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Chapter 17 - Deconstructing Hashimoto Encephalopathy

from Section 3 - Specific Syndromes and Diseases

Published online by Cambridge University Press:  27 January 2022

Josep Dalmau
Affiliation:
Universitat de Barcelona
Francesc Graus
Affiliation:
Universitat de Barcelona
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Summary

This chapter critically reviews the diagnostic criteria of Hashimoto encephalopathy (HE) and the misuse of this diagnosis. HE is usually considered in patients with subacute cognitive deterioration, myoclonus, change in behaviour, or seizures, accompanied by normal or non-specific MRI and CSF findings, normal thyroid function or mild hypothyroidism, increased serum levels of thyroid peroxidase (TPO) antibodies, and clinical response to steroids. The beneficial effect of steroids was emphasized by renaming the disease ‘steroid-responsive encephalopathy associated with autoimmune thyroiditis’ (SREAT). However, the diagnosis of HE has several important limitations. One is that there are no specific biomarkers of the disease. Moreover, the specificity of TPO antibodies is poor as they are also found in 13% of healthy persons. The significance of antibodies against the amino (NH2)-terminal domain of α-enolase, considered a potential biomarker of HE, is also unclear. Another limitation is that the diagnostic confirmation of HE depends on steroid-responsiveness. However, the clinical criteria and paraclinical findings do not identify the patients that will respond to steroids (<30%). Finally, most patients reported with HE are not investigated for neuronal surface antibodies. Overall, the weaknesses of the criteria and their misuse characterizing as HE any neurological syndrome with positive TPO antibodies that responds to steroids, raise doubts about the clinical usefulness of the term HE.

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Publisher: Cambridge University Press
Print publication year: 2022

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References

Hauser, W, Fitzcharles, MA. Facts and myths pertaining to fibromyalgia. Dialogues Clin Neurosci 2018;20:5362.Google Scholar
Chong, JY, Rowland, LP, Utiger, RD. Hashimoto encephalopathy: syndrome or myth? Arch Neurol 2003;60:164171.Google Scholar
Chen, KA, Brilot, F, Dale, RC, Lafferty, AR, Andrews, PI. Hashimoto’s encephalopathy and anti-MOG antibody encephalitis: 50 years after Lord Brain’s description. Eur J Paediatr Neurol 2017;21:898901.CrossRefGoogle ScholarPubMed
Mirabelli-Badenier, M, Biancheri, R, Morana, G, et al. Anti-NMDAR encephalitis misdiagnosed as Hashimoto’s encephalopathy. Eur J Paediatr Neurol 2014;18:7274.CrossRefGoogle ScholarPubMed
Montagna, G, Imperiali, M, Agazzi, P, et al. Hashimoto’s encephalopathy: a rare proteiform disorder. Autoimmunity Rev 2016;15:466476.CrossRefGoogle ScholarPubMed
Laurent, C, Capron, J, Quillerou, B, et al. Steroid-responsive encephalopathy associated with autoimmune thyroiditis (SREAT): characteristics, treatment and outcome in 251 cases from the literature. Autoimmunity Rev 2016;15:11291133.Google Scholar
Brain, L, Jellinek, EH, Ball, K. Hashimoto’s disease and encephalopathy. Lancet 1966;2:512514.Google Scholar
Thrush, DC, Boddie, HG. Episodic encephalopathy associated with thyroid disorders. J Neurol Neurosurg Psychiatry 1974;37:696700.Google Scholar
Becker, KL, Ferguson, RH, Mc, CW. The connective-tissue diseases and symptoms associated with Hashimoto’s thyroiditis. N Engl J Med 1963;268:277280.Google Scholar
