Tract-specific damage at spinal cord level in pure hereditary spastic paraplegia type 4: a diffusion tensor imaging study
Background SPG4 is a subtype of hereditary spastic paraplegia (HSP), an upper motor neuron disorder characterized by axonal degeneration of the corticospinal tracts and the fasciculus gracilis. The few neuroimaging studies that have focused on the spinal cord in HSP are based mainly on the analysis...
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Published in | Journal of neurology Vol. 269; no. 6; pp. 3189 - 3203 |
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Main Authors | , , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Berlin/Heidelberg
Springer Berlin Heidelberg
01.06.2022
Springer Nature B.V |
Subjects | |
Online Access | Get full text |
ISSN | 0340-5354 1432-1459 1432-1459 |
DOI | 10.1007/s00415-021-10933-8 |
Cover
Abstract | Background
SPG4 is a subtype of hereditary spastic paraplegia (HSP), an upper motor neuron disorder characterized by axonal degeneration of the corticospinal tracts and the fasciculus gracilis. The few neuroimaging studies that have focused on the spinal cord in HSP are based mainly on the analysis of structural characteristics.
Methods
We assessed diffusion-related characteristics of the spinal cord using diffusion tensor imaging (DTI), as well as structural and shape-related properties in 12 SPG4 patients and 14 controls. We used linear mixed effects models up to T3 in order to analyze the global effects of 'group' and 'clinical data' on structural and diffusion data. For DTI, we carried out a region of interest (ROI) analysis in native space for the whole spinal cord, the anterior and lateral funiculi, and the dorsal columns. We also performed a voxelwise analysis of the spinal cord to study local diffusion-related changes.
Results
A reduced cross-sectional area was observed in the cervical region of SPG4 patients, with significant anteroposterior flattening. DTI analyses revealed significantly decreased fractional anisotropy (FA) and increased radial diffusivity at all the cervical and thoracic levels, particularly in the lateral funiculi and dorsal columns. The FA changes in SPG4 patients were significantly related to disease severity, measured as the Spastic Paraplegia Rating Scale score.
Conclusions
Our results in SPG4 indicate tract-specific axonal damage at the level of the cervical and thoracic spinal cord. This finding is correlated with the degree of motor disability. |
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AbstractList | SPG4 is a subtype of hereditary spastic paraplegia (HSP), an upper motor neuron disorder characterized by axonal degeneration of the corticospinal tracts and the fasciculus gracilis. The few neuroimaging studies that have focused on the spinal cord in HSP are based mainly on the analysis of structural characteristics.BACKGROUNDSPG4 is a subtype of hereditary spastic paraplegia (HSP), an upper motor neuron disorder characterized by axonal degeneration of the corticospinal tracts and the fasciculus gracilis. The few neuroimaging studies that have focused on the spinal cord in HSP are based mainly on the analysis of structural characteristics.We assessed diffusion-related characteristics of the spinal cord using diffusion tensor imaging (DTI), as well as structural and shape-related properties in 12 SPG4 patients and 14 controls. We used linear mixed effects models up to T3 in order to analyze the global effects of 'group' and 'clinical data' on structural and diffusion data. For DTI, we carried out a region of interest (ROI) analysis in native space for the whole spinal cord, the anterior and lateral funiculi, and the dorsal columns. We also performed a voxelwise analysis of the spinal cord to study local diffusion-related changes.METHODSWe assessed diffusion-related characteristics of the spinal cord using diffusion tensor imaging (DTI), as well as structural and shape-related properties in 12 SPG4 patients and 14 controls. We used linear mixed effects models up to T3 in order to analyze the global effects of 'group' and 