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1 ry amyloidosis with a concomitant monoclonal gammopathy.
2 marrow and the presence of an IgM monoclonal gammopathy.
3 racutaneous manifestations, and a monoclonal gammopathy.
4 me (FS) is a rare complication of monoclonal gammopathy.
5 era of individuals with a form of monoclonal gammopathy.
6 ge, 42-80 years) of the IBM patients without gammopathy.
7 ogy in patients who do not have a monoclonal gammopathy.
8 of patients will have persistent monoclonal gammopathy.
9 amate than patients with indolent monoclonal gammopathies.
10 ) cells across the progression of monoclonal gammopathies.
11 implicated in the pathogenesis of monoclonal gammopathies.
12 ed gammopathies and some sporadic monoclonal gammopathies.
13 disease have an increased risk of monoclonal gammopathies.
14 replication in the persistence of monoclonal gammopathy.1 It has been known for some time that patien
16 Further investigation revealed a monoclonal gammopathy, a unique patterning of subcutaneous fat reti
17 rized by urticarial exanthema and monoclonal gammopathy accompanied by systemic symptoms such as feve
18 ) are preceded by an asymptomatic monoclonal gammopathy (AMG), classified as either monoclonal gammop
19 y underlie both Gaucher's disease-associated gammopathies and some sporadic monoclonal gammopathies.
21 alignancy characterized by an IgM monoclonal gammopathy and bone marrow (BM) infiltration with lympho
22 (21%) patients were positive for monoclonal gammopathy and had a faster rate of recurrence and graft
23 ew the causal association between monoclonal gammopathy and neuropathy, and critically review the rec
24 unknown, but in many patients the monoclonal gammopathy and other B-cell abnormalities can be reverse
25 on have an increased incidence of monoclonal gammopathy and plasma cell dyscrasias.2,3 The exact mech
26 a causal relationship between the monoclonal gammopathy and the renal damage and because the signific
27 ambda J lambda rearrangements in lambda-type gammopathies, and that of other Abs to thymus-dependent
28 cterized by an urticarial rash, a monoclonal gammopathy, and clinical, histological, and biological s
29 current urticarial rash and a monoclonal IgM gammopathy, and two of the following minor criteria: rec
35 by recurrent urticarial rash and monoclonal gammopathy, associated with clinical and biological sign
36 stics of human disease, including monoclonal gammopathy, BM infiltration with lytic bone lesions, and
38 2% of age-matched controls, had a monoclonal gammopathy characterized as IgG lambda in 9 patients, Ig
39 (MIDD) is a rare complication of monoclonal gammopathy characterized by deposition of monoclonal Ig
40 ain human sera from patients with monoclonal gammopathies contain factors that induce myelin repair i
42 In conclusion, FS associated with monoclonal gammopathy does not appear to confer an additional risk
43 in 305 patients with asymptomatic monoclonal gammopathy enrolled in S0120 under the auspices of SWOG.
44 ical and laboratory findings with monoclonal gammopathy evaluation and, if indicated, TTR gene testin
45 pheral neuropathy associated with monoclonal gammopathies has been advanced by recent clinical studie
46 t not nonprogressive myeloma or premalignant gammopathy, have a marked deficiency of ligand-dependent
47 iated skeletal destruction, serum monoclonal gammopathy, immune suppression, and end-organ sequelae.
