Zobrazeno 1 - 10
of 42
pro vyhledávání: '"Marcelo A. Costa Lima"'
Autor:
Raquel Garcia Rocco da Silva, Marcelo A. Costa Lima, Claudia de Melo Moura, Jorge Luiz Luescher, Ludmila Nascimento Rodrigues Campos, Daniel de Souza e Silva, Márcia Gonçalves Ribeiro
Publikováno v:
Arquivos de Neuro-Psiquiatria, Vol 82, Iss 12, Pp 001-009 (2024)
Background It is believed that genetic factors play a role in the development and severity of neural injury among people with distal symmetrical polyneuropathy (DSP), because some genes are involved in specific biological pathways, acting in differen
Externí odkaz:
https://doaj.org/article/4df90882a0be4ebcbb243c4d69839b4c
Autor:
Carolina Monteiro Leite de Castro, Carolina Oliveto Bastos Pereira, Joissy Aprigio, Marcelo A. Costa Lima, Márcia G. Ribeiro, Márcia Rodrigues Amorim
Publikováno v:
Human Cell. 35:849-855
Aneuploidies, such as Down syndrome (DS), are the leading cause of pregnancy loss. Abnormalities in aurora kinase proteins result in genomic instability and aneuploidy, mainly in tumors. Thus, polymorphisms in Aurora kinase genes could influence the
Autor:
Joissy Aprigio, Carolina M. L. de Castro, Marcelo A. Costa Lima, Márcia G. Ribeiro, Iêda M. Orioli, Márcia R. Amorim
Publikováno v:
J Community Genet
Down syndrome is the main genetic cause of intellectual disability. Many studies describe the clinical characteristics of DS patients; however, few have investigated the clinical profile of mothers who have children with DS. Advanced maternal age (
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a403ad9135987d9b3b30b653aef287a3
https://europepmc.org/articles/PMC10104982/
https://europepmc.org/articles/PMC10104982/
Autor:
Clarice Pagani Savastano, Kênia Balbi El-Jaick, Marcelo Aguiar Costa-Lima, Cristina Maria Batista Abath, Sebastiano Bianca, Denise Pontes Cavalcanti, Têmis Maria Félix, Gioacchino Scarano, Juan Clinton Llerena Jr, Fernando Regla Vargas, Miguel Ângelo Martins Moreira, Hector N. Seuánez, Eduardo Enrique Castilla, Iêda Maria Orioli
Publikováno v:
Genetics and Molecular Biology, Vol 37, Iss 1 suppl 1, Pp 250-262 (2014)
Holoprosencephaly (HPE) is a spectrum of brain and facial malformations primarily reflecting genetic factors, such as chromosomal abnormalities and gene mutations. Here, we present a clinical and molecular analysis of 195 probands with HPE or microfo
Externí odkaz:
https://doaj.org/article/2c49f53a85b04a1988e64794050857aa
Publikováno v:
ID on line REVISTA DE PSICOLOGIA. 14:979-987
Resumo: A lipodistrofia é definida pelas alterações na distribuição da gordura corporal e este estudo objetiva averiguar as contribuições da massagem modeladora quando associada ao creme lipolítico de café no tratamento da lipodistrofia loca
Autor:
Márcia R. Amorim, Thereza Quirico-Santos, Cláudia de Melo Moura, Márcia Gonçalves Ribeiro, Hazel N. Barboza, Marcelo Aguiar Costa-Lima, Joissy Aprigio
Publikováno v:
Journal of Molecular Neuroscience. 70:1410-1414
Down syndrome (DS) is the most common form of mental disability of genetic etiology. Nondisjunction of chromosome 21 is the leading cause of the syndrome. In general, free trisomy 21 cases originate from missegregation in maternal meiosis. Several re
Publikováno v:
Brazilian Journal of Health Review. 3:6502-6513
Publikováno v:
Human cell. 35(1)
Publikováno v:
Culturas e história dos povos indígenas 2
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::43455418bb5a2929eb20e5e4e079596f
https://doi.org/10.22533/at.ed.3512123073
https://doi.org/10.22533/at.ed.3512123073