BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

196 related articles for article (PubMed ID: 29771426)

  • 41. Low frequency of factor V Leiden and prothrombin G20210A mutations in patients with hepatic venous outflow tract obstruction in northern India: a case-control study.
    Kumar SI; Kumar A; Srivastava S; Saraswat VA; Aggarwal R
    Indian J Gastroenterol; 2005; 24(5):211-5. PubMed ID: 16361766
    [TBL] [Abstract][Full Text] [Related]  

  • 42. Prevalence of the factor V Leiden mutation in portal and hepatic vein thrombosis.
    Das R; Garewal G; Chawla Y; Dhiman RK
    Gut; 1998 Jul; 43(1):147. PubMed ID: 9771422
    [No Abstract]   [Full Text] [Related]  

  • 43. Factor V G1691A (Leiden) is a major etiological factor in Egyptian Budd-Chiari syndrome patients.
    Abdel Ghaffar TY; Elsayed SM; Sakr MA; Elsobky ES; Abdelhakam SM; Yousuf S; Eğin Y; Akar N
    Turk J Haematol; 2011 Dec; 28(4):299-305. PubMed ID: 27264587
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Multiple thrombophilic factors in a patient with Budd-Chiari syndrome.
    Brancaccio V; Iannaccone L; Margaglione M; Guardascione MA; Amitrano L
    Clin Lab Haematol; 2002 Feb; 24(1):61-3. PubMed ID: 11843901
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Budd-Chiari syndrome: combination of genetic defects and the use of oral contraceptives leading to hypercoagulability.
    Minnema MC; Janssen HL; Niermeijer P; de Man RA
    J Hepatol; 2000 Sep; 33(3):509-12. PubMed ID: 11020010
    [TBL] [Abstract][Full Text] [Related]  

  • 46. Subacute Budd-Chiari syndrome associated with polycythemia vera and factor V Leiden mutation.
    Simsek S; Verheesen RV; Haagsma EB; Lourens J
    Neth J Med; 2000 Aug; 57(2):62-7. PubMed ID: 10924943
    [TBL] [Abstract][Full Text] [Related]  

  • 47. Budd-Chiari syndrome with underlying homozygous factor V Leiden and heterozygous methylenetetrahydrofolate reductase mutations.
    Barada KA; Azar CR; Otrock ZK; Taher AT
    J Gastroenterol; 2005 Oct; 40(10):1002-3. PubMed ID: 16261441
    [No Abstract]   [Full Text] [Related]  

  • 48. Transjugular intrahepatic portosystemic shunt for severe jaundice in patients with acute Budd-Chiari syndrome.
    He FL; Wang L; Zhao HW; Fan ZH; Zhao MF; Dai S; Yue ZD; Liu FQ
    World J Gastroenterol; 2015 Feb; 21(8):2413-8. PubMed ID: 25741149
    [TBL] [Abstract][Full Text] [Related]  

  • 49. [Apoptosis of pathological tissues and expression of apoptosis-related genes in hepatic venous stricture Budd-Chiari syndrome].
    Wang CX; Huang ZQ; Liang FQ; Li R; Peng Z
    Zhonghua Yi Xue Za Zhi; 2005 Apr; 85(13):912-5. PubMed ID: 16029531
    [TBL] [Abstract][Full Text] [Related]  

  • 50. JAK2V617F mutation as a marker of a latent myeloproliferative disorder in a patient with Budd-Chiari syndrome and factor V Leiden mutation.
    Plumé G; Vayá A; Ferrando F; Mira Y; Orbis F
    Thromb Haemost; 2007 Sep; 98(3):681-2. PubMed ID: 17849060
    [No Abstract]   [Full Text] [Related]  

  • 51. Budd-Chiari Syndrome and antithrombin III deficiency.
    McClure S; Dincsoy HP; Glueck H
    Am J Clin Pathol; 1982 Aug; 78(2):236-41. PubMed ID: 7102823
    [TBL] [Abstract][Full Text] [Related]  

  • 52. [Budd-Chiari syndrome in children and adolescents: therapeutic radiological intervention].
    Wang L; Zu MH; Gu YM; Xu H; Zhang QQ; Wei N; Xu W; Cui YF; Teng F; Hua QJ
    Zhonghua Er Ke Za Zhi; 2013 Aug; 51(8):590-4. PubMed ID: 24225289
    [TBL] [Abstract][Full Text] [Related]  

  • 53. Factor V Leiden and antiphospholipid antibodies are significant risk factors for ischemic stroke in children.
    Kenet G; Sadetzki S; Murad H; Martinowitz U; Rosenberg N; Gitel S; Rechavi G; Inbal A
    Stroke; 2000 Jun; 31(6):1283-8. PubMed ID: 10835445
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Prospective evaluation of the prevalence of factor V Leiden mutation in portal or hepatic vein thrombosis.
    Denninger MH; Helley D; Valla D; Guillin MC
    Thromb Haemost; 1997 Oct; 78(4):1297-8. PubMed ID: 9365003
    [No Abstract]   [Full Text] [Related]  

  • 55. Factor V leiden mutation and Budd-Chiari syndrome.
    Mohanty D; Shetty S; Narayanan TS; Abraham P
    Blood; 1998 Sep; 92(5):1838-9. PubMed ID: 9716618
    [No Abstract]   [Full Text] [Related]  

  • 56. A Nationwide Analysis of Budd-Chiari Syndrome in the United States.
    Alukal JJ; Zhang T; Thuluvath PJ
    J Clin Exp Hepatol; 2021; 11(2):181-187. PubMed ID: 33746442
    [TBL] [Abstract][Full Text] [Related]  

  • 57. Hepatic outflow obstruction (Budd-Chiari syndrome). Experience with 177 patients and a review of the literature.
    Dilawari JB; Bambery P; Chawla Y; Kaur U; Bhusnurmath SR; Malhotra HS; Sood GK; Mitra SK; Khanna SK; Walia BS
    Medicine (Baltimore); 1994 Jan; 73(1):21-36. PubMed ID: 8309360
    [TBL] [Abstract][Full Text] [Related]  

  • 58. Acquired and Heritable Thrombophilia in Indian Patients With Pediatric Deep Venous Thrombosis (DVT).
    Pai N; Ghosh K; Shetty S
    Clin Appl Thromb Hemost; 2014 Sep; 20(6):573-6. PubMed ID: 23406614
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Budd-Chiari syndrome associated with homozygous factor V Leiden mutation.
    Garewal G; Das R; Chawla Y; Dhiman RK
    Br J Haematol; 1999 Jun; 105(3):842. PubMed ID: 10354159
    [No Abstract]   [Full Text] [Related]  

  • 60. Pseudo-homozygous activated protein C resistance due to coinheritance of heterozygous factor V Leiden mutation and type I factor V deficiency. Variable expression when analyzed by different activated protein C resistance functional assays.
    Delahousse B; Iochmann S; Pouplard C; Fimbel B; Charbonnier B; Gruel Y
    Blood Coagul Fibrinolysis; 1997 Nov; 8(8):503-9. PubMed ID: 9491268
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 10.