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Results: 8

Related Articles by Review for PubMed (Select 23152587)

1.

Novel mutation in VCP gene causes atypical amyotrophic lateral sclerosis.

González-Pérez P, Cirulli ET, Drory VE, Dabby R, Nisipeanu P, Carasso RL, Sadeh M, Fox A, Festoff BW, Sapp PC, McKenna-Yasek D, Goldstein DB, Brown RH Jr, Blumen SC.

Neurology. 2012 Nov 27;79(22):2201-8. doi: 10.1212/WNL.0b013e318275963b. Epub 2012 Nov 14.

2.

The multiple faces of valosin-containing protein-associated diseases: inclusion body myopathy with Paget's disease of bone, frontotemporal dementia, and amyotrophic lateral sclerosis.

Nalbandian A, Donkervoort S, Dec E, Badadani M, Katheria V, Rana P, Nguyen C, Mukherjee J, Caiozzo V, Martin B, Watts GD, Vesa J, Smith C, Kimonis VE.

J Mol Neurosci. 2011 Nov;45(3):522-31. doi: 10.1007/s12031-011-9627-y. Epub 2011 Sep 3. Review.

PMID:
21892620
3.

A Brazilian family with hereditary inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia.

Fanganiello RD, Kimonis VE, Côrte CC, Nitrini R, Passos-Bueno MR.

Braz J Med Biol Res. 2011 Apr;44(4):374-80. Epub 2011 Mar 11. Review.

4.

Valosin-containing protein and the pathogenesis of frontotemporal dementia associated with inclusion body myopathy.

Guinto JB, Ritson GP, Taylor JP, Forman MS.

Acta Neuropathol. 2007 Jul;114(1):55-61. Epub 2007 Apr 25. Review.

PMID:
17457594
5.

[On intra-familial clinical diversities of a familial amyotrophic lateral sclerosis with a point mutation of Cu/Zn superoxide dismutase (Asn 86-Ser].

Maeda T, Kurahashi K, Matsunaga M, Inoue K, Inoue M.

No To Shinkei. 1997 Sep;49(9):847-51. Review. Japanese.

PMID:
9311004
6.

[Frontotemporal dementia (FTD) and genetic mutations including progranulin gene].

Arai T, Hasegawa M, Nishihara M, Nonaka T, Kametani F, Yoshida M, Hashizume Y, Beach TG, Morita M, Nakano I, Oda T, Tsuchiya K, Akiyama H.

Rinsho Shinkeigaku. 2008 Nov;48(11):990-3. Review. Japanese.

PMID:
19198141
7.

Familial amyotrophic lateral sclerosis from north India: case report and brief review.

Kulshreshtha D, Singh AK, Maurya PK, Thacker AK.

Neurol India. 2014 Mar-Apr;62(2):210-1. doi: 10.4103/0028-3886.132421. Review. No abstract available.

8.

Amyotrophic Lateral Sclerosis Genetic Studies: From Genome-wide Association Mapping to Genome Sequencing.

He J, Mangelsdorf M, Fan D, Bartlett P, Brown MA.

Neuroscientist. 2014 Nov 5. pii: 1073858414555404. [Epub ahead of print] Review.

PMID:
25378359
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