Lista de obras -

A family study of DRD3 rs6280, SLC1A2 rs3794087 and MAPT rs1052553 variants in essential tremor

artículo científico publicado en 2016

A polymorphism located at an ATG transcription start site of the heme oxygenase-2 gene is associated with classical Parkinson's disease.

artículo científico publicado en 2011

Advances in understanding genomic markers and pharmacogenetics of Parkinson's disease

artículo científico publicado en 2016

Alcohol consumption and risk for Parkinson's disease: a systematic review and meta-analysis

scientific article published on 28 August 2018

Alcohol dehydrogenase 2 genotype and allelic variants are not associated with the risk for essential tremor

artículo científico publicado en 2007

Alcohol dehydrogenase 2 genotype and risk for migraine.

artículo científico publicado en 2009

An Update on the Neurochemistry of Essential Tremor

scientific article published on 01 January 2020

An Update on the Role of Nitric Oxide in the Neurodegenerative Processes of Parkinson's Disease

artículo científico publicado en 2016

An association study between Heme oxygenase-1 genetic variants and Parkinson's disease

artículo científico publicado en 2014

Anti-Inflammatory Effects of Amantadine and Memantine: Possible Therapeutics for the Treatment of Covid-19?

artículo científico publicado en 2020

Association Between Vitamin D Receptor rs731236 (Taq1) Polymorphism and Risk for Restless Legs Syndrome in the Spanish Caucasian Population.

artículo científico publicado en 2015

Association Between the rs1229984 Polymorphism in the Alcohol Dehydrogenase 1B Gene and Risk for Restless Legs Syndrome.

artículo científico publicado en 2017

Association between restless legs syndrome and other movement disorders

artículo científico publicado en 2019

Association between the missense alcohol dehydrogenase rs1229984T variant with the risk for Parkinson's disease in women

scientific article published on 27 November 2018

COMT gene and risk for Parkinson's disease: a systematic review and meta-analysis

artículo científico publicado en 2014

CYP2C19 polymorphism and risk for essential tremor

artículo científico publicado en 2006

Cerebrospinal fluid biochemical studies in patients with Parkinson's disease: toward a potential search for biomarkers for this disease.

artículo científico publicado en 2014

Changes at the CYP2C locus and disruption of CYP2C8/9 linkage disequilibrium in patients with essential tremor

artículo científico publicado en 2007

Delta-amino-levulinic acid dehydratase gene and essential tremor

artículo científico publicado en 2017

Diamine oxidase rs10156191 and rs2052129 variants are associated with the risk for migraine

artículo científico publicado en 2015

Dopamine receptor D3 (DRD3) gene rs6280 variant and risk for restless legs syndrome

artículo científico publicado en 2013

Dopamine receptor D3 (DRD3) genotype and allelic variants and risk for essential tremor.

artículo científico publicado en 2009

Drug and xenobiotic biotransformation in the blood-brain barrier: a neglected issue. ⬇️

artículo científico publicado en 2014

Gamma-Aminobutyric Acid (Gaba) Receptors Rho (Gabrr) Gene Polymorphisms and Risk for Migraine.

artículo científico

Gamma-aminobutyric acid (GABA) receptor rho (GABRR) polymorphisms and risk for essential tremor

artículo científico publicado en 2010

Gamma-aminobutyric acid (GABA) receptors GABRA4, GABRE, and GABRQ gene polymorphisms and risk for migraine

artículo científico publicado en 2018

Gamma-aminobutyric acid (GABA) receptors genes polymorphisms and risk for restless legs syndrome

artículo científico publicado en 2018

Gamma-aminobutyric acid GABRA4, GABRE, and GABRQ receptor polymorphisms and risk for essential tremor

artículo científico publicado en 2011

Genetics of restless legs syndrome: An update

artículo científico publicado en 2017

Genome-wide association study raised biomarker SLC1A2 rs3794087 and essential tremor: is it too early to say?

artículo científico publicado en 2013

Genomic and pharmacogenomic biomarkers of Parkinson's disease.

