Zobrazeno 1 - 10
of 85
pro vyhledávání: '"Walter Pinto"'
Autor:
Cylmara Aziz, Armando Morales, Walter Pinto, Vanessa Fanchini, Luis Dell Aquila, Carine Sangaleti, Rosilene Elias, Maria Dalboni
Publikováno v:
Frontiers in Pediatrics, Vol 11 (2023)
AimThis prospective pilot study evaluated inflammatory and intestinal barrier biomarkers and the effects of a synbiotic in obese adolescents.MethodsEighteen obese and 20 eutrophic adolescents were evaluated for body composition using bioimpedance ana
Externí odkaz:
https://doaj.org/article/ab42f829d32b4bd6921ac88cbc8ea049
Publikováno v:
Revista Interdisciplinar em Cultura e Sociedade, Vol 0, Iss 0, Pp 248-264 (2020)
RESUMO Recuerdos de niñez y mocedad (1908) é uma obra autobiográfica do escritor Miguel de Unamuno (1864 – 1936), na qual o autor narra diversas experiências da infância e adolescência. Nela, Unamuno aborda algumas lembranças que, por se ma
Externí odkaz:
https://doaj.org/article/5352567241b2497a893f045500c54c85
Publikováno v:
Revista Brasileira de Anestesiologia, Vol 59, Iss 4, Pp 387-395 (2009)
JUSTIFICATIVA E OBJETIVOS: O bloqueio de plexo cervical permite avaliação neurológica durante a endarterctomia, além de manter analgesia pós-operatória. A clonidina é agonista alfa2 com efeito analgésico em diferentes bloqueios. O objetivo de
Externí odkaz:
https://doaj.org/article/423bfb893b6b4cc9b152a30d169582b1
Autor:
Heliane Guerra Serra, Carmen Sílvia Bertuzzo, Mônica Corso Pereira, Cláudio Lúcio Rossi, Walter Pinto Júnior, Ilma Aparecida Paschoal
Publikováno v:
Jornal Brasileiro de Pneumologia, Vol 34, Iss 12, Pp 1019-1025 (2008)
OBJETIVO: Determinar a concentração de alfa 1-antitripsina (AAT) e a prevalência dos alelos S e Z em indivíduos sintomáticos respiratórios crônicos. MÉTODOS: Pacientes com tosse crônica e dispnéia foram submetidos à avaliação clínica, e
Externí odkaz:
https://doaj.org/article/4738f6a393a94ae68da7898dc458509c
Autor:
Kelly Santos, Sofia H.V. Lemos-Marini, Maria T.M. Baptista, Luciana Cardoso Bonadia, Walter Pinto Júnior, Carmen Sílvia Bertuzzo
Publikováno v:
Genetics and Molecular Biology, Vol 29, Iss 1, Pp 41-44 (2006)
Turner syndrome (TS) is an interesting model for investigating the association between methylenetetrahydrofolate reductase (MTHFR) gene polymorphisms and non-disjunction because of the high frequency of chromosomal mosaicism among patients with this
Externí odkaz:
https://doaj.org/article/ae247afd9e92467e9b7143a735f66ed5
Autor:
David Enrique Aguilar Rodriguez, Carmen Silvia Passos Lima, Gustavo Jacob Lourenço, Maria Estela Figueiredo, Jorge David Aivazoglu Carneiro, Luiz Gonzaga Tone, Juan Clinton Llerena Jr., Raquel Alves Toscano, Silvia Brandalise, Walter Pinto Júnior, Fernando Ferreira Costa, Carmen Sílvia Bertuzzo
Publikováno v:
Genetics and Molecular Biology, Vol 28, Iss 2, Pp 205-209 (2005)
Fanconi anaemia (FA) is a recessive autosomal disease determined by mutations in genes of at least eleven complementation groups, with distinct distributions in different populations. As far as we know, there are no reports regarding the molecular ch
Externí odkaz:
https://doaj.org/article/0382fe48f2db4ba8964845241ca988ae
Autor:
Gregório Lorenzo Acácio, Ricardo Barini, Walter Pinto Júnior, Renato Luís Silveira Ximenes, Heverton Pettersen, Marcos Faria
Publikováno v:
São Paulo Medical Journal, Vol 119, Iss 1, Pp 19-23 (2001)
CONTEXT: The literature shows an association between several ultrasound markers and chromosome abnormality. Among these, measurement of nuchal translucency has been indicated as a screening method for aneuploidy. The trisomy of chromosome 21 has been
Externí odkaz:
https://doaj.org/article/33b671a1f95343e782e68b339c516269
Autor:
Iscia Lopes-Cendesi, Hélio G.A. Teive, Maria E Calcagnotto, Jaderson C. da Costa, Francisco Cardoso, Erika Viana, Jaime A. Maciel, João Radvany, Walter O. Arruda, Paulo C. Trevisol-Bittencourt, Pedro Rosa Neto, Isabel Silveira, Carlos E. Steiner, Walter Pinto-Júnior, André S. Santos, Ylmar Correa Neto, Lineu C. Werneck, Abelardo Q.C. Araújo, Gerson Carakushansky, Luiz R. Mello, Laura B. Jardim, Guy A. Rouleau
Publikováno v:
Arquivos de Neuro-Psiquiatria, Vol 55, Iss 3B, Pp 519-529 (1997)
Spinocerebellar ataxia type 1 (SCA1), spinocerebellar ataxia type 2 (SCA2) and Machado-Joseph disease or spinocerebellar ataxia type 3 (MJD/SCA3) are three distinctive forms of autosomal dominant spinocerebellar ataxia (SCA) caused by expansions of a
Externí odkaz:
https://doaj.org/article/02bdfc208fe340e890a607549bd42d95
Autor:
Iscia Lopes-Cendes, Carlos E. Steiner, Isabel Silveira, Walter Pinto-Junior, Jayme A. Maciel, Guy A. Rouleau
Publikováno v:
Arquivos de Neuro-Psiquiatria, Vol 54, Iss 3, Pp 412-418 (1996)
The spinocerebellar ataxias (SCAs) are a clinically and genetically heterogeneous group of late onset neurodegenerative disorders. To date, seven different genes causing autosomal dominant SCA have been mapped: SCA1, SCA2, Machado-Joseph disease (MJD
Externí odkaz:
https://doaj.org/article/5b31715fe1f8445cb5004d81276957d1
Autor:
Walter O. Arruda, Rogério S. Clemente, Ricardo Ramina, Ari A. Pedrozo, Rui F. Pilotto, Walter Pinto Jr., Luiz F. Bleggi-torres
Publikováno v:
Arquivos de Neuro-Psiquiatria, Vol 53, Iss 2, Pp 312-317 (1995)
The authors describe a family with three members affected by glioblastoma. The proband patient, a 7 year-old girl, developed a rare complication, a pulmonary metastasis. Chromosomal analysis of her peripheral blood lymphocytes showed a normal karyoty
Externí odkaz:
https://doaj.org/article/68712e182097433ab8b9a97fd1da3087