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1 s a rare disorder associated with monoclonal gammopathy.
2 ry amyloidosis with a concomitant monoclonal gammopathy.
3 marrow and the presence of an IgM monoclonal gammopathy.
4 racutaneous manifestations, and a monoclonal gammopathy.
5 me (FS) is a rare complication of monoclonal gammopathy.
6 era of individuals with a form of monoclonal gammopathy.
7 ge, 42-80 years) of the IBM patients without gammopathy.
8 ogy in patients who do not have a monoclonal gammopathy.
9  of patients will have persistent monoclonal gammopathy.
10 al reorganization of AL and other monoclonal gammopathies.
11 amate than patients with indolent monoclonal gammopathies.
12 ) cells across the progression of monoclonal gammopathies.
13 implicated in the pathogenesis of monoclonal gammopathies.
14 ed gammopathies and some sporadic monoclonal gammopathies.
15 disease have an increased risk of monoclonal gammopathies.
16 replication in the persistence of monoclonal gammopathy.1 It has been known for some time that patien
17 nts (91.9%) with monoclonal immunoglobulin G gammopathy, 20 (58.8%) had kappa light chains.
18  multiple myeloma (8% vs. 0), and monoclonal gammopathy (22% vs. 16%).
19 ropoietin and erythrocytosis; (3) monoclonal gammopathy; (4) perinephric fluid collections; and (5) i
20  Further investigation revealed a monoclonal gammopathy, a unique patterning of subcutaneous fat reti
21 rized by urticarial exanthema and monoclonal gammopathy accompanied by systemic symptoms such as feve
22 ) are preceded by an asymptomatic monoclonal gammopathy (AMG), classified as either monoclonal gammop
23 y underlie both Gaucher's disease-associated gammopathies and some sporadic monoclonal gammopathies.
24  symptomatic patients) had both a monoclonal gammopathy and a hereditary variant.
25 alignancy characterized by an IgM monoclonal gammopathy and bone marrow (BM) infiltration with lympho
26 e always preceded by a detectable monoclonal gammopathy and by elevated biomarkers of organ involveme
27  (21%) patients were positive for monoclonal gammopathy and had a faster rate of recurrence and graft
28 ew the causal association between monoclonal gammopathy and neuropathy, and critically review the rec
29 unknown, but in many patients the monoclonal gammopathy and other B-cell abnormalities can be reverse
30 on have an increased incidence of monoclonal gammopathy and plasma cell dyscrasias.2,3 The exact mech
31 a causal relationship between the monoclonal gammopathy and the renal damage and because the signific
32 ambda J lambda rearrangements in lambda-type gammopathies, and that of other Abs to thymus-dependent
33 ogic workup revealed an IgG kappa monoclonal gammopathy, and bone marrow biopsy confirmed smoldering
34 cterized by an urticarial rash, a monoclonal gammopathy, and clinical, histological, and biological s
35  with C3G had GN unrelated to the monoclonal gammopathy, and one with PGNMID did not complete the fir
36 hy, organomegaly, endocrinopathy, monoclonal gammopathy, and skin changes (POEMS) syndrome is a rare
37 current urticarial rash and a monoclonal IgM gammopathy, and two of the following minor criteria: rec
38 ey diseases associated with other monoclonal gammopathies are being recognized.
39                                   Monoclonal gammopathies are frequently complicated by kidney lesion
40                   The IgG and IgA monoclonal gammopathies are rarely associated with specific neuropa
41                               IgD monoclonal gammopathies are uncommon.
42 (MGUS) is the most commonly found monoclonal gammopathy associated with neuropathy.
43  by recurrent urticarial rash and monoclonal gammopathy, associated with clinical and biological sign
44                 Clarkson disease [monoclonal gammopathy-associated idiopathic systemic capillary leak
45              Clarkson disease, or monoclonal gammopathy-associated idiopathic systemic capillary leak
46 ofluorescence in the diagnosis of monoclonal gammopathy-associated kidney diseases.
47 sis with precision therapy in the monoclonal gammopathy-associated kidney disorders.
