Medicina
Facultad
Instituto de Investigación Sanitaria Hospital 12 de Octubre
Madrid, EspañaPublicacións en colaboración con investigadores/as de Instituto de Investigación Sanitaria Hospital 12 de Octubre (254)
2024
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A Multifunctionalized Potyvirus-Derived Nanoparticle That Targets and Internalizes into Cancer Cells
International Journal of Molecular Sciences, Vol. 25, Núm. 8
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A case of myotonic dystrophy type 1 with severe dilated cardiomyopathy: an unusual presenting manifestation of the most common muscular dystrophy in adults
Neurological Sciences
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A new mutation in the Parkinson's-related FBXO7 gene impairs mitochondrial and proteasomal function
FEBS Journal
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Assessing the clinical benefit, safety, and patient-reported outcomes with the use of the PAHcare™ digital platform in pulmonary arterial hypertension: a pilot study
Frontiers in Public Health, Vol. 12
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Association between neutrophil to lymphocyte ratio and inflammatory biomarkers in patients with a first episode of psychosis
Journal of Psychiatric Research, Vol. 172, pp. 334-339
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Cerebral Venous Sinus Thrombosis Following Scrub Typhus Meningoencephalitis in a Pregnant Woman
Neurohospitalist
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Challenging neurological presentation: Scrub typhus with meningoencephalitis and multiple cranial nerve involvement
Neurology and Clinical Neuroscience
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Cognitive Impairment in Neurological Diseases
International Journal of Molecular Sciences
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Comment on the article titled “Impact of sex on outcome after pulmonary endarterectomy for chronic thromboembolic pulmonary hypertension” published by J. Chan et al
Journal of Heart and Lung Transplantation
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Congenital myasthenia syndrome with demyelinating sensorimotor neuropathy responsive to salbutamol monotherapy: a novel clinical phenotype of CHRNE mutation
Neurological Sciences
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Correction to: A case of myotonic dystrophy type 1 with severe dilated cardiomyopathy: an unusual presenting manifestation of the most common muscular dystrophy in adults (Neurological Sciences, (2024), 10.1007/s10072-024-07535-3)
Neurological Sciences
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Correction to: Detection of kinase domain mutations in BCR::ABL1 leukemia by ultra-deep sequencing of genomic DNA (Scientific Reports, (2022), 12, 1, (13057), 10.1038/s41598-022-17271-3)
Scientific Reports
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Data source integration: a key tool for optimizing resources and prioritizing areas for improvement in clinical practice and epidemiology
Revista Espanola de Cardiologia
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Decreased oxytocin levels related to social cognition impairment in borderline personality disorder
Acta Psychiatrica Scandinavica, Vol. 149, Núm. 6, pp. 458-466
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Detection of auditory hallucinations from electroencephalographic brain–computer interface signals
Cognitive Systems Research, Vol. 83
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Diabetic striatopathy and other acute onset de novo movement disorders in hyperglycemia
Diabetes and Metabolic Syndrome: Clinical Research and Reviews, Vol. 18, Núm. 3
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Distal hereditary motor neuronopathy as a new phenotype associated with variants in BAG3
Journal of Neurology, Vol. 271, Núm. 2, pp. 986-994
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Engineered T cells secreting anti-BCMA T cell engagers control multiple myeloma and promote immune memory in vivo
Science translational medicine, Vol. 16, Núm. 734, pp. eadg7962
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Evolution of the impact of the COVID-19 pandemic on heart transplant recipients: Decreasing risk, improving perspective
Transplant Infectious Disease, Vol. 26, Núm. 2
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Expanding the genetic and phenotypic spectrum of congenital myasthenic syndrome: new homozygous VAMP1 splicing variants in 2 novel individuals
Journal of Human Genetics, Vol. 69, Núm. 5, pp. 187-196