Literature DB >> 31286011

Abnormal DaTSCAN and Atypical Parkinsonism in SCA12.

Anna Latorre1,2, Claudia Del Gamba1,3, Elisa Menozzi1,4, Bettina Balint1,5, Florian Brugger6, Kailash P Bhatia1.   

Abstract

Entities:  

Year:  2019        PMID： 31286011      PMCID： PMC6592799          DOI： 10.1002/mdc3.12751

Source DB:  PubMed          Journal:  Mov Disord Clin Pract        ISSN： 2330-1619


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  12 in total

Review 1.  SCA12: an unusual mutation leads to an unusual spinocerebellar ataxia.

Authors:  S E Holmes; E O Hearn; C A Ross; R L Margolis
Journal:  Brain Res Bull       Date:  2001 Oct-Nov 1       Impact factor: 4.077

Review 2.  Why is SCA12 different from other SCAs?

Authors:  S E Holmes; E O'Hearn; R L Margolis
Journal:  Cytogenet Genome Res       Date:  2003       Impact factor: 1.636

3.  Coincidence of a large SCA12 repeat allele with a case of Creutzfeld-Jacob disease.

Authors:  Y Hellenbroich; W Schulz-Schaeffer; M F Nitschke; J Köhnke; G Händler; K Bürk; E Schwinger; C Zühlke
Journal:  J Neurol Neurosurg Psychiatry       Date:  2004-06       Impact factor: 10.154

4.  Nigrostriatal denervation sine parkinsonism.

Authors:  Kristoffer Haugarvoll; Laurence A Bindoff; Charalampos Tzoulis
Journal:  Brain       Date:  2016-01-25       Impact factor: 13.501

Review 5.  Movement disorders in spinocerebellar ataxias.

Authors:  Judith van Gaalen; Paola Giunti; Bart P van de Warrenburg
Journal:  Mov Disord       Date:  2011-03-02       Impact factor: 10.338

6.  Evidence of a common founder for SCA12 in the Indian population.

Authors:  S Bahl; K Virdi; U Mittal; M P Sachdeva; A K Kalla; S E Holmes; E O'Hearn; R L Margolis; S Jain; A K Srivastava; M Mukerji
Journal:  Ann Hum Genet       Date:  2005-09       Impact factor: 1.670

7.  Clinical behaviour of spinocerebellar ataxia type 12 and intermediate length abnormal CAG repeats in PPP2R2B.

Authors:  Achal K Srivastava; Amit Takkar; Ajay Garg; Mohammed Faruq
Journal:  Brain       Date:  2016-11-17       Impact factor: 13.501

8.  Molecular and clinical correlation in five Indian families with spinocerebellar ataxia 12.

Authors:  A K Srivastava; S Choudhry; M S Gopinath; S Roy; M Tripathi; S K Brahmachari; S Jain
Journal:  Ann Neurol       Date:  2001-12       Impact factor: 10.422

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

Authors:  Ludger Schöls; Matthias Reimold; Kay Seidel; Christoph Globas; Kathrin Brockmann; Till Karsten Hauser; Georg Auburger; Katrin Bürk; Wilfred den Dunnen; Gerald Reischl; Horst-Werner Korf; Ewout R Brunt; Udo Rüb
Journal:  Brain       Date:  2015-09-11       Impact factor: 13.501

Review 10.  "Atypical" atypical parkinsonism: new genetic conditions presenting with features of progressive supranuclear palsy, corticobasal degeneration, or multiple system atrophy-a diagnostic guide.

Authors:  Maria Stamelou; Niall P Quinn; Kailash P Bhatia
Journal:  Mov Disord       Date:  2013-05-29       Impact factor: 10.338
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  1 in total

1.  Clinical, Radiological, and Genetic Profile of Spinocerebellar Ataxia 12: A Hospital-Based Cohort Analysis.

Authors:  Valakunja Harikrishna Ganaraja; Vikram V Holla; Albert Stezin; Nitish Kamble; Ravi Yadav; Meera Purushottam; Sanjeev Jain; Pramod Kumar Pal
Journal:  Tremor Other Hyperkinet Mov (N Y)       Date:  2022-04-21
  1 in total

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