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List of works by Tanya Gurevich

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

scientific article published on 16 December 2016

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

scientific article published on 11 July 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

scientific article published on 30 March 2018

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

scientific article

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

scientific article published on 19 July 2016

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

scientific article published in January 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

scientific article published on 30 May 2018

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

scientific article

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

scientific article

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

scientific article

Gait alterations in healthy carriers of the LRRK2 G2019S mutation.

scientific article

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

scientific article

Health-related quality of life in multiple system atrophy

scientific article published in June 2006

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

scientific article

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

scientific article

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

scientific article published on 4 November 2015

Lower cognitive performance in healthy G2019S LRRK2 mutation carriers

scientific article

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

scientific article published on 21 February 2019

Neural correlates of executive functions in healthy G2019S LRRK2 mutation carriers

scientific article

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

scientific article published on 21 March 2015

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

scientific article published on 15 October 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

scientific article

Red flags for multiple system atrophy

scientific article published in June 2008

Reorganization of corticostriatal circuits in healthy G2019S LRRK2 carriers

scientific article

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

scientific article published on 13 February 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

scientific article published on 06 September 2011

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

scientific article published on 5 February 2013

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

scientific article

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

scientific article