The corpus callosum in the diagnosis of multiple sclerosis and other CNS demyelinating and inflammatory diseases

Case 39-2000

Rochester, C. L., & Kradin, R. L. (2000) · New England Journal of Medicine · doi:10.1056/nejm200012213432509 · Cited by 3,875 · see citing works

Anti-NMDA-receptor encephalitis: case series and analysis of the effects of antibodies

Dalmau, J., Gleichman, A. J., Hughes, E. G., Rossi, J. E., Peng, X., Lai, M., Dessain, S. K., Rosenfeld, M. R., Balice-Gordon, R., & Lynch, D. R. (2008) · The Lancet Neurology · doi:10.1016/s1474-4422(08)70224-2 · Cited by 3,488 · see citing works

Acute disseminated encephalomyelitis, multiphasic disseminated encephalomyelitis and multiple sclerosis in children

Dale, R. C. (2000) · Brain · doi:10.1093/brain/123.12.2407 · Cited by 703 · see citing works

Brain Abnormalities in Neuromyelitis Optica

Pittock, S. J., Lennon, V. A., Krecke, K. N., Wingerchuk, D. M., Lucchinetti, C. F., & Weinshenker, B. G. (2006) · Archives of Neurology · doi:10.1001/archneur.63.3.390 · Cited by 677 · see citing works

Histopathologic correlate of hypointense lesions on T1-weighted spin-echo MRI in multiple sclerosis

van Walderveen, M. A. A., Kamphorst, W., Scheltens, P., van Waesberghe, J. H. T. M., Ravid, R., Valk, J., Polman, C. H., & Barkhof, F. (1998) · Neurology · doi:10.1212/wnl.50.5.1282 · Cited by 656 · see citing works

Neurologic Manifestations in Primary Sjögren Syndrome

Delalande, S., Seze, J. D., Fauchais, A. L., HACHULLA, E., Stojkovic, T., Ferriby, D., Dubucquoi, S., Pruvo, J., Vermersch, P., & Hatron, P. (2004) · Medicine · doi:10.1097/01.md.0000141099.53742.16 · Cited by 642 · see citing works

Clinically mild encephalitis/encephalopathy with a reversible splenial lesion

Tada, H., Takanashi, J., Barkovich, A. J., Oba, H., Maeda, M., Tsukahara, H., Suzuki, M., Yamamoto, T., Shimono, T., Ichiyama, T., et al. (2004) · Neurology · doi:10.1212/01.wnl.0000144274.12174.cb · Cited by 554 · see citing works

Clinical and neuroradiologic features of acute disseminated encephalomyelitis in children

Hynson, J. L., Kornberg, A. J., Coleman, L. T., Shield, L. K., Harvey, A. S., & Kean, M. J. (2001) · Neurology · doi:10.1212/wnl.56.10.1308 · Cited by 536 · see citing works

Clinical and radiographic spectrum of pathologically confirmed tumefactive multiple sclerosis

Lucchinetti, C. F., Gavrilova, R. H., Metz, I., Parisi, J. E., Scheithauer, B. W., Weigand, S., Thomsen, K., Mandrekar, J., Altintas, A., Erickson, B. J., et al. (2008) · Brain · doi:10.1093/brain/awn098 · Cited by 493 · see citing works

Myelin-oligodendrocyte glycoprotein antibodies in adults with a neuromyelitis optica phenotype

Kitley, J., Woodhall, M., Waters, P., Leite, M. I., Devenney, E., Craig, J., Palace, J., & Vincent, A. (2012) · Neurology · doi:10.1212/wnl.0b013e31826aac4e · Cited by 445 · see citing works

Regional axonal loss in the corpus callosum correlates with cerebral white matter lesion volume and distribution in multiple sclerosis

Evangelou, N. (2000) · Brain · doi:10.1093/brain/123.9.1845 · Cited by 416 · see citing works

The Pathology of an Autoimmune Astrocytopathy: Lessons Learned from Neuromyelitis Optica

Lucchinetti, C. F., Guo, Y. X., Popescu, B. F. G., Fujihara, K., Itoyama, Y., & Misu, T. (2013) · Brain Pathology · doi:10.1111/bpa.12099 · Cited by 415 · see citing works

Microangiopathy of the brain and retina

Susac, J. O., Hardman, J. M., & Selhorst, J. B. (1979) · Neurology · doi:10.1212/wnl.29.3.313 · Cited by 383 · see citing works

Chronic lymphocytic inflammation with pontine perivascular enhancement responsive to steroids (CLIPPERS)

Pittock, S. J., Debruyne, J., Krecke, K. N., Giannini, C., van den Ameele, J., Herdt, V. D., McKeon, A. B., Fealey, R. D., Weinshenker, B. G., Aksamit, A. J., et al. (2010) · Brain · doi:10.1093/brain/awq164 · Cited by 372 · see citing works

MRI findings in Susac’s syndrome

Susac, J. O., Murtagh, F. R., Egan, R. A., Berger, J. R., Bakshi, R., Lincoff, N. S., Gean, A. D., Galetta, S. L., Fox, R. J., Costello, F., et al. (2003) · Neurology · doi:10.1212/01.wnl.0000103880.29693.48 · Cited by 323 · see citing works

Role of MRI in the differentiation of ADEM from MS in children

Callen, D. J. A., Shroff, M. M., Branson, H. M., Li, D. K., Lotze, T. E., Stephens, D., & Banwell, B. (2008) · Neurology · doi:10.1212/01.wnl.0000338630.20412.45 · Cited by 247 · see citing works

Distinct lesion morphology at 7-T MRI differentiates neuromyelitis optica from multiple sclerosis

Sinnecker, T., Dörr, J., Pfueller, C. F., Harms, L., Ruprecht, K., Jarius, S., Brück, W., Niendorf, T., Wuerfel, J., & Paul, F. (2012) · Neurology · doi:10.1212/wnl.0b013e3182648bc8 · Cited by 214 · see citing works

Characteristic brain magnetic resonance imaging abnormalities in central nervous system aquaporin-4 autoimmunity

Kim, W., Park, M. S., Lee, S. H., Kim, S., Jung, I. J., Takahashi, T., Misu, T., Fujihara, K., & Kim, H. J. (2010) · Multiple Sclerosis Journal · doi:10.1177/1352458510376640 · Cited by 194 · see citing works

CNS Vasculitis in Autoimmune Disease: MR Imaging Findings and Correlation with Angiography

Pomper, M. G., Miller, T. J., Stone, J. H., Tidmore, W. C., & Hellmann, D. B. (2024) · American Journal of Neuroradiology · doi:10.3174/ajnr.45-12.s76 · Cited by 193 · see citing works

Clinical Implications of Splenium Magnetic Resonance Imaging Signal Changes

Doherty, M. J., Jayadev, S., Watson, N. F., Konchada, R., & Hallam, D. K. (2005) · Archives of Neurology · doi:10.1001/archneur.62.3.433 · Cited by 187 · see citing works

Perivenous demyelination: association with clinically defined acute disseminated encephalomyelitis and comparison with pathologically confirmed multiple sclerosis

Young, N. P., Weinshenker, B. G., Parisi, J. E., Scheithauer, B. W., Giannini, C., Roemer, S. F., Thomsen, K. M., Mandrekar, J. N., Erickson, B. J., & Lucchinetti, C. F. (2010) · Brain · doi:10.1093/brain/awp321 · Cited by 186 · see citing works

Susac's Syndrome — Update

Rennebohm, R. M., Susac, J. O., Egan, R. A., & Daroff, R. B. (2010) · Journal of the Neurological Sciences · doi:10.1016/j.jns.2010.08.032 · Cited by 186 · see citing works

MRI of the corpus callosum in multiple sclerosis: association with disability

Öztürk, A., Smith, S., Gordon‐Lipkin, E. M., Harrison, D. M., Shiee, N., Pham, D., Caffo, B., Calabresi, P. A., & Reich, D. (2010) · Multiple Sclerosis Journal · doi:10.1177/1352458509353649 · Cited by 178 · see citing works

Abnormal corpus callosum: a sensitive and specific indicator of multiple sclerosis.

