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13. ALS-FTD complex disorder due to C9ORF72 gene mutation: description of first Polish family. Siuda J; Lewicka T; Bujak M; Opala G; Golenia A; Slowik A; van Blitterswijk M; Baker M; Ertekin-Taner N; Wszolek ZK; Rademakers R Eur Neurol; 2014; 72(1-2):64-71. PubMed ID: 24861139 [TBL] [Abstract][Full Text] [Related]
14. Cognitive and clinical characteristics of patients with amyotrophic lateral sclerosis carrying a C9orf72 repeat expansion: a population-based cohort study. Byrne S; Elamin M; Bede P; Shatunov A; Walsh C; Corr B; Heverin M; Jordan N; Kenna K; Lynch C; McLaughlin RL; Iyer PM; O'Brien C; Phukan J; Wynne B; Bokde AL; Bradley DG; Pender N; Al-Chalabi A; Hardiman O Lancet Neurol; 2012 Mar; 11(3):232-40. PubMed ID: 22305801 [TBL] [Abstract][Full Text] [Related]
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18. Clinical and pathological features of amyotrophic lateral sclerosis caused by mutation in the C9ORF72 gene on chromosome 9p. Stewart H; Rutherford NJ; Briemberg H; Krieger C; Cashman N; Fabros M; Baker M; Fok A; DeJesus-Hernandez M; Eisen A; Rademakers R; Mackenzie IR Acta Neuropathol; 2012 Mar; 123(3):409-17. PubMed ID: 22228244 [TBL] [Abstract][Full Text] [Related]
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20. Multiple system atrophy and amyotrophic lateral sclerosis in a family with hexanucleotide repeat expansions in C9orf72. Goldman JS; Quinzii C; Dunning-Broadbent J; Waters C; Mitsumoto H; Brannagan TH; Cosentino S; Huey ED; Nagy P; Kuo SH JAMA Neurol; 2014 Jun; 71(6):771-4. PubMed ID: 24733620 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]