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 *

149 related articles for article (PubMed ID: 16295492)

  • 1. Hereditary coagulation factor X deficiency--a clinico-haematological profile of 5 cases from Varanasi.
    Shukla J; Boyal R; Singh VP
    Indian J Pathol Microbiol; 2004 Apr; 47(2):259-61. PubMed ID: 16295492
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Hereditary coagulation factor X deficiency.
    Kumar A; Mishra KL; Kumar A; Mishra D
    Indian Pediatr; 2005 Dec; 42(12):1240-2. PubMed ID: 16424563
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Inherited factor X deficiency in two brothers.
    Barik S; Budhraja A; Bhalla M; Diwan S
    Indian J Pathol Microbiol; 1997 Jan; 40(1):63-5. PubMed ID: 9145616
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [Hereditary deficiency of coagulation factor X. Study of 10 cases in a family in Mexico].
    Chávez-Vela JJ; Ambriz R; Pizzuto J; Paz Reyna M; Avilés A; Morales M; Herrera J; Sinco A
    Rev Invest Clin; 1983; 35(4):309-14. PubMed ID: 6672929
    [No Abstract]   [Full Text] [Related]  

  • 5. Factor X deficiency--a rare disorder.
    Trivedi S; Bhatia J; Jain S; Toprani TH
    Indian J Pathol Microbiol; 2004 Apr; 47(2):223-4. PubMed ID: 16295475
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Rare inherited coagulation disorders in India.
    Kashyap R; Saxena R; Choudhry VP
    Haematologia (Budap); 1996; 28(1):13-9. PubMed ID: 9283899
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Congenital factor X deficiency of coagulation revealed by epistaxis.
    Atmani S; Aouragh R; El-Alaoui K; Bouharrou A; Hida M
    Saudi Med J; 2006 Aug; 27(8):1265-6. PubMed ID: 16883471
    [No Abstract]   [Full Text] [Related]  

  • 8. A further inherited variant of coagulation factor X.
    Parkin JD; Madaras F; Sweet B; Castaldi PA
    Aust N Z J Med; 1974 Dec; 4(6):561-4. PubMed ID: 4533945
    [No Abstract]   [Full Text] [Related]  

  • 9. Factor X deficiency in North Pakistan.
    Anwar M; Hamdani SN; Ayyub M; Ali W
    J Ayub Med Coll Abbottabad; 2004; 16(3):1-4. PubMed ID: 15631360
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Rare coagulation disorders: a study of 70 cases in the Egyptian population.
    Abdelwahab M; Khaddah N
    Haemophilia; 2012 Sep; 18(5):e386-8. PubMed ID: 22845778
    [No Abstract]   [Full Text] [Related]  

  • 11. [Probably inherited factor X deficiency. Report of a case (author's transl)].
    García León L; Gerzso Rivera F; González Constandse R
    Rev Invest Clin; 1981; 33(4):395-7. PubMed ID: 7330513
    [No Abstract]   [Full Text] [Related]  

  • 12. Factor X deficiency in a cat.
    Gookin JL; Brooks MB; Catalfamo JL; Bunch SE; Muñana KR
    J Am Vet Med Assoc; 1997 Sep; 211(5):576-9. PubMed ID: 9290823
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Diagnosis of Stuart-Prower disease].
    Papaian LP; Fedorova ZD; Medved' RI; Khrolova PV
    Probl Gematol Pereliv Krovi; 1977 Mar; 22(3):46-9. PubMed ID: 854510
    [No Abstract]   [Full Text] [Related]  

  • 14. Prophylaxis in rare coagulation disorders -- factor X deficiency.
    Auerswald G
    Thromb Res; 2006; 118 Suppl 1():S29-31. PubMed ID: 16574201
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Congenital factor X (Stuart-Prower factor) deficiency: a family study.
    Jain D; Bhargava M; Arya LS
    Indian Pediatr; 1988 Nov; 25(11):1120-4. PubMed ID: 3248882
    [No Abstract]   [Full Text] [Related]  

  • 16. Congenital FX deficiency combined with other clotting defects or with other abnormalities: a critical evaluation of the literature.
    Girolami A; Ruzzon E; Tezza F; Scandellari R; Scapin M; Scarparo P
    Haemophilia; 2008 Mar; 14(2):323-8. PubMed ID: 18081833
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Routine preoperative coagulation screening detects a rare bleeding disorder.
    Jonnavithula N; Durga P; Pochiraju R; Anne KK; Ramachandran G
    Anesth Analg; 2009 Jan; 108(1):76-8. PubMed ID: 19095834
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Factors X Nice I and II: two novel missense mutations (Met-40Val and Pro304Ser) in patient with coagulation factor X deficiency.
    Miyata T; Fischer F; Umeyama H; Appert A; Jambou D; Kato H
    Thromb Haemost; 1998 Oct; 80(4):709-10. PubMed ID: 9799000
    [No Abstract]   [Full Text] [Related]  

  • 19. Congenital bleeding disorders of the vitamin K-dependent clotting factors.
    Girolami A; Scandellari R; Scapin M; Vettore S
    Vitam Horm; 2008; 78():281-374. PubMed ID: 18374200
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Clinical and coagulation studies in 3 cases of congenital factor X deficiency and review of reported cases in Japan (author's transl)].
    Mori K; Sakai H; Suzuki S; Nakano N; Tachiya H; Sugai K; Goto Y
    Nihon Ketsueki Gakkai Zasshi; 1980 Jun; 43(3):572-86. PubMed ID: 7223329
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 8.