Gean, A. D., Vezina, L. G., Marton, K. I., Stimac, G. K., Peyster, R. G., Taveras, J. M., & Davis, K. R. (1991) · Radiology · doi:10.1148/radiology.180.1.2052698 · Cited by 177 · see citing works

Suspected multiple sclerosis: MR imaging with a thin-section fast FLAIR pulse sequence.

Hashemi, R. H. E. A., Bradley, W. G., Chen, D. Y., Jordan, J. E., Queralt, J. A., Cheng, A. E., & Henrie, J. N. (1995) · Radiology · doi:10.1148/radiology.196.2.7617868 · Cited by 174 · see citing works

Lesion morphology at 7 Tesla MRI differentiates Susac syndrome from multiple sclerosis

Wuerfel, J., Sinnecker, T., Ringelstein, E., Jarius, S., Schwindt, W., Niendorf, T., Paul, F., Kleffner, I., & Dörr, J. (2012) · Multiple Sclerosis · doi:10.1177/1352458512441270 · Cited by 165 · see citing works

The Arteries of the Corpus Callosum: A Microsurgical Anatomic Study

Türe, U., Yasargil, M. G., & Krisht, A. F. (1996) · Neurosurgery · doi:10.1097/00006123-199612000-00001 · Cited by 164 · see citing works

Tumefactive demyelination: an approach to diagnosis and management

Hardy, T. A., & Chataway, J. (2013) · Journal of Neurology Neurosurgery & Psychiatry · doi:10.1136/jnnp-2012-304498 · Cited by 164 · see citing works

Pathology, histochemistry and immunocytochemistry of lesions in acute multiple sclerosis

Adams, C. W. M., Poston, R. N., & Buk, S. J. (1989) · Journal of the Neurological Sciences · doi:10.1016/0022-510x(89)90144-5 · Cited by 163 · see citing works

“Cloud‐like enhancement” is a magnetic resonance imaging abnormality specific to neuromyelitis optica

Ito, S., Mori, M., Makino, T., Hayakawa, S., & Kuwabara, S. (2009) · Annals of Neurology · doi:10.1002/ana.21753 · Cited by 161 · see citing works

The pathological spectrum of CNS inflammatory demyelinating diseases

Hu, W., & Lucchinetti, C. (2009) · Seminars in Immunopathology · doi:10.1007/s00281-009-0178-z · Cited by 157 · see citing works

Expanding the clinical, radiological and neuropathological phenotype of chronic lymphocytic inflammation with pontine perivascular enhancement responsive to steroids (CLIPPERS)

Simon, N. G., Parratt, J. D. E., Barnett, M. H., Buckland, M. E., Gupta, R., Hayes, M. W., Masters, L. T., & Reddel, S. (2011) · Journal of Neurology Neurosurgery & Psychiatry · doi:10.1136/jnnp-2011-301054 · Cited by 151 · see citing works

Susac Syndrome

MAGRO, C. M. J., Poe, J. C., Lubow, M., & Susac, J. O. (2011) · American Journal of Clinical Pathology · doi:10.1309/ajcperi7lc4vnfyk · Cited by 140 · see citing works

Clinical, paraclinical and serological findings in Susac syndrome: an international multicenter study

Jarius, S., Kleffner, I., Dörr, J., Sastre‐Garriga, J., Illés, Z., Eggenberger, E., Chalk, C., Ringelstein, M., Aktaş, O., Montalbán, X., et al. (2014) · Journal of Neuroinflammation · doi:10.1186/1742-2094-11-46 · Cited by 130 · see citing works

A brief review of Susac syndrome

Kleffner, I., Duning, T., Lohmann, H., Deppe, M., Basel, T. J., Promesberger, J., Dörr, J., Schwindt, W., & Ringelstein, E. B. (2012) · Journal of the Neurological Sciences · doi:10.1016/j.jns.2012.05.021 · Cited by 126 · see citing works

Cerebral and corpus callosum atrophy in systemic lupus erythematosus

Appenzeller, S., Rondina, J. M., Li, L. M., Costallat, L. T. L., & Cendes, F. (2005) · Arthritis & Rheumatism · doi:10.1002/art.21271 · Cited by 126 · see citing works

Long-term Outcomes of CLIPPERS (Chronic Lymphocytic Inflammation With Pontine Perivascular Enhancement Responsive to Steroids) in a Consecutive Series of 12 Patients

Taïeb, G., Duflos, C., Renard, D., Audoin, B., Kaphan, E., Pelletier, J., Limousin, N., Tranchant, C., Kremer, S., Seze, J. D., et al. (2012) · Archives of Neurology · doi:10.1001/archneurol.2012.122 · Cited by 125 · see citing works

Multiple sclerosis and acute disseminated encephalomyelitis diagnosed in children after long‐term follow‐up: comparison of presenting features

Alper, G. P., Heyman, R. A., & WANG, L. (2009) · Developmental Medicine & Child Neurology · doi:10.1111/j.1469-8749.2008.03136.x · Cited by 123 · see citing works

The formation of inflammatory demyelinated lesions in cerebral white matter

Maggi, P., Macri, S. M. C., Gaitán, M. I., Leibovitch, E., Wholer, J. E., Knight, H. L., Ellis, M., Wu, T., Silva, A. C., Massacesi, L., et al. (2014) · Annals of Neurology · doi:10.1002/ana.24242 · Cited by 110 · see citing works

The ovoid lesion: a new MR observation in patients with multiple sclerosis.

Horowitz, A. L., Kaplan, R. D., Grewe, G., White, R. T., & Salberg, L. M. (1989) · PubMed Central · Cited by 104 · see citing works

Magnetic resonance imaging of neurosarcoidosis.

Ginat, D. T., Dhillon, G. S., & Almast, J. (2011) · Europe PMC (PubMed Central) · doi:10.4103/2156-7514.76693 · Cited by 101 · see citing works

Occurrence of acute large and edematous callosal lesions in neuromyelitis optica

Nakamura, M., Misu, T., Fujihara, K., Miyazawa, I., Nakashima, I., Takahashi, T., Watanabe, S., & Itoyama, Y. (2009) · Multiple Sclerosis Journal · doi:10.1177/1352458509103301 · Cited by 98 · see citing works

A practical approach to diagnosing adult onset leukodystrophies

Ahmed, R. M., Murphy, E., Davagnanam, I., Parton, M. J., Schott, J. M., Mummery, C. J., Rohrer, J. D., Lachmann, R., Houlden, H., Fox, N. C., et al. (2013) · Journal of Neurology Neurosurgery & Psychiatry · doi:10.1136/jnnp-2013-305888 · Cited by 95 · see citing works

Corpus callosum and subcallosal-periventricular lesions in multiple sclerosis: detection with MR.

