0010 21f0 LO 1 Patient's Religious Preference
0010 4000 LT 1 Patient Comments
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0012 0010 LO 1 Clinical Trial Sponsor Name
0012 0020 LO 1 Clinical Trial Protocol ID
0012 0021 LO 1 Clinical Trial Protocol Name
0018 003a ST 1 Intervention Description
0018 0040 IS 1 Cine Rate
0018 0050 DS 1 Slice Thickness
-0018 0060 DS 1 KVP
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0018 0070 IS 1 Counts Accumulated
0018 0071 CS 1 Acquisition Termination Condition
0018 0072 DS 1 Effective Duration
0018 9027 CS 1 Spatial Pre-saturation
0018 9028 CS 1 Tagging
0018 9029 CS 1 Oversampling Phase
-0018 9022 CS 1 Blood Signal Nulling
0018 9030 FD 1 Tag Spacing First Dimension
0018 9032 CS 1 Geometry of k-Space Traversal
0018 9033 CS 1 Segmented k-Space Traversal
0018 9344 CS 1 Contrast/Bolus Agent Phase
0018 9345 FD 1 CTDIvol
0018 a001 SQ 1 Contributing Equipment Sequence
-0018 a002 DT 1 Contribution DateTime
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0018 a003 ST 1 Contribution Description
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0020 000d UI 1 Study Instance UID
0020 000e UI 1 Series Instance UID
0020 0010 SH 1 Study ID
0020 9228 UL 1 Concatenation Frame Offset Number
0020 9238 LO 1 Functional Group Private Creator
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0022 0001 US 1 Light Path Filter Pass-Through Wavelength
0022 0002 US 2 Light Path Filter Pass Band
0022 0003 US 1 Image Path Filter Pass-Through Wavelength
0028 9145 SQ 1 Pixel Value Transformation Sequence
0028 9235 CS 1 Signal Domain Rows
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0032 000a CS 1 Study Status ID
0032 000c CS 1 Study Priority ID
0032 0012 LO 1 Study ID Issuer
0050 0016 DS 1 Device Diameter
0050 0017 CS 1 Device Diameter Units
0050 0018 DS 1 Device Volume
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0050 0020 LO 1 Device Description
0054 0000 UL 1 Group Length
0088 0904 LO 1 Topic Title
0088 0906 ST 1 Topic Subject
0088 0910 LO 1 Topic Author
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0100 0000 UL 1 Group Length
0100 0410 CS 1 SOP Instance Status
3002 0041 CS 1 Fluence Data Source
3002 0042 DS 1 Fluence Data Scale
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3004 0001 CS 1 DVH Type
3004 0002 CS 1 Dose Units
3004 0004 CS 1 Dose Type
300e 0005 TM 1 Review Time
300e 0008 PN 1 Reviewer Name
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4000 0010 LT 1-n Text Arbitrary (RET)
4000 4000 LT 1-n Text Comments (RET)