'clinical data' on structural and diffusion data. For DTI, we carried out a region of interest (ROI) analysis in native space for the whole spinal cord, the anterior and lateral funiculi, and the dorsal columns. We also performed a voxelwise analysis of the spinal cord to study local diffusion-related changes.A reduced cross-sectional area was observed in the cervical region of SPG4 patients, with significant anteroposterior flattening. DTI analyses revealed significantly decreased fractional anisotropy (FA) and increased radial diffusivity at all the cervical and thoracic levels, particularly in the lateral funiculi and dorsal columns. The FA changes in SPG4 patients were significantly related to disease severity, measured as the Spastic Paraplegia Rating Scale score.RESULTSA reduced cross-sectional area was observed in the cervical region of SPG4 patients, with significant anteroposterior flattening. DTI analyses revealed significantly decreased fractional anisotropy (FA) and increased radial diffusivity at all the cervical and thoracic levels, particularly in the lateral funiculi and dorsal columns. The FA changes in SPG4 patients were significantly related to disease severity, measured as the Spastic Paraplegia Rating Scale score.Our results in SPG4 indicate tract-specific axonal damage at the level of the cervical and thoracic spinal cord. This finding is correlated with the degree of motor disability.CONCLUSIONSOur results in SPG4 indicate tract-specific axonal damage at the level of the cervical and thoracic spinal cord. This finding is correlated with the degree of motor disability. SPG4 is a subtype of hereditary spastic paraplegia (HSP), an upper motor neuron disorder characterized by axonal degeneration of the corticospinal tracts and the fasciculus gracilis. The few neuroimaging studies that have focused on the spinal cord in HSP are based mainly on the analysis of structural characteristics. We assessed diffusion-related characteristics of the spinal cord using diffusion tensor imaging (DTI), as well as structural and shape-related properties in 12 SPG4 patients and 14 controls. We used linear mixed effects models up to T3 in order to analyze the global effects of 'group' and 'clinical data' on structural and diffusion data. For DTI, we carried out a region of interest (ROI) analysis in native space for the whole spinal cord, the anterior and lateral funiculi, and the dorsal columns. We also performed a voxelwise analysis of the spinal cord to study local diffusion-related changes. A reduced cross-sectional area was observed in the cervical region of SPG4 patients, with significant anteroposterior flattening. DTI analyses revealed significantly decreased fractional anisotropy (FA) and increased radial diffusivity at all the cervical and thoracic levels, particularly in the lateral funiculi and dorsal columns. The FA changes in SPG4 patients were significantly related to disease severity, measured as the Spastic Paraplegia Rating Scale score. Our results in SPG4 indicate tract-specific axonal damage at the level of the cervical and thoracic spinal cord. This finding is correlated with the degree of motor disability. BackgroundSPG4 is a subtype of hereditary spastic paraplegia (HSP), an upper motor neuron disorder characterized by axonal degeneration of the corticospinal tracts and the fasciculus gracilis. The few neuroimaging studies that have focused on the spinal cord in HSP are based mainly on the analysis of structural characteristics.MethodsWe assessed diffusion-related characteristics of the spinal cord using diffusion tensor imaging (DTI), as well as structural and shape-related properties in 12 SPG4 patients and 14 controls. We used linear mixed effects models up to T3 in order to analyze the global effects of 'group' and 'clinical data' on structural and diffusion data. For DTI, we carried out a region of interest (ROI) analysis in native space for the whole spinal cord, the anterior and lateral funiculi, and the dorsal columns. We also performed a voxelwise analysis of the spinal cord to study local