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1 tt's lymphoma, nasopharyngeal carcinoma, and Hodgkin's disease.
2  effective in locally extensive and advanced Hodgkin's disease.
3 tutively activated in the malignant cells of Hodgkin's disease.
4 bulky mediastinal stage I/II or stage III/IV Hodgkin's disease.
5 nge, 2.65 to 29.88 years) after diagnosis of Hodgkin's disease.
6 The risk of breast cancer is increased after Hodgkin's disease.
7 men for children with relapsed or refractory Hodgkin's disease.
8 or effect on risk of second malignancy after Hodgkin's disease.
9  with heavily pretreated relapsed/refractory Hodgkin's disease.
10 tment with doxorubicin, and the diagnosis of Hodgkin's disease.
11 ervical-thoracic CT imaging of patients with Hodgkin's disease.
12 nd pairs in B-cell lymphoid malignancies and Hodgkin's disease.
13 eloid leukemia 17 months after treatment for Hodgkin's disease.
14  malignant neoplasms (SMNs) in children with Hodgkin's disease.
15 t biopsy samples from patients with relapsed Hodgkin's disease.
16 sion in EBV-induced lymphoproliferations and Hodgkin's disease.
17 apy for patients with relapsed or refractory Hodgkin's disease.
18 curring in untreated Reed-Sternberg cells of Hodgkin's disease.
19 ses of T- and null-cell NHL, and 18 cases of Hodgkin's disease.
20 athologically verified stage III or stage IV Hodgkin's disease.
21  31.6 years (mean, 13.1) after treatment for Hodgkin's disease.
22  have value in the treatment of EBV-positive Hodgkin's disease.
23 g cells and their variants from six cases of Hodgkin's disease.
24 year-old white girl diagnosed with stage IIa Hodgkin's disease.
25 ll lymphoma of T-cell lineage, and five with Hodgkin's disease.
26 eveloped AML 16 months from the diagnosis of Hodgkin's disease.
27 patients with nodular lymphocyte-predominant Hodgkin's disease.
28 OS in pediatric patients with advanced-stage Hodgkin's disease.
29 taneous T-cell lymphomas, and 5/38 classical Hodgkin's disease.
30 and autografting in the sustained control of Hodgkin's disease.
31 ells occur in nodular lymphocyte-predominant Hodgkin's disease.
32 5 years, and 12.2 years, respectively, after Hodgkin's disease.
33  developed multiple myeloma 16.5 years after Hodgkin's disease.
34 ted a 41% complete response in patients with Hodgkin's disease.
35 ased CD30+ lymphoproliferative disorders and Hodgkin's disease.
36 me patients with Epstein-Barr virus-positive Hodgkin's disease.
37 aining for CD95 was seen in 9 of 10 cases of Hodgkin's disease.
38 7 B- and 5 T-cell lymphomas, and 10 cases of Hodgkin's disease.
39 tment, age at treatment, sex, and time after Hodgkin's disease.
40 ho were treated with radiation for childhood Hodgkin's disease.
41  factor superfamily and a surface marker for Hodgkin's disease.
42 possible localization of primary extra nodal Hodgkin's disease.
43 ts who had prior mediastinal irradiation for Hodgkin's disease.
44  lymphomas and approximately 40% of cases of Hodgkin's disease.
45 c patients with unfavorable presentations of Hodgkin's disease.
46  been identified as effective treatments for Hodgkin's disease.
47 eive newer, combined modality treatments for Hodgkin's disease.
48 e standard regimen for treatment of advanced Hodgkin's disease.
49 xistence of chronic lymphocytic leukemia and Hodgkin's disease.
50  MOPP/ABV hybrid are effective therapies for Hodgkin's disease.
51  relapse after combined-modality therapy for Hodgkin's disease.
52 d with at least 35 Gy to the mediastinum for Hodgkin's disease.
53 d these regimens as initial chemotherapy for Hodgkin's disease.
54 ked in the first 5 years, predominantly from Hodgkin's disease.
55 monoclonal antibody (mAb)-based therapies of Hodgkin's disease.
56 an association between cigarette smoking and Hodgkin's disease.
