Cargando…

Correction: CAG Repeats Determine Brain Atrophy in Spinocerebellar Ataxia 17: A VBM Study

Detalles Bibliográficos
Autores principales:	Reetz, Kathrin, Kleiman, Alexandra, Klein, Christine, Lencer, Rebekka, Zuehlke, Christine, Brockmann, Kathrin, Rolfs, Arndt, Binkofski, Ferdinand
Formato:	Texto
Lenguaje:	English
Publicado:	Public Library of Science 2011
Materias:	Correction
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3031635/ http://dx.doi.org/10.1371/annotation/e30b739b-114e-445a-b07b-7e2a8efa2668

Ejemplares similares

CAG Repeats Determine Brain Atrophy in Spinocerebellar Ataxia 17: A VBM Study
por: Reetz, Kathrin, et al.
Publicado: (2011)

Brain atrophy measures in preclinical and manifest spinocerebellar ataxia type 2
por: Reetz, Kathrin, et al.
Publicado: (2018)

Expansion, mosaicism and interruption: mechanisms of the CAG repeat mutation in spinocerebellar ataxia type 1
por: Kraus-Perrotta, Cara, et al.
Publicado: (2016)

Spinocerebellar ataxia 17: full phenotype in a 41 CAG/CAA repeats carrier
por: Origone, Paola, et al.
Publicado: (2018)

CAG repeat length does not associate with the rate of cerebellar degeneration in spinocerebellar ataxia type 3
por: Huang, Shang-Ran, et al.
Publicado: (2016)

Population Genetics and New Insight into Range of CAG Repeats of Spinocerebellar Ataxia Type 3 in the Han Chinese Population
por: Gan, Shi-Rui, et al.
Publicado: (2015)

Patterns of CAG repeat instability in the central nervous system and periphery in Huntington’s disease and in spinocerebellar ataxia type 1
por: Mouro Pinto, Ricardo, et al.
Publicado: (2020)

Structural Insights Reveal the Dynamics of the Repeating r(CAG) Transcript Found in Huntington’s Disease (HD) and Spinocerebellar Ataxias (SCAs)
por: Tawani, Arpita, et al.
Publicado: (2015)

Association between Proton Magnetic Resonance Spectroscopy Measurements and CAG Repeat Number in Patients with Spinocerebellar Ataxias 2, 3, or 6
por: Wang, Po-Shan, et al.
Publicado: (2012)

Spinocerebellar ataxia type 2 in seven Korean families: CAG trinucleotide expansion and clinical characteristics.
por: Kim, J. M., et al.
Publicado: (1999)

Cognition in Trinucleotide Repeat Spinocerebellar Ataxias: A Review
por: Agarwal, Ayush, et al.
Publicado: (2022)

Functionally Relevant Maculopathy and Optic Atrophy in Spinocerebellar Ataxia Type 1
por: Oertel, Frederike Cosima, et al.
Publicado: (2020)

A clinical report of the massive CAG repeat expansion in spinocerebellar ataxia type 2: Severe onset in a Mexican child and review previous cases
por: Sánchez-Corona, José, et al.
Publicado: (2020)

An understanding of spinocerebellar ataxia
por: Ramachandra, N.B., et al.
Publicado: (2015)

Parkinsonism in Spinocerebellar Ataxia
por: Park, Hyeyoung, et al.
Publicado: (2015)

Spinocerebellar ataxia: an update
por: Sullivan, Roisin, et al.
Publicado: (2018)

Radiological hints for differentiation of cerebellar multiple system atrophy from spinocerebellar ataxia
por: Chen, Hung-Chieh, et al.
Publicado: (2022)

Postural Tremor and Ataxia Progression in Spinocerebellar Ataxias
por: Gan, Shi-Rui, et al.
Publicado: (2017)

Spinocerebellar ataxia 7 (SCA7) in Indian population: predilection of ATXN7-CAG expansion mutation in an ethnic population
por: Faruq, Mohammed, et al.
Publicado: (2015)

Altered Velocity Processing in Schizophrenia during Pursuit Eye Tracking
por: Nagel, Matthias, et al.
Publicado: (2012)

A longitudinal VBM study monitoring treatment with erythropoietin in patients with Friedreich ataxia
por: Santner, Wolfram, et al.
Publicado: (2014)

Cell biology of spinocerebellar ataxia
por: Orr, Harry T.
Publicado: (2012)

Cognitive dysfunction in spinocerebellar ataxias
por: Teive, Helio Afonso Ghizoni, et al.
Publicado: (2009)

Neuroradiological Findings in the Spinocerebellar Ataxias
por: Meira, Alex Tiburtino, et al.
Publicado: (2019)

Minidumbbell structures formed by ATTCT pentanucleotide repeats in spinocerebellar ataxia type 10
por: Guo, Pei, et al.
Publicado: (2020)

Stage-dependent biomarker changes in spinocerebellar ataxia type 3
por: Faber, Jennifer, et al.
Publicado: (2023)

Quantitative evaluation of upper limb ataxia in spinocerebellar ataxias
por: Kishimoto, Yoshiyuki, et al.
Publicado: (2022)

Tau and neurofilament light‐chain as fluid biomarkers in spinocerebellar ataxia type 3
por: Garcia‐Moreno, Hector, et al.
Publicado: (2022)

Spinocerebellar Ataxia 12 Patients have better Quality of Life than Spinocerebellar Ataxia 1 and 2
por: Dabla, Surekha, et al.
Publicado: (2022)

Regional Brain and Spinal Cord Volume Loss in Spinocerebellar Ataxia Type 3
por: Faber, Jennifer, et al.
Publicado: (2021)

Genetic and molecular aspects of spinocerebellar ataxias
por: Honti, Viktor, et al.
Publicado: (2005)

Decreasing fall risk in spinocerebellar ataxia
por: Santos de Oliveira, Laura Alice, et al.
Publicado: (2015)

Spinocerebellar ataxia-10 with paranoid schizophrenia
por: Trikamji, Bhavesh, et al.
Publicado: (2015)

Spinocerebellar Ataxia Type 31 with Blepharospasm
por: Itaya, Sakiko, et al.
Publicado: (2018)

Diagnosis of Spinocerebellar Ataxia in the West Indies
por: Yearwood, Ashley K., et al.
Publicado: (2018)

Nonmotor symptoms in spinocerebellar ataxias (SCAs)
por: Moro, Adriana, et al.
Publicado: (2019)

Aberrant Cerebellar Circuitry in the Spinocerebellar Ataxias
por: Robinson, Katherine J., et al.
Publicado: (2020)

Functionality and disease severity in spinocerebellar ataxias
por: da CRUZ, Geanison Castro, et al.
Publicado: (2022)

Ancestral Origin of the ATTCT Repeat Expansion in Spinocerebellar Ataxia Type 10 (SCA10)
por: Almeida, Teresa, et al.
Publicado: (2009)

Transgenic Models of Spinocerebellar Ataxia Type 10: Modeling a Repeat Expansion Disorder
por: McFarland, Karen N., et al.
Publicado: (2012)

Cannot write session to /tmp/vufind_sessions/sess_d0dml15cgnq3s4tfe6mp6ssln0