推荐同事 机构合作 中文 繁體中文 English 한국어 日本語 Português Español

美国ACCDON公司旗下品牌

021-33361733，021-33632861

chinasupport@letpub.com

登录 注册 新注册优惠

Chronic Diarrhea in Children, Malabsorption Syndromes, Protein Losing Enteropathy

R Chan… - … Diseases of Childhood: A Practical Guide …, 2011 - books.google.com
... Congenital intestinal enterocyte brush border enzyme deficiencies and epithelial dysplasias
(neonatal diarrheas): The intestinal brush border is a complex system of enzymes and transporters,
and malfunction in these leads to carbohydrate malabsorption and diarrhea. ...
Related articles

Identification of novel mutations in the proton-coupled folate transporter (PCFT-SLC46A1) associated with hereditary folate malabsorption

DS Shin, K Mahadeo, SH Min, N Diop-Bove… - Molecular Genetics and …, 2011 - Elsevier
... Medicine (Baltimore). 81 (2002) 51-68. [5] S. Jebnoun, S. Kacem, CH Mokrani, A.
Chabchoub, N. Khrouf, J. Zittoun, A Family Study of Congenital Malabsorption of
Folate, J.Inherit.Metab Dis. 24 (2001) 749-750. [6] BA Kamen ...
Cited by 1 - Related articles - All 2 versions

Congenital Disorders of Digestion and Absorption

[PDF] from yimg.comD Mogul… - Diarrhea, 2011 - Springer
... Key Words: Congenital diarrhea, Glucose–galactose malabsorption, Lactase deficiency,
Sucrase–isomaltase deficiency, Adult-type hypolactasia, Fructose malabsorption, Fanconi–Bickel
syndrome, Enterokinase deficiency, Trypsinogen deficiency, Lysinuric protein intolerance ...
Related articles - All 4 versions

An unusual presentation of a congenital intrahepatic arterioportal fistula in an infant with Down syndrome

JN Bogert, DD Potter, S Crow, GM Arteaga… - Journal of Pediatric …, 2011 - Elsevier
... Received 28 June 2010; revised 10 August 2010; accepted 11 August 2010. Available online
14 January 2011. Abstract. Congenital intrahepatic arterioportal fistula is a rare entity that most
often presents with symptoms of portal hypertension and malabsorption. ...
Related articles - All 3 versions

Selected Disorders of Malabsorption

Z Siddiqui, AS Osayande - Primary Care: Clinics in Office Practice, 2011 - Elsevier
... These disorders may be congenital or acquired and include cystic fibrosis and Shwachman-
Diamond syndrome; the rare congenital lactase deficiency; glucose-galactose malabsorption;
sucrase-isomaltase deficiency; adult-type hypolactasia leading to acquired lactose ...

联系我们 | 站点地图 | 友情链接 | 授权代理商 | 加入我们

© 2010-2024 中国: LetPub上海分公司    网站备案号：沪ICP备10217908号-1    沪公网安备号：31010402006960

增值电信业务经营许可证：沪B2-20211595

礼翰商务信息咨询（上海）有限公司      办公地址：上海市徐汇区漕溪北路88号圣爱大厦1803室

United States: Tel: 1-781-202-9968 Address: 400 5th Ave, Suite 530, Waltham, Massachusetts 02451