Factor X Deficiency
暂无分享,去创建一个
[1] Pagana. mosby's diagnostic&labaratory test refrence , 2015 .
[2] N. Josephson,et al. Factor X deficiency and pregnancy: preconception counselling and therapeutic options , 2012, Haemophilia : the official journal of the World Federation of Hemophilia.
[3] A. Lombardi,et al. Persistent validity of a classification of congenital factor X defects based on clotting, chromogenic and immunological assays even in the molecular biology era , 2011, Haemophilia : the official journal of the World Federation of Hemophilia.
[4] P. Kouides,et al. Diagnosis and treatment of inherited factor X deficiency , 2008, Haemophilia : the official journal of the World Federation of Hemophilia.
[5] A. Girolami,et al. Congenital factor X deficiencies with a defect only or predominantly in the extrinsic or in the intrinsic system: A critical evaluation , 2008, American journal of hematology.
[6] F. Peyvandi,et al. Phenotype and genotype report on homozygous and heterozygous patients with congenital factor X deficiency , 2008, Haematologica.
[7] A. Batorova,et al. Factor X deficiency: clinical manifestation of 102 subjects from Europe and Latin America with mutations in the factor 10 gene , 2006, Haemophilia : the official journal of the World Federation of Hemophilia.
[8] A. Lombardi,et al. A novel type I factor X variant (factor X Cys350Phe) due to loss of a disulfide bond in the catalytic domain , 2003, Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis.
[9] A. Lombardi,et al. Conformation sensitive gel electrophoresis for detection of factor X gene mutations. , 2002, Thrombosis research.
[10] D. Perry,et al. Factor X deficiency. , 2002, Blood reviews.
[11] G. Palù,et al. A dysfunctional factor X (factor X San Giovanni Rotondo) present at homozygous and double heterozygous level: identification of a novel microdeletion (delC556) and missense mutation (Lys(408)-->Asn) in the factor X gene. A study of an Italian family. , 2001, Thrombosis research.
[12] P. Mannucci,et al. Congenital factor X deficiency: spectrum of bleeding symptoms in 32 Iranian patients , 1998, British journal of haematology.
[13] J. Miletich,et al. Factor XSt. Louis II , 1996, The Journal of Biological Chemistry.
[14] A. Thompson,et al. Factors XWenatchee I and II: compound heterozygosity involving two variant proteins. , 1995, Biochimica et biophysica acta.
[15] M. Hertzberg. Biochemistry of factor X. , 1994, Blood reviews.
[16] R. Huber,et al. Structure of human des(1-45) factor Xa at 2.2 A resolution. , 1993, Journal of molecular biology.
[17] C. Hougie,et al. Stuart clotting defect. II. Genetic aspects of a new hemorrhagic state. , 1957, The Journal of clinical investigation.
[18] C. Hougie,et al. Stuart clotting defect. I. Segregation of an hereditary hemorrhagic state from the heterogeneous group heretofore called stable factor (SPCA, proconvertin, factor VII) deficiency. , 1957, The Journal of clinical investigation.
[19] K. Denson,et al. A ‘New’ Coagulation Defect , 1956, British journal of haematology.
[20] R. Pfeiffer,et al. Deficiency of coagulation factors VII and X associated with deletion of a chromosome 13 (q34). Evidence from two cases with 46,XY,t(13;Y)(q11;q34) , 2004, Human Genetics.
[21] H. Blacklock,et al. Factor X deficiency. , 1987, The New Zealand medical journal.
[22] A. Girolami. Tentative and updated classification of factor X variants. , 1986, Acta haematologica.