Magnetic resonance imaging markers of Parkinson's disease nigrostriatal signature
Abstract
One objective of modern neuroimaging is to identify markers that can aid in diagnosis, disease progression monitoring and long-term drug impact analysis. In this study, Parkinson-associated physiopathological modifications were characterized in six subcortical structures by simultaneously measuring quantitative magnetic resonance parameters sensitive to complementary tissue characteristics (i.e. volume atrophy, iron deposition and microstructural damage). Thirty patients with Parkinson's disease and 22 control subjects underwent 3-T magnetic resonance imaging with T₂*-weighted, whole-brain T₁-weighted and diffusion tensor imaging scans. The mean R₂* value, mean diffusivity and fractional anisotropy in the pallidum, putamen, caudate nucleus, thalamus, substantia nigra and red nucleus were compared between patients with Parkinson's disease and control subjects. Comparisons were also performed using voxel-based analysis of R₂*, mean diffusivity and fractional anisotropy maps to determine which subregion of the basal ganglia showed the greater difference for each parameter. Averages of each subregion were then used in a logistic regression analysis. Compared with control subjects, patients with Parkinson's disease displayed significantly higher R₂* values in the substantia nigra, lower fractional anisotropy values in the substantia nigra and thalamus, and higher mean diffusivity values in the thalamus. Voxel-based analyses confirmed these results and, in addition, showed a significant difference in the mean diffusivity in the striatum. The combination of three markers was sufficient to obtain a 95% global accuracy (area under the receiver operating characteristic curve) for discriminating patients with Parkinson's disease from controls. The markers comprising discriminating combinations were R₂* in the substantia nigra, fractional anisotropy in the substantia nigra and mean diffusivity in the putamen or caudate nucleus. Remarkably, the predictive markers involved the nigrostriatal structures that characterize Parkinson's physiopathology. Furthermore, highly discriminating combinations included markers from three different magnetic resonance parameters (R₂*, mean diffusivity and fractional anisotropy). These findings demonstrate that multimodal magnetic resonance imaging of subcortical grey matter structures is useful for the evaluation of Parkinson's disease and, possibly, of other subcortical pathologies.
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
Imaging methods such as MRI and transcranial sonography were not able to substantiate the relation between total iron concentration and disease severity because of the absence of accurate quantification for iron content in different brain areas.
“Imaging methods, such as MRI and transcranial sonography, were not able to substantiate the relation between total iron concentration and disease severity because of the absence of accurate quantification for the iron content in different brain areas.104,105”
From The role of iron in brain ageing and neurodegenerative disorders (2014) · cites this paper as [104]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Cites
Hughes, A. J., Daniel, S. E., Kilford, L., & Lees, A. J. (1992) · Journal of Neurology, Neurosurgery & Psychiatry · doi:10.1136/jnnp.55.3.181 · Cited by 10,378 · see citing works
Parallel organization of functionally segregated circuits linking basal ganglia and cortex
Alexander, G. E., DeLong, M. R., & Strick, P. L. (1986) · Annual Review of Neuroscience · doi:10.1146/annurev.ne.09.030186.002041 · Cited by 8,527 · see citing works
AGEING AND PARKINSON'S DISEASE: SUBSTANTIA NIGRA REGIONAL SELECTIVITY
FEARNLEY, J. M., & LEES, A. J. (1991) · Brain · doi:10.1093/brain/114.5.2283 · Cited by 3,529 · see citing works
