Epilepsias mioclônicas progressivas

um grupo de doenças a espera de tratamento

Authors

  • Marcelo Masruha Rodrigues Professor Adjunto do Setor de Neurologia Infantil, Departamento de Neurologia e Neurocirurgia – UNIFESP/EPM, São Paulo-SP, Brasil

DOI:

https://doi.org/10.34024/rnc.2010.v18.8426

Keywords:

editorial

Abstract

.

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References

Shahwan A, Farrell M, Delanty N. Progressive myoclonic epilepsies: a review of genetic and therapeutic aspects. Lancet Neurol 2005;4:239-48.

Siqueira LF. Epilepsias Mioclônicas Progressivas: revisão de aspectos clínicos e moleculares. Rev Neurocienc 2010;18:561-71.

Siqueira LF. Progressive myoclonic epilepsies: review of clinical, molecular and therapeutic aspects. J Neurol 2010;257:1612-9.

Galliciotti G, Glatzel M, Kinter J, Kozlov SV, Cinelli P, Rulicke T, et al. Accumulation of mutant neuroserpin precedes development of clinical symptoms in familial encephalopathy with neuroserpin inclusion bodies. Am J Pathol 2007;170:1305-13.

Bhatia KP, Brown P, Gregory R, Lennox GG, Manji H, Thompson PD, et al. Progressive myoclonic ataxia associated with coeliac disease. The myoclonus is of cortical origin, but the pathology is in the cerebellum. Brain 1995;118(Pt 5):1087-93.

Gonzalez S, Rodrigo L, Salas-Puig J, Astudillo A, Fuentes D, LopezVazquez A, et al. [Progressive myoclonic ataxia associated with antibodies against Purkinje cells in a celiac patient]. Rev Esp Enferm Dig 2005;97:918-21.

Published

2010-12-31

Issue

Section

Editorial

How to Cite

1.
Rodrigues MM. Epilepsias mioclônicas progressivas: um grupo de doenças a espera de tratamento. Rev Neurocienc [Internet]. 2010 Dec. 31 [cited 2025 Dec. 13];18(4):427-8. Available from: https://periodicos.unifesp.br/index.php/neurociencias/article/view/8426