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Location matters - Genotype-phenotype correlation in LRSAM1 mutations associated with rare Charcot-Marie-Tooth neuropathy CMT2P.
Neuromuscul Disord. 2021 Feb;31(2):123-133. doi: 10.1016/j.nmd.2020.11.011. Epub 2020 Nov 28.
Neuromuscul Disord. 2021.
PMID: 33414056
Incidence and geographical variation of amyotrophic lateral sclerosis (ALS) in Southern Germany--completeness of the ALS registry Swabia.
Uenal H, Rosenbohm A, Kufeldt J, Weydt P, Goder K, Ludolph A, Rothenbacher D, Nagel G; ALS registry Study Group.
Uenal H, et al.
PLoS One. 2014 Apr 10;9(4):e93932. doi: 10.1371/journal.pone.0093932. eCollection 2014.
PLoS One. 2014.
PMID: 24722455
Free PMC article.
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Can lesions to the motor cortex induce amyotrophic lateral sclerosis?
Rosenbohm A, Kassubek J, Weydt P, Marroquin N, Volk AE, Kubisch C, Huppertz HJ, Weber M, Andersen PM, Weishaupt JH, Ludolph AC; ALS Schwaben Register Group.
Rosenbohm A, et al.
J Neurol. 2014 Feb;261(2):283-90. doi: 10.1007/s00415-013-7185-7. Epub 2013 Nov 20.
J Neurol. 2014.
PMID: 24253481
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Implementation of a population-based epidemiological rare disease registry: study protocol of the amyotrophic lateral sclerosis (ALS)--registry Swabia.
Nagel G, Unal H, Rosenbohm A, Ludolph AC, Rothenbacher D; ALS Registry Study Group.
Nagel G, et al.
BMC Neurol. 2013 Feb 17;13:22. doi: 10.1186/1471-2377-13-22.
BMC Neurol. 2013.
PMID: 23414001
Free PMC article.
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