Zobrazeno 1 - 10
of 164
pro vyhledávání: '"M. J. Larrieu"'
Publikováno v:
Scandinavian Journal of Haematology. 28:233-237
Washed red blood cells (WRC) have been used for replacing the blood loss in haemophilia A patients with antibody to Factor VIII. Levels of VIII coagulant activity (VIII:C), VIII coagulant antigen (VIII:CAg) and VIII related antigen (VIIIR:Ag) have be
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3d0eab75a822372ec507473c6eb524d0
https://doi.org/10.1111/j.1600-0609.1982.tb00520.x
https://doi.org/10.1111/j.1600-0609.1982.tb00520.x
Publikováno v:
British Journal of Haematology. 50:531-535
Antithrombin III concentrates were administered to a patient with hereditary AT III deficiency undergoing orthopaedic surgery. The plasma AT III level (heparin cofactor activity) was maintained at values in excess of 100% postoperatively. A mean dose
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::26e25c51386d5b6bdb498212c8a3e974
https://doi.org/10.1111/j.1365-2141.1982.00479.x-i1
https://doi.org/10.1111/j.1365-2141.1982.00479.x-i1
Publikováno v:
Blood Coagulation & Fibrinolysis. 4:679-687
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4fa2fb67aed6f790b33e4182389efa9c
https://doi.org/10.1097/00001721-199310000-00003
https://doi.org/10.1097/00001721-199310000-00003
Publikováno v:
Blood coagulationfibrinolysis : an international journal in haemostasis and thrombosis. 4(5)
The aim of this study was to investigate the interactions of t-PA and plasminogen with fibrin derived from an abnormal fibrinogen detected in a 40-year-old male patient who had had an episode of thrombophlebitis with pulmonary embolism. An abnormal f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::a52b7b682f63a2d64cb9b23d846d66ce
https://pubmed.ncbi.nlm.nih.gov/8292717
https://pubmed.ncbi.nlm.nih.gov/8292717
Publikováno v:
Thrombosis and haemostasis. 63(2)
The association of a variant of antithrombin III (AT III Bligny) and protein C deficiency is described in a 36-year-old patient having suffered from severe thrombotic episodes. His mother has protein C deficiency and showed a single episode of thromb
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::ef7f7803de313c68083c64e5ea64f08e
https://pubmed.ncbi.nlm.nih.gov/2363123
https://pubmed.ncbi.nlm.nih.gov/2363123
Publikováno v:
Nouvelle revue francaise d'hematologie. 32(2)
A prenatal diagnosis for fetal disease was performed at 20 weeks gestation in a severely affected patient with type IIA von Willebrand disease. In the fetal cord blood sample obtained under ultrasound guidance, the level of von Willebrand ristocetin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::330b5f50e54ae7e4aadfb555eea9d160
https://pubmed.ncbi.nlm.nih.gov/2115990
https://pubmed.ncbi.nlm.nih.gov/2115990
Publikováno v:
Journal of Clinical Pathology. 28:690-695
Factor VIII activity and factor VIII related--or Willebrand--antigen were studied in 49 known carriers of haemophilia A and 31 normal women, and the data were analysed by four statistical approaches. Sixteen per cent of normals and 18% of carriers we
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7b68a93871e31529f090aa7b401ba703
https://doi.org/10.1136/jcp.28.9.690
https://doi.org/10.1136/jcp.28.9.690
Publikováno v:
The Journal of Bone & Joint Surgery. 69:264-269
Synovectomy of twenty-three elbows was done in eighteen patients, eight to twenty-five years old, who had severe hemophilia and were followed for eighteen to seventy months. Episodes of bleeding recurred in four elbows, and moderate pain persisted in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fb5297325cde32a8b5c0af98b42e27fb
https://doi.org/10.2106/00004623-198769020-00015
https://doi.org/10.2106/00004623-198769020-00015
Publikováno v:
Blood. 65:496-500
A qualitative defect of antithrombin III (AT III) has been demonstrated over three generations in eight members of an Italian family by the discrepancy between a normal amount of antigen and decreased antithrombin and anti-Xa activity in the presence
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::422a027b934ee73e58d5da23fd0ebe5c
https://doi.org/10.1182/blood.v65.2.496.bloodjournal652496
https://doi.org/10.1182/blood.v65.2.496.bloodjournal652496
Publikováno v:
Vox Sanguinis. 53:37-43
Forty-six subjects (44 HIV antibody-positive) with some degree of immune deficiency (at least TH/TS ratio below 1) were randomly distributed into 4 treatment groups. Each group was assigned to 1 of 4 products to be used exclusively for a 1-year perio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::98a5b0efbf399b7a577b396a9c678c2b
https://doi.org/10.1111/j.1423-0410.1987.tb04911.x
https://doi.org/10.1111/j.1423-0410.1987.tb04911.x