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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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