Title Issue Date
The T1048I mutation in ATP7A gene causes an unusual Menkes disease presentation León-García, Gregorio; Santana, Alfredo ; Villegas-Sepúlveda, Nicolás; Pérez-González, Concepción; Henrríquez-Esquíroz, José M., et al Issued date: 2012 DOI: 10.1186/1471-2431-12-150 Source: BMC Pediatrics,v. 12 (150). SJR: 1,174 - Q1 JCR: 1,982 - Q2 SCIE Artículo
Application of non-invasive neuromodulation in children with neurodevelopmental disorders to improve their sleep quality and constipation Báez Suárez, Aníbal ; Padrón Rodríguez, Iraya; Castellano Moreno, Elizabeth; González González, Erica; Quintana Montesdeoca, María Del Pino , et al Issued date: 2023 DOI: 10.1186/s12887-023-04307-4 Source: BMC Pediatr, [ISSN 1471-2431], v. 23 (465), (2023). SJR: 0,688 - Q2 JCR: 2,0 - Q2 SCIE MIAR ICDS: 10,8 Artículo
Does HLA explain the high incidence of childhood-onset type 1 diabetes in the Canary Islands? The role of Asp57 <i>DQB1</i> molecules Novoa Medina, Yeray ; Marcelino-Rodriguez, Itahisa; Martel Suárez, Nicolás Alfonso ; Barreiro Bautista, Marta; Rivas-Garcia, Eva, et al Issued date: 2024 DOI: 10.1186/s12887-024-04983-w Source: Bmc Pediatrics, [ISSN 1471-2431], v. 24, 569, (Septiembre 2024) SJR: 0,688 - Q2 JCR: 2,0 - Q2 SCIE MIAR ICDS: 10,8 Artículo