Zobrazeno 1 - 10
of 37
pro vyhledávání: '"Maria Claúdia Nogueira Zerbini"'
Autor:
Cláudia Regina Gomes Cardim Mendes de Oliveira, Berenice Bilharino Mendonça, Olavo Pires de Camargo, Emilia Modolo Pinto, Sérgio Antonio Barbosa Nascimento, Maria do Rosario D. O. Latorre, Maria Claúdia Nogueira Zerbini
Publikováno v:
Clinics, Vol 62, Iss 2, Pp 167-174 (2007)
OBJECTIVE: To investigate the biological behavior of classical and atypical osteoblastomas in comparison to osteosarcomas. METHODS: Based on histological parameters, 30 osteoblastomas were subclassified as classical osteoblastomas (23/30) or atypical
Externí odkaz:
https://doaj.org/article/43b938f085264ef08c7aed4ddefb1c83
Autor:
Luís Alberto de Pádua Covas Lage, Vinícius Araújo Soares, Thales Dalessandro Meneguin, Hebert Fabrício Culler, Cadiele Oliana Reichert, Mayara D’Auria Jacomassi, Diego Gomes Cândido Reis, Maria Cláudia Nogueira Zerbini, Renata de Oliveira Costa, Vanderson Rocha, Juliana Pereira
Publikováno v:
Radiation Oncology, Vol 17, Iss 1, Pp 1-12 (2022)
Abstract Background Primary central nervous system lymphoma (PCNSL) is a rare and aggressive malignancy. Although potentially curable, its prognosis remains dismal. Its treatment is based on high-doses of methotrexate (HD-MTX) and rituximab, followed
Externí odkaz:
https://doaj.org/article/47cb8f4628334d5b80fdc3e5ff284e53
Autor:
Barbara Brito da Conceição, Isadora Pontes Cavalcante, Jean Lucas Kremer, Thais Barabba Auricino, Eduarda Corrêa Bento, Maria Claudia Nogueira Zerbini, Maria Candida Barisson Villares Fragoso, Claudimara Ferini Pacicco Lotfi
Publikováno v:
Archives of Endocrinology and Metabolism, Vol 64, Iss 4, Pp 390-401 (2020)
ABSTRACT Objective To analyze the morphological and functional characteristics of primary macronodular adrenal hyperplasia (PMAH) nodules carrying or not carrying ARMC5 mutations and the consequences of the presence of mutations in terms of the patte
Externí odkaz:
https://doaj.org/article/6f30d993c36d44a4be9daed88dda3200
Autor:
Diego Gomes Candido Reis, Débora Levy, Luís Alberto de Pádua Covas Lage, Hebert Fabrício Culler, Vanderson Rocha, Sérgio Paulo Bydlowski, Maria Cláudia Nogueira Zerbini, Juliana Pereira
Publikováno v:
Brain and Behavior, Vol 11, Iss 4, Pp n/a-n/a (2021)
Abstract Background PCNSL is a rare extranodal NHL with poor prognosis. Tumorigenesis has been associated with hyperactivation of BCR downstream and NFkB pathways. We studied the prognosis of the relative expression profile of target genes of NFkB pa
Externí odkaz:
https://doaj.org/article/d3bb88e603f643259f29152b3a6a5a8f
Autor:
Patrícia Lacerda Bellodi, Marisa Dolhnikoff, Alfredo Luiz Jacomo, Alexander Augusto de Lima Jorge, Alexandre Archanjo Ferraro, Ana Claudia Camargo Gonçalves Germani, Ana Cristina Aoun Tannuri, Beatriz Helena Carvalho Tess, Bruno Caramelli, Denise Maria Avancini Costa Malheiros, Iolanda de Fátima Lopes Calvo Tibério, José Pinhata Otoch, Luiz Fernando Ferraz da Silva, Luiz Henrique Martins Castro, Maria Cláudia Nogueira Zerbini, Milton de Arruda Martins, Rogério de Souza, Rossana Pulcineli Vieira Francisco
Publikováno v:
Clinics, Vol 76 (2021)
BACKGROUND: Even students with previous academic success may face challenges that affect their academic performance. Many medical schools offer programs to students at the risk of academic failure, to ensure that they succeed in the course. OBJECTIVE