Simon, J. H., Holtås, S., Schiffer, R. B., Rudick, R. A., Herndon, R. M., Kido, D. K., & Utz, R. (1986) · Radiology · doi:10.1148/radiology.160.2.3726114 · Cited by 93 · see citing works

Clinical and diagnostic aspects of multiple sclerosis and acute monophasic encephalomyelitis in pediatric patients: a single centre prospective study

Atzori, M., Battistella, P. A., de Perini, P., Calabrese, M., Fontanin, M., Laverda, A., Suppiej, A., Drigo, P., Grossi, P., Rinaldi, L., et al. (2008) · Multiple Sclerosis Journal · doi:10.1177/1352458508098562 · Cited by 91 · see citing works

Multiple sclerosis vs acute disseminated encephalomyelitis in childhood

Brass, S. D., Caramanos, Z., Santos, C. A. Q., Dilenge, M.-E., Lapierre, Y., & Rosenblatt, B. (2003) · Pediatric Neurology · doi:10.1016/s0887-8994(03)00235-2 · Cited by 88 · see citing works

The Magnetic Resonance Imaging Appearance of Monophasic Acute Disseminated Encephalomyelitis

Marin, S. E., & Callen, D. J. A. (2013) · Neuroimaging Clinics of North America · doi:10.1016/j.nic.2012.12.005 · Cited by 84 · see citing works

Corpus callosum atrophy is strongly associated with cognitive impairment in multiple sclerosis: Results of a 17-year longitudinal study

Granberg, T., Martola, J., Bergendal, G., Shams, S., Damangir, S., Aspelin, P., Fredrikson, S., & Wiberg, M. K. (2014) · Multiple Sclerosis Journal · doi:10.1177/1352458514560928 · Cited by 81 · see citing works

PERIVENTRICULAR LESIONS IN MULTIPLE SCLEROSIS: THEIR PERIVENOUS ORIGIN AND RELATIONSHIP TO GRANULAR EPENDYMITIS

Adams, C. W. M., Abdulla, Y. H., Torres, E. M., & Poston, R. N. (1987) · Neuropathology and Applied Neurobiology · doi:10.1111/j.1365-2990.1987.tb00177.x · Cited by 78 · see citing works

Brain magnetic resonance imaging findings in relapsing neuromyelitis optica

Cabrera-Gómez, J. A., Sotolongo, L. Q., González‐Quevedo, A., Lima, S., Real-González, Y., Cristòfol-Corominas, M., Romero-García, K., Ugarte-Sánchez, C., Jordán-González, J., de la Nuez, J. G., et al. (2007) · Multiple Sclerosis Journal · doi:10.1177/1352458506070725 · Cited by 77 · see citing works

The corpus callosum, a unique white-matter tract: anatomic features that may explain sparing in Binswanger disease and resistance to flow of fluid masses.

Moody, D. M., Bell, M. A., & CHALLA, V. R. (1989) · PubMed · Cited by 73 · see citing works

Cerebral white matter lesions in primary Sjögren's syndrome: a controlled study.

Coates, T., Slavotinek, J., Rischmueller, M., Schultz, D. W., Anderson, C. S., Dellamelva, M., Sage, M., & Gordon, T. P. (1999) · PubMed · Cited by 73 · see citing works

Conventional and Advanced Imaging in Neuromyelitis Optica

Barnett, Y., Sutton, I., Ghadiri, M., Masters, L. T., Zivadinov, R., & Barnett, M. H. (2013) · American Journal of Neuroradiology · doi:10.3174/ajnr.a3592 · Cited by 66 · see citing works

MRI findings in central nervous system systemic lupus erythematosus are associated with immunoserological parameters and hypertension

Cs�p�ny, T., Bereczki, D., Koll�r, J., Sikula, J., Kiss, E. V., & Csiba, L. (2003) · Journal of Neurology · doi:10.1007/s00415-003-0223-0 · Cited by 64 · see citing works

Brain histopathology in three cases of Susac's syndrome: implications for lesion pathogenesis and treatment: Figure 1

Hardy, T. A., O’Brien, B., Gerbis, N., Barnett, M. H., Reddel, S. W., Brewer, J. M., Herkes, G., Silberstein, P., Garsia, R. J., Watson, J. D. G., et al. (2014) · Journal of Neurology Neurosurgery & Psychiatry · doi:10.1136/jnnp-2014-308240 · Cited by 63 · see citing works

Corpus callosum index and long-term disability in multiple sclerosis patients

Yaldizli, Ö., Atefy, R., Gass, A., Sturm, D., Glassl, S., Tettenborn, B., & Putzki, N. (2010) · Journal of Neurology · doi:10.1007/s00415-010-5503-x · Cited by 63 · see citing works

Kawasaki disease complicated by mild encephalopathy with a reversible splenial lesion (MERS)

Takanashi, J., Shirai, K., Sugawara, Y., Okamoto, Y., Obonai, T., & Terada, H. (2011) · Journal of the Neurological Sciences · doi:10.1016/j.jns.2011.11.022 · Cited by 62 · see citing works

Immunopathogenesis of Neuromyelitis Optica

Levy, M., Wildemann, B., Jarius, S., Arellano, B., Sasidharan, S., Weber, M. S., & Stüve, O. (2014) · Advances in immunology · doi:10.1016/b978-0-12-800100-4.00006-4 · Cited by 61 · see citing works

Distinguishing Susac’s syndrome from multiple sclerosis

Buzzard, K. A., Reddel, S., Yiannikas, C., Riminton, S., Barnett, M. H., & Hardy, T. A. (2014) · Journal of Neurology · doi:10.1007/s00415-014-7628-9 · Cited by 52 · see citing works

Subcallosal Striations: Early Findings of Multiple Sclerosis on Sagittal, Thin-Section, Fast FLAIR MR Images

Palmer, S. L., Bradley, W. G., Chen, D.-Y., & Patel, S. (1999) · Radiology · doi:10.1148/radiology.210.1.r99ja38149 · Cited by 51 · see citing works

White matter abnormalities in primary Sjogren syndrome

Akasbi, M., Berenguer, J., Saiz, A., Brito‐Zerón, P., Pérez-De-Lis, M., Bové, A., Díaz‐Lagares, C., Retamozo, S., Blanco, Y., Pérez-Álvarez, R., et al. (2011) · QJM · doi:10.1093/qjmed/hcr218 · Cited by 49 · see citing works

An MRI review of acquired corpus callosum lesions

Renard, D., Castelnovo, G., Campello, C., Bouly, S., Floch, A. L., Thouvenot, É., Waconge, A., & Taïeb, G. (2014) · Journal of Neurology Neurosurgery & Psychiatry · doi:10.1136/jnnp-2013-307072 · Cited by 49 · see citing works

Acute Disseminated Encephalomyelitis in North Indian Children: Clinical Profile and Follow-Up

SINGHI, P. D., Ray, M., Singhi, S. C., & Khandelwal, N. (2006) · Journal of Child Neurology · doi:10.1177/08830738060210100201 · Cited by 48 · see citing works