artículo científico publicado en 2014

H1-MAPT and the risk for familial essential tremor

artículo científico publicado en 2012

Heme Oxygenase 1 and 2 Common Genetic Variants and Risk for Essential Tremor.

artículo científico publicado en 2015

Heme Oxygenase-1 and 2 Common Genetic Variants and Risk for Multiple Sclerosis

artículo científico publicado en 2016

Heme Oxygenase-1 and 2 Common Genetic Variants and Risk for Restless Legs Syndrome.

artículo científico publicado en 2015

Hereditary Coproporphyria Associated with the Q306X Mutation in the Coproporphyrin Oxidase Gene Presenting with Acute Ataxia

artículo científico publicado en 2013

Histamine-N-methyl transferase polymorphism and risk for migraine

artículo científico publicado en 2008

Influence of age and gender in motor performance in healthy subjects

artículo científico publicado en 2010

LINGO1 and risk for essential tremor: results of a meta-analysis of rs9652490 and rs11856808.

artículo científico publicado en 2012

LINGO1 gene analysis in Parkinson's disease phenotypes.

artículo científico publicado en 2011

LINGO1 rs9652490 and rs11856808 are not associated with the risk of Parkinson’s disease: Results of a meta-analysis

article

LINGO1 rs9652490 and rs11856808 polymorphisms are not associated with risk for multiple sclerosis

artículo científico publicado en 2013

MAPT gene rs1052553 variant is not associated with the risk for multiple sclerosis

artículo científico publicado en 2013

MAPT1 gene rs1052553 variant is unrelated with the risk for restless legs syndrome.

artículo científico publicado en 2012

Missense Gamma-Aminobutyric Acid Receptor Polymorphisms Are Associated with Reaction Time, Motor Time, and Ethanol Effects in Vivo.

artículo científico publicado en 2018

Missense mutations in TENM4, a regulator of axon guidance and central myelination, cause essential tremor

artículo científico publicado en 2015

NAT2 polymorphisms and risk for Parkinson's disease: a systematic review and meta-analysis

artículo científico publicado en 2016

NQO1 gene rs1800566 variant is not associated with risk for multiple sclerosis

artículo científico publicado en 2014

Neuronal Nitric Oxide Synthase (nNOS, NOS1) rs693534 and rs7977109 Variants and Risk for Migraine

artículo científico publicado en 2015

Neuronal nitric oxide synthase (nNOS, NOS1) rs693534 and rs7977109 variants and risk for restless legs syndrome

artículo científico publicado en 2014

No association of the SLC1A2 rs3794087 allele with risk for essential tremor in the Spanish population

artículo científico publicado en 2013

Nonsynonymous polymorphisms of histamine-metabolising enzymes in patients with Parkinson's disease

artículo científico publicado en 2007

PITX3 and risk for Parkinson's disease: a systematic review and meta-analysis.

artículo científico

Paraoxonase 1 (PON1) polymorphisms and risk for migraine

scientific article published on 21 April 2010

Paraoxonase 1 Polymorphisms Are Not Related with the Risk for Multiple Sclerosis

artículo científico publicado en 2009

SLC1A2 rs3794087 variant and risk for essential tremor: a systematic review and meta-analysis.

artículo científico

SLC1A2 rs3794087 variant and risk for migraine

artículo científico publicado en 2013

Serum vitamin D, vitamin D receptor and binding protein genes polymorphisms in restless legs syndrome

artículo científico publicado en 2020

The GSTP1 gene variant rs1695 is not associated with an increased risk of multiple sclerosis

artículo científico publicado en 2014

The nonsynonymous Thr105Ile polymorphism of the histamine N-methyltransferase is associated to the risk of developing essential tremor

artículo científico publicado en 2008

The potential of LINGO-1 as a therapeutic target for essential tremor.

