Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Aryadnne L, Schactae"'
Autor:
Clarissa M. Comim, Jaime A. Soares, Adriano Alberti, Viviane Freiberger, Letícia Ventura, Paula Dias, Aryadnne L. Schactae, Leoberto R. Grigollo, Amanda V. Steckert, Daniel F. Martins, Rudy J. Nodari Junior, Mariz Vainzof, João Quevedo
Publikováno v:
Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP
Universidade de São Paulo (USP)
instacron:USP
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::71777723d58785a6c5e66a8fd830a870
https://doi.org/10.1007/s10072-022-05928-w
https://doi.org/10.1007/s10072-022-05928-w
Autor:
Clarissa M. Comim, Jaime A. Soares, Adriano Alberti, Viviane Freiberger, Letícia Ventura, Paula Dias, Aryadnne L. Schactae, Leoberto R. Grigollo, Amanda V. Steckert, Daniel F. Martins, Rudy J. Nodari Junior, Mariz Vainzof, João Quevedo
Publikováno v:
Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP
Universidade de São Paulo (USP)
instacron:USP
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c8a45cf40d1bbd8071aa23ee79214db7
Autor:
Clarissa M, Comim, Jaime A, Soares, Adriano, Alberti, Viviane, Freiberger, Letícia, Ventura, Paula, Dias, Aryadnne L, Schactae, Leoberto R, Grigollo, Amanda V, Steckert, Daniel F, Martins, Rudy J Nodari, Junior, Mariz, Vainzof, João, Quevedo
Publikováno v:
Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical NeurophysiologyReferences. 43(7)
Congenital Muscular Dystrophy type 1D (MDC1D) is characterized by a hypoglycosylation of α-dystroglycan protein (α-DG), and this may be strongly implicated in increased skeletal muscle tissue degeneration and abnormal brain development, leading to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::d610e037b55d37396702f33211e48e3a
https://pubmed.ncbi.nlm.nih.gov/35353268
https://pubmed.ncbi.nlm.nih.gov/35353268
Autor:
Aryadnne L. Schactae, Daphne Palmas, Monique Michels, Felipe Dal-Pizzol, Mariz Vainzof, Clarissa M. Comim, Jaqueline S. Generoso, Tatiana Barichello
Publikováno v:
Current Neurovascular Research. 14:60-64
Congenital Muscular Dystrophy type 1D (CMD1D) is characterized by an abnormal glycosylation of α-DG (α-dystroglycan) and is associated to the central nervous system (CNS) abnormalities such as cognitive impairment. The purpose of the research was t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a9fafb7bc481b4113ba4c0c1519760ef
https://doi.org/10.2174/1567202613666161201204549
https://doi.org/10.2174/1567202613666161201204549
Autor:
Mariz Vainzof, Clarissa M. Comim, Aryadnne L. Schactae, Francielle Mina, Letícia Ventura, João Quevedo, Diogo Dominguini, Jaime A. Soares, Viviane Freiberger
Publikováno v:
Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP
Universidade de São Paulo (USP)
instacron:USP
Congenital muscular dystrophies 1D (CMD1D) present a mutation on the LARGE gene and are characterized by an abnormal glycosylation of α-dystroglycan (α-DG), strongly implicated as having a causative role in the development of central nervous system
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bb708ebb9ca8ab98f15ff995662dd1a9