57 er were treated for clinical stage IA to IIB Hodgkin's disease.
58 APEC-B in patients with previously untreated Hodgkin's disease.
59 or II) disease or advanced (stage III or IV) Hodgkin's disease.
60  is an important preventable risk factor for Hodgkin's disease.
61 -term follow-up care in patients treated for Hodgkin's disease.
62 ctal cancer (10.8, 1.3-38.8; two cases), and Hodgkin's disease (11.4, 1.4-41.3; two cases).
63 ter steroid treatment (T5) in 40 patients (7 Hodgkin's Disease, 13 Acute Myeloblastic Leukemia, 5 Acu
64 s reacted with the BSAP antisera, whereas in Hodgkin's disease, 2 of 4 (50%) nodular lymphocytic pred
65 ll neoplasms, nodular lymphocyte-predominant Hodgkin's disease (7 cases), CD4+ cutaneous T-cell lymph
66 n KS and NHL, only angiosarcoma (36.7-fold), Hodgkin's disease (7.6-fold), multiple myeloma (4.5-fold
67 ific deaths at 25 years were 9.8%+/-1.6% for Hodgkin's disease, 8.1%+/-2.6% for second malignancy, 4.
68 n of a child who had completed treatment for Hodgkin's disease, a PET study strongly suggested recurr
69 st were those for lung cancer, leukemia, and Hodgkin's disease (all 99.9%).
70 e median age at diagnosis was 24.6 years for Hodgkin's disease and 42.6 years for breast cancer.
71 of the EBV-positive, GC-associated lymphomas Hodgkin's disease and Burkitt's lymphoma.
72 lated CD30+ forms of lymphoma, such as CD30+ Hodgkin's disease and CD30+ cutaneous T-cell lymphoma.
73       The autopsy confirmed the existence of Hodgkin's disease and chronic lymphocytic leukemia.
74 asis to understand the genes responsible for Hodgkin's disease and develop novel diagnostic markers a
75 nfect on and suggests an association between Hodgkin's disease and HIV-1 infection.
76 in splenectomized patients in remission from Hodgkin's disease and in healthy Afro-Caribbean subjects
77                  Patients with CD30+ tumors (Hodgkin's disease and Ki-1+ non-Hodgkin's lymphoma) freq
78                  All other tumors, including Hodgkin's disease and lymphomatoid papulosis, were ALK1-
79 le association between radiation therapy for Hodgkin's disease and mesothelioma.
80 roved useful in the staging and follow-up of Hodgkin's disease and non-Hodgkin's lymphoma (especially
81 ), and may be helpful to distinguish between Hodgkin's disease and non-Hodgkin's lymphoma in difficul
82                     There was one death from Hodgkin's disease and one death from an M5 acute leukemi
83 ular adverse effect of radiation exposure in Hodgkin's disease and other types of cancer manifesting
84 on library with TrAb sera from patients with Hodgkin's disease and paraneoplastic cerebellar degenera
85 ly untreated stages III2A, IIIB, IVA, or IVB Hodgkin's disease and patients in first relapse after ra
86 d of therapy is rarely seen in patients with Hodgkin's disease and should be considered a manifestati
87 erature on breast cancer after treatment for Hodgkin's disease and show that high risk is particularl
88 ole of radiotherapy and high-dose therapy in Hodgkin's disease and the non-Hodgkin's lymphomas.
89 s expressed by vascular endothelial cells in Hodgkin's disease and various solid tumors in mice and h
90 otomy could be safely avoided in early-stage Hodgkin's disease and whether chemotherapy should be a p
91 durable responses in melanoma, renal cancer, Hodgkin's diseases and lung cancer.
92 isorders, including posttransplant lymphoma, Hodgkin's disease, and Burkitt's lymphoma, as well as na
93 e expression in nasopharyngeal carcinoma and Hodgkin's disease, and differs from the full spectrum of
94 ers, such as nasopharyngeal carcinoma (NPC), Hodgkin's disease, and gastric carcinoma.
