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pro vyhledávání: '"Peter H. Mackie"'
Autor:
Peter H. Mackie, Antonio Piga, Antonella Roetto, Karen Livesey, Jennifer J. Pointon, Clara Camaschella, Giuliana Barbabietola, Filomena Daraio, Alison T. Merryweather-Clarke, Kathryn J.H. Robson
Hemochromatosis type 4 is an atypical hemochromatosis characterized by dominant inheritance, increased serum ferritin, normal transferrin saturation, and prevalent iron deposition in the reticuloendothelial (RE) cells rather than in hepatocytes. Hete
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9c8cfa703011fd5e96c757c18f4d1287
https://doi.org/10.1182/blood-2002-03-0693
https://doi.org/10.1182/blood-2002-03-0693
Autor:
Peter H. Mackie, Rajeev Joshi, Anil Lakhani, Daniel Catovsky, Janet E. Ropner, Andrew G. Bosanquet, Estella Matutes, Henri Grech, Stella J. Bowcock, Patrick D Thornton, Ian D. C. Douglas
Publikováno v:
Annals of Hematology. 82:759-765
Abnormalities of the p53 gene are known to confer detrimental effects in chronic lymphocytic leukaemia (CLL) and are associated with short survival. We have used high dose methylprednisolone (HDMP) to treat 25 patients with advanced refractory CLL of
Publikováno v:
Archives of Internal Medicine. 140:127
• A patient had hereditary angioneurotic edema coincident with systemic lupus erythematosus. This condition resulted in loss of hair, arthralgia, leukoplakia, colitis, and a nephrotic syndrome due to proliferative glomerulonephritis. The renal lesi
Periodical
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