Iron, brain ageing and neurodegenerative disorders
Zecca, L., Youdim, M. B. H., Riederer, P., Connor, J. R., & Crichton, R. R. (2004) · Nature Reviews Neuroscience · doi:10.1038/nrn1537 · Cited by 1,801 · see citing works
Self-initiated versus externally triggered movements
Jahanshahi, M., Jenkins, I. H., Brown, R. G., MARSDEN, C. D., Passingham, R. E., & Brooks, D. J. (1995) · Brain · doi:10.1093/brain/118.4.913 · Cited by 999 · see citing works
Increased nigral iron content in postmortem parkinsonian brain
Dexter, D. T., Wells, F. R., Agid, F., Agid, Y., Lees, A. J., Jenner, P., & Marsden, C. D. (1987) · The Lancet · doi:10.1016/s0140-6736(87)91361-4 · Cited by 963 · see citing works
The diagnosis of Parkinson’s disease
Tolosa, E., Wenning, G., & Poewe, W. (2006) · The Lancet Neurology · doi:10.1016/s1474-4422(05)70285-4 · Cited by 902 · see citing works
Self-initiated versus externally triggered movements
Jenkins, I. H., Jahanshahi, M., Jueptner, M., Passingham, R. E., & Brooks, D. J. (2000) · Brain · doi:10.1093/brain/123.6.1216 · Cited by 746 · see citing works
Burton, E. J. (2004) · Brain · doi:10.1093/brain/awh088 · Cited by 643 · see citing works
Playford, E. D., Jenkins, I. H., Passingham, R. E., Nutt, J. G., Frackowiak, R. S. J., & Brooks, D. J. (1992) · Annals of Neurology · doi:10.1002/ana.410320206 · Cited by 611 · see citing works
Cortical motor reorganization in akinetic patients with Parkinson's disease
Sabatini, U., Boulanouar, K., Fabre, N., Martin, F., Carel, C., Colonnese, C., Bozzao, L., Berry, I., Montastruc, J., Chollet, F., et al. (2000) · Brain · doi:10.1093/brain/123.2.394 · Cited by 592 · see citing works
Self-citationSelective Increase of Iron in Substantia Nigra Zona Compacta of Parkinsonian Brains
Sofic, E., Paulus, W., Jellinger, K. A., Riederer, P. F., & Youdim, M. B. H. (1991) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.1991.tb02017.x · Cited by 523 · see citing works
Molecular diffusion, tissue microdynamics and microstructure
Bihan, D. L. (1995) · NMR in Biomedicine · doi:10.1002/nbm.1940080711 · Cited by 497 · see citing works
High-resolution diffusion tensor imaging in the substantia nigra of de novo Parkinson disease
Vaillancourt, D. E., Spraker, M. B., Prodoehl, J., Abraham, I. E., Corcos, D. M., Zhou, X. J., Comella, C. L., & Little, D. M. (2009) · Neurology · doi:10.1212/01.wnl.0000340982.01727.6e · Cited by 438 · see citing works
Normal aging in the central nervous system: Quantitative MR diffusion-tensor analysis
Abe, O., Aoki, S., Hayashi, N., Yamada, H., Kunimatsu, A., Mori, H., Yoshikawa, T., Okubo, T., & Ohtomo, K. (2002) · Neurobiology of Aging · doi:10.1016/s0197-4580(01)00318-9 · Cited by 420 · see citing works
Deichmann, R., Schwarzbauer, C., & Turner, R. (2003) · NeuroImage · doi:10.1016/j.neuroimage.2003.09.062 · Cited by 391 · see citing works
Gelman, N., Gorell, J. M., Barker, P. B., Savage, R. M., Spickler, E. M., Windham, J. P., & Knight, R. A. (1999) · Radiology · doi:10.1148/radiology.210.3.r99fe41759 · Cited by 373 · see citing works
Midbrain iron content in early Parkinson disease
Martin, W. R. W., Wieler, M., & Gee, M. (2008) · Neurology · doi:10.1212/01.wnl.0000286384.31050.b5 · Cited by 355 · see citing works
Increased iron‐related MRI contrast in the substantia nigra in Parkinson's disease
Gorell, J. M., Ordidge, R. J., Brown, G. G., Deniau, J.-C., Buderer, N. M. F., & Helpern, J. A. (1995) · Neurology · doi:10.1212/wnl.45.6.1138 · Cited by 324 · see citing works
Assessment of relative brain iron concentrations using T2‐weighted and T2*‐weighted MRI at 3 Tesla
Ordidge, R. J., Gorell, J. M., Deniau, J. C., Knight, R. A., & Helpern, J. A. (1994) · Magnetic Resonance in Medicine · doi:10.1002/mrm.1910320309 · Cited by 318 · see citing works
Cerebral atrophy and its relation to cognitive impairment in Parkinson disease
