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1 cance (MGUS) is an asymptomatic premalignant plasma cell disorder.
2 ry systemic amyloidosis (AL) is an incurable plasma cell disorder.
3 Primary systemic amyloidosis (AL) is a fatal plasma cell disorder.
4 loma, primary amyloidosis (AL), or a related plasma cell disorder.
5 iple myeloma (SMM) is an asymptomatic clonal plasma cell disorder.
6 -chain (AL) amyloidosis is a rare, incurable plasma cell disorder.
7 entary to conventional methods of evaluating plasma cell disorders.
8 plant had complete responses of their clonal plasma cell disorders.
9 om had biopsy-proven amyloidosis with clonal plasma cell disorders.
10 al light chain deposits is a complication of plasma cell disorders.
11 tablished in the diagnosis and monitoring of plasma cell disorders.
12 termined significance (MGUS), a premalignant plasma-cell disorder, among persons 50 years of age or o
13 Patients with symptomatic AL, a measurable plasma cell disorder, and adequate hematologic and renal
14 he polyradiculoneuropathy and the monoclonal plasma cell disorder, and at least 1 of the other 3 majo
15 mplete response or persistence of the clonal plasma cell disorder, and change in the function of orga
18 he proportion of patients with a preexisting plasma cell disorder has never been determined by labora
19 phomas (HR, 1.81; 95% CI, 1.12 to 2.93), and plasma cell disorders (HR, 2.42; 95% CI, 1.08 to 5.41),
20 loid light-chain) amyloidosis is an uncommon plasma cell disorder in which depositions of amyloid lig
21 in patients with multiple myeloma and other plasma cell disorders, including smouldering multiple my
22 is occurs in myeloma, but not in the limited plasma cell disorder monoclonal gammopathy of unknown si
24 esses to multiple myeloma or another related plasma cell disorder (PCD) at a rate of approximately 1%
25 ized by peripheral neuropathy (PN), a clonal plasma cell disorder (PCD), organomegaly, endocrinopathy
26 enotype is associated with the initiation of plasma-cell disorders rather than the progression of MGU
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