2024

1. A wide scope, pan-comparative, systematic meta-analysis of the efficacy of prophylactic strategies for cardiac surgery-associated acute kidney injury

   Biomedicine and Pharmacotherapy, Vol. 178

2. Accounting for Visual Field Abnormalities when Using Eye-tracking to Diagnose Reading Problems in Neurological Degeneration

   Journal of Eye Movement Research, Vol. 17, Núm. 2

3. Additional file 10 of Clinical exome analysis and targeted gene repair of the c.1354dupT variant in iPSC lines from patients with PROM1-related retinopathies exhibiting diverse phenotypes

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4. Additional file 10 of Clinical exome analysis and targeted gene repair of the c.1354dupT variant in iPSC lines from patients with PROM1-related retinopathies exhibiting diverse phenotypes

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5. Additional file 11 of Clinical exome analysis and targeted gene repair of the c.1354dupT variant in iPSC lines from patients with PROM1-related retinopathies exhibiting diverse phenotypes

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6. Additional file 11 of Clinical exome analysis and targeted gene repair of the c.1354dupT variant in iPSC lines from patients with PROM1-related retinopathies exhibiting diverse phenotypes

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7. Additional file 6 of Clinical exome analysis and targeted gene repair of the c.1354dupT variant in iPSC lines from patients with PROM1-related retinopathies exhibiting diverse phenotypes

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8. Additional file 6 of Clinical exome analysis and targeted gene repair of the c.1354dupT variant in iPSC lines from patients with PROM1-related retinopathies exhibiting diverse phenotypes

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9. Additional file 7 of Clinical exome analysis and targeted gene repair of the c.1354dupT variant in iPSC lines from patients with PROM1-related retinopathies exhibiting diverse phenotypes

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10. Additional file 7 of Clinical exome analysis and targeted gene repair of the c.1354dupT variant in iPSC lines from patients with PROM1-related retinopathies exhibiting diverse phenotypes

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11. Additional file 8 of Clinical exome analysis and targeted gene repair of the c.1354dupT variant in iPSC lines from patients with PROM1-related retinopathies exhibiting diverse phenotypes

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12. Additional file 8 of Clinical exome analysis and targeted gene repair of the c.1354dupT variant in iPSC lines from patients with PROM1-related retinopathies exhibiting diverse phenotypes

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13. Additional file 9 of Clinical exome analysis and targeted gene repair of the c.1354dupT variant in iPSC lines from patients with PROM1-related retinopathies exhibiting diverse phenotypes

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14. Additional file 9 of Clinical exome analysis and targeted gene repair of the c.1354dupT variant in iPSC lines from patients with PROM1-related retinopathies exhibiting diverse phenotypes

    figshare

15. Clinical and genetic characterization of patients with eye diseases included in the Spanish Rare Diseases Patient Registry

    Orphanet Journal of Rare Diseases, Vol. 19, Núm. 1

16. Clinical exome analysis and targeted gene repair of the c.1354dupT variant in iPSC lines from patients with PROM1-related retinopathies exhibiting diverse phenotypes

    Stem Cell Research and Therapy, Vol. 15, Núm. 1

17. Decision-making concordance in thoracic drain management: Is necessary previous experience?

    Cirugia Espanola

18. Identification and characterization of a new pathologic mutation in a large Leber hereditary optic neuropathy pedigree

    Orphanet Journal of Rare Diseases, Vol. 19, Núm. 1

19. Novel risk loci for COVID-19 hospitalization among admixed American populations

    eLife, Vol. 13

20. Oxidative Stress Mediates Epigenetic Modifications and the Expression of miRNAs and Genes Related to Apoptosis in Diabetic Retinopathy Patients

    Journal of Clinical Medicine, Vol. 13, Núm. 1