Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Amin Karimi-Moghadam"'
Publikováno v:
Cellular and Molecular Neurobiology
Parkinson disease (PD) is known as a common progressive neurodegenerative disease which is clinically diagnosed by the manifestation of numerous motor and nonmotor symptoms. PD is a genetically heterogeneous disorder with both familial and sporadic f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d8037433b44769e0b87158fec800e8a3
http://europepmc.org/articles/PMC6061130
http://europepmc.org/articles/PMC6061130
Publikováno v:
Genes & Genomics. 39:433-443
Leber’s congenital amaurosis (LCA) is considered as one of the main causes of congenital blindness. In view of the genetically heterogeneous nature of the disease, indirect diagnosis using linkage analysis has proven to be useful in molecular diagn
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ea1c23ba2d95e79fef3e72b1dd8240e3
https://doi.org/10.1007/s13258-016-0467-6
https://doi.org/10.1007/s13258-016-0467-6
Publikováno v:
Acta neurologica Belgica. 120(3)
Glutamate is considered as the predominant excitatory neurotransmitter in the mammalian central nervous systems (CNS). Alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid receptors (AMPARs) are the main glutamate-gated ionotropic channels that m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6476b2eb3729742ba7e57708cf988234
https://pubmed.ncbi.nlm.nih.gov/32152997
https://pubmed.ncbi.nlm.nih.gov/32152997