about
The impact of the relaxivity definition on the quantitative measurement of glycosaminoglycans in cartilage by the MRI dGEMRIC methodAnimal models of osteoarthritis: classification, update, and measurement of outcomesQuantitative MRI using T1ρ and T2 in human osteoarthritic cartilage specimens: correlation with biochemical measurements and histologySubject-specific analysis of joint contact mechanics: application to the study of osteoarthritis and surgical planningTheory of MRI contrast in the annulus fibrosus of the intervertebral discThe influences of different spatial resolutions on the characteristics of T2 relaxation times in articular cartilage: A coarse-graining study of the microscopic magnetic resonance imaging data.Image interpolation improves the zonal analysis of cartilage T2 relaxation in MRI.High-resolution measurements of the multilayer ultra-structure of articular cartilage and their translational potential.On the measurement of multi-component T2 relaxation in cartilage by MR spectroscopy and imagingMR imaging of articular cartilage physiology.Dependencies of multi-component T2 and T1ρ relaxation on the anisotropy of collagen fibrils in bovine nasal cartilageReversed laminar appearance of articular cartilage by T1-weighting in 3D fat-suppressed spoiled gradient recalled echo (SPGR) imagingUltrashort-echo time MR imaging of the patella with bicomponent analysis: correlation with histopathologic and polarized light microscopic findings.In vivo 3.0-tesla magnetic resonance T1rho and T2 relaxation mapping in subjects with intervertebral disc degeneration and clinical symptoms.Further studies on the anisotropic distribution of collagen in articular cartilage by μMRI.Molecular origin of a loading-induced black layer in the deep region of articular cartilage at the magic angleAnisotropic analysis of multi-component T2 and T1ρ relaxations in achilles tendon by NMR spectroscopy and microscopic MRI.Changes in Proton Dynamics in Articular Cartilage Caused by Phosphate Salts and Fixation Solutions.T₁ρ MRI of human musculoskeletal system.Magnetic Resonance Imaging of Cartilage Repair: A ReviewDetecting structural changes in early experimental osteoarthritis of tibial cartilage by microscopic magnetic resonance imaging and polarised light microscopy.Depth and orientational dependencies of MRI T(2) and T(1ρ) sensitivities towards trypsin degradation and Gd-DTPA(2-) presence in articular cartilage at microscopic resolutionMRI properties of a unique hypo-intense layer in degraded articular cartilage.MRI of articular cartilage at microscopic resolutionMulti-components of T2 relaxation in ex vivo cartilage and tendonNovel contrast mechanisms at 3 Tesla and 7 TeslaDamages to the extracellular matrix in articular cartilage due to cryopreservation by microscopic magnetic resonance imaging and biochemistry.The collagen fibril structure in the superficial zone of articular cartilage by microMRI.Imaging cartilage physiology.Dual inversion recovery ultrashort echo time (DIR-UTE) imaging and quantification of the zone of calcified cartilage (ZCC).Comparison of Three Methods to Quantify Repair Cartilage Collagen Orientation.Multimodal quantitative magnetic resonance imaging for lumbar intervertebral disc degeneration.Resolution 'scaling law' in MRI of articular cartilage.Local tissue properties of human osteoarthritic cartilage correlate with magnetic resonance T(1) rho relaxation timesThe basic science of articular cartilage: structure, composition, and function.MRI rotating frame relaxation measurements for articular cartilage assessment.Magic angle effect plays a major role in both T1rho and T2 relaxation in articular cartilage.Evaluation of Lumbar Intervertebral Disc Degeneration Using T1ρ and T2 Magnetic Resonance Imaging in a Rabbit Disc Injury Model.
P2860
Q24653383-4AF013F6-757C-4CF6-9293-3D1B9268CA37Q28072990-33A96F66-B3E4-4E6B-B843-71529B473350Q28386961-281D5F37-064F-44B0-B7FF-BBD5CB617344Q28679547-F0B91618-FA3F-441B-8845-90BE9E8A292BQ31036347-5068E10F-16D4-4F28-A22F-906F1652DD34Q31107911-0831CEB8-380E-4522-B1B7-1CAF5A6A20FBQ33638794-53AE23DA-66E6-4057-9480-05A6DD10D761Q33771682-1F16936B-6D80-4FF3-953D-E78F6159A033Q33811947-17CB2A9C-2BF7-4349-929E-12DE100860F2Q33930002-F605EC82-BB5A-4DC1-9EE8-C4BF121A6C39Q33970776-5E07AE09-FE01-46F5-99E3-5E2203AFA342Q34106304-B641C5E1-3189-4F0D-AD04-D3EC9DE8800AQ34288337-223B32BD-20E5-4EEA-BA6A-7559595C22FEQ34334325-BFB49BCB-61FB-4AB1-B243-375D2CEB650FQ34494265-4BFB9FB9-14BC-4251-B202-F9F50EBD18AEQ34518592-32419EF5-AA86-493E-B6B2-FCB00F9ECB76Q34561764-BD8B48DF-19CE-4B32-8855-30B4113D1E8DQ34622574-DF6047DB-7A92-49F3-A13A-5E2DED393DDEQ34725693-D0B26ACA-4922-4A01-95C0-E1D60FFEFA52Q34991542-A0BBD6D3-89F1-46E7-8AF1-0E3B348D54E0Q35554161-3D70D588-006E-42A7-85BD-095ECF902E22Q35786115-9D308DF5-A831-4188-A817-BABAEF7AF3CDQ36276860-FCF86948-1687-4177-B84D-ED75ED6AE6A8Q36765429-0F045E6F-B38D-4520-A3D7-CBFCE454F65EQ37188993-FDEF3D1D-8148-4F6A-9962-9EFD8C170ED2Q37292519-756B65AE-D1EB-4F4D-BC5F-E6D54C2FB29FQ37344175-D547FB8A-83D6-472A-A06A-4661626F2B49Q37392191-26602BF5-0E53-4A0A-A401-EC2EADAE4DB8Q40231309-650AF5F0-BD02-44D3-B08D-B07EF952FA7EQ40501710-023EEC7C-48A0-48BF-ABC1-D08C793F0B07Q40840885-42E8F4EB-9721-4648-9EF5-720E55777998Q41672245-7DE2A39D-331D-473F-BE13-273B8C6A71F2Q41827143-F49BDADC-105D-4E99-B31A-77DD3AB90327Q42088682-89ACE734-8781-4382-9F02-93293225F207Q42094020-693EA5AC-BBE8-45E4-9B16-9E29C838F52AQ43144599-75186857-F62F-4D35-86F0-ED77671E2D99Q46157337-C8193E48-F636-4A73-9A29-5E8C57825B08Q54944043-E6D90DF0-9356-46FC-A3BA-80595606C786
P2860
description
scientific article published on 01 September 1997
@en
wetenschappelijk artikel
@nl
name
Origin of cartilage laminae in MRI
@en
Origin of cartilage laminae in MRI
@nl
type
label
Origin of cartilage laminae in MRI
@en
Origin of cartilage laminae in MRI
@nl
prefLabel
Origin of cartilage laminae in MRI
@en
Origin of cartilage laminae in MRI
@nl
P2093
P356
P1476
Origin of cartilage laminae in MRI
@en
P2093
N Burton-Wurster
T Farquhar
P304
P356
10.1002/JMRI.1880070518
P407
P50
P577
1997-09-01T00:00:00Z