Ana
Rojo Sebastian
Profesor/a Asociado/a en CC. de la Salud
Publications (30) Ana Rojo Sebastian publications
2020
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Vitamin B6 deficiency in patients with parkinson disease treated with levodopa/carbidopa
Clinical Neuropharmacology, Vol. 43, Núm. 5, pp. 151-157
2019
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Dementia
Medicine (Spain), Vol. 12, Núm. 74, pp. 4329-4337
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Diagnostic and therapeutic protocol of cognitive disturbances in patients with movement disorders
Medicine (Spain), Vol. 12, Núm. 74, pp. 4376-4380
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Elderly patient with dementia: complex therapeutic decisions
Medicine (Spain), Vol. 12, Núm. 74, pp. 4381-4384
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Other degenerative dementias. Dementia with Lewy bodies, dementia in Parkinson's disease, frontotemporal dementia and vascular dementia
Medicine (Spain), Vol. 12, Núm. 74, pp. 4347-4356
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The Spectrum of Movement Disorders in 18-p Deletion Syndrome
Movement Disorders Clinical Practice
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Therapeutic aspects in dementias
Medicine (Spain), Vol. 12, Núm. 74, pp. 4357-4366
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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Beyond cervical lipomas: Myoclonus, gait disorder and multisystem involvement leading to mitochondrial disease
BMJ Case Reports, Vol. 2017
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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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The high prevalence of impulse control behaviors in patients with early-onset Parkinson's disease: A cross-sectional multicenter study
Journal of the Neurological Sciences, Vol. 368, pp. 150-154
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 Restless Legs Syndrome
Medicine (United States), Vol. 94, Núm. 34, pp. e1448
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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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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Suicidal ideation in a European Huntington's disease population
Journal of Affective Disorders, Vol. 151, Núm. 1, pp. 248-258
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β-defensin genomic copy number does not influence the age of onset in huntington’s disease
Journal of Huntington's Disease, Vol. 2, Núm. 1, pp. 107-124