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Nature, ISSN 0028-0836, 05/2010, Volume 465, Issue 7295, pp. 223 - 226
Amyotrophic lateral sclerosis (ALS) has its onset in middle age and is a progressive disorder characterized by degeneration of motor neurons of the primary... 
OPEN-ANGLE GLAUCOMA | COMPLEX | PROTEIN | GENE | MULTIDISCIPLINARY SCIENCES | EXPRESSION | NEMO | MYOSIN-VI | Amyotrophic Lateral Sclerosis - physiopathology | Humans | Middle Aged | Transcription Factor TFIIIA - genetics | Cytoplasm - metabolism | Male | NF-kappa B - metabolism | Cytoplasm - pathology | Transcription Factor TFIIIA - metabolism | Mutation, Missense - genetics | DNA-Binding Proteins - metabolism | Young Adult | Base Sequence | Aged, 80 and over | Adult | Female | Child | Superoxide Dismutase - metabolism | NF-kappa B - agonists | Amino Acid Sequence | NF-kappa B - antagonists & inhibitors | Amyotrophic Lateral Sclerosis - genetics | Japan | Mutant Proteins - genetics | Transcription Factor TFIIIA - chemistry | Exons - genetics | Mutant Proteins - metabolism | Mutation - genetics | Transcription Factor TFIIