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 *

101 related articles for article (PubMed ID: 5698876)

  • 21. Severe factor VII deficiency caused by a novel point mutation (Arg353Pro) combined with a rare Cys22Arg mutation.
    Zhidong W; Xiaojun H
    Thromb Haemost; 2007 Sep; 98(3):687-8. PubMed ID: 17849063
    [No Abstract]   [Full Text] [Related]  

  • 22. [Factor VII deficiency revealed by intracranial hemorrhage].
    Sfaihi Ben Mansour L; Thabet A; Aloulou H; Turki H; Chabchoub I; Mhiri F; Mnif Z; Ben Ali H; Kammoun T; Hachicha M
    Arch Pediatr; 2009 Jul; 16(7):1024-7. PubMed ID: 19409767
    [TBL] [Abstract][Full Text] [Related]  

  • 23. [Inherited coagulation factor VII deficiency caused by double heterozygotic mutations Arg304Gln and Arg304Trp].
    Ding QL; Wang HL; Wang XF; Wang MS; Fu QH; Wu WM; Hu YQ; Wang ZY
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2003 Aug; 20(4):279-83. PubMed ID: 12903033
    [TBL] [Abstract][Full Text] [Related]  

  • 24. First report of a FVII-deficient Indian patient carrying double heterozygous mutations in the FVII gene.
    Ahmed RP; Biswas A; Kannan M; Bhattacharya M; Geisen C; Seifried E; Oldenburg J; Saxena R
    Thromb Res; 2005; 115(6):535-6. PubMed ID: 15792686
    [No Abstract]   [Full Text] [Related]  

  • 25. [Molecular analysis of two pedigrees with hereditary F VII deficiency].
    Chu H; Wang H; Wang X; Guo X; Qu B; Duan B; Yin J; Kang W; Wang Z
    Zhonghua Xue Ye Xue Za Zhi; 2002 Mar; 23(3):130-3. PubMed ID: 12015065
    [TBL] [Abstract][Full Text] [Related]  

  • 26. [Congenital factor VII deficiency (author's transl)].
    Fernández de Castro Pombo M; Torreblanca J; Cuesta García MV; Crespo E; Fernández Pavón A
    An Esp Pediatr; 1980 Jul; 13(7):611-8. PubMed ID: 7416654
    [TBL] [Abstract][Full Text] [Related]  

  • 27. [Studies on inherited coagulation factor VII deficiency and tissue factor abnormality in a pedigree].
    Ding QL; Wang XF; Xu GQ; Huang XP; Hu YQ; Wu WM; Fu QH; Wang HL; Wang ZY
    Zhonghua Xue Ye Xue Za Zhi; 2006 Mar; 27(3):150-3. PubMed ID: 16792912
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Homozygous nonsense mutation (Cys72-->stop) in the human F7 gene: a not life-threatening mutation despite the absence of circulating factor VII.
    Chafa O; Fischer AM; Reghis A; Tapon-Bretaudiere J
    J Thromb Haemost; 2005 Jan; 3(1):175-7. PubMed ID: 15634284
    [No Abstract]   [Full Text] [Related]  

  • 29. [Factor VII deficiency--case report].
    Kuliszkiewicz-Janus M; Dereń-Wagemann I; Kasza R; Kuliczkowski K
    Pol Arch Med Wewn; 2006 Sep; 116(3):873-5. PubMed ID: 18652281
    [TBL] [Abstract][Full Text] [Related]  

  • 30. [Intracranial hemorrhage in an infant with congenital factor VII deficiency].
    De Sanctis C; Lumare A; Sardella M; Dogliani P; Lange M
    Minerva Pediatr; 1972 Mar; 24(8):312-20. PubMed ID: 5016067
    [No Abstract]   [Full Text] [Related]  

  • 31. [Subcutaneous hematomas, reduced Quick value. Factor VII deficiency].
    Osterwalder P; Koch J; Von Felten A
    Praxis (Bern 1994); 1998 Jul; 87(29-30):958-60. PubMed ID: 9737176
    [No Abstract]   [Full Text] [Related]  

  • 32. "Congenital deficiency of Factor VII. Case reports of non-identical twins".
    Jain SC; Quadri MI; Garewal G; Bhakoo ON; Das KC
    Indian Pediatr; 1979 Sep; 16(9):809-13. PubMed ID: 536024
    [No Abstract]   [Full Text] [Related]  

  • 33. [A case of familial proconvertine (factor VII) deficiency].
    Mallet EC; Roche B; Bataille H; Parlier G
    Arch Fr Pediatr; 1991 Dec; 48(10):737. PubMed ID: 1793352
    [No Abstract]   [Full Text] [Related]  

  • 34. Coagulation factor VII. (Biochemistry, role in blood coagulation, methods of assay, congenital deficiencies and relationship with thrombosis).
    Mariani G; Mandelli F
    Ric Clin Lab; 1983; 13(3):287-98. PubMed ID: 6606207
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Factor VII deficiency: clinical manifestation of 717 subjects from Europe and Latin America with mutations in the factor 7 gene.
    Herrmann FH; Wulff K; Auerswald G; Schulman S; Astermark J; Batorova A; Kreuz W; Pollmann H; Ruiz-Saez A; De Bosch N; Salazar-Sanchez L;
    Haemophilia; 2009 Jan; 15(1):267-80. PubMed ID: 18976247
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Factor VII deficiency: a double heterozygote of an Arg402Stop with a deletion of the C-terminal five amino acids and a Thr359Met.
    Okamoto M; Katsuda I; Ohshika Y; Maruyama F; Ezaki K; Emi N; Ichihara Y
    Eur J Haematol; 2009 May; 82(5):405-7. PubMed ID: 19141116
    [No Abstract]   [Full Text] [Related]  

  • 37. 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]  

  • 38. Homozygous 2bp deletion in the human factor VII gene: a non-lethal mutation that is associated with a complete absence of circulating factor VII.
    Peyvandi F; Mannucci PM; Jenkins PV; Lee A; Coppola R; Perry DJ
    Thromb Haemost; 2000 Oct; 84(4):635-7. PubMed ID: 11057862
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Factor VII deficiency: immunological characterization of genetic variants and detection of carriers.
    Mariani G; Mazzucconi MG; Hermans J; Ciavarella N; Faiella A; Hassan HJ; Mannucci PM; Nenci GG; Orlando M; Romoli D; Mandelli F
    Br J Haematol; 1981 May; 48(1):7-14. PubMed ID: 7248191
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Factor VII verona coagulation disorder: double heterozygosis with an abnormal factor VII and heterozygous factor VII deficiency.
    Girolami A; Falezza G; Patrassi G; Stenico M; Vettore L
    Blood; 1977 Oct; 50(4):603-10. PubMed ID: 901936
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 6.