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1 Castleman disease (CD) describes a group of at least 4 d
2 Castleman disease (CD) in the context of human immunodef
3 Castleman disease (CD) is a lymphoproliferative disorder
4 Castleman disease (CD) is a rare hematologic disorder ch
5 Castleman disease (CD), a heterogeneous group of disorde
6 Castleman disease can occur in association with autoimmu
7 Castleman disease was initially described over 50 years
8 Castleman disease, an unusual condition of unknown cause
9 Castleman's Awareness & Research Effort/Castleman Diseas
10 Castleman's disease is a rare primary disease of the lym
14 less commonly primary effusion lymphoma and Castleman's disease; these neoplastic diseases are repor
17 si's sarcoma, primary effusion lymphoma, and Castleman's disease are the major malignancies associate
18 si's sarcoma, primary effusion lymphoma, and Castleman's disease, encodes several pathogenically impo
23 herapies successful in the treatment of both Castleman disease and associated autoimmune disease.
26 ganomegaly, potentially including coexisting Castleman disease, endocrinopathy, monoclonal plasma cel
27 tic pemphigus (including 10 with concomitant Castleman's disease) nor from 19 patients with pemphigus
28 Inclusion criteria were pathology-confirmed Castleman's disease in multiple nodes and minimum clinic
29 nd at least 1 of the other 3 major criteria (Castleman disease, sclerotic bone lesions, or elevated V
35 ng of pathogenic cell types and cytokines in Castleman disease have allowed the development of target
36 from January, 1995, with keywords including "Castleman's disease" and "giant lymph node hyperplasia".
37 ) are associated with Kaposi's sarcoma (KS), Castleman's disease, and body cavity-based lymphomas (BC
38 V-8) and its etiologic associations with KS, Castleman's disease, and primary effusion lymphomas.
39 ional criteria were included: a bone lesion, Castleman disease, organomegaly (or lymphadenopathy), en
52 gent of Kaposi sarcoma (KS) and multicentric Castleman disease (MCD), a life-threatening, virally ind
59 ry effusion lymphoma (PEL), and multicentric Castleman disease, encodes four interferon regulatory fa
66 phoma (PEL) cell lines, PEL and multicentric Castleman's disease (MCD) tumors, Kaposi's sarcoma lesio
67 ry effusion lymphoma (PEL), and multicentric Castleman's disease (MCD), all of which are viewed as cy
68 ry effusion lymphoma (PEL), and multicentric Castleman's disease (MCD), in addition to an MCD-related
69 iated Kaposi's sarcoma, PEL and multicentric Castleman's disease (MCD), in addition to proinflammator
70 ry effusion lymphoma (PEL), and multicentric Castleman's disease (MCD), three diseases that frequentl
80 ry effusion lymphoma (PEL), and multicentric Castleman's disease through autocrine or paracrine mecha
81 lopment of Kaposi's sarcoma and multicentric Castleman's disease, as well as a rare form of B cell ly
82 h primary effusion lymphoma and multicentric Castleman's disease, as well as its namesake Kaposi's sa
116 primary effusion lymphoma, and multicentric Castleman's disease; in all of these diseases, interleuk
117 ated with both malignancies and multicentric Castleman's disease; the latter is a rare angiolymphopro
119 ful treatment of HIV-associated multicentric Castleman disease (HIV+MCD) with rituximab-based approac
122 oma (KS) herpesvirus-associated multicentric Castleman disease (KSHV-MCD) is a lymphoproliferative di
123 a herpesvirus (KSHV)-associated multicentric Castleman disease (KSHV-MCD) is characterized by severe
124 recognition of KSHV-associated multicentric Castleman disease (MCD) as a distinct lymphoproliferativ
125 a herpesvirus (KSHV)-associated multicentric Castleman disease (MCD) is a lymphoproliferative disorde
126 a herpesvirus (KSHV)-associated multicentric Castleman disease (MCD) is a lymphoproliferative inflamm
127 a herpesvirus (KSHV)-associated multicentric Castleman disease (MCD) is a polyclonal B-cell lymphopro
129 lymphoma (PEL), KSHV-associated multicentric Castleman disease (MCD), and KS inflammatory cytokine sy
130 itary (EC) PEL, KSHV-associated multicentric Castleman disease (MCD), KSHV+ diffuse large B-cell lymp
133 aposi sarcoma, HHV-8-associated multicentric Castleman disease with microlymphomas and a severe hemop
134 on lymphoma and KSHV-associated multicentric Castleman disease, which are B-cell lymphoproliferative
139 ted in KSHV-positive cells from multicentric Castleman's disease (MCD) and Kaposi's sarcoma (KS) lesi
145 clinical subtype of idiopathic multicentric Castleman disease (iMCD), consists of a constellation of
146 t-line treatment for idiopathic multicentric Castleman disease on the basis of durable efficacy and s
148 of 128 patients with idiopathic multicentric Castleman's disease had a diagnosis of a separate malign
149 -line treatments for idiopathic multicentric Castleman's disease included corticosteroids (47/128 [37
150 Clinical features of idiopathic multicentric Castleman's disease included multicentric lymphadenopath
151 128 patients with idiopathic multicentric Castleman's disease met all inclusion criteria for the s
152 ed information about idiopathic multicentric Castleman's disease represents a major challenge for cli
153 or 127 patients with idiopathic multicentric Castleman's disease were presented from clinical trials,
154 ent, and outcomes of idiopathic multicentric Castleman's disease, which accounts for at least 33% of
158 (UCD) or the dominant focus in multicentric Castleman's disease (MCD), nature of the surgical approa
159 ted with human herpesvirus-8 in multicentric Castleman's disease support lytic replication, so that c
160 K1 was readily detected in multicentric Castleman's disease tissues, whereas it was not detected
164 ncluding Kaposi's sarcoma (KS), multicentric Castleman's disease (MCD), and primary effusion lymphoma
165 inked to Kaposi's sarcoma (KS), multicentric Castleman's disease (MCD), and primary effusion lymphoma
166 found in Kaposi's sarcoma (KS), multicentric Castleman's disease, and primary effusion lymphomas.
