Zobrazeno 1 - 10
of 61
pro vyhledávání: '"Francisco Barros‐Angueira"'
Autor:
Paula Sánchez-Pintos, Maria José Camba-Garea, Beatriz Martin López-Pardo, Jose A. Cocho de Juan, M. Dolores Bóveda, Sofia Barbosa-Gouveia, Maria E Vázquez-Mosquera, Francisco Barros-Angueira, Raquel Fernández Patiño, Maria L. Couce
Publikováno v:
BMC Pediatrics, Vol 24, Iss 1, Pp 1-6 (2024)
Abstract Background The recommended diet attitude in the recently described galactose mutarotase (GALM) deficiency is not yet established. We describe two 9-years twins who remain asymptomatic despite prolonged partial dietary liberalization from 18
Externí odkaz:
https://doaj.org/article/328914c3c58d4540a861bf9746e623c8
Determination and diagnostic value of CA9 mRNA in peripheral blood of patients with oral leukoplakia
Autor:
Manuel Torres López, Mario Pérez Sayáns, Cintia Chamorro Petronacci, Francisco Barros Angueira, Pilar Gándara Vila, Alejandro Lorenzo Pouso, Abel García García
Publikováno v:
Journal of Enzyme Inhibition and Medicinal Chemistry, Vol 33, Iss 1, Pp 951-955 (2018)
Background: Oral leukoplakia is one of the most common oral premalignant disorder. The classical evaluation through tissue biopsy is not always valid to evaluate the risk of malignization. Material and methods: RT-qPCR was performed on 47 blood sampl
Externí odkaz:
https://doaj.org/article/e13750b8f80a4200b1cf1a76feec21da
Autor:
Mario Pérez‐Sayáns, Cintia M. Chamorro‐Petronacci, Susana B. Bravo, María E. Padín‐Iruegas, Esteban Guitián‐Fernández, Francisco Barros‐Angueira, Rita Quintas‐Rey, Abel García‐García
Publikováno v:
Oral Diseases.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5775184ff2cbf9d73d98bbfe62e8a80d
https://doi.org/10.1111/odi.14572
https://doi.org/10.1111/odi.14572
Autor:
Carmen González Mao, Susana Romero Santos, Daisy Castiñeiras Ramos, Cristina Collazo Abal, Francisco Barros Angueira, Emilio C. Pazos Lago
Publikováno v:
Advances in Laboratory Medicine, Vol 2, Iss 4, Pp 567-570 (2021)
Objectives Hereditary xanthinuria is a rare, autosomal and recessive disorder characterized by severe hypouricemia and increased xanthine excretion, caused by a deficiency of xanthine dehydrogenase/oxidase (XDH/XO, EC: 1.17.1.4/1.17.3.2) in type I, o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ec051192232672d3609aa9de714d0432
https://doi.org/10.1515/almed-2021-0018
https://doi.org/10.1515/almed-2021-0018
Autor:
Nabil Alberto Sabbagh Casado, Francisco Barros Angueira, Daniel Apolinar García Estévez, Beatriz Quintáns
Publikováno v:
Neurology Perspectives. 2:53-55
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5389071529e9866252751fdb9641f476
https://doi.org/10.1016/j.neurop.2021.10.006
https://doi.org/10.1016/j.neurop.2021.10.006
Autor:
Francisco Barros-Angueira, Tamara Lourido-Cebreiro, María Luisa Pérez del Molino, Ana Casal-Mouriño, Ana Palacios-Bartolomé, Luis Valdés, Tara Pereiro-Brea
Publikováno v:
Archivos de Bronconeumología. 56:60-62
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::831e945a262276cbf12b26ba6f122b85
https://doi.org/10.1016/j.arbres.2019.07.011
https://doi.org/10.1016/j.arbres.2019.07.011
Determination and diagnostic value of CA9 mRNA in peripheral blood of patients with oral leukoplakia
Autor:
Alejandro Ismael Lorenzo Pouso, Manuel Torres López, Francisco Barros Angueira, Pilar Gándara Vila, Cintia Micaela Chamorro Petronacci, Mario Pérez Sayáns, Abel García García
Publikováno v:
Journal of Enzyme Inhibition and Medicinal Chemistry, Vol 33, Iss 1, Pp 951-955 (2018)
Journal of Enzyme Inhibition and Medicinal Chemistry
Journal of Enzyme Inhibition and Medicinal Chemistry
Background: Oral leukoplakia is one of the most common oral premalignant disorder. The classical evaluation through tissue biopsy is not always valid to evaluate the risk of malignization. Material and methods: RT-qPCR was performed on 47 blood sampl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::61647ee134a19a4a2bb16bba5d334d89
https://doi.org/10.1080/14756366.2018.1466120
https://doi.org/10.1080/14756366.2018.1466120
Autor:
Goitzane Marcaida, David Albuquerque, Alicia Amadoz, Francisco Barros Angueira, Fátima Gimeno Ferrer, Juan Carlos Ferrer García, Carolina Monzó, Raquel Rodríguez López
Publikováno v:
Indian Journal of Case Reports. 3:171-174
Reduced genetic variability in isolated populations promotes the prevalence of long contiguous stretches of homozygosity (LCSH) that may carry deleterious mutations, manifesting recessive syndromes such as Alstrom syndrome (OMIM # 203800), caused pri
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0ddf56d6ef4d8b5ec4adc31e9db4efe1
https://doi.org/10.32677/ijcr.2017.v03.i04.001
https://doi.org/10.32677/ijcr.2017.v03.i04.001
Autor:
Mario Pérez-Sayáns, Mercedes Gallas-Torreira, José-Manuel Aguirre-Urizar, Francisco Barros-Angueira, Abel García-García, Rodríguez-Tojo Mj, J. M. Suárez-Peñaranda
Publikováno v:
Biotechnic & Histochemistry. 90:439-444
We described earlier the possible role of ATPaseC1 expression as a diagnostic and prognostic marker for oral cancer; others have reported its use for tumors of the lung and breast. We assessed ATPaseC1 expression in a sample of oral squamous cell car
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3976275fb3238d2a66d81b0ee1e85393
https://doi.org/10.3109/10520295.2015.1023357
https://doi.org/10.3109/10520295.2015.1023357
Autor:
Francisco Sousa Santos, Lidia Castro-Feijoo, Teresa Rego, Francisco Barros Angueira, Paloma Cabanas Rodriguez, Manuel Castro-Gago, Carmen Gomez Lado, Jesus Barreiro Conde
Publikováno v:
HORMONES. 16
Monocarboxylate transporter 8 (MCT8) is an active and specific thyroid hormone transporter into neurons. MCT8 mutations cause an X-linked condition known as Allan-Herndon-Dudley syndrome and are characterized by impaired psychomotor development and t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8349301dd3e6deb1697693eeecaaa006
https://doi.org/10.14310/horm.2002.1733
https://doi.org/10.14310/horm.2002.1733