Zobrazeno 1 - 10
of 15
pro vyhledávání: '"NATALIA P MENA"'
Autor:
Olimpo García-Beltrán, Natalia P Mena, Pabla Aguirre, Germán Barriga-González, Antonio Galdámez, Edgar Nagles, Tatiana Adasme, Cecilia Hidalgo, Marco T Núñez
Publikováno v:
PLoS ONE, Vol 12, Iss 12, p e0189043 (2017)
Iron accumulation, oxidative stress and calcium signaling dysregulation are common pathognomonic signs of several neurodegenerative diseases, including Parkinson´s and Alzheimer's diseases, Friedreich ataxia and Huntington's disease. Given their the
Externí odkaz:
https://doaj.org/article/07513b7a3cd840afac3e9920a4d04929
Autor:
Beatriz Escamilla-Cabrera, Sergio Luis-Lima, Eduardo Gallego-Valcarce, Nuria Victoria Sánchez-Dorta, Natalia Negrín-Mena, Laura Díaz-Martín, Coriolano Cruz-Perera, Ana Monserrat Hernández-Valles, Federico González-Rinne, María José Rodríguez-Gamboa, Sara Estupiñán-Torres, Rosa Miquel-Rodríguez, María Ángeles Cobo-Caso, Patricia Delgado-Mallén, Gema Fernández-Suárez, Ana González-Rinne, Grimanesa Hernández-Barroso, Alejandra González-Delgado, Armando Torres-Ramírez, Alejandro Jiménez-Sosa, Alberto Ortiz, Flavio Gaspari, Domingo Hernández-Marrero, Esteban Luis Porrini
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-11 (2024)
Abstract The error of estimated glomerular filtration rate (eGFR) and its consequences in predialysis are unknown. In this prospective multicentre study, 315 predialysis patients underwent measured GFR (mGFR) by the clearance of iohexol and eGFR by 5
Externí odkaz:
https://doaj.org/article/fc3f8f8208c544e4b00036312130c06a
Autor:
Pabla Aguirre, Natalia P Mena, Carlos M Carrasco, Yorka Muñoz, Patricio Pérez-Henríquez, Rodrigo A Morales, Bruce K Cassels, Carolina Méndez-Gálvez, Olimpo García-Beltrán, Christian González-Billault, Marco T Núñez
Publikováno v:
PLoS ONE, Vol 10, Iss 12, p e0144848 (2015)
Neuronal death in Parkinson's disease (PD) is often preceded by axodendritic tree retraction and loss of neuronal functionality. The presence of non-functional but live neurons opens therapeutic possibilities to recover functionality before clinical
Externí odkaz:
https://doaj.org/article/07e3dcd9b356406682ba92db1457d413
Publikováno v:
Biological Research, Vol 39, Iss 1, Pp 191-193 (2006)
Hepcidin (Hepc) is a 25 amino acid cationic peptide with broad antibacterial and antifungal actions. A likely role for Hepc in iron metabolism was suggested by the observation that mice having disruption of the gene encoding the transcription factor
Externí odkaz:
https://doaj.org/article/1bb47e8de4e24c6aa46d2e7f6a3ff8da
Autor:
Raúl Morales Febles, Domingo Marrero Miranda, Alejandro Jiménez Sosa, Ana González Rinne, Coriolano Cruz Perera, Ana Elena Rodríguez-Rodríguez, Alejandra Álvarez González, Laura Díaz Martín, Natalia Negrín Mena, Cristian Acosta Sørensen, Lourdes Pérez Tamajón, Aurelio Rodríguez Hernández, Federico González Rinne, Aday Dorta González, Eusebio Ledesma Pérez, Alejandra González Delgado, Alberto Domínguez-Rodríguez, Maria del Carmen García Baute, Armando Torres Ramírez, Esteban Porrini
Publikováno v:
Sports Medicine - Open, Vol 9, Iss 1, Pp 1-13 (2023)
Abstract Background Post-transplant diabetes mellitus (PTDM) beyond 12 months (late PTDM) is a severe complication after renal transplantation. Late PTDM develops mostly in subjects with prediabetes. Although exercise may have a potential role in pre
Externí odkaz:
https://doaj.org/article/e05af955a77d440a8894ccbc3371c696
Autor:
Leopoldo Garduño-Vieyra, Raul Rua Martinez, Natalia Rodriguez Mena, Isabel De la Fuente Batta
Publikováno v:
Journal of Ophthalmology, Iss 4, Pp 79-80 (2023)
Horner Syndrome results from an interruption of the sympathetic innervation of the eye. This pathway is a chain of three neurons which originate in the hypothalamus, travels down to spinal cord at the level of lower cervical and upper thoracic levels
Externí odkaz:
https://doaj.org/article/ac9da947ce5d4e0f9c248ebceab22a93
Publikováno v:
Journal of Ophthalmology, Iss 2, Pp 63-64 (2023)
Gyrus atrophy is a rare autosomal recessive hereditary disease secondary to a mutation of the OAT gene on chromosome 10 which results in a deficiency of the mitochondrial enzyme ornithine aminotransferase that causes a 20-fold increase in serum conce
Externí odkaz:
https://doaj.org/article/6e317e18470b4b63bf431c95e825f17b
Akademický článek
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Autor:
Christian S. Lobsiger, Etienne C. Hirsch, Anne Laure Bulteau, Jean-Michel Camadro, Natalia P. Mena, Annick Prigent, Irene Lee, Françoise Auchère
Publikováno v:
Free Radical Biology and Medicine
Free Radical Biology and Medicine, 2017, ⟨10.1016/j.freeradbiomed.2017.03.036⟩
Free Radical Biology and Medicine, Elsevier, 2017, ⟨10.1016/j.freeradbiomed.2017.03.036⟩
Free Radical Biology and Medicine, 2017, ⟨10.1016/j.freeradbiomed.2017.03.036⟩
Free Radical Biology and Medicine, Elsevier, 2017, ⟨10.1016/j.freeradbiomed.2017.03.036⟩
International audience; Compelling evidence suggests that mitochondrial dysfunction leading to reactive oxygen species (ROS) production and protein oxidation could represent a critical event in the pathogenesis of Parkinson's disease (PD). Pioneering
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fb0cf548053989b868427e2e83fd7184
https://hal.sorbonne-universite.fr/hal-01501657
https://hal.sorbonne-universite.fr/hal-01501657
Publikováno v:
Migraciones, Iss 48, Pp 1-20 (2020)
Los enfoques convencionales sobre las migraciones han tendido a considerar frecuentemente a los inmigrantes como sujetos pasivos en sus procesos de incorporación a las sociedades de recepción. En cambio, cada vez contamos con más muestras de la in
Externí odkaz:
https://doaj.org/article/d9ff59ea29a14af59d533b6284424dad