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Central ibotenate lesion placement and extent was assessed post-mortem in NeuN-immunolabeled tissue sections.
Disease extent was assessed in all patients by radionuclide bone scan in which the number of affected sites was counted.
At the time of diagnosis, local tumor extent was assessed using computed tomography (CT) and/or magnetic resonance imaging (MRI).
Organ damage was measured using Vasculitis Damage Index (VDI), and disease extent was assessed by Disease Extent Index (DEI) [ 17, 18].
Disease extent was assessed using the Disease Extent Index (DEI) and disease activity using the Birmingham Vasculitis Activity Score (BVAS) at the time point when the sera were collected from the GPA, EGPA and MPA patients [ 19, 20].
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Extent is assessed by percent of involved BSA and the "rule of nine".
Tumour size and extent were assessed by multi-detector computed tomography (CT) of the chest, abdomen and pelvis and/or F18 positron emission tomography (PET).
The size of the tumor, its location, and cranial extent were assessed in all patients by a combination of magnetic resonance imaging and transrectal ultrasound.
The extent of wear was assessed by scanning electron microscopy.
The extent of wastage was assessed using scanning electron microscopy and weight loss techniques.
The extent of IGC was assessed by metallurgical cross-sectional images.
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