diffusion-related changes.ResultsA reduced cross-sectional area was observed in the cervical region of SPG4 patients, with significant anteroposterior flattening. DTI analyses revealed significantly decreased fractional anisotropy (FA) and increased radial diffusivity at all the cervical and thoracic levels, particularly in the lateral funiculi and dorsal columns. The FA changes in SPG4 patients were significantly related to disease severity, measured as the Spastic Paraplegia Rating Scale score.ConclusionsOur results in SPG4 indicate tract-specific axonal damage at the level of the cervical and thoracic spinal cord. This finding is correlated with the degree of motor disability. Background SPG4 is a subtype of hereditary spastic paraplegia (HSP), an upper motor neuron disorder characterized by axonal degeneration of the corticospinal tracts and the fasciculus gracilis. The few neuroimaging studies that have focused on the spinal cord in HSP are based mainly on the analysis of structural characteristics. Methods We assessed diffusion-related characteristics of the spinal cord using diffusion tensor imaging (DTI), as well as structural and shape-related properties in 12 SPG4 patients and 14 controls. We used linear mixed effects models up to T3 in order to analyze the global effects of 'group' and 'clinical data' on structural and diffusion data. For DTI, we carried out a region of interest (ROI) analysis in native space for the whole spinal cord, the anterior and lateral funiculi, and the dorsal columns. We also performed a voxelwise analysis of the spinal cord to study local diffusion-related changes. Results A reduced cross-sectional area was observed in the cervical region of SPG4 patients, with significant anteroposterior flattening. DTI analyses revealed significantly decreased fractional anisotropy (FA) and increased radial diffusivity at all the cervical and thoracic levels, particularly in the lateral funiculi and dorsal columns. The FA changes in SPG4 patients were significantly related to disease severity, measured as the Spastic Paraplegia Rating Scale score. Conclusions Our results in SPG4 indicate tract-specific axonal damage at the level of the cervical and thoracic spinal cord. This finding is correlated with the degree of motor disability. |
Author | Sobrido, María-Jesús Carmona, Susanna Grandas, Francisco Catalina, Irene Navas-Sánchez, Francisco J. Desco, Manuel Muñoz-Blanco, José L. Ordoñez-Ugalde, Andrés Marcos-Vidal, Luis Alemán-Gómez, Yasser Romero, Julia Lillo, Laura Guzmán-de-Villoria, Juan A. Fernández-Pena, Alberto de Blas, Daniel Martín Quintáns, Beatriz |
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CitedBy_id | crossref_primary_10_1016_j_nicl_2022_103213 crossref_primary_10_1007_s00234_025_03543_y crossref_primary_10_1080_14737159_2022_2118048 crossref_primary_10_3390_biology13110909 |
Cites_doi | 10.1371/journal.pone.0117666 10.1002/jmri.25622 10.1016/0022-3956(75)90026-6 10.1016/j.neuroimage.2011.01.007 10.3109/21678421.2013.852589 10.1016/j.neuroimage.2008.03.061 10.3389/fneur.2020.00399 10.1212/01.wnl.0000219042.60538.92 10.3174/ajnr.A7017 10.1097/RLI.0000000000000394 10.1016/j.neuroimage.2015.10.019 10.3390/brainsci9100268 10.1093/hmg/ddl431 10.1212/01.wnl.0000228242.53336.90 10.1016/j.neuroimage.2018.09.081 10.1093/brain/awv178 10.1159/000090294 10.1136/jmg.37.10.759 10.1002/nbm.782 10.1007/s00415-020-10387-4 10.1001/jamaneurol.2013.1956 10.1002/ana.24641 10.1007/s002340050495 10.3389/fnins.2020.00325 10.1016/j.neuroimage.2012.06.081 10.1016/j.neuroimage.2014.01.060 10.1111/j.1440-1789.2005.00620.x 10.1002/ana.25571 10.1016/j.ejpn.2016.02.001 10.3174/ajnr.A1483 10.1093/jnen/62.11.1166 10.1155/2014/719520 10.1212/WNL.55.1.89 10.1016/j.neuroimage.2014.04.051 10.1136/jnnp.44.10.871 10.1016/j.neuroimage.2016.08.016 10.1016/j.neuroimage.2019.116137 10.1016/j.neuroimage.2015.06.040 10.3389/fneur.2018.01117 10.1016/j.neuroimage.2016.10.009 10.1371/journal.pone.0224078 10.17219/acem/116754 10.1038/s42003-020-1093-z 10.1016/j.neuroimage.2017.10.041 10.1002/mrm.26054 10.1016/j.neuroimage.2005.01.028 10.1016/j.neuroimage.2011.02.014 10.1111/j.1365-2990.2004.00587.x 10.1007/s00234-005-1415-3 10.1016/j.neuroimage.2016.06.058 |
