Detalhe da pesquisa
1.
[Phenotypic and genetic analysis of a Chinese pedigree affected with Hereditary antithrombin deficiency due to a novel variant of SERPINC1 gene].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 41(3): 312-316, 2024 Mar 10.
Artigo
em Zh
| MEDLINE | ID: mdl-38448020
2.
[Analysis of two pedigrees affected with inherited dysfibrinogenemia due to a novel c.1115 T>A variant of the FGB gene].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 39(6): 587-591, 2022 Jun 10.
Artigo
em Zh
| MEDLINE | ID: mdl-35773760
3.
Predictive and prognostic values of preoperative platelet parameters in patients with gynecological tumors.
J Clin Lab Anal
; 34(7): e23295, 2020 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-32170805
4.
[A case of inherited afibrinogenemia caused by an IVS7-12A>G splice mutation of FGG gene].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 37(12): 1391-1394, 2020 Dec 10.
Artigo
em Zh
| MEDLINE | ID: mdl-33306830
5.
[Clinical and genetic analysis of a pedigree affected with type I hereditary antithrombin deficiency due to a g.2736dupT variant of the AT gene].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 37(11): 1250-1252, 2020 Nov 10.
Artigo
em Zh
| MEDLINE | ID: mdl-33179232
6.
[Analysis of a pedigree affected with congenital dysfibrinogenemia due to a novel Gly31Glu mutation of FGA gene].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 36(9): 901-904, 2019 Sep 10.
Artigo
em Zh
| MEDLINE | ID: mdl-31515786
7.
[Clinical and genotypic analysis of two Chinese pedigrees affected with hereditary coagulable factor VII deficiency].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 36(3): 221-224, 2019 Mar 10.
Artigo
em Zh
| MEDLINE | ID: mdl-30835350
8.
The analysis of false prolongation of the activated partial thromboplastin time (activator: silica): Interference of C-reactive protein.
J Clin Lab Anal
; 32(8): e22571, 2018 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-29756266
9.
[Phenotypic and genetic analysis of two pedigrees affected with hereditary coagulation FXII deficiency].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 35(6): 800-803, 2018 Dec 10.
Artigo
em Zh
| MEDLINE | ID: mdl-30512149
10.
[Identification of compound heterozygous mutations p.Gly400Val and p.Arg532Ter of the F11 gene in a Chinese patient with hereditary factor XI deficiency].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 35(4): 522-526, 2018 Aug 10.
Artigo
em Zh
| MEDLINE | ID: mdl-30098248
11.
[Genotypic and phenotypic analysis of a case with inherited coagulation factor X deficiency].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 35(4): 544-547, 2018 Aug 10.
Artigo
em Zh
| MEDLINE | ID: mdl-30098253
12.
Acquired Factor V Inhibitor with Symptoms and Titer of Inhibitor Differences: Report of Two Cases.
Acta Haematol
; 141(3): 148-150, 2019.
Artigo
em Inglês
| MEDLINE | ID: mdl-30783058
13.
[Clinical and genetic analysis of 8 Chinese pedigrees with inherited dysfibrinogenemia].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 31(2): 134-9, 2014 Apr.
Artigo
em Zh
| MEDLINE | ID: mdl-24711018
14.
Phenotypic and genetic analyses of four cases of coagulation factor XII deficiency.
Hematology
; 27(1): 802-808, 2022 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-35866546
15.
Economical and easily detectable markers of digestive tumors: platelet parameters.
Biomark Med
; 15(3): 157-166, 2021 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-33474972
16.
[Genetic Diagnosis and Phenotype Analysis for 3 Patients with Hereditary Coagulation Factor â ¦ Deficiency].
Zhongguo Shi Yan Xue Ye Xue Za Zhi
; 27(3): 904-910, 2019 Jun.
Artigo
em Zh
| MEDLINE | ID: mdl-31204952
17.
Antithrombotic Effect of shRNA Target F12 Mediated by Adeno-Associated Virus.
Mol Ther Nucleic Acids
; 16: 295-301, 2019 Jun 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-30959404