Zobrazeno 1 - 10
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pro vyhledávání: '"Paula Sancho"'
Plastic contamination of sandy beaches along the southern Baltic – a one season field survey results
Autor:
Mikołaj Mazurkiewicz, Paula Sancho Martinez, Weronika Konwent, Kajetan Deja, Lech Kotwicki, Jan Marcin Węsławski
Publikováno v:
Oceanologia, Vol 64, Iss 4, Pp 769-780 (2022)
The subject of this study was microplastics (>32 µm), large micro-/macroplastics (>2 mm) and plastic litter (visible by naked eye) contamination on sandy beaches and in coastal waters along the Polish coast of the Baltic Sea. Microplastics were stud
Externí odkaz:
https://doaj.org/article/835c9433db4e41208296b24ec746ce7a
Plastic contamination of sandy beaches along the southern Baltic – a one season field survey results
Autor:
Mazurkiewicz, Mikołaj, Martinez, Paula Sancho, Konwent, Weronika, Deja, Kajetan, Kotwicki, Lech, Węsławski, Jan Marcin
Publikováno v:
In Oceanologia October-December 2022 64(4):769-780
Autor:
Marta Correa‐Vela, Vincenzo Lupo, Marta Montpeyó, Paula Sancho, Anna Marcé‐Grau, Jorge Hernández‐Vara, Alejandra Darling, Alison Jenkins, Sandra Fernández‐Rodríguez, Cristina Tello, Laura Ramírez‐Jiménez, Belén Pérez, Ángel Sánchez‐Montáñez, Alfons Macaya, María J. Sobrido, Marta Martinez‐Vicente, Belén Pérez‐Dueñas, Carmen Espinós
Publikováno v:
Annals of Clinical and Translational Neurology, Vol 7, Iss 8, Pp 1436-1442 (2020)
Abstact FBXO7 is implicated in the ubiquitin–proteasome system and parkin‐mediated mitophagy. FBXO7defects cause a levodopa‐responsive parkinsonian‐pyramidal syndrome(PPS). Methods: We investigated the disease molecular bases in a child with
Externí odkaz:
https://doaj.org/article/5962ad217fd2467d95a29552c3e8210a
Publikováno v:
Spanish Journal of Medicine, Vol 2, Iss 1 (2022)
Background and objective: The aim of this study was to evaluate the accuracy of computed tomography (CT) attenuation values in differentiating transudates from exudates; a controversial issue in the literature. Methods: A total of 317 consecutive pat
Externí odkaz:
https://doaj.org/article/c3a8e1f367bd474fb7cc677c63cccf15
Autor:
Dolores Martínez-Rubio, Isabel Hinarejos, Paula Sancho, Nerea Gorría-Redondo, Raquel Bernadó-Fonz, Cristina Tello, Clara Marco-Marín, Itxaso Martí-Carrera, María Jesús Martínez-González, Ainhoa García-Ribes, Raquel Baviera-Muñoz, Isabel Sastre-Bataller, Irene Martínez-Torres, Anna Duat-Rodríguez, Patrícia Janeiro, Esther Moreno, Leticia Pías-Peleteiro, Mar O’Callaghan Gordo, Ángeles Ruiz-Gómez, Esteban Muñoz, Maria Josep Martí, Ana Sánchez-Monteagudo, Candela Fuster, Amparo Andrés-Bordería, Roser Maria Pons, Silvia Jesús-Maestre, Pablo Mir, Vincenzo Lupo, Belén Pérez-Dueñas, Alejandra Darling, Sergio Aguilera-Albesa, Carmen Espinós
Publikováno v:
International Journal of Molecular Sciences, Vol 23, Iss 19, p 11847 (2022)
Our clinical series comprises 124 patients with movement disorders (MDs) and/or ataxia with cerebellar atrophy (CA), many of them showing signs of neurodegeneration with brain iron accumulation (NBIA). Ten NBIA genes are accepted, although isolated c
Externí odkaz:
https://doaj.org/article/65e1319d27ad461db2e041f1cb14beef
Publikováno v:
Educação & Formação, Vol 5, Iss 3 (2020)