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Keywords | Hereditary spastic paraplegia Spinal cord Corticospinal tract Diffusion tensor imaging |
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References | De Leener, Mangeat, Dupont (CR38) 2017; 46 List, Kohl, Winkler (CR7) 2019; 9 Tournier, Smith, Raffelt (CR30) 2019; 202 Andersson, Sotiropoulos (CR31) 2016; 125 Hourani, El-Hajj, Barada (CR15) 2009; 30 Lin, Zheng, Ma (CR6) 2020; 11 Song, Yoshino, Le (CR46) 2005 Wharton, McDermott, Grierson (CR50) 2003; 62 Da Graça, De Rezende, Vasconcellos (CR11) 2019; 10 Hedera, Eldevik, Maly (CR13) 2005; 47 Smith, Nichols (CR42) 2009; 44 Patzig, Bochmann, Lutz (CR22) 2019 Schüle, Holland-Letz, Klimpe (CR25) 2006; 67 Servelhere, Casseb, de Lima (CR17) 2021; 42 Branco, De Albuquerque, De Andrade (CR19) 2014 Pisharady, Eberly, Cheong (CR24) 2020 Rezende, De Albuquerque, Lamas (CR10) 2015; 10 Klawiter, Schmidt, Trinkaus (CR21) 2011 Tu, Williams, Lescher (CR48) 2016; 79 Gros, De Leener, Badji (CR35) 2019 Beaulieu (CR44) 2002 Schmitz-Hübsch, Du Montcel, Baliko (CR27) 2006; 66 Lindsey, Bushby, Lusher (CR43) 2000 Kellner, Dhital, Kiselev, Reisert (CR29) 2016; 76 Folstein, Folstein, McHugh (CR26) 1975; 12 De Leener, Kadoury, Cohen-Adad (CR34) 2014 Harding (CR1) 1981; 44 Navas-Sánchez, Fernández-Pena, Martín de Blas (CR9) 2021; 268 Wolanczyk, Bladowska, Koltowska (CR23) 2020 White, Ince, Lusher (CR4) 2000; 55 Andersson, Graham, Zsoldos, Sotiropoulos (CR32) 2016; 141 Winkler, Ridgway, Webster (CR41) 2014; 92 Solowska, Baas (CR2) 2015; 138 Krabbe, Nielsen, Fallentin (CR18) 1997; 39 Montanaro, Vavla, Frijia (CR8) 2020; 14 Veraart, Novikov, Christiaens (CR28) 2016; 142 De Leener, Fonov, Collins (CR37) 2018 Sperfeld, Baumgartner, Kassubek (CR12) 2006; 54 Kuru, Sakai, Konagaya (CR5) 2005; 25 Loureiro, Brandão, Ruano (CR14) 2013; 70 De Leener, Lévy, Dupont (CR33) 2017 Jones, Knösche, Turner (CR45) 2013 DeLuca, Ebers, Esiri (CR3) 2004; 30 Tarrade, Fassier, Courageot (CR49) 2006; 15 Masciullo, Tessa, Perazza (CR16) 2016 Kronlage, Pitarokoili, Schwarz (CR47) 2017; 52 Ullmann, Pelletier Paquette, Thong, Cohen-Adad (CR36) 2014 Moccia, Prados, Filippi (CR20) 2019 Raffelt, Tournier, Fripp (CR39) 2011; 56 Lévy, Benhamou, Naaman (CR40) 2015 B De Leener (10933_CR38) 2017; 46 DK Jones (10933_CR45) 2013 KD White (10933_CR4) 2000; 55 MF Folstein (10933_CR26) 1975; 12 EC Klawiter (10933_CR21) 2011 J List (10933_CR7) 2019; 9 B De Leener (10933_CR33) 2017 C Beaulieu (10933_CR44) 2002 M Masciullo (10933_CR16) 2016 JZ Lin (10933_CR6) 2020; 11 JL Loureiro (10933_CR14) 2013; 70 E Ullmann (10933_CR36) 2014 A Tarrade (10933_CR49) 2006; 15 K Krabbe (10933_CR18) 1997; 39 SB Wharton (10933_CR50) 2003; 62 J Veraart (10933_CR28) 2016; 142 B De Leener (10933_CR37) 2018 TJR Rezende (10933_CR10) 2015; 10 B De Leener (10933_CR34) 2014 M Patzig (10933_CR22) 2019 D Montanaro (10933_CR8) 2020; 14 LMT Branco (10933_CR19) 2014 M Moccia (10933_CR20) 2019 JLR Andersson (10933_CR32) 2016; 141 M Kronlage (10933_CR47) 2017; 52 R Schüle (10933_CR25) 2006; 67 AD Sperfeld (10933_CR12) 2006; 54 PK Pisharady (10933_CR24) 2020 AE Harding (10933_CR1) 1981; 44 D Raffelt (10933_CR39) 2011; 56 T Schmitz-Hübsch (10933_CR27) 2006; 66 JM Solowska (10933_CR2) 2015; 138 E Kellner (10933_CR29) 2016; 76 M Wolanczyk (10933_CR23) 2020 S Lévy (10933_CR40) 2015 FJ Navas-Sánchez (10933_CR9) 2021; 268 JC Lindsey (10933_CR43) 2000 C Gros (10933_CR35) 2019 S Kuru (10933_CR5) 2005; 25 AM Winkler (10933_CR41) 2014; 92 JD Tournier (10933_CR30) 2019; 202 R Hourani (10933_CR15) 2009; 30 SM Smith (10933_CR42) 2009; 44 JLR Andersson (10933_CR31) 2016; 125 P Hedera (10933_CR13) 2005; 47 KR Servelhere (10933_CR17) 2021; 42 FF Da Graça (10933_CR11) 2019; 10 TW Tu (10933_CR48) 2016; 79 SK Song (10933_CR46) 2005 GC DeLuca (10933_CR3) 2004; 30 |