95 of HIV-associated non-Hodgkin's lymphoma and Hodgkin's disease, and include further work on virologic
96                                              Hodgkin's disease, and lymphomatoid papulosis, and to es
97 stic leukemia, chronic myelogenous leukemia, Hodgkin's disease, and non-Hodgkin's lymphoma.
98 the management of early stage breast cancer, Hodgkin's disease, and to a lesser extent other thoracic
99 erse non-Hodgkin's lymphomas overexpress the Hodgkin's disease antigen CD30 (CD30(hi)), a tumor necro
100 cell lymphomas and leukemias and variants of Hodgkin's disease are collected and defined.
101   Unusual types of NHL and manifestations of Hodgkin's disease are seen in HIV-infected individuals a
102 , B-lineage leukemias, multiple myeloma, and Hodgkin's disease, as well as certain carcinomas.
103 rrent disease were alive without evidence of Hodgkin's disease at the time of last follow-up.
104 berg cells in nodular lymphocyte-predominant Hodgkin's disease, belong to the B-cell lineage.
105 negative cases, including three NHL and four Hodgkin's disease biopsy samples.
106  age, diagnosis of non-Hodgkin's lymphoma or Hodgkin's disease, bone marrow involvement, prior radiat
107 e marrow transplant (BMT) can cure recurrent Hodgkin's disease, but more than half of patients will p
108 the number of genes known to be expressed in Hodgkin's disease by 20-fold to 2,666 named genes.
109 tric patients with stages I and II favorable Hodgkin's disease can be cured with limited therapy that
110             Pediatric patients with low-risk Hodgkin's disease can be cured with therapy without an a
111                       Finally, eleven of the Hodgkin's disease cases were also subjected to Southern
112                                   All of the Hodgkin's disease cases, eight of the large-cell lymphom
113 caspase-3 is commonly expressed in classical Hodgkin's disease (CHD); however, the biological signifi
114 ighty-two patients with previously untreated Hodgkin's disease, clinical stages I/II (plus mediastina
115 ogeneity and paucity of "malignant" cells in Hodgkin's disease continue to limit our ability to artic
116                                  Therapy for Hodgkin's disease continues to evolve toward the most ef
117 IV and developing non-Hodgkin's lymphoma and Hodgkin's disease continues to improve as insights into
118                                     Cultured Hodgkin's disease-derived (HD) cell lines, however, were
119 ker for Reed-Sternberg cells and variants of Hodgkin's disease (except L&H types), and may be helpful
120  demonstrated that patients with early-stage Hodgkin's disease experience a short-term decrease in QO
121  29 B and 2 T cell lymphomas, and 9 cases of Hodgkin's disease expressed CD95.
122 nal diagnosis of bone tumor, brain tumor, or Hodgkin's disease; female sex; and an income less than $
123         The malignant Reed-Sternberg cell of Hodgkin's disease, first described a century ago, has re
124                    Additionally, 17 cases of Hodgkin's disease fixed in B5 and formalin were compared
125 ve palliation with low toxicity in recurrent Hodgkin's disease following transplant.
126 fective treatment strategy for patients with Hodgkin's disease for whom induction chemotherapy fails.
127 , whereas patients with multiple myeloma and Hodgkin's disease had worse outcomes as a result of high
128                  The successful treatment of Hodgkin's disease has been associated with an increased
129 ticular, extended follow-up of patients with Hodgkin's disease has revealed an increased risk of brea
130 sfully treated children and adolescents with Hodgkin's disease have a substantial risk for the occurr
131             Patients treated for early-stage Hodgkin's disease have a sustained excess mortality risk
132 -AIDS-defining cancers, germ cell tumors and Hodgkin's disease, have been reported in the setting of
133 rative disorders (PTLD); however, reports of Hodgkin's disease (HD) after transplantation are rare.
134 n expression was also studied in 51 cases of Hodgkin's disease (HD) and 17 large B-cell lymphomas (LB
135  carcinoma, from infectious mononucleosis to Hodgkin's disease (HD) and Burkitt's lymphoma.