Externí odkaz:
https://doaj.org/article/f816f0189c3c41fabbe65e55fe0ad997
Autor:
Beatriz Marinho de Paula Mariani, Mirian Yumie Nishi, Ingrid Quevedo Wanichi, Vania Balderrama Brondani, Amanda Meneses Ferreira Lacombe, Helaine Charchar, Maria Adelaide Albergaria Pereira, Victor Srougi, Fabio Yoshiaki Tanno, Filippo Ceccato, Daniela Regazzo, Mattia Barbot, Gianluca Occhi, Nora Maria Elvira Albiger, Marcelo Vieira-Corrêa, Claudio Elias Kater, Carla Scaroni, José Luis Chambô, Maria Claudia Nogueira Zerbini, Berenice B. Mendonca, Madson Q. Almeida, Maria Candida Barisson Villares Fragoso
Publikováno v:
Frontiers in Endocrinology, Vol 11 (2020)
Objective: Germline ARMC5 mutations are considered to be the main genetic cause of primary macronodular adrenal hyperplasia (PMAH). PMAH is associated with high variability of cortisol secretion caused from subclinical hypercortisolism to overt Cushi
Externí odkaz:
https://doaj.org/article/d26e5bf5debf46b8b1a8f741ad6b4046
Autor:
Fernanda Bernardi Bertonha, Silvia Yumi Bando, Leandro Rodrigues Ferreira, Paulo Chaccur, Christiana Vinhas, Maria Claudia Nogueira Zerbini, Magda Maria Carneiro-Sampaio, Carlos Alberto Moreira-Filho
Publikováno v:
PLoS ONE, Vol 15, Iss 4, p e0227547 (2020)
The human thymus suffers a transient neonatal involution, recovers and then starts a process of decline between the 1st and 2nd years of life. Age-related morphological changes in thymus were extensively investigated, but the genomic mechanisms under
Externí odkaz:
https://doaj.org/article/f2ec8f26eadb4911a222db31d90aec0e
Autor:
Suellen Serafini, Maria Mercês Santos, Ana Cristina Aoun Tannuri, Maria Claudia Nogueira Zerbini, Maria Cecília de Mendonça Coelho, Josiane de Oliveira Gonçalves, Uenis Tannuri
Publikováno v:
Diagnostic Pathology, Vol 12, Iss 1, Pp 1-5 (2017)
Abstract Background Hematoxylin-eosin (HE) staining of a full-thickness rectal wall fragment is classically used for the diagnosis of Hirschsprung disease (HD). However, this technique requires large fragments for a better diagnosis. Additionally, th
Externí odkaz:
https://doaj.org/article/bab686ca950f4b03a9f60daa53d47d9c
Autor:
Luis Alberto de Pádua Covas Lage, Tamara Carvalho dos Santos Cabral, Renata de Oliveira Costa, Marianne de Castro Gonçalves, Debora Levy, Maria Cláudia Nogueira Zerbini, Juliana Pereira
Publikováno v:
Revista Brasileira de Hematologia e Hemoterapia, Vol 37, Iss 4, Pp 277-284 (2015)
Nodal peripheral T-cell lymphomas are a rare group of neoplasms derived from post-thymic and activated T lymphocytes. A review of scientific articles listed in PubMed, Lilacs, and the Cochrane Library databases was performed using the term "periphera
Externí odkaz:
https://doaj.org/article/ddd5a7632a65403d98ee78c9c2233c12
Autor:
Denise de Fatima Forteski, Fernanda Calil Machado Netto, Andrea Barranjard Vannucci Lomonte, Bruno César Cavalcanti dos Anjos, Maria Claudia Nogueira Zerbini, Cristiano Augusto de Freitas Zerbini
Publikováno v:
Revista Brasileira de Reumatologia, Vol 54, Iss 4, Pp 326-329 (2014)
A doença de Castleman (DC) é uma desordem linfoproliferativa policlonal, também conhecida como hiperplasia nodular gigante ou hiperplasia angiofolicular linfoide. Esta é uma doença rara que está frequentemente associada ao vírus da imunodefici
Externí odkaz:
https://doaj.org/article/3af6bb5dd9ac451ca3afbf87d4626128