48 group of patients with ISCLS have monoclonal gammopathy-associated SCLS (also known as Clarkson disea
49 rgan involvement in patients with monoclonal gammopathies at higher risk to develop the disease.
50 stics of human disease, including monoclonal gammopathy, BM infiltration with lytic bone lesions, and
51                  In patients with monoclonal gammopathies, C-reactive protein may be a more specific
52 2% of age-matched controls, had a monoclonal gammopathy characterized as IgG lambda in 9 patients, Ig
53  (MIDD) is a rare complication of monoclonal gammopathy characterized by deposition of monoclonal Ig
54 ain human sera from patients with monoclonal gammopathies contain factors that induce myelin repair i
55 t results led us to consider that monoclonal gammopathy could be the cause of this entity.
56              In patients with monoclonal IgG gammopathies, diagnosis is definite if three minor crite
57 ion in the immunoglobulin M (IgM) monoclonal gammopathy disease spectrum remains poorly understood.
58 In conclusion, FS associated with monoclonal gammopathy does not appear to confer an additional risk
59 in 305 patients with asymptomatic monoclonal gammopathy enrolled in S0120 under the auspices of SWOG.
60 ical and laboratory findings with monoclonal gammopathy evaluation and, if indicated, TTR gene testin
61 an screen subjects who have known monoclonal gammopathy for amyloid organ dysfunction and damage, all
62 pheral neuropathy associated with monoclonal gammopathies has been advanced by recent clinical studie
63 t not nonprogressive myeloma or premalignant gammopathy, have a marked deficiency of ligand-dependent
64 iated skeletal destruction, serum monoclonal gammopathy, immune suppression, and end-organ sequelae.
65  Ophthalmologists should consider monoclonal gammopathies in unexplained bilateral interstitial kerat
66 emia/small lymphocytic lymphoma), monoclonal gammopathy in 20%, and multiple myeloma in 6%.
67 tor in child GP patients and with monoclonal gammopathy in adult GP patients, who frequently showed I
68             The high frequency of monoclonal gammopathy in adult patients with C3 glomerulopathy (C3G
69 ion ameliorates Gaucher's disease-associated gammopathy in mice.
70 rasias.2,3 The exact mechanism of monoclonal gammopathy in patients with HIV infection is unknown, bu
71                                   Monoclonal gammopathy in several patients may have potential clinic
72 lification was detected in 67% of monoclonal gammopathies, including monoclonal gammopathy of undeter
73 globulin in 33% of sporadic human monoclonal gammopathies is also specific for the lysolipids LGL1 an
74 ical progression in patients with monoclonal gammopathies is associated with an acquired but potentia
75 l disease, the persistence of the monoclonal gammopathy is associated with high rates of recurrence a
76 d because the significance of the monoclonal gammopathy is no longer undetermined.
77 mouse models of Gaucher's disease-associated gammopathy is reactive against lyso-glucosylceramide (LG
78 ears before diagnosis to detect a monoclonal gammopathy (M-Ig).
79        All patients had serum monoclonal IgM gammopathy (median, 2.6 g/L; range, 0.1-40 g/L).
80 ing and serum electrophoresis for monoclonal gammopathy (MG or M-protein).
81 on, the presence of non-malignant monoclonal gammopathy (MG) can be causally associated with kidney d
82              A high prevalence of monoclonal gammopathy (MG) has been observed in HIV-infected patien
83  predictors of finding lesions of monoclonal gammopathy (MG) of renal significance (MGRS) on kidney b
84 s that is usually associated with monoclonal gammopathy (MG).
85  with chronic kidney disease with monoclonal gammopathy (MG).
86     Detection of light chain (LC) monoclonal gammopathies (MGs) traditionally relies on serum free LC
87 ls compared with the marrow in preneoplastic gammopathy (monoclonal gammopathy of undetermined signif
88 ere we show that patients with preneoplastic gammopathy mount a vigorous T cell response to autologou
89 tudies might seek to identify, with biclonal gammopathy multiple myeloma as an investigative model, t
90  study, we identified patients with biclonal gammopathy multiple myeloma by central laboratory analys
91                                     Biclonal gammopathy multiple myeloma is characterised by the coex
92                    44 patients with biclonal gammopathy multiple myeloma with IgG or IgA MGUS clones
93 results show that, in patients with biclonal gammopathy multiple myeloma, anti-multiple myeloma thera
94 py in patients newly diagnosed with biclonal gammopathy multiple myeloma.
