Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Juan M. Suarez"'
Publikováno v:
Phytotaxa. 479:44-54
Leucocoprinus brunneosporus sp. nov., collected at the Santa Catalina Reserve (Buenos Aires, Argentina), is proposed as a new species. We performed separate phylogenetic analyses of the nuclear rDNA large subunit (28S) and the complete nuclear rDNA i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c9212930399585f630e5cb385287f217
https://doi.org/10.11646/phytotaxa.479.1.3
https://doi.org/10.11646/phytotaxa.479.1.3
Publikováno v:
Darwiniana, nueva serie, Volume: 8, Issue: 2, Pages: 438-448, Published: DEC 2020
CONICET Digital (CONICET)
Consejo Nacional de Investigaciones Científicas y Técnicas
instacron:CONICET
CONICET Digital (CONICET)
Consejo Nacional de Investigaciones Científicas y Técnicas
instacron:CONICET
Se citan por primera vez tres nuevas especies de Agaricomycetes para la Argentina: Cortinarius casimiri var. hoffmannii, Lactarius hepaticus y Mycena margarita. En el presente trabajo se proveen descripciones completas e ilustraciones de las mismas c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1984ce4748854129934b7d56add12f27
https://doi.org/10.14522/darwiniana.2020.82.888
https://doi.org/10.14522/darwiniana.2020.82.888
Autor:
David Gómez-Fernández, Ana Romero-González, Juan M. Suárez-Rivero, Paula Cilleros-Holgado, Mónica Álvarez-Córdoba, Rocío Piñero-Pérez, José Manuel Romero-Domínguez, Diana Reche-López, Alejandra López-Cabrera, Salvador Ibáñez-Mico, Marta Castro de Oliveira, Andrés Rodríguez-Sacristán, Susana González-Granero, José Manuel García-Verdugo, José A. Sánchez-Alcázar
Publikováno v:
Antioxidants, Vol 13, Iss 8, p 1023 (2024)
Mutations in the lipoyltransferase 1 (LIPT1) gene are rare inborn errors of metabolism leading to a fatal condition characterized by lipoylation defects of the 2-ketoacid dehydrogenase complexes causing early-onset seizures, psychomotor retardation,
Externí odkaz:
https://doaj.org/article/3e5f8306564c49ea85740f0320439a87
Autor:
Marta Talaverón-Rey, Mónica Álvarez-Córdoba, Irene Villalón-García, Suleva Povea-Cabello, Juan M. Suárez-Rivero, David Gómez-Fernández, Ana Romero-González, Alejandra Suárez-Carrillo, Manuel Munuera-Cabeza, Paula Cilleros-Holgado, Diana Reche-López, Rocío Piñero-Pérez, José A. Sánchez-Alcázar
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 18, Iss 1, Pp 1-23 (2023)
Abstract Background Neurodegeneration with brain iron accumulation (NBIA) disorders are a group of neurodegenerative diseases that have in common the accumulation of iron in the basal nuclei of the brain which are essential components of the extrapyr
Externí odkaz:
https://doaj.org/article/a9c9d7d4ff2e4fdeafccf4fbfe00f6d4
Autor:
Mónica Álvarez-Córdoba, Diana Reche-López, Paula Cilleros-Holgado, Marta Talaverón-Rey, Irene Villalón-García, Suleva Povea-Cabello, Juan M. Suárez-Rivero, Alejandra Suárez-Carrillo, Manuel Munuera-Cabeza, Rocío Piñero-Pérez, José A. Sánchez-Alcázar
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 17, Iss 1, Pp 1-16 (2022)
Abstract Background Neurodegeneration with brain iron accumulation (NBIA) is a group of rare neurogenetic disorders frequently associated with iron accumulation in the basal nuclei of the brain characterized by progressive spasticity, dystonia, muscl
Externí odkaz:
https://doaj.org/article/25dc1fcca1da406d810dd2635ade6c2f
Autor:
