English  |  正體中文  |  简体中文  |  Total items :0  
Visitors :  53284211    Online Users :  687
Project Commissioned by the Ministry of Education
Project Executed by National Taiwan University Library
 
臺灣學術機構典藏系統 (Taiwan Academic Institutional Repository, TAIR)
About TAIR

Browse By

News

Copyright

Related Links

"lin j s"

Return to Browse by Author
Sorting by Title Sort by Date

Showing items 16-25 of 148  (15 Page(s) Totally)
<< < 1 2 3 4 5 6 7 8 9 10 > >>
View [10|25|50] records per page

Institution Date Title Author
臺大學術典藏 2021-05-25T06:36:04Z Factor V Arg306 → Gly mutation is not associated with activated protein C resistance and is rare in Taiwanese Chinese MING-CHING SHEN; Lin J.-S.; Tsay W.
臺大學術典藏 2021-05-25T06:36:04Z Factor V arg306-> Gly is not a risk factor for venous thrombophilia in Taiwanese Chinese Lin J.S.; MING-CHING SHEN; Tsai W.; Lin B.; Lin B.B.; Hong M.H.
臺大學術典藏 2021-05-25T06:36:03Z Novel mutations in the factor VII gene of Taiwanese factor VII-deficient patients MING-CHING SHEN; Lin J.-S.; Lin S.-W.; Yang W.-S.; Lin B.
臺大學術典藏 2021-05-25T06:36:02Z Age, sex and vitamin status affect plasma level of homocysteine, but hyperhomocysteinaemia is possibly not an important risk factor for venous thrombophilia in Taiwanese Chinese Lin J.-S.; MING-CHING SHEN; Cheng W.-C.; Tsay W.; Wang Y.-C.; Lin B.-B.; Hung M.-H.
臺大學術典藏 2021-05-25T06:36:01Z A first Taiwanese Chinese family of type 2B von Willebrand disease with R1306W mutation MING-CHING SHEN; Lin J.-S.; Lin D.S.-Y.; Hsu S.-C.; Lin B.
臺大學術典藏 2021-05-25T06:36:00Z A novel mutation with Ins C (882-883) of the factor X gene in a Taiwanese Chinese factor X-deficient family MING-CHING SHEN; Lin J.-S.; Lin D.S.-Y.; Lin S.-W.; Lin B.
臺大學術典藏 2021-05-25T06:35:58Z Hyperhomacysteinemia, deep vein thrombosis and vitamin B12 deficiency in a metformin-treated diabetic patient Lin H.-Y.; Chung C.-Y.; Chang C.-S.; Wang M.-L.; Lin J.-S.; MING-CHING SHEN
臺大學術典藏 2021-05-25T06:35:56Z Nattokinase decreases plasma levels of fibrinogen, factor VII, and factor VIII in human subjects Hsia C.-H.; MING-CHING SHEN; Lin J.-S.; Wen Y.-K.; Hwang K.-L.; Cham T.-M.; Yang N.-C.
臺大學術典藏 2021-05-25T06:35:51Z Characterization of hereditary factor XI deficiency in Taiwanese patients: identification of three novel and two common mutations Lin H.-Y.;Lin C.-Y.;Hung M.-H.;Kuo S.-F.;Lin J.-S.;Ming-Ching Shen; Lin H.-Y.; Lin C.-Y.; Hung M.-H.; Kuo S.-F.; Lin J.-S.; MING-CHING SHEN
臺大學術典藏 2021-05-25T06:35:50Z A family with an MYH9-related disorder with different phenotypes masquerading as immune thrombocytopaenia: an underreported disorder in Taiwan Huang Y.-C.;Shih Y.-H.;Lin C.-Y.;Chiu P.-F.;Kuo S.-F.;Lin J.-S.;Ming-Ching Shen; Huang Y.-C.; Shih Y.-H.; Lin C.-Y.; Chiu P.-F.; Kuo S.-F.; Lin J.-S.; MING-CHING SHEN

Showing items 16-25 of 148  (15 Page(s) Totally)
<< < 1 2 3 4 5 6 7 8 9 10 > >>
View [10|25|50] records per page