144 related articles for article (PubMed ID: 24684277)
1. Clinical presentation and molecular basis of congenital antithrombin deficiency in children: a cohort study.
Kumar R; Chan AK; Dawson JE; Forman-Kay JD; Kahr WH; Williams S
Br J Haematol; 2014 Jul; 166(1):130-9. PubMed ID: 24684277
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. Antithrombin heparin binding site deficiency: A challenging diagnosis of a not so benign thrombophilia.
Orlando C; Heylen O; Lissens W; Jochmans K
Thromb Res; 2015 Jun; 135(6):1179-85. PubMed ID: 25837307
[TBL] [Abstract][Full Text] [Related]
4. Thrombotic risk according to SERPINC1 genotype in a large cohort of subjects with antithrombin inherited deficiency.
Alhenc-Gelas M; Plu-Bureau G; Hugon-Rodin J; Picard V; Horellou MH;
Thromb Haemost; 2017 Jun; 117(6):1040-1051. PubMed ID: 28300866
[TBL] [Abstract][Full Text] [Related]
5. Clinical and laboratory characteristics of paediatric and adolescent index cases with venous thromboembolism and antithrombin deficiency. An observational multicentre cohort study.
Limperger V; Franke A; Kenet G; Holzhauer S; Picard V; Junker R; Heller C; Gille C; Manner D; Kurnik K; Knoefler R; Mesters R; Halimeh S; Nowak-Göttl U
Thromb Haemost; 2014 Sep; 112(3):478-85. PubMed ID: 24966143
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. Novel SERPINC1 missense mutation (Cys462Tyr) causes disruption of the 279Cys-462Cys disulfide bond and leads to type Ⅰ hereditary antithrombin deficiency.
Zhang F; Gui Y; Lu Y; Liu D; Chen H; Qin X; Li S
Clin Biochem; 2020 Nov; 85():38-42. PubMed ID: 32745482
[TBL] [Abstract][Full Text] [Related]
8. Inherited risk factors in low-risk venous thromboembolism in patients under 45 years.
Yilmaz S; Gunaydin S
Interact Cardiovasc Thorac Surg; 2015 Jan; 20(1):21-3. PubMed ID: 25326427
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. Impact of SERPINC1 mutation on thrombotic phenotype in children with congenital antithrombin deficiency-first analysis of the International Society on Thrombosis and Haemostasis pediatric antithrombin deficiency database and biorepository.
Kumar R; Bakeer N; Dawson J; Al-Mughairy A; Stanek J; Dunn A; Male C; Chan A; Williams S
J Thromb Haemost; 2023 May; 21(5):1248-1257. PubMed ID: 36764659
[TBL] [Abstract][Full Text] [Related]
11. Hereditary deficiency of protein C or protein S confers increased risk of arterial thromboembolic events at a young age: results from a large family cohort study.
Mahmoodi BK; Brouwer JL; Veeger NJ; van der Meer J
Circulation; 2008 Oct; 118(16):1659-67. PubMed ID: 18824642
[TBL] [Abstract][Full Text] [Related]
12. A rare case of unprovoked venous thromboembolism manifestation in a young patient with antithrombin Type IIB deficiency combined with inferior vena cava anomaly from Lithuania.
Saulytė-Trakymienė S; Adomaitienė I; Unkrig S; Oldenburg J; Ivaškevičius V
Hamostaseologie; 2017; 37(S 01):S26-S31. PubMed ID: 29582922
[TBL] [Abstract][Full Text] [Related]
13. Molecular basis of antithrombin deficiency.
Luxembourg B; Delev D; Geisen C; Spannagl M; Krause M; Miesbach W; Heller C; Bergmann F; Schmeink U; Grossmann R; Lindhoff-Last E; Seifried E; Oldenburg J; Pavlova A
Thromb Haemost; 2011 Apr; 105(4):635-46. PubMed ID: 21264449
[TBL] [Abstract][Full Text] [Related]
14.
Gemmati D; Longo G; Franchini E; Araujo Silva J; Gallo I; Lunghi B; Moratelli S; Maestri I; Serino ML; Tisato V
Genes (Basel); 2021 Jun; 12(6):. PubMed ID: 34207366
[TBL] [Abstract][Full Text] [Related]
15. Clinical and laboratory characteristics of children with venous thromboembolism and protein C-deficiency: an observational Israeli-German cohort study.
Limperger V; Klostermeier UC; Kenet G; Holzhauer S; Alhenc Gelas M; Finckh U; Junker R; Heller C; Zieger B; Kurnik K; Knöfler R; Mesters R; Halimeh S; Nowak-Göttl U
Br J Haematol; 2014 Nov; 167(3):385-93. PubMed ID: 25039884
[TBL] [Abstract][Full Text] [Related]
16. High prevalence of congenital thrombophilia in patients with pregnancy-related or idiopathic venous thromboembolism/pulmonary embolism.
Ikejiri M; Wada H; Yamada N; Nakamura M; Fujimoto N; Nakatani K; Matsuda A; Ogihara Y; Matsumoto T; Kamimoto Y; Ikeda T; Katayama N; Ito M
Int J Hematol; 2017 Mar; 105(3):272-279. PubMed ID: 27766527
[TBL] [Abstract][Full Text] [Related]
17. Venous thromboembolism in neonates and children.
Kenet G; Nowak-Göttl U
Best Pract Res Clin Haematol; 2012 Sep; 25(3):333-44. PubMed ID: 22959549
[TBL] [Abstract][Full Text] [Related]
18. Impact of high-risk thrombophilia status on recurrence among children with a first non-central-venous-catheter-associated VTE: an observational multicentre cohort study.
Limperger V; Kenet G; Goldenberg NA; Heller C; Holzhauer S; Junker R; Klostermeier UC; Knoefler R; Kurnik K; Krümpel A; Mesters R; Stach M; Young G; Nowak-Göttl U
Br J Haematol; 2016 Oct; 175(1):133-40. PubMed ID: 27329967
[TBL] [Abstract][Full Text] [Related]
19. [Hereditary deficiency of antithrombin III, protein C, protein S and factor XII in 121 patients with venous or arterial thrombosis].
Miljić P; Rolović Z; Elezović I; Antunović P; Stanojević M; Colović M
Srp Arh Celok Lek; 1999; 127(1-2):21-7. PubMed ID: 10377836
[TBL] [Abstract][Full Text] [Related]
20. Hypoglycosylation is a common finding in antithrombin deficiency in the absence of a SERPINC1 gene defect.
de la Morena-Barrio ME; Martínez-Martínez I; de Cos C; Wypasek E; Roldán V; Undas A; van Scherpenzeel M; Lefeber DJ; Toderici M; Sevivas T; España F; Jaeken J; Corral J; Vicente V
J Thromb Haemost; 2016 Aug; 14(8):1549-60. PubMed ID: 27214821
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]