Found: 17
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Gene4MND: An Integrative Genetic Database and Analytic Platform for Motor Neuron Disease.
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- Frontiers in Molecular Neuroscience, 2021, v. 13, p. N.PAG, doi. 10.3389/fnmol.2021.644202
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- Article
Association of variants in the KIF1A gene with amyotrophic lateral sclerosis.
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- Translational Neurodegeneration, 2022, v. 11, n. 1, p. 1, doi. 10.1186/s40035-022-00320-2
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Association of variants in the KIF1A gene with amyotrophic lateral sclerosis.
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- Translational Neurodegeneration, 2022, v. 11, n. 1, p. 1, doi. 10.1186/s40035-022-00320-2
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- Article
Association Between Vitamins and Amyotrophic Lateral Sclerosis: A Center-Based Survey in Mainland China.
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- Frontiers in Neurology, 2020, p. 1, doi. 10.3389/fneur.2020.00488
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A Novel Potentially Pathogenic Rare Variant in the DNAJC7 Gene Identified in Amyotrophic Lateral Sclerosis Patients From Mainland China.
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- Frontiers in Genetics, 2020, v. 11, p. N.PAG, doi. 10.3389/fgene.2020.00821
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Brain metabolic signatures in patients with genetic and nongenetic amyotrophic lateral sclerosis.
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- CNS Neuroscience & Therapeutics, 2023, v. 29, n. 9, p. 2530, doi. 10.1111/cns.14193
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- Article
Mitochondrial genome variations are associated with amyotrophic lateral sclerosis in patients from mainland China.
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- Journal of Neurology, 2022, v. 269, n. 2, p. 805, doi. 10.1007/s00415-021-10659-7
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Genetic and clinical analyses of spinocerebellar ataxia type 8 in mainland China.
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- Journal of Neurology, 2019, v. 266, n. 12, p. 2979, doi. 10.1007/s00415-019-09519-2
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- Article
ALS-plus related clinical and genetic study from China.
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- Neurological Sciences, 2023, v. 44, n. 10, p. 3557, doi. 10.1007/s10072-023-06843-4
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Mutation and clinical analysis of the CLCC1 gene in amyotrophic lateral sclerosis patients from Central South China.
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- Annals of Clinical & Translational Neurology, 2024, v. 11, n. 1, p. 79, doi. 10.1002/acn3.51934
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The Clinical and Ploynucleotide Repeat Expansion Analysis of ATXN2, NOP56, AR and C9orf72 in Patients With ALS From Mainland China.
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- Frontiers in Neurology, 2022, v. 13, p. 1, doi. 10.3389/fneur.2022.811202
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- Article
Profiling the Genome-Wide Landscape of Short Tandem Repeats by Long-Read Sequencing.
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- Frontiers in Genetics, 2022, v. 13, p. 1, doi. 10.3389/fgene.2022.810595
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- Article
Association of TRMT2B gene variants with juvenile amyotrophic lateral sclerosis.
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- Frontiers of Medicine, 2024, v. 18, n. 1, p. 68, doi. 10.1007/s11684-023-1005-y
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- Article
Mutation analysis of MFSD8 in an amyotrophic lateral sclerosis cohort from mainland China.
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- European Journal of Neuroscience, 2021, v. 53, n. 4, p. 1197, doi. 10.1111/ejn.15058
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Genetic and clinical analysis of TP73 gene in amyotrophic lateral sclerosis patients from Chinese mainland.
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- Frontiers in Aging Neuroscience, 2023, v. 15, p. 01, doi. 10.3389/fnagi.2023.1114022
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- Article
Evaluation of Peripheral Immune Activation in Amyotrophic Lateral Sclerosis.
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- Frontiers in Neurology, 2021, v. 12, p. 1, doi. 10.3389/fneur.2021.628710
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- Article
Detection of changes in synaptic density in amyotrophic lateral sclerosis patients using <sup>18</sup>F‐SynVesT‐1 positron emission tomography.
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- European Journal of Neurology, 2022, v. 29, n. 10, p. 2934, doi. 10.1111/ene.15451
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- Article