Detalles de la búsqueda
1.
Chinese guidelines for treatment of adult primary immune thrombocytopenia.
Int J Hematol
; 107(6): 615-623, 2018 Jun.
Artículo
en Inglés
| MEDLINE | ID: mdl-29619624
2.
The Resistance Phenotype and Molecular Epidemiology of Klebsiella pneumoniae in Bloodstream Infections in Shanghai, China, 2012-2015.
Front Microbiol
; 8: 250, 2017.
Artículo
en Inglés
| MEDLINE | ID: mdl-28280486
3.
Factor X Shanghai and disruption of translocation to the endoplasmic reticulum.
Haematologica
; 90(12): 1659-64, 2005 Dec.
Artículo
en Inglés
| MEDLINE | ID: mdl-16330440
4.
Characterization of molecular defect of 13387-9delG mutated antithrombin in inherited type I antithrombin deficiency.
Blood Coagul Fibrinolysis
; 16(2): 149-55, 2005 Mar.
Artículo
en Inglés
| MEDLINE | ID: mdl-15741804
5.
[Inherited coagulation factor VII deficiency caused by double heterozygotic mutations Arg304Gln and Arg304Trp].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 20(4): 279-83, 2003 Aug.
Artículo
en Zh
| MEDLINE | ID: mdl-12903033
6.
[Molecular genetic analysis for a pedigree with severe hereditary coagulation factor VII deficiency].
Zhonghua Nei Ke Za Zhi
; 42(10): 692-6, 2003 Oct.
Artículo
en Zh
| MEDLINE | ID: mdl-14633462
7.
[Two novel factor V gene mutations associated with congenital coagulation factor V deficiency, study of one pedigree].
Zhonghua Yi Xue Za Zhi
; 83(4): 312-5, 2003 Feb 25.
Artículo
en Zh
| MEDLINE | ID: mdl-12812650
8.
[Genetic analysis of a Chinese family with inherited afibrinogenemia].
Zhonghua Yi Xue Za Zhi
; 83(23): 2054-7, 2003 Dec 10.
Artículo
en Zh
| MEDLINE | ID: mdl-14703415
9.
[Type I hereditary protein C deficiency due to C5498T mutation in protein C gene].
Zhonghua Yi Xue Za Zhi
; 83(19): 1694-7, 2003 Oct 10.
Artículo
en Zh
| MEDLINE | ID: mdl-14642106
10.
[Molecular mechanisms of two novel mutations of factor XIII gene resulting in hereditary coagulation deficiency].
Zhonghua Yi Xue Za Zhi
; 83(24): 2158-61, 2003 Dec 25.
Artículo
en Zh
| MEDLINE | ID: mdl-14720426
11.
[Studies on inherited coagulation factor VII deficiency and tissue factor abnormality in a pedigree].
Zhonghua Xue Ye Xue Za Zhi
; 27(3): 150-3, 2006 Mar.
Artículo
en Zh
| MEDLINE | ID: mdl-16792912
12.
[The inherited coagulation factor XI deficiency caused by intronic mutation IVS J-4delgttg].
Zhonghua Xue Ye Xue Za Zhi
; 26(3): 144-7, 2005 Mar.
Artículo
en Zh
| MEDLINE | ID: mdl-15946525
13.
[Severe hereditary coagulation factor V deficiency caused by two novel heterozygous mutations].
Zhonghua Xue Ye Xue Za Zhi
; 26(3): 129-32, 2005 Mar.
Artículo
en Zh
| MEDLINE | ID: mdl-15946520
14.
[Study on the molecular mechanism of antithrombin gene C2759T (Leu99Phe) mutation causing antithrombin deficiency].
Zhonghua Xue Ye Xue Za Zhi
; 26(3): 148-51, 2005 Mar.
Artículo
en Zh
| MEDLINE | ID: mdl-15946526
15.
[Non-viral vector mediating human coagulation factor VIII gene expression in mouse 32D cell line].
Zhongguo Shi Yan Xue Ye Xue Za Zhi
; 12(6): 721-5, 2004 Dec.
Artículo
en Zh
| MEDLINE | ID: mdl-15631647
16.
[Double heterozygous mutations of non-canonical splice (IVS1a + 5g > a) and His348Gln caused inherited coagulation factor VII deficiency].
Zhonghua Xue Ye Xue Za Zhi
; 25(3): 139-42, 2004 Mar.
Artículo
en Zh
| MEDLINE | ID: mdl-15182580
17.
[In vivo transfection and expression of human coagulant factor VIII cDNA in mice].
Zhongguo Shi Yan Xue Ye Xue Za Zhi
; 12(2): 188-93, 2004 Apr.
Artículo
en Zh
| MEDLINE | ID: mdl-15157331
18.
[Identification of two novel factor XI non-sense mutation Trp228stop and Trp383stop in a Chinese pedigree of congenital factor XI deficiency].
Zhonghua Xue Ye Xue Za Zhi
; 24(3): 126-8, 2003 Mar.
Artículo
en Zh
| MEDLINE | ID: mdl-12697122
19.
[Prothrombin deficiency resulted from a homozygous Glu29 to Gly mutation in the prothrombin gene].
Zhonghua Xue Ye Xue Za Zhi
; 24(9): 449-51, 2003 Sep.
Artículo
en Zh
| MEDLINE | ID: mdl-14575584
20.
[Effective and stable in vitro expression of human coagulation factor VIII by retrovirus-based plasmid vector coupled with polyamidoamine dendrimer].
Zhonghua Xue Ye Xue Za Zhi
; 24(9): 464-6, 2003 Sep.
Artículo
en Zh
| MEDLINE | ID: mdl-14575588