The previously unrecognised association of myoclonus in two patients with LHON with the 11778/ND4 pathogenic mutationis described. EEG failed to disclose epileptic figures, and a back averaging study suggested that myoclonus was cortical inorigin in both patients.

Leber's hereditary optic neuropathy (LHON/11778) with myoclonus: report of two cases / V., C., M. L., V., R., L., Meletti, S., R., V., F., P., G. L., M., F., B., A., B., P., M.. - In: JOURNAL OF NEUROLOGY, NEUROSURGERY AND PSYCHIATRY. - ISSN 0022-3050. - 71:6(2001), pp. 813-816. [10.1136/jnnp.71.6.813]

Leber's hereditary optic neuropathy (LHON/11778) with myoclonus: report of two cases

MELETTI, Stefano;
2001-01-01

Abstract

The previously unrecognised association of myoclonus in two patients with LHON with the 11778/ND4 pathogenic mutationis described. EEG failed to disclose epileptic figures, and a back averaging study suggested that myoclonus was cortical inorigin in both patients.
2001
Leber's hereditary optic neuropathy (LHON/11778) with myoclonus: report of two cases / V., C., M. L., V., R., L., Meletti, S., R., V., F., P., G. L., M., F., B., A., B., P., M.. - In: JOURNAL OF NEUROLOGY, NEUROSURGERY AND PSYCHIATRY. - ISSN 0022-3050. - 71:6(2001), pp. 813-816. [10.1136/jnnp.71.6.813]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11381/3058202
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