[Mucolipidosis type II (I-cell disease)].
作者信息
Szigeti R, Konyár E, Görgényi A, Schaff Z, Klujber L, Jellinek H
出版信息
Orv Hetil. 1975 Feb 9;116(6):313-6.
PMID:163018
Abstract
摘要
相似文献
1
[Mucolipidosis type II (I-cell disease)].[II型黏脂贮积症（I型细胞病）]
Orv Hetil. 1975 Feb 9;116(6):313-6.
2
3
4
[Case of dysostosis multiplex with features of mucolipidosis II (I-cell disease)].[伴有黏脂贮积症II（I型细胞病）特征的多发性骨发育异常病例]
Pol Przegl Radiol Med Nukl. 1974 Sep-Oct;38(5):617-22.
5
6
Apparent allelism of the Hurler, Scheie, and Hurler/Scheie syndromes.胡勒氏综合征、谢伊氏综合征和胡勒/谢伊氏综合征的明显等位基因现象。
Am J Med Genet. 1984 Jul;18(3):547-56. doi: 10.1002/ajmg.1320180324.
7
[Mucopolysaccharidosis type II (Hurler-Hunter) in siblings. Electron microscopic study].[同胞中的黏多糖贮积症II型（胡尔勒-亨特综合征）。电子显微镜研究]
Sb Ved Pr Lek Fak Karlovy Univerzity Hradci Kralove. 1972;15(2):173-9.
8
A method for the quantitative determination of urinary glycosaminoglycans.
Clin Chim Acta. 1976 Aug 2;70(3):427-32. doi: 10.1016/0009-8981(76)90356-9.
9
[Arachnoid cysts in the Hurler-Hunter syndrome].
Ann Radiol (Paris). 1968;11(5):453-69.
10
[Type II mucolipidosis (I-cell disease)].[II型粘脂贮积症（I-细胞病）]
Arch Fr Pediatr. 1973 Jun-Jul;30(6):577-93.
Zotero 插件