CNS Involvement in Primary Sjögren Syndrome: Assessment of Gray and White Matter Changes With MRI and Voxel-Based Morphometry

Tzarouchi, L. C., Tsifetaki, N., Konitsiotis, S., Zikou, A. K., Astrakas, L. G., Drosos, A. A., & Argyropoulou, M. I. (2011) · American Journal of Roentgenology · doi:10.2214/ajr.10.5984 · Cited by 47 · see citing works

Neurosarcoidosis Mimicry of Multiple Sclerosis

Scott, T. F. M., Yandora, K. A., Kunschner, L. J., & Schramke, C. J. (2010) · The Neurologist · doi:10.1097/nrl.0b013e3181b287df · Cited by 47 · see citing works

Focal transient lesions of the corpus callosum in systemic lupus erythematosus

Appenzeller, S., Faria, A. V., Marini, R., Costallat, L. T. L., & Cendes, F. (2006) · Clinical Rheumatology · doi:10.1007/s10067-005-0174-1 · Cited by 46 · see citing works

Limited utility of current MRI criteria for distinguishing multiple sclerosis from common mimickers: primary and secondary CNS vasculitis, lupus and Sjogren’s syndrome

Kim, S. S., Richman, D. P., Johnson, W. O., Hald, J. K., & Agius, M. A. (2013) · Multiple Sclerosis Journal · doi:10.1177/1352458513491329 · Cited by 43 · see citing works

MR imaging findings of spinal dural involvement with Wegener granulomatosis.

Albayram, S., Kizilkilie, O., Adaletli, İ., Erdogan, N., Koçer, N., & Işlak, C. (2002) · PubMed Central · Cited by 42 · see citing works

Corpus Callosum Atrophy – A Simple Predictor of Multiple Sclerosis Progression: A Longitudinal 9-Year Study

Vaněčková, M., Kalinčík, T., Krásenský, J., Horáková, D., Havrdová, E., Hrebikova, T., & Seidl, Z. (2012) · European Neurology · doi:10.1159/000337683 · Cited by 39 · see citing works

Evaluation of Parenchymal Neuro-Behçet Disease by Using Susceptibility-Weighted Imaging

Albayram, S., Saip, S., Hasıloğlu, Z. I., Teke, M., Ceyhan, E., Tütüncü, M., Selçuk, H., Kina, A., & Sıva, A. (2011) · American Journal of Neuroradiology · doi:10.3174/ajnr.a2477 · Cited by 39 · see citing works

Cerebral and Cerebellar Volume Loss in Children and Adolescents with Systemic Lupus Erythematosus: A Review of Clinically Acquired Brain Magnetic Resonance Imaging

Muscal, E., Traipe, E., de Guzman, M. M., Myones, B. L., Brey, R. L., & Hunter, J. V. (2010) · The Journal of Rheumatology · doi:10.3899/jrheum.090983 · Cited by 38 · see citing works

Diffuse and heterogeneous T2-hyperintense lesions in the splenium are characteristic of neuromyelitis optica

Makino, T., Ito, S., Mori, M., Yonezu, T., Ogawa, Y., & Kuwabara, S. (2012) · Multiple Sclerosis Journal · doi:10.1177/1352458512454772 · Cited by 38 · see citing works

Arterial vascularization patterns of the splenium: An anatomical study

Kahiloğulları, G., Cömert, A., Özdemir, M. B., Brohi, R. A., Özgüral, O., Esmer, A. F., Egemen, N., & Karahan, S. T. (2012) · Clinical Anatomy · doi:10.1002/ca.22114 · Cited by 35 · see citing works

Neuroimaging features of acute disseminated encephalomyelitis in childhood

Richer, L. P., Sinclair, D. B., & Bhargava, R. (2004) · Pediatric Neurology · doi:10.1016/j.pediatrneurol.2004.07.004 · Cited by 30 · see citing works

Corpus Callosum Atrophy Correlates with Gray Matter Atrophy in Patients with Multiple Sclerosis

Klawiter, E. C., Ceccarelli, A., Arora, A., Jackson, J. S., Bakshi, S., Kim, G., Miller, J. R., Tauhid, S., von Gizycki, C., Bakshi, R., et al. (2014) · Journal of Neuroimaging · doi:10.1111/jon.12124 · Cited by 29 · see citing works

The ependymal "Dot-Dash" sign: an MR imaging finding of early multiple sclerosis.

Lisanti, C. J., Asbach, P., & Bradley, W. G. (2005) · PubMed Central · Cited by 25 · see citing works

A case of primary Sjögren’s syndrome presenting primarily with central nervous system vasculitic involvement

Hasıloğlu, Z. I., Albayram, S., Tasmali, K., Erer, B., Selçuk, H., & Işlak, C. (2011) · Rheumatology International · doi:10.1007/s00296-011-1824-z · Cited by 23 · see citing works

Case 24-2011

Bienfang, D. C., McKenna, M. J., Papaliodis, G. N., González, R. G., & Stemmer-Rachamimov, A. O. (2011) · New England Journal of Medicine · doi:10.1056/nejmcpc1011324 · Cited by 20 · see citing works

A clinically isolated syndrome: A challenging entity

Kurne, A., Işıkay, İ. Ç., Karlı-Oğuz, K., Kalyoncu, U., Aydın, Ö. F., Çalgünerı, M., & Karabudak, R. (2008) · Journal of Neurology · doi:10.1007/s00415-008-0882-y · Cited by 17 · see citing works

The venous vascularization of the corpus callosum in man

Wolfram-Gabel, R., & Maillot, C. (1992) · Surgical and Radiologic Anatomy · doi:10.1007/bf01628038 · Cited by 16 · see citing works

MR imaging findings of the corpus callosum region in the differentiation between multiple sclerosis and neuromyelitis optica

Chen, Z., Feng, F., Yang, Y., Li, J., & Ma, L. (2012) · European Journal of Radiology · doi:10.1016/j.ejrad.2012.02.010 · Cited by 14 · see citing works

Reversible Splenial Lesion Syndrome in Pediatric Systemic Lupus Erythematosus: Figure 1.

Soon, G. S., Rodan, L. H., Laughlin, S., Laxer, R. M., Benseler, S. M., & Silverman, E. D. (2012) · The Journal of Rheumatology · doi:10.3899/jrheum.120390 · Cited by 11 · see citing works

Pseudotumoral brain lesion as the presenting feature of primary Sjögren's syndrome

Sassi, S. B., Nabli, F., Boubaker, A., Ghorbel, I. B., Neji, S., & Hentati, F. (2014) · Journal of the Neurological Sciences · doi:10.1016/j.jns.2014.01.027 · Cited by 9 · see citing works

Magnetic Resonance Imaging Abnormalities in the Corpus Callosum of a Patient With Neuropsychiatric Lupus

Fogel, B. L., Cardenas, D., & Ovbiagele, B. I. (2006) · The Neurologist · doi:10.1097/01.nrl.0000237119.00864.d7 · Cited by 9 · see citing works

Infarction of the Corpus Callosum: A Manifestation of Giant Cell Arteritis

Lempel, J. K., Bernstein, S. L., & Kalina, P. (2011) · American Journal of Neuroradiology · doi:10.3174/ajnr.a2763 · Cited by 7 · see citing works

Acute Disseminated Encephalomyelitis and Mucocutaneous Ulcerations

Lackmann, G.-M., Lyding, S., Scherer, A., & Niehues, T. (2004) · Neuropediatrics · doi:10.1055/s-2004-820995 · Cited by 7 · see citing works

Neuro-Behçet avec atteinte du corps calleux

Maarouf, A., Hadj-Henni, L., Caucheteux, N., Renkes, C., Serre, I., Bakchine, S., & Tourbah, A. (2011) · Revue Neurologique · doi:10.1016/j.neurol.2010.10.010 · Cited by 5 · see citing works

[Clinical features and neuroimaging findings of 12 patients with acute disseminated encephalomyelitis involved in corpus callosum].