artículo científico publicado en 2015

The relationship between Parkinson's disease and essential tremor: review of clinical, epidemiologic, genetic, neuroimaging and neuropathological data, and data on the presence of cardinal signs of parkinsonism in essential tremor

artículo científico publicado en 2012

The solute carrier family 1 (glial high affinity glutamate transporter), member 2 gene, SLC1A2, rs3794087 variant and assessment risk for restless legs syndrome

artículo científico publicado en 2013

Thr105Ile (rs11558538) polymorphism in the histamine N-methyltransferase (HNMT) gene and risk for Parkinson disease: A PRISMA-compliant systematic review and meta-analysis

artículo científico publicado en 2016

Thr105Ile (rs11558538) polymorphism in the histamine-1-methyl-transferase (HNMT) gene and risk for restless legs syndrome

artículo científico publicado en 2016

Two common nonsynonymous paraoxonase 1 (PON1) gene polymorphisms and brain astrocytoma and meningioma.

artículo científico publicado en 2010

Vitamin D3 receptor ( VDR ) gene rs2228570 (Fok1) and rs731236 (Taq1) variants are not associated with the risk for multiple sclerosis: results of a new study and a meta-analysis

artículo científico publicado en 2013

Lista de obras de

A family study of DRD3 rs6280, SLC1A2 rs3794087 and MAPT rs1052553 variants in essential tremor

A polymorphism located at an ATG transcription start site of the heme oxygenase-2 gene is associated with classical Parkinson's disease.

Advances in understanding genomic markers and pharmacogenetics of Parkinson's disease

Alcohol consumption and risk for Parkinson's disease: a systematic review and meta-analysis

Alcohol dehydrogenase 2 genotype and allelic variants are not associated with the risk for essential tremor

Alcohol dehydrogenase 2 genotype and risk for migraine.

An Update on the Neurochemistry of Essential Tremor

An Update on the Role of Nitric Oxide in the Neurodegenerative Processes of Parkinson's Disease

An association study between Heme oxygenase-1 genetic variants and Parkinson's disease

Anti-Inflammatory Effects of Amantadine and Memantine: Possible Therapeutics for the Treatment of Covid-19?

Association Between Vitamin D Receptor rs731236 (Taq1) Polymorphism and Risk for Restless Legs Syndrome in the Spanish Caucasian Population.

Association Between the rs1229984 Polymorphism in the Alcohol Dehydrogenase 1B Gene and Risk for Restless Legs Syndrome.

Association between restless legs syndrome and other movement disorders

Association between the missense alcohol dehydrogenase rs1229984T variant with the risk for Parkinson's disease in women

COMT gene and risk for Parkinson's disease: a systematic review and meta-analysis

CYP2C19 polymorphism and risk for essential tremor

Cerebrospinal fluid biochemical studies in patients with Parkinson's disease: toward a potential search for biomarkers for this disease.

Changes at the CYP2C locus and disruption of CYP2C8/9 linkage disequilibrium in patients with essential tremor

Delta-amino-levulinic acid dehydratase gene and essential tremor

Diamine oxidase rs10156191 and rs2052129 variants are associated with the risk for migraine

Dopamine receptor D3 (DRD3) gene rs6280 variant and risk for restless legs syndrome

Dopamine receptor D3 (DRD3) genotype and allelic variants and risk for essential tremor.

Drug and xenobiotic biotransformation in the blood-brain barrier: a neglected issue. ⬇️

Gamma-Aminobutyric Acid (Gaba) Receptors Rho (Gabrr) Gene Polymorphisms and Risk for Migraine.

Gamma-aminobutyric acid (GABA) receptor rho (GABRR) polymorphisms and risk for essential tremor

Gamma-aminobutyric acid (GABA) receptors GABRA4, GABRE, and GABRQ gene polymorphisms and risk for migraine

Gamma-aminobutyric acid (GABA) receptors genes polymorphisms and risk for restless legs syndrome

Gamma-aminobutyric acid GABRA4, GABRE, and GABRQ receptor polymorphisms and risk for essential tremor

Genetics of restless legs syndrome: An update

Genome-wide association study raised biomarker SLC1A2 rs3794087 and essential tremor: is it too early to say?

