Spinal and bulbar muscular atrophy: Kennedy's disease and its first description by Hiroshi Kawahara in 1897 von Teive, H.A.G., Coutinho, L., Cardoso, F.E.C., Tsuji, S.

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May Parkinson's disease be a protective factor against CNS involvement by SARS-CoV2? von Spina Tensini, F., Spina Tensini, T., Franklin, G.L., Teive, H.A.G.

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Phenotype in parkinsonian and nonparkinsonian LRRK2 G2019S mutation carriers von MARRAS, C, SCHUELE, B, CHUANG, R. S.-I, ZADIKOF, C, STEEVES, T, PRAKASH, K. M, DE BIE, R. M. A, ADELI, G, THOMSEN, T, JOHANSEN, K. K, TEIVE, H. A, ASANTE, A, MUNHOZ, R. P, REGINOLD, W, LANG, A. E, ROGAEVA, E, LANGSTON, J. W, KASTEN, M, MEANEY, C, KLEIN, C, WADIA, P. M, LIM, S.-Y

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Consensus Paper: Neurophysiological Assessments of Ataxias in Daily Practice von Ilg, W., Branscheidt, M., Butala, A., Celnik, P., de Paola, L., Horak, F. B., Schöls, L., Teive, H. A. G., Vogel, A. P., Zee, D. S., Timmann, D.

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An open study of botulinum-A toxin treatment of trigeminal neuralgia von PIOVESAN, E. J, TEIVE, H. G, KOWACS, P. A, DELLA COLETTA, M. V, WERNECK, L. C, SILBERSTEIN, S. D

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Non-motor symptoms in patients with hereditary spastic paraplegia caused by SPG4 mutations von Servelhere, K. R., Faber, I., Saute, J. A. M., Moscovich, M., D'Abreu, A., Jardim, L. B., Teive, H. A. G., Lopes-Cendes, I., Franca Jr, M. C.

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The locked-in syndrome: The early French descriptions von Teive, H.A.G., Ferreira, M.G., Coutinho, L., Camargo, C.H.F., Munhoz, R.P., Walusinski, O.

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Zolpidem in movement disorders after cardiac arrest von Arruda, W.O, Silva, M.S, Bertholdo, D.B, Munhoz, R.P, Teive, H.A.G

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Autonomic dysfunction in hereditary spastic paraplegia type 4 von González‐Salazar, C., Takazaki, K. A. G., Martinez, A. R. M., Pimentel‐Silva, L. R., Jacinto‐Scudeiro, L. A., Nakagawa, É. Y., Fujiwara Murakami, C. E., Saute, J. A. M., Pedroso, J. L., Barsottini, O. G. P., Teive, H. A. G., França Jr, M. C.

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Clinical phenotype of Brazilian families with spinocerebellar ataxia 10 von TEIVE, H. A. G, ROA, B. B, RASKIN, S, FANG, P, ARRUDA, W. O, CORREA, Y. NETO, GAO, R, WERNECK, L. C, ASHIZAWA, T

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SPG4-related hereditary spastic paraplegia: frequency and mutation spectrum in Brazil von França Jr, M.C., Dogini, D.B., D'Abreu, A., Teive, H.A.G., Munhoz, R.P., Raskin, S., Moro, A., Melo, C.C., Gomes, A.P., Saute, J.A.M., Jardim, L.B., Lopes-Cendes, I.

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Migraine, subarachnoid haemorrhage, thunderclap headache and vertigo – Differential diagnosis in Florence + The Machine’s “DRUMMING SONG” von Branco Germiniani, F, Roza, T.H, Kahakura Pedro, M, Piovesan, E, Teive, H

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And the words are meaningless- apahasia in Florence + The Machine’s “all this and heaven too” von Branco Germiniani, F, Roza, T.H, Kahakura Pedro, M, Piovesan, E, Teive, H

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Central nervous system paracoccidioidomycosis: clinical features and laboratorial findings von de Almeida, S.M, Queiroz-Telles, F, Teive, H.A.G, Ribeiro, C.E.L, Werneck, L.C

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Leão's cortical spreading depression : From experimental artifact to physiological principle von TEIVE, H. A. G, KOWACS, P. A, MARANHAO FILHO, P, PIOVESAN, E. J, WERNECK, L. C

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Acute allergic reaction following injection of generic, government-provided botulinum toxin a (GGP-BTA) for hemifacial spasm von Branco Germiniani, F, Teive, H, Scola, R.H, Brito, R.N, Scavasine, V, Canever, M.M, Mannarino Borges, C, Ribas, G, Miksza Thölken, K.F, Zuneda Serafini, S

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Symptom onset of spinocerebellar ataxia type 10 in pregnancy and puerperium von Teive, H.A.G, Arruda, W.O, Raskin, S, Munhoz, R.P, Zavala, J.A, Werneck, L.C, Ashizawa, T

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Skin biopsy in Lafora disease: Genotype-phenotype correlations and diagnostic pitfalls von ANDRADE, D. M, ACKERLEY, C. A, MINETT, T. S. C, TEIVE, H. A. G, BOHLEGA, S, SCHERER, S. W, MINASSIAN, B. A

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New parkin mutations and atypical phenotypes in families with autosomal recessive parkinsonism von RAWAL, N, PERIQUET, M, HORSTINK, M. W. I. M, DOS SANTOS BELE, W, BROUSOLLE, E, DESTEE, A, MIZUNO, Y, FARRER, M, DELEUZE, J.-F, DE MICHELE, G, AGID, Y, DÜRR, A, LOHMANN, E, BRICE, A, LÜCKING, C. B, TEIVE, H. A, AMBROSIO, G, RASKIN, S, LINCOLN, S, HATTORI, N, GUIMARAES, J

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Huntington's disease-like 2 and apparent ancestry von Rodrigues, GGR, Teive, HAG, Tumas, V

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