Differential corticospinal tract degeneration in homozygous 'D90A' SOD-1 ALS and sporadic ALS.
BACKGROUND: The homogeneous genotype and stereotyped phenotype of a unique familial form of amyotrophic lateral sclerosis (ALS) (patients homozygous for aspartate-to-alanine mutations in codon 90 (homD90A) superoxide dismutase 1) provides an ideal model for studying genotype/phenotype interactions a...
المؤلفون الرئيسيون: | Blain, C, Brunton, S, Williams, VC, Leemans, A, Turner, MR, Andersen, P, Catani, M, Stanton, B, Ganesalingham, J, Jones, D, Williams, S, Leigh, P, Simmons, A |
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التنسيق: | Journal article |
اللغة: | English |
منشور في: |
2011
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مواد مشابهة
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Differential corticospinal tract degeneration in homozygous 'D90A' SOD-1 ALS and sporadic ALS
حسب: Blain, C, وآخرون
منشور في: (2011) -
Diffusion tensor imaging in sporadic and familial (D90A SOD1) forms of amyotrophic lateral sclerosis.
حسب: Stanton, B, وآخرون
منشور في: (2009) -
Abnormal cortical excitability in sporadic but not homozygous D90A SOD1 ALS.
حسب: Turner, M, وآخرون
منشور في: (2005) -
Cortical 5-HT1A receptor binding in patients with homozygous D90A SOD1 vs sporadic ALS.
حسب: Turner, M, وآخرون
منشور في: (2007) -
Diffusion tensor imaging reveals white matter differences between sporadic and familial forms of amyotrophic lateral sclerosis
حسب: Stanton, B, وآخرون
منشور في: (2008)