Recent Cerebellum and Related Publications from Center Members:
Duvick, L., Southern, W. M., Benzow, K. A., Burch, Z. N., Handler, H. P., Mitchell, J. S., Kuivinen, H., Gadiparthi, U., Yang, P., Soles, A., Sheeler, C. A., Rainwater, O., Serres, S., Lind, E. B., Nichols-Meade, T., You, Y., O'Callaghan, B., Zoghbi, H. Y., Cvetanovic, M., Wheeler, V. C., … Orr, H. T. (2024). Mapping SCA1 regional vulnerabilities reveals neural and skeletal muscle contributions to disease. JCI insight, https://doi.org/10.1172/jci.insight.176057
Hamel, K., Moncada, E. L., Sheeler, C., Rosa, J. G., Gilliat, S., Zhang, Y., & Cvetanovic, M. (2024). Cerebellar Heterogeneity and Selective vulnerability in Spinocerebellar Ataxia Type 1 (SCA1). Neurobiology of disease, https://doi.org/10.1016/j.nbd.2024.106530
Sbrocco, K., Borgenheimer, E., Zhang, Y., Koob, M., & Cvetanovic, M. (2024). Cerebellar contribution to cognitive deficits and prefrontal cortex dysfunction in Spinocerebellar Ataxia Type 1 (SCA1). bioRxiv : the preprint server for biology, https://doi.org/10.1101/2024.07.10.602931
Soles, A., Grittner, J., Douglas, K., Yang, P., Barnett, R., Chau, C., Cosiquien, R., Duvick, L., Rainwater, O., Serres, S., Orr, H., Dougherty, B., & Cvetanovic, M. (2024). A Neural Basis for Mutant ATAXIN-1 Induced Respiratory Dysfunction in Mouse Models of Spinocerebellar Ataxia Type 1. bioRxiv : the preprint server for biology, https://doi.org/10.1101/2024.08.20.608114
Nietz, A. K., Popa, L. S., Carter, R. E., Gerhart, M. L., Manikonda, K., Ranum, L. P. W., & Ebner, T. J. (2024). Cerebral cortical functional hyperconnectivity in a mouse model of spinocerebellar ataxia type 8 (SCA8). bioRxiv : the preprint server for biology, https://doi.org/10.1101/2024.06.20.599947
Froula, J. M., Rose, J. J., Krook-Magnuson, C., & Krook-Magnuson, E. (2024). Distinct functional classes of CA1 hippocampal interneurons are modulated by cerebellar stimulation in a coordinated manner. bioRxiv : the preprint server for biology, https://doi.org/10.1101/2024.05.14.594213
Streng M. L. (2023). The bidirectional relationship between the cerebellum and seizure networks: a double-edged sword. Current opinion in behavioral sciences, https://doi.org/10.1016/j.cobeha.2023.101327
Lai, R. Y. et al (2024). Fatigue Impacts Quality of Life in People with Spinocerebellar Ataxias. Movement disorders clinical practice, https://doi.org/10.1002/mdc3.14006
Selvadurai, L. P. et al (2024). The Cerebellar Cognitive Affective/Schmahmann Syndrome Scale in Spinocerebellar Ataxias. Cerebellum (London, England), https://doi.org/10.1007/s12311-023-01651-0
Uebachs, M., Wegner, P., Schaaf, S., Kugai, S., Jacobi, H., Kuo, S. H., Ashizawa, T., Fluck, J., EUROSCA study group, ESMI study group, RISCA study group, CRC-SCA study group, SCA Registry study group, Klockgether, T., & Faber, J. (2024). SCAview: an Intuitive Visual Approach to the Integrative Analysis of Clinical Data in Spinocerebellar Ataxias. Cerebellum (London, England), https://doi.org/10.1007/s12311-023-01546-0
Petit, E. et al (2024). SARA captures disparate progression and responsiveness in spinocerebellar ataxias. Journal of neurology, https://doi.org/10.1007/s00415-024-12475-1
Abou Chaar et al(2024). Clinical, Radiological and Pathological Features of a Large American Cohort of Spinocerebellar Ataxia (SCA27B). Annals of neurology, https://doi.org/10.1002/ana.27060
Rezende, T. J. R. et al (2024). Sensitivity of Advanced Magnetic Resonance Imaging to Progression over Six Months in Early Spinocerebellar Ataxia. Movement disorders : official journal of the Movement Disorder Society, https://doi.org/10.1002/mds.29934
