JULIÁN
BENITO LEÓN
Profesor asociado
Hospital Universitario de Salamanca
Salamanca, EspañaPublicacions en col·laboració amb investigadors/es de Hospital Universitario de Salamanca (18)
2022
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Vitamin D Receptor and Binding Protein Gene Variants in Patients with Essential Tremor
Molecular Neurobiology, Vol. 59, Núm. 6, pp. 3458-3466
2020
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Memory and Executive Dysfunction Predict Complex Activities of Daily Living Impairment in Amnestic Multi-Domain Mild Cognitive Impairment
Journal of Alzheimer's disease : JAD, Vol. 75, Núm. 3, pp. 1061-1069
2019
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Neurological disorders in central Spain, second survey: Feasibility pilot observational study
Journal of Medical Internet Research, Vol. 21, Núm. 1
2017
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Delta-amino-levulinic acid dehydratase gene and essential tremor
European Journal of Clinical Investigation, Vol. 47, Núm. 5, pp. 348-356
2013
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No association of the SLC1A2 rs3794087 allele with risk for essential tremor in the Spanish population
Pharmacogenetics and Genomics, Vol. 23, Núm. 11, pp. 587-590
2012
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H1-MAPT and the risk for familial essential tremor
PLoS ONE, Vol. 7, Núm. 7
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Impact of apathy on health-related quality of life in recently diagnosed Parkinson's disease: The ANIMO study
Movement Disorders, Vol. 27, Núm. 2, pp. 211-218
2011
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Gamma-aminobutyric acid (GABA) receptor rho (GABRR) polymorphisms and risk for essential tremor
Journal of Neurology, Vol. 258, Núm. 2, pp. 203-211
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Gamma-aminobutyric acid GABRA4, GABRE, and GABRQ receptor polymorphisms and risk for essential tremor
Pharmacogenetics and Genomics, Vol. 21, Núm. 7, pp. 436-439
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Methods and design of the baseline survey of the neurological disorders in Salamanca (NEDISA) cohort: A population-based study in Central-Western Spain
Neuroepidemiology, Vol. 36, Núm. 1, pp. 62-68
2010
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Does the combination of the MMSE and clock drawing test (mini-clock) improve the detection of mild Alzheimer's disease and mild cognitive impairment?
Journal of Alzheimer's Disease, Vol. 22, Núm. 3, pp. 889-896
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Paraoxonase 1 (PON1) polymorphisms and risk for essential tremor
European Journal of Neurology, Vol. 17, Núm. 6, pp. 879-881
2009
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Dopamine Receptor D3 (DRD3) genotype and allelic variants and risk for essential tremor
Movement Disorders, Vol. 24, Núm. 13, pp. 1910-1915
2008
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Glutathione-S-transferase P1 polymorphism and risk for essential tremor
European Journal of Neurology, Vol. 15, Núm. 3, pp. 234-238
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The nonsynonymous Thr105Ile polymorphism of the histamine N-methyltransferase is associated to the risk of developing essential tremor
NeuroMolecular Medicine, Vol. 10, Núm. 4, pp. 356-361
2007
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Alcohol dehydrogenase 2 genotype and allelic variants are not associated with the risk for essential tremor
Clinical Neuropharmacology, Vol. 30, Núm. 4, pp. 196-200
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Changes at the CYP2C locus and disruption of CYP2C8/9 linkage disequilibrium in patients with essential tremor
NeuroMolecular Medicine, Vol. 9, Núm. 2, pp. 195-204
2006
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CYP2C19 polymorphism and risk for essential tremor
European Neurology, Vol. 56, Núm. 2, pp. 119-123