Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Giulia Mennella"'
Autor:
Chiara Gemelli, Alessandro Geroldi, Sara Massucco, Lucia Trevisan, Ilaria Callegari, Lucio Marinelli, Giulia Ursino, Mehrnaz Hamedani, Giulia Mennella, Silvia Stara, Giovanni Maggi, Laura Mori, Cristina Schenone, Fabio Gotta, Serena Patrone, Alessia Mammi, Paola Origone, Valeria Prada, Lucilla Nobbio, Paola Mandich, Angelo Schenone, Emilia Bellone, Marina Grandis
Publikováno v:
Life, Vol 12, Iss 3, p 402 (2022)
Charcot–Marie–Tooth (CMT) disease is the most commonly inherited neurological disorder. This study includes patients affected by CMT during regular follow-ups at the CMT clinic in Genova, a neuromuscular university center in the northwest of Ital
Externí odkaz:
https://doaj.org/article/6a0ea7e07bf84bfa957c4bd6181b2c97
Autor:
Angelo Schenone, Michael E. Shy, Valeria Prada, Marina Grandis, Riccardo Zuccarino, Cristina Schenone, Giulia Mennella
Publikováno v:
Neurological Sciences. 43:2759-2764
Charcot-Marie-Tooth (CMT) disease is the most common hereditary neuropathy with an estimated prevalence of 1 person affected on 2500. Frequent symptoms include distal weakness and muscle wasting, sensory loss, reduced deep tendon reflexes, and skelet
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d65d6f50753a54d9b8381fd00df349e3
https://doi.org/10.1007/s10072-021-05646-9
https://doi.org/10.1007/s10072-021-05646-9
Autor:
Riccardo Zuccarino, Emilia Bellone, Giulia Mennella, Angelo Schenone, Marina Grandis, Giulia Robbiano, Mehrnaz Hamedani, Valeria Prada
Publikováno v:
Journal of the peripheral nervous system : JPNSREFERENCES. 25(4)
The symptomatology of Charcot-Marie-Tooth (CMT) disease mainly involves the feet and the hands. To date, there is no consensus on how to evaluate hand function in CMT. The aim of this study is to correlate the data of the engineered glove Hand Test S
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3d1bd2532aad46203f088ffbf0b5f544
https://pubmed.ncbi.nlm.nih.gov/33140522
https://pubmed.ncbi.nlm.nih.gov/33140522