Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Luigino de Marco"'
Publikováno v:
Blut Zeitschrift für die Gesamte Blutforschung. 31:107-112
Ellagic acid solutions, regardless of the concentration, failed to alter platelet aggregation induced by ADP, Adrenalin, Collagen, Thrombofax and Ristocetin in normal and in factor XII deficient plasma. A moderate inhibition was noted after addition
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::204173016d0481bd6d89b09e854cf229
https://doi.org/10.1007/bf01633726
https://doi.org/10.1007/bf01633726
Publikováno v:
Acta Haematologica. 56:151-159
Platelet aggregation in citrated and heparinized plasma by ionophore A 23187 and Ristocetin was studied in normal subjects and in patients with von Willebrand's disease and congenital afibrinogenemia. Aggregation by ionophore was normal in all groups
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8858f418ae065dd67cdb3ac48a82b467
https://doi.org/10.1159/000207932
https://doi.org/10.1159/000207932
Publikováno v:
Acta Haematologica. 56:27-38
A newly recognized patient with the factor X Friuli coagulation disorder is presented. The propositus is a 10-year-old boy who presented excessive bleeding after a tooth extraction. This is the 11th patient with this peculiar coagulation disorder dis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::83cc93e3a483a42d72d1983f78b5756c
https://doi.org/10.1159/000207916
https://doi.org/10.1159/000207916
Publikováno v:
Blut. 28(1)
A patient with a congenital deficiency of factor V and factor VIII is described (brother/sister incest). The deficiency of the two factors was accompanied by a life-long bleeding tendency. A peculiar family history is added.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0b0a11335e62935f87c7903426645a18
https://pubmed.ncbi.nlm.nih.gov/4810902
https://pubmed.ncbi.nlm.nih.gov/4810902
Publikováno v:
Blut. 31(4)
Platelet aggregation by various inductors was studied in citrated and heparinized plasma of the following groups of subjects: Normal, hemophilia A, combined factor V and factor VIII deficiency, v. Willeprand's disease and congenital afibrinognemia. T
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c17fba35cce8a61f6ecb381f486fa90b
https://pubmed.ncbi.nlm.nih.gov/1080679
https://pubmed.ncbi.nlm.nih.gov/1080679
Publikováno v:
Blut. 30(2)
Platelet adhesiveness and aggregation were studied in three patients with congenital afibrinogenemia. The results obtained may be summarized as follows: The retention of platelets to a glass-bead filter determined with the Salzman method was signific
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c9402dc379edcaafd5c335242df480e2
https://pubmed.ncbi.nlm.nih.gov/1111662
https://pubmed.ncbi.nlm.nih.gov/1111662