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Year Number of Results
2005 1
2006 1
2009 1
2010 1
2012 2
2013 1
2014 1
2016 1
2022 1
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Page 1
Analysis of EEG patterns and genotypes in patients with Angelman syndrome.
Vendrame M, Loddenkemper T, Zarowski M, Gregas M, Shuhaiber H, Sarco DP, Morales A, Nespeca M, Sharpe C, Haas K, Barnes G, Glaze D, Kothare SV. Vendrame M, et al. Among authors: morales a. Epilepsy Behav. 2012 Mar;23(3):261-5. doi: 10.1016/j.yebeh.2011.11.027. Epub 2012 Feb 16. Epilepsy Behav. 2012. PMID: 22341959
Loss of humoral response 3 months after SARS-CoV-2 vaccination in the CKD spectrum: the multicentric SENCOVAC study.
Quiroga B, Soler MJ, Ortiz A, Bernat A, Muñoz Díaz AB, Jarava Mantecón CJ, Gómez Pérez VO, Calderón González C, Cervienka M, Mazuecos A, Cazorla JM, Carnerero Di Riso M, Martínez S, Ortega Diaz M, Lucena Valverde R, Sánchez Márquez MG, Lancho Novillo C, González Parra E, Gracia-Iguacel C, Rodrigo De Tomas MT, Aguilar Cervera MC, Giorgi M, Muñoz Ramos P, Macías Carmona N, Toapanta N, Cigarrán S, Ruiz San Millán JC, Santana Estupiñán R, Crespo M, Villacorta Linaza B, Jimeno Martín MI, Rodríguez-Osorio Jiménez L, Soriano S, González Ferri D, Pizarro Sánchez MS, Yugueros A, Leyva A, Rojas J, Gansevoort RT, de Sequera P; SENCOVAC collaborative network. Quiroga B, et al. Nephrol Dial Transplant. 2022 Apr 25;37(5):994-999. doi: 10.1093/ndt/gfac007. Nephrol Dial Transplant. 2022. PMID: 35022757 No abstract available.
Infantile onset spinocerebellar ataxia caused by compound heterozygosity for Twinkle mutations and modeling of Twinkle mutations causing recessive disease.
Pierce SB, Gulsuner S, Stapleton GA, Walsh T, Lee MK, Mandell JB, Morales A, Klevit RE, King MC, Rogers RC. Pierce SB, et al. Among authors: morales a. Cold Spring Harb Mol Case Stud. 2016 Jul;2(4):a001107. doi: 10.1101/mcs.a001107. Cold Spring Harb Mol Case Stud. 2016. PMID: 27551684 Free PMC article.