95 d tumor bed in 23 patients with premalignant gammopathy, nonprogressive myeloma, or progressive multi
96 only 15% of patients, included 21 monoclonal gammopathies of renal significance; 15 multiple myelomas
97 bone marrow trephine samples from monoclonal gammopathies of undetermined significance (MGUS) and fro
98 paraprotein target (paratargs) in monoclonal gammopathies of undetermined significance (MGUS), multip
99 n can be identified as in myeloma/monoclonal gammopathies of undetermined significance (MGUS).
100 tients (29 AL, 23 MM, and 9 MGUS [monoclonal gammopathies of undetermined significance]) were studied
101 light-chain (AL) amyloidosis, and monoclonal gammopathy of clinical significance (MGCS), all of which
102      It focuses on the concept of monoclonal gammopathy of clinical significance, which can have a la
103 OMAD to be included in neurologic monoclonal gammopathy of clinical significance.
104   M-protein concentrations at the monoclonal gammopathy of indeterminate potential (MGIP) level were
105          Given the propensity for monoclonal gammopathy of macular significance to transform into mal
106 tive disorder that we have termed monoclonal gammopathy of macular significance.
107 und in 89% of patients, including monoclonal gammopathy of renal significance (65%) and symptomatic l
108                                   Monoclonal gammopathy of renal significance (MGRS) defines disorder
109                                   Monoclonal gammopathy of renal significance (MGRS) is increasingly
110                          The term monoclonal gammopathy of renal significance (MGRS) was introduced b
111                Recently, the term monoclonal gammopathy of renal significance (MGRS) was introduced t
112       Hematological diagnosis was monoclonal gammopathy of renal significance in 30 (60%), multiple m
113       Hematological diagnosis was monoclonal gammopathy of renal significance in 64% and symptomatic
114                 We think the term monoclonal gammopathy of renal significance is most helpful to indi
115 bone marrow biopsy which revealed Monoclonal Gammopathy of renal significance, triggering a HUS and t
116 as determined in 63 patients with monoclonal gammopathy of uncertain significance (MGUS) and 198 pati
117 s of normal plasma cells (PCs) to monoclonal gammopathy of uncertain significance (MGUS) and multiple
118  human controls and patients with monoclonal gammopathy of uncertain significance expressed higher le
119         Aberrant demethylation in monoclonal gammopathy of uncertain significance occurred primarily
120 bjects representing premalignant (monoclonal gammopathy of uncertain significance), early, and advanc
121 CGH on 25 cases of MM, 4 cases of monoclonal gammopathy of uncertain significance, and 1 case of Wald
122 cal study in a person with advanced ALS, IgA gammopathy of unclear significance, and B lymphopenia, C
123 ent course of disease that mimics monoclonal gammopathy of undermined significance, whereas others ha
124 oma (SMM) bridges the gap between monoclonal gammopathy of undetermined significance (a mostly premal
125  with WM and 10 patients with IgM monoclonal gammopathy of undetermined significance (IgM MGUS).
