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Less than 1% plasma cells in the bone marrow were considered insufficient for testing.
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Therefore, carcinomatosis of the bone marrow was considered as a potential cause of pancytopenia.
The bone marrow is considered the most important dose-limiting organ besides the kidneys [1, 2, 4].
Presently, bone marrow is considered as a prime source of MSCs; however, there are some drawbacks and limitations in use of these MSCs for cell therapy.
Memory B cells are not thought to reside in the BM [30] and CD19+ IgM− IgD− cells in bone marrow are considered to be pro- and pre-B cells [29], [31] [33].
The bone marrow is considered to be an important storage of parasites in Leishmania-infected dogs, although little is known about cellular genesis in this organ during canine visceral leishmaniasis (CVL).
Bone marrow was considered an extranodal site.
The liver, spleen, and bone marrow are considered high-risk organs for LCH [ 12, 13].
Endothelial progenitor cell (EPC) mobilization from the bone marrow was considered to improve outcome after ischemic stroke.
Tumour cells residing in bone marrow are considered to mirror the efficacy of the metastatic process throughout the body.
aPatients with more than 25% of blast cells in the bone marrow are considered to have acute-B-cell leukaemia.
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