Please use this identifier to cite or link to this item: http://hdl.handle.net/2445/178020
Title: Proceedings of the tenth international meeting on neuroacanthocytosis syndromes
Author: Masana Nadal, Mercè
Rodríguez Allué, Manuel José
Alberch i Vié, Jordi, 1959-
Keywords: Malalties hereditàries
Corea de Huntington
Genetic diseases
Huntington's chorea
Issue Date: 21-May-2021
Abstract: The 10th International Meeting on Neuroacanthocytosis Syndromes was held online on March 10th12th, 2021. The COVID19 pandemic situation made our planned meeting in Barcelona on March 2020 to be suspended by one year, and finally took place online. The meeting followed the previous nine international symposia, the last of which was held in Dresden, Germany in March, 2018. The setting of the meeting encouraged interactions, exchange of ideas and networking opportunities among the high number of participants from around the globe, including scientists, neurologists and specially patients and caregivers. A total of 27 oral communications were distributed in 8 sessions with topics ranging from molecular and cellular functions of VPS13 genes and proteins, their involvement in Neuroacanthocytosis Syndromes and finally clinical aspects and patients care. In addition, 5 posters were presented. Altogether, scientists and neurologists discussed recent advances and set the bases for next steps, action points, and future studies in close collaboration with the patients associations, which are always actively involved in the whole process.
Note: Reproducció del document publicat a: https://doi.org/10.5334/tohm.622
It is part of: Tremor and Other Hyperkinetic Movements, 2021, vol. 11, num. 1, p. 1-19
URI: http://hdl.handle.net/2445/178020
Related resource: https://doi.org/10.5334/tohm.622
ISSN: 2160-8288
Appears in Collections:Articles publicats en revistes (IDIBAPS: Institut d'investigacions Biomèdiques August Pi i Sunyer)
Articles publicats en revistes (Institut de Neurociències (UBNeuro))
Articles publicats en revistes (Biomedicina)

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