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 *

103 related articles for article (PubMed ID: 6701468)

  • 1. Factor XI deficiency in an Arab Moslem family in Israel.
    Aghai E; Yaniv I; David M
    Scand J Haematol; 1984 Mar; 32(3):327-31. PubMed ID: 6701468
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Hereditary plasma thromboplastin antecedent (PTA, FXI) deficiency in a Saudi family.
    al-Adhadh AN
    Clin Lab Haematol; 1988; 10(3):307-14. PubMed ID: 3180697
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Definition of the bleeding tendency in factor XI-deficient kindreds--a clinical and laboratory study.
    Bolton-Maggs PH; Patterson DA; Wensley RT; Tuddenham EG
    Thromb Haemost; 1995 Feb; 73(2):194-202. PubMed ID: 7792729
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Factor XI (PTA) deficiency in an English-American kindred.
    Zacharski LR; French EE
    Thromb Haemost; 1978 Feb; 39(1):215-22. PubMed ID: 580496
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Factor XI deficiency in Ashkenazi Jews in Israel.
    Asakai R; Chung DW; Davie EW; Seligsohn U
    N Engl J Med; 1991 Jul; 325(3):153-8. PubMed ID: 2052060
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Co-existence of Bernard Soulier syndrome and factor XI deficiency in a family: a unified pathology?
    Ghosh K; Nair S; Shetty S; Rajapurkar M; Mohanty D
    Platelets; 2005 Mar; 16(2):85-9. PubMed ID: 15823864
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Hereditary deficiency of factor XI in a Portuguese family, the propositus of which had Behçet's disease (author's transl)].
    Le Roux G; Baledent F; Daupleix D; Larmignat P; Lortholary P
    Nouv Presse Med; 1981 May; 10(22):1829-31. PubMed ID: 7232172
    [TBL] [Abstract][Full Text] [Related]  

  • 8. High gene frequency of factor XI (PTA) deficiency in Ashkenazi Jews.
    Seligsohn U
    Blood; 1978 Jun; 51(6):1223-8. PubMed ID: 647126
    [No Abstract]   [Full Text] [Related]  

  • 9. Inheritance and bleeding in factor XI deficiency.
    Bolton-Maggs PH; Young Wan-Yin B; McCraw AH; Slack J; Kernoff PB
    Br J Haematol; 1988 Aug; 69(4):521-8. PubMed ID: 3408688
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Definition of the population at risk of bleeding due to factor XI deficiency in Ashkenazic Jews and the value of activated partial thromboplastin time in its detection.
    Seligsohn U; Modan M
    Isr J Med Sci; 1981 Jun; 17(6):413-5. PubMed ID: 7263201
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Combined deficiencies of Factor VIII (AHF) and Factor XI (PTA).
    Lian EC; Deykin D; Harkness DR
    Am J Hematol; 1976; 1(3):319-24. PubMed ID: 998619
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Four novel FXI gene mutations in three factor XI- deficient patients.
    de Raucourt E; de Mazancourt P; Quélin F
    Blood Coagul Fibrinolysis; 2008 Apr; 19(3):240-2. PubMed ID: 18388506
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Molecular genetics aspects of factor XI deficiency and Glanzmann thrombasthenia.
    Seligsohn U; Peretz H
    Haemostasis; 1994; 24(2):81-5. PubMed ID: 7959366
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Severe factor XI deficiency in an Arab family associated with a novel mutation in exon 11.
    Wistinghausen B; Reischer A; Oddoux C; Ostrer H; Nardi M; Karpatkin M
    Br J Haematol; 1997 Dec; 99(3):575-7. PubMed ID: 9401068
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Plasma thromboplastin antecedent (Factor XI) deficiency in a black family.
    Niskanen EO; Saito H; Cline MJ
    Arch Intern Med; 1981 Jun; 141(7):936-7. PubMed ID: 7235815
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Novel homozygous large deletion including the 5' part of the SPATA7 gene in a consanguineous Israeli Muslim Arab family.
    Mayer AK; Mahajnah M; Zobor D; Bonin M; Sharkia R; Wissinger B
    Mol Vis; 2015; 21():306-15. PubMed ID: 25814828
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Factor XI deficiency: genetic and clinical studies of a single kindred.
    Litz CE; Swaim WR; Dalmasso AP
    Am J Hematol; 1988 May; 28(1):8-12. PubMed ID: 3369441
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Hemorrhagic diathesis due to a familial, isolated Factor-XI(PTA)-deficiency].
    Lehmann W; Bruhn HD; Lehmann H
    Med Welt; 1973 Apr; 24(17):701-3. PubMed ID: 4750932
    [No Abstract]   [Full Text] [Related]  

  • 19. A cluster of factor XI-deficient patients due to a new mutation (Ile 436 Lys) in northeastern Italy.
    Girolami A; Scarparo P; Bonamigo E; Santarossa L; Cristiani A; Moro S; Lombardi AM
    Eur J Haematol; 2012 Mar; 88(3):229-36. PubMed ID: 21999818
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Two common mutations causing factor XI deficiency in Ashkenazi Jews may point to a European origin.
    Zoossmann-Diskin A
    Blood; 1995 Oct; 86(8):3267-8. PubMed ID: 7579427
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 6.