Liu, J., Qiao, W.-Y., Dong, Q., Zhang, H., Zheng, K.-H., Qian, H., & Qi, X. (2012) · PubMed · Cited by 5 · see citing works

Atypical Presentation of Neuropsychiatric Lupus With Acanthosis Nigricans

Miquel, J., Hadj-Rabia, S., Boddaert, N., Lascelles, K., & Bahi‐Buisson, N. (2012) · Pediatric Neurology · doi:10.1016/j.pediatrneurol.2012.06.005 · Cited by 4 · see citing works

Marchiafava–Bignami disease-like lesions due to central nervous system lupus

Kashiwagi, Y., Horiuchi, T., Harashima, C., Matsubara, F., & Harashima, S. (2010) · BMJ Case Reports · doi:10.1136/bcr.08.2010.3269 · Cited by 4 · see citing works

Advances and Challenges in Neuropsychiatric Systemic Lupus Erythematosus

Zandi, M. S. (2010) · Cited by 3 · see citing works

Neurosarcoidosis with bilateral subependymal periventricular lesions.

Raets, I., & Vandevenne, J. E. (2007) · PubMed · Cited by 1 · see citing works

Diagnosis of multiple sclerosis: progress and challenges

Brownlee, W. J., Hardy, T. A., Fazekas, F., & Miller, D. H. (2017) · The Lancet · doi:10.1016/s0140-6736(16)30959-x · Cited by 701 · see citing works

Uncovering convolutional neural network decisions for diagnosing multiple sclerosis on conventional mri using layer-wise relevance propagation

Eitel, F., Soehler, E., Bellmann-Strobl, J., Brandt, A. U., Ruprecht, K., Giess, R. M., Kuchling, J., Asseyer, S., Weygandt, M., Haynes, J.-D., et al. (2019) · NeuroImage: Clinical · doi:10.1016/j.nicl.2019.102003 · Cited by 171 · see citing works

Atypical inflammatory demyelinating syndromes of the CNS

Hardy, T. A., Reddel, S. W., Barnett, M. H., Palace, J., Lucchinetti, C. F., & Weinshenker, B. G. (2016) · The Lancet Neurology · doi:10.1016/s1474-4422(16)30043-6 · Cited by 161 · see citing works

A review on brain structures segmentation in magnetic resonance imaging

González-Villà, S., Oliver, A., Valverde, S., Wang, L., Reyer Zwiggelaar, A., & Lladó, X. (2016) · Artificial Intelligence in Medicine · doi:10.1016/j.artmed.2016.09.001 · Cited by 132 · see citing works

Neuroinflammation and Its Association with Cognition, Neuronal Markers and Peripheral Inflammation after Chemotherapy for Breast Cancer

Schroyen, G., Blommaert, J., Weehaeghe, D. V., Sleurs, C., Vandenbulcke, M., Dedoncker, N., Hatse, S., Goris, A., Koole, M., Smeets, A., et al. (2021) · Cancers · doi:10.3390/cancers13164198 · Cited by 70 · see citing works

Structural properties of the human corpus callosum: Multimodal assessment and sex differences

Björnholm, L., Nikkinen, J., Kiviniemi, V. J., Nordström, T., Niemelä, S., Drakesmith, M., Evans, J. J., Pike, G. B., Veijola, J. M., & Paus, T. (2017) · NeuroImage · doi:10.1016/j.neuroimage.2017.02.056 · Cited by 57 · see citing works

Cytotoxic lesions of the corpus callosum: a systematic review

Moors, S., Nakhostin, D., Ilchenko, D., Kulcsár, Z., Starkey, J., Winklhofer, S. F.-X., & Ineichen, B. V. (2023) · European Radiology · doi:10.1007/s00330-023-10524-3 · Cited by 53 · see citing works

Pseudotumoral demyelinating lesions: diagnostic approach and long-term outcome

Hardy, T. A. (2019) · Current Opinion in Neurology · doi:10.1097/wco.0000000000000683 · Cited by 52 · see citing works

Computational methods for corpus callosum segmentation on MRI: A systematic literature review

Cover, G. S., Herrera, W. G., Bento, M., Appenzeller, S., & Rittner, L. (2017) · Computer Methods and Programs in Biomedicine · doi:10.1016/j.cmpb.2017.10.025 · Cited by 42 · see citing works

Diagnosis, Differential Diagnosis and Misdiagnosis of Susac Syndrome

Triplett, J. D., Qiu, J., O'Brien, B., Gopinath, S., Trewin, B., Spring, P. J., Shaffi, M., Ip, J., Chan, F., Chen, L., et al. (2022) · European Journal of Neurology · doi:10.1111/ene.15317 · Cited by 41 · see citing works

Pathological cut-offs of global and regional brain volume loss in multiple sclerosis

Uher, T., Vaněčková, M., Krásenský, J., Sobíšek, L., Týblová, M., Volná, J., Seidl, Z., Bergsland, N., Dwyer, M. G., Zivadinov, R., et al. (2017) · Multiple Sclerosis Journal · doi:10.1177/1352458517742739 · Cited by 41 · see citing works

Misdiagnoses and delay of diagnoses in Moyamoya angiopathy—a large Caucasian case series

Graf, J., Schwitalla, J. C., Albrecht, P., Veltkamp, R. C., Berlit, P., Hartung, H., Aktaş, O., & Kraemer, M. (2019) · Journal of Neurology · doi:10.1007/s00415-019-09245-9 · Cited by 40 · see citing works

Diffusion tensor imaging findings in the multiple sclerosis patients and their relationships to various aspects of disability

Pokryszko‐Dragan, A., Banaszek, A., Nowakowska-Kotas, M. M., Jeżowska-Jurczyk, K., Dziadkowiak, E., Gruszka, E., Zagrajek, M., Bilińska, M. M., Budrewicz, S. P., Sąsiadek, M. J., et al. (2018) · Journal of the Neurological Sciences · doi:10.1016/j.jns.2018.06.007 · Cited by 39 · see citing works

Lesion topographies in multiple sclerosis diagnosis: A reappraisal

Arrambide, G., Tintore, M., Auger, C., Río, J., Castilló, J., Vidal-Jordana, A., Galán, I., Nos, C., Comabella, M., Mitjana, R., et al. (2017) · Neurology · doi:10.1212/wnl.0000000000004715 · Cited by 38 · see citing works

Air Pollution-Related Brain Metal Dyshomeostasis as a Potential Risk Factor for Neurodevelopmental Disorders and Neurodegenerative Diseases

Cory‐Slechta, D. A., Sobolewski, M., & Oberdörster, G. (2020) · Atmosphere · doi:10.3390/atmos11101098 · Cited by 36 · see citing works

