Found: 9
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BDNF Val66Met polymorphism is associated with cognitive impairment in Italian patients with Parkinson’s disease.
- Published in:
- European Journal of Neurology, 2009, v. 16, n. 11, p. 1240, doi. 10.1111/j.1468-1331.2009.02706.x
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- Article
Mutations in the lamin B1 gene are not present in multiple sclerosis.
- Published in:
- European Journal of Neurology, 2009, v. 16, n. 4, p. 544, doi. 10.1111/j.1468-1331.2009.02536.x
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- Article
A non-synonymous SNP within membrane metalloendopeptidase-like 1 (MMEL1) is associated with multiple sclerosis.
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- Genes & Immunity, 2010, v. 11, n. 8, p. 660, doi. 10.1038/gene.2010.36
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- Article
HLA-class I markers and multiple sclerosis susceptibility in the Italian population.
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- Genes & Immunity, 2010, v. 11, n. 2, p. 173, doi. 10.1038/gene.2009.101
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- Article
Variations of the perforin gene in patients with multiple sclerosis.
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- Genes & Immunity, 2008, v. 9, n. 5, p. 438, doi. 10.1038/gene.2008.35
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- Article
A sequence variation in the MOG gene is involved in multiple sclerosis susceptibility in Italy.
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- Genes & Immunity, 2008, v. 9, n. 1, p. 7, doi. 10.1038/sj.gene.6364437
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- Article
A Trans-Specific Polymorphism in ZC3HAV1 Is Maintained by Long-Standing Balancing Selection and May Confer Susceptibility to Multiple Sclerosis.
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- Molecular Biology & Evolution, 2012, v. 29, n. 6, p. 1599, doi. 10.1093/molbev/mss002
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- Article
DNA Length Polymorphism of Tetranucleotide Repeat at the 5′ Side of the Myelin Basic Protein Gene in Russian Multiple Sclerosis Patients.
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- Molecular Biology, 2003, v. 37, n. 6, p. 849, doi. 10.1023/B:MBIL.0000008353.74758.c7
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- Article
Intervening on the Developmental Course of Children With Borderline Intellectual Functioning With a Multimodal Intervention: Results From a Randomized Controlled Trial.
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- Frontiers in Psychology, 2020, v. 11, p. 1, doi. 10.3389/fpsyg.2020.00679
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- Article