136 large-cell lymphomas (DLCL) and 128 cases of Hodgkin's disease (HD) and discusses the clinical featur
137 homa (BL), post-transplant B cell lymphomas, Hodgkin's disease (HD) and nasopharyngeal carcinoma (NPC
138 y (HDT) with autologous stem cell rescue for Hodgkin's disease (HD) and non-Hodgkin's lymphoma (NHL)
139                          Accurate staging of Hodgkin's disease (HD) and non-Hodgkin's lymphoma (NHL)
140  patients with a history of presumably cured Hodgkin's disease (HD) and non-Hodgkin's lymphoma (NHL).
141 as documented survival benefits for relapsed Hodgkin's disease (HD) and non-Hodgkin's lymphoma (NHL).
142  carboxy (C)-terminal mutations occurring in Hodgkin's disease (HD) and reactive tissues from two dif
143 men who are exposed to chest irradiation for Hodgkin's disease (HD) are at increased risk of breast c
144                         Approximately 40% of Hodgkin's disease (HD) cases in Western countries carry
145 ts Study Group cohort of 1,380 children with Hodgkin's disease (HD) diagnosed between 1955 and 1986 i
146                    Epstein Barr virus (EBV)+ Hodgkin's disease (HD) expresses clearly identified tumo
147 m 190 patients with histologically confirmed Hodgkin's disease (HD) for the presence of Epstein-Barr
148 the Hodgkin's Reed-Sternberg (H-RS) cells in Hodgkin's disease (HD) had the greatest abundance of hsp
149                 The treatment of early-stage Hodgkin's disease (HD) has evolved from radiotherapy alo
150 non-Hodgkin's lymphoma (NHL) in 48 patients, Hodgkin's disease (HD) in 14 patients, other neoplastic
151 sted to have an impact on the development of Hodgkin's disease (HD) in women.
152                                              Hodgkin's disease (HD) is a lymphoid malignancy characte
153                                              Hodgkin's disease (HD) is a lymphoma characterized by a
154                                              Hodgkin's disease (HD) is a malignancy that displays a b
155                                              Hodgkin's disease (HD) is an example of a malignancy whi
156 lymphoma with the characteristic features of Hodgkin's disease (HD) occasionally develops in patients
157                                  A subset of Hodgkin's disease (HD) patients have detectable Epstein-
158               Thirty-nine previously treated Hodgkin's disease (HD) patients were immunized with 7-va
159 ineteen patients with relapsed or refractory Hodgkin's disease (HD) received high-dose therapy follow
160 mphoma (ALCL) and the Reed-Sternberg cell of Hodgkin's disease (HD) remains largely uncertain.
161             Refinement in managing pediatric Hodgkin's disease (HD) requires understanding of factors
162     Cardiovascular status was assessed in 48 Hodgkin's disease (HD) survivors at a median of 14.3 yea
163  and risk factors for stroke among childhood Hodgkin's disease (HD) survivors.
164 in patients with lymphocyte-predominant (LP) Hodgkin's disease (HD) to determine whether these patien
165 CL), other non-Hodgkin's lymphomas (NHL), or Hodgkin's disease (HD) were eligible if their cancer was
166 ield radiotherapy in patients with favorable Hodgkin's disease (HD) who have been laparotomy-staged.
167 heral T cell, 13 with low-grade NHL, 31 with Hodgkin's disease (HD), and 6 with lymphomatoid papulosi
168  nasopharyngeal carcinoma (NPC), a subset of Hodgkin's disease (HD), and in EBV-associated lymphoprol
169  six had lymphoplasmacytic lymphoma, six had Hodgkin's disease (HD), and one each had diffuse large B
170 ted tumors such as nasopharyngeal carcinoma, Hodgkin's disease (HD), and T/NK lymphomas.
171  and Reed-Sternberg (HRS) cells of classical Hodgkin's disease (HD), but its clinical significance re
172  mortality after the successful treatment of Hodgkin's disease (HD), little is known about the molecu
173 dian, 40) with non-Hodgkin's lymphoma (NHL), Hodgkin's disease (HD), multiple myeloma (MM), or acute
174 n 1982 and 1995 were included in this study: Hodgkin's disease (HD), n = 12; intermediate/high-grade
175 -424 of EBNA-4 in 25 cases of EBV-associated Hodgkin's disease (HD), nine cases of AIDS-related non-H
176  Reed-Sternberg (RS) cells of EBV-associated Hodgkin's disease (HD).
177 Reed-Sternberg (HRS) cells of EBV-associated Hodgkin's disease (HD).
178 diopulmonary protectant during treatment for Hodgkin's disease (HD).
