Lista de obras - Tanya Gurevich - Dominio Público Uruguay

A "dose" effect of mutations in the GBA gene on Parkinson's disease phenotype

artículo científico publicado en 2016

A cognitive fMRI study in non-manifesting LRRK2 and GBA carriers

artículo científico publicado en 2016

A voxel-based morphometry and diffusion tensor imaging analysis of asymptomatic Parkinson's disease-related G2019S LRRK2 mutation carriers

article

Altered reward-related neural responses in non-manifesting carriers of the Parkinson disease related LRRK2 mutation

article

Application of the Movement Disorder Society prodromal criteria in healthy G2019S-LRRK2 carriers

artículo científico publicado en 2018

Appreciation of humor is decreased among patients with Parkinson's disease

artículo científico publicado en 2011

Arm swing as a potential new prodromal marker of Parkinson's disease

artículo científico publicado en 2016

Association of sequence alterations in the putative promoter of RAB7L1 with a reduced parkinson disease risk

artículo científico publicado en 2012

Axial motor clues to identify atypical parkinsonism: A multicentre European cohort study

scholarly article by Carlijn D J M Borm et al published 8 June 2018 in Parkinsonism and Related Disorders

Cerebral Imaging Markers of GBA and LRRK2 Related Parkinson's Disease and Their First-Degree Unaffected Relatives

artículo científico publicado en 2018

Decreased expression of B cell related genes in leukocytes of women with Parkinson's disease

artículo científico publicado en 2011

Fall risk and gait in Parkinson's disease: the role of the LRRK2 G2019S mutation.

artículo científico publicado en 2013

Fighting the risk of developing Parkinson's disease; clinical counseling for first degree relatives of patients with Parkinson's disease.

artículo científico publicado en 2011

Gait alterations in healthy carriers of the LRRK2 G2019S mutation.

artículo científico publicado en 2011

Genome-wide mapping of IBD segments in an Ashkenazi PD cohort identifies associated haplotypes

artículo científico publicado en 2014

Health-related quality of life in multiple system atrophy

artículo científico publicado en 2006

Hierarchical Data-Driven Analysis of Clinical Symptoms Among Patients With Parkinson's Disease.

artículo científico publicado en 2019

High Frequency of GBA Gene Mutations in Dementia With Lewy Bodies Among Ashkenazi Jews

artículo científico publicado en 2016

Intact working memory in non-manifesting LRRK2 carriers--an fMRI study

artículo científico publicado en 2015

Lower cognitive performance in healthy G2019S LRRK2 mutation carriers

artículo científico publicado en 2012

Network abnormalities among non-manifesting Parkinson disease related LRRK2 mutation carriers

artículo científico publicado en 2019

Neural correlates of executive functions in healthy G2019S LRRK2 mutation carriers

artículo científico publicado en 2013

Nonmotor symptoms in healthy Ashkenazi Jewish carriers of the G2019S mutation in the LRRK2 gene

artículo científico publicado en 2015

Parkinson disease phenotype in Ashkenazi Jews with and without LRRK2 G2019S mutations

artículo científico publicado en 2013

Parkinson's disease phenotype is influenced by the severity of the mutations in the GBA gene

article

Presentation, diagnosis, and management of multiple system atrophy in Europe: final analysis of the European multiple system atrophy registry

artículo científico publicado en 2010

Red flags for multiple system atrophy

artículo científico publicado en 2008

Reorganization of corticostriatal circuits in healthy G2019S LRRK2 carriers

artículo científico publicado en 2014

Subthalamic Neurons Encode Both Single- and Multi-Limb Movements in Parkinson's Disease Patients

artículo científico publicado en 2017

Survival rates among Parkinson's disease patients who carry mutations in the LRRK2 and GBA genes

article

The age at motor symptoms onset in LRRK2-associated Parkinson's disease is affected by a variation in the MAPT locus: a possible interaction

artículo científico publicado en 2011

The natural history of multiple system atrophy: a prospective European cohort study

artículo científico publicado en 2013

The p.L302P mutation in the lysosomal enzyme gene SMPD1 is a risk factor for Parkinson disease

artículo científico publicado en 2013

Two Ethnic Clusters with Huntington Disease in Israel: The Case of Mountain Jews and Karaites

artículo científico publicado en 2017

Lista de obras de Tanya Gurevich

A "dose" effect of mutations in the GBA gene on Parkinson's disease phenotype

A cognitive fMRI study in non-manifesting LRRK2 and GBA carriers

A voxel-based morphometry and diffusion tensor imaging analysis of asymptomatic Parkinson's disease-related G2019S LRRK2 mutation carriers

Altered reward-related neural responses in non-manifesting carriers of the Parkinson disease related LRRK2 mutation

Application of the Movement Disorder Society prodromal criteria in healthy G2019S-LRRK2 carriers

Appreciation of humor is decreased among patients with Parkinson's disease

Arm swing as a potential new prodromal marker of Parkinson's disease

Association of sequence alterations in the putative promoter of RAB7L1 with a reduced parkinson disease risk

Axial motor clues to identify atypical parkinsonism: A multicentre European cohort study

Cerebral Imaging Markers of GBA and LRRK2 Related Parkinson's Disease and Their First-Degree Unaffected Relatives

Decreased expression of B cell related genes in leukocytes of women with Parkinson's disease

Fall risk and gait in Parkinson's disease: the role of the LRRK2 G2019S mutation.

Fighting the risk of developing Parkinson's disease; clinical counseling for first degree relatives of patients with Parkinson's disease.

Gait alterations in healthy carriers of the LRRK2 G2019S mutation.

Genome-wide mapping of IBD segments in an Ashkenazi PD cohort identifies associated haplotypes

Health-related quality of life in multiple system atrophy

Hierarchical Data-Driven Analysis of Clinical Symptoms Among Patients With Parkinson's Disease.

High Frequency of GBA Gene Mutations in Dementia With Lewy Bodies Among Ashkenazi Jews

Intact working memory in non-manifesting LRRK2 carriers--an fMRI study

Lower cognitive performance in healthy G2019S LRRK2 mutation carriers

Network abnormalities among non-manifesting Parkinson disease related LRRK2 mutation carriers

Neural correlates of executive functions in healthy G2019S LRRK2 mutation carriers

Nonmotor symptoms in healthy Ashkenazi Jewish carriers of the G2019S mutation in the LRRK2 gene

Parkinson disease phenotype in Ashkenazi Jews with and without LRRK2 G2019S mutations

Parkinson's disease phenotype is influenced by the severity of the mutations in the GBA gene

Presentation, diagnosis, and management of multiple system atrophy in Europe: final analysis of the European multiple system atrophy registry

Red flags for multiple system atrophy

Reorganization of corticostriatal circuits in healthy G2019S LRRK2 carriers

Subthalamic Neurons Encode Both Single- and Multi-Limb Movements in Parkinson's Disease Patients

Survival rates among Parkinson's disease patients who carry mutations in the LRRK2 and GBA genes

The age at motor symptoms onset in LRRK2-associated Parkinson's disease is affected by a variation in the MAPT locus: a possible interaction

The natural history of multiple system atrophy: a prospective European cohort study

The p.L302P mutation in the lysosomal enzyme gene SMPD1 is a risk factor for Parkinson disease

Two Ethnic Clusters with Huntington Disease in Israel: The Case of Mountain Jews and Karaites