WordNet

of or relating to or inside the intestines; "intestinal disease" (同)enteric, enteral

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1. 小腸内細菌過剰繁殖の治療 treatment of small intestinal bacterial overgrowth
2. 胃腸上皮化生 gastric intestinal metaplasia
3. 慢性偽性腸閉塞 chronic intestinal pseudo obstruction
4. 成人における腸管虚血の概要 overview of intestinal ischemia in adults
5. 小腸内細菌過剰繁殖の病因および発症機序 etiology and pathogenesis of small intestinal bacterial overgrowth

Lymphangiomatous Lesions of the Gastrointestinal Tract: A Clinicopathologic Study and Comparison Between Adults and Children.

Lawless ME1, Lloyd KA1, Swanson PE1, Upton MP1, Yeh MM2.
American journal of clinical pathology.Am J Clin Pathol.2015 Oct;144(4):563-9. doi: 10.1309/AJCPO8TW6EMAJSRP.
OBJECTIVES: Lymphangiomatous lesions involving the gastrointestinal (GI) tract remain incompletely characterized, and their clinical and histopathologic features have not been systematically evaluated. The distinction between a primary lymphatic malformation (lymphangioma) and a dilation of existing
PMID 26386077

Functional Dissection of the CCBE1 Protein: A Crucial Requirement for the Collagen Repeat Domain.

Roukens MG1, Peterson-Maduro J1, Padberg Y1, Jeltsch M1, Leppänen VM1, Bos FL1, Alitalo K1, Schulte-Merker S1, Schulte D2.
Circulation research.Circ Res.2015 May 8;116(10):1660-9. doi: 10.1161/CIRCRESAHA.116.304949. Epub 2015 Mar 26.
RATIONALE: Collagen- and calcium-binding EGF domain-containing protein 1 (CCBE1) is essential for lymphangiogenesis in vertebrates and has been associated with Hennekam syndrome. Recently, CCBE1 has emerged as a crucial regulator of vascular endothelial growth factor-C (VEGFC) signaling.OBJECTIVE: C
PMID 25814692

A novel CCBE1 mutation leading to a mild form of hennekam syndrome: case report and review of the literature.

Frosk P1,2, Chodirker B3,4, Simard L5, El-Matary W6, Hanlon-Dearman A7, Schwartzentruber J8, Majewski J9; FORGE Canada Consortium, Rockman-Greenberg C10,11.
BMC medical genetics.BMC Med Genet.2015 Apr 30;16:28. doi: 10.1186/s12881-015-0175-0.
BACKGROUND: Mutations in CCBE1 have been found to be responsible for a subset of families with autosomal recessive Hennekam syndrome. Hennekam syndrome is defined as the combination of generalized lymphatic dysplasia (ie. lymphedema and lymphangiectasia), variable intellectual disability and charact
PMID 25925991

腸リンパ管拡張症 : 約 21,200 件
腸管リンパ管拡張症 : 44 件
腸壁リンパ管拡張症 : 33 件

関: alimentary system、bowel、digestive system、enteric、enteric canal、entero、gastrointestinal、gastrointestinal system、GI、gut、intestinal tract、intestine

リンク元	「腸リンパ管拡張症」
関連記事	「intestinal」