126            Immunoglobulin M (IgM) monoclonal gammopathy of undetermined significance (IgM-MGUS) and a
127  58 patients with WM, 77 with IgM monoclonal gammopathy of undetermined significance (IgM-MGUS), 84 w
128 othelial cells from patients with monoclonal gammopathy of undetermined significance (MGECs) and endo
129 s from subjects with MM (n = 16), monoclonal gammopathy of undetermined significance (MGUS) (n = 6),
130 somes from multiple myeloma (MM), monoclonal gammopathy of undetermined significance (MGUS) and healt
131 4+ CD25+ T cells in patients with monoclonal gammopathy of undetermined significance (MGUS) and in pa
132 arly pathogenesis of premalignant monoclonal gammopathy of undetermined significance (MGUS) and malig
133                                   Monoclonal gammopathy of undetermined significance (MGUS) and multi
134 rrow specimens from patients with monoclonal gammopathy of undetermined significance (MGUS) and multi
135 ignant non-immunoglobulin M (IgM) monoclonal gammopathy of undetermined significance (MGUS) and multi
136 ly expressed in plasma cells from monoclonal gammopathy of undetermined significance (MGUS) and multi
137 eceded by the precursor states of monoclonal gammopathy of undetermined significance (MGUS) and smold
138                                   Monoclonal gammopathy of undetermined significance (MGUS) and smold
139  (MM) is consistently preceded by monoclonal gammopathy of undetermined significance (MGUS) and smold
140 ant plasma cell dyscrasia such as monoclonal gammopathy of undetermined significance (MGUS) and smold
141                     Patients with monoclonal gammopathy of undetermined significance (MGUS) are at in
142                                   Monoclonal gammopathy of undetermined significance (MGUS) can progr
143 ering of the precursor condition, monoclonal gammopathy of undetermined significance (MGUS) has been
144 lls in the blood of patients with monoclonal gammopathy of undetermined significance (MGUS) has been
145 r et al showed that patients with monoclonal gammopathy of undetermined significance (MGUS) have incr
146 e reported a higher prevalence of monoclonal gammopathy of undetermined significance (MGUS) in Africa
147                                   Monoclonal gammopathy of undetermined significance (MGUS) is a comm
148                                   Monoclonal gammopathy of undetermined significance (MGUS) is a plas
149                                   Monoclonal gammopathy of undetermined significance (MGUS) is a prec
150                                   Monoclonal gammopathy of undetermined significance (MGUS) is a prem
151                                   Monoclonal gammopathy of undetermined significance (MGUS) is a prem
152                                   Monoclonal gammopathy of undetermined significance (MGUS) is an asy
153                                   Monoclonal gammopathy of undetermined significance (MGUS) is an asy
154                                   Monoclonal gammopathy of undetermined significance (MGUS) is an asy
155                                   Monoclonal gammopathy of undetermined significance (MGUS) is associ
156                                   Monoclonal gammopathy of undetermined significance (MGUS) is associ
157                                   Monoclonal gammopathy of undetermined significance (MGUS) is define
158               We examined whether monoclonal gammopathy of undetermined significance (MGUS) is increa
159                                   Monoclonal gammopathy of undetermined significance (MGUS) is presen
160                               IgM monoclonal gammopathy of undetermined significance (MGUS) is the mo
161  Whether this dichotomy exists in monoclonal gammopathy of undetermined significance (MGUS) is uncert
162   The association of obesity with monoclonal gammopathy of undetermined significance (MGUS) is unknow
163                                   Monoclonal gammopathy of undetermined significance (MGUS) is, in ma
164                                 A monoclonal gammopathy of undetermined significance (MGUS) occurs in
165 to quantitate adverse outcomes of monoclonal gammopathy of undetermined significance (MGUS) of the im
166 pathy (AMG), classified as either monoclonal gammopathy of undetermined significance (MGUS) or asympt
167                            Unlike monoclonal gammopathy of undetermined significance (MGUS) or non-Ho
168   At diagnosis, most patients had monoclonal gammopathy of undetermined significance (MGUS) or smolde
169 nditions recognized clinically as monoclonal gammopathy of undetermined significance (MGUS) or smolde
170 eceded by precursor states termed monoclonal gammopathy of undetermined significance (MGUS) or smolde
171 (MM) patients (n = 8740) and 5652 monoclonal gammopathy of undetermined significance (MGUS) patients
172  in 90% of immunoglobulin M (IgM) monoclonal gammopathy of undetermined significance (MGUS) patients.