48 tor in child GP patients and with monoclonal gammopathy in adult GP patients, who frequently showed I
51 rasias.2,3 The exact mechanism of monoclonal gammopathy in patients with HIV infection is unknown, bu
53 lification was detected in 67% of monoclonal gammopathies, including monoclonal gammopathy of undeter
54 globulin in 33% of sporadic human monoclonal gammopathies is also specific for the lysolipids LGL1 an
55 ical progression in patients with monoclonal gammopathies is associated with an acquired but potentia
56 l disease, the persistence of the monoclonal gammopathy is associated with high rates of recurrence a
58 mouse models of Gaucher's disease-associated gammopathy is reactive against lyso-glucosylceramide (LG
61 ls compared with the marrow in preneoplastic gammopathy (monoclonal gammopathy of undetermined signif
62 ere we show that patients with preneoplastic gammopathy mount a vigorous T cell response to autologou
63 tudies might seek to identify, with biclonal gammopathy multiple myeloma as an investigative model, t
64 study, we identified patients with biclonal gammopathy multiple myeloma by central laboratory analys
67 results show that, in patients with biclonal gammopathy multiple myeloma, anti-multiple myeloma thera
69 d tumor bed in 23 patients with premalignant gammopathy, nonprogressive myeloma, or progressive multi
70 only 15% of patients, included 21 monoclonal gammopathies of renal significance; 15 multiple myelomas
71 paraprotein target (paratargs) in monoclonal gammopathies of undetermined significance (MGUS), multip
73 tients (29 AL, 23 MM, and 9 MGUS [monoclonal gammopathies of undetermined significance]) were studied
77 as determined in 63 patients with monoclonal gammopathy of uncertain significance (MGUS) and 198 pati
78 s of normal plasma cells (PCs) to monoclonal gammopathy of uncertain significance (MGUS) and multiple
80 bjects representing premalignant (monoclonal gammopathy of uncertain significance), early, and advanc
81 CGH on 25 cases of MM, 4 cases of monoclonal gammopathy of uncertain significance, and 1 case of Wald
82 ent course of disease that mimics monoclonal gammopathy of undermined significance, whereas others ha
83 oma (SMM) bridges the gap between monoclonal gammopathy of undetermined significance (a mostly premal
85 58 patients with WM, 77 with IgM monoclonal gammopathy of undetermined significance (IgM-MGUS), 84 w
86 s from subjects with MM (n = 16), monoclonal gammopathy of undetermined significance (MGUS) (n = 6),
87 somes from multiple myeloma (MM), monoclonal gammopathy of undetermined significance (MGUS) and healt
88 4+ CD25+ T cells in patients with monoclonal gammopathy of undetermined significance (MGUS) and in pa
89 arly pathogenesis of premalignant monoclonal gammopathy of undetermined significance (MGUS) and malig
91 rrow specimens from patients with monoclonal gammopathy of undetermined significance (MGUS) and multi
92 ignant non-immunoglobulin M (IgM) monoclonal gammopathy of undetermined significance (MGUS) and multi
93 ly expressed in plasma cells from monoclonal gammopathy of undetermined significance (MGUS) and multi
94 eceded by the precursor states of monoclonal gammopathy of undetermined significance (MGUS) and smold
95 ant plasma cell dyscrasia such as monoclonal gammopathy of undetermined significance (MGUS) and smold
98 ering of the precursor condition, monoclonal gammopathy of undetermined significance (MGUS) has been
99 lls in the blood of patients with monoclonal gammopathy of undetermined significance (MGUS) has been
100 r et al showed that patients with monoclonal gammopathy of undetermined significance (MGUS) have incr
101 e reported a higher prevalence of monoclonal gammopathy of undetermined significance (MGUS) in Africa
111 Whether this dichotomy exists in monoclonal gammopathy of undetermined significance (MGUS) is uncert
112 The association of obesity with monoclonal gammopathy of undetermined significance (MGUS) is unknow
115 to quantitate adverse outcomes of monoclonal gammopathy of undetermined significance (MGUS) of the im
116 pathy (AMG), classified as either monoclonal gammopathy of undetermined significance (MGUS) or asympt
118 At diagnosis, most patients had monoclonal gammopathy of undetermined significance (MGUS) or smolde
119 eceded by precursor states termed monoclonal gammopathy of undetermined significance (MGUS) or smolde
120 (MM) patients (n = 8740) and 5652 monoclonal gammopathy of undetermined significance (MGUS) patients
121 in 90% of immunoglobulin M (IgM) monoclonal gammopathy of undetermined significance (MGUS) patients.
123 ith AL-amyloidosis secondary to a monoclonal gammopathy of undetermined significance (MGUS) referred
124 ation from immunoglobulin-M (IgM) monoclonal gammopathy of undetermined significance (MGUS) remain un
126 patients is more consistent with monoclonal gammopathy of undetermined significance (MGUS) than with
127 study the risk of progression of monoclonal gammopathy of undetermined significance (MGUS) to lympho
128 y a role in the transformation of monoclonal gammopathy of undetermined significance (MGUS) to MM.