Shein, M, Apter, A, Dickerman, Z, Tyano, S, Gadoth, N. Encephalopathy in compensated Hashimoto thyroiditis: a clinical expression of autoimmune cerebral vasculitis. Brain Dev 1986;8:6064.Google Scholar
Latinville, D, Bernardi, O, Cougoule, JP, et al. [Hashimoto’s thyroiditis and myoclonic encephalopathy. Pathogenic hypothesis]. Rev Neurol (Paris) 1985;141:5558.Google Scholar
Shaw, PJ, Walls, TJ, Newman, PK, Cleland, PG, Cartlidge, NE. Hashimoto’s encephalopathy: a steroid-responsive disorder associated with high anti-thyroid antibody titers – report of 5 cases. Neurology 1991;41:228233.Google Scholar
Kothbauer-Margreiter, I, Sturzenegger, M, Komor, J, Baumgartner, R, Hess, CW. Encephalopathy associated with Hashimoto thyroiditis: diagnosis and treatment. J Neurol 1996;243:585593.Google Scholar
v Maydell, B, Kopp, M, v Komorowski, G, et al. Hashimoto encephalopathy: is it underdiagnosed in pediatric patients? Neuropediatrics 2002;33:8689.CrossRefGoogle ScholarPubMed
Ghika-Schmid, F, Ghika, J, Regli, F, et al. Hashimoto’s myoclonic encephalopathy: an underdiagnosed treatable condition? Mov Disord 1996;11:555562.Google Scholar
Sunil, GS, Mariash, CN. Hashimoto’s encephalitis. J Clin Endocrinol Metab 2001;86:947.Google Scholar
Peschen-Rosin, R, Schabet, M, Dichgans, J. Manifestation of Hashimoto’s encephalopathy years before onset of thyroid disease. Eur Neurol 1999;41:7984.Google Scholar
Selim, M, Drachman, DA. Ataxia associated with Hashimoto’s disease: progressive non-familial adult onset cerebellar degeneration with autoimmune thyroiditis. J Neurol Neurosurg Psychiatry 2001;71:8187.Google Scholar
Caselli, RJ, Boeve, BF, Scheithauer, BW, O’Duffy, JD, Hunder, GG. Nonvasculitic autoimmune inflammatory meningoencephalitis (NAIM): a reversible form of encephalopathy. Neurology 1999;53:15791581.CrossRefGoogle Scholar
Chong, JY, Rowland, LP. What’s in a NAIM? Hashimoto encephalopathy, steroid-responsive encephalopathy associated with autoimmune thyroiditis, or nonvasculitic autoimmune meningoencephalitis? Arch Neurol 2006;63:175176.Google Scholar
Josephs, KA, Rubino, FA, Dickson, DW. Nonvasculitic autoimmune inflammatory meningoencephalitis. Neuropathology 2004;24:149152.CrossRefGoogle ScholarPubMed
Schiess, N, Pardo, CA. Hashimoto’s encephalopathy. Ann N Y Acad Sci 2008;1142:254265.CrossRefGoogle ScholarPubMed
Striano, P, Pagliuca, M, Andreone, V, et al. Unfavourable outcome of Hashimoto encephalopathy due to status epilepticus: one autopsy case. J Neurol 2006;253:248249.CrossRefGoogle ScholarPubMed
Oide, T, Tokuda, T, Yazaki, M, et al. Anti-neuronal autoantibody in Hashimoto’s encephalopathy: neuropathological, immunohistochemical, and biochemical analysis of two patients. J Neurol Sci 2004;217:712.Google Scholar
Duffey, P, Yee, S, Reid, IN, Bridges, LR. Hashimoto’s encephalopathy: postmortem findings after fatal status epilepticus. Neurology 2003;61:11241126.Google Scholar
Nolte, KW, Unbehaun, A, Sieker, H, Kloss, TM, Paulus, W. Hashimoto encephalopathy: a brainstem vasculitis? Neurology 2000;54:769770.CrossRefGoogle ScholarPubMed
Castillo, P, Woodruff, B, Caselli, R, et al. Steroid-responsive encephalopathy associated with autoimmune thyroiditis. Arch Neurol 2006;63:197202.Google Scholar
Ergul, AB, Altuner Torun, Y, Altug, U, et al. Congenital hemophilia A presenting with hashimoto’s encephalopathy and myocarditis: the first reported case. J Pediatr Hematol Oncol 2018;40:e435e438.Google Scholar
Cooper, BL, Appel, SE, Ammar, HM. A young female with urinary retention: Hashimoto’s encephalopathy. Am J Emerg Med 2017;35:943.e941943.e942.CrossRefGoogle Scholar
Graus, F, Titulaer, MJ, Balu, R, et al. A clinical approach to diagnosis of autoimmune encephalitis. Lancet Neurol 2016;15:391404.Google Scholar
Litmeier, S, Pruss, H, Witsch, E, Witsch, J. Initial serum thyroid peroxidase antibodies and long-term outcomes in SREAT. Acta Neurol Scand 2016;134:452457.Google Scholar
Mattozzi, S, Sabater, L, Escudero, D, et al. Hashimoto encephalopathy in the 21st century. Neurology 2020;94:e217e224.Google Scholar
Hollowell, JG, Staehling, NW, Flanders, WD, et al. Serum TSH, T(4), and thyroid antibodies in the United States population (1988 to 1994): National Health and Nutrition Examination Survey (NHANES III). J Clin Endocrinol Metab 2002;87:489499.Google Scholar
Sinclair, D. Analytical aspects of thyroid antibodies estimation. Autoimmunity 2008;41:4654.Google Scholar
Ochi, H, Horiuchi, I, Araki, N, et al. Proteomic analysis of human brain identifies alpha-enolase as a novel autoantigen in Hashimoto’s encephalopathy. FEBS Lett 2002;528:197202.Google Scholar
Gitlits, VM, Toh, BH, Sentry, JW. Disease association, origin, and clinical relevance of autoantibodies to the glycolytic enzyme enolase. J Investig Med 2001;49:138145.Google Scholar
Vermeulen, N, Arijs, I, Joossens, S, et al. Anti-alpha-enolase antibodies in patients with inflammatory bowel disease. Clin Chem 2008;54:534541.Google Scholar
Pratesi, F, Moscato, S, Sabbatini, A, et al. Autoantibodies specific for alpha-enolase in systemic autoimmune disorders. J Rheumatol 2000;27:109115.Google Scholar
Adamus, G, Amundson, D, Seigel, GM, Machnicki, M. Anti-enolase-alpha autoantibodies in cancer-associated retinopathy: epitope mapping and cytotoxicity on retinal cells. J Autoimmun 1998;11:671677.Google Scholar
Yoneda, M, Fujii, A, Ito, A, et al. High prevalence of serum autoantibodies against the amino terminal of alpha-enolase in Hashimoto’s encephalopathy. J Neuroimmunol 2007;185:195200.Google Scholar
Fujii, A, Yoneda, M, Ito, T, et al. Autoantibodies against the amino terminal of alpha-enolase are a useful diagnostic marker of Hashimoto’s encephalopathy. J Neuroimmunol 2005;162:130136.CrossRefGoogle ScholarPubMed
Kishitani, T, Matsunaga, A, Ikawa, M, et al. Limbic encephalitis associated with anti-NH2-terminal of alpha-enolase antibodies: a clinical subtype of Hashimoto encephalopathy. Medicine (Baltimore) 2017;96:e6181.CrossRefGoogle ScholarPubMed
Hayashi, Y, Yamada, M, Kimura, A, et al. Clinical findings of a probable case of MM2-cortical-type sporadic Creutzfeldt-Jakob disease with antibodies to anti-N-terminus of alpha-enolase. Prion 2017;11:454464.Google Scholar
Ferracci, F, Bertiato, G, Moretto, G. Hashimoto’s encephalopathy: epidemiologic data and pathogenetic considerations. J Neurol Sci 2004;217:165168.CrossRefGoogle ScholarPubMed
Dubey, D, Pittock, SJ, Kelly, CR, et al. Autoimmune encephalitis epidemiology and a comparison to infectious encephalitis. Ann Neurol 2018;83:166177.Google Scholar
Grande, ML, Constantino, A, Rayo, JI, et al. Brain hypoperfusion on Tc-99 m-ethylene dicysteine diethyl ester single-photon emission computed tomography in Hashimoto’s encephalopathy. Indian J Nucl Med 2013;28:102104.Google Scholar
Yeh, SJ, Tsai, LK, Tang, SC, Jeng, JS. Pin-point pupils with drowsiness as a presentation of Hashimoto’s encephalopathy mimicking pontine infarction. Acta neurologica Taiwanica 2014;23:1923.Google Scholar
Zimmermann, P, Stranzinger, E. Steroid-responsive encephalopathy associated with Hashimoto thyroiditis. Pediatr Radiol 2012;42:891893.Google Scholar
Hirose, D, Hirao, K, Kaneko, Y, et al. Case of Hashimoto’s encephalopathy showing atypical clinical course with magnetic resonance imaging abnormalities. Geriatr Gerontol Intl 2017;17:12351237.Google Scholar
Bonmann, E, Prumbaum, M, Stippich, C, Ringleb, P, Sliwka, U. Hashimoto encephalopathy: rare cause of stroke in young patient. Neurologist 2009;15:342344.CrossRefGoogle ScholarPubMed
Yildiz, OK, Segmen, H, Oztoprak, I, Bolayir, E, Topaktas, S. Posterior reversible encephalopathy and alexia without agraphia in a patient with Hashimoto’s encephalopathy. Neurol Sci 2010;31:523525.CrossRefGoogle Scholar
Lalanne, L, Meriot, ME, Ruppert, E, et al. Attempted infanticide and suicide inaugurating catatonia associated with Hashimoto’s encephalopathy: a case report. BMC Psychiatry 2016;16:13.CrossRefGoogle ScholarPubMed
Liu, MY, Zhang, SQ, Hao, Y, Zheng, HM. Paroxysmal kinesigenic dyskinesia as the initial symptom of Hashimoto encephalopathy. CNS Neurosci Therapeut 2012;18:271273.CrossRefGoogle ScholarPubMed
Georgiev, D, Kojovic, M, Klanjscek, G, Dolenc-Groselj, L. Hashimoto encephalopathy associated rapid onset narcolepsy type 1. Sleep Med 2017;29:9495.Google Scholar
Olmez, I, Moses, H, Sriram, S, et al. Diagnostic and therapeutic aspects of Hashimoto’s encephalopathy. J Neurol Sci 2013;331:6771.CrossRefGoogle ScholarPubMed
Ramcharan, K, Hosein, N, Teelucksingh, JD, Rampersad, F, Teelucksingh, S. Prominent bilateral hand tremor in hashimoto’s encephalopathy: a video demonstration. Tremor Other Hyperkinet Mov 2016;6:419.Google Scholar
Schnedl, WJ, Mirzaei, S, Wallner-Liebmann, SJ, et al. Improvement of cerebral hypoperfusion with levothyroxine therapy in Hashimoto’s encephalopathy demonstrated by (99 m)Tc-HMPAO-SPECT. Eur Thyroid J 2013;2:116119.Google Scholar
Zhao, W, Li, J, Wang, J, et al. A case of Hashimoto encephalopathy: clinical manifestation, imaging, pathology, treatment, and prognosis. Neurologist 2011;17:141143.CrossRefGoogle ScholarPubMed
Zhu, Y, Yang, H, Xiao, F. Hashimoto’s encephalopathy: a report of three cases and relevant literature reviews. Intl J Clin Exp Med 2015;8:1681716826.Google ScholarPubMed
He, L, Li, M, Long, XH, Li, XP, Peng, Y. A case of Hashimoto’s encephalopathy misdiagnosed as viral encephalitis. Am J Case Rep 2013;14:366369.Google Scholar
Uwatoko, H, Yabe, I, Sato, S, et al. Hashimoto’s encephalopathy mimicking a brain tumor and its pathological findings: a case report. J Neurol Sci 2018;394:141143.Google Scholar
Chang, T, Riffsy, MT, Gunaratne, PS. Hashimoto encephalopathy: clinical and MRI improvement following high-dose corticosteroid therapy. Neurologist 2010;16:394396.Google Scholar
Graham, BR, Shiff, N, Nour, M, et al. Hashimoto encephalopathy presenting with stroke-like episodes in an adolescent female: a case report and literature review. Pediatr Neurol 2016;59:6270.Google Scholar
Gresa-Arribas, N, Titulaer, MJ, Torrents, A, et al. Antibody titres at diagnosis and during follow-up of anti-NMDA receptor encephalitis: a retrospective study. Lancet Neurol 2014;13:167177.Google Scholar
Guasp, M, Modena, Y, Armangue, T, Dalmau, J, Graus, F. Clinical features of seronegative, but CSF antibody-positive, anti-NMDA receptor encephalitis. Neurol Neuroimmunol Neuroinflamm 2020;7:e659.Google Scholar
Gabilondo, I, Saiz, A, Galan, L, et al. Analysis of relapses in anti-NMDAR encephalitis. Neurology 2011;77:996999.Google Scholar
Kayser, MS, Titulaer, MJ, Gresa-Arribas, N, Dalmau, J. Frequency and characteristics of isolated psychiatric episodes in anti-N-methyl-d-aspartate receptor encephalitis. JAMA Neurol 2013;70:11331139.Google Scholar
Koros, C, Economou, A, Mastorakos, G, et al. A selective memory deficit caused by autoimmune encephalopathy associated with Hashimoto thyroiditis. Cogn Behav Neurol 2012;25:144148.Google Scholar
Laycock, K, Chaudhuri, A, Fuller, C, et al. A novel assessment and treatment approach to patients with Hashimoto’s encephalopathy. Endocrinol Diabetes Metab Case Rep 2018;2018:17-0117.Google Scholar
Sheetal, SK, Mathew, R, Peethambaran, B. Hashimoto’s encephalopathy as a treatable cause of corticobasal disease. Ann Indian Acad Neurol 2016;19:285286.Google Scholar
Gliebus, G, Lippa, CF. Cerebrospinal immunoglobulin level changes and clinical response to treatment of Hashimoto’s encephalopathy. Am J Alzheimer Dis Other Dementia 2009;24:373376.CrossRefGoogle ScholarPubMed
de Holanda, NC, de Lima, DD, Cavalcanti, TB, Lucena, CS, Bandeira, F. Hashimoto’s encephalopathy: systematic review of the literature and an additional case. J Neuropsychiatr Clin Neurosci 2011;23:384390.Google Scholar
Aquino, RT, Mutarelli, EG. Hashimoto’s encephalopathy. Arq Neuropsiquiatr 2009;67:724725.Google Scholar
Mijajlovic, M, Mirkovic, M, Dackovic, J, Zidverc-Trajkovic, J, Sternic, N. Clinical manifestations, diagnostic criteria and therapy of Hashimoto’s encephalopathy: report of two cases. J Neurol Sci 2010;288:194196.Google Scholar
Chong, CS, Leung, JL, Wong, IH, Ng, PW, Miao, MY. Presenile dementia: a case of Hashimoto’s encephalopathy. E Asian Arch Psychiatr 2011;21:3236.Google Scholar
Guirgis, H, Amar, C. A Case of Hashimoto’s encephalopathy presenting with acute psychosis. J Neuropsychiatr Clin Neurosci 2014;26:E1E2.Google Scholar
Lee, Y, House, EM. Treatment of steroid-resistant Hashimoto encephalopathy with misidentification delusions and catatonia. Psychosomatics 2017;58:322327.Google Scholar
Segers, K, Braconnier, P, Corazza, F, et al. Subacute cognitive deterioration with high serum anti-thyroid peroxidase antibodies: two cases and a plea for pragmatism. Psychogeriatrics 2013;13:175179.Google Scholar
Vivek, AK, Arun, AB, Menon, V, Kandasamy, P. Acute polymorphic psychosis as a presenting feature of Hashimoto’s encephalopathy. Asian J Psychiatr 2016;19:1920.CrossRefGoogle ScholarPubMed
Horikoshi, S, Miura, I, Kunii, Y, et al. Hashimoto encephalopathy with high plasma monoamine metabolite levels: a case report. Neuropsychiatr Dis Treat 2017;13:10431045.Google Scholar
Liu, CY, Tseng, MC, Lin, PH. Encephalopathy associated with autoimmune thyroid disease (Hashimoto’s thyroiditis) presenting as depression: a case report. Gen Hosp Psychiatry 2011;33:641.e647649.CrossRefGoogle ScholarPubMed
Chang, JS, Chang, TC. Hashimoto’s encephalopathy: report of three cases. J Formosan Med Assoc 2014;113:862866.Google Scholar
Normann, C, Frase, L, Berger, M, Nissen, C. Steroid-responsive depression. BMJ Case Rep 2013;2013:bcr2013009101.Google Scholar
Endres, D, Perlov, E, Riering, AN, et al. Steroid-responsive chronic schizophreniform syndrome in the context of mildly increased antithyroid peroxidase antibodies. Front Psychiatry 2017;8:64.Google Scholar
Endres, D, Perlov, E, Stich, O, et al. Steroid responsive encephalopathy associated with autoimmune thyroiditis (SREAT) presenting as major depression. BMC Psychiatry 2016;16:184.Google Scholar
Prat, S, Jouan, Y, Magnant, J, Graux, J, El-Hage, W. Hashimoto encephalopathy diagnosis after 40 years of a schizophrenia-like disorder. Schizophr Res 2012;139:269270.Google Scholar
Lin, YT, Liao, SC. Hashimoto encephalopathy presenting as schizophrenia-like disorder. Cogn Behav Neurol 2009;22:197201.Google Scholar
Boban, M, Malojcic, B. Rumination syndrome in a patient with Hashimoto’s encephalopathy. J Neuropsychiatr Clin Neurosci 2011;23:E11E12.Google Scholar
