Literature DB >> 22670877

Combined fulminant frontotemporal dementia and amyotrophic lateral sclerosis associated with an I113T SOD1 mutation.

Jonathan S Katz1, Hans D Katzberg, Susan C Woolley, Stefan L Marklund, Peter M Andersen.   

Abstract

Mutations in the gene for superoxide dismutase type 1 cause amyotrophic lateral sclerosis (ALS), but are not thought to be associated with frontotemporal dementia (FTD). A lack of detailed case reports is one reason, among others, for this skepticism. This case report comments on a patient with familial ALS caused by I113T mutation in the SOD1 gene presenting with progressive cognitive and behavioral decline two years before developing progressive motor degeneration. In conclusion, this case provides evidence that SOD1 mutations can be associated with FTD.

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Year:  2012        PMID: 22670877     DOI: 10.3109/17482968.2012.678365

Source DB:  PubMed          Journal:  Amyotroph Lateral Scler        ISSN: 1471-180X


  7 in total

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Review 2.  From animal models to human disease: a genetic approach for personalized medicine in ALS.

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Review 3.  Frontotemporal dementia: a bridge between dementia and neuromuscular disease.

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Review 4.  Modelling amyotrophic lateral sclerosis in rodents.

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5.  A truncating SOD1 mutation, p.Gly141X, is associated with clinical and pathologic heterogeneity, including frontotemporal lobar degeneration.

Authors:  Masataka Nakamura; Kevin F Bieniek; Wen-Lang Lin; Neill R Graff-Radford; Melissa E Murray; Monica Castanedes-Casey; Pamela Desaro; Matthew C Baker; Nicola J Rutherford; Janice Robertson; Rosa Rademakers; Dennis W Dickson; Kevin B Boylan
Journal:  Acta Neuropathol       Date:  2015-04-28       Impact factor: 17.088

6.  De novo mutations in SOD1 are a cause of ALS.

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Journal:  J Neurol Neurosurg Psychiatry       Date:  2021-09-13       Impact factor: 10.154

7.  Effects of 3D culturing conditions on the transcriptomic profile of stem-cell-derived neurons.

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Journal:  Nat Biomed Eng       Date:  2018-04-09       Impact factor: 25.671

  7 in total

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