Results 211 to 220 of about 23,927 (264)
IgG4-related sclerosing cholangitis associated with essential thrombocythemia: A case report. [PDF]
Wu ZN, Ji R, Xiao Y, Wang YD, Zhao CY.
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Dystonia during pegylated interferon alpha therapy in a case with essential thrombocythemia and cerebral infarction. [PDF]
Zhang P +6 more
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[IgM- κ and IgM- λ biclonal POEMS syndrome combined with essential thrombocythemia: a case report]. [PDF]
Wang J, Wu F, Zhai ZM.
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Essential thrombocythemia: nutritional management in weight loss and malnutrition. [PDF]
Brum ISDC +8 more
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Management of Essential Thrombocythemia in a Patient With a History of Thrombotic Thrombocytopenic Purpura. [PDF]
Johnson S +3 more
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[Essential thrombocythemia: conventional therapy].
A. Grossi +4 more
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Seminars in Hematology, 2005
Significant progress in our understanding of the molecular pathogenesis of essential thrombocythemia (ET) and the other Philadelphia (Ph) chromosome-negative myeloproliferative disorders (MPDs) has recently been achieved. Unfortunately, the diagnosis of ET still relies on a set of exclusion criteria developed years ago, as recent advances have yet to ...
Guido, Finazzi, Claire, Harrison
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Significant progress in our understanding of the molecular pathogenesis of essential thrombocythemia (ET) and the other Philadelphia (Ph) chromosome-negative myeloproliferative disorders (MPDs) has recently been achieved. Unfortunately, the diagnosis of ET still relies on a set of exclusion criteria developed years ago, as recent advances have yet to ...
Guido, Finazzi, Claire, Harrison
openaire +4 more sources
Best Practice & Research Clinical Haematology, 2003
Essential thrombocythaemia is a myeloproliferative disorder that results from the transformation of a multipotent haematopoietic progenitor. Its diagnosis can be challenging and its optimal management has been controversial, largely because of a virtual absence of randomised trials.
Claire N, Harrison, Anthony R, Green
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Essential thrombocythaemia is a myeloproliferative disorder that results from the transformation of a multipotent haematopoietic progenitor. Its diagnosis can be challenging and its optimal management has been controversial, largely because of a virtual absence of randomised trials.
Claire N, Harrison, Anthony R, Green
openaire +3 more sources

