Alberto Bergareche
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View article: Home-based transcranial static magnetic field stimulation of the motor cortex for treating levodopa-induced dyskinesias in Parkinson's disease: A randomized controlled trial
Home-based transcranial static magnetic field stimulation of the motor cortex for treating levodopa-induced dyskinesias in Parkinson's disease: A randomized controlled trial Open
•tSMS is a portable, inhibitory, non-invasive brain stimulation technique.•Repeated sessions of home-based tSMS of the motor cortex are feasible and safe.•tSMS may provide subjective benefit for the treatment of levodopa-induced dyskinesia…
View article: A Set of Reliable Samples for the Study of Biomarkers for the Early Diagnosis of Parkinson’s Disease
A Set of Reliable Samples for the Study of Biomarkers for the Early Diagnosis of Parkinson’s Disease Open
Background: The identification of biomarkers for the early diagnosis of Parkinson’s Disease (PD) might improve treatment and avoid complications. However, the search of such biomarkers is a real challenge. The main reason for this is that …
View article: A More Homogeneous Phenotype in Parkinson's Disease Related to R1441G Mutation in the LRRK2 Gene
A More Homogeneous Phenotype in Parkinson's Disease Related to R1441G Mutation in the LRRK2 Gene Open
Parkinson's disease (PD) is characterized by a great clinical heterogeneity. Nevertheless, the biological drivers of this heterogeneity have not been completely elucidated and are likely to be complex, arising from interactions between gen…
View article: Two cases of opercular myoclonic‐anarthric status epilepticus
Two cases of opercular myoclonic‐anarthric status epilepticus Open
Opercular myoclonic‐anarthric status epilepticus (OMASE) is a rare form of epilepsia partialis continua presenting as fluctuating dysarthria, or even anarthria. The condition is caused by an epileptogenic lesion involving the opercular cor…
View article: Whole-exome sequencing associates novel<i>CSMD1</i>gene mutations with familial Parkinson disease
Whole-exome sequencing associates novel<i>CSMD1</i>gene mutations with familial Parkinson disease Open
We conclude that the CSMD1 mutations identified in this study might be responsible for the PD phenotype observed in our examined patients. This, along with previous reported studies, may suggest the complement pathway as an importan…
View article: A protective personal factor against disability and dependence in the elderly: an ordinal regression analysis with nine geographically-defined samples from Spain
A protective personal factor against disability and dependence in the elderly: an ordinal regression analysis with nine geographically-defined samples from Spain Open
View article: SCN4A Pore Mutation Pathogenetically Contributes to Autosomal Dominant Essential Tremor and May Increase Susceptibility to Epilepsy
SCN4A Pore Mutation Pathogenetically Contributes to Autosomal Dominant Essential Tremor and May Increase Susceptibility to Epilepsy Open
View article: Box plot of plasma α-synuclein levels in Controls, iPD patients and <i>LRRK2</i> PD patients.
Box plot of plasma α-synuclein levels in Controls, iPD patients and <i>LRRK2</i> PD patients. Open
A) Total α-synuclein (ng/ml). B) α-Synuclein oligomers in Counts Per Second (CPS). C) % Ratio Oligomers to total α-synuclein. Boxes show the minimum, maximum and median level for each group, together with the lower and…
View article: <i>SCN4A</i>pore mutation pathogenetically contributes to autosomal dominant essential tremor and may increase susceptibility to epilepsy
<i>SCN4A</i>pore mutation pathogenetically contributes to autosomal dominant essential tremor and may increase susceptibility to epilepsy Open
Essential tremor (ET) is the most prevalent movement disorder, affecting millions of people in the USA. Although a positive family history is one of the most important risk factors for ET, the genetic causes of ET remain unknown. In an att…
View article: <i>SORT1</i> Mutation Resulting in Sortilin Deficiency and p75 <sup>NTR</sup> Upregulation in a Family With Essential Tremor
<i>SORT1</i> Mutation Resulting in Sortilin Deficiency and p75 <sup>NTR</sup> Upregulation in a Family With Essential Tremor Open
*These authors contributed equally to this work.Essential tremor (ET) is the most prevalent movement disorder affecting millions of people in the United States. Although a positive family history is one of the most important risk factors f…
View article: Parkinson's Disease Case Ascertainment in the EPIC Cohort: The NeuroEPIC4PD Study
Parkinson's Disease Case Ascertainment in the EPIC Cohort: The NeuroEPIC4PD Study Open
Background/Aims: Large epidemiological prospective studies represent an important opportunity for investigating risk factors for rare diseases such as Parkinson's disease (PD). Here we describe the procedures we used for asce…
View article: Parkin and &lt;i&gt;LRRK2&lt;/i&gt;/Dardarin Mutations in Early Onset Parkinson’s Disease in the Basque Country (Spain)
Parkin and <i>LRRK2</i>/Dardarin Mutations in Early Onset Parkinson’s Disease in the Basque Country (Spain) Open
We have performed a complete screening of the Parkin gene (PRKN2) and looked for p.Gly2019Ser (G2019S) and p.Arg1441Gly (R1441G) LRRK2/dardarin gene mutations in twenty seven patients with Parkinson’s disease (PD) with an age at onset youn…