Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Teresa Gago"'
Publikováno v:
American Journal of Hematology. 76:163-171
Antithrombin (AT), the most important coagulation serine proteases inhibitor, plays an important role in maintaining the hemostatic balance. Inherited AT deficiency, mainly characterized by predisposition to recurrent venous thromboembolism, is trans
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::79b483486c5739e67b21757c7cd931aa
https://doi.org/10.1002/ajh.20067
https://doi.org/10.1002/ajh.20067
Publikováno v:
Thrombosis research. 128(3)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4b3fcf3799d0597dfe1e9b58395cbb63
https://pubmed.ncbi.nlm.nih.gov/21621249
https://pubmed.ncbi.nlm.nih.gov/21621249
Publikováno v:
American journal of hematology. 76(2)
Antithrombin (AT), the most important coagulation serine proteases inhibitor, plays an important role in maintaining the hemostatic balance. Inherited AT deficiency, mainly characterized by predisposition to recurrent venous thromboembolism, is trans
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::7058684402caac608e934a42ebcb679f
https://pubmed.ncbi.nlm.nih.gov/15164384
https://pubmed.ncbi.nlm.nih.gov/15164384
Autor:
A. N. G. Tavares, João Lavinha, Teresa Gago, John H. McVey, Célia Ventura, Dezsö David, Ana I. M. Santos
Publikováno v:
Scopus-Elsevier
Europe PubMed Central
Europe PubMed Central
SummaryCoagulation factor XI (FXI) deficiency is an inherited autosomal recessive mild bleeding disorder. In this study, we report the molecular genetic analysis of FXI deficiency in six unrelated families of Portuguese origin. The Jewish type II mut
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f714eab6cb70571da2510812bb0ee101
http://www.scopus.com/inward/record.url?eid=2-s2.0-0033708931&partnerID=MN8TOARS
http://www.scopus.com/inward/record.url?eid=2-s2.0-0033708931&partnerID=MN8TOARS
Publikováno v:
Europe PubMed Central
SummaryWe report the application of single-stranded conformation polymorphism (SSCP) analysis to the screening of 15 functionally important Protein S (PS) gene (PSα) regions (4.243 Kb) in 6 unrelated families with PS deficiencies. Direct sequencing
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b6da2c647592cbc28e6c7be5e39920ee
http://europepmc.org/abstract/med/9031443
http://europepmc.org/abstract/med/9031443