Lista de obras -

A painless burn due to lack of painkillers.

artículo científico publicado en 2014

A search for SNCA 3' UTR variants identified SNP rs356165 as a determinant of disease risk and onset age in Parkinson's disease.

artículo científico publicado en 2011

Alpha-synuclein transcript isoforms in three different brain regions from Parkinson's disease and healthy subjects in relation to the SNCA rs356165/rs11931074 polymorphisms.

artículo científico publicado en 2014

Amyloid precursor protein gene (APP) variation in late-onset Alzheimer's disease.

artículo científico publicado en 2011

Analysis of theMicro-RNA-133andPITX3genes in Parkinson's disease

article

Association between an alpha(2) macroglobulin DNA polymorphism and late-onset Alzheimer's disease

scientific article published on 01 October 1999

Autoimmune post-herpes simplex encephalitis of adults and teenagers

artículo científico publicado en 2015

Chronic migraine does not increase posterior circulation territory (PCT) infarct-like lesions.

artículo científico publicado en 2013

Cluster-like headache heralding cerebral venous thrombosis

artículo científico publicado en 2008

Cryoglobulinaemic neuropathy: a further cause of bilateral sciatic neuropathy.

artículo científico publicado en 2008

FGF20 rs12720208 SNP and microRNA-433 variation: no association with Parkinson's disease in Spanish patients.

artículo científico publicado en 2010

Inflammatory bowel disease: an increased risk factor for neurologic complications

artículo científico publicado en 2014

Ipsilateral reversible diaphragmatic paralysis after pons stroke.

artículo científico publicado en 2011

LRRK2 mutations are a common cause of Parkinson's disease in Spain

article

Lack of association between protocadherin 11-X/Y (PCDH11X and PCDH11Y) polymorphisms and late onset Alzheimer's disease.

artículo científico publicado en 2011

Late-onset Alzheimer's disease is associated with mitochondrial DNA 7028C/haplogroup H and D310 poly-C tract heteroplasmy.

artículo científico publicado en 2011

MiRNA profile in the substantia nigra of Parkinson's disease and healthy subjects.

artículo científico publicado en 2014

Mitochondrial DNA polymorphisms/haplogroups in hereditary spastic paraplegia

artículo científico publicado en 2011

Mutational screening of PARKIN identified a 3' UTR variant (rs62637702) associated with Parkinson's disease.

artículo científico publicado en 2012

Mutational spectrum of the SPG4 (SPAST) and SPG3A (ATL1) genes in Spanish patients with hereditary spastic paraplegia.

artículo científico publicado en 2010

Netrin-1 receptor antibodies in thymoma-associated neuromyotonia with myasthenia gravis.

artículo científico publicado en 2017

Neurologic disorders associated with inflammatory bowel disease.

artículo científico publicado en 2011

Peripheral neuropathy: an underreported neurologic manifestation of inflammatory bowel disease.

artículo científico

Profile of microRNAs in the plasma of Parkinson's disease patients and healthy controls

artículo científico publicado en 2013

SPG7 mutational screening in spastic paraplegia patients supports a dominant effect for some mutations and a pathogenic role for p.A510V

artículo científico publicado en 2012

Sudden paraplegia after lumbar puncture as a clue in the diagnosis of a patient with spinal dural arteriovenous fistula.

artículo científico publicado en 2017

The challenge of drug-induced aseptic meningitis revisited

artículo científico publicado en 2014

The screening of the 3'UTR sequence of LRRK2 identified an association between the rs66737902 polymorphism and Parkinson's disease

artículo científico publicado en 2014

Trigeminal mononeuropathy: first clinical manifestation of breast cancer

scientific article published on 01 January 2005

Trunk muscle involvement in late-onset Pompe disease: Study of thirty patients

article

[Neuralgic amyotrophy associated to hepatitis E virus infection]

scientific article published on 24 March 2015

Lista de obras de

A painless burn due to lack of painkillers.

A search for SNCA 3' UTR variants identified SNP rs356165 as a determinant of disease risk and onset age in Parkinson's disease.

Alpha-synuclein transcript isoforms in three different brain regions from Parkinson's disease and healthy subjects in relation to the SNCA rs356165/rs11931074 polymorphisms.

Amyloid precursor protein gene (APP) variation in late-onset Alzheimer's disease.

Analysis of theMicro-RNA-133andPITX3genes in Parkinson's disease

Association between an alpha(2) macroglobulin DNA polymorphism and late-onset Alzheimer's disease

Autoimmune post-herpes simplex encephalitis of adults and teenagers

Chronic migraine does not increase posterior circulation territory (PCT) infarct-like lesions.

Cluster-like headache heralding cerebral venous thrombosis

Cryoglobulinaemic neuropathy: a further cause of bilateral sciatic neuropathy.

FGF20 rs12720208 SNP and microRNA-433 variation: no association with Parkinson's disease in Spanish patients.

Inflammatory bowel disease: an increased risk factor for neurologic complications

Ipsilateral reversible diaphragmatic paralysis after pons stroke.

LRRK2 mutations are a common cause of Parkinson's disease in Spain

Lack of association between protocadherin 11-X/Y (PCDH11X and PCDH11Y) polymorphisms and late onset Alzheimer's disease.

Late-onset Alzheimer's disease is associated with mitochondrial DNA 7028C/haplogroup H and D310 poly-C tract heteroplasmy.

MiRNA profile in the substantia nigra of Parkinson's disease and healthy subjects.

Mitochondrial DNA polymorphisms/haplogroups in hereditary spastic paraplegia

Mutational screening of PARKIN identified a 3' UTR variant (rs62637702) associated with Parkinson's disease.

Mutational spectrum of the SPG4 (SPAST) and SPG3A (ATL1) genes in Spanish patients with hereditary spastic paraplegia.

Netrin-1 receptor antibodies in thymoma-associated neuromyotonia with myasthenia gravis.

Neurologic disorders associated with inflammatory bowel disease.

Peripheral neuropathy: an underreported neurologic manifestation of inflammatory bowel disease.

Profile of microRNAs in the plasma of Parkinson's disease patients and healthy controls

SPG7 mutational screening in spastic paraplegia patients supports a dominant effect for some mutations and a pathogenic role for p.A510V

Sudden paraplegia after lumbar puncture as a clue in the diagnosis of a patient with spinal dural arteriovenous fistula.

The challenge of drug-induced aseptic meningitis revisited

The screening of the 3'UTR sequence of LRRK2 identified an association between the rs66737902 polymorphism and Parkinson's disease

Trigeminal mononeuropathy: first clinical manifestation of breast cancer

Trunk muscle involvement in late-onset Pompe disease: Study of thirty patients

[Neuralgic amyotrophy associated to hepatitis E virus infection]