FACULTAD DE CIENCIAS DE LA SALUD
Facultad/Centro de investigación
José Augusto
García-Agúndez Pérez-Coca
Publicaciones en las que colabora con José Augusto García-Agúndez Pérez-Coca (18)
2021
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Exome-wide rare variant analysis in familial essential tremor
Parkinsonism and Related Disorders, Vol. 82, pp. 109-116
2018
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Gamma-aminobutyric acid (GABA) receptors genes polymorphisms and risk for restless legs syndrome
Pharmacogenomics Journal, Vol. 18, Núm. 4, pp. 565-577
2017
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Association between the rs1229984 polymorphism in the alcohol dehydrogenase 1B gene and risk for restless legs syndrome
Sleep, Vol. 40, Núm. 12
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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
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Thr105Ile (rs11558538) polymorphism in the histamine-1-methyl-transferase (HNMT) gene and risk for restless legs syndrome
Journal of Neural Transmission, Vol. 124, Núm. 3, pp. 285-291
2016
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A family study of DRD3 rs6280, SLC1A2 rs3794087 and MAPT rs1052553 variants in essential tremor
Neurological Research, Vol. 38, Núm. 10, pp. 880-887
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Heme Oxygenase-1 and 2 Common Genetic Variants and Risk for Multiple Sclerosis
Scientific Reports, Vol. 6
2015
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Neuronal nitric oxide synthase (nNOS, NOS1) rs693534 and rs7977109 variants and risk for restless legs syndrome
Journal of Neural Transmission, Vol. 122, Núm. 6, pp. 819-823
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Association between Vitamin D receptor rs731236 (Taq1) polymorphism and risk for restless legs syndrome in the Spanish caucasian population
Medicine (United States), Vol. 94, Núm. 47, pp. e2125
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Heme Oxygenase 1 and 2 Common Genetic Variants and Risk for Essential Tremor
Medicine, Vol. 94, Núm. 24, pp. e968
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Heme Oxygenase-1 and 2 Common Genetic Variants and Risk for Restless Legs Syndrome
Medicine (United States), Vol. 94, Núm. 34, pp. e1448
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Missense mutations in TENM4, a regulator of axon guidance and central myelination, cause essential tremor
Human Molecular Genetics, Vol. 24, Núm. 20, pp. 5677-5686
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TREM2 R47H variant and risk of essential tremor: A cross-sectional international multicenter study
Parkinsonism and Related Disorders, Vol. 21, Núm. 3, pp. 306-309
2014
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The solute carrier family 1 (glial high affinity glutamate transporter), member 2 gene, SLC1A2, rs3794087 variant and assessment risk for restless legs syndrome
Sleep Medicine, Vol. 15, Núm. 2, pp. 266-268
2013
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Dopamine receptor D3 (DRD3) gene rs6280 variant and risk for restless legs syndrome
Sleep Medicine
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Fused in sarcoma (FUS) gene mutations are not a frequent cause of essential tremor in europeans
Neurobiology of Aging, Vol. 34, Núm. 10, pp. 2441.e9-2441.e11
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MAPT1 gene rs1052553 variant is unrelated with the risk for restless legs syndrome
Journal of Neural Transmission, Vol. 120, Núm. 3, pp. 463-467
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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