173                  Hypercalcemia in monoclonal gammopathy of undetermined significance (MGUS) presents
174                                   Monoclonal gammopathy of undetermined significance (MGUS) progresse
175 ith AL-amyloidosis secondary to a monoclonal gammopathy of undetermined significance (MGUS) referred
176 ation from immunoglobulin-M (IgM) monoclonal gammopathy of undetermined significance (MGUS) remain un
177                                   Monoclonal gammopathy of undetermined significance (MGUS) represent
178  patients is more consistent with monoclonal gammopathy of undetermined significance (MGUS) than with
179  study the risk of progression of monoclonal gammopathy of undetermined significance (MGUS) to lympho
180 y a role in the transformation of monoclonal gammopathy of undetermined significance (MGUS) to MM.
181           The transformation from monoclonal gammopathy of undetermined significance (MGUS) to multip
182 cogenic drivers of progression of monoclonal gammopathy of undetermined significance (MGUS) to multip
183 s that determine progression from monoclonal gammopathy of undetermined significance (MGUS) to multip
184 dering multiple myeloma (SMM) and monoclonal gammopathy of undetermined significance (MGUS) to multip
185 hat the clinical progression from monoclonal gammopathy of undetermined significance (MGUS) to multip
186 leading the transformation of the monoclonal gammopathy of undetermined significance (MGUS) to myelom
187 ple myeloma (MM) and premalignant monoclonal gammopathy of undetermined significance (MGUS) tumors: a
188 ate the outcomes of patients with monoclonal gammopathy of undetermined significance (MGUS) with COVI
189  untreated active myeloma, 14 had monoclonal gammopathy of undetermined significance (MGUS), 10 had d
190                                   Monoclonal gammopathy of undetermined significance (MGUS), a precur
191 om two out of eight patients with monoclonal gammopathy of undetermined significance (MGUS), a precur
192 re suggested to jointly influence monoclonal gammopathy of undetermined significance (MGUS), a precur
193                 The prevalence of monoclonal gammopathy of undetermined significance (MGUS), a premal
194  detected in 5 of 5 patients with monoclonal gammopathy of undetermined significance (MGUS), an early
195 sed multiple myeloma (MM), 5 with monoclonal gammopathy of undetermined significance (MGUS), and 31 h
196  multiple myeloma, three cases of monoclonal gammopathy of undetermined significance (MGUS), and five
197 da immunoglobulin light chains in monoclonal gammopathy of undetermined significance (MGUS), as detec
198 ones of a subset of patients with monoclonal gammopathy of undetermined significance (MGUS), asymptom
199 ties to multiple myeloma (MM) and monoclonal gammopathy of undetermined significance (MGUS), but its
200 tions have been identified in the monoclonal gammopathy of undetermined significance (MGUS), but thei
201           In 728 Swedish cases of monoclonal gammopathy of undetermined significance (MGUS), followed
202 l clone, referred to as secondary monoclonal gammopathy of undetermined significance (MGUS), have bee
203 Plasma cell dyscrasias, including monoclonal gammopathy of undetermined significance (MGUS), multiple
204 n plasma cells from patients with monoclonal gammopathy of undetermined significance (MGUS), smolderi
205 eloma is consistently preceded by monoclonal gammopathy of undetermined significance (MGUS), which is
206 myeloma to a benign form known as monoclonal gammopathy of undetermined significance (MGUS), which re
207 e an increased fracture risk with monoclonal gammopathy of undetermined significance (MGUS).
208  from a premalignant stage called monoclonal gammopathy of undetermined significance (MGUS).
209 applicators to assess the risk of monoclonal gammopathy of undetermined significance (MGUS).
210 logy of multiple myeloma (MM) and monoclonal gammopathy of undetermined significance (MGUS).
211 onoclonal gammopathies, including monoclonal gammopathy of undetermined significance (MGUS).
212 m a common benign PC tumor called Monoclonal Gammopathy of Undetermined Significance (MGUS).
213 le myeloma (MM) and its precursor monoclonal gammopathy of undetermined significance (MGUS).
214 ded by an asymptomatic condition, monoclonal gammopathy of undetermined significance (MGUS).
215 a premalignant condition known as monoclonal gammopathy of undetermined significance (MGUS).