Wu, S., Liu, P., Cvetanovic, M., & Lin, W. (2024). Endoplasmic reticulum associated degradation preserves neurons viability by maintaining endoplasmic reticulum homeostasis. Frontiers in neuroscience, https://doi.org/10.3389/fnins.2024.1437854
Kim, L. H., Heck, D. H., & Sillitoe, R. V. (2024). Cerebellar Functions Beyond Movement and Learning. Annual review of neuroscience, https://doi.org/10.1146/annurev-neuro-100423-104943
Lee, A. S., Arefin, T. M., Gubanova, A., Stephen, D. N., Liu, Y., Lao, Z., Krishnamurthy, A., De Marco García, N. V., Heck, D. H., Zhang, J., Rajadhyaksha, A. M., & Joyner, A. L. (2024). Cerebellar output neurons impair non-motor behaviors by altering development of extracerebellar connectivity. bioRxiv : the preprint server for biology, https://doi.org/10.1101/2024.07.08.602496
Beckinghausen, J., Ortiz-Guzman, J., Lin, T., Bachman, B., Salazar Leon, L. E., Liu, Y., Heck, D. H., Arenkiel, B. R., & Sillitoe, R. V. (2024). Author Correction: The cerebellum contributes to generalized seizures by altering activity in the ventral posteromedial nucleus. Communications biology, https://doi.org/10.1038/s42003-024-05885-4
Labounek, R. et al (2024). Body size interacts with the structure of the central nervous system: A multi-center in vivo neuroimaging study. bioRxiv : the preprint server for biology, https://doi.org/10.1101/2024.04.29.591421
Rezende, T. J. R. et al (2024). Genotype-specific spinal cord damage in spinocerebellar ataxias: an ENIGMA-Ataxia study. Journal of neurology, neurosurgery, and psychiatry, https://doi.org/10.1136/jnnp-2023-332696
Tejwani, L. et al (2024). Longitudinal single-cell transcriptional dynamics throughout neurodegeneration in SCA1. Neuron, https://doi.org/10.1016/j.neuron.2023.10.039
Morrison, L. M., Huang, H., Handler, H. P., Fu, M., Bushart, D. D., Pappas, S. S., Orr, H. T., & Shakkottai, V. G. (2023). Increased intrinsic membrane excitability is associated with hypertrophic olivary degeneration in spinocerebellar ataxia type 1. bioRxiv : the preprint server for biology, https://doi.org/10.1101/2023.10.23.563657
Rezende, T. J. R. et al (2024). Genotype-specific spinal cord damage in spinocerebellar ataxias: an ENIGMA-Ataxia study. Journal of neurology, neurosurgery, and psychiatry, https://doi.org/10.1136/jnnp-2023-332696
Ferreira, M. et al(2024). Cerebellar Volumetry in Ataxias: Relation to Ataxia Severity and Duration. Cerebellum (London, England), https://doi.org/10.1007/s12311-024-01659-0
Weber, N., Buchholz, M., Rädke, A., Faber, J., Schmitz-Hübsch, T., Jacobi, H., Klockgether, T., Hoffmann, W., Michalowsky, B., EUROSCA study group, & ESMI study group (2024). Factors Influencing Health-Related Quality of Life of Patients with Spinocerebellar Ataxia. Cerebellum (London, England), https://doi.org/10.1007/s12311-024-01657-2
Rudolph, S., Badura, A., Lutzu, S., Pathak, S. S., Thieme, A., Verpeut, J. L., Wagner, M. J., Yang, Y. M., & Fioravante, D. (2023). Cognitive-Affective Functions of the Cerebellum. The Journal of neuroscience : the official journal of the Society for Neuroscience, https://doi.org/10.1523/JNEUROSCI.1451-23.2023
Adanyeguh, I. M., Joers, J. M., Deelchand, D. K., Hutter, D. H., Eberly, L. E., Guo, B., Iltis, I., Bushara, K. O., Henry, P. G., & Lenglet, C. (2023). Brain MRI detects early-stage alterations and disease progression in Friedreich ataxia. Brain communications, https://doi.org/10.1093/braincomms/fcad196
Hengel, H. et al (2023). The frequency of non-motor symptoms in SCA3 and their association with disease severity and lifestyle factors. Journal of neurology, https://doi.org/10.1007/s00415-022-11441-z
