Departamento de Cirurxía e Especialidades Médico-Cirúrxicas
Departamento
Hospital Universitario de Salamanca
Salamanca, EspañaPublicacións en colaboración con investigadores/as de Hospital Universitario de Salamanca (28)
2024
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Standardization of the definition of the types of oncological colectomy. Delphi method for consensus of experts of the Spanish Association of Surgeons
Cirugia Espanola, Vol. 102, Núm. 9, pp. 484-494
2023
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Single-cell immune profiling of Meniere Disease patients
Clinical Immunology, Vol. 252
2022
2021
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Burden of rare variants in synaptic genes in patients with severe tinnitus: An exome based extreme phenotype study
EBioMedicine, Vol. 66
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Clinical and cytokine profile in patients with early and late onset meniere disease
Journal of Clinical Medicine, Vol. 10, Núm. 18
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Hydroxyethyl starch and acute kidney injury in high-risk patients undergoing cardiac surgery: A prospective multicenter study
Journal of Clinical Anesthesia, Vol. 73
2020
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Burden of Rare Variants in the OTOG Gene in Familial Meniere's Disease
Ear and Hearing, Vol. 41, Núm. 6, pp. 1598-1605
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Heparan sulfate in human cutaneous Meissner's and Pacinian corpuscles
Anatomical Record, Vol. 303, Núm. 8, pp. 2262-2273
2019
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Ageing of the somatosensory system at the periphery: age-related changes in cutaneous mechanoreceptors
Journal of Anatomy, Vol. 234, Núm. 6, pp. 839-852
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Class I and Class II small leucine-rich proteoglycans in human cutaneous pacinian corpuscles
Annals of Anatomy, Vol. 224, pp. 62-72
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Differential proinflammatory signature in vestibular migraine and meniere disease
Frontiers in Immunology, Vol. 10, Núm. JUN
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Multicentric study on total pancreatectomies
Cirugia Espanola, Vol. 97, Núm. 7, pp. 377-384
2018
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Proinflammatory cytokines and response to molds in mononuclear cells of patients with Meniere disease
Scientific Reports, Vol. 8, Núm. 1
2017
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Extended phenotype and clinical subgroups in unilateral Meniere disease: A cross-sectional study with cluster analysis
Clinical Otolaryngology, Vol. 42, Núm. 6, pp. 1172-1180
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Regulation of Fn14 receptor and NF-κB underlies inflammation in Meniere's disease
Frontiers in Immunology, Vol. 8, Núm. DEC
2016
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A novel missense variant in PRKCB segregates low-frequency hearing loss in an autosomal dominant family with Meniere's disease
Human Molecular Genetics, Vol. 25, Núm. 16, pp. 3407-3415
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Clinical subgroups in bilateral meniere disease
Frontiers in Neurology, Vol. 7, Núm. OCT
2015
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Common variants of NFE2L2 gene predisposes to acute respiratory distress syndrome in patients with severe sepsis
Critical Care, Vol. 19, Núm. 1
2014
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Familial clustering and genetic heterogeneity in Meniere's disease
Clinical Genetics, Vol. 85, Núm. 3, pp. 245-252