Corpus callosum involvement: a useful clue for differentiating Fabry Disease from Multiple Sclerosis

Cocozza, S., Olivo, G., Riccio, E., Russo, C., Pontillo, G., Ugga, L., Migliaccio, S., Rosa, D. D., Feriozzi, S., Veroux, M., et al. (2017) · Neuroradiology · doi:10.1007/s00234-017-1829-8 · Cited by 35 · see citing works

Clinical Presentation and Outcomes of Acute Disseminated Encephalomyelitis in Adults Worldwide: Systematic Review and Meta-Analysis

Li, K., Li, M., Wen, L., Wang, Q., Ding, X., & Wang, J. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.870867 · Cited by 33 · see citing works

Lesions in the Splenium of the Corpus Callosum on MRI in Children: A Review

Kontzialis, M. S., Soares, B. P., & Huisman, T. A. G. M. (2017) · Journal of Neuroimaging · doi:10.1111/jon.12455 · Cited by 33 · see citing works

Immune-mediated conditions affecting the brain, eye and ear (BEE syndromes)

Triplett, J. D., Buzzard, K. A., Lubomski, M., Riminton, S., Barnett, M. H., Welgampola, M. S., Halmagyi, G. M., Nguyen, M., Landau, K., Lee, A. G., et al. (2019) · Journal of Neurology Neurosurgery & Psychiatry · doi:10.1136/jnnp-2018-319002 · Cited by 33 · see citing works

The spectrum of immune-mediated and inflammatory lesions of the brainstem

Law, L. Y., Riminton, S., Nguyen, M., Barnett, M. H., Reddel, S., & Hardy, T. A. (2019) · Neurology · doi:10.1212/wnl.0000000000008015 · Cited by 34 · see citing works

Diagnosis and Prediction of Relapses in Susac Syndrome: A New Use for MR Postcontrast FLAIR Leptomeningeal Enhancement

Coulette, S., Lecler, A., Saragoussi, É., Zuber, K., Savatovsky, J., Deschamps, R., Gout, O., Sabben, C., Aboab, J., Affortit, A., et al. (2019) · American Journal of Neuroradiology · doi:10.3174/ajnr.a6103 · Cited by 32 · see citing works

Tumefactive demyelination: updated perspectives on diagnosis and management

Sánchez, P., Chan, F., & Hardy, T. A. (2021) · Expert Review of Neurotherapeutics · doi:10.1080/14737175.2021.1971077 · Cited by 27 · see citing works

Obesity and White Matter Neuroinflammation Related Edema in Alzheimer’s Disease Dementia Biomarker Negative Cognitively Normal Individuals

Ly, M. J., Raji, C. A., Yu, G. Z., Wang, Q., Wang, Y., Schindler, S. E., An, H., Samara, A., Eisenstein, S. A., Hershey, T. G., et al. (2021) · Journal of Alzheimer s Disease · doi:10.3233/jad-201242 · Cited by 26 · see citing works

Corpus Callosum Structural Integrity Is Associated With Postural Control Improvement in Persons With Multiple Sclerosis Who Have Minimal Disability

Peterson, D. S., Gera, G., Horak, F. B., & Fling, B. W. (2016) · Neurorehabilitation and neural repair · doi:10.1177/1545968316680487 · Cited by 26 · see citing works

Advanced MR diffusion imaging and chemotherapy‐related changes in cerebral white matter microstructure of survivors of childhood bone and soft tissue sarcoma?

Sleurs, C., Lemiere, J., Christiaens, D., Billiet, T., Peeters, R., Sunaert, S., Uyttebroeck, A., & Deprez, S. (2018) · Human Brain Mapping · doi:10.1002/hbm.24082 · Cited by 26 · see citing works

Clinical and imaging features distinguishing Susac syndrome from primary angiitis of the central nervous system

Marrodán, M., Acosta, J., Alessandro, L., Fernández, V., Contentti, E. C., Arakaki, N., Köhler, A., Fiol, M., Ameriso, S. F., & Correale, J. D. (2018) · Journal of the Neurological Sciences · doi:10.1016/j.jns.2018.09.029 · Cited by 25 · see citing works

Characterization of variations in IL23A and IL23R genes: possible roles in multiple sclerosis and other neuroinflammatory demyelinating diseases

Li, F.-F., Zhu, X., Yan, P., Jin, M.-H., Yue, H., Zhang, Q., Fu, J. X., & Liu, S. (2016) · Aging · doi:10.18632/aging.101058 · Cited by 23 · see citing works

CNS vasculopathies: Challenging mimickers of primary angiitis of the central nervous system

Cho, T. A., & Jones, A. (2020) · Best Practice & Research Clinical Rheumatology · doi:10.1016/j.berh.2020.101569 · Cited by 24 · see citing works

Susac syndrome: neurological update (clinical features, long-term observational follow-up and management of sixteen patients)

Bose, S., Papathanasiou, A., Karkhanis, S., Appleton, J. P., King, D. S., Batra, R., Mollan, S. P., & Jacob, S. (2023) · Journal of Neurology · doi:10.1007/s00415-023-11891-z · Cited by 21 · see citing works

The neuro-otology of Susac syndrome

Hardy, T. A., Taylor, R. L., Qiu, J. X., O’Brien, B., Gopinath, S., Trewin, B. P., Spring, P. J., Shaffi, M., Bolitho, S., Garsia, R. J., et al. (2020) · Journal of Neurology · doi:10.1007/s00415-020-10086-0 · Cited by 21 · see citing works

Callosal lesions on magnetic resonance imaging with multiple sclerosis, neuromyelitis optica spectrum disorder and acute disseminated encephalomyelitis

Cai, M., Zhang, Y., Zheng, Y., Fang, W. J., & Ding, M. (2019) · Multiple Sclerosis and Related Disorders · doi:10.1016/j.msard.2019.04.019 · Cited by 20 · see citing works

Corpus callosum involvement in MOG antibody-associated disease in comparison to AQP4-IgG-seropositive neuromyelitis optica spectrum disorder and multiple sclerosis

Chia, N., Redenbaugh, V., Chen, J. J.-W., Pittock, S. J., & Flanagan, E. P. (2023) · Multiple Sclerosis Journal · doi:10.1177/13524585221150743 · Cited by 18 · see citing works

The impact of cancer and chemotherapy during pregnancy on child neurodevelopment: A multimodal neuroimaging analysis

Blommaert, J., Radwan, A., Sleurs, C., Maggen, C., van Gerwen, M., Wolters, V., Christiaens, D., Peeters, R., Dupont, P., Sunaert, S., et al. (2020) · EClinicalMedicine · doi:10.1016/j.eclinm.2020.100598 · Cited by 17 · see citing works

Pathologic and MRI analysis in acute atypical inflammatory demyelinating lesions

Ayrignac, X., Rigau, V., Lhermitte, B., Vincent, T., de Champfleur, N. M., Dalliere, C. C., Charif, M., Collongues, N., Seze, J. D., Hebbadj, S., et al. (2019) · Journal of Neurology · doi:10.1007/s00415-019-09328-7 · Cited by 14 · see citing works

Demyelination and impaired oligodendrogenesis in the corpus callosum following lead exposure

