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Items: 1 to 20 of 70

1.

An MND/ALS phenotype associated with C9orf72 repeat expansion: abundant p62-positive, TDP-43-negative inclusions in cerebral cortex, hippocampus and cerebellum but without associated cognitive decline.

Troakes C, Maekawa S, Wijesekera L, Rogelj B, Siklós L, Bell C, Smith B, Newhouse S, Vance C, Johnson L, Hortobágyi T, Shatunov A, Al-Chalabi A, Leigh N, Shaw CE, King A, Al-Sarraj S.

Neuropathology. 2012 Oct;32(5):505-14. doi: 10.1111/j.1440-1789.2011.01286.x. Epub 2011 Dec 19.

PMID:
22181065
2.

[Clinical and pathological spectrum of TDP-43 associated ALS].

Onodera O, Yokoseki A, Tan CF, Ishihara T, Nishiira Y, Toyoshima Y, Kakita A, Nishizawa M, Takahashi H.

Rinsho Shinkeigaku. 2010 Nov;50(11):940-2. Review. Japanese.

PMID:
21921519
3.

Current insights into the C9orf72 repeat expansion diseases of the FTLD/ALS spectrum.

Cruts M, Gijselinck I, Van Langenhove T, van der Zee J, Van Broeckhoven C.

Trends Neurosci. 2013 Aug;36(8):450-9. doi: 10.1016/j.tins.2013.04.010. Epub 2013 Jun 7. Review.

PMID:
23746459
4.

[FTLD/ALS as TDP-43 proteinopathies].

Ishihara T, Ariizumi Y, Shiga A, Yokoseki A, Sato T, Toyoshima Y, Kakita A, Takahashi H, Nishizawa M, Onodera O.

Rinsho Shinkeigaku. 2010 Nov;50(11):1022-4. Review. Japanese.

PMID:
21921552
5.

The neuropathology associated with repeat expansions in the C9ORF72 gene.

Mackenzie IR, Frick P, Neumann M.

Acta Neuropathol. 2014 Mar;127(3):347-57. doi: 10.1007/s00401-013-1232-4. Epub 2013 Dec 20. Review.

PMID:
24356984
6.

Amyotrophic lateral sclerosis and frontotemporal lobar degeneration: a spectrum of TDP-43 proteinopathies.

Geser F, Lee VM, Trojanowski JQ.

Neuropathology. 2010 Apr;30(2):103-12. doi: 10.1111/j.1440-1789.2009.01091.x. Epub 2010 Jan 25. Review.

7.

ALS and FTLD: two faces of TDP-43 proteinopathy.

Liscic RM, Grinberg LT, Zidar J, Gitcho MA, Cairns NJ.

Eur J Neurol. 2008 Aug;15(8):772-80. doi: 10.1111/j.1468-1331.2008.02195.x. Review.

8.

[Yuasa-Mitsuyama disease].

Mitsuyama Y.

Brain Nerve. 2011 Feb;63(2):109-18. Review. Japanese.

PMID:
21301035
9.

Molecular basis of amyotrophic lateral sclerosis.

Liscic RM, Breljak D.

Prog Neuropsychopharmacol Biol Psychiatry. 2011 Mar 30;35(2):370-2. doi: 10.1016/j.pnpbp.2010.07.017. Epub 2010 Jul 23. Review.

PMID:
20655970
10.

Recent advances in the genetics of the ALS-FTLD complex.

Morris HR, Waite AJ, Williams NM, Neal JW, Blake DJ.

Curr Neurol Neurosci Rep. 2012 Jun;12(3):243-50. doi: 10.1007/s11910-012-0268-5. Review.

PMID:
22477152
11.

Molecular pathology and genetic advances in amyotrophic lateral sclerosis: an emerging molecular pathway and the significance of glial pathology.

Ince PG, Highley JR, Kirby J, Wharton SB, Takahashi H, Strong MJ, Shaw PJ.

Acta Neuropathol. 2011 Dec;122(6):657-71. doi: 10.1007/s00401-011-0913-0. Epub 2011 Nov 22. Review.

PMID:
22105541
12.

Neuropathology of Amyotrophic Lateral Sclerosis and Its Variants.

Saberi S, Stauffer JE, Schulte DJ, Ravits J.

Neurol Clin. 2015 Nov;33(4):855-76. doi: 10.1016/j.ncl.2015.07.012. Review.

13.

Amyotrophic lateral sclerosis.

Wijesekera LC, Leigh PN.

Orphanet J Rare Dis. 2009 Feb 3;4:3. doi: 10.1186/1750-1172-4-3. Review.

14.

Cytoplasmic inclusions of TDP-43 in neurodegenerative diseases: a potential role for caspases.

Rohn TT.

Histol Histopathol. 2009 Aug;24(8):1081-6. doi: 10.14670/HH-24.1081. Review.

15.

TDP-43: the relationship between protein aggregation and neurodegeneration in amyotrophic lateral sclerosis and frontotemporal lobar degeneration.

Baloh RH.

FEBS J. 2011 Oct;278(19):3539-49. doi: 10.1111/j.1742-4658.2011.08256.x. Epub 2011 Aug 24. Review.

16.

Molecular basis of ALS and FTD: implications for translational studies.

Liščić RM.

Arh Hig Rada Toksikol. 2015 Dec;66(4):285-90. doi: 10.1515/aiht-2015-66-2679. Review.

PMID:
26751860
17.

Frontotemporal dementias: update on recent developments in molecular genetics and neuropathology.

Liscić RM.

Arh Hig Rada Toksikol. 2009 Mar;60(1):117-22. doi: 10.2478/10004-1254-60-2009-1921. Review.

PMID:
19329383
18.

The role of transactive response DNA-binding protein-43 in amyotrophic lateral sclerosis and frontotemporal dementia.

Mackenzie IR, Rademakers R.

Curr Opin Neurol. 2008 Dec;21(6):693-700. doi: 10.1097/WCO.0b013e3283168d1d. Review.

19.

RNA-binding proteins with prion-like domains in ALS and FTLD-U.

Gitler AD, Shorter J.

Prion. 2011 Jul-Sep;5(3):179-87. doi: 10.4161/pri.5.3.17230. Epub 2011 Jul 1. Review.

20.

An amyloid-like cascade hypothesis for C9orf72 ALS/FTD.

Edbauer D, Haass C.

Curr Opin Neurobiol. 2016 Feb;36:99-106. doi: 10.1016/j.conb.2015.10.009. Epub 2015 Nov 8. Review.

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