Nagano‐Saito, A., Washimi, Y., Arahata, Y., et al. (2005) · Neurology · doi:10.1212/01.wnl.0000149510.41793.50 · Cited by 284 · see citing works
The Metabolism of Neuronal Iron and Its Pathogenic Role in Neurological Disease: Review
Moos, T., & Morgan, E. H. (2004) · Annals of the New York Academy of Sciences · doi:10.1196/annals.1306.002 · Cited by 234 · see citing works
Early pathological changes in the parkinsonian brain demonstrated by diffusion tensor MRI
Yoshikawa, K. (2004) · Journal of Neurology Neurosurgery & Psychiatry · doi:10.1136/jnnp.2003.021873 · Cited by 232 · see citing works
Iron in the basal ganglia in Parkinson's disease
Griffiths, P. D., Dobson, B. R., Jones, G. R., & Clarke, D. T. (1999) · Brain · doi:10.1093/brain/122.4.667 · Cited by 229 · see citing works
The Evolution of Diagnosis in Early Parkinson Disease
Jankovic, J. J. (2000) · Archives of Neurology · doi:10.1001/archneur.57.3.369 · Cited by 229 · see citing works
Structural Brain Changes in Parkinson Disease With Dementia
Summerfield, C., Junqué, C., TOLOSA, E. S., Salgado‐Pineda, P., Gómez‐Ansón, B., Martı́, M. J., Pástor, P., Ramírez‐Ruiz, B., & Mercader, J. (2005) · Archives of Neurology · doi:10.1001/archneur.62.2.281 · Cited by 228 · see citing works
Ghaemi, M. (2002) · Journal of Neurology Neurosurgery & Psychiatry · doi:10.1136/jnnp.73.5.517 · Cited by 224 · see citing works
Brain iron deposition in Parkinson's disease imaged using the PRIME magnetic resonance sequence
Graham, J. (2000) · Brain · doi:10.1093/brain/123.12.2423 · Cited by 223 · see citing works
Supplementary and Primary Sensory Motor Area Activity in Parkinson's Disease
Rascol, O. (1992) · Archives of Neurology · doi:10.1001/archneur.1992.00530260044017 · Cited by 223 · see citing works
Self-citationCase control study of diffusion tensor imaging in Parkinson's disease
Chan, L.-L., Rumpel, H., Yap, K., Lee, E., Loo, H.-V., Ho, G.-L., Fook-Chong, S. M. C., Yuen, Y., & Tan, E.-K. (2007) · Journal of Neurology Neurosurgery & Psychiatry · doi:10.1136/jnnp.2007.121525 · Cited by 188 · see citing works
Feldmann, Á., Illés, Z., Kosztolányi, P., Illes, E., Mike, A., Kövér, F., Balás, I., Kovács, N., & Nagy, F. T. (2007) · Movement Disorders · doi:10.1002/mds.21765 · Cited by 182 · see citing works
MR evaluation of age-related increase of brain iron in young adult and older normal males
Bartzokis, G., Beckson, M., Hance, D. B., Marx, P., Foster, J., & Marder, S. R. (1997) · Magnetic Resonance Imaging · doi:10.1016/s0730-725x(96)00234-2 · Cited by 181 · see citing works
Menke, R., Scholz, J., Miller, K. L., Deoni, S., Jbabdi, S., Matthews, P. M., & Zarei, M. (2009) · NeuroImage · doi:10.1016/j.neuroimage.2009.05.017 · Cited by 175 · see citing works
Cherubini, A., Péran, P., Caltagirone, C., Sabatini, U., & Spalletta, G. (2009) · NeuroImage · doi:10.1016/j.neuroimage.2009.06.035 · Cited by 173 · see citing works
Self-citationSleepiness in Parkinson's disease: A controlled study
Brodsky, M. A., Godbold, J., Roth, T., & Olanow, C. W. (2003) · Movement Disorders · doi:10.1002/mds.10429 · Cited by 169 · see citing works
Voxel‐based morphometry detects cortical atrophy in the Parkinson variant of multiple system atrophy
Brenneis, C., Seppi, K., Schocke, M. F., Müller, J., Luginger, E., Bösch, S., Löscher, W. N., Büchel, C., Poewe, W., & Wenning, G. K. (2003) · Movement Disorders · doi:10.1002/mds.10502 · Cited by 167 · see citing works
Baudrexel, S., Nürnberger, L., Rüb, U., Seifried, C., Klein, J. C., Deller, T., Steinmetz, H., Deichmann, R., & Hilker, R. (2010) · NeuroImage · doi:10.1016/j.neuroimage.2010.03.005 · Cited by 160 · see citing works
Price, S. L., Paviour, D. C., Scahill, R. I., Stevens, J., Rossor, M. N., Lees, A. J., & Fox, N. C. (2004) · NeuroImage · doi:10.1016/j.neuroimage.2004.06.013 · Cited by 152 · see citing works
Olfactory Impairment Predicts Brain Atrophy in Parkinson's Disease: Figure 1.