216  preceded by the precursor state, monoclonal gammopathy of undetermined significance (MGUS).
217  myeloma and its precursor state, monoclonal gammopathy of undetermined significance (MGUS); however,
218  than 500 untreated patients with monoclonal gammopathy of undetermined significance (MGUS; n = 14),
219 s relatively common and occurs in monoclonal gammopathy of undetermined significance (MGUS; n=17), sm
220 l [CI], 1.31-17.86; P = .018) and monoclonal gammopathy of undetermined significance (OR, 5.94; 95% C
221 rrow in preneoplastic gammopathy (monoclonal gammopathy of undetermined significance [MGUS]).
222 acroglobulinemia [WM], 6 with IgM monoclonal gammopathy of undetermined significance [MGUS], and 5 no
223 ls (B cells, normal plasma cells, monoclonal gammopathy of undetermined significance [MGUS], presenta
224         They are seen rarely as a monoclonal gammopathy of undetermined significance and are present
225 ypic profiles between AL and both monoclonal gammopathy of undetermined significance and MM PCs.
226 te potential (CHIP), analogous to monoclonal gammopathy of undetermined significance and monoclonal B
227 luding asymptomatic states called monoclonal gammopathy of undetermined significance and smoldering m
228 precursor states of MM, including monoclonal gammopathy of undetermined significance and smoldering M
229 m precursor conditions, including monoclonal gammopathy of undetermined significance and smoldering m
230 oreover, analyses of samples from monoclonal gammopathy of undetermined significance and smouldering
231         Our goal was to develop a monoclonal gammopathy of undetermined significance and smouldering
232 one marrow involvement similar to monoclonal gammopathy of undetermined significance at diagnosis, th
233 criteria were newly diagnosed MM, monoclonal gammopathy of undetermined significance at high risk for
234         SMM is distinguished from monoclonal gammopathy of undetermined significance by a much higher
235                                   Monoclonal gammopathy of undetermined significance isotype; monoclo
236  healthy donors and patients with monoclonal gammopathy of undetermined significance or other plasma
237 ment cells in transformation from monoclonal gammopathy of undetermined significance or smoldering mu
238 s who were 18 years or older with monoclonal gammopathy of undetermined significance or smouldering m
239 matic precursor conditions-either monoclonal gammopathy of undetermined significance or smouldering m
240 rum adiponectin concentrations in monoclonal gammopathy of undetermined significance patients who sub
241 terials and Methods Patients with monoclonal gammopathy of undetermined significance prospectively un
242 nt disease stages, from 23.66% in monoclonal gammopathy of undetermined significance to 3.23% in MMs
243 d model of genetic evolution from monoclonal gammopathy of undetermined significance to MM.
244 n that parallels progression from monoclonal gammopathy of undetermined significance to MM.
245                      An IgG kappa monoclonal gammopathy of undetermined significance was found.
246  Plasma cells in 10 patients with monoclonal gammopathy of undetermined significance were not stained
247 s can help identify patients with monoclonal gammopathy of undetermined significance who are developi
248 y be the presenting feature); and monoclonal gammopathy of undetermined significance with atypical cl
249 characteristics that evolves from monoclonal gammopathy of undetermined significance, a highly preval
250 S from neuropathy associated with monoclonal gammopathy of undetermined significance, additional crit
251 in amyloidosis, multiple myeloma, monoclonal gammopathy of undetermined significance, and non-parapro
252  Monoclonal B-cell lymphocytosis, monoclonal gammopathy of undetermined significance, and T-cell clon
253 n from the non-malignant disorder monoclonal gammopathy of undetermined significance, are poorly unde
254 amyloidosis, multiple myeloma and monoclonal gammopathy of undetermined significance, immunoreactive
255 reexisting plasma cell disorders, monoclonal gammopathy of undetermined significance, or smoldering m
256 plasma cells from healthy donors, monoclonal gammopathy of undetermined significance, smoldering MM,
257 f paraproteinemia in a setting of monoclonal gammopathy of undetermined significance, smoldering plas
258 on to delineate the complexity of monoclonal gammopathy of undetermined significance, smouldering MM
259 in both multiple myeloma (MM) and monoclonal gammopathy of undetermined significance, suggesting that
260 tients with IgG/IgA (but not IgM) monoclonal gammopathy of undetermined significance, supporting a ro
261 MM, whereas nonprogressor SMM has monoclonal gammopathy of undetermined significance-like characteris
262  myeloproliferative disorder, and monoclonal gammopathy of undetermined significance.