Genomic and pharmacogenomic biomarkers of Parkinson's disease.

H1-MAPT and the risk for familial essential tremor

Heme Oxygenase 1 and 2 Common Genetic Variants and Risk for Essential Tremor.

Heme Oxygenase-1 and 2 Common Genetic Variants and Risk for Multiple Sclerosis

Heme Oxygenase-1 and 2 Common Genetic Variants and Risk for Restless Legs Syndrome.

Hereditary Coproporphyria Associated with the Q306X Mutation in the Coproporphyrin Oxidase Gene Presenting with Acute Ataxia

Histamine-N-methyl transferase polymorphism and risk for migraine

Influence of age and gender in motor performance in healthy subjects

LINGO1 and risk for essential tremor: results of a meta-analysis of rs9652490 and rs11856808.

LINGO1 gene analysis in Parkinson's disease phenotypes.

LINGO1 rs9652490 and rs11856808 are not associated with the risk of Parkinson’s disease: Results of a meta-analysis

LINGO1 rs9652490 and rs11856808 polymorphisms are not associated with risk for multiple sclerosis

MAPT gene rs1052553 variant is not associated with the risk for multiple sclerosis

MAPT1 gene rs1052553 variant is unrelated with the risk for restless legs syndrome.

Missense Gamma-Aminobutyric Acid Receptor Polymorphisms Are Associated with Reaction Time, Motor Time, and Ethanol Effects in Vivo.

Missense mutations in TENM4, a regulator of axon guidance and central myelination, cause essential tremor

NAT2 polymorphisms and risk for Parkinson's disease: a systematic review and meta-analysis

NQO1 gene rs1800566 variant is not associated with risk for multiple sclerosis

Neuronal Nitric Oxide Synthase (nNOS, NOS1) rs693534 and rs7977109 Variants and Risk for Migraine

Neuronal nitric oxide synthase (nNOS, NOS1) rs693534 and rs7977109 variants and risk for restless legs syndrome

No association of the SLC1A2 rs3794087 allele with risk for essential tremor in the Spanish population

Nonsynonymous polymorphisms of histamine-metabolising enzymes in patients with Parkinson's disease

PITX3 and risk for Parkinson's disease: a systematic review and meta-analysis.

Paraoxonase 1 (PON1) polymorphisms and risk for migraine

Paraoxonase 1 Polymorphisms Are Not Related with the Risk for Multiple Sclerosis

SLC1A2 rs3794087 variant and risk for essential tremor: a systematic review and meta-analysis.

SLC1A2 rs3794087 variant and risk for migraine

Serum vitamin D, vitamin D receptor and binding protein genes polymorphisms in restless legs syndrome

The GSTP1 gene variant rs1695 is not associated with an increased risk of multiple sclerosis

The nonsynonymous Thr105Ile polymorphism of the histamine N-methyltransferase is associated to the risk of developing essential tremor

The potential of LINGO-1 as a therapeutic target for essential tremor.

The relationship between Parkinson's disease and essential tremor: review of clinical, epidemiologic, genetic, neuroimaging and neuropathological data, and data on the presence of cardinal signs of parkinsonism in essential tremor

The solute carrier family 1 (glial high affinity glutamate transporter), member 2 gene, SLC1A2, rs3794087 variant and assessment risk for restless legs syndrome

Thr105Ile (rs11558538) polymorphism in the histamine N-methyltransferase (HNMT) gene and risk for Parkinson disease: A PRISMA-compliant systematic review and meta-analysis

Thr105Ile (rs11558538) polymorphism in the histamine-1-methyl-transferase (HNMT) gene and risk for restless legs syndrome

Two common nonsynonymous paraoxonase 1 (PON1) gene polymorphisms and brain astrocytoma and meningioma.

Vitamin D3 receptor ( VDR ) gene rs2228570 (Fok1) and rs731236 (Taq1) variants are not associated with the risk for multiple sclerosis: results of a new study and a meta-analysis