Haider, AS, Alam, M, Adetutu, E, et al. Autoimmune schizophrenia? Psychiatric manifestations of Hashimoto’s encephalitis. Cureus 2016;8:e672.Google Scholar
Al-Busaidi, M, Burad, J, Al-Belushi, A, Gujjar, A. Super refractory status epilepticus in Hashimoto’s encephalopathy. Oman Med J 2017;32:247250.Google Scholar
Yu, HJ, Lee, J, Seo, DW, Lee, M. Clinical manifestations and treatment response of steroid in pediatric Hashimoto encephalopathy. J Child Neurol 2014;29:938942.Google Scholar
Visée, H, Mabiglia, C, Vanderaspoilden, V, Gazagnes, MD, Glibert, G. Recurrent status epilepticus associated with Hashimoto’s encephalopathy. Epilepsy Behav Case Rep 2013;1:113117.Google Scholar
Bektas, O, Yilmaz, A, Kendirli, T, Siklar, Z, Deda, G. Hashimoto encephalopathy causing drug-resistant status epilepticus treated with plasmapheresis. Pediatr Neurol 2012;46:132135.CrossRefGoogle ScholarPubMed
Hilberath, JM, Schmidt, H, Wolf, GK. Steroid-responsive encephalopathy associated with autoimmune thyroiditis (SREAT): case report of reversible coma and status epilepticus in an adolescent patient and review of the literature. Eur J Pediatr 2014;173:12631273.Google Scholar
Monti, G, Pugnaghi, M, Ariatti, A, et al. Non-convulsive status epilepticus of frontal origin as the first manifestation of Hashimoto’s encephalopathy. Epileptic Disord 2011;13:253258.Google Scholar
Spatola, M, Petit-Pedrol, M, Simabukuro, MM, et al. Investigations in GABAA receptor antibody-associated encephalitis. Neurology 2017;88:10121020.Google Scholar
Maureille, A, Fenouil, T, Joubert, B, et al. Isolated seizures are a common early feature of paraneoplastic anti-GABAB receptor encephalitis. J Neurol 2019;266:195206.Google Scholar
Hacohen, Y, Joseph, S, Kneen, R, et al. Limbic encephalitis associated with elevated antithyroid antibodies. J Child Neurol 2014;29:769773.Google Scholar
Graus, F, Escudero, D, Oleaga, L, et al. Syndrome and outcome of antibody-negative limbic encephalitis. Eur J Neurol 2018;25:10111016.CrossRefGoogle ScholarPubMed
Termsarasab, P, Pitakpatapee, Y, Frucht, SJ, Srivanitchapoom, P. Steroid-responsive encephalopathy associated with autoimmune thyroiditis (SREAT) presenting with pure cerebellar ataxia. Tremor Other Hyperkinet Mov 2018;8:585.Google Scholar
Matsunaga, A, Ikawa, M, Fujii, A, et al. Hashimoto’s encephalopathy as a treatable adult-onset cerebellar ataxia mimicking spinocerebellar degeneration. Eur Neurol 2013;69:1420.Google Scholar
Marignier, R, Chenevier, F, Rogemond, V, et al. Metabotropic glutamate receptor type 1 autoantibody-associated cerebellitis: a primary autoimmune disease? Arch Neurol 2010;67:627630.Google Scholar
Yaguchi, H, Yabe, I, Takahashi, H, et al. Identification of anti-Sez6l2 antibody in a patient with cerebellar ataxia and retinopathy. J Neurol 2014;261:224226.CrossRefGoogle Scholar
Honorat, JA, Lopez-Chiriboga, AS, Kryzer, TJ, et al. Autoimmune septin-5 cerebellar ataxia. Neurol Neuroimmunol Neuroinflamm 2018;5:e474.Google Scholar
Rukmangadachar, LA, Dandapat, S, Bit-Ivan, EN, Peng, YY. Hashimoto’s encephalopathy: presenting with epilepsia partialis continua and a frontal lobe lesion. Clin Case Rep 2018;6:136142.CrossRefGoogle Scholar
Spatola, M, Sabater, L, Planaguma, J, et al. Encephalitis with mGluR5 antibodies: symptoms and antibody effects. Neurology 2018;90:e1964e1972.Google Scholar
Gini, B, Lovato, L, Cianti, R, et al. Novel autoantigens recognized by CSF IgG from Hashimoto’s encephalitis revealed by a proteomic approach. J Neuroimmunol 2008;196:153158.Google Scholar

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