Zobrazeno 1 - 10
of 86
pro vyhledávání: '"Beiras Iglesias A"'
Autor:
J. Víctor Álvarez, Carolina Herrero Filgueira, Alexandre de la Fuente González, Cristóbal Colón Mejeras, Andrés Beiras Iglesias, Shunji Tomatsu, José Blanco Méndez, Asteria Luzardo Álvarez, María Luz Couce, Francisco J. Otero Espinar
Publikováno v:
Pharmaceutics, Vol 11, Iss 10, p 522 (2019)
Mucopolysaccharidosis IVA (Morquio A) is a rare inherited metabolic disease caused by deficiency of the lysosomal enzyme N-acetylgalatosamine-6-sulfate-sulfatase (GALNS). Until now, treatments employed included hematopoietic stem cell transplantation
Externí odkaz:
https://doaj.org/article/a123f631e56c40dab3d1d83b018f860e
Autor:
Javier Iglesias-Gonzalez, Sofía Sánchez-Iglesias, Andrés Beiras-Iglesias, Estefanía Méndez-Álvarez, Ramón Soto-Otero
Publikováno v:
Molecular Neurobiology. 54:563-570
Numerous studies have highlighted the potential of aluminium as an aetiological factor for some neurodegenerative disorders, particularly Alzheimer's disease and Parkinson's disease. Our previous studies have shown that aluminium can cause oxidative
Akademický článek
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Autor:
José Cameselle-Teijeiro, María Jesús Ladra, Ihab Abdulkader, Paula Soares, Catarina Eloy, Manuel Sobrinho-Simões, Francisco Xabier Varela Barreiro, Andrés Beiras-Iglesias
Publikováno v:
Virchows Archiv. 465:359-364
The present study describes in depth a case of Riedel thyroiditis (RT) to clarify its pathogenesis and its putative inclusion in the spectrum of IgG4-related disease. We report the clinicopathological, immunohistochemical, and ultrastructural feature
Autor:
Couce Ml, Blanco Méndez J, Colón Mejeras C, González Af, Beiras Iglesias A, Otero Espinar Fj, Shunji Tomatsu, Herrero Filgueira C, Luzardo Álvarez A, Álvarez Jv
Publikováno v:
Minerva. Repositorio Institucional de la Universidad de Santiago de Compostela
instname
Pharmaceutics
Pharmaceutics, Vol 11, Iss 10, p 522 (2019)
Volume 11
Issue 10
instname
Pharmaceutics
Pharmaceutics, Vol 11, Iss 10, p 522 (2019)
Volume 11
Issue 10
Mucopolysaccharidosis IVA (Morquio A) is a rare inherited metabolic disease caused by deficiency of the lysosomal enzyme N-acetylgalatosamine-6-sulfate-sulfatase (GALNS). Until now, treatments employed included hematopoietic stem cell transplantation
Autor:
Javier Iglesias-Gonzalez, Ramón Soto-Otero, Andrés Beiras-Iglesias, Estefanía Méndez-Álvarez, Sofía Sánchez-Iglesias
Publikováno v:
Journal of Neuroscience Methods. 213:39-42
Isolated mitochondria are widely used in metabolic and oxidative stress studies for neurodegenerative diseases. In the present work, the influence of EGTA and EDTA has been tested on a sucrose-based differential centrifugation protocol in order to es
Autor:
Miguel A. Martín, David Dacruz-Alvarez, Pintos-Martínez E, Andrés Beiras-Iglesias, Francisco Martínez-Azorín, Joaquín Arenas, Manuel Castro-Gago
Publikováno v:
Braindevelopment. 38(1)
Choline kinase beta gene ( CHKB ) mutations have been identified in Megaconial Congenital Muscular Dystrophy (MDCMC) patients, a very rare inborn error of metabolism with 21 cases reported worldwide. We report the case of a Spanish boy of Caucasian o
Publikováno v:
RUNA. Repositorio da Consellería de Sanidade e Sergas
Servizo Galego de Saúde (SERGAS)
Servizo Galego de Saúde (SERGAS)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::3341b7f297e346d801787be071816c4f
http://hdl.handle.net/20.500.11940/8162
http://hdl.handle.net/20.500.11940/8162
Akademický článek
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Autor:
Francisco Martínez-Azorín, Miguel A. Martín, David Dacruz-Alvarez, Pintos-Martínez E, Aitor Delmiro, Manuel Castro-Gago, Joaquín Arenas, Andrés Beiras-Iglesias
Publikováno v:
European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society. 18(6)
Background Choline kinase beta gene (CHKB) mutations have been identified in Megaconial Congenital Muscular Dystrophy (MDCMC) patients, but never in patients with an additional combined deficiency of complexes I, III and IV and mitochondrial DNA (mtD