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Carotid agenesis and absence of bifurcation, asymptomatic and incidental, during the study of cognitive impairment: a case report. Neurologia (Engl Ed). 2021 Jul 8:S2173-5808(21)00104-8. doi: 10.1016/j.nrleng.2020.11.010. Epub ahead of print. PMID: 34247975.F.I: 0.870
Alpha-protein kinase 3 (ALPK3) truncating variants are a cause of autosomal dominant hypertrophic cardiomyopathy. Transfus Apher Sci. 2021 Aug 25:103259. doi: 10.1016/j.transci.2021.103259. Online ahead of print.PMID: 34462218. F.I.:1.285
Genetic Variants in PGE2 Receptors Modulate the Risk of Nephrosclerosis and Clinical Outcomes in These Patients.. J Pers Med. 2021 Aug 6;11(8):772. doi: 10.3390/jpm11080772.PMID: 34442416 F.I.:4.945
Monoclonal gammopathy of undetermined significance and evolution to myeloma: Experience in 153 patients]. Semergen. 2021 Aug 31:S1138-3593(21)00216-1. doi: 10.1016/j.semerg.2021.05.011. Online ahead of print.PMID: 34479794. F.I.
Incidence and factors associated with COVID-19 in 13 hemodialysis units. Int Urol Nephrol. 2021 Jun 18:1–2. doi: 10.1007/s11255-021-02918-3. Epub ahead of print. PMID: 34143370; PMCID: PMC8212577.F.I.:1.843
Relationship between sleep quality and cognitive performance in patients with epilepsy. Epilepsy Behav. 2021 Jun 16;122:108127. doi: 10.1016/j.yebeh.2021.108127. Epub ahead of print. PMID: 34147020.F.I.:2.508
Implantation of a biochemical and genetic screening programme for family hypercholesterolaemia. Clin Investig Arterioscler. 2021 Jun 3:S
Cardiovascular risk assessment after one-year acute ischemic stroke based on uric acid levels and renal dysfunction. A clinical study. Int J Neurosci. 2021 Jun;131(6):609-614. doi: 10.1080/00207454.2020.1750395. Epub 2020 Apr 13. PMID: 32228334.F.I.:5.374