Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Lucia Ilaria Manfredini"'
Autor:
Giuseppe Bonapace, Rosa Gullace, Daniela Concolino, Grazia Iannello, Radha Procopio, Monica Gagliardi, Gennarina Arabia, Gaetano Barbagallo, Angela Lupo, Lucia Ilaria Manfredini, Grazia Annesi, Aldo Quattrone
Publikováno v:
Heliyon, Vol 5, Iss 6, Pp e01954- (2019)
Background: Fragile X-associated tremor/ataxia syndrome is a late-onset neurodegenerative disorder that affects about 40% of carriers of CGG-repeat expansions in the premutation range within the fragile X gene (FMR1). Main clinical features include i
Externí odkaz:
https://doaj.org/article/80ec8d5ad1604445bfccd2b43d380b3f
Autor:
Grazia Iannello, Radha Procopio, Monica Gagliardi, Lucia Ilaria Manfredini, Daniela Concolino, Giuseppe Bonapace, Gaetano Barbagallo, Grazia Annesi, Gennarina Arabia, Rosa Gullace, Angela Lupo, Aldo Quattrone
Publikováno v:
Heliyon, Vol 5, Iss 6, Pp e01954-(2019)
Heliyon (Londen) 5 (2019): e01954. doi:10.1016/j.heliyon.2019.e01954
info:cnr-pdr/source/autori:Bonapace, Giuseppe; Gullace, Rosa; Concolino, Daniela; Iannello, Grazia; Procopio, Radha; Gagliardi, Monica; Arabia, Gennarina; Barbagallo, Gaetano; Lupo, Angela; Manfredini, Lucia Ilaria; Annesi, Grazia; Quattrone, Aldo/titolo:Intracellular FMRpolyG-Hsp70 complex in fibroblast cells from a patient affected by fragile X tremor ataxia syndrome/doi:10.1016%2Fj.heliyon.2019.e01954/rivista:Heliyon (Londen)/anno:2019/pagina_da:e01954/pagina_a:/intervallo_pagine:e01954/volume:5
Heliyon
Heliyon (Londen) 5 (2019): e01954. doi:10.1016/j.heliyon.2019.e01954
info:cnr-pdr/source/autori:Bonapace, Giuseppe; Gullace, Rosa; Concolino, Daniela; Iannello, Grazia; Procopio, Radha; Gagliardi, Monica; Arabia, Gennarina; Barbagallo, Gaetano; Lupo, Angela; Manfredini, Lucia Ilaria; Annesi, Grazia; Quattrone, Aldo/titolo:Intracellular FMRpolyG-Hsp70 complex in fibroblast cells from a patient affected by fragile X tremor ataxia syndrome/doi:10.1016%2Fj.heliyon.2019.e01954/rivista:Heliyon (Londen)/anno:2019/pagina_da:e01954/pagina_a:/intervallo_pagine:e01954/volume:5
Heliyon
Background Fragile X-associated tremor/ataxia syndrome is a late-onset neurodegenerative disorder that affects about 40% of carriers of CGG-repeat expansions in the premutation range within the fragile X gene (FMR1). Main clinical features include in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8a8fb37b1ac2a93e5617e3e58f387732
http://www.sciencedirect.com/science/article/pii/S2405844019355653
http://www.sciencedirect.com/science/article/pii/S2405844019355653
Autor:
Daniela Concolino, Gennarina Arabia, Aldo Quattrone, Radha Procopio, Giuseppe Bonapace, Monica Gagliardi, Grazia Annesi, Grazia Iannello, Lucia Ilaria Manfredini, Rosa Gullace, Gaetano Barbagallo, Angela Lupo
Fragile X associated tremor/ataxia syndrome (FXTAS) is a late-onset neurodegenerative disorder that affects about 25% of carriers of CGG repeat expansions (55,200 repeats) in the premutation range within the fragile X gene (FMR1). Main clinical featu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::693ed385229af722d982daf5642ea5d2
https://doi.org/10.1101/278416
https://doi.org/10.1101/278416
