Juan José
Tellería Orriols
Investigador no período 2017-2021
Universidad de Valladolid
Valladolid, EspañaPublicacións en colaboración con investigadores/as de Universidad de Valladolid (11)
2022
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Fatal Respiratory Failure in a Term Newborn Due to Non-previously Described Compound Heterozygous ABCA3 Mutations
Journal of Neonatology, Vol. 36, Núm. 3, pp. 250-254
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Genetic profiles to identify talents in elite endurance athletes and professional football players
PLoS ONE, Vol. 17, Núm. 9 September
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Pathophysiology of Age-Related Macular Degeneration: Implications for Treatment
Ophthalmic Research, Vol. 65, Núm. 6, pp. 615-636
2021
2020
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Exome sequencing identifies PEX6 mutations in three cases diagnosed with Retinitis Pigmentosa and hearing impairment
Molecular Vision, Vol. 26, pp. 216-225
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Genotype scores in energy and iron-metabolising genes are higher in elite endurance athletes than in nonathlete controls
Applied Physiology, Nutrition and Metabolism, Vol. 45, Núm. 11, pp. 1225-1231
2019
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CALCA and TRPV1 genes polymorphisms are related to a good outcome in female chronic migraine patients treated with OnabotulinumtoxinA
Journal of Headache and Pain, Vol. 20, Núm. 1
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Liver-Metabolizing Genes and Their Relationship to the Performance of Elite Spanish Male Endurance Athletes; a Prospective Transversal Study
Sports Medicine - Open, Vol. 5, Núm. 1
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Novel presenilin 1 mutation (p.Thr-Pro116-117Ser-Thr) in a Spanish family with early-onset Alzheimer's disease
Neurobiology of Aging, Vol. 84, pp. 238.e19-238.e24
2018
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Polymorphisms in receptors involved in opsonic and nonopsonic phagocytosis, and correlation with risk of infection in oncohematology patients
Infection and Immunity, Vol. 86, Núm. 12
2017
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Neuropatía auditiva autosómica dominante y variante DIAPH3 (c.-173C>T)
Acta Otorrinolaringologica Espanola, Vol. 68, Núm. 3, pp. 183-185