179 y on the potential for fertility of men with Hodgkin's disease (HD).
180 st cancer, non-Hodgkin's lymphoma (NHL), and Hodgkin's disease (HD).
181 T cells in patients who had been treated for Hodgkin's disease (HD).
182 he immunohistochemical detection of LMP2A in Hodgkin's disease (HD).
183 -Barr virus (EBV) is etiologically linked to Hodgkin's disease (HD).
184  Reed-Sternberg (RS) cells of EBV-associated Hodgkin's disease (HD).
185 hly expressed on the Reed Sternberg cells of Hodgkin's disease (HD).
186 h aggressive non-Hodgkin's lymphoma (NHL) or Hodgkin's disease (HD).
187 with diffuse large B-cell lymphoma (n = 12), Hodgkin's disease (HD; n = 12), multiple myeloma (n = 2)
188 y disease is effective in bulky and advanced Hodgkin's disease in a multi-institutional setting.
189 s of this study show that, in advanced-stage Hodgkin's disease in children, equivalent results can be
190 mbination chemotherapy regimens for advanced Hodgkin's disease in pediatric patients.
191 o cure acute childhood leukemia and advanced Hodgkin's disease in the 1960s and early 1970s overcame
192                The management of early-stage Hodgkin's disease in the United States is controversial.
193 rd therapy for children and adolescents with Hodgkin's disease includes combination chemotherapy and
194                                   Relapse of Hodgkin's disease increased the risk of second malignanc
195 ednisone (NOVP) combination chemotherapy for Hodgkin's disease increases the frequencies of the speci
196 ar lymphomas, 3 mantle cell lymphomas, and 2 Hodgkin's disease) involving GIT.
197 tra nodal and extra lymphatic propagation of Hodgkin's disease is a characteristic of the fourth stag
198                                              Hodgkin's disease is a common malignancy of the lymphoid
199  alone in selected patients with early-stage Hodgkin's disease is associated with disease control rat
200 urate disease status in patients treated for Hodgkin's disease is discussed, along with recommendatio
201 tion for patients with early-stage/favorable Hodgkin's disease is highly effective and without demons
202                                     Although Hodgkin's disease is highly responsive to treatments tha
203 major consequence of successful treatment of Hodgkin's disease is the development of second malignant
204 biological significance of its expression in Hodgkin's disease is unknown.
205 ong the highest reported in association with Hodgkin's disease, is unusual.
206 ransplant-related mortality rates decline in Hodgkin's disease, it is predicted that cure rates and l
207                   Exclusion of deaths due to Hodgkin's disease led to small changes in the estimates
208                       We found that in fresh Hodgkin's disease lymph node biopsies, a subset of HRS c
209 elated cancers, elevated SIRs were found for Hodgkin's disease (male, 8.0; female, 6.4; heterosexuall
210 lso present in the cytoplasmic domain of the Hodgkin's disease marker, CD30, and binds TRAF3 in vitro
211  C promoter or Cp) in Burkitt's lymphoma and Hodgkin's disease may play an important role in the path
212                                     However, Hodgkin's disease may produce several inhibitory effects
213 ts, alternative malignancies were diagnosed (Hodgkin's disease; metastatic neuroendocrine carcinoma;
214 ectal cancer incidence and mortality, and of Hodgkin's disease mortality were increased.
