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1 hole-brain radiotherapy improves survival in primary central nervous system lymphoma.
2 be studied for newly diagnosed and recurrent primary central nervous system lymphoma.
3 cular disease or as secondary involvement by primary central nervous system lymphoma.
4 inetics to water- and lipid-soluble drugs in primary central nervous system lymphomas.
5 h the acquired immunodeficiency syndrome and primary central nervous system lymphoma (AIDS-PCNSL) is
6 agnosis of primary vitreoretinal lymphoma or primary central nervous system lymphoma and can regress
7 , particularly for responsive tumors such as primary central nervous system lymphoma and oligodendrog
8 ly among individuals with low-grade gliomas, primary central nervous system lymphoma and those underg
9 lymphoma, 5 (9%) Burkitt lymphoma, 10 (18%) primary central nervous system lymphoma, and 7 (13%) oth
10 n spinal fluid is useful in the diagnosis of primary central nervous system lymphoma, and monitoring
12 induced frequent responses in patients with primary central nervous system lymphoma but was associat
14 ients with uncommon histological variants of primary central nervous system lymphoma have been publis
15 e cerebrospinal fluid (CSF) in patients with primary central nervous system lymphoma; however, the CS
16 intraocular lymphoma (PIOL) is a variant of primary central nervous system lymphoma in which lymphom
17 best mode for treatment of PIOL or recurrent primary central nervous system lymphoma involving only t
19 Salvage therapy for progressive or recurrent primary central nervous system lymphoma is an area of ac
29 se 2 study for patients with newly diagnosed primary central nervous system lymphoma (PCNSL) using in
30 chemotherapy is the mainstay of treatment of primary central nervous system lymphoma (PCNSL), but rel
35 affecting the brain (cerebral toxoplasmosis, primary central nervous system lymphoma, progressive mul
38 Future studies on the biology of recurrent primary central nervous system lymphoma should help to c
39 t progress has been made in the treatment of primary central nervous system lymphoma since the time w
40 To evaluate whether the chemosensitivity of primary central nervous system lymphomas to water-solubl
41 sis of primary vitreoretinal lymphoma and/or primary central nervous system lymphoma was made within
42 d with primary vitreoretinal lymphoma and/or primary central nervous system lymphoma were analyzed.
43 AIDS-primary effusion lymphoma; 1 of 4 AIDS-primary central nervous system lymphoma), with 9 of 39 (
44 e neurocognitive deficits among survivors of primary central nervous system lymphoma without residual
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