These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

110 related articles for article (PubMed ID: 15338392)

  • 1. Renovascular hypertension due to antithrombin deficiency in childhood.
    Miura K; Takahashi T; Takahashi I; Komatsu M; Tsuchida S; Mikami T; Suzuki T; Takahashi S; Takada G
    Pediatr Nephrol; 2004 Nov; 19(11):1294-6. PubMed ID: 15338392
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Hereditary antithrombin deficiency resulting in severe neonatal thrombosis].
    Niklassen US; Ingerslev J; Birkebaek NH
    Ugeskr Laeger; 2000 Nov; 162(45):6081-2. PubMed ID: 11107947
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. Inherited antithrombin deficiency and end stage renal disease.
    Hara T; Naito K
    Med Sci Monit; 2005 Nov; 11(11):RA346-54. PubMed ID: 16258410
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Report of a novel kindred with antithrombin heparin-binding site variant (47 Arg to His): demand for an automated progressive antithrombin assay to detect molecular variants with low thrombotic risk.
    Rossi E; Chiusolo P; Za T; Marietti S; Ciminello A; Leone G; De Stefano V
    Thromb Haemost; 2007 Sep; 98(3):695-7. PubMed ID: 17849067
    [No Abstract]   [Full Text] [Related]  

  • 6. Successful therapy with argatroban for superior mesenteric vein thrombosis in a patient with congenital antithrombin deficiency.
    Muta T; Okamura T; Kawamoto M; Ichimiya H; Yamanaka M; Wada Y; Urata M; Kayamori Y; Hamasaki N; Kato K; Eto T; Gondo H; Shibuya T
    Eur J Haematol; 2005 Aug; 75(2):167-70. PubMed ID: 16000134
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Mutations in the shutter region of antithrombin result in formation of disulfide-linked dimers and severe venous thrombosis.
    Corral J; Huntington JA; González-Conejero R; Mushunje A; Navarro M; Marco P; Vicente V; Carrell RW
    J Thromb Haemost; 2004 Jun; 2(6):931-9. PubMed ID: 15140129
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Genotype phenotype correlation in a pediatric population with antithrombin deficiency.
    Kovac M; Mitic G; Djilas I; Kuzmanovic M; Serbic O; Lekovic D; Tomic B; Bereczky Z
    Eur J Pediatr; 2019 Oct; 178(10):1471-1478. PubMed ID: 31359133
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. Molecular bases of antithrombin deficiency in French families: identification of seven novel mutations in the antithrombin gene.
    Picard V; Bura A; Emmerich J; Alhenc-Gelas M; Biron C; Houbouyan-Reveillard LL; Molho P; Labatide-Alanore A; Sié P; Toulon P; Verdy E; Aiach M
    Br J Haematol; 2000 Sep; 110(3):731-4. PubMed ID: 10997988
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Incidence and features of thrombosis in children with inherited antithrombin deficiency.
    de la Morena-Barrio B; Orlando C; de la Morena-Barrio ME; Vicente V; Jochmans K; Corral J
    Haematologica; 2019 Dec; 104(12):2512-2518. PubMed ID: 30975910
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [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]  

  • 13. 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]  

  • 14. 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]  

  • 15. [Thrombosis of the renal artery in a 2-month-old child: presentation of a case].
    Pérez-Arbej JA; Valdivia Uría JG; López López JA; Taberner Llop J
    Arch Esp Urol; 1986 Oct; 39(8):563-7. PubMed ID: 3827322
    [No Abstract]   [Full Text] [Related]  

  • 16. Antithrombin gene mutation 5356-5364*delCTT with type I deficiency and early-onset thrombophilia and a brief review of the antithrombin alpha-helix D molecular pathology.
    Steiner M; Steiner B; Rolfs A; Wangnick M; Burstein C; Freund M; Schuff-Werner P
    Ann Hematol; 2005 Jan; 84(1):56-8. PubMed ID: 15309521
    [No Abstract]   [Full Text] [Related]  

  • 17. A novel mutation p.Met1Val in SERPINC1 gene causes hereditary antithrombin deficiency in a Chinese family with thrombotic disease.
    Zeng M; Jia K; Liu M; Wang M; Yang L; Xie H
    Thromb Res; 2023 Dec; 232():104-107. PubMed ID: 37976729
    [No Abstract]   [Full Text] [Related]  

  • 18. Spontaneous recanalization of renal artery stenosis in childhood Takayasu arteritis: A case report.
    Wiggelinkhuizen J; Cremin BJ; Cywes S
    S Afr Med J; 1980 Jan; 57(3):96-8. PubMed ID: 6105718
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Antithrombin III deficiency in a patient with multifocal osteonecrosis.
    Kubo T; Tsuji H; Yamamoto T; Nakahara H; Nakagawa M; Hirasawa Y
    Clin Orthop Relat Res; 2000 Sep; (378):306-11. PubMed ID: 10987006
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Identification of Regulatory Mutations in SERPINC1 Affecting Vitamin D Response Elements Associated with Antithrombin Deficiency.
    Toderici M; de la Morena-Barrio ME; Padilla J; Miñano A; Antón AI; Iniesta JA; Herranz MT; Fernández N; Vicente V; Corral J
    PLoS One; 2016; 11(3):e0152159. PubMed ID: 27003919
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.