167 vestigated in patients with KS, multicentric Castleman disease (MCD), and primary effusion lymphoma.
168 rus (HIV)-infected men with KS, multicentric Castleman disease, or primary effusion lymphoma and 8 HI
170 oma, primary effusion lymphoma, multicentric Castleman's disease, and KSHV inflammatory cytokine synd
172 nt of three human malignancies: multicentric Castleman's disease, primary effusion lymphoma, and Kapo
173 3%) patients with HHV8-negative multicentric Castleman's disease from 1923 cases of multicentric Cast
174 The cause of HHV8-negative multicentric Castleman's disease is idiopathic; such cases are called
175 plasia to monoclonal neoplasia: multicentric Castleman's disease (CD), Kaposi's sarcoma (KS), and pri
176 reported as a heralding sign of multicentric Castleman disease (MCD) and other lymphoproliferative di
179 on lymphoma (PEL) and a form of multicentric Castleman's disease (MCD) are both caused by Kaposi sarc
183 (KS), the plasmablastic form of multicentric Castleman's disease, and primary effusion lymphoma.
184 (KS), the plasmablastic form of multicentric Castleman's disease, and primary effusion lymphoma.
193 effusion lymphoma (PEL) and/or multicentric Castleman disease (MCD), and in 18 (60.0%) of 30 HIV(+),
194 er primary effusion lymphoma or multicentric Castleman disease B-cell malignancies, and from polyclon
196 rimary effusion lymphoma (PEL), multicentric Castleman disease (MCD), and MCD-associated plasmablasti
197 rimary effusion lymphoma (PEL), multicentric Castleman's disease (MCD), and the inflammation-driven n
198 rimary effusion lymphoma (PEL), multicentric Castleman's disease, and two inflammatory diseases.
199 tuximab in posttrans-plantation multicentric Castleman disease patients and non-neoplastic HHV8-assoc
200 HIV-associated plasmablastic multicentric Castleman disease is an increasingly frequent diagnosis.
203 tent lymphadenopathy resembling multicentric Castleman disease in rhesus macaques (RMs) coinfected wi
204 ogic agent of Kaposi's sarcoma, multicentric Castleman's disease, and AIDS-associated primary effusio
205 tive agent of Kaposi's sarcoma, multicentric Castleman's disease, and primary effusion lymphoma.
206 e for patients with symptomatic multicentric Castleman's disease and well tolerated with prolonged ex
208 ive agent of two B cell tumors, multicentric Castleman disease (MCD) and primary effusion lymphoma (P
209 etiologic agent for KS tumors, multicentric Castleman's disease, and primary effusion lymphomas.
211 erpesvirus 8 is associated with multicentric Castleman disease (MCD) and primary effusion lymphoma (P
213 ase (2 with visceral KS, 1 with multicentric Castleman disease, and 1 with primary effusion lymphoma)
215 etermine the cellular and molecular basis of Castleman Disease (CD), we analyze the spatial proteome
216 ces in understanding the biological basis of Castleman disease have provided new targets for therapeu
219 systematic review of 404 published cases of Castleman's disease to identify the role of the surgeon
224 This review focuses on the intersection of Castleman disease and autoimmunity with an emphasis on s
226 enesis, both involved in the pathogenesis of Castleman disease, may provide additional unique therape
229 Rational approaches to the treatment of Castleman disease have begun to have an impact on diseas
230 ling the multicentric plasma cell variant of Castleman's disease, characterized by persistent angiofo
231 there is mild FDG localization within pelvic Castleman's disease with standard uptake values lower th
232 ma-herpesvirus that causes Kaposi's sarcoma, Castleman's disease and primary effusion lymphomas in tr
234 recent progress has been coordinated by the Castleman Disease Collaborative Network (CDCN), and furt
236 cal location of the only focus in unicentric Castleman's disease (UCD) or the dominant focus in multi
237 hieving long-term remission in patients with Castleman disease and associated autoimmune features.