Zobrazeno 1 - 10
of 533
pro vyhledávání: '"Ana Maria Martins"'
Autor:
Ana Maria Martins dos Santos, Vanessa Pereira Corrêa, Núbia Carelli Pereira de Avelar, Cesar de Oliveira, Ione Jayce Ceola Schneider
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-10 (2024)
Abstract Low serum 25(OH)D levels (
Externí odkaz:
https://doaj.org/article/6c6d5bf3a4cc44a5b5fabc55d4e39e0d
Autor:
Natalia Cristina Aguirre, Pamela Victoria Villalba, Martín Nahuel García, Carla Valeria Filippi, Juan Gabriel Rivas, María Carolina Martínez, Cintia Vanesa Acuña, Augusto J. López, Juan Adolfo López, Pablo Pathauer, Dino Palazzini, Leonel Harrand, Javier Oberschelp, Martín Alberto Marcó, Esteban Felipe Cisneros, Rocío Carreras, Ana Maria Martins Alves, José Carlos Rodrigues, H. Esteban Hopp, Dario Grattapaglia, Eduardo Pablo Cappa, Norma Beatriz Paniego, Susana Noemí Marcucci Poltri
Publikováno v:
Frontiers in Genetics, Vol 15 (2024)
Eucalyptus dunnii is one of the most important Eucalyptus species for short-fiber pulp production in regions where other species of the genus are affected by poor soil and climatic conditions. In this context, E. dunnii holds promise as a resource to
Externí odkaz:
https://doaj.org/article/d140ac3618824575893330f6135efd79
Autor:
Ida Vanessa Doederlein Schwartz, Andrea Amaro Quesada, Erlane Marques Ribeiro, Ana Maria Martins, Daniel Reda Fenga Vilela, André Pessoa
Publikováno v:
Arquivos de Neuro-Psiquiatria, Vol 81, Iss 07, Pp 685-695 (2023)
Background Phenylketonuria (PKU) is an inborn error of metabolism caused by deficient activity of phenylalanine hydroxylase. In Brazil, the National Neonatal Screening Program enables early treatment of patients with PKU, which prevents them from dev
Externí odkaz:
https://doaj.org/article/1d2b4216fdda4986b600f447e5ef8cc4
Autor:
Barbara C.F. Ramos, Carolina S. Aranda, Rita S.B. Cardona, Ana Maria Martins, Dirceu Solé, Sue Ann C. Clemens, Ralf Clemens
Publikováno v:
Jornal de Pediatria, Vol 99, Iss , Pp S70-S80 (2023)
Objective: Through a literature review, make recommendations regarding immunizations in people living with Inborn Error of Metabolism (IEM) in Brazil, assess the possible impact on metabolic decompensations after immunization, and if this specific po
Externí odkaz:
https://doaj.org/article/d944206726334807810ffb036af7cb35
Autor:
Paulo C. Gregório, Gilson Biagini, Regiane S. da Cunha, Júlia Budag, Ana Maria Martins, Lara Valiño Rivas, Elberth M. Schiefer, Maria Dolores Sánchez-Niño, Alberto Ortiz, Andréa E. M. Stinghen, Fellype C. Barreto
Publikováno v:
Kidney & Blood Pressure Research, Pp 1-10 (2022)
Background and Aims: Inflammation and endothelial damage play a pivotal role in Fabry disease (FD) manifestations. In daily clinical practice, FD is mainly monitored by traditional biomarkers of target organ injury, such as serum creatinine and prote
Externí odkaz:
https://doaj.org/article/8ff34d0a10fe41c88d672644d3fe72b9
Autor:
Ione Jayce Ceola Schneider, Tauana Prestes Schmidt, Ana Maria Martins dos Santos, Vanessa Pereira Correa, Leandro Pereira Garcia, Cesar de Oliveira, Maria Alice Franzoi
Publikováno v:
Dialogues in Health, Vol 1, Iss , Pp 100010- (2022)
Background: The aim of this study was to report the overall survival and baseline factors associated with OS for breast, cervical and ovarian cancer in Florianópolis, Southern Brazil, a region with quality-of-life indicators comparable to high-incom
Externí odkaz:
https://doaj.org/article/8ed159470d5a409abf7b3568092f18f2
Autor:
Ione Jayce Ceola Schneider, Tauana Prestes Schmidt, Vanessa Pereira Correa, Ana Maria Martins dos Santos, Bruna Vanti da Rocha, Leandro Pereira Garcia, Roger Flores Ceccon
Publikováno v:
Revista de Saúde Pública, Vol 56 (2022)
ABSTRACT OBJECTIVE To estimate the probability of survival and prognostic factors for tobacco-related neoplasms in a population-based cohort. METHODS This is a cohort with data from the Population-Based Cancer Registry of Florianópolis, southern Bra
Externí odkaz:
https://doaj.org/article/4c47e8a8cc7141ce944f83277cfc7caa
Autor:
Christoph Wanner, Ulla Feldt‐Rasmussen, Ana Jovanovic, Aleš Linhart, Meng Yang, Elvira Ponce, Eva Brand, Dominique P. Germain, Derralynn A. Hughes, John L. Jefferies, Ana Maria Martins, Albina Nowak, Bojan Vujkovac, Frank Weidemann, Michael L. West, Alberto Ortiz
Publikováno v:
ESC Heart Failure, Vol 7, Iss 3, Pp 825-834 (2020)
Abstract Aims Long‐term treatment effect studies in large female Fabry patient groups are challenging to design because of phenotype heterogeneity and lack of appropriate comparison groups, and have not been reported. We compared long‐term cardio
Externí odkaz:
https://doaj.org/article/d245bf80912e439eb9ef9a86af5c8b32
Autor:
Rachel Sayuri Honjo, Evelyn Cristina Nuñez Vaca, Gabriela Nunes Leal, Deipara Monteiro Abellan, Nana Miura Ikari, Marcelo Biscegli Jatene, Ana Maria Martins, Chong Ae Kim
Publikováno v:
BMC Medical Genetics, Vol 21, Iss 1, Pp 1-8 (2020)
Abstract Background The Mucopolysaccharidosis type VI (MPS VI), also known as Maroteaux-Lamy syndrome (OMIM 253200) is an autosomal recessive lysosomal disorder, caused by the deficiency of the enzyme N-acetylgalactosamine 4-sulfatase (also known as
Externí odkaz:
https://doaj.org/article/7cdb8dec43974bb7b44713da18cf9cd0
Autor:
Patrícia Varela, Gianna Mastroianni Kirsztajn, Fabiana L. Motta, Renan P. Martin, Lauro T. Turaça, Henrique L. F. Ferrer, Caio P. Gomes, Priscila Nicolicht, Maryana Mara Marins, Juliana G. Pessoa, Marion C. Braga, Vânia D’Almeida, Ana Maria Martins, João B. Pesquero
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 15, Iss 1, Pp 1-12 (2020)
Abstract Background Fabry disease is a rare X-linked inherited disorder caused by deficiency of α-Galactosidase A. Hundreds of mutations and non-coding haplotypes in the GLA gene have been described; however, many are variants of unknown significanc
Externí odkaz:
https://doaj.org/article/9a7dc0be8c6041e5b97f74e6d93ed7cd