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1 of tumorigenesis and the design of rational biological therapy.
2 eous stimulation, novel drug approaches, and biological therapies.
3 rticularly those who do not respond to other biological therapies.
4 lytic VV in combination with conventional or biological therapies.
5 d use include the use of antimetabolites and biological therapies.
6 a combination of loco-regional and targeted biological therapies.
7 dvances in the fast expanding field of these biological therapies.
8 nse, and summarise the role of antibodies in biological therapies.
9 nt in surgical and radiation techniques, and biological therapies.
10 n of clinical trials should explore emerging biological therapies.
11 e of 33%, with use of topical therapy (60%), biological therapy (66%, mostly anti-tumor necrosis fact
13 e resulted in renewed interest in the use of biological therapies, although only subsets of individua
14 se-modifying antirheumatic drugs (DMARDs) to biological therapies and a more technical focus on dynam
15 ed patients with severe psoriasis initiating biological therapy and matched controls not receiving sy
16 lone individuals who receive chemotherapy or biological therapy and should be continued for 6-12 mont
24 ted vasculitis is increasing, and many novel biological therapies are now entering the drug developme
28 ules, and accessory molecules are targets of biological therapy, but the relevance of these targets i
29 acizumab in combination with chemotherapy or biological therapy, compared with chemotherapy alone, wa
30 -dose biological drugs to 55 for combination biological therapy, compared with traditional DMARDs.
32 aches--including preliminary experience with biological therapies directed at tumor necrosis factor a
33 Recent studies of both nonbiological and biological therapies for arthritis-related uveitis are d
35 tegral to the potential development of novel biological therapies for autoinflammatory diseases, incl
39 opportunities and risks inherent in a novel biological therapy for a progressive neurologic disease.
43 ey cancer is a devastating disease; however, biological therapies have achieved some limited success.
49 re is ongoing debate about the role of newer biological therapies in prevention, treatment or even as
50 of an inhibitory Lt betaR-Ig as a candidate biological therapy in demyelinating disorders, because i
51 tudy on the pharmacogenetics of FcgammaR and biological therapy in psoriasis suggest a role with clin
56 ation associated with immune-suppressive and biological therapies is emerging to be an important caus
57 An intrinsic problem with developing new biological therapies is the difficulty in determining th
58 ns involved in the immunological pathways of biological therapy may account for the differences obser
59 for some profoundly deaf patients, potential biological therapies must extend hearing restoration to
69 reasingly diagnosed in patients treated with biological therapies such as monoclonal antibodies that
71 iles in assessing early treatment effects in biological therapies such as vaccines awaits further val
73 eatment continues to be a challenge, but new biological therapies, such as humanised antibodies again
74 risk of viral reactivation when prescribing biological therapies, thereby facilitating the request f
75 nt experiments demonstrate the potential for biological therapies to regenerate or remyelinate axons
76 overy of inner ear function and suggest that biological therapies to treat deafness may be suitable f
77 as amalgam, composites, and metallic alloys, biological therapies utilize mesenchymal stem cells, del
78 acizumab in combination with chemotherapy or biological therapy was compared with chemotherapy or bio
80 In most patients, systemic administration of biological therapies with cytokines is associated with s
81 Objective: To investigate the association of biological therapy with changes in coronary artery disea
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