Neuroimaging Of Ataxias

dc.creatorD' Abreu A.
dc.creatorCendes F.
dc.date2013
dc.date2015-06-25T19:09:17Z
dc.date2015-11-26T15:07:19Z
dc.date2015-06-25T19:09:17Z
dc.date2015-11-26T15:07:19Z
dc.date.accessioned2018-03-28T22:17:44Z
dc.date.available2018-03-28T22:17:44Z
dc.identifier
dc.identifierCurrent Clinical Neurology. Humana Press Inc., v. 44, n. , p. 227 - 245, 2013.
dc.identifier15590585
dc.identifier10.1007/978-1-62703-471-5_14
dc.identifierhttp://www.scopus.com/inward/record.url?eid=2-s2.0-84897396514&partnerID=40&md5=6f08cd6cf602243cbb57d769e0792602
dc.identifierhttp://www.repositorio.unicamp.br/handle/REPOSIP/88267
dc.identifierhttp://repositorio.unicamp.br/jspui/handle/REPOSIP/88267
dc.identifier2-s2.0-84897396514
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/1257428
dc.descriptionAtaxia is characterized by incoordination of movement and loss of equilibrium. The role of imaging studies in the differential diagnosis of ataxias is fundamental, and it is considered by most the main first evaluation in order to exclude symptomatic ataxias. In contrast, in progressive ataxias that include both hereditary and sporadic degenerative ataxias, neuroimaging studies play a dual role: they may assist in the diagnosis at times, but more importantly, they are essential research tools in the discovery of surrogate markers of disease progression and a better understanding of disease pathophysiology.
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dc.descriptionKlockgether, T., Sporadic ataxia with adult onset: Classification and diagnostic criteria (2010) Lancet Neurol, 9, pp. 94-104
dc.descriptionAbele, M., Burk, K., Schols, L., The aetiology of sporadic adult-onset ataxia (2002) Brain, 125, pp. 961-968
dc.descriptionWhaley, N.R., Fujioka, S., Wszolek, Z.K., Autosomal dominant cerebellar ataxia type I: A review of the phenotypic and genotypic characteristics (2011) Orphanet J Rare Dis, 6, p. 33
dc.descriptionDegardin, A., Dobbelaere, D., Vuillaume, I., Spinocerebellar ataxia: A rational approach to aetiological diagnosis (2012) Cerebellum, 11 (1), pp. 289-299
dc.descriptionBrusse, E., Maat-Kievit, J.A., van Swieten, J.C., Diagnosis and management of early- and late-onset cerebellar ataxia (2007) Clin Genet, 71, pp. 12-24
dc.descriptionKöllensperger, M., Wenning, G.K., Assessing disease progression with MRI in atypical parkinsonian disorders (2009) Mov Disord, 24, pp. S699-S702
dc.descriptionPaulson, H.L., The spinocerebellar ataxias (2009) J Neuroophthalmol, 29, pp. 227-237
dc.descriptionViau, M., Boulanger, Y., Characterization of ataxias with magnetic resonance imaging and spectroscopy (2004) Parkinsonism Relat Disord, 10, pp. 335-351
dc.descriptionDöhlinger, S., Hauser, T.-K., Borkert, J., Luft, A., Schulz, J., Magnetic resonance imaging in spinocerebellar ataxias (2008) Cerebellum, 7, pp. 204-214
dc.descriptionOrmerod, I.E., Harding, A.E., Miller, D.H., Magnetic resonance imaging in degenerative ataxic disorders (1994) J Neurol Neurosurg Psychiatry, 57, pp. 51-57
dc.descriptionNagaoka, U., Suzuki, Y., Kawanami, T., Regional differences in genetic subgroup frequency in hereditary cerebellar ataxia, and a morphometrical study of brain MR images in SCA1, MJD and SCA6 (1999) J Neurol Sci, 164, pp. 187-194
dc.descriptionMurata, Y., Kawakami, H., Yamaguchi, S., Characteristic magnetic resonance imaging findings in spinocerebellar ataxia 6 (1998) Arch Neurol, 55, pp. 1348-1352
dc.descriptionMurata, Y., Yamaguchi, S., Kawakami, H., Characteristic magnetic resonance imaging findings in Machado-Joseph disease (1998) Arch Neurol, 55, pp. 33-37
dc.descriptionJacobi, H., Hauser, T.-K., Giunti, P., Spinocerebellar ataxia types 1, 2, 3 and 6: The clinical spectrum of ataxia and morphometric brainstem and cerebellar findings (2012) Cerebellum, 11, pp. 1-12
dc.descriptionOnodera, O., Idezuka, J., Igarashi, S., Progressive atrophy of cerebellum and brainstem as a function of age and the size of the expandedCAGrepeats in theMJD1gene in Machado-Joseph disease (1998) Ann Neurol, 43, pp. 288-296
dc.descriptionAbe, Y., Tanaka, F., Matsumoto, M., CAGrepeat number correlates with the rate of brainstem and cerebellar atrophy in Machado-Joseph disease (1998) Neurology, 51, pp. 882-884
dc.descriptionHorimoto, Y., Matsumoto, M., Yuasa, H., Brainstem in Machado-Joseph disease: Atrophy or small size? (2008) Eur J Neurol, 15, pp. 102-105
dc.descriptionYoshizawa, T., Watanabe, M., Frusho, K., Shoji, S., Magnetic resonance imaging demonstrates differential atrophy of pontine base and tegmentum in Machado-Joseph disease (2003) J Neurol Sci, 215, pp. 45-50
dc.descriptionD'abreu, A., Franca, M.C., Yasuda, C.L., Souza, M.S.A., Lopes-Cendes, I., Cendes, F., Thalamic volume and dystonia in Machado-Joseph disease (2011) J Neuroimaging, 21, pp. e91-e93
dc.descriptionGiuffrida, S., Saponara, R., Restivo, D.A., Supratentorial atrophy in spinocerebellar ataxia type 2: MRI study of 20 patients (1999) J Neurol, 246, pp. 383-388
dc.descriptionYing, S.H.M., Choi, S.I.B., Perlman, S.L.M., Baloh, R.W.M., Zee, D.S.M., Toga, A.W.P., Pontine and cerebellar atrophy correlate with clinical disability in SCA2 (2006) Neurology, 66, pp. 424-426
dc.descriptionBang, O.Y., Lee, P.H., Kim, S.Y., Kim, H.J., Huh, K., Pontine atrophy precedes cerebellar degeneration in spinocerebellar ataxia 7: MRI-based volumetric analysis (2004) J Neurol Neurosurg Psychiatry, 75, pp. 1452-1456
dc.descriptionLukas, C., Hahn, H., Bellenberg, B., Spinal cord atrophy in spinocerebellar ataxia type 3 and 6 (2008) J Neurol, 255, pp. 1244-1249
dc.descriptionGinestroni, A., della Nave, R., Tessa, C., Brain structural damage in spinocerebellar ataxia type 1 (2008) J Neurol, 255, pp. 1153-1158
dc.descriptionD'agata, F., Caroppo, P., Boghi, A., Linking coordinative and executive dysfunctions to atrophy in spinocerebellar ataxia 2 patients (2011) Brain Struct Funct, 216, pp. 275-288
dc.descriptionD'abreu, A., França Jr., M.C., Yasuda, C.L., Campos, B.A.G., Lopes-Cendes, I., Cendes, F., Neocortical atrophy in Machado-Joseph disease: A longitudinal neuroimaging study (2011) J Neuroimaging, , doi:101111/j1552-6569201100614×2011
dc.descriptionAlcauter, S., Barrios, F.A., Diaz, R., Fernandez-Ruiz, J., Gray and white matter alterations in spinocerebellar ataxia type 7: An in vivo DTI and VBM study (2011) Neuroimage, 55, pp. 1-7
dc.descriptionReetz, K., Kleiman, A., Klein, C., CAG repeats determine brain atrophy in spinocerebellar ataxia 17: A VBM study (2011) PLoS One, 6, pp. e15125
dc.descriptionReetz, K., Lencer, R., Hagenah, J., Structural changes associated with progression of motor deficits in spinocerebellar ataxia 17 (2010) Cerebellum, 9, pp. 210-217
dc.descriptionGoel, G., Pal, P.K., Ravishankar, S., Gray matter volume deficits in spinocerebellar ataxia: An optimized voxel based morphometric study (2011) Parkinsonism Relat Disord, 17, pp. 521-527
dc.descriptionGuerrini, L., Lolli, F., Ginestroni, A., Brainstem neurodegeneration correlates with clinical dysfunction in SCA1 but not in SCA2. A quantitative volumetric, diffusion and proton spectroscopy MR study (2004) Brain, 127, pp. 1785-1795
dc.descriptionSchulz, J.B., Borkert, J., Wolf, S., Visualization, quantification and correlation of brain atrophy with clinical symptoms in spinocerebellar ataxia types 1, 3 and 6 (2010) Neuroimage, 49, pp. 158-168
dc.descriptionLukas, C., Schöls, L., Bellenberg, B., Dissociation of grey and white matter reduction in spinocerebellar ataxia type 3 and 6: A voxel-based morphometry study (2006) Neurosci Lett, 408, pp. 230-235
dc.descriptionMandelli, M.L., de Simone, T., Minati, L., Diffusion tensor imaging of spinocerebellar ataxias types 1 and 2 (2007) Am J Neuroradiol, 28, pp. 1996-2000
dc.descriptiondella Nave, R., Ginestroni, A., Tessa, C., Brain white matter damage in SCA1 and SCA2. An in vivo study using voxel-based morphometry, histogram analysis of mean diffusivity and tract-based spatial statistics (2008) Neuroimage, 43, pp. 10-19
dc.descriptionSolodkin, A., Peri, E., Chen, E., Ben-Jacob, E., Gomez, C., Loss of intrinsic organization of cerebellar networks in spinocerebellar ataxia type 1: Correlates with disease severity and duration (2011) Cerebellum, 10, pp. 218-232
dc.descriptionÖz, G., Hutter, D., Tkác, I., Neurochemical alterations in spinocerebellar ataxia type 1 and their correlations with clinical status (2010) Mov Disord, 25, pp. 1253-1261
dc.descriptionÖz, G., Iltis, I., Hutter, D., Thomas, W., Bushara, K., Gomez, C., Distinct neurochemical profiles of spinocerebellar ataxias 1, 2, 6, and cerebellar multiple system atrophy (2011) Cerebellum, 10, pp. 208-217
dc.descriptionBoesch, S.M., Schocke, M., Bürk, K., Proton magnetic resonance spectroscopic imaging reveals differences in spinocerebellar ataxia types 2 and 6 (2001) J Magn Reson Imaging, 13, pp. 553-559
dc.descriptionBoesch, S.M., Wolf, C., Seppi, K., Felber, S., Wenning, G.K., Schocke, M., Differentiation of SCA2 from MSA-C using proton magnetic resonance spectroscopic imaging (2007) J Magn Reson Imaging, 25, pp. 564-569
dc.descriptionHadjivassiliou, M., Wallis, L.I., Hoggard, N., Grünewald, R.A., Griffiths, P.D., Wilkinson, I.D., MR spectroscopy and atrophy in Gluten, Friedreich's and SCA6 ataxias (2011) Acta Neurol Scand, , doi:10.1111/j.1600-0404.2011.01620.x
dc.descriptionD'abreu, A., Franca, M., Appenzeller, S., Lopes-Cendes, I., Cendes, F., Axonal dysfunction in the deep white matter in Machado-Joseph disease (2009) J Neuroimaging, 19, pp. 9-12
dc.descriptionYabe, I., Tha, K.K., Yokota, T., Estimation of skeletal muscle energy metabolism in Machado- Joseph disease using P-31-MR spectroscopy (2011) Mov Disord, 26, pp. 165-168
dc.descriptionWullner, U., Reimold, M., Abele, M., Dopamine transporter positron emission tomography in spinocerebellar ataxias type 1, 2, 3, and 6 (2005) Arch Neurol, 62, pp. 1280-1285
dc.descriptionHonjo, K., Ohshita, T., Kawakami, H., Quantitative assessment of cerebral blood flow in genetically confirmed spinocerebellar ataxia type 6 (2004) Arch Neurol, 61, pp. 933-937
dc.descriptionEtchebehere, E.C., Cendes, F., Lopes-Cendes, I., Pereira, J.A., Lima, M.C., Sansana, C.R., Silva, C.A., Camargo, E.E., Brain single-photon emission computed tomography and magnetic resonance imaging in Machado-Joseph disease (2001) Arch Neurol, 58, pp. 1257-1263
dc.descriptionTaniwaki, T.S.T., Kobayashi, T., Kuwabara, Y., Otsuka, M., Ichiya, Y., Masuda, K., Goto, I., Positron emission tomography (PET) in Machado-Joseph disease (1997) J Neurol Sci, 145, pp. 63-67
dc.descriptionWang, P.S., Liu, R.S., Yang, B.H., Soong, B.W., Regional patterns of cerebral glucose metabolism in spinocerebellar ataxia type 2, 3 and 6-a voxel-based FDG-positron emission tomography analysis (2007) J Neurol, 254, pp. 838-845
dc.descriptionBoesch, S.M., Donnemiller, E., Müller, J., Abnormalities of dopaminergic neurotransmission in SCA2: A combined 123I-βCIT and 123I-IBZM SPECT study (2004) Mov Disord, 19, pp. 1320-1325
dc.descriptionYen, T.C., Tzen, K.Y., Chen, M.C., Dopamine transporter concentration is reduced in asymptomatic Machado-Joseph disease gene carriers (2002) J Nucl Med, 43, pp. 153-159
dc.descriptionSoong, B.W., Liu, R.S., Positron emission tomography in asymptomatic gene carriers of Machado-Joseph disease (1998) J Neurol Neurosurg Psychiatry, 64, pp. 499-504
dc.descriptionKim, J.-M., Lee, J.-Y., Kim, H.J., The wide clinical spectrum and nigrostriatal dopaminergic damage in spinocerebellar ataxia type 6 (2010) J Neurol Neurosurg Psychiatry, 81, pp. 529-532
dc.descriptionSoong, B., Liu, R., Wu, L., Lu, Y., Lee, H., Metabolic characterization of spinocerebellar ataxia type 6 (2001) Arch Neurol, 58, pp. 300-304
dc.descriptionKoeppen, A.H., Friedreich's ataxia: Pathology, pathogenesis, and molecular genetics (2011) J Neurol Sci, 303, pp. 1-12
dc.descriptionKoeppen, A., Morral, J., McComb, R., Feustel, P., The neuropathology of late-onset Friedreich's ataxia (2011) Cerebellum, 10, pp. 96-103
dc.descriptionde Michele, G., Di Salle, F., Filla, A., Magnetic resonance imaging in "typical" and "late onset" Friedreich's disease and early onset cerebellar ataxia with retained tendon reflexes (1995) Ital J Neurol Sci, 16, pp. 303-308
dc.descriptionBhidayasiri, R., Perlman, S.L., Pulst, S.M., Geschwind, D.H., Late-onset Friedreich ataxia: Phenotypic analysis, magnetic resonance imaging findings, and review of the literature (2005) Arch Neurol, 62, pp. 1865-1869
dc.descriptionAkhlaghi, H., Corben, L., Georgiou-Karistianis, N., Superior cerebellar peduncle atrophy in Friedreich's ataxia correlates with disease symptoms (2011) Cerebellum, 10, pp. 81-87
dc.descriptionFrança, M., D'abreu, A., Yasuda, C., A combined voxel-based morphometry and 1H-MRS study in patients with Friedreich's ataxia (2009) J Neurol, 256, pp. 1114-1120
dc.descriptiondella Nave, R., Ginestroni, A., Giannelli, M., Brain structural damage in Friedreich's ataxia (2008) J Neurol Neurosurg Psychiatry, 79, pp. 82-85
dc.descriptionIltis, I., Hutter, D., Bushara, K.O., 1H MR spectroscopy in Friedreich's ataxia and ataxia with oculomotor apraxia type 2 (2010) Brain Res, 1358, pp. 200-210
dc.descriptiondella Nave, R., Ginestroni, A., Tessa, C., Brain white matter tracts degeneration in Friedreich ataxia.An in vivo MRI study using tract-based spatial statistics and voxel-based morphometry (2008) Neuroimage, 40, pp. 19-25
dc.descriptionRizzo, G., Tonon, C., Valentino, M.L., Brain diffusion-weighted imaging in Friedreich's ataxia (2011) Mov Disord, 26, pp. 705-712
dc.descriptionAnheim, M., Tranchant, C., Koenig, M., The autosomal recessive cerebellar ataxias (2012) N Engl J Med, 366, pp. 636-646
dc.descriptionPalau, F., Espinos, C., Autosomal recessive cerebellar ataxias (2006) Orphanet J Rare Dis, 1, p. 47
dc.descriptionAnheim, M., Fleury, M., Monga, B., Epidemiological, clinical, paraclinical and molecular study of a cohort of 102 patients affected with autosomal recessive progressive cerebellar ataxia from Alsace, Eastern France: Implications for clinical management (2010) Neurogenetics, 11, pp. 1-12
dc.descriptionChun, H.H., Gatti, R.A., Ataxia-telangiectasia, an evolving phenotype (2004) DNA Repair, 3, pp. 1187-1196
dc.descriptionTavani, F., Zimmerman, R.A., Berry, G.T., Sullivan, K., Gatti, R., Bingham, P., Ataxia-telangiectasia: The pattern of cerebellar atrophy on MRI (2003) Neuroradiology, 45, pp. 315-319
dc.descriptionCiemins, J.J., Horowitz, A.L., Abnormal white matter signal in ataxia telangiectasia (2000) Am J Neuroradiol, 21, pp. 1483-1485
dc.descriptionWallis, L.I., Griffiths, P.D., Ritchie, S.J., Romanowski, C.A.J., Darwent, G., Wilkinson, I.D., Proton spectroscopy and imaging at 3 T in ataxia-telangiectasia (2007) Am J Neuroradiol, 28, pp. 79-83
dc.descriptionFirat, A.K., Muammer, K.H., Firat, Y., Yakinci, C., Quantitative evaluation of brain involvement in ataxia telangiectasia by diffusion weighted MR imaging (2005) Eur J Radiol, 56, pp. 192-196
dc.descriptionBerry-Kravis, E., Abrams, L., Coffey, S.M., Fragile X-associated tremor/ataxia syndrome: Clinical features, genetics, and testing guidelines (2007) Mov Disord, 22, pp. 2018-2030
dc.descriptionHashimoto, R., Javan, A.K., Tassone, F., Hagerman, R.J., Rivera, S.M., A voxel-based morphometry study of grey matter loss in fragile X-associated tremor/ataxia syndrome (2011) Brain, 134, pp. 863-878
dc.descriptionAdams, J.S., Adams, P.E., Nguyen, D., Volumetric brain changes in females with fragile X-associated tremor/ataxia syndrome (FXTAS) (2007) Neurology, 69, pp. 851-859
dc.descriptionHashimoto, R.-I., Srivastava, S., Tassone, F., Hagerman, R.J., Rivera, S.M., Diffusion tensor imaging in male premutation carriers of the fragile X mental retardation gene (2011) Mov Disord, 26, pp. 1329-1336
dc.descriptionHashimoto, R., Backer, K.C., Tassone, F., Hagerman, R.J., Rivera, S.M., An fMRI study of the prefrontal activity during the performance of a working memory task in premutation carriers of the fragile X mental retardation 1 gene with and without fragile X-associated tremor/ataxia syndrome (FXTAS) (2011) J Psychiatr Res, 45, pp. 36-43
dc.descriptionMartin, M.-H., Bouchard, J.-P., Sylvain, M., St-Onge, O., Truchon, S., Autosomal recessive spastic ataxia of Charlevoix-Saguenay: A report of MR imaging in 5 Patients (2007) Am J Neuroradiol, 28, pp. 1606-1608
dc.descriptionGazulla, J., Vela, A.C., Marín, M.A., Is the ataxia of Charlevoix-Saguenay a developmental disease? (2011) Med Hypotheses, 77, pp. 347-352
dc.descriptionShimazaki, H., Takiyama, Y., Honda, J., Middle cerebellar peduncles and pontine T2 hypointensities in ARSACS (2013) J Neuroimaging, 23 (1), pp. 82-85
dc.descriptionAnheim, M., Monga, B., Fleury, M., Ataxia with oculomotor apraxia type 2: Clinical, biological and genotype/phenotype correlation study of a cohort of 90 patients (2009) Brain, 132, pp. 2688-2698
dc.descriptionWenning, G.K., Litvan, I., Tolosa, E., Milestones in atypical and secondary Parkinsonisms (2011) Mov Disord, 26, pp. 1083-1095
dc.descriptionJuh, R., Pae, C.-U., Lee, C.-U., Voxel based comparison of glucose metabolism in the differential diagnosis of the multiple system atrophy using statistical parametric mapping (2005) Neurosci Res, 52, pp. 211-219
dc.descriptionPaviour, D.C., Price, S.L., Jahanshahi, M., Lees, A.J., Fox, N.C., Regional brain volumes distinguish PSP, MSA-P, and PD: MRI-based clinico-radiological correlations (2006) Mov Disord, 21, pp. 989-996
dc.descriptionNicoletti, G., Fera, F., Condino, F., MRImaging of middle cerebellar peduncle width: Differentiation of multiple system atrophy from Parkinson disease 1 (2006) Radiology, 239, pp. 825-830
dc.descriptionLee, J.-Y., Yun, J., Shin, C.-W., Kim, H.-J., Jeon, B., Putaminal abnormality on 3-T magnetic resonance imaging in early parkinsonism-predominant multiple system atrophy (2010) J Neurol, 257, pp. 2065-2070
dc.descriptionKwon, K.-Y., Choi, C.G., Kim, J.S., Lee, M.C., Chung, S.J., Comparison of brain MRI and 18F-FDG PET in the differential diagnosis of multiple system atrophy from Parkinson's disease (2007) Mov Disord, 22, pp. 2352-2358
dc.descriptionKwon, K.Y., Choi, C.G., Kim, J.S., Lee, M.C., Chung, S.J., Diagnostic value of brain MRI and 18F-FDG PET in the differentiation of parkinsonian type multiple system atrophy from Parkinson's disease (2008) Eur J Neurol, 15, pp. 1043-1049
dc.descriptionBlain, C.R.V.M., Barker, G.J.P., Jarosz, J.M.M., Measuring brain stem and cerebellar damage in parkinsonian syndromes using diffusion tensor MRI (2006) Neurology, 67, pp. 2199-2205
dc.descriptionWatanabe, H., Saito, Y., Terao, S., Progression and prognosis in multiple system atrophy (2002) Brain, 125, pp. 1070-1083
dc.descriptionMarrannes, J., Mulleners, E., Hot cross bun sign in a patient with SCA-2 (2009) JBR-BTR, 92, p. 263
dc.descriptionLee, Y.C., Liu, C.S., Wu, H.M., Wang, P.S., Chang, M.H., Soong, B.W., The 'hot cross bun' sign in the patients with spinocerebellar ataxia (2009) Eur J Neurol, 16, pp. 513-516
dc.descriptionMinnerop, M., Specht, K., Ruhlmann, J., Voxel-based morphometry and voxel-based relaxometry in multiple system atrophy-a comparison between clinical subtypes and correlations with clinical parameters (2007) Neuroimage, 36, pp. 1086-1095
dc.descriptionPellecchia, M.T., Barone, P., Mollica, C., Diffusion-weighted imaging in multiple system atrophy: A comparison between clinical subtypes (2009) Mov Disord, 24, pp. 689-696
dc.descriptionWang, P.-S., Wu, H.-M., Lin, C.-P., Soong, B.-W., Use of diffusion tensor imaging to identify similarities and differences between cerebellar and Parkinsonism forms of multiple system atrophy (2011) Neuroradiology, 53, pp. 471-481
dc.descriptionBhattacharya, K., Saadia, D., Eisenkraft, B., Brain magnetic resonance imaging in multiplesystem atrophy and Parkinson disease: A diagnostic algorithm (2002) Arch Neurol, 59, pp. 835-842
dc.descriptionKanazawa, M., Shimohata, T., Terajima, K., Quantitative evaluation of brainstem involvement in multiple system atrophy by diffusion-weighted MR imaging (2004) J Neurol, 251, pp. 1121-1124
dc.descriptionBrenneis, C., Boesch, S.M., Egger, K.E., Cortical atrophy in the cerebellar variant of multiple system atrophy: A voxel-based morphometry study (2006) Mov Disord, 21, pp. 159-165
dc.descriptionHauser, T.-K., Luft, A., Skalej, M., Visualization and quantification of disease progression in multiple system atrophy (2006) Mov Disord, 21, pp. 1674-1681
dc.descriptionSpecht, K., Minnerop, M., Abele, M., Reul, J., Wullner, U., Klockgether, T., In vivo voxel-based morphometry in multiple system atrophy of the cerebellar type (2003) Arch Neurol, 60, pp. 1431-1435
dc.descriptionTha, K.K., Terae, S., Yabe, I., Microstructural white matter abnormalities of multiple system atrophy: In vivo topographic illustration by using diffusion-tensor MR imaging (2010) Radiology, 255, pp. 563-569
dc.descriptionShiga, K., Yamada, K., Yoshikawa, K., Mizuno, T., Nishimura, T., Nakagawa, M., Local tissue anisotropy decreases in cerebellopetal fibers and pyramidal tract in multiple system atrophy (2005) J Neurol, 252, pp. 589-596
dc.descriptionTakado, Y., Igarashi, H., Terajima, K., Brainstem metabolites in multiple system atrophy of cerebellar type: 3.0-T magnetic resonance spectroscopy study (2011) Mov Disord, 26, pp. 1297-1302
dc.languageen
dc.publisherHumana Press Inc.
dc.relationCurrent Clinical Neurology
dc.rightsfechado
dc.sourceScopus
dc.titleNeuroimaging Of Ataxias
dc.typeArtículos de revistas


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