Zobrazeno 1 - 10
of 73
pro vyhledávání: '"O. Margaret Garson"'
Autor:
A. Manoharan, O. Margaret Garson
Publikováno v:
Scandinavian Journal of Haematology. 17:10-16
The familial occurrence of polycythaemia vera (PV) is rare, with only 3 authentic reports in the world literature. This paper describes a family of 8 females, 3 of whom have PV and another has pernicious anaemia. Clinical and haematological data is p
Autor:
O. Margaret Garson, Wendy J. Milligan
Publikováno v:
Scandinavian Journal of Haematology. 12:256-262
A young female presenting with lymphoblastic leukaemia was found to have an abnormal genotype due to a reciprocal translocation between chromosomes B and D. The father and twin sisters of the propositus were also found to possess the trans-location.
Autor:
Wendy J. Milligan, O. Margaret Garson
Publikováno v:
Scandinavian Journal of Haematology. 9:186-192
Three male patients with chronic granulocytic leukaemia were found by direct bone marrow chromosome studies to belong to a cytogenetically defined variant of this disorder. In addition to possessing the Philadelphia chromosome, the leukaemic cells la
Autor:
Adrian L. Polglase, David Gunter, Andrew R. Moot, Vicky Thursfield, O. Margaret Garson, Graham G. Giles
Publikováno v:
ANZ Journal of Surgery. 73:289-293
Background: The objective of the present study was to investigate the relationship between colorectal and prostate cancer. Methods: All Victorian men who developed metachronous colorectal and prostate cancer with the first primary diagnosed between 1
Autor:
Christina Rudduck, Lisa M Ooms, Lynda J. Campbell, O. Margaret Garson, Vickie Vrazas, Jeff Szer
Publikováno v:
American Journal of Hematology. 49:15-20
Chromosomal in situ hybridization (ISH) has extended the scope of cytogenetic analysis to nondividing cells by the use of chromosome-specific probes detected by nonisotopic techniques. This provides a rapid and sensitive method for identifying chromo
Publikováno v:
Genes, Chromosomes and Cancer. 10:213-216
The cell line CIPL38 was derived from the pleural effusion of a patient with small cell lung cancer. The karyotype was hyperdiploid and complex with a variable number of marker chromosomes. Two of the markers had large homogeneously staining regions
Publikováno v:
International Journal of Cancer. 55:390-393
While loss of the Y chromosome from the karyotype of tumor cells has frequently been found in a number of human malignancies of different types, structural alterations are a much less common finding. Prompted by the high frequency of cytogenetic Y ch
Publikováno v:
Genes, Chromosomes and Cancer. 7:213-218
Parathyroid hormone-related protein (PTHRP) is expressed in a large number of tumors and is the mediator of parathyroid hormone-like effects seen in humoral hypercalcemia of malignancy. The gene coding for PTHRP has been localised to the short arm of
Autor:
Robyn Lukeis, O. Margaret Garson
Publikováno v:
Journal of Histotechnology. 15:253-261
The identification of specific chromosomal abnormalities in the malignant lymphomas has both clinical and biological significance. Translocations t(14;18) and t(8;14) (with variant translocations t(2;8) and t(8;22)) in particular are associated with
Autor:
John Bashford, James S. Wiley, Martin B. Van Der Weyden, Michael F. Buckley, O. Margaret Garson, Jeff Szer
Publikováno v:
British Journal of Haematology. 79:331-334
Summary We describe the clinical experience of a male patient with acute promyelocytic leukaemia, relapsing after sex-mismatched allogeneic bone marrow transplantation and treated with all-trans-retinoic acid. Resolution of the coagulopathy was obser