220 related articles for article (PubMed ID: 23807486)
1. Antithrombin Rybnik: a new point mutation (nt 683 G>T) associated with type I antithrombin deficiency in a patient with venous thromboembolism and recurrent superficial venous thrombosis.
Szymańska M; Alhenc-Gelas M; Undas A
Blood Coagul Fibrinolysis; 2013 Jul; 24(5):579-80. PubMed ID: 23807486
[No Abstract] [Full Text] [Related]
2. Arterial and venous thrombosis and prothrombotic fibrin clot phenotype in a Polish family with type 1 antithrombin deficiency (antithrombin Krakow).
Celinska-Lowenhoff M; Iwaniec T; Alhenc-Gelas M; Musial J; Undas A
Thromb Haemost; 2011 Aug; 106(2):379-81. PubMed ID: 21655678
[No Abstract] [Full Text] [Related]
3. Homozygous antithrombin deficiency type II (99 Leu to Phe mutation) and childhood thromboembolism.
Kuhle S; Lane DA; Jochmanns K; Male C; Quehenberger P; Lechner K; Pabinger I
Thromb Haemost; 2001 Oct; 86(4):1007-11. PubMed ID: 11686316
[TBL] [Abstract][Full Text] [Related]
4. Impact of the type of SERPINC1 mutation and subtype of antithrombin deficiency on the thrombotic phenotype in hereditary antithrombin deficiency.
Luxembourg B; Pavlova A; Geisen C; Spannagl M; Bergmann F; Krause M; Alesci S; Seifried E; Lindhoff-Last E
Thromb Haemost; 2014 Feb; 111(2):249-57. PubMed ID: 24196373
[TBL] [Abstract][Full Text] [Related]
5. Successful outcome in a pregnant woman with homozygous antithrombin deficiency.
Alguel G; Jochmans K; Simanek R; Ay C; Quehenberger P; Langer M; Pabinger I
Thromb Haemost; 2007 Dec; 98(6):1377-8. PubMed ID: 18064341
[No Abstract] [Full Text] [Related]
6. Hereditary Antithrombin Deficiency Presenting with Deep Venous Thrombosis During the Second Pregnancy.
Yamashita M; Komaki T; Tashiro K; Inada Y; Iwata A; Ogawa M; Morishita E; Miura SI
Intern Med; 2020 Jan; 59(2):235-239. PubMed ID: 31554754
[TBL] [Abstract][Full Text] [Related]
7. Regulatory regions of SERPINC1 gene: identification of the first mutation associated with antithrombin deficiency.
de la Morena-Barrio ME; Antón AI; Martínez-Martínez I; Padilla J; Miñano A; Navarro-Fernández J; Águila S; López MF; Fontcuberta J; Vicente V; Corral J
Thromb Haemost; 2012 Mar; 107(3):430-7. PubMed ID: 22234719
[TBL] [Abstract][Full Text] [Related]
8. Molecular basis of type I antithrombin deficiency in two women with recurrent venous thromboembolism in the first trimester of pregnancy.
Xia Y; Lu QY; Lu YL; Dai J; Ding QL; Wang XF; Xi XD; Wang HL
Blood Cells Mol Dis; 2012 Apr; 48(4):254-9. PubMed ID: 22424603
[TBL] [Abstract][Full Text] [Related]
9. Creation of an additional glycosylation site as a mechanism for type I antithrombin deficiency.
Fitches AC; Lewandowski K; Olds RJ
Thromb Haemost; 2001 Oct; 86(4):1023-7. PubMed ID: 11686319
[TBL] [Abstract][Full Text] [Related]
10. Antithrombin deficiency in three Japanese families: one novel and two reported point mutations in the antithrombin gene.
Maruyama K; Morishita E; Karato M; Kadono T; Sekiya A; Goto Y; Sato T; Nomoto H; Omi W; Tsuzura S; Imai H; Asakura H; Ohtake S; Nakao S
Thromb Res; 2013 Aug; 132(2):e118-23. PubMed ID: 23809926
[TBL] [Abstract][Full Text] [Related]
11. High long-term absolute risk of recurrent venous thromboembolism in patients with hereditary deficiencies of protein S, protein C or antithrombin.
Brouwer JL; Lijfering WM; Ten Kate MK; Kluin-Nelemans HC; Veeger NJ; van der Meer J
Thromb Haemost; 2009 Jan; 101(1):93-9. PubMed ID: 19132194
[TBL] [Abstract][Full Text] [Related]
12. Antithrombin deficiency and decreased protein C activity in a young man with venous thromboembolism: a case report.
Wang D; Tian M; Cui G; Wang DW
Front Med; 2018 Jun; 12(3):319-323. PubMed ID: 28861852
[TBL] [Abstract][Full Text] [Related]
13. Antithrombin III deficiency in Indian patients with deep vein thrombosis: identification of first India based AT variants including a novel point mutation (T280A) that leads to aggregation.
Bhakuni T; Sharma A; Rashid Q; Kapil C; Saxena R; Mahapatra M; Jairajpuri MA
PLoS One; 2015; 10(3):e0121889. PubMed ID: 25811371
[TBL] [Abstract][Full Text] [Related]
14. A novel mutation of antithrombin deficiency in six family siblings and the clinical combat.
Nadir Y; Hoffman R; Corral J; Barak Y; Hasin T; Keren-Politansky A; Brenner B
Thromb Haemost; 2015 Oct; 114(4):859-61. PubMed ID: 26177694
[No Abstract] [Full Text] [Related]
15. A series of 10 Polish patients with thromboembolic events and antithrombin deficiency: two new c.1154-1 G>C and c.1219-534 A>G SERPINC1 gene splicing mutations.
Wójcik M; de la Morena-Barrio ME; Michalik J; Wypasek E; Kopytek M; Corral J; Undas A
Blood Coagul Fibrinolysis; 2019 Jul; 30(5):193-198. PubMed ID: 31157679
[TBL] [Abstract][Full Text] [Related]
16. Antithrombin deficiency in Brazilian patients with venous thrombosis: molecular characterization of a single splice site mutation, an insertion and a de novo point mutation.
Arnaldi LA; Pretti FA; Zampieri JP; Ramos CF; Arruda VR; Annichino-Bizzacchi JM
Thromb Res; 2001 Dec; 104(6):397-403. PubMed ID: 11755949
[TBL] [Abstract][Full Text] [Related]
17. Five novel and four recurrent point mutations in the antithrombin gene causing venous thrombosis.
Nagaizumi K; Inaba H; Amano K; Suzuki M; Arai M; Fukutake K
Int J Hematol; 2003 Jul; 78(1):79-83. PubMed ID: 12894857
[TBL] [Abstract][Full Text] [Related]
18. It's all in your genes.
Versteeg HH; Rodger M
Thromb Res; 2018 Sep; 169():157. PubMed ID: 30170635
[No Abstract] [Full Text] [Related]
19. Compound heterozygosity involving Antithrombin Cambridge II (p.Ala416Ser) in antithrombin deficiency.
Águila S; Martínez-Martínez I; Collado M; Llamas P; Antón AI; Martínez-Redondo C; Padilla J; Miñano A; de la Morena-Barrio ME; Garcia-Avello Á; Vicente V; Corral J
Thromb Haemost; 2013 Mar; 109(3):556-8. PubMed ID: 23329010
[No Abstract] [Full Text] [Related]
20. Inherited antithrombin deficiency: a review.
Patnaik MM; Moll S
Haemophilia; 2008 Nov; 14(6):1229-39. PubMed ID: 19141163
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]