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MeSH Review

Factor X Deficiency

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Disease relevance of Factor X Deficiency


High impact information on Factor X Deficiency


Chemical compound and disease context of Factor X Deficiency


Biological context of Factor X Deficiency


Analytical, diagnostic and therapeutic context of Factor X Deficiency


  1. Acquired factor X deficiency and amyloidosis treated with melphalan and prednisone. Levin, M., Chokas, W. N. Engl. J. Med. (1987) [Pubmed]
  2. Characterization of amyloid deposits and P component from a patient with factor X deficiency reveals proteins derived from a lambda VI light chain. Cohen, D., Pras, M., Franklin, E.C., Frangione, B. Am. J. Med. (1983) [Pubmed]
  3. Steroid hormone-responsive secondary factor X deficiency. Hamasaki, A., Ishii, K., Yamaguchi, K., Sunamoto, M., Ozaki, H., Yanagita, M., Wakatsuki, Y., Horiuchi, H., Nakahata, Y., Kita, T. Thromb. Haemost. (1998) [Pubmed]
  4. Factor X Nagoya 1 and Nagoya 2: a CRM- factor X deficiency and a dysfunctional CRM+ factor X deficiency characterized by substitution of Arg306 by Cys and of Gly366 by Ser, respectively. Miyata, T., Kojima, T., Suzuki, K., Umeyama, H., Yamazaki, T., Kamiya, T., Toyoda, H., Kato, H. Thromb. Haemost. (1998) [Pubmed]
  5. Molecular analysis of the genotype-phenotype relationship in factor X deficiency. Millar, D.S., Elliston, L., Deex, P., Krawczak, M., Wacey, A.I., Reynaud, J., Nieuwenhuis, H.K., Bolton-Maggs, P., Mannucci, P.M., Reverter, J.C., Cachia, P., Pasi, K.J., Layton, D.M., Cooper, D.N. Hum. Genet. (2000) [Pubmed]
  6. Severe factor X deficiency treated with heparin-added prothrombin complex concentrate. Apak, H., Celkan, T., Ozkan, A., Yüksel, L., Bilgi, Z., Yildiz, I. Ann. Hematol. (2003) [Pubmed]
  7. Acquired and transient factor X deficiency associated with sodium valproate treatment. Gallais, V., Bredoux, H., le Roux, G., Laroche, L. Eur. J. Haematol. (1996) [Pubmed]
  8. Factor X deficiency during treatment of relapsed acute myeloid leukaemia with amsacrine. Carter, C., Winfield, D.A. Clinical and laboratory haematology. (1988) [Pubmed]
  9. Hereditary coagulation factor X deficiency. Kumar, A., Mishra, K.L., Kumar, A., Mishra, D. Indian pediatrics. (2005) [Pubmed]
  10. Progressive systemic sclerosis with the nephrotic syndrome and acquired factor X deficiency. Eiser, A.R., Zilversmit, R., Neff, M.S., Grishman, E., Slifkin, R.F. American journal of nephrology. (1986) [Pubmed]
  11. Successful treatment of transient acquired factor X deficiency by plasmapheresis with concomitant intravenous immunoglobulin and steroid therapy. Smith, S.V., Liles, D.K., White, G.C., Brecher, M.E. Am. J. Hematol. (1998) [Pubmed]
  12. Presurgical plasma exchange is ineffective in correcting amyloid associated factor X deficiency. Barker, B., Altuntas, F., Paranjape, G., Sarode, R. Journal of clinical apheresis. (2004) [Pubmed]
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