263 ive premalignant condition termed monoclonal gammopathy of undetermined significance.
264 eloma cells, even in asymptomatic monoclonal gammopathy of undetermined significance.
265 ave shown limited efficacy in IgM monoclonal gammopathy of undetermined significance.
266 rease in MM cell proliferation in monoclonal gammopathy of undetermined significance/smoldering MM co
267                                   Monoclonal gammopathy of unknown significance (MGUS) and smoldering
268 tion of SOCS1 and SYK; (5) MM and monoclonal gammopathy of unknown significance (MGUS) had infrequent
269 ients with MM, chronic leukemias, monoclonal gammopathy of unknown significance (MGUS), PBC, and heal
270 the precursor malignant condition monoclonal gammopathy of unknown significance (MGUS).
271 e myeloma (MM) and its precursor, monoclonal gammopathy of unknown significance (MGUS).
272 Although the high prevalence of a monoclonal gammopathy of unknown significance in SCLS suggests a pa
273  the limited plasma cell disorder monoclonal gammopathy of unknown significance or in nonmyeloma hema
274 patients with multiple myeloma or monoclonal gammopathy of unknown significance sequentially underwen
275  5 with smoldering MM, and 4 with monoclonal gammopathy of unknown significance) and 20 individuals w
276 a, marginal-zone lymphoma, or IgM monoclonal gammopathy of unknown significance.
277  T-cell populations, analogous to monoclonal gammopathy of unknown significance.
278 that the patient had unrecognized monoclonal gammopathy of unknown significance.
279 s with indolent smoldering MM and monoclonal gammopathy of unknown significance.
280 s through a premalignant state of monoclonal gammopathy of unknown significance; however, the molecul
281 ere at high risk for developing a monoclonal gammopathy on the basis of Black race or a family histor
282 onstellation of lambda-restricted monoclonal gammopathy, plasma cell rimming around lymphoid aggregat
283                                   Polyclonal gammopathy pretransplant is common with 17% of all patie
284        Paraproteinemia relates to monoclonal gammopathy-producing pathologic antibodies with serous m
285 unexpected low rate of detectable monoclonal gammopathy, questioning the reality of an underlying clo
286 mmune GN, autoinflammatory GN and monoclonal gammopathy-related GN.
287 d by the International Kidney and Monoclonal Gammopathy Research Group (IKMG) in 2012.
288  xenografts from patients with preneoplastic gammopathy showed progressive growth, suggesting that th
289 Its differentiation from other IgM-producing gammopathies such as Waldenstrom macroglobulinemia (WM)
290 tiple myeloma (MM) are 2 distinct monoclonal gammopathies that involve the same cellular compartment:
291 RS) was introduced to distinguish monoclonal gammopathies that result in the development of kidney di
292 s, a form of renal involvement by monoclonal gammopathy that mimics immune-complex glomerulonephritis
293 iple myeloma is the most frequent monoclonal gammopathy to involve the kidney; however, a growing num
294 ge renal disease and known benign monoclonal gammopathy underwent kidney transplantation at Westchest
295 nt somatic mutation in benign monoclonal IgM gammopathy, Waldenstrom's macroglobulinemia, and diffuse
296            The mean age of IBM patients with gammopathy was 60.6 years (range, 35-77 years), compared
297                                   Monoclonal gammopathy was of IgG type in 47 (94%) patients.
298                               All monoclonal gammopathies were associated with an increased likelihoo
299 ge, is frequently associated with monoclonal gammopathies, which often recognize various muscle compo
300  focused on defining differences between IgM gammopathies (WM/IgM-MGUS) compared with controls, and s

 
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