215 S leads to a significantly increased risk of Hodgkin's disease, multiple myeloma, brain cancer, and s
216  of follow-up, 71 fatal events resulted from Hodgkin's disease (n=36), second malignancies (n=14), in
217 nfection including posttransplant lymphomas, Hodgkin's disease, nasopharyngeal carcinoma, and AIDS-re
218 methylated and silent in Burkitt's lymphoma, Hodgkin's disease, nasopharyngeal carcinoma, and nasal l
219  and B strains contrasts with EBV-associated Hodgkin's disease, nasopharyngeal carcinoma, and post-tr
220 apy and low-dose radiotherapy in early stage Hodgkin's disease need our attention in rigorously desig
221 d be generated ex vivo from 13 patients with Hodgkin's disease: nine with active relapsed disease and
222  clonality of nodular lymphocyte-predominant Hodgkin's disease (NLPHD) and the relationship to compos
223              Nodular lymphocyte predominance Hodgkin's disease (NLPHD) is characterized by the presen
224 caspase-3 in nodular lymphocyte predominance Hodgkin's disease (NLPHD) was evaluated by immunohistoch
225  reticulum cell, for the neoplastic cells of Hodgkin's disease, notably in nodular sclerosis type.
226  and histology other than nodular sclerosing Hodgkin's disease (NSHD).
227 's transformation occurred in 9 patients and Hodgkin's disease occurred in 4 patients.
228 mokers had a significantly increased risk of Hodgkin's disease (odds ratio (OR) = 1.8, 95% confidence
229                          Primary extra nodal Hodgkin's disease of bone is manifested with painful swe
230  chronic lymphocytic leukemia (one patient), Hodgkin's disease (one patient), and adult T-cell leukem
231  of cholestasis, but not pruritus of uremia, Hodgkin's disease, or atopic dermatitis.
232                     Certain types of cancer (Hodgkin's disease, osteosarcoma/Ewing's sarcoma, rhabdom
233  contrast, Burkitt's lymphoma (P=0.0047) and Hodgkin's disease (P=0.016) were only observed in late P
234 healthy men and to repeated samples of eight Hodgkin's disease patients before treatment, 35-50 days
235  tumors in pathologically staged and treated Hodgkin's disease patients followed for long intervals t
236  52 patients, compared with three (4%) of 68 Hodgkin's disease patients in a comparison cohort who di
237 nd Marrow Transplant Registry (ABMTR) on 122 Hodgkin's disease patients who failed to achieve complet
238                                              Hodgkin's disease patients who never achieve complete re
239  whole saliva flow rates were measured in 11 Hodgkin's disease patients who received therapeutic dose
240 re reported only for NHL patients, excluding Hodgkin's disease patients.
241 59 children and adolescents with unfavorable Hodgkin's disease received three alternating cycles (tot
242                          Sixty patients with Hodgkin's disease, refractory to or at first recurrence
243 gents in the etiology of solid cancers after Hodgkin's disease require detailed investigation.
244                       Survivors of pediatric Hodgkin's disease require lifelong evaluation and cancer
245 lymphoma and nodular lymphocyte predominance Hodgkin's disease, respectively).
246 mortality from all causes, causes other than Hodgkin's disease, second tumors, and cardiac disease re
247 er (PTLD; SIR = 54.3; 95% CI, 39.5 to 41.1), Hodgkin's disease (SIR = 14.8; 95% CI, 3.9 to 32.9), or
248                                              Hodgkin's disease (SIR = 2.5; 95% CI 1.5-3.9), and anal
249 motherapy regimen plus radiotherapy to bulky Hodgkin's disease sites.
250 es in non-AIDS-defining malignancies such as Hodgkin's disease, skin, lung, anal, and kidney cancers
251 n a randomized clinical trial in early-stage Hodgkin's disease (Southwest Oncology Group [SWOG] 9133)
252                                              Hodgkin's disease stage, patient age, splenectomy, and t
253 elangiectasia (AT) gene, ATM, in a cohort of Hodgkin's disease survivors with secondary malignancies.
254 neoplasms were observed in this cohort of 52 Hodgkin's disease survivors, with 18 patients (35%) deve
255 opment of secondary neoplasms in a subset of Hodgkin's disease survivors.
256  is an effective treatment for all stages of Hodgkin's disease that present with a large mediastinal
257                      In 50% of patients with Hodgkin's disease, the tumor cells are EBV antigen-posit
258                                   Aggressive Hodgkin's disease therapy is successful, but patients ha
259  active in both nasopharyngeal carcinoma and Hodgkin's disease tissues.
