The genetics and neuropathology of amyotrophic lateral sclerosis-Reference-Cited by-同舟云学术

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The genetics and neuropathology of amyotrophic lateral sclerosis

Published:2012-08-02 Issue:3 Volume:124 Page:339-352
ISSN:0001-6322
Container-title:Acta Neuropathologica
language:en
Short-container-title:Acta Neuropathol

Author:

Al-Chalabi Ammar,Jones Ashley,Troakes Claire,King Andrew,Al-Sarraj Safa,van den Berg Leonard H.

Publisher

Springer Science and Business Media LLC

Subject

Cellular and Molecular Neuroscience,Neurology (clinical),Pathology and Forensic Medicine

Link

http://link.springer.com/content/pdf/10.1007/s00401-012-1022-4.pdf

Reference133 articles.

1. Al-Chalabi A, Andersen PM, Nilsson P et al (1999) Deletions of the heavy neurofilament subunit tail in amyotrophic lateral sclerosis. Hum Mol Genet 8:157–164. doi: 10.1093/hmg/8.2.157

2. Al-Chalabi A, Fang F, Hanby MF et al (2010) An estimate of amyotrophic lateral sclerosis heritability using twin data. J Neurol Neurosurg Psychiatry 81:1324–1326. doi: 10.1136/jnnp.2010.207464

3. Al-Chalabi A, Lewis CM (2011) Modelling the effects of penetrance and family size on rates of sporadic and familial disease. Hum Hered 71:281–288. doi: 10.1159/000330167

4. Al-Saif A, Al-Mohanna F, Bohlega S (2011) A mutation in sigma-1 receptor causes juvenile amyotrophic lateral sclerosis. Ann Neurol 70:913–919. doi: 10.1002/ana.22534

5. Al-Sarraj S, King A, Troakes C et al (2011) p62 positive, TDP-43 negative, neuronal cytoplasmic and intranuclear inclusions in the cerebellum and hippocampus define the pathology of C9orf72-linked FTLD and MND/ALS. Acta Neuropathol 122:691–702. doi: 10.1007/s00401-011-0911-2

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