Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Andrés Beiras-Iglesias"'
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::337039c1bf454c0cddde9ada65702252
https://doi.org/10.1007/s12035-015-9650-z
https://doi.org/10.1007/s12035-015-9650-z
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a9e8055ca6a8cd46f708b0337dc0b430
https://doi.org/10.1007/s00428-014-1626-2
https://doi.org/10.1007/s00428-014-1626-2
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::29679ff436e9eb80929498a47cf874e8
https://doi.org/10.1016/j.jneumeth.2012.12.005
https://doi.org/10.1016/j.jneumeth.2012.12.005
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c2a35df456467f3141ff8b70a08c1904
https://pubmed.ncbi.nlm.nih.gov/26006750
https://pubmed.ncbi.nlm.nih.gov/26006750
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::30653160e8d377638707d599f1ea7158
https://pubmed.ncbi.nlm.nih.gov/24997086
https://pubmed.ncbi.nlm.nih.gov/24997086
Autor:
M I Novo-Rodríguez, Adela Alonso, Jesús Eirís-Puñal, Pintos-Martínez E, Joaquín Arenas, Yolanda Campos, Manuel Castro-Gago, Andrés Beiras-Iglesias
Publikováno v:
Journal of Child Neurology. 14:131-135
We report the case of a 3-year-old girl, the only child of a nonconsanguineous couple without relevant antecedents, who was born with hydranencephalic-hydrocephalic syndrome diagnosed by ultrasonography at gestation week 28, and who was treated durin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::83bf8223d0b64fa6ff77d5dbf8f22083
https://doi.org/10.1177/088307389901400213
https://doi.org/10.1177/088307389901400213
Autor:
Pintos-Martínez E, Francisco Martínez-Azorín, Joaquín Arenas, Andrés Beiras-Iglesias, David Dacruz-Alvarez, Manuel Castro-Gago, Miguel Martín
Publikováno v:
Brain and Development. 38:783
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::38add6b87b7475ac089383c48eba4be0
https://doi.org/10.1016/j.braindev.2016.04.009
https://doi.org/10.1016/j.braindev.2016.04.009
Autor:
Andrés Beiras Iglesias, Juan José González Agúndez, Virginia Fernández Redondo, Fernando Valdés Tascón, Juan Manuel Calzada González, Eduardo Iglesias García
Publikováno v:
Actas Dermo-Sifiliográficas. 93:175-177
The presence of melanotic cells in the dermis is known with the term of dermal melanocytosis. Inside this concept we find the blue nevus or the Mongolian spot. We report a 55-year-old woman that referred for 10 years the appearance of a pigmented les
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::140cd56bb38446af82b209fdf3810add
https://doi.org/10.1016/s0001-7310(02)76552-6
https://doi.org/10.1016/s0001-7310(02)76552-6
Autor:
Sagrario Maroto, Yolanda Campos, Pintos-Martínez E, Joaquín Arenas, Manuel Castro-Gago, Jesús Eirís-Puñal, Andrés Beiras-Iglesias
Publikováno v:
Journal of child neurology. 11(2)
We report the case histories of two 6-month-old girls, both with young, nonconsanguineous parents, referred to us for suspected blindness. In both cases, Leber's congenital amaurosis was diagnosed. Due to persistently high lactic acid levels in blood
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::46302581acd0440b2fa615fc43145157
https://pubmed.ncbi.nlm.nih.gov/8881986
https://pubmed.ncbi.nlm.nih.gov/8881986