Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Ekatrina Fedotova"'
Autor:
Galina Baydakova, A E Kopytova, Irina Miliukhina, Ekatrina Fedotova, Ekaterina Yur'evna Zakharova, A. F. Yakimovskii, Mikhael Nikolaev, Sergey N. Illarioshkin, S.N. Pchelina, A. Emelyanov, A A Timofeeva, Konstantin Senkevich, O. Berkovich
Publikováno v:
Movement Disorders. 33:1325-1330
INTRODUCTION Glucocerebrosidase 1 mutations, the most common genetic contributor to Parkinson's disease (PD), have been associated with decreased glucocerebrosidase enzymatic activity in PD patients with glucocerebrosidase 1 mutations (glucocerebrosi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::76b69a16c59a3482f638ba48ff78b8a9
https://doi.org/10.1002/mds.27393
https://doi.org/10.1002/mds.27393
Autor:
Sofya, Pchelina, Galina, Baydakova, Mikhael, Nikolaev, Konstantin, Senkevich, Anton, Emelyanov, Alena, Kopytova, Irina, Miliukhina, Andrey, Yakimovskii, Alla, Timofeeva, Olga, Berkovich, Ekatrina, Fedotova, Sergey, Illarioshkin, Ekaterina, Zakharova
Publikováno v:
Movement disorders : official journal of the Movement Disorder Society. 33(8)
Glucocerebrosidase 1 mutations, the most common genetic contributor to Parkinson's disease (PD), have been associated with decreased glucocerebrosidase enzymatic activity in PD patients with glucocerebrosidase 1 mutations (glucocerebrosidase 1-PD). H
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::0447ae74afff462e9d1ff8965cc1fa94
https://pubmed.ncbi.nlm.nih.gov/30192031
https://pubmed.ncbi.nlm.nih.gov/30192031