Lista de obras -

Autosomal dominant palatal myoclonus and spinal cord atrophy

artículo científico publicado en 2002

CMT4A: identification of a Hispanic GDAP1 founder mutation

artículo científico publicado en 2003

Cerebrospinal fluid proteomic patterns discriminate Parkinson's disease and multiple system atrophy

artículo científico publicado en 2012

Clinical aspects and pathology of Alexander disease, and morphological and functional alteration of astrocytes induced by GFAP mutation

artículo científico publicado en 2011

Clozapine, but not haloperidol, enhances glial D-serine and L-glutamate release in rat frontal cortex and primary cultured astrocytes

artículo científico publicado en 2012

Decrease in plasma levels of α-synuclein is evident in patients with Parkinson's disease after elimination of heterophilic antibody interference

artículo científico publicado en 2015

Demyelinating and axonal features of Charcot-Marie-Tooth disease with mutations of myelin-related proteins (PMP22, MPZ and Cx32): a clinicopathological study of 205 Japanese patients

artículo científico publicado en 2003

Early-onset parkinsonism in a pedigree with phosphoglycerate kinase deficiency and a heterozygous carrier: do PGK-1 mutations contribute to vulnerability to parkinsonism?

artículo científico publicado en 2017

Effect of lamotrigine and carbamazepine on corticotropin-releasing factor-associated serotonergic transmission in rat dorsal raphe nucleus

scientific journal article

Enhancement of visual attention precedes the emergence of novel metaphor interpretations

artículo científico publicado en 2015

Evaluation of factors associated with elevated levels of platelet-derived microparticles in the acute phase of cerebral infarction

artículo científico publicado en 2009

Fine mapping of 16q-linked autosomal dominant cerebellar ataxia type III in Japanese families.

artículo científico publicado en 2004

Idiopathic thrombocytopenic purpura and mononeuropathy multiplex

artículo científico publicado en 2003

Inactivation of the putamen selectively impairs reward history-based action selection ⬇️

artículo científico publicado el 6 de febrero de 2011

Increased expression and secretion of r-Gsp protein, rat counterpart of complement C1s precursor, during cyclic AMP-induced differentiation in rat C6 glioma cells

scientific journal article

Knockdown of the Drosophila fused in sarcoma (FUS) homologue causes deficient locomotive behavior and shortening of motoneuron terminal branches.

artículo científico publicado en 2012

Local tissue anisotropy decreases in cerebellopetal fibers and pyramidal tract in multiple system atrophy.

artículo científico publicado en 2005

Molecular mechanism of rigid spine with muscular dystrophy type 1 caused by novel mutations of selenoprotein N gene

artículo científico publicado en 2006

Mollaret cells detected in a patient with varicella-zoster virus meningitis

artículo científico publicado en 2012

Mutation of TDP1, encoding a topoisomerase I-dependent DNA damage repair enzyme, in spinocerebellar ataxia with axonal neuropathy

artículo científico publicado en 2002

Predictive markers of blood cytokine and chemokine in recurrent brain infarction

artículo científico publicado en 2009

Regulation of axonal elongation and pathfinding from the entorhinal cortex to the dentate gyrus in the hippocampus by the chemokine stromal cell-derived factor 1 alpha

scientific journal article

Somatotopic organization of thalamocortical projection fibers as assessed with MR tractography

artículo científico publicado en 2007

The TRK-fused gene is mutated in hereditary motor and sensory neuropathy with proximal dominant involvement

artículo científico publicado en 2012

Ventricular Temperatures in Idiopathic Normal Pressure Hydrocephalus (iNPH) Measured with DWI-based MR Thermometry

artículo científico publicado en 2015

White matter loss in the splenium of the corpus callosum in a case of posterior cortical atrophy: a diffusion tensor imaging study

artículo científico publicado en 2004

[Wide spectrum of hereditary motor sensory neuropathy (HMSN)].

artículo científico publicado en 2009

p62/SQSTM1-dependent autophagy of Lewy body-like α-synuclein inclusions

artículo científico publicado en 2012

Lista de obras de

Autosomal dominant palatal myoclonus and spinal cord atrophy

CMT4A: identification of a Hispanic GDAP1 founder mutation

Cerebrospinal fluid proteomic patterns discriminate Parkinson's disease and multiple system atrophy

Clinical aspects and pathology of Alexander disease, and morphological and functional alteration of astrocytes induced by GFAP mutation

Clozapine, but not haloperidol, enhances glial D-serine and L-glutamate release in rat frontal cortex and primary cultured astrocytes

Decrease in plasma levels of α-synuclein is evident in patients with Parkinson's disease after elimination of heterophilic antibody interference

Demyelinating and axonal features of Charcot-Marie-Tooth disease with mutations of myelin-related proteins (PMP22, MPZ and Cx32): a clinicopathological study of 205 Japanese patients

Early-onset parkinsonism in a pedigree with phosphoglycerate kinase deficiency and a heterozygous carrier: do PGK-1 mutations contribute to vulnerability to parkinsonism?

Effect of lamotrigine and carbamazepine on corticotropin-releasing factor-associated serotonergic transmission in rat dorsal raphe nucleus

Enhancement of visual attention precedes the emergence of novel metaphor interpretations

Evaluation of factors associated with elevated levels of platelet-derived microparticles in the acute phase of cerebral infarction

Fine mapping of 16q-linked autosomal dominant cerebellar ataxia type III in Japanese families.

Idiopathic thrombocytopenic purpura and mononeuropathy multiplex

Inactivation of the putamen selectively impairs reward history-based action selection ⬇️

Increased expression and secretion of r-Gsp protein, rat counterpart of complement C1s precursor, during cyclic AMP-induced differentiation in rat C6 glioma cells

Knockdown of the Drosophila fused in sarcoma (FUS) homologue causes deficient locomotive behavior and shortening of motoneuron terminal branches.

Local tissue anisotropy decreases in cerebellopetal fibers and pyramidal tract in multiple system atrophy.

Molecular mechanism of rigid spine with muscular dystrophy type 1 caused by novel mutations of selenoprotein N gene

Mollaret cells detected in a patient with varicella-zoster virus meningitis

Mutation of TDP1, encoding a topoisomerase I-dependent DNA damage repair enzyme, in spinocerebellar ataxia with axonal neuropathy

Predictive markers of blood cytokine and chemokine in recurrent brain infarction

Regulation of axonal elongation and pathfinding from the entorhinal cortex to the dentate gyrus in the hippocampus by the chemokine stromal cell-derived factor 1 alpha

Somatotopic organization of thalamocortical projection fibers as assessed with MR tractography

The TRK-fused gene is mutated in hereditary motor and sensory neuropathy with proximal dominant involvement

Ventricular Temperatures in Idiopathic Normal Pressure Hydrocephalus (iNPH) Measured with DWI-based MR Thermometry

White matter loss in the splenium of the corpus callosum in a case of posterior cortical atrophy: a diffusion tensor imaging study

[Wide spectrum of hereditary motor sensory neuropathy (HMSN)].

p62/SQSTM1-dependent autophagy of Lewy body-like α-synuclein inclusions