Liu, L. L., Emir, U. E., Gu, H., Sang, L. T., Sawiak, S. J., Cannon, J. R., Du, Y., & Zheng, W. (2024) · Toxicological Sciences · doi:10.1093/toxsci/kfae100 · Cited by 12 · see citing works

Data-Driven Corpus Callosum Parcellation Method Through Diffusion Tensor Imaging

Cover, G. S., Pereira, M. B., Bento, M., Appenzeller, S., & Rittner, L. (2017) · IEEE Access · doi:10.1109/access.2017.2761701 · Cited by 12 · see citing works

Streamline density and lesion volume reveal a postero–anterior gradient of corpus callosum damage in multiple sclerosis

Petracca, M., Schiavi, S., Battocchio, M., Mendili, M. M. E., Fleysher, L., Daducci, A., & Inglese, M. (2020) · European Journal of Neurology · doi:10.1111/ene.14214 · Cited by 10 · see citing works

MRI of Transcallosal White Matter Helps to Predict Motor Impairment in Multiple Sclerosis

Cordani, C., Preziosa, P., Valsasina, P., Meani, A., Pagani, E., Morozumi, T., Rocca, M. A., & Filippi, M. (2021) · Radiology · doi:10.1148/radiol.2021210922 · Cited by 10 · see citing works

Corpus callosum index correlates with brain volumetry and disability in multiple sclerosis patients

Sugijono, S. E., Mulyadi, R., Firdausia, S., Prihartono, J., & Estiasari, R. (2020) · Neurosciences · doi:10.17712/nsj.2020.3.20190093 · Cited by 9 · see citing works

The Spectrum of Acute Disseminated Encephalomyelitis and Mild Encephalopathy with Reversible Splenial Lesion

Sáenz‐Farret, M., Cansino-Torres, M. A., Sandoval-Rodríguez, V., Navarro-Ibarra, R., & Zúñiga‐Ramírez, C. (2019) · Case Reports in Neurological Medicine · doi:10.1155/2019/9272074 · Cited by 9 · see citing works

Effect of fluoxetine on proliferation and/or survival of microglia and oligodendrocyte progenitor cells in the fornix and corpus callosum of the mouse brain

Fukushima, S., Kurganov, E., Hiratsuka, D., & Miyata, S. (2020) · Pharmacological Reports · doi:10.1007/s43440-020-00079-1 · Cited by 9 · see citing works

A Novel Mouse Model for Cerebral Inflammatory Demyelination in X‐Linked Adrenoleukodystrophy: Insights into Pathogenesis and Potential Therapeutic Targets

Hashemi, E., Srivastava, I. N., Aguirre, A., Yoseph, E., Kaushal, E., Awani, A., Ryu, J. K., Akassoglou, K., Talebian, S., Chu, P., et al. (2024) · Annals of Neurology · doi:10.1002/ana.27117 · Cited by 8 · see citing works

Successful Treatment of Incomplete Susac Syndrome with Simultaneous Corticosteroids and Plasmapheresis Followed by Rituximab

Reedy, M. B., Wang, Y., Beinlich, B. R., & Rose, W. N. (2021) · Case Reports in Neurological Medicine · doi:10.1155/2021/5591559 · Cited by 7 · see citing works

Thalamus Atrophy in the Peri-Pregnancy Period in Clinically Stable Multiple Sclerosis Patients: Preliminary Results

Rościszewska-Żukowska, I., Podyma, M., Stasiołek, M., & Siger, M. (2021) · Brain Sciences · doi:10.3390/brainsci11101270 · Cited by 7 · see citing works

Exquisite response to intravenous immunoglobulin in Susac syndrome during pregnancy

Gómez‐Figueroa, E., Garcia-Trejo, S., García-Santos, R. A., Pesqueira, G. Q., & Calleja-Castillo, J. M. (2017) · eNeurologicalSci · doi:10.1016/j.ensci.2017.12.004 · Cited by 7 · see citing works

Sex hormones secondary players in Susac's syndrome

Alungulese, A. L., Soldevilla, M. Á. G., Martínez, D. B., & Mañas, R. G. (2020) · Multiple Sclerosis and Related Disorders · doi:10.1016/j.msard.2020.102373 · Cited by 6 · see citing works

Behavioral Impairment and Amnesia at the Onset of Susac Syndrome

Masjuan, M., Ivanovski, T., Ezcurra, H. S., & Oliver, E. R. (2023) · Cureus · doi:10.7759/cureus.38089 · Cited by 4 · see citing works

Case report: Breaking CNS immuno-privilege: TNFα-inhibitor triggers aseptic meningitis in a patient with rheumatoid arthritis

Kassabian, B., Facco, M., Miscioscia, A., Carraro, S., Rinaldi, F., Gallo, P., & Puthenparampil, M. (2024) · Frontiers in Immunology · doi:10.3389/fimmu.2024.1432360 · Cited by 4 · see citing works

Delirium as presentation of late-onset and relapsing Susac syndrome

Betend, R., Humm, A. M., & Medlin, F. (2017) · BMJ Case Reports · doi:10.1136/bcr-2017-220494 · Cited by 4 · see citing works

Lifespan trajectories of the morphology and tractography of the corpus callosum: A 5.0 T MRI study

Chen, X., Liu, X., Zhong, X., Ren, J., Wang, H., Song, X., Fan, C., Xu, J., Li, C., Wang, L., et al. (2024) · Brain Research · doi:10.1016/j.brainres.2024.149413 · Cited by 3 · see citing works

Automatic callosal fiber convergence plane computation through DTI-based divergence map

Cover, G. S., Bento, M., Rittner, L., & Pinheiro, G. R. (2018) · SPIE Medical Imaging: Biomedical Applications in Molecular, Structural, and Functional Imaging · doi:10.1117/12.2293381 · Cited by 3 · see citing works

Demographic, ocular and associated neurological findings in corpus callosum malformations

Kızıltunç, P. B., Şahlı, E., Idil, A. M., & Atilla, H. (2021) · The Turkish Journal of Pediatrics · doi:10.24953/turkjped.2021.02.013 · Cited by 3 · see citing works

Mapping the complexity of multiple sclerosis: a novel perspective on genetic, environmental, and neurobiological insights

Omidi, A., Zolfaghari, A., Mirab, S. M., Bafghi, M. H., Khosravi, M., Safdari, F., & Shirani, K. (2025) · Molecular Biology Reports · doi:10.1007/s11033-025-10572-6 · Cited by 2 · see citing works

Reversible splenial lesion syndrome: A differential diagnosis of corpus callosum lesions

Fernández, C. G., López, P. A., Caride, A., & Contentti, E. C. (2018) · Neurology Psychiatry and Brain Research · doi:10.1016/j.npbr.2018.07.004 · Cited by 2 · see citing works

Case report: Reversible splenial lesion syndrome preceding the onset of multiple sclerosis

Mauritz, M., Kliushnikova, D., Otto, F., Harrer, A., Moser, T., Radlberger, R. F., Kleindienst, W., Trinka, E., & Wipfler, P. (2025) · Frontiers in Immunology · doi:10.3389/fimmu.2024.1517719 · Cited by 1 · see citing works

Corpus callosum indices are correlated with disability and cognitive performance in patients with multiple sclerosis: A systematic review and meta-analysis

Tabibian, F., Hoseini, E., Motahharynia, A., Azimzadeh, K., Kafieh, R., Amini, Z., & Adibi, I. (2025) · Multiple Sclerosis and Related Disorders · doi:10.1016/j.msard.2025.106522 · Cited by 1 · see citing works

Anomalies de signal du corps calleux : quels diagnostic évoquer ?

