Brain atrophy measures in preclinical and manifest spinocerebellar ataxia type 2

Antisense oligonucleotide therapy for spinocerebellar ataxia type 2

(2017) Daniel R. Scoles et al.   NATURE

Brain imaging findings in idiopathic REM sleep behavior disorder (RBD) – A systematic review on potential biomarkers for neurodegeneration

(2017) Julia Heller et al.   SLEEP MEDICINE REVIEWS

Spinocerebellar ataxia type 2: Measures of saccade changes improve power for clinical trials

(2016) Roberto Rodríguez-Labrada et al.   MOVEMENT DISORDERS

No parkinsonism in SCA2 and SCA3 despite severe neurodegeneration of the dopaminergic substantia nigra

(2015) Ludger Schöls et al.   BRAIN

Functional connectivity changes related to cognitive and motor performance in spinocerebellar ataxia type 2

(2015) Carlos R. Hernandez-Castillo et al.   MOVEMENT DISORDERS

Modifications of resting state networks in spinocerebellar ataxia type 2

(2015) Sirio Cocozza et al.   MOVEMENT DISORDERS

Extensive White Matter Alterations and Its Correlations with Ataxia Severity in SCA 2 Patients

(2015) Carlos R. Hernandez-Castillo et al.   PLoS One

Comprehensive Study of Early Features in Spinocerebellar Ataxia 2: Delineating the Prodromal Stage of the Disease

(2014) Luis Velázquez-Pérez et al.   CEREBELLUM

Parahippocampal gray matter alterations in Spinocerebellar Ataxia Type 2 identified by voxel based morphometry

(2014) Roberto E. Mercadillo et al.   JOURNAL OF THE NEUROLOGICAL SCIENCES

Progression of Brain Atrophy in Spinocerebellar Ataxia Type 2: A Longitudinal Tensor-Based Morphometry Study

(2014) Mario Mascalchi et al.   PLoS One

Genotype-specific patterns of atrophy progression are more sensitive than clinical decline in SCA1, SCA3 and SCA6

(2013) Kathrin Reetz et al.   BRAIN

Biological and clinical characteristics of individuals at risk for spinocerebellar ataxia types 1, 2, 3, and 6 in the longitudinal RISCA study: analysis of baseline data

(2013) Heike Jacobi et al.   LANCET NEUROLOGY

Supratentorial and infratentorial damage in spinocerebellar ataxia 2: A diffusion-weighted MRI study

(2013) Elena Salvatore et al.   MOVEMENT DISORDERS

Linking coordinative and executive dysfunctions to atrophy in spinocerebellar ataxia 2 patients

(2011) Federico D’Agata et al.   Brain Structure & Function

MRI Shows a Region-Specific Pattern of Atrophy in Spinocerebellar Ataxia Type 2

(2011) Brian C. Jung et al.   CEREBELLUM

Sleep Disorders in Spinocerebellar Ataxia Type 2 Patients

(2011) Luis Velázquez-Pérez et al.   Neurodegenerative Diseases

Spinocerebellar Ataxia Type 2 (SCA2): Identification of Early Brain Degeneration in One Monozygous Twin in the Initial Disease Stage

(2010) Franziska Hoche et al.   CEREBELLUM

Distinct Neurochemical Profiles of Spinocerebellar Ataxias 1, 2, 6, and Cerebellar Multiple System Atrophy

(2010) Gülin Öz et al.   CEREBELLUM

Subtle rapid eye movement sleep abnormalities in presymptomatic spinocerebellar ataxia type 2 gene carriers

(2010) Roberto Rodríguez-Labrada et al.   MOVEMENT DISORDERS

Estimation of the age at onset in spinocerebellar ataxia type 2 Cuban patients by survival analysis

(2009) LE Almaguer-Mederos et al.   CLINICAL GENETICS

Molecular epidemiology of spinocerebellar ataxias in Cuba: Insights into SCA2 founder effect in Holguin

(2009) Luis Velázquez Pérez et al.   NEUROSCIENCE LETTERS

Brain white matter tracts degeneration in Friedreich ataxia. An in vivo MRI study using tract-based spatial statistics and voxel-based morphometry

(2008) Riccardo Della Nave et al.   NEUROIMAGE

Brain white matter damage in SCA1 and SCA2. An in vivo study using voxel-based morphometry, histogram analysis of mean diffusivity and tract-based spatial statistics

(2008) Riccardo Della Nave et al.   NEUROIMAGE