Zobrazeno 1 - 10
of 1 032
pro vyhledávání: '"J, del Castillo"'
Autor:
María Domínguez-Ruiz, Silvia Murillo-Cuesta, Julio Contreras, Marta Cantero, Gema Garrido, Belén Martín-Bernardo, Elena Gómez-Rosas, Almudena Fernández, Francisco J. del Castillo, Lluís Montoliu, Isabel Varela-Nieto, Ignacio del Castillo
Publikováno v:
BMC Genomics, Vol 25, Iss 1, Pp 1-14 (2024)
Abstract Inherited hearing impairment is a remarkably heterogeneous monogenic condition, involving hundreds of genes, most of them with very small ( 90 dB SPL) that correlates with specific structural abnormalities in the cochlea. We show that Gjb2 e
Externí odkaz:
https://doaj.org/article/005dfd86e59541f7888dab03f10a4e7b
Publikováno v:
Resuscitation Plus, Vol 17, Iss , Pp 100563- (2024)
Long-term outcome studies after pediatric cardiac arrest (CA) are few. They require a CA registry and dedicated outcome teams. Learning about the long-term outcomes is very important for developing prognostication guidelines, improving post-cardiac c
Externí odkaz:
https://doaj.org/article/9c506bd9b3214876b0c0914c00350a2e
Autor:
David Saceda-Corralo, Daniel Ortega-Quijano, Gloria Muñoz-Martín, Óscar M. Moreno-Arrones, Cristina Pindado-Ortega, Tuntas Rayinda, Ana Melián-Olivera, Carlos Azcárraga-Llobet, Patricia Burgos-Blasco, María Elena Castañeda-Bermúdez, Francisco J. del Castillo, Sergio Vañó-Galván
Publikováno v:
Acta Dermato-Venereologica, Vol 103 (2023)
The pathogenesis of frontal fibrosing alopecia has been linked to specific genetic variants. CYP1B1 codes for a component of the cytochrome p450 machinery that is involved in the metabolism of xenobiotic oestrogens. The study of the prevalence of pol
Externí odkaz:
https://doaj.org/article/be955e9abfdc4860baca2e10900c357d
Autor:
María Domínguez-Ruiz, Laura Ruiz-Palmero, Paula I. Buonfiglio, Irene García-Vaquero, Elena Gómez-Rosas, Marina Goñi, Manuela Villamar, Matías Morín, Miguel A. Moreno-Pelayo, Ana B. Elgoyhen, Francisco J. del Castillo, Viviana Dalamón, Ignacio del Castillo
Publikováno v:
Biomedicines, Vol 11, Iss 11, p 2943 (2023)
Non-syndromic hearing impairment (NSHI) is a very heterogeneous genetic condition, involving over 130 genes. Mutations in GJB2, encoding connexin-26, are a major cause of NSHI (the DFNB1 type), but few other genes have significant epidemiological con
Externí odkaz:
https://doaj.org/article/992bbf9bae834364a262f8b6f33463a6
Autor:
Sinziana Stanescu, Patricia Correcher Medina, Francisco J. del Castillo, Olga Alonso Luengo, Luis Maria Arto Millan, Amaya Belanger Quintana, Maria Camprodon Gomez, Lydia Diez Langhetée, Oscar Garcia Campos, Ana Matas Garcia, Jimena Perez-Moreno, Barbara Rubio Gribble, Nuria Visa-Reñé, Pilar Giraldo-Castellano, Mar O’Callaghan Gordo
Publikováno v:
Biomedicines, Vol 11, Iss 10, p 2861 (2023)
This was a retrospective, multicenter study that aimed to report the characteristics of type 3 Gaucher disease (GD3) patients in Spain, including the genotype, phenotype, therapeutic options, and treatment responses. A total of 19 patients with GD3 f
Externí odkaz:
https://doaj.org/article/5e5a3a4353424e60994aaa7c5732e1bf
Autor:
Juan M. Reyes, Magda V. Gutierrez‐Ardila, Hugo Madariaga, William Otero, Renato Guzman, Jorge Izquierdo, David J. Del Castillo, Mauricio Abello, Patricia Velez, Dario Ponce de Leon, Tatjana Lukic, Luisa F. Amador, Natalia Castaño
Publikováno v:
Health Science Reports, Vol 6, Iss 3, Pp n/a-n/a (2023)
Abstract Background and Aims A noninterventional prospective study was performed in Colombia and Peru. The aim was to describe the impact of access to treatment on Patient‐reported outcomes (PRO) in patients with Rheumatoid arthritis (RA) after fai
Externí odkaz:
https://doaj.org/article/8e84558703914c9580497121a51f6405
Autor:
Miguel Piris-Villaespesa, Alberto Álvarez-Larrán, Adolfo Saez-Marín, Claudia Nuñez-Torrón, Gloria Muñoz-Martin, Ricardo Sánchez, Francisco J. del Castillo, Jesús Villarrubia, Javier Lopez-Jimenez, Joaquin Martinez-Lopez, Valentin Garcia-Gutierrez
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-7 (2021)
Abstract In 2016, the WHO included haemoglobin values within normal ranges as a diagnostic criterion for Polycythaemia Vera (PV). Since then, concerns have arisen that a large number of patients are undergoing unnecessary screening for PV. To address
Externí odkaz:
https://doaj.org/article/560245e2949f4728a1b3dea54258ebdf
Autor:
Summer Ramsay-Burrough, Daniel P. Marron, Keith C. Armstrong, Trevor J. Del Castillo, Richard N. Zare, Robert M. Waymouth
Publikováno v:
Journal of the American Chemical Society. 145:2282-2293
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b2db588140703854f2f295209874aaf8
https://doi.org/10.1021/jacs.2c10667
https://doi.org/10.1021/jacs.2c10667
Publikováno v:
Acta Horticulturae. :149-152
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::99d938c4b468c8c7537e8603274ccdbe
https://doi.org/10.17660/actahortic.2022.1351.24
https://doi.org/10.17660/actahortic.2022.1351.24
Autor:
Matthew J. Chalkley, Trevor J. Del Castillo, Benjamin D. Matson, Joseph P. Roddy, Jonas C. Peters
Publikováno v:
ACS Central Science, Vol 3, Iss 3, Pp 217-223 (2017)
Externí odkaz:
https://doaj.org/article/92b0709cd1a7420bbdf591b530197d8c