Comparison of the clinical and cognitive features of genetically positive ALS patients from the largest tertiary center in Serbia
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Title
Comparison of the clinical and cognitive features of genetically positive ALS patients from the largest tertiary center in Serbia
Authors
Keywords
ALS, Genetics, Cognition, SOD1, C9orf72
Journal
JOURNAL OF NEUROLOGY
Volume 264, Issue 6, Pages 1091-1098
Publisher
Springer Nature
Online
2017-04-25
DOI
10.1007/s00415-017-8495-y
References
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Note: Only part of the references are listed.- Mutant SOD1 mediated pathogenesis of Amyotrophic Lateral Sclerosis
- (2016) Simran J. Kaur et al. GENE
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- Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: a cross-sectional study
- (2012) Elisa Majounie et al. LANCET NEUROLOGY
- Extensive genetics of ALS: A population-based study in Italy
- (2012) A. Chio et al. NEUROLOGY
- Genetic Overlap between Apparently Sporadic Motor Neuron Diseases
- (2012) Marka van Blitterswijk et al. PLoS One
- Expanded GGGGCC Hexanucleotide Repeat in Noncoding Region of C9ORF72 Causes Chromosome 9p-Linked FTD and ALS
- (2011) Mariely DeJesus-Hernandez et al. NEURON
- G41SSOD1mutation: A common ancestor for six ALS Italian families with an aggressive phenotype
- (2010) Stefania Battistini et al. Amyotrophic Lateral Sclerosis
- D90A-SOD1 mutation in ALS: The first report of heterozygous Italian patients and unusual findings
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- (2010) S. Millecamps et al. JOURNAL OF MEDICAL GENETICS
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- (2009) P. Wicks et al. JOURNAL OF NEUROLOGY
- Heterozygous SOD1 D90A mutation presenting as slowly progressive predominant upper motor neuron amyotrophic lateral sclerosis
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- A CASE OF ALS-FTD IN A LARGE FALS PEDIGREE WITH A K17I ANG MUTATION
- (2009) M. A. van Es et al. NEUROLOGY
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- (2009) Lokesh C Wijesekera et al. Orphanet Journal of Rare Diseases
- Mutations in FUS, an RNA Processing Protein, Cause Familial Amyotrophic Lateral Sclerosis Type 6
- (2009) C. Vance et al. SCIENCE
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