Juan M. Suárez-Rivero, Carmen J. Pastor-Maldonado, Suleva Povea-Cabello, Mónica Álvarez-Córdoba, Irene Villalón-García, Marta Talaverón-Rey, Alejandra Suárez-Carrillo, Manuel Munuera-Cabeza, Diana Reche-López, Paula Cilleros-Holgado, Rocío Piñero-Perez, José A. Sánchez-Alcázar
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 17, Iss 1, Pp 1-23 (2022)
Abstract Background Mitochondrial diseases represent one of the most common groups of genetic diseases. With a prevalence greater than 1 in 5000 adults, such diseases still lack effective treatment. Current therapies are purely palliative and, in mos
Externí odkaz:
https://doaj.org/article/36b1121325ae4a249c38c5ee37bf18fa
Autor:
Mónica Álvarez-Córdoba, Marta Talaverón-Rey, Irene Villalón-García, Suleva Povea-Cabello, Juan M. Suárez-Rivero, Alejandra Suárez-Carrillo, Manuel Munuera-Cabeza, Joaquín J. Salas, José A. Sánchez-Alcázar
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 16, Iss 1, Pp 1-16 (2021)
Abstract Background Neurodegeneration with brain iron accumulation (NBIA) is a group of genetic neurological disorders frequently associated with iron accumulation in the basal nuclei of the brain characterized by progressive spasticity, dystonia, mu
Externí odkaz:
https://doaj.org/article/6bc379513f8b46b78c586b7fa2c6900e
Autor:
Irene Villalón-García, Mónica Álvarez-Córdoba, Suleva Povea-Cabello, Marta Talaverón-Rey, Marina Villanueva-Paz, Raquel Luzón-Hidalgo, Juan M. Suárez-Rivero, Alejandra Suárez-Carrillo, Manuel Munuera-Cabeza, Joaquín J. Salas, Rafael Falcón-Moya, Antonio Rodríguez-Moreno, José A. Armengol, José A. Sánchez-Alcázar
Publikováno v:
Neurobiology of Disease, Vol 165, Iss , Pp 105649- (2022)
Background: PLA2G6-Associated Neurodegeneration (PLAN) is a rare neurodegenerative disease with autosomal recessive inheritance, which belongs to the NBIA (Neurodegeneration with Brain Iron Accumulation) group. Although the pathogenesis of the diseas
Externí odkaz:
https://doaj.org/article/7c54399a42554a24a0660b56caed3833
Autor:
Juan M. Suárez-Rivero, Carmen J. Pastor-Maldonado, Ana Romero-González, David Gómez-Fernandez, Suleva Povea-Cabello, Mónica Álvarez-Córdoba, Irene Villalón-García, Marta Talaverón-Rey, Alejandra Suárez-Carrillo, Manuel Munuera-Cabeza, José A. Sánchez-Alcázar
Publikováno v:
Frontiers in Pharmacology, Vol 13 (2022)
Mitochondrial diseases are genetic disorders caused by mutations in genes in the nuclear DNA (nDNA) and mitochondrial DNA (mtDNA) that encode mitochondrial structural or functional proteins. Although considered “rare” due to their low incidence,
Externí odkaz:
https://doaj.org/article/137e3b95f7344feabec2bf2b74fa35c0
Autor:
Juan M. Suárez-Rivero, Juan López-Pérez, Inés Muela-Zarzuela, Carmen Pastor-Maldonado, Paula Cilleros-Holgado, David Gómez-Fernández, Mónica Álvarez-Córdoba, Manuel Munuera-Cabeza, Marta Talaverón-Rey, Suleva Povea-Cabello, Alejandra Suárez-Carrillo, Rocío Piñero-Pérez, Diana Reche-López, José M. Romero-Domínguez, José Antonio Sánchez-Alcázar
Publikováno v:
Metabolites, Vol 13, Iss 3, p 416 (2023)
Neurodegenerative diseases are characterized by the progressive loss of neurons, synapses, dendrites, and myelin in the central and/or peripheral nervous system. Actual therapeutic options for patients are scarce and merely palliative. Although they
Externí odkaz:
https://doaj.org/article/c3f0aea027c14196ac709180971dfef3