553.x. Epub 2011 Nov 17.
- BACKGROUND: Junctional epidermolysis bullosa, type Herlitz (JEB-H) is a lethal, autosomal recessive blistering disease caused by null mutations in the genes coding for the lamina lucida/densa adhesion protein laminin-332 (LAMB3, LAMA3 and LAMC2).OBJECTIVES: To present the diagnostic features and mol
- PMID 21801158
- Atypical epidermolysis bullosa simplex with a missense keratin 14 mutation p.Arg125Cys.
- Tsuruta D, Sowa J, Tateishi C, Obase Y, Tsubura A, Fukumoto T, Ishii M, Kobayashi H, Sakaguchi S, Hashimoto T, Hamada T.SourceDepartment of Dermatology, Kurume University School of Medicine, and Kurume University Institute of Cutaneous Cell Biology, Fukuoka, Japan. tsuruta_daisuke@med.kurume-u.ac.jp
- The Journal of dermatology.J Dermatol.2011 Dec;38(12):1177-9. doi: 10.1111/j.1346-8138.2011.01302.x. Epub 2011 Oct 3.
- Epidermolysis bullosa (EB) is a group of hereditary autosomal dominant bullous diseases. EB is divided into four major phenotypes: intraepidermal EB (or EB simplex), junctional EB, dermolytic EB and mixed EB (Kindler syndrome). EB simplex is further divided into three subtypes: localized EB simplex,
- PMID 21967011
Japanese Journal
- Two Dogs with Juvenile-Onset Skin Diseases with Involvement of Extremities
- YOON Ji-Seon,MINAMI Tomohiko,TAKIZAWA Yasuko,SEKIGUCHI Maiko,YABUZOE Atsushi,IDE Kaori,NISHIFUJI Koji,IWASAKI Toshiroh
- Journal of Veterinary Medical Science 72(11), 1513-1516, 2010
- … Thus, the findings in case 1 were compatible to those in junctional epidermolysis bullosa, while those in case 2 were compatible to dermatomyositis-like disease. …
- NAID 130000307670
- Complete maternal isodisomy causing reduction to homozygosity for a novel LAMB3 mutation in Herlitz junctional epidermolysis bullosa
- CASTORI Marco,FLORIDDIA Giovanna,PISANESCHI Elisa,COVACIU Claudia,PARADISI Mauro,TORRENTE Isabella,CASTIGLIA Daniele
- Journal of dermatological science 51(1), 58-61, 2008-07-01
- NAID 10024119475
Related Links
- Junctional epidermolysis bullosa (JEB) is characterized by fragility of the skin and mucous membranes, manifest by blistering with little or no trauma. Blistering may be severe and granulation tissue can form on the skin around the ...
- Junctional epidermolysis bullosa (JEB) is one of the major forms of epidermolysis bullosa, a group of genetic conditions that cause the skin to be very fragile and to blister easily. Blisters and skin erosions form in ...
Related Pictures
★リンクテーブル★
| リンク元 | 「水疱症」「表皮水疱症」「接合部型表皮水疱症」「JEB」 |
| 拡張検索 | 「lethal junctional epidermolysis bullosa」 |
| 関連記事 | 「junction」「junctional」「epidermolysis」 |
「水疱症」
- 遺伝性水疱症(先天性水疱症)
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- Dowling-Meara型（重症型）
- Kobner型（中等症型）
- Weber-Cockayne型（軽症型）
- 筋ジストロフィー合併型
- Herlitz型
- 非Herlitz型
- 幽門閉鎖症合併型
- Hallopeau-Siemens劣性型
- 非Hallopeau-Siemens劣性型
- 優性型
- その他の遺伝性水疱症
- ヘイリー・ヘイリー病 Hailey-Hailey disease = 家族性良性慢性天疱瘡]] familial benign chronic pemphigus
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- 自己免疫性水疱症（後天性水疱症） autoimmuno blistering disease
「表皮水疱症」
表皮水疱症
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-
- Dowling-Meara型（重症型）
- Kobner型（中等症型）
- Weber-Cockayne型（軽症型）
- 筋ジストロフィー合併型
- Herlitz型
- 非Herlitz型
- 幽門閉鎖症合併型
- Hallopeau-Siemens劣性型
- 非Hallopeau-Siemens劣性型
- 優性型
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「接合部型表皮水疱症」
「JEB」
[★] 接合部型表皮水疱症 junctional epidermolysis bullosa
「lethal junctional epidermolysis bullosa」
「junction」
- n.
「junctional」
- adj.
- 接合部の