Zobrazeno 1 - 10
of 71
pro vyhledávání: '"Isabel Nascimento"'
Autor:
Isabel Nascimento dos Santos, Jorginete de Jesus Damião, Maria de Jesus Mendes da Fonseca, Cláudia dos Santos Cople‐Rodrigues, Odaleia Barbosa de Aguiar
Publikováno v:
Jornal de Pediatria (Versão em Português), Vol 95, Iss 3, Pp 306-313 (2019)
Objective: To examine the associations between food insecurity (IA) and social support in families of children with sickle‐cell disease (DF). Methods: This cross‐sectional study in families of 190 children from five to nine years old in follow‐
Externí odkaz:
https://doaj.org/article/02d21ffe7df24c85a24515d4a613a833
Autor:
Isabel Nascimento Santos, Jorginete de Jesus Damião, Ana Cecília Travassos Freitas, Vanessa Monteiro Voll, Cláudia dos Santos Cople Rodrigues, Odaleia Barbosa de Aguiar
Publikováno v:
Demetra, Vol 15, Iss 0, Pp e49173-e49173 (2020)
Objective: To describe the clinical, social and nutritional characteristics of children with sickle cell disease aged 5 to 9 years. Method: Cross-sectional study carried out in 2015-2016 with a random sample of 190 children receiving care at a refere
Externí odkaz:
https://doaj.org/article/6823570c22b542259a8b22eb6c2b66ba
Publikováno v:
Cell Reports, Vol 10, Iss 12, Pp 1974-1981 (2015)
SARM1 function and nicotinamide mononucleotide adenylyltransferase 2 (NMNAT2) loss both promote axon degeneration, but their relative relationship in the process is unknown. Here, we show that NMNAT2 loss and resultant changes to NMNAT metabolites oc
Externí odkaz:
https://doaj.org/article/8ad2162bda0d4a0682c72aef15edbd5d
Autor:
Clévio Nóbrega, Isabel Nascimento-Ferreira, Isabel Onofre, David Albuquerque, Nicole Déglon, Luís Pereira de Almeida
Publikováno v:
PLoS ONE, Vol 9, Iss 8, p e100086 (2014)
Machado-Joseph disease or Spinocerebellar ataxia type 3 is a progressive fatal neurodegenerative disorder caused by the polyglutamine-expanded protein ataxin-3. Recent studies demonstrate that RNA interference is a promising approach for the treatmen
Externí odkaz:
https://doaj.org/article/33775b10d91a45f49bd22670e237f3b3
Autor:
Clévio Nóbrega, Isabel Nascimento-Ferreira, Isabel Onofre, David Albuquerque, Hirokazu Hirai, Nicole Déglon, Luís Pereira de Almeida
Publikováno v:
PLoS ONE, Vol 8, Iss 1, p e52396 (2013)
Machado-Joseph disease (MJD) or spinocerebellar ataxia type 3 (SCA3) is an autosomal dominantly-inherited neurodegenerative disorder caused by the over-repetition of a CAG codon in the MJD1 gene. This expansion translates into a polyglutamine tract t
Externí odkaz:
https://doaj.org/article/34ddcc2006da447481516d0368af541a
Autor:
Lígia Sousa-Ferreira, Manuel Garrido, Isabel Nascimento-Ferreira, Clévio Nobrega, Ana Santos-Carvalho, Ana Rita Alvaro, Joana Rosmaninho-Salgado, Manuella Kaster, Sebastian Kügler, Luís Pereira de Almeida, Claudia Cavadas
Publikováno v:
PLoS ONE, Vol 6, Iss 7, p e22333 (2011)
Neuropeptide Y (NPY) produced by arcuate nucleus (ARC) neurons has a strong orexigenic effect on target neurons. Hypothalamic NPY levels undergo wide-ranging oscillations during the circadian cycle and in response to fasting and peripheral hormones (
Externí odkaz:
https://doaj.org/article/1e57eedd30f442f78020be3db427627d
Autor:
Andreia Veloza, Isabel Manita, Catarina Coelho, Catarina Saraiva, Isabel Nascimento, Ana Oliveira, Maria C Cordeiro, Jorge Portugal
Publikováno v:
Acta Médica Portuguesa, Vol 23, Iss 2 (2010)
Thyroid adenolipomas or thyrolipomas are rare benign neoplasms composed of mature adipose tissue and glandular elements. The most common clinical manifestation is a slowly enlarging neck mass. If thyroid fine-needle aspiration biopsy discloses a mixe
Externí odkaz:
https://doaj.org/article/d8323d86cea44d52a0f32c432172ce9b
Autor:
Sandro Alves, Isabel Nascimento-Ferreira, Gwennaëlle Auregan, Raymonde Hassig, Noëlle Dufour, Emmanuel Brouillet, Maria C Pedroso de Lima, Philippe Hantraye, Luís Pereira de Almeida, Nicole Déglon
Publikováno v:
PLoS ONE, Vol 3, Iss 10, p e3341 (2008)
Recent studies have demonstrated that RNAi is a promising approach for treating autosomal dominant disorders. However, discrimination between wild-type and mutant transcripts is essential, to preserve wild-type expression and function. A single nucle
Externí odkaz:
https://doaj.org/article/2766a5d9287248fead8a3c51410d315a
Autor:
Santos, Isabel Nascimento dos, Damião, Jorginete de Jesus, Fonseca, Maria de Jesus Mendes da, Cople‐Rodrigues, Cláudia dos Santos, Aguiar, Odaleia Barbosa de
Publikováno v:
In Jornal de Pediatria (Versão em Português) May-June 2019 95(3):306-313