260 blastoid cell lines and are also detected in Hodgkin's disease tissues.
261 creening of patients who have recovered from Hodgkin's disease to aid early diagnosis and ensure the
262 roup followed a cohort of 1380 children with Hodgkin's disease to determine the incidence of second n
263  neck and chest are obtained at diagnosis of Hodgkin's disease to establish disease extent, plan radi
264 his may be useful in assigning children with Hodgkin's disease to risk-adapted therapy.
265               Most patients who present with Hodgkin's disease today can be cured of their disease.
266 A striking finding was observed for cases of Hodgkin's disease (total 187 cases).
267      A cohort of 5,519 British patients with Hodgkin's disease treated during 1963 through 1993 was a
268 ns in children and adolescents with low-risk Hodgkin's disease treated with vinblastine, doxorubicin,
269 s enrolled onto two Pediatric Oncology Group Hodgkin's disease treatment protocols.
270 ith lymphomatoid papulosis (fourteen cases), Hodgkin's disease (twelve cases), and CD30+ large-cell l
271 ren), Kaposi's sarcoma (KS; three children), Hodgkin's disease (two children), vaginal carcinoma in s
272  and in the FRC and endothelium of classical Hodgkin's disease, two tumor types that also showed an a
273 ith diagnosed relapsed or primary refractory Hodgkin's disease underwent this treatment.
274 fects for smoking in relation to the risk of Hodgkin's disease using data from the Selected Cancers S
275 lative risk for invasive breast cancer after Hodgkin's disease was 4.7 (95% confidence interval, 3.4
276 ond neoplasm 15 years after the diagnosis of Hodgkin's disease was 7.0 percent (95 percent confidence
277 it was observed that successful treatment of Hodgkin's disease was associated with risk of a second m
278 ldren and adolescents with stages III and IV Hodgkin's disease was conducted by the Children's Cancer
279  The risk for developing breast cancer after Hodgkin's disease was greatest in women who were under t
280 ne cases of breast cancer in 65 survivors of Hodgkin's disease were analyzed.
281 odular sclerosing and lymphocyte predominant Hodgkin's disease were derived from an unusual B-cell li
282 age (PS) IA to IIA or clinical stage (CS) IA Hodgkin's disease were entered onto a single-arm prospec
283 escents with stages IIB, IIIA2, IIIB, and IV Hodgkin's disease were randomized to receive eight cycle
284  clinical stage IA to IIA supradiaphragmatic Hodgkin's disease were randomized without staging laparo
285       Adult patients (N = 856) with advanced Hodgkin's disease were randomly assigned to treatment wi
286 0 and April 1993, 56 pediatric patients with Hodgkin's disease were treated on a single-arm trial at
287 diatric patients with clinical stage I to IV Hodgkin's disease were treated with chemotherapy and low
288 inical stages I and II, favorable (nonbulky) Hodgkin's disease were treated with four cycles of VAMP
289       One hundred ten children with low-risk Hodgkin's disease were treated with four cycles of VAMP
290 patients with laparotomy staged (PS) IA-IIIB Hodgkin's disease were treated with radiation therapy (R
291 like B-cell chronic lymphocytic leukemia and Hodgkin's disease, where IL-13 modulates apoptosis or tu
292 m patients with nasopharyngeal carcinoma and Hodgkin's disease, where LMP1 is also found.
293                                Patients with Hodgkin's disease, which is either refractory or recurs
294 lants should be considered for patients with Hodgkin's disease who do not achieve complete remission
295 We analyzed retrospectively 81 patients with Hodgkin's disease who had serial [(18)F]FDG-PET scans pe
296 acial zygomycosis in a 24-year-old male with Hodgkin's disease who underwent chemotherapy and autolog
297  control populations, survivors of pediatric Hodgkin's disease who were treated before 1990 face an i
298 secutive, previously untreated patients with Hodgkin's disease who were younger than 20 years of age
299 ms focus on obtaining a relapse-free cure of Hodgkin's disease with judicious use of radiation and al
300  = cisplatinum), in a group of patients with Hodgkin's disease with such poor risk characteristics.

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