Epileptic syndrome with myoclonus as manifestation of adult-onset CblC deficiency
J Neurol
.
2022 Sep;269(9):5173-5178.
doi: 10.1007/s00415-022-11129-4.
Epub 2022 Apr 11.
Authors
Roberta Di Giacomo
#
1
,
Ettore Salsano
#
2
,
Francesco Deleo
3
,
Chiara Pastori
3
,
Giuseppe Didato
3
,
Andrea Stabile
3
,
Rosalba Ferrario
4
,
Anna Rita Giovagnoli
4
,
Chiara Benzoni
2
,
Lidia Sarro
5
,
Elisa Visani
3
,
Laura Canafoglia
3
Affiliations
1
Epilepsy Unit, Fondazione IRCCS Istituto Neurologico Carlo Besta, Via Celoria 11, 20133, Milan, Italy. roberta.digiacomo@istituto-besta.it.
2
Unit of Rare Neurodegenerative and Neurometabolic Diseases, Fondazione IRCCS Istituto Neurologico Carlo Besta, Milan, Italy.
3
Epilepsy Unit, Fondazione IRCCS Istituto Neurologico Carlo Besta, Via Celoria 11, 20133, Milan, Italy.
4
Neurology and Neuropathology Unit, Fondazione IRCCS Istituto Neurologico Carlo Besta, Milan, Italy.
5
Department of Neurology, Martini Hospital, ASL Città Di Torino, Torino, Italy.
#
Contributed equally.
PMID:
35403876
DOI:
10.1007/s00415-022-11129-4
No abstract available
Publication types
Letter
Research Support, Non-U.S. Gov't
MeSH terms
Adult
Electroencephalography
Epileptic Syndromes*
Humans
Myoclonus* / diagnosis
Myoclonus* / etiology
Grants and funding
grant NET2013-02355313/Ministero della Salute
grant RF-2016-02363230/Ministero della Salute