PuSH - Publication Server of Helmholtz Zentrum München

5 Records found.
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1.
Müller, K.* et al.: Comprehensive analysis of the mutation spectrum in 301 German ALS families. J. Neurol. Neurosurg. Psychiatr. 89, 817-827 (2018)
2.
Lehmer, C.* et al.: Poly-GP in cerebrospinal fluid links C9orf72-associated dipeptide repeat expression to the asymptomatic phase of ALS/FTD. EMBO Mol. Med. 9, 859-868 (2017)
3.
Brenner, D.* et al.: NEK1 mutations in familial amyotrophic lateral sclerosis. Brain 139:e28 (2016)
4.
Freischmidt, A.* et al.: Haploinsufficiency of TBK1 causes familial ALS and fronto-temporal dementia. Nat. Neurosci. 18, 631-636 (2015)
5.
Müller, K.* et al.: Two novel mutations in conserved codons indicate that CHCHD10 is a gene associated with motor neuron disease. Brain 137:e309 (2014)