Zobrazeno 1 - 10
of 74
pro vyhledávání: '"Per Stavem"'
Publikováno v:
Scandinavian Journal of Haematology. 14:24-34
A patient with a plasma cell proliferative disorder and a monoclonal IgG-kappa protein in the serum was observed over a period of four years. Two unusual features were seen in this patient: (1) An apparently benign course in spite of relatively large
Autor:
Per Stavem
Publikováno v:
Scandinavian Journal of Haematology. 8:396-399
Cumulative frequency diagrams display the magnitude of a symptom or sign, as well as the frequency, thus adding another dimension to the graphic figure. One particular sign, like e. g. splenic enlargement in different diseases, may be illustrated by
Publikováno v:
Scandinavian Journal of Haematology. 10:153-160
Two sisters had a congenital hypochromic anaemia in spite of hyperferraemia with a fully saturated serum transferrin, and in spite of heavy iron deposits in the liver. Bone marrow iron was reduced. The anaemia was markedly increased during pregnancy,
Autor:
Per Stavem, Stein A. Evensen
Publikováno v:
Acta Medica Scandinavica. 219:79-83
An intermittent combination chemotherapy program was initiated in 1971–79 in 172 patients, aged 15–59 years, with acute leukemia (131 myelogenous (AML) and 41 lymphoblastic (ALL)). Sixteen patients with AML and 6 with ALL have survived for more t
Publikováno v:
Scandinavian Journal of Haematology. 13:266-275
A patient with IgG myeloma is reported in whom about 30 % of the plasma cells contained one or more hyaline intranuclear inclusions which were characterized by light, immunofluorescence and electron microscopy. Our results suggest that the intranucle
Autor:
Per Stavem, Kåre Berg
Publikováno v:
Scandinavian Journal of Haematology. 10:202-208
A macromolecular serum component, platelet stain preventing factor (PSPF), possessing the capacity to prevent staining of platelets, has been observed in the serum of an apparently healthy person. The factor is active only when EDTA is present, and i
Publikováno v:
Scandinavian Journal of Haematology. 26:149-152
A 17-year-old woman had acute myeloid leukaemia (AML) with a leucocyte count of about 100 times 109/1. The great majority of the leucocytes were immature. About half of them were without granules; in the other half the granules were usually scanty, b
Publikováno v:
Acta medica Scandinavica
A routine medical examination revealed a markedly increased ESR in a 40-year-old man. Further studies showed an enlarged spleen and a marked polyclonal increase of serum globulins. Splenectomy was performed, revealing a solitary plasmocytoma which we
Publikováno v:
Scandinavian Journal of Haematology. 17:241-250
Studies of blood lymphocytes from 4 patients with pure red cell aplasia were performed with lymphocyte surface markers, and with various in vitro tests for lymphocyte functions. Pathologically low B-lymphocyte values were found. In contrast, no marke
Publikováno v:
Scandinavian Journal of Haematology. 21:355-359
A patient is reported to have an in between type of acute myeloid leukaemia, namely acute eosinophilomyelomonocytic leukaemia. The blasts in the peripheral blood showed a definite transition towards immature monocytes. The bone marrow contained 65 %