Wattendorf, E., Welge–Lüssen, A., Fiedler, K., Bilecen, D., Wolfensberger, M., Fuhr, P., Hummel, T. R., & Westermann, B. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.1909-09.2009 · Cited by 152 · see citing works
Morphological differences in Parkinson’s disease with and without rest tremor
Benninger, D. H., Thees, S., Kollias, S., Bassetti, C. L., & Waldvogel, D. (2009) · Journal of Neurology · doi:10.1007/s00415-009-0092-2 · Cited by 139 · see citing works
Ramírez‐Ruiz, B., Martı́, M. J., Tolosa, E., David Bartrés-faz, A., Summerfield, C., Salgado‐Pineda, P., Gómez‐Ansón, B., & Junqué, C. (2005) · Journal of Neurology · doi:10.1007/s00415-005-0864-2 · Cited by 138 · see citing works
Hippocampal head atrophy predominance in Parkinson’s disease with hallucinations and with dementia
Ibarretxe‐Bilbao, N., Ramírez‐Ruiz, B., Tolosa, E., Martı́, M. J., Valldeoriola, F., Bargalló, N., & Junqué, C. (2008) · Journal of Neurology · doi:10.1007/s00415-008-0885-8 · Cited by 134 · see citing works
Ibarretxe‐Bilbao, N., Ramírez‐Ruiz, B., Junqué, C., Martí, M. J., Valldeoriola, F., Bargalló, N., Juanes, S., & Tolosa, E. (2009) · Journal of Neurology Neurosurgery & Psychiatry · doi:10.1136/jnnp.2009.179655 · Cited by 133 · see citing works
Frontal atrophy correlates with behavioural changes in progressive supranuclear palsy
Cordato, N. J., Pantelis, C., Halliday, G. M., Velakoulis, D., Wood, S. J., Stuart, G. W., Currie, J. N., Soo, M. Y. S., Olivieri, G., Broe, G. A., et al. (2002) · Brain · doi:10.1093/brain/awf082 · Cited by 133 · see citing works
Imaging neurodegeneration in Parkinson's disease
Pavese, N., & Brooks, D. J. (2008) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2008.10.003 · Cited by 130 · see citing works
Boska, M. D., Hasan, K. M., Kibuule, D., Banerjee, R., McIntyre, E. M., Nelson, J. A., Hahn, T., Gendelman, H. E., & Mosley, R. L. (2007) · Neurobiology of Disease · doi:10.1016/j.nbd.2007.02.010 · Cited by 128 · see citing works
Increasing striatal iron content associated with normal aging
Martin, W. R. W., Ye, F. Q., & Allen, P. S. (1998) · Movement Disorders · doi:10.1002/mds.870130214 · Cited by 122 · see citing works
Do published criteria improve clinical diagnostic accuracy in multiple system atrophy?