130 s that determine progression from monoclonal gammopathy of undetermined significance (MGUS) to multip
131 hat the clinical progression from monoclonal gammopathy of undetermined significance (MGUS) to multip
132 leading the transformation of the monoclonal gammopathy of undetermined significance (MGUS) to myelom
133 ple myeloma (MM) and premalignant monoclonal gammopathy of undetermined significance (MGUS) tumors: a
134 untreated active myeloma, 14 had monoclonal gammopathy of undetermined significance (MGUS), 10 had d
135 om two out of eight patients with monoclonal gammopathy of undetermined significance (MGUS), a precur
138 detected in 5 of 5 patients with monoclonal gammopathy of undetermined significance (MGUS), an early
139 sed multiple myeloma (MM), 5 with monoclonal gammopathy of undetermined significance (MGUS), and 31 h
140 multiple myeloma, three cases of monoclonal gammopathy of undetermined significance (MGUS), and five
141 da immunoglobulin light chains in monoclonal gammopathy of undetermined significance (MGUS), as detec
142 ones of a subset of patients with monoclonal gammopathy of undetermined significance (MGUS), asymptom
143 ties to multiple myeloma (MM) and monoclonal gammopathy of undetermined significance (MGUS), but its
144 tions have been identified in the monoclonal gammopathy of undetermined significance (MGUS), but thei
146 l clone, referred to as secondary monoclonal gammopathy of undetermined significance (MGUS), have bee
147 Plasma cell dyscrasias, including monoclonal gammopathy of undetermined significance (MGUS), multiple
148 n plasma cells from patients with monoclonal gammopathy of undetermined significance (MGUS), smolderi
149 eloma is consistently preceded by monoclonal gammopathy of undetermined significance (MGUS), which is
150 myeloma to a benign form known as monoclonal gammopathy of undetermined significance (MGUS), which re
159 myeloma and its precursor state, monoclonal gammopathy of undetermined significance (MGUS); however,
160 than 500 untreated patients with monoclonal gammopathy of undetermined significance (MGUS; n = 14),
161 s relatively common and occurs in monoclonal gammopathy of undetermined significance (MGUS; n=17), sm
162 l [CI], 1.31-17.86; P = .018) and monoclonal gammopathy of undetermined significance (OR, 5.94; 95% C
164 ls (B cells, normal plasma cells, monoclonal gammopathy of undetermined significance [MGUS], presenta
166 ypic profiles between AL and both monoclonal gammopathy of undetermined significance and MM PCs.
167 te potential (CHIP), analogous to monoclonal gammopathy of undetermined significance and monoclonal B
168 one marrow involvement similar to monoclonal gammopathy of undetermined significance at diagnosis, th
170 healthy donors and patients with monoclonal gammopathy of undetermined significance or other plasma
171 ment cells in transformation from monoclonal gammopathy of undetermined significance or smoldering mu
172 rum adiponectin concentrations in monoclonal gammopathy of undetermined significance patients who sub
175 Plasma cells in 10 patients with monoclonal gammopathy of undetermined significance were not stained
176 s can help identify patients with monoclonal gammopathy of undetermined significance who are developi
177 characteristics that evolves from monoclonal gammopathy of undetermined significance, a highly preval
178 S from neuropathy associated with monoclonal gammopathy of undetermined significance, additional crit
179 in amyloidosis, multiple myeloma, monoclonal gammopathy of undetermined significance, and non-parapro
180 n from the non-malignant disorder monoclonal gammopathy of undetermined significance, are poorly unde
181 amyloidosis, multiple myeloma and monoclonal gammopathy of undetermined significance, immunoreactive
182 reexisting plasma cell disorders, monoclonal gammopathy of undetermined significance, or smoldering m
183 plasma cells from healthy donors, monoclonal gammopathy of undetermined significance, smoldering MM,
184 f paraproteinemia in a setting of monoclonal gammopathy of undetermined significance, smoldering plas
185 tients with IgG/IgA (but not IgM) monoclonal gammopathy of undetermined significance, supporting a ro
191 tion of SOCS1 and SYK; (5) MM and monoclonal gammopathy of unknown significance (MGUS) had infrequent
192 ients with MM, chronic leukemias, monoclonal gammopathy of unknown significance (MGUS), PBC, and heal
193 Although the high prevalence of a monoclonal gammopathy of unknown significance in SCLS suggests a pa
194 the limited plasma cell disorder monoclonal gammopathy of unknown significance or in nonmyeloma hema
195 patients with multiple myeloma or monoclonal gammopathy of unknown significance sequentially underwen
196 5 with smoldering MM, and 4 with monoclonal gammopathy of unknown significance) and 20 individuals w
200 s through a premalignant state of monoclonal gammopathy of unknown significance; however, the molecul
201 onstellation of lambda-restricted monoclonal gammopathy, plasma cell rimming around lymphoid aggregat
204 xenografts from patients with preneoplastic gammopathy showed progressive growth, suggesting that th
205 tiple myeloma (MM) are 2 distinct monoclonal gammopathies that involve the same cellular compartment:
206 RS) was introduced to distinguish monoclonal gammopathies that result in the development of kidney di
207 s, a form of renal involvement by monoclonal gammopathy that mimics immune-complex glomerulonephritis
208 iple myeloma is the most frequent monoclonal gammopathy to involve the kidney; however, a growing num
209 ge renal disease and known benign monoclonal gammopathy underwent kidney transplantation at Westchest
210 nt somatic mutation in benign monoclonal IgM gammopathy, Waldenstrom's macroglobulinemia, and diffuse
213 ge, is frequently associated with monoclonal gammopathies, which often recognize various muscle compo
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