Literature DB >> 7482420

Protein C deficiency: a database of mutations, 1995 update. On behalf of the Subcommittee on Plasma Coagulation Inhibitors of the Scientific and Standardization Committee of the ISTH.

P H Reitsma1, F Bernardi, R G Doig, S Gandrille, J S Greengard, H Ireland, M Krawczak, B Lind, G L Long, S R Poort.   

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Year:  1995        PMID: 7482420

Source DB:  PubMed          Journal:  Thromb Haemost        ISSN: 0340-6245            Impact factor:   5.249


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  37 in total

1.  Superior sagittal sinus and inferior vena cava thrombosis with acute Budd-Chiari syndrome.

Authors:  A Kakar; C S Agarwal; A Arora
Journal:  Postgrad Med J       Date:  1998-09       Impact factor: 2.401

2.  Myeloid/natural killer cell precursor acute leukemia accompanied by homozygous protein C deficiency.

Authors:  Takashi Shimamoto; Akihiro Nakajima; Tomoko Katagiri; Yoshikazu Ito; Kazuma Ohyashiki
Journal:  Int J Hematol       Date:  2003-08       Impact factor: 2.490

3.  Gly74Ser mutation in protein C causes thrombosis due to a defect in protein S-dependent anticoagulant function.

Authors:  Changming Chen; Likui Yang; Bruno O Villoutreix; Xuefeng Wang; Qiulan Ding; Alireza R Rezaie
Journal:  Thromb Haemost       Date:  2017-04-13       Impact factor: 5.249

4.  A delayed presentation of homozygous protein C deficiency in a series of children: a report on two molecular defects.

Authors:  Abdullah A Baothman; Enaam AlSobhi; Hassan A Khayat; Raed E Alsulami; Abdulaziz S Alkahtani; Abdelraheem A Al-Thobyani; Yousef I Marzouk; Mohammad A Abdelaal
Journal:  Clin Case Rep       Date:  2017-02-06

5.  Definite diagnosis in Japanese patients with protein C deficiency by identification of causative PROC mutations.

Authors:  Akira Takagi; Ryoko Tanaka; Daisuke Nakashima; Yuta Fujimori; Takayuki Yamada; Kaoru Okumura; Takashi Murate; Midori Yamada; Yasuo Horikoshi; Koji Yamamoto; Akira Katsumi; Tadashi Matsushita; Tomoki Naoe; Tetsuhito Kojima
Journal:  Int J Hematol       Date:  2009-04-17       Impact factor: 2.490

6.  Recurrent cerebellar infarction associated with hereditary heterozygous protein C deficiency in a 35-year-old woman: A case report and genetic study on the pedigree.

Authors:  Pingping Li; Chao Qin
Journal:  Exp Ther Med       Date:  2018-07-25       Impact factor: 2.447

7.  Impairment of protein C secretion in protein C-deficient patients carrying an Asp297 mutation.

Authors:  Jun Yamanouchi; Takaaki Hato; Toshiyuki Niiya; Tatsuya Hayashi; Koji Suzuki; Masaki Yasukawa
Journal:  Int J Hematol       Date:  2011-07-09       Impact factor: 2.490

8.  Gly197Arg mutation in protein C causes recurrent thrombosis in a heterozygous carrier.

Authors:  Yeling Lu; Hemant Giri; Bruno O Villoutreix; Qiulan Ding; Xuefeng Wang; Alireza R Rezaie
Journal:  J Thromb Haemost       Date:  2020-04-09       Impact factor: 5.824

9.  Use of human protein C concentrates in the treatment of patients with severe congenital protein C deficiency.

Authors:  Sabine Kroiss; Manuela Albisetti
Journal:  Biologics       Date:  2010-03-24

10.  Severe congenital protein C deficiency: the use of protein C concentrates (human) as replacement therapy for life-threatening blood-clotting complications.

Authors:  Paul N Knoebl
Journal:  Biologics       Date:  2008-06
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