Osaki, Y., Ben‐Shlomo, Y., Wenning, G. K., Daniel, S. E., Hughes, A., Lees, A. J., Mathias, C. J., & Quinn, N. P. (2002) · Neurology · doi:10.1212/01.wnl.0000028690.15001.00 · Cited by 119 · see citing works
Volume and iron content in basal ganglia and thalamus
Péran, P., Cherubini, A., Luccichenti, G., Hagberg, G. E., Démonet, J., Rascol, O., Celsis, P., Caltagirone, C., Spalletta, G., & Sabatini, U. (2009) · Human Brain Mapping · doi:10.1002/hbm.20698 · Cited by 116 · see citing works
Self-citationGriffiths, P. D., & Crossman, A. R. (1993) · Dementia and Geriatric Cognitive Disorders · doi:10.1159/000107298 · Cited by 113 · see citing works
Lhermitte, J., Kraus, W. M., & McAlpine, D. (1924) · Journal of Neurology Neurosurgery & Psychiatry · doi:10.1136/jnnp.s1-5.19.195 · Cited by 103 · see citing works
Voxel‐based analysis of R2* maps in the healthy human brain
Péran, P., Hagberg, G. E., Luccichenti, G., Cherubini, A., Brainovich, V., Celsis, P., Caltagirone, C., & Sabatini, U. (2007) · Journal of Magnetic Resonance Imaging · doi:10.1002/jmri.21204 · Cited by 88 · see citing works
Self-citationMagnetic field correlation imaging
Jensen, J. H., Chandra, R., Ramani, A., Lu, H., Johnson, G., Lee, P., Kaczynski, K., & Helpern, J. A. (2006) · Magnetic Resonance in Medicine · doi:10.1002/mrm.20907 · Cited by 85 · see citing works
Characterization of white matter fiber bundles with T relaxometry and diffusion tensor imaging
Cherubini, A., Péran, P., Hagberg, G. E., Varsi, A. E., Luccichenti, G., Caltagirone, C., Sabatini, U., & Spalletta, G. (2009) · Magnetic Resonance in Medicine · doi:10.1002/mrm.21978 · Cited by 70 · see citing works
Self-citationChanges in diagnosis with follow-up in an incident cohort of patients with parkinsonism
Caslake, R., Moore, J. N., Gordon, J. C., Harris, C. E., & Counsell, C. E. (2008) · Journal of Neurology Neurosurgery & Psychiatry · doi:10.1136/jnnp.2008.144501 · Cited by 69 · see citing works
Anatomy of the Substantia Nigra and Subthalamic Nucleus on MR Imaging
Massey, L. A., & Yousry, T. A. (2009) · Neuroimaging Clinics of North America · doi:10.1016/j.nic.2009.10.001 · Cited by 53 · see citing works
Transcranial ultrasound as a risk marker for Parkinson's disease
Berg, D. (2009) · Movement Disorders · doi:10.1002/mds.22540 · Cited by 39 · see citing works
Popolizio, T., Pollice, S., & Scarabino, T. (2017) · Springer eBooks · doi:10.1007/978-3-319-44174-0 · Cited by 11 · see citing works
High-Field Neuroimaging in Parkinson’s Disease
Péran, P., Luccichenti, G., Cherubini, A., et al. (2006) · Springer eBooks · doi:10.1007/3-540-31776-7_16 · Cited by 8 · see citing works
Self-citationIncreased activity of surviving locus ceruleus neurons in Alzheimer's disease
Moser (1999) · Pure Amsterdam UMC · doi:10.1002/1531-8249(199901)45:1
Flagged first, then by citations
Research works printed but not linked: 2
- Lehermitte JKW, McAlpine MA. On the occurrence of abnormal deposits of iron in the brain in Parkinson's disease with special reference to its location. J Neurol Psychopathol 1924; 5: 195-208.
- Schulz JB, Skalej M, Wedekind D, Luft AR, Abele M, Voigt K, et al. Magnetic resonance imaging-based volumetry differentiates idiopathic Parkinson's syndrome from multiple system atrophy and progressive supranuclear palsy. Ann Neurol 1999; 45: 65-74.
