Co-occurrence of amyotrophic lateral sclerosis and Leber's hereditary optic neuropathy: is mitochondrial dysfunction a modifier?

J Neurol. 2023 Jan;270(1):559-564. doi: 10.1007/s00415-022-11355-w. Epub 2022 Sep 6.

Giulia Amore¹, Veria Vacchiano^{1

2}, Chiara La Morgia^{1

2}, Maria L Valentino^{1

2}, Leonardo Caporali³, Claudio Fiorini³, Danara Ormanbekova³, Fabrizio Salvi⁴, Anna Bartoletti-Stella⁵, Sabina Capellari^{1

3}, Rocco Liguori^{1

2}, Valerio Carelli^{6

7

8}

¹ Department of Biomedical and Neuromotor Sciences (DIBINEM), University of Bologna, Bologna, Italy.
² IRCCS Istituto delle Scienze Neurologiche di Bologna, UOC Clinica Neurologica, Bologna, Italy.
³ IRCCS Istituto delle Scienze Neurologiche di Bologna, Programma di Neurogenetica, Bologna, Italy.
⁴ IRCCS Istituto delle Scienze Neurologiche di Bologna, Programma SLA Atassia Amiloidosi e Miastenia, Bologna, Italy.
⁵ Department of Experimental, Diagnostic and Specialty Medicine, DIMES University of Bologna, Bologna, Italy.
⁶ Department of Biomedical and Neuromotor Sciences (DIBINEM), University of Bologna, Bologna, Italy. valerio.carelli@unibo.it.
⁷ IRCCS Istituto delle Scienze Neurologiche di Bologna, Programma di Neurogenetica, Bologna, Italy. valerio.carelli@unibo.it.
⁸ Bellaria Hospital, Via Altura 3, 40139, Bologna, Italy. valerio.carelli@unibo.it.

No abstract available

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