Zobrazeno 1 - 10
of 19
pro vyhledávání: '"A. G. Papayannis"'
Publikováno v:
Scandinavian Journal of Haematology. 18:301-308
15 patients with preleukaemia were cytogenetically studied during the preleukaemic state by using the G-banding staining technique. It was found that 9 patients had a completely normal karyotype, while the other 6 showed various chromosomal abnormali
Publikováno v:
Blood. 38:745-758
Two families have been studied, members of which have a lifelong hemorrhagic diathesis. In both families, a platelet functional abnormality has been found, with the coagulation mechanism intact. Findings common to both families were a prolonged bleed
Publikováno v:
British Journal of Haematology. 24:435-441
Summary. Two families are described in which many members were shown to have increased platclet adhesiveness, using a modification of the Salzman techniquc. The abnormality appears to be inherited as an autosomal dominant characteristic. In addition,
Publikováno v:
Human Genetics. 48:109-111
Publikováno v:
Annals of clinical research. 6(4)
Publikováno v:
The British journal of surgery. 64(2)
Platelet function tests were performed on 15 patients undergoing major operation preoperatively, during anaesthesia and 30 minutes and 3 hours after the beginning of operation. It was found that during anaesthesia platelet retention in a glass bead c
Publikováno v:
The Journal of antimicrobial chemotherapy. 3(4)
Publikováno v:
Scandinavian journal of haematology. 29(1)
A 73-year-old patient who had polycythaemia vera (PV), and who 6 years later developed chronic lymphocytic leukaemia (CCL) is described. 2 years after the appearance of CLL, the polycythaemic phase showed a remission following treatment with phleboto
Publikováno v:
Scandinavian journal of haematology. 24(2)
24 patients with preleukaemia were cytogenetically studied by the G-banding staining technique. All patients developed later frank acute non-lymphocytic leukaemia and died. 13 patients had a completely normal karyotype (NN-patients) with a median sur
Publikováno v:
Scandinavian journal of haematology. 12(2)
Erythrocyte δ-ALA dehydratase activity was quantitatively measured in 33 normal subjects and 50 patients with homozygous b-thalassaemia. It was found that, a) In thalassaemic erythrocytes the activity of this enzyme was usually higher than in the no