Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Renáta Lázár"'
Autor:
Luciana Beatriz Mendes Gomes, Renata Lazari Sandoval, Camila Bragança Xavier, Tatiana Strava Correa, Raquel Midori Koga Matuda, Zenaide Silva de Souza, Luiz Guilherme Cernaglia Aureliano de Lima, Mariana Petaccia de Macedo, Filomena Marino Carvalho, Daniele Assad Suzuki
Publikováno v:
Case Reports in Oncology, Vol 17, Iss 1, Pp 1-9 (2024)
Malignant mixed müllerian tumor (MMMT) is a rare neoplasm, consisting of carcinomatous (epithelial) and sarcomatous (mesenchymal) components that most commonly arise in the endometrium and more infrequently in the ovaries, fallopian tube, cervix, an
Externí odkaz:
https://doaj.org/article/c7114bc99ed947dabb1548b4fbd062a6
Autor:
Edit Hermesz, Renáta Lázár, Hajnalka Orvos, Petra Talapka, Ágnes Ferencz, Krisztina N. Dugmonits, Szabolcs Zahorán
Publikováno v:
British Journal of Haematology. 174:932-941
Summary Pregnancy is a state associated with an enhanced metabolism and demand for O2, which may lead to the overproduction of reactive oxygen species (ROS) and hence to oxidative stress. An elevated ROS level may result in delayed development and a
Publikováno v:
Redox Report. 20:103-108
Objective: Multiple pregnancy is associated with an enhanced metabolism and demand for O2, which may lead to the overproduction of reactive oxygen species and the development of oxidative stress. The degree of oxidative damage depends on the level of
Autor:
Renata Lazari Sandoval, Cibele Masotti, Mariana Petaccia de Macedo, Maurício Fernando Silva Almeida Ribeiro, Ana Carolina Rathsam Leite, Sibele Inacio Meireles, Rodrigo Medeiros Bovolin, Fernando Costa Santini, Rodrigo Ramella Munhoz, Denis Leonardo Fontes Jardim, Artur Katz, Anamaria Aranha Camargo, Gustavo dos Santos Fernandes, Maria Isabel Achatz
Publikováno v:
JCO Global Oncology, Vol , Iss 7, Pp 1141-1150 (2021)
PURPOSELi-Fraumeni syndrome (LFS) is rare in the worldwide population, but it is highly prevalent in the Brazilian population because of a founder mutation, TP53 p.R337H, accounting for 0.3% of south and southeastern population. Clinical criteria for
Externí odkaz:
https://doaj.org/article/6a8c6059217b4076af1e7479ce18af74
Autor:
Bruno Augusto Alves Martins, Reinaldo Falluh Filho, Romulo Medeiros de Almeida, Renata Lazari Sandoval
Publikováno v:
Journal of Coloproctology, Vol 41, Iss 04, Pp 443-446 (2021)
Introduction Most cases of colorectal cancer (CRC) occur sporadically; however, ∼ 3% to 6% of all CRCs are related to inherited syndromes, such as Lynch syndrome and familial adenomatous polyposis (FAP). The adenomatous polyposis coli (APC) and mut
Externí odkaz:
https://doaj.org/article/7db6e988481a48249f14ca450faf9f67
Autor:
Ana Carolina Rathsam Leite, Daniele Assad Suzuki, Allan Anderson Lima Pereira, Natalia Polidorio Machado, Romualdo Barroso-Sousa, Tatiana Strava Correa, Fernanda Cesar Moura, Igor Alexandre Protzner Morbeck, Brenda Pires Gumz, Luiza Dib Batista Bugiato Faria, Gustavo dos Santos Fernandes, Renata Lazari Sandoval
Publikováno v:
Frontiers in Oncology, Vol 12 (2022)
BackgroundIdentifying individuals at a higher risk of developing cancer is a major concern for healthcare providers. Cancer predisposition syndromes are the underlying cause of cancer aggregation and young-onset tumors in many families. Germline gene
Externí odkaz:
https://doaj.org/article/c5d6f477aa174347acc50a372bfb16d2
Autor:
Renata Lazari Sandoval, Natalia Polidorio, Ana Carolina Rathsam Leite, Mariana Cartaxo, Janina Pontes Pisani, Carla Vanessa Quirino, Loureno Cezana, Natálya Gonçalves Pereira, Allan Andresson Lima Pereira, Benedito Mauro Rossi, Maria Isabel Achatz
Publikováno v:
Frontiers in Oncology, Vol 12 (2022)
Breast cancer (BC) is the most prevalent malignancy in women with Li-Fraumeni syndrome (LFS). The literature on BC in LFS is limited due to its rarity worldwide. A TP53 founder pathogenic variant (c.1010G>A; p.R337H) is responsible for the higher pre
Externí odkaz:
https://doaj.org/article/e4027b7cb5df4ac3a42df4ae9ba8d4d5
Autor:
Renata Lazari Sandoval, Ana Carolina Rathsam Leite, Daniel Meirelles Barbalho, Daniele Xavier Assad, Romualdo Barroso, Natalia Polidorio, Carlos Henrique Dos Anjos, Andréa Discaciati de Miranda, Ana Carolina Salles de Mendonça Ferreira, Gustavo Dos Santos Fernandes, Maria Isabel Achatz
Publikováno v:
PLoS ONE, Vol 16, Iss 2, p e0247363 (2021)
Brazil is the largest country in South America and the most genetically heterogeneous. The aim of the present study was to determine the prevalence of germline pathogenic variants (PVs) in Brazilian patients with breast cancer (BC) who underwent gene
Externí odkaz:
https://doaj.org/article/8adb010a05334b4faa15e8f38084f104
Publikováno v:
Brazilian Journal of Oral Sciences, Vol 3, Iss 11 (2015)
Maxillofacial defects caused by cancer treatment are a huge problem, affecting the quality of life of patients. Some of these deformities are minimized using facial epistheses, which needs some additional retenion devices, like glasses or skin adhesi
Externí odkaz:
https://doaj.org/article/cccac220b6794498846c72d8fa258bc1
Autor:
Renata Lazari Sandoval, Daniel Henrique Koga, Lígia Schmitd Buloto, Ricardo Suzuki, Luciano Lauria Dib
Publikováno v:
Journal of Applied Oral Science, Vol 11, Iss 4, Pp 337-341 (2003)
Background. Oral mucositis is a common complication of some malignancies treatment, causing therapeutic modifications due to patient's debilitation, which often interferes with the prognosis of the disease. Many attempts have been made to find an opt
Externí odkaz:
https://doaj.org/article/f4d8232fd25848798f2308afba057c9f