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Miguel Lucas

University of Seville

98

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2293

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Lipoid proteinosis or Urbach-Wiethe disease: Description of a new case with cerebral involvement.

2017 Neurologia
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Lipoidoproteinosis o enfermedad de Urbach-Wiethe: a propósito de un nuevo caso con afectación cerebral

2017 Neurologia
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Analysis of CCM1 expression uncovers novel minor-form exons and variable splicing patterns

2016 Genes & Genomics
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Dominant‐negative mutation p.Arg324Thr in KCNA1 impairs Kv1.1 channel function in episodic ataxia

2016 Movement Disorders
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Free kappa light chains in cerebrospinal fluid as a biomarker to assess risk conversion to multiple sclerosis

2015
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A new risk variant for multiple sclerosis at the immunoglobulin heavy chain locus associates with intrathecal IgG, IgM index and oligoclonal bands

2015 Multiple Sclerosis Journal
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Mutation prevalence of cerebral cavernous malformation genes in Spanish patients.

2014 PLOS ONE
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Genome-Wide Pharmacogenomic Study Of Response To Cannabinoids In MS Spasticity Patients (P1.185)

2014 Neurology
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HERV-W polymorphism in chromosome X is associated with multiple sclerosis risk and with differential expression of MSRV

2014 Retrovirology
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Clinical and Molecular Study of the Extracellular Matrix Protein 1 Gene in a Spanish Family with Lipoid Proteinosis

2014 Journal of Clinical Neurology
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