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Biomarkers in osteoarthritis can be categorised using the burden of disease, investigative, prognostic, efficacy of intervention, diagnostic and safety classification.
Remoteness of residence when diagnosed with breast cancer will be categorised using the ARIA+ classification, which is a measure of accessibility and remoteness based on geographical location [ 59].
They also argue that the idea that genetic resources can be categorised using the concepts of rival and excludable goods makes sense of various observations (e.g. that it seems difficult for prokaryotes to prevent other prokaryotes from eventually exploiting a particular genetic resource).
The European Germ Cell Cancer Consensus Group (EGCCCG) recommend that TNM staging be used [ 10] (Table 1) and that patients be categorised using the International Germ Cell Cancer Collaborative Group (IGCCCG) classification which stratifies patients into good, intermediate and poor prognostic groups.
Biomarkers in osteoarthritis can be categorised using the five-point burden of disease, investigative, prognostic, efficacy of intervention and diagnostic (BIPED) classification scheme, which was developed by the Osteoarthritis Biomarkers Network with the aim of providing a common framework for communication in the field.
After the double review, each record will be categorised using the following criteria: (1) both authors agree on inclusion; (2) one author recommends inclusion; (3) both authors are unsure; (4) one author recommends exclusion and the other is unsure or (5) both authors agree on exclusion.
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BMI was categorised using the WHO categorisation (World Health Organization Consultation on Obesity, 1998): BMI <18.5 (underweight), 18.5 24.9 (normal), 25.0 29.9 (preobese/overweight) and ⩾30.0 (obese).
Body mass index was categorised using the WHO categorisation (World Health Organization Consultation on Obesity, 1998): BMI <18.5 (underweight), 18.5 24.9 (normal), 25.0 29.9 (preobese/overweight) and ≥30.0 kg/m (obese).
Pathologies were categorised using the diagram shown in Fig. 1 [6].
Toxicity was categorised using the National Cancer Institute Common Toxicity Criteria (version 2.0).
All visual fields were categorised using the classification defined by Wild et al. (2009) [ 22].
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