Cited by
Sorted by citations
The role of iron in brain ageing and neurodegenerative disorders
Ward, R. J., Zucca, F. A., Duyn, J. H., Crichton, R. R., & Zecca, L. (2014) · The Lancet Neurology · doi:10.1016/s1474-4422(14)70117-6 · Cited by 1,819 · see citing works
Obeso, J. A., Stamelou, M., Goetz, C. G., Poewe, W., Lang, A. E., Weintraub, D., Burn, D., Halliday, G. M., Bezard, E., Przedborski, S., et al. (2017) · Movement Disorders · doi:10.1002/mds.27115 · Cited by 859 · see citing works
Functional network disruption in the degenerative dementias
Pievani, M., de Haan, W., Wu, T., Seeley, W. W., & Frisoni, G. B. (2011) · The Lancet Neurology · doi:10.1016/s1474-4422(11)70158-2 · Cited by 481 · see citing works
Neurite orientation dispersion and density imaging (NODDI) and free‐water imaging in Parkinsonism
Mitchell, T., Archer, D. B., Chu, W. T., Coombes, S. A., Lai, S., Wilkes, B. J., McFarland, N. R., Okun, M. S., Black, M. L., Herschel, E., et al. (2019) · Human Brain Mapping · doi:10.1002/hbm.24760 · Cited by 118 · see citing works
Surova, Y., Lampinen, B., Nilsson, M., Lätt, J., Hall, S., Widner, H., study, S. B., van Westen, D., & Hansson, O. (2016) · PLOS ONE · doi:10.1371/journal.pone.0157755 · Cited by 51 · see citing works
Dopaminergic system and dream recall: an MRI study in Parkinson's disease patients
De Gennaro, L., Lanteri, O., Piras, F., Scarpelli, S., Assogna, F., Ferrara, M., Caltagirone, C., & Spalletta, G. (2016) · Human Brain Mapping · doi:10.1002/hbm.23095 · Cited by 45 · see citing works
Self-citationWorking memory training impacts the mean diffusivity in the dopaminergic system
Takeuchi, H., Taki, Y., Nouchi, R., Hashizume, H., Sekiguchi, A., Kotozaki, Y., Nakagawa, S., Miyauchi, C. M., Sassa, Y., & Kawashima, R. (2015) · Brain Structure and Function · doi:10.1007/s00429-014-0845-2 · Cited by 35 · see citing works
Gröger, A., & Berg, D. (2012) · Journal of Neural Transmission · doi:10.1007/s00702-012-0873-0 · Cited by 34 · see citing works
- Authors
- Péran, P., Cherubini, A., Assogna, F., Piras, F., Quattrocchi, C., Peppe, A., Celsis, P., Rascol, O., Démonet, J.-F., Stefani, A., Pierantozzi, M., Pontieri, F. E., Caltagirone, C., Spalletta, G., & Sabatini, U.
- Affiliations
- Université Toulouse III - Paul Sabatier (FR)
- Fondazione Santa Lucia (IT)
- University of Rome Tor Vergata (IT)
- Sapienza University of Rome (IT)
- ORCID
- Venue
- Brain
- Publisher
- Oxford University Press (OUP)
- Published
- 2010-08-23
- Volume
- 133
- Issue
- 11
- Pages
- 3423-3433
- ISSN
- 0006-8950 (ISSN-L)
- 1460-2156
- OpenAlex
- W2133955737
- Cited by
- 399
- References
- 60
- Citations by year
- 2026: 2 · 2025: 10 · 2024: 15 · 2023: 14 · 2022: 18 · 2021: 26 · 2020: 26 · 2019: 29 · 2018: 30 · 2017: 37 · 2016: 35 · 2015: 37 · 2014: 26 · 2013: 42 · 2012: 30
- FWCI
- 17.53
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Brain (publishedVersion)
- PubMed (publishedVersion)
- HAL (submittedVersion)
- Cineca Institutional Research Information System (Tor Vergata University) (submittedVersion)
- IRIS Research product catalog (Sapienza University of Rome) (submittedVersion)
- Institutional Research Information System (Università degli Studi di Trento) (submittedVersion)
- Funders
- Institut National de la Santé et de la Recherche Médicale
- Ministero della Salute
- Direction de l’hospitalisation et de l’offre de Soins
- Topics
- Health Sciences › Medicine › Neurology › Parkinson's Disease Mechanisms and Treatments
- Health Sciences › Medicine › Radiology, Nuclear Medicine and Imaging › Advanced MRI Techniques and Applications
- Health Sciences › Medicine › Neurology › Neurological disorders and treatments
- Keywords
- Parkinson's disease, nigrostriatal pathway, R2* mapping, iron accumulation, diffusion tensor imaging, fractional anisotropy, mean diffusivity, substantia nigra, putamen, caudate nucleus, thalamus, red nucleus, globus pallidus, basal ganglia, subcortical gray matter, diagnostic biomarkers, voxel-based analysis
- MeSH terms
- Aged, Corpus Striatum, Female, Humans, Magnetic Resonance Imaging, Male, Middle Aged, Parkinson Disease, Substantia Nigra, Biomarkers
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review