[Trypsinogen pseudo-deficiency caused by congenital enterokinase deficiency. Clinical study]. - Suppr | 超能文献

[Trypsinogen pseudo-deficiency caused by congenital enterokinase deficiency. Clinical study].

作者信息

Polonovski C, Laplane R, Alison F, Navarro J

出版信息

Arch Fr Pediatr. 1970;27(7):677-88.

Abstract

摘要

文献AI研究员

20分钟写一篇综述，助力文献阅读效率提升50倍。

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

文档翻译

学术文献翻译模型，支持多种主流文档格式。

相似文献

1

[Trypsinogen pseudo-deficiency caused by congenital enterokinase deficiency. Clinical study].

Arch Fr Pediatr. 1970;27(7):677-88.

2

[Trypsinogen pseudo-deficiency caused by congenital enterokinase deficiency. Enzyme study].先天性肠激酶缺乏导致的胰蛋白酶原假性缺乏。酶学研究

Arch Fr Pediatr. 1970;27(7):689-702.

3

[Activity and Km of enterokinase in 3 cases of congenital deficiency of this enzyme].[3例先天性肠激酶缺乏症患者的肠激酶活性及米氏常数]

Nouv Presse Med. 1972 Jul 8;1(28):1898.

4

The activation of human pancreatic proteinases. Studies on human pancreatic juice and duodenal juice of four children with intestinal enterokinase deficiency.人胰蛋白酶的激活。对四名肠激酶缺乏症儿童的胰液和十二指肠液的研究。

Acta Paediatr Scand. 1971 May;60(3):369.

5

[Congenital enterokinase deficiency].[先天性肠激酶缺乏症]

Pediatrie. 1977 Apr-May;32(3):297-301.

6

Role of bile acids in the activation of trypsinogen by enterokinase: disturbance of trypsinogen activation in patients with intrahepatic biliary atresia.胆汁酸在肠激酶激活胰蛋白酶原中的作用：肝内胆管闭锁患者胰蛋白酶原激活障碍

Gastroenterology. 1974 Apr;66(4):548-55.

7

The interrelationships of the pancreatic enzymes.胰腺酶之间的相互关系。

Gut. 1972 May;13(5):398-412. doi: 10.1136/gut.13.5.398.

8

Presence of colipase in a congenital pancreatic lipase deficiency.先天性胰腺脂肪酶缺乏症中辅脂酶的存在情况。

Biochim Biophys Acta. 1972 Sep 7;280(1):205-11. doi: 10.1016/0005-2760(72)90227-5.

9

Intestinal enterokinase deficiency. A newly-recognized disorder of protein digestion.肠内肠激酶缺乏症。一种新发现的蛋白质消化紊乱疾病。

Arch Dis Child. 1970 Oct;45(243):651-5. doi: 10.1136/adc.45.243.651.

10

Intestinal enterokinase deficiency.

Lancet. 1969 Apr 19;1(7599):812-3. doi: 10.1016/s0140-6736(69)92071-6.

引用本文的文献

1

Enterokinase deficiency associated with novel TMPRSS15 gene mutations: a case report.与新型TMPRSS15基因突变相关的肠激酶缺乏症：一例报告。

Front Pediatr. 2025 Jan 29;13:1484208. doi: 10.3389/fped.2025.1484208. eCollection 2025.

2

Enteropeptidase: a gene associated with a starvation human phenotype and a novel target for obesity treatment.肠肽酶：与饥饿人类表型相关的基因，也是肥胖治疗的新靶点。

PLoS One. 2012;7(11):e49612. doi: 10.1371/journal.pone.0049612. Epub 2012 Nov 21.

3

Mutations in the proenteropeptidase gene are the molecular cause of congenital enteropeptidase deficiency.肠肽酶原基因的突变是先天性肠肽酶缺乏症的分子病因。

Am J Hum Genet. 2002 Jan;70(1):20-5. doi: 10.1086/338456. Epub 2001 Nov 21.

4

Intestinal enterokinase deficiency. Occurrence in two sibs and age dependency of clinical expression.肠内肠激酶缺乏症。在两名同胞中的发生情况及临床表型的年龄依赖性。

Arch Dis Child. 1975 Apr;50(4):277-82. doi: 10.1136/adc.50.4.277.