Mahmoud, M., Laifi, S., Arous, A., DRISSI, C., Nagi, S., & Hamouda, M. B. (2020) · Pratique Neurologique - FMC · doi:10.1016/j.praneu.2019.10.010 · Cited by 1 · see citing works

Inflammatory and Demyelinating Diseases of the Corpus Callosum

Ott, K., & Tubbs, R. S. (2023) · Springer eBooks · doi:10.1007/978-3-031-38114-0_22 · Cited by 1 · see citing works

White Matter Magnetic Resonance Diffusion Measures in Multiple Sclerosis with Overactive Bladder

Yang, X., Liechti, M. D., Kanber, B., Sudre, C. H., Castellazzi, G., Zhang, J., Yiannakas, M. C., Gonzales, G., Prados, F., Toosy, A., et al. (2024) · Brain Sciences · doi:10.3390/brainsci14100975 · Cited by 1 · see citing works

Síndrome de Susac. Caso clínico y revisión

Phoebe Ramos, Y., Leandro Rodríguez, H., Carolina Peralta, C., & Francisca Montoya, S. (2018) · Revista de otorrinolaringología y cirugía de cabeza y cuello · doi:10.4067/s0717-75262018000200167 · Cited by 1 · see citing works

Cases of Susac syndrome misdiagnosed with multiple sclerosis

Polekhina, N. V., Сурнина, З. В., Коновалов, Р. Н., & Zakharova, M. N. (2019) · Journal of Neurology & Stroke · doi:10.15406/jnsk.2019.09.00400 · Cited by 1 · see citing works

What can smudge the 'tough body' corpus callosum?

Elkider, M., & O'Toole, O. (2017) · PubMed

Multiple Brain Hyperintensities (T2/FLAIR), Common

Jhaveri, M. D., Salzman, K. L., Ross, J. S., Moore, K. R., Osborn, A. G., & Ho, C. Y. (2018) · Elsevier eBooks · doi:10.1016/b978-0-323-44308-1.50151-3

A Multiple Sclerosis Mimiker with Good Recovery following Specific Therapy: Susac Syndrome

Clerici, V. T. (2021) · Journal of Ophthalmology Research Reviews & Reports · doi:10.47363/jorrr/2021(2)112

Framework for the analysis of the corpus callosum microstructure along its extension

da Costa, A. L. (2018) · doi:10.47749/t/unicamp.2018.1082471

Multiple Brain Hyperintensities (T2/FLAIR), Less Common

Jhaveri, M. D., Salzman, K. L., Ross, J. S., Moore, K. R., Osborn, A. G., & Ho, C. Y. (2018) · Elsevier eBooks · doi:10.1016/b978-0-323-44308-1.50226-9

Susac syndrome

Weerakkody, Y., Gaillard, F., & Sharma, R. (2010) · Radiopaedia.org · doi:10.53347/rid-10736

Ablación automática de tumores en el contexto del aprendizaje automático

Orozco, A. A., Arias, H. F. G., & Cardona, H. D. V. (2022) · Universidad Tecnológica de Pereira eBooks · doi:10.22517/9789587225839

The diagnostic signature of Susac’s syndrome

Hardy, T. A. (2022) · Journal of Clinical Neuroscience · doi:10.1016/j.jocn.2022.07.023

Sclérose en plaque : signe de la crête-de-coq

Onka, B., Mohamed, D. A., Tessi, R. T. Y., Bizimana, W., Jiddane, M., Fikri, M., & Touarsa, F. (2022) · Journal d imagerie diagnostique et interventionnelle · doi:10.1016/j.jidi.2022.03.012

Understanding MRI Features of Multiple Sclerosis: Based on the 2017 McDonald Criteria

Yang, J. (2023) · Journal of Multiple Sclerosis and Neuroimmunology · doi:10.59578/jmsni.2023.14.1.1

Susac syndrome: challenges of interpreting treatment data in a rare disease

Hardy, T. A. (2024) · The Lancet Rheumatology · doi:10.1016/s2665-9913(24)00267-4

Training a Vision Transformer Model on Shape Signatures for Quality Control of MRI Corpus Callosum Segmentations

Silva, S. S., Rodrigues, J., Júlio, P. R., Appenzeller, S., & Rittner, L. (2024) · International Symposium on Medical Information Processing and Analysis (SIPAIM) · doi:10.1109/sipaim62974.2024.10783553

Gender-Associated Variation in Morphometric Analysis of the Corpus Callosum: A Hospital-Based Cross-Sectional Study Using 3.0 Tesla MRI

Eleyadath, A. B., Panchal, P., Ghosh, S. K., & Kumar, S. (2025) · Cureus · doi:10.7759/cureus.97742

Structural brain changes in subacute spinal cord injury: an analysis of diffusion kurtosis imaging and diffusion tensor imaging metrics with clinical correlation

Christiaanse, E., Sritharan, J., Wyss, P. O., Scheel‐Sailer, A., Leemans, A., Verma, R. K., Luca, A. D., & Zito, G. A. (2025) · Frontiers in Neuroscience · doi:10.3389/fnins.2025.1652416

Smoldering neuroinflammation in progressive multiple sclerosis: mechanisms, imaging biomarkers, and therapeutic opportunities

Wang, M., Zhu, B.-C., & 毛西京 (2026) · Frontiers in Immunology · doi:10.3389/fimmu.2026.1901957

Long-Term Morphine Treatment Enhances Proteasome-Dependent Degradation of Gβ in Human Neuroblastoma SH-SY5Y Cells: Correlation with Onset of Adenylate Cyclase Sensitization

Moulédous, L., Neasta, J., Uttenweiler‐Joseph, S., Stella, A., Matondo, M., Corbani, M., Monsarrat, B., & Meunier, J. (2005) · Molecular Pharmacology · doi:10.1124/mol.105.013391 · Cited by 37 · see citing works

Effets d'un traitement chronique par la morphine sur le protéome des cellules de neuroblastome humain SH-SY5Y

Moulédous, L. (2007) · HAL

A general role for adaptations in G-proteins and the cyclic AMP system in mediating the chronic actions of morphine and cocaine on neuronal function

Terwilliger, R. Z., Beitner‐Johnson, D., Sevarino, K. A., Crain, S. M., & Nestler, E. J. (1991) · Brain Research · doi:10.1016/0006-8993(91)91111-d · Cited by 534 · see citing works

Alterations in the expression of G-proteins and regulation of adenylate cyclase in human neuroblastoma SH-SY5Y cells chronically exposed to low-efficacy μ-opioids

Ammer, H., & Schulz, R. (1993) · Biochemical Journal · doi:10.1042/bj2950263 · Cited by 42 · see citing works

Morphine dependence in human neuroblastoma SH-SY5Y cells is associated with adaptive changes in both the quantity and functional interaction of PGE1 receptors and stimulatory G proteins

Ammer, H., & Schulz, R. (1996) · Brain Research · doi:10.1016/0006-8993(95)01265-6 · Cited by 32 · see citing works