[Glanzmann's disease: diagnostic study of 6 patients].
作者信息
Quiroga T, Mezzano D, Aranda E, Montesinos M, Foradori A, Bull P, Schuh W, Morales M, Vargas L
出版信息
Rev Med Chil. 1985 Nov;113(11):1076-83.
PMID:3879773
Abstract
摘要
相似文献
1
[Glanzmann's disease: diagnostic study of 6 patients].[血小板无力症：6例患者的诊断研究]
Rev Med Chil. 1985 Nov;113(11):1076-83.
2
Diagnosis of heterozygotes in Glanzmann's thrombasthenia.
Thromb Haemost. 1982 Oct 29;48(2):217-21.
3
Diagnostic tool for Glanzmann's thrombasthenia clinicopathologic spectrum.用于Glanzmann血小板无力症临床病理谱的诊断工具。
J Coll Physicians Surg Pak. 2008 Feb;18(2):91-4.
4
Glanzmann's thrombasthenia: diagnosis supplemented by HP1-1D monoclonal antibody.血小板无力症：HP1-1D单克隆抗体辅助诊断
Taiwan Yi Xue Hui Za Zhi. 1986 May;85(5):488-94.
5
Glanzmann's thrombasthenia.
J Postgrad Med. 1980 Jul;26(3):210-2.
6
[Monoclonal antibodies in the diagnosis of Glanzmann's thrombasthenia].
Bol Med Hosp Infant Mex. 1988 Nov;45(11):776-80.
7
Platelet aggregation, adhesion and adenosine diphosphate release in thrombopathia (platelet factor 3 deficiency). A comparison with Glanzmann's thrombasthenia and von Willebrand's disease.血小板病（血小板因子3缺乏症）中的血小板聚集、黏附及二磷酸腺苷释放。与Glanzmann血小板无力症和血管性血友病的比较。
Am J Med. 1967 Oct;43(4):570-8. doi: 10.1016/0002-9343(67)90180-5.
8
Inherited disorders of platelet function in pediatric clinical practice: a diagnostic challenge.儿科临床实践中的遗传性血小板功能障碍：一项诊断挑战。
Klin Padiatr. 2010 May;222(3):203-8. doi: 10.1055/s-0030-1249660. Epub 2010 May 31.
9
Prenatal diagnosis of Glanzmann's thrombasthenia.血小板无力症的产前诊断
Lancet. 1985;2(8469-70):1419. doi: 10.1016/s0140-6736(85)92579-6.
10
Prenatal diagnosis of a molecular variant of Glanzmann's thrombasthenia.血小板无力症分子变异型的产前诊断
Curr Stud Hematol Blood Transfus. 1988(55):180-3. doi: 10.1159/000415441.
Zotero 插件