Elena
Pintos Martínez
Complexo Hospitalario Universitario de Santiago
Santiago de Compostela, EspañaPublications in collaboration with researchers from Complexo Hospitalario Universitario de Santiago (24)
2022
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Health related quality of life following open versus minimally invasive total gastrectomy for cancer: Results from a randomized clinical trial
European Journal of Surgical Oncology, Vol. 48, Núm. 3, pp. 553-560
2021
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Correction to: Open versus minimally invasive total gastrectomy after neoadjuvant chemotherapy: results of a European randomized trial (Gastric Cancer, (2021), 24, 1, (258-271), 10.1007/s10120-020-01109-w)
Gastric Cancer
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Open versus minimally invasive total gastrectomy after neoadjuvant chemotherapy: results of a European randomized trial
Gastric Cancer, Vol. 24, Núm. 1, pp. 258-271
2018
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Scrotal Peripheral Primitive Neuroectodermal Tumor
Current Urology, Vol. 12, Núm. 1, pp. 50-53
2016
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Congenital neurogenic muscular atrophy in megaconial myopathy due to a mutation in CHKB gene
Brain and Development, Vol. 38, Núm. 1, pp. 167-172
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Erratum: Corrigendum to “Congenital neurogenic muscular atrophy in megaconial myopathy due to a mutation in CHKB gene” (Brain and Development (2016) 38(1) (167–172) (S0387760415001023) (10.1016/j.braindev.2015.05.008))
Brain and Development
2014
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Exome sequencing identifies a CHKB mutation in Spanish patient with Megaconial Congenital Muscular Dystrophy and mtDNA depletion
European Journal of Paediatric Neurology, Vol. 18, Núm. 6, pp. 796-800
2011
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Primary adenosine monophosphate (AMP) deaminase deficiency in a hypotonic infant
Journal of Child Neurology, Vol. 26, Núm. 6, pp. 734-737
2008
2007
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Pontocerebellar hypoplasia type 1: A case report
Revista de Neurologia, Vol. 44, Núm. 5, pp. 281-284
2006
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Epidemiology of pediatric mitochondrial respiratory chain disorders in northwest Spain
Pediatric Neurology, Vol. 34, Núm. 3, pp. 204-211
2005
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Aspectos actuales de las miopatías congénitas estructurales
Revista Espanola de Pediatria, Vol. 61, Núm. 2, pp. 114-125
2004
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Aspectos actuales de las distrofias musculares congénitas
Revista Espanola de Pediatria, Vol. 60, Núm. 6, pp. 451-467
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Mitochondrial encephalomyopathies and West's syndrome: A frequently underdiagnosed association
Revista de Neurologia, Vol. 39, Núm. 7, pp. 618-623
2003
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Lipomatosis simétrica múltiple asociada a polineuropatía, atrofia de cerebelo y citopatía mitocondrial
Revista de Neurologia, Vol. 36, Núm. 11, pp. 1026-1029
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Mixed hypotonia, neurological regression and atrophy of the cerebellum: Manifestations that suggest infantile neuroaxonal dystrophy
Revista de Neurologia, Vol. 37, Núm. 1, pp. 25-28
2002
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A new congenital myopathy [5]
Acta Paediatrica, International Journal of Paediatrics
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Fibroma cemento osificante del cráneo
Neurocirugia, Vol. 13, Núm. 6, pp. 495-497
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Muscular dystrophy due to a deficit of γ-sarcoglycan. A report of three patients with the Δ-521T mutation
Revista de Neurologia