Facultad de Ciencia y Tecnología
Centro
Hospital Universitario La Fe
Valencia, EspañaPublicaciones en colaboración con investigadoras/es de Hospital Universitario La Fe (19)
2023
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Decoding the molecular heterogeneity of pediatric monomorphic post–solid organ transplant lymphoproliferative disorders
Blood, Vol. 142, Núm. 5, pp. 434-445
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Extracting relevant predictive variables for COVID-19 severity prognosis: An exhaustive comparison of feature selection techniques
PLoS ONE, Vol. 18, Núm. 4 April
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Impact of outdoor air pollution on severity and mortality in COVID-19 pneumonia
Science of the Total Environment, Vol. 894
2022
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Association of TYR SNP rs1042602 with Melanoma Risk and Prognosis
Life, Vol. 12, Núm. 12
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Diverse mutations and structural variations contribute to Notch signaling deregulation in paediatric T-cell lymphoblastic lymphoma
Pediatric Blood and Cancer, Vol. 69, Núm. 11
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Mitochondrial bioenergetics boost macrophage activation, promoting liver regeneration in metabolically compromised animals
Hepatology, Vol. 75, Núm. 3, pp. 550-566
2020
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Distinct molecular profile of IRF4-rearranged large B-cell lymphoma
Blood, Vol. 135, Núm. 4, pp. 274-286
2018
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Scedosporium and Lomentospora: An updated overview of underrated opportunists
Medical Mycology, Vol. 56, pp. S102-S125
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What to consider when pseudohypoparathyroidism is ruled out: IPPSD and differential diagnosis
BMC Medical Genetics, Vol. 19, Núm. 1
2017
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TIAM1 variants improve clinical outcome in neuroblastoma
Oncotarget, Vol. 8, Núm. 28, pp. 45286-45297
2014
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Rapid and specific detection of section Fumigati and Aspergillus fumigatus in human samples using a new multiplex real-time PCR
Diagnostic Microbiology and Infectious Disease, Vol. 80, Núm. 2, pp. 111-118
2013
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The aspHS gene as a new target for detecting Aspergillus fumigatus during infections by quantitative real-time PCR
Medical Mycology, Vol. 51, Núm. 5, pp. 545-554
2012
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Detection of hypomethylation syndrome among patients with epigenetic alterations at the GNAS locus
Journal of Clinical Endocrinology and Metabolism, Vol. 97, Núm. 6
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Novel mutations in MEN1, CDKN1B and AIP genes in patients with multiple endocrine neoplasia type 1 syndrome in Spain
Clinical Endocrinology, Vol. 76, Núm. 5, pp. 719-724
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Simultaneous analysis of the expression of 14 genes with individual prognostic value in myelodysplastic syndrome patients at diagnosis: WT1 detection in peripheral blood adversely affects survival
Annals of Hematology, Vol. 91, Núm. 12, pp. 1887-1895
2010
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Intragenic GNAS deletion involving exon A/B in pseudohypoparathyroidism type 1A resulting in an apparent loss of exon A/B methylation: Potential for misdiagnosis of pseudohypoparathyroidism type 1B
Journal of Clinical Endocrinology and Metabolism, Vol. 95, Núm. 2, pp. 765-771
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New mechanisms involved in paternal 20q disomy associated with pseudohypoparathyroidism
European Journal of Endocrinology, Vol. 163, Núm. 6, pp. 953-962
2007
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The majority of cases of neonatal diabetes in Spain can be explained by known genetic abnormalities
Diabetic Medicine, Vol. 24, Núm. 7, pp. 707-713
1996
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¿ Qué variables predicen la aparición de un bloqueo de rama derecha del haz de his y su evolución tras el trasplante cardíaco?
Revista Espanola de Cardiologia, Vol. 49, Núm. 5, pp. 328-333