Este artigo resulta da análise do romance A triste história de Eredegalda do livro Enquanto o sono não vem, editora Rocco, 2013. Em 2017, esse livro foi retirado das escolas públicas brasileiras por tematizar o incesto. A polêmica ensejou debate
Externí odkaz:
https://doaj.org/article/b1b7a06e086a44bc9f28b198956758c2
Autor:
Paula Sancho, Amparo Andrés-Bordería, Nerea Gorría-Redondo, Katia Llano, Dolores Martínez-Rubio, María Eugenia Yoldi-Petri, Luba Blumkin, Pablo Rodríguez de la Fuente, Fernando Gil-Ortiz, Leonor Fernández-Murga, Ana Sánchez-Monteagudo, Vincenzo Lupo, Belén Pérez-Dueñas, Carmen Espinós, Sergio Aguilera-Albesa
Publikováno v:
International Journal of Molecular Sciences, Vol 22, Iss 5, p 2505 (2021)
(1) Background: A non-progressive congenital ataxia (NPCA) phenotype caused by β-III spectrin (SPTBN2) mutations has emerged, mimicking spinocerebellar ataxia, autosomal recessive type 14 (SCAR14). The pattern of inheritance, however, resembles that
Externí odkaz:
https://doaj.org/article/fc6a808cdc5c49769f2b6e655f50897f
Publikováno v:
Antioxidants, Vol 9, Iss 10, p 1020 (2020)
The syndromes of neurodegeneration with brain iron accumulation (NBIA) encompass a group of invalidating and progressive rare diseases that share the abnormal accumulation of iron in the basal ganglia. The onset of NBIA disorders ranges from infancy
Externí odkaz:
https://doaj.org/article/ac9fe3fff7084b0c9614b8aebba6b30b
Publikováno v:
European Journal of Investigation in Health, Psychology and Education, Vol 4, Iss 2, Pp 131-140 (2014)
La enfermedad de Alzheimer se ha convertido en una de las dolencias más prevalentes y que más preocupa en nuestra sociedad por el impacto que genera tanto en el paciente como en familiares y cuidadores. Debido en gran medida a que los tratamientos
Externí odkaz:
https://doaj.org/article/0ebcf0ecdf314f879d6a1c14120319ea
Autor:
Dolores Martínez-Rubio, Ángela Rodríguez-Prieto, Paula Sancho, Carmen Navarro-González, Nerea Gorría-Redondo, Javier Miquel-Leal, Clara Marco-Marín, Alison Jenkins, Mario Soriano-Navarro, Alberto Hernández, Belén Pérez-Dueñas, Pietro Fazzari, Sergio Aguilera-Albesa, Carmen Espinós
Publikováno v:
HUMAN MOLECULAR GENETICS
r-CIPF. Repositorio Institucional Producción Científica del Centro de Investigación Principe Felipe (CIPF)
instname
r-IIS La Fe. Repositorio Institucional de Producción Científica del Instituto de Investigación Sanitaria La Fe
Scientia
r-CIPF. Repositorio Institucional Producción Científica del Centro de Investigación Principe Felipe (CIPF)
instname
r-IIS La Fe. Repositorio Institucional de Producción Científica del Instituto de Investigación Sanitaria La Fe
Scientia
17 páginas, 8 figuras
Peroxiredoxin 3 (PRDX3) encodes a mitochondrial antioxidant protein, which is essential for the control of reactive oxygen species homeostasis. So far, PRDX3 mutations are involved in mild-to-moderate progressive juvenile
Peroxiredoxin 3 (PRDX3) encodes a mitochondrial antioxidant protein, which is essential for the control of reactive oxygen species homeostasis. So far, PRDX3 mutations are involved in mild-to-moderate progressive juvenile
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3cdcc3ce146164c11fcb0a4936001ae4
https://pubmed.ncbi.nlm.nih.gov/35766882
https://pubmed.ncbi.nlm.nih.gov/35766882