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1 e wherever needed and to develop a consensus wherever possible.
2 rough additional computations or experiments wherever possible.
3 long-term treatment goals and should be used wherever possible.
4 propriate clinical trials for their patients wherever possible.
5 ctivity to their cyclopentadienyl analogues, wherever possible.
6 er, conservation should clearly be proactive wherever possible.
7 studies of combination chemotherapy regimens wherever possible.
8 es, use patterns, and hazard classifications wherever possible.
9 rgical and anatomical-pathological findings, wherever possible.
10 t 1 month, 3 months, and 1 year post-stroke, wherever possible.
11 d be preferred in structural studies over FA wherever possible.
12 individuals and to compare the final outcome wherever possible.
13 he mechanistic origins of these distinctions wherever possible.
14 oxide (CO2) emissions, and provide solutions wherever possible.
15 ticular reference to Alzheimers disease (AD) wherever possible.
16  and repeat revascularization) were reported wherever possible.
17 utational back end runs operations on-demand wherever possible, allowing for interactive prediction o
18 cies should be identified to a species level wherever possible and cover estimated.
19      Rhodamine-phalloidin labelling was used wherever possible, and revealed that the cytoskeleton ha
20                                              Wherever possible, assessments are based on systematic r
21                                              Wherever possible, attempts have been made to interrelat
22 individuality and context-dependence should, wherever possible, be incorporated into future studies i
23 h the elucidation of gut hormone action and, wherever possible, highlight therapeutic implications of
24  site for percutaneous coronary intervention wherever possible in line with current best evidence.
25 -domain interaction data should be exploited wherever possible in the analysis and prediction of prot
26                                              Wherever possible, known biochemical and electrophysiolo
27 t, empirical and is based on the correction, wherever possible, of any underlying cause, attention to
28 here recent and current approaches focusing, wherever possible, on applications to real data (particu
29 nt goal setting practice genuinely involves, wherever possible, patients as collaborative partners.
30 y (MedPAC) has recommended using claims data wherever possible to measure clinical quality.
31                           We draw attention, wherever possible, to pathological factors common to mul
32 been given a standard nomenclature, designed wherever possible, to provide a consistent identity with
33 new classification system is proposed, based wherever possible, upon embryology and genetics.
34                                              Wherever possible, we attempt to transplant SCID patient
35                                              Wherever possible, we emphasize the application of these
36  we must abandon the monkey model, only that wherever possible, we should test whether generalization
37  parts of the tree of life, we seek to work, wherever possible, with the communities actively generat