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1 ctivity to their cyclopentadienyl analogues, wherever possible.
2 rgical and anatomical-pathological findings, wherever possible.
3 rough additional computations or experiments wherever possible.
4 long-term treatment goals and should be used wherever possible.
5 propriate clinical trials for their patients wherever possible.
6 er, conservation should clearly be proactive wherever possible.
7 studies of combination chemotherapy regimens wherever possible.
8 ticular reference to Alzheimers disease (AD) wherever possible.
9 and repeat revascularization) were reported wherever possible.
10 e wherever needed and to develop a consensus wherever possible.
14 h the elucidation of gut hormone action and, wherever possible, highlight therapeutic implications of
15 site for percutaneous coronary intervention wherever possible in line with current best evidence.
16 -domain interaction data should be exploited wherever possible in the analysis and prediction of prot
18 t, empirical and is based on the correction, wherever possible, of any underlying cause, attention to
19 here recent and current approaches focusing, wherever possible, on applications to real data (particu
20 nt goal setting practice genuinely involves, wherever possible, patients as collaborative partners.
22 been given a standard nomenclature, designed wherever possible, to provide a consistent identity with
26 we must abandon the monkey model, only that wherever possible, we should test whether generalization
27 parts of the tree of life, we seek to work, wherever possible, with the communities actively generat
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