References_xml | – volume: 10 year: 2015 ident: CR10 article-title: Multimodal MRI-based study in patients with SPG4 mutations publication-title: PLoS ONE doi: 10.1371/journal.pone.0117666 – volume: 46 start-page: 1209 year: 2017 end-page: 1219 ident: CR38 article-title: Topologically preserving straightening of spinal cord MRI publication-title: J Magn Reson Imaging doi: 10.1002/jmri.25622 – volume: 12 start-page: 189 year: 1975 end-page: 198 ident: CR26 article-title: “Mini-mental state”. A practical method for grading the cognitive state of patients for the clinician publication-title: J Psychiatr Res doi: 10.1016/0022-3956(75)90026-6 – year: 2011 ident: CR21 article-title: Radial diffusivity predicts demyelination in ex vivo multiple sclerosis spinal cords publication-title: Neuroimage doi: 10.1016/j.neuroimage.2011.01.007 – year: 2014 ident: CR19 article-title: Spinal cord atrophy correlates with disease duration and severity in amyotrophic lateral sclerosis publication-title: Amyotroph Lateral Scler Front Degener doi: 10.3109/21678421.2013.852589 – volume: 44 start-page: 83 year: 2009 end-page: 98 ident: CR42 article-title: Threshold-free cluster enhancement: addressing problems of smoothing, threshold dependence and localisation in cluster inference publication-title: Neuroimage doi: 10.1016/j.neuroimage.2008.03.061 – volume: 11 start-page: 399 year: 2020 ident: CR6 article-title: Cortical damage associated with cognitive and motor impairment in hereditary spastic paraplegia: evidence of a novel SPAST mutation publication-title: Front Neurol doi: 10.3389/fneur.2020.00399 – volume: 66 start-page: 1717 year: 2006 end-page: 1720 ident: CR27 article-title: Scale for the assessment and rating of ataxia: development of a new clinical scale publication-title: Neurology doi: 10.1212/01.wnl.0000219042.60538.92 – volume: 42 start-page: 610 year: 2021 end-page: 615 ident: CR17 article-title: Spinal cord gray and white matter damage in different hereditary spastic paraplegia subtypes publication-title: Am J Neuroradiol doi: 10.3174/ajnr.A7017 – volume: 52 start-page: 701 year: 2017 end-page: 707 ident: CR47 article-title: Diffusion tensor imaging in chronic inflammatory demyelinating polyneuropathy publication-title: Invest Radiol doi: 10.1097/RLI.0000000000000394 – volume: 125 start-page: 1063 year: 2016 end-page: 1078 ident: CR31 article-title: An integrated approach to correction for off-resonance effects and subject movement in diffusion MR imaging publication-title: Neuroimage doi: 10.1016/j.neuroimage.2015.10.019 – volume: 9 start-page: 268 year: 2019 ident: CR7 article-title: Ascending axonal degeneration of the corticospinal tract in pure hereditary spastic paraplegia: a cross-sectional DTI study publication-title: Brain Sci doi: 10.3390/brainsci9100268 – volume: 15 start-page: 3544 year: 2006 end-page: 3558 ident: CR49 article-title: A mutation of spastin is responsible for swellings and impairment of transport in a region of axon characterized by changes in microtubule composition publication-title: Hum Mol Genet doi: 10.1093/hmg/ddl431 – volume: 67 start-page: 430 year: 2006 end-page: 434 ident: CR25 article-title: The spastic paraplegia rating scale (SPRS): a reliable and valid measure of disease severity publication-title: Neurology doi: 10.1212/01.wnl.0000228242.53336.90 – year: 2019 ident: CR35 article-title: Automatic segmentation of the spinal cord and intramedullary multiple sclerosis lesions with convolutional neural networks publication-title: Neuroimage doi: 10.1016/j.neuroimage.2018.09.081 – volume: 138 start-page: 2471 year: 2015 end-page: 2484 ident: CR2 article-title: Hereditary spastic paraplegia SPG4: what is known and not known about the disease publication-title: Brain doi: 10.1093/brain/awv178 – volume: 54 start-page: 181 year: 2006 end-page: 185 ident: CR12 article-title: Magnetic resonance investigation of the upper spinal cord in pure and complicated hereditary spastic paraparesis publication-title: Eur Neurol doi: 10.1159/000090294 – year: 2000 ident: CR43 article-title: Mutation analysis of the spastin gene (SPG4) in patients with hereditary spastic paraparesis publication-title: J Med Genet doi: 10.1136/jmg.37.10.759 – year: 2002 ident: CR44 article-title: The basis of anisotropic water diffusion in the nervous system—a technical review publication-title: NMR Biomed doi: 10.1002/nbm.782 – volume: 268 start-page: 2429 year: 2021 end-page: 2440 ident: CR9 article-title: Thalamic atrophy in patients with pure hereditary spastic paraplegia type 4 publication-title: J Neurol doi: 10.1007/s00415-020-10387-4 – volume: 70 start-page: 481 year: 2013 end-page: 487 ident: CR14 article-title: Autosomal dominant spastic paraplegias: a review of 89 families resulting from a Portuguese survey publication-title: JAMA Neurol doi: 10.1001/jamaneurol.2013.1956 – volume: 79 start-page: 907 year: 2016 end-page: 920 ident: CR48 article-title: Radiological-pathological correlation of diffusion tensor and magnetization transfer imaging in a closed head traumatic brain injury model publication-title: Ann Neurol doi: 10.1002/ana.24641 – volume: 39 start-page: 724 year: 1997 end-page: 727 ident: CR18 article-title: MRI of autosomal dominant pure spastic paraplegia publication-title: Neuroradiology doi: 10.1007/s002340050495 – volume: 14 start-page: 325 year: 2020 ident: CR8 article-title: Multimodal MRI longitudinal assessment of white and gray matter in different SPG types of hereditary spastic paraparesis publication-title: Front Neurosci doi: 10.3389/fnins.2020.00325 – year: 2013 ident: CR45 article-title: White matter integrity, fiber count, and other fallacies: the do’s and don’ts of diffusion MRI publication-title: Neuroimage doi: 10.1016/j.neuroimage.2012.06.081 – volume: 92 start-page: 381 year: 2014 end-page: 397 ident: CR41 article-title: Permutation inference for the general linear model publication-title: Neuroimage doi: 10.1016/j.neuroimage.2014.01.060 – volume: 25 start-page: 346 year: 2005 end-page: 352 ident: CR5 article-title: Autopsy case of hereditary spastic paraplegia with thin corpus callosum showing severe gliosis in the cerebral white matter publication-title: Neuropathology doi: 10.1111/j.1440-1789.2005.00620.x – year: 2019 ident: CR20 article-title: Longitudinal spinal cord atrophy in multiple sclerosis using the generalized boundary shift integral publication-title: Ann Neurol doi: 10.1002/ana.25571 – year: 2016 ident: CR16 article-title: Hereditary spastic paraplegia: novel mutations and expansion of the phenotype variability in SPG56 publication-title: Eur J Paediatr Neurol doi: 10.1016/j.ejpn.2016.02.001 – volume: 30 start-page: 936 year: 2009 end-page: 940 ident: CR15 article-title: MR imaging findings in autosomal recessive hereditary spastic paraplegia publication-title: Am J Neuroradiol doi: 10.3174/ajnr.A1483 – volume: 62 start-page: 1166 year: 2003 end-page: 1177 ident: CR50 article-title: The cellular and molecular pathology of the motor system in hereditary spastic paraparesis due to mutation of the Spastin gene publication-title: J Neuropathol Exp Neurol doi: 10.1093/jnen/62.11.1166 – year: 2014 ident: CR36 article-title: Automatic labeling of vertebral levels using a robust template-based approach publication-title: Int J Biomed Imaging doi: 10.1155/2014/719520 – volume: 55 start-page: 89 year: 2000 end-page: 94 ident: CR4 article-title: Clinical and pathologic findings in hereditary spastic paraparesis with spastin mutation publication-title: Neurology doi: 10.1212/WNL.55.1.89 – year: 2014 ident: CR34 article-title: Robust, accurate and fast automatic segmentation of the spinal cord publication-title: Neuroimage doi: 10.1016/j.neuroimage.2014.04.051 – volume: 44 start-page: 871 year: 1981 end-page: 883 ident: CR1 article-title: Hereditary “pure” spastic paraplegia: a clinical and genetic study of 22 families publication-title: J Neurol Neurosurg Psychiatry doi: 10.1136/jnnp.44.10.871 – volume: 142 start-page: 394 year: 2016 end-page: 406 ident: CR28 article-title: Denoising of diffusion MRI using random matrix theory publication-title: Neuroimage doi: 10.1016/j.neuroimage.2016.08.016 – volume: 202 year: 2019 ident: CR30 article-title: MRtrix3: a fast, flexible and open software framework for medical image processing and visualisation publication-title: Neuroimage doi: 10.1016/j.neuroimage.2019.116137 – year: 2015 ident: CR40 article-title: White matter atlas of the human spinal cord with estimation of partial volume effect publication-title: Neuroimage doi: 10.1016/j.neuroimage.2015.06.040 – volume: 10 start-page: 1117 year: 2019 ident: CR11 article-title: Neuroimaging in hereditary spastic paraplegias: Current use and future perspectives publication-title: Front Neurol doi: 10.3389/fneur.2018.01117 – year: 2017 ident: CR33 article-title: SCT: Spinal Cord Toolbox, an open-source software for processing spinal cord MRI data publication-title: Neuroimage doi: 10.1016/j.neuroimage.2016.10.009 – year: 2019 ident: CR22 article-title: Measurement of structural integrity of the spinal cord in patients with amyotrophic lateral sclerosis using diffusion tensor magnetic resonance imaging publication-title: PLoS ONE doi: 10.1371/journal.pone.0224078 – year: 2020 ident: CR23 article-title: Diffusion tensor imaging of normal-appearing cervical spinal cords in patients with multiple sclerosis: correlations with clinical evaluation and cerebral diffusion tensor imaging changes. Preliminary experience publication-title: Adv Clin Exp Med doi: 10.17219/acem/116754 – year: 2020 ident: CR24 article-title: Tract-specific analysis improves sensitivity of spinal cord diffusion MRI to cross-sectional and longitudinal changes in amyotrophic lateral sclerosis publication-title: Commun Biol doi: 10.1038/s42003-020-1093-z – year: 2018 ident: CR37 article-title: PAM50: Unbiased multimodal template of the brainstem and spinal cord aligned with the ICBM152 space publication-title: Neuroimage doi: 10.1016/j.neuroimage.2017.10.041 – volume: 76 start-page: 1574 year: 2016 end-page: 1581 ident: CR29 article-title: Gibbs-ringing artifact removal based on local subvoxel-shifts publication-title: Magn Reson Med doi: 10.1002/mrm.26054 – year: 2005 ident: CR46 article-title: Demyelination increases radial diffusivity in corpus callosum of mouse brain publication-title: Neuroimage doi: 10.1016/j.neuroimage.2005.01.028 – volume: 56 start-page: 1171 year: 2011 end-page: 1180 ident: CR39 article-title: Symmetric diffeomorphic registration of fibre orientation distributions publication-title: Neuroimage doi: 10.1016/j.neuroimage.2011.02.014 – volume: 30 start-page: 576 year: 2004 end-page: 584 ident: CR3 article-title: The extent of axonal loss in the long tracts in hereditary spastic paraplegia publication-title: Neuropathol Appl Neurobiol doi: 10.1111/j.1365-2990.2004.00587.x – volume: 47 start-page: 730 year: 2005 end-page: 734 ident: CR13 article-title: Spinal cord magnetic resonance imaging in autosomal dominant hereditary spastic paraplegia publication-title: Neuroradiology doi: 10.1007/s00234-005-1415-3 – volume: 141 start-page: 556 year: 2016 end-page: 572 ident: CR32 article-title: Incorporating outlier detection and replacement into a non-parametric framework for movement and distortion correction of diffusion MR images publication-title: Neuroimage doi: 10.1016/j.neuroimage.2016.06.058 – year: 2015 ident: 10933_CR40 publication-title: Neuroimage doi: 10.1016/j.neuroimage.2015.06.040 – volume: 92 start-page: 381 year: 2014 ident: 10933_CR41 publication-title: Neuroimage doi: 10.1016/j.neuroimage.2014.01.060 – volume: 67 start-page: 430 year: 2006 ident: 10933_CR25 publication-title: Neurology doi: 10.1212/01.wnl.0000228242.53336.90 – year: 2013 ident: 10933_CR45 publication-title: Neuroimage doi: 10.1016/j.neuroimage.2012.06.081 – volume: 55 start-page: 89 year: 2000 ident: 10933_CR4 publication-title: Neurology doi: 10.1212/WNL.55.1.89 – year: 2011 ident: 10933_CR21 publication-title: Neuroimage doi: 10.1016/j.neuroimage.2011.01.007 – year: 2014 ident: 10933_CR34 publication-title: Neuroimage doi: 10.1016/j.neuroimage.2014.04.051 – volume: 62 start-page: 1166 year: 2003 ident: 10933_CR50 publication-title: J Neuropathol Exp Neurol doi: 10.1093/jnen/62.11.1166 – volume: 125 start-page: 1063 year: 2016 ident: 10933_CR31 publication-title: Neuroimage doi: 10.1016/j.neuroimage.2015.10.019 – volume: 25 start-page: 346 year: 2005 ident: 10933_CR5 publication-title: Neuropathology doi: 10.1111/j.1440-1789.2005.00620.x – volume: 30 start-page: 936 year: 2009 ident: 10933_CR15 publication-title: Am J Neuroradiol doi: 10.3174/ajnr.A1483 – volume: 30 start-page: 576 year: 2004 ident: 10933_CR3 publication-title: Neuropathol Appl Neurobiol doi: 10.1111/j.1365-2990.2004.00587.x – volume: 268 start-page: 2429 year: 2021 ident: 10933_CR9 publication-title: J Neurol doi: 10.1007/s00415-020-10387-4 – volume: 11 start-page: 399 year: 2020 ident: 10933_CR6 publication-title: Front Neurol doi: 10.3389/fneur.2020.00399 – volume: 141 start-page: 556 year: 2016 ident: 10933_CR32 publication-title: Neuroimage doi: 10.1016/j.neuroimage.2016.06.058 – volume: 47 start-page: 730 year: 2005 ident: 10933_CR13 publication-title: Neuroradiology doi: 10.1007/s00234-005-1415-3 – year: 2019 ident: 10933_CR35 publication-title: Neuroimage doi: 10.1016/j.neuroimage.2018.09.081 – volume: 66 start-page: 1717 year: 2006 ident: 10933_CR27 publication-title: Neurology doi: 10.1212/01.wnl.0000219042.60538.92 – volume: 10 start-page: 1117 year: 2019 ident: 10933_CR11 publication-title: Front Neurol doi: 10.3389/fneur.2018.01117 – volume: 202 year: 2019 ident: 10933_CR30 publication-title: Neuroimage doi: 10.1016/j.neuroimage.2019.116137 – volume: 15 start-page: 3544 year: 2006 ident: 10933_CR49 publication-title: Hum Mol Genet doi: 10.1093/hmg/ddl431 – volume: 10 year: 2015 ident: 10933_CR10 publication-title: PLoS ONE doi: 10.1371/journal.pone.0117666 – volume: 46 start-page: 1209 year: 2017 ident: 10933_CR38 publication-title: J Magn Reson Imaging doi: 10.1002/jmri.25622 – volume: 79 start-page: 907 year: 2016 ident: 10933_CR48 publication-title: Ann Neurol doi: 10.1002/ana.24641 – volume: 14 start-page: 325 year: 2020 ident: 10933_CR8 publication-title: Front Neurosci doi: 10.3389/fnins.2020.00325 – year: 2019 ident: 10933_CR22 publication-title: PLoS ONE doi: 10.1371/journal.pone.0224078 – volume: 12 start-page: 189 year: 1975 ident: 10933_CR26 publication-title: J Psychiatr Res doi: 10.1016/0022-3956(75)90026-6 – volume: 44 start-page: 83 year: 2009 ident: 10933_CR42 publication-title: Neuroimage doi: 10.1016/j.neuroimage.2008.03.061 – volume: 142 start-page: 394 year: 2016 ident: 10933_CR28 publication-title: Neuroimage doi: 10.1016/j.neuroimage.2016.08.016 – volume: 138 start-page: 2471 year: 2015 ident: 10933_CR2 publication-title: Brain doi: 10.1093/brain/awv178 – year: 2020 ident: 10933_CR24 publication-title: Commun Biol doi: 10.1038/s42003-020-1093-z – year: 2020 ident: 10933_CR23 publication-title: Adv Clin Exp Med doi: 10.17219/acem/116754 – year: 2014 ident: 10933_CR36 publication-title: Int J Biomed Imaging doi: 10.1155/2014/719520 – volume: 9 start-page: 268 year: 2019 ident: 10933_CR7 publication-title: Brain Sci doi: 10.3390/brainsci9100268 – year: 2005 ident: 10933_CR46 publication-title: Neuroimage doi: 10.1016/j.neuroimage.2005.01.028 – year: 2000 ident: 10933_CR43 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SPG4 is a subtype of hereditary spastic paraplegia (HSP), an upper motor neuron disorder characterized by axonal degeneration of the corticospinal... SPG4 is a subtype of hereditary spastic paraplegia (HSP), an upper motor neuron disorder characterized by axonal degeneration of the corticospinal tracts and... BackgroundSPG4 is a subtype of hereditary spastic paraplegia (HSP), an upper motor neuron disorder characterized by axonal degeneration of the corticospinal... |
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SubjectTerms | Anisotropy Dorsal columns Hereditary spastic paraplegia Image processing Magnetic resonance imaging Medicine Medicine & Public Health Neurodegeneration Neuroimaging Neurology Neuroradiology Neurosciences Original Communication Paralysis Patients Pyramidal tracts Spasticity Spinal cord Thorax |
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Title | Tract-specific damage at spinal cord level in pure hereditary spastic paraplegia type 4: a diffusion tensor imaging study |
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