Nanclares, C., Noriega-Prieto, J. A., Labrada-Moncada, F. E., Cvetanovic, M., Araque, A., & Kofuji, P. (2023). Altered calcium signaling in Bergmann glia contributes to spinocerebellar ataxia type-1 in a mouse model of SCA1. Neurobiology of disease, https://doi.org/10.1016/j.nbd.2023.106318
Soles, A., Selimovic, A., Sbrocco, K., Ghannoum, F., Hamel, K., Moncada, E. L., Gilliat, S., & Cvetanovic, M. (2023). Extracellular Matrix Regulation in Physiology and in Brain Disease. International journal of molecular sciences, https://doi.org/10.3390/ijms24087049
Mathews, P. J., Paradis, A. L., Cvetanovic, M., Carlson, E. S., & Parker, K. L. (2023). Editorial: Unraveling the complex and multifaceted role of the cerebellum in health and disease. Frontiers in systems neuroscience, https://doi.org/10.3389/fnsys.2023.1155939
Cvetanovic, M., & Gray, M. (2023). Contribution of Glial Cells to Polyglutamine Diseases: Observations from Patients and Mouse Models. Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics, https://doi.org/10.1007/s13311-023-01357-5
Duvick, L., Southern, W. M., Benzow, K., Burch, Z. N., Handler, H. P., Mitchell, J. S., Kuivinen, H., Gadiparthi, U. K., Yang, P., Soles, A., Scheeler, C., Rainwater, O., Serres, S., Lind, E., Nichols-Meade, T., O'Callaghan, B., Zoghbi, H. Y., Cvetanovic, M., Wheeler, V. C., Ervasti, J. M., … Orr, H. T. (2023). Delineating regional vulnerability in the neurodegenerative disease SCA1 using a conditional mutant ATXN1 mouse. bioRxiv : the preprint server for biology, https://doi.org/10.1101/2023.02.08.527710
Rosa, J. G., Hamel, K., Soles, A., Sheeler, C., Borgenheimer, E., Gilliat, S., Sbrocco, K., Ghanoum, F., Handler, H. P., Forster, C., Rainwater, O., & Cvetanovic, M. (2023). BDNF is altered in a brain-region specific manner and rescues deficits in Spinocerebellar Ataxia Type 1. Neurobiology of disease, https://doi.org/10.1016/j.nbd.2023.106023
Handler, H. P., Duvick, L., Mitchell, J. S., Cvetanovic, M., Reighard, M., Soles, A., Mather, K. B., Rainwater, O., Serres, S., Nichols-Meade, T., Coffin, S. L., You, Y., Ruis, B. L., O'Callaghan, B., Henzler, C., Zoghbi, H. Y., & Orr, H. T. (2023). Decreasing mutant ATXN1 nuclear localization improves a spectrum of SCA1-like phenotypes and brain region transcriptomic profiles. Neuron, https://doi.org/10.1016/j.neuron.2022.11.017
McLoughlin, H. S., Gundry, K., Rainwater, O., Schuster, K. H., Wellik, I. G., Zalon, A. J., Benneyworth, M. A., Eberly, L. E., & Öz, G. (2023). Antisense Oligonucleotide Silencing Reverses Abnormal Neurochemistry in Spinocerebellar Ataxia 3 Mice. Annals of neurology, 94(4), 658–671. https://doi.org/10.1002/ana.26713
Deelchand, D. K., Eberly, L. E., McCarten, J. R., Hemmy, L. S., Auerbach, E. J., & Marjańska, M. (2023). Scyllo-inositol: Transverse relaxation time constant at 3 T and concentration changes associated with aging and alcohol use. NMR in biomedicine, https://doi.org/10.1002/nbm.4929
Adanyeguh, I. M., Joers, J. M., Deelchand, D. K., Hutter, D. H., Eberly, L. E., Guo, B., Iltis, I., Bushara, K. O., Henry, P. G., & Lenglet, C. (2023). Brain MRI detects early-stage alterations and disease progression in Friedreich ataxia. Brain communications, https://doi.org/10.1093/braincomms/fcad196
Pisharady, P. K., Eberly, L. E., Adanyeguh, I. M., Manousakis, G., Guliani, G., Walk, D., & Lenglet, C. (2023). Multimodal MRI improves diagnostic accuracy and sensitivity to longitudinal change in amyotrophic lateral sclerosis. Communications medicine, https://doi.org/10.1038/s43856-023-00318-5
Guo, B., Eberly, L. E., Henry, P. G., Lenglet, C., & Lock, E. F. (2023). Multiway sparse distance weighted discrimination. Journal of computational and graphical statistics, https://doi.org/10.1080/10618600.2022.2099404
Zarate, N., Gundry, K., Yu, D., Casby, J., Eberly, L. E., Öz, G., & Gomez-Pastor, R. (2023). Neurochemical correlates of synapse density in a Huntington's disease mouse model. Journal of neurochemistry, https://doi.org/10.1111/jnc.15714
Hope, J., Beckerle, T., Cheng, P. H., Viavattine, Z., Feldkamp, M., Fausner, S., Saxena, K., Ko, E., Hryb, I., Carter, R., Ebner, T., & Kodandaramaiah, S. (2023). Brain-wide neural recordings in mice navigating physical spaces enabled by a cranial exoskeleton. bioRxiv : the preprint server for biology, https://doi.org/10.1101/2023.06.04.543578
Nietz, A. K., Streng, M. L., Popa, L. S., Carter, R. E., Flaherty, E. B., Aronson, J. D., & Ebner, T. J. (2023). To be and not to be: wide-field Ca2+ imaging reveals neocortical functional segmentation combines stability and flexibility. Cerebral cortex, https://doi.org/10.1093/cercor/bhac523
West, S. L., Gerhart, M. L., & Ebner, T. J. (2023). Wide-field calcium imaging of cortical activation and functional connectivity in externally- and internally-driven locomotion. Research square, https://doi.org/10.21203/rs.3.rs-2776902/v1
Gray, M. M., Naik, A., Ebner, T. J., & Carter, R. E. (2023). Altered brain state during episodic dystonia in tottering mice decouples primary motor cortex from limb kinematics. Dystonia, https://doi.org/10.3389/dyst.2023.10974
Cramer, S. W., Haley, S. P., Popa, L. S., Carter, R. E., Scott, E., Flaherty, E. B., Dominguez, J., Aronson, J. D., Sabal, L., Surinach, D., Chen, C. C., Kodandaramaiah, S. B., & Ebner, T. J. (2023). Wide-field calcium imaging reveals widespread changes in cortical functional connectivity following mild traumatic brain injury in the mouse. Neurobiology of disease, https://doi.org/10.1016/j.nbd.2022.105943
Brændholt, M., Kluger, D. S., Varga, S., Heck, D. H., Gross, J., & Allen, M. G. (2023). Breathing in waves: Understanding respiratory-brain coupling as a gradient of predictive oscillations. Neuroscience and biobehavioral reviews, https://doi.org/10.1016/j.neubiorev.2023.105262
Beckinghausen, J., Ortiz-Guzman, J., Lin, T., Bachman, B., Salazar Leon, L. E., Liu, Y., Heck, D. H., Arenkiel, B. R., & Sillitoe, R. V. (2023). The cerebellum contributes to generalized seizures by altering activity in the ventral posteromedial nucleus. Communications biology, https://doi.org/10.1038/s42003-023-05100-w
Allen, M., Varga, S., & Heck, D. H. (2023). Respiratory rhythms of the predictive mind. Psychological review, https://doi.org/10.1037/rev0000391
Heck, D. H., Fox, M. B., Correia Chapman, B., McAfee, S. S., & Liu, Y. (2023). Cerebellar control of thalamocortical circuits for cognitive function: A review of pathways and a proposed mechanism. Frontiers in systems neuroscience, https://doi.org/10.3389/fnsys.2023.1126508
Heck, D. H., & Varga, S. (2023). "The great mixing machine": multisensory integration and brain-breath coupling in the cerebral cortex. Pflugers Archiv : European journal of physiology, https://doi.org/10.1007/s00424-022-02738-z
Adanyeguh, I. M., Henry, P. G., & Deelchand, D. K. (2023). Prospective motion correction for cervical spinal cord MRS. Magnetic resonance in medicine, https://doi.org/10.1002/mrm.29836
Öz, G., Cocozza, S., Henry, P. G., Lenglet, C., Deistung, A., Faber, J., Schwarz, A. J., Timmann, D., Van Dijk, K. R. A., Harding, I. H., & AGI Working Group on MRI Biomarkers (2023). Correction to: MR Imaging in Ataxias: Consensus Recommendations by the Ataxia Global Initiative Working Group on MRI Biomarkers. Cerebellum (London, England), https://doi.org/10.1007/s12311-023-01589-3
Rezende, T. J. R., Adanyeguh, I. M., Arrigoni, F., Bender, B., Cendes, F., Corben, L. A., Deistung, A., Delatycki, M., Dogan, I., Egan, G. F., Göricke, S. L., Georgiou-Karistianis, N., Henry, P. G., Hutter, D., Jahanshad, N., Joers, J. M., Lenglet, C., Lindig, T., Martinez, A. R. M., Martinuzzi, A., … França, M. C., Jr (2023). Progressive Spinal Cord Degeneration in Friedreich's Ataxia: Results from ENIGMA-Ataxia. Movement disorders : official journal of the Movement Disorder Society, https://doi.org/10.1002/mds.29261
Kauppinen, R. A., Thothard, J., Leskinen, H. P. P., Pisharady, P. K., Manninen, E., Kettunen, M., Lenglet, C., Gröhn, O. H. J., Garwood, M., & Nissi, M. J. (2023). Axon fiber orientation as the source of T1 relaxation anisotropy in white matter: A study on corpus callosum in vivo and ex vivo. Magnetic resonance in medicine, https://doi.org/10.1002/mrm.29667
Kauppinen, R. A., Thotland, J., Pisharady, P. K., Lenglet, C., & Garwood, M. (2023). White matter microstructure and longitudinal relaxation time anisotropy in human brain at 3 and 7 T. NMR in biomedicine, https://doi.org/10.1002/nbm.4815
Wei, C., Benzow, K., Koob, M. D., Gomez, C. M., & Du, X. (2023). The Transcription Factor, α1ACT, Acts Through a MicroRNA Network to Regulate Neurogenesis and Cell Death During Neonatal Cerebellar Development. Cerebellum (London, England), https://doi.org/10.1007/s12311-022-01431-2
Streng, M. L., Froula, J. M., & Krook-Magnuson, E. (2023). The cerebellum's understated role and influences in the epilepsies. Neurobiology of disease, https://doi.org/10.1016/j.nbd.2023.106160
Liu, M., Liu, H., Feng, F., Krook-Magnuson, E., & Dudley, S. C. (2023). TRPM7 kinase mediates hypomagnesemia-induced seizure-related death. Scientific reports, https://doi.org/10.1038/s41598-023-34789-2
Stieve, B. J., Smith, M. M., & Krook-Magnuson, E. (2023). LINCs Are Vulnerable to Epileptic Insult and Fail to Provide Seizure Control via On-Demand Activation. eNeuro, https://doi.org/10.1523/ENEURO.0195-22.2022
Thompson, L. M., & Orr, H. T. (2023). HD and SCA1: Tales from two 30-year journeys since gene discovery. Neuron, https://doi.org/10.1016/j.neuron.2023.09.036
Orr H. T. (2023). Cholecystokinin Activation of Cholecystokinin 1 Receptors: a Purkinje Cell Neuroprotective Pathway. Cerebellum (London, England), https://doi.org/10.1007/s12311-022-01428-x
Bartelt, L. C., Switonski, P. M., Adamek, G., Carvalho, J., Duvick, L. A., Jarrah, S. I., McLoughlin, H. S., Scoles, D. R., Pulst, S. M., Orr, H. T., Hull, C., Lowe, C. B., & La Spada, A. R. (2023). Purkinje-Enriched snRNA-seq in SCA7 Cerebellum Reveals Zebrin Identity Loss as a Central Feature of Polyglutamine Ataxias. bioRxiv : the preprint server for biology, https://doi.org/10.1101/2023.03.19.533345
Coffin, S. L., Durham, M. A., Nitschke, L., Xhako, E., Brown, A. M., Revelli, J. P., Villavicencio Gonzalez, E., Lin, T., Handler, H. P., Dai, Y., Trostle, A. J., Wan, Y. W., Liu, Z., Sillitoe, R. V., Orr, H. T., & Zoghbi, H. Y. (2023). Disruption of the ATXN1-CIC complex reveals the role of additional nuclear ATXN1 interactors in spinocerebellar ataxia type 1. Neuron, https://doi.org/10.1016/j.neuron.2023.02.030
Coffin, S. L., Durham, M. A., Nitschke, L., Xhako, E., Brown, A. M., Revelli, J. P., Villavicencio Gonzalez, E., Lin, T., Handler, H. P., Dai, Y., Trostle, A. J., Wan, Y. W., Liu, Z., Sillitoe, R. V., Orr, H. T., & Zoghbi, H. Y. (2023). Disruption of the ATXN1-CIC complex reveals the role of additional nuclear ATXN1 interactors in spinocerebellar ataxia type 1. Neuron, https://doi.org/10.1016/j.neuron.2022.11.016
McLoughlin, H. S., Gundry, K., Rainwater, O., Schuster, K. H., Wellik, I. G., Zalon, A. J., Benneyworth, M. A., Eberly, L. E., & Öz, G. (2023). Antisense Oligonucleotide Silencing Reverses Abnormal Neurochemistry in Spinocerebellar Ataxia 3 Mice. Annals of neurology, https://doi.org/10.1002/ana.26713
Buchholz, M., Weber, N., Rädke, A., Faber, J., Schmitz-Hübsch, T., Jacobi, H., Xie, F., Klockgether, T., Michalowsky, B., EUROSCA study group, & ESMI study group (2023). Health-Related Quality of Life in Patients with Spinocerebellar Ataxia: a Validation Study of the EQ-5D-3L. Cerebellum (London, England), https://doi.org/10.1007/s12311-023-01597-3
Mengel, D., Wellik, I. G., Schuster, K. H., Jarrah, S. I., Wacker, M., Ashraf, N. S., Öz, G., Synofzik, M., Costa, M. D. C., & McLoughlin, H. S. (2023). Blood levels of neurofilament light are associated with disease progression in a mouse model of spinocerebellar ataxia type 3. Disease models & mechanisms, https://doi.org/10.1242/dmm.050144
Peek, A. L., Rebbeck, T. J., Leaver, A. M., Foster, S. L., Refshauge, K. M., Puts, N. A., Oeltzschner, G., & MRS Expert Panel (2023). A comprehensive guide to MEGA-PRESS for GABA measurement. Analytical biochemistry, https://doi.org/10.1016/j.ab.2023.115113
Faber, J., Berger, M., Carlo, W., Hübener-Schmid, J., Schaprian, T., Santana, M. M., Grobe-Einsler, M., Onder, D., Koyak, B., Giunti, P., Garcia-Moreno, H., Gonzalez-Robles, C., Lima, M., Raposo, M., Melo, A. R. V., de Almeida, L. P., Silva, P., Pinto, M. M., van de Warrenburg, B. P., van Gaalen, J., … Klockgether, T. (2023). Stage-dependent biomarker changes in spinocerebellar ataxia type 3. medRxiv : the preprint server for health sciences, https://doi.org/10.1101/2023.04.21.23287817
Chao, O. Y., Pathak, S. S., Zhang, H., Augustine, G. J., Christie, J. M., Kikuchi, C., Taniguchi, H., & Yang, Y. M. (2023). Social memory deficit caused by dysregulation of the cerebellar vermis. Nature communications, https://doi.org/10.1038/s41467-023-41744-2
Levings, D. C., Pathak, S. S., Yang, Y. M., & Slattery, M. (2023). Limited Expression of Nrf2 in Neurons Across the Central Nervous System. bioRxiv : the preprint server for biology, https://doi.org/10.1101/2023.05.09.540014
Wang, S. Y., Yao, X., Yang, Y. M., Chen, D., Wang, R. W., & Xie, F. J. (2023). Super-rational aspiration promotes cooperation in the asymmetric game with peer exit punishment and reward. Heliyon, https://doi.org/10.1016/j.heliyon.2023.e16729
Chao, O. Y., Nikolaus, S., Yang, Y. M., & Huston, J. P. (2022). Neuronal circuitry for recognition memory of object and place in rodent models. Neuroscience and biobehavioral reviews, https://doi.org/10.1016/j.neubiorev.2022.104855
Abdelfattah AS, Ahuja S, Akkin T, et al. (2022) Neurophotonic tools for microscopic measurements and manipulation: status report. Neurophotonics. doi:10.1117/1.NPh.9.S1.013001
Joers, J. M., Adanyeguh, I. M., Deelchand, D. K., Hutter, D. H., Eberly, L. E., Iltis, I., Bushara, K. O., Lenglet, C., & Henry, P. G. (2022). Spinal cord magnetic resonance imaging and spectroscopy detect early-stage alterations and disease progression in Friedreich ataxia. Brain communications, https://doi.org/10.1093/braincomms/fcac246
Park, Y. W., Joers, J. M., Guo, B., Hutter, D., Bushara, K., Adanyeguh, I. M., Eberly, L. E., Öz, G., & Lenglet, C. (2022). Corrigendum: Assessment of cerebral and cerebellar white matter microstructure in spinocerebellar ataxias 1, 2, 3, and 6 using diffusion MRI. Frontiers in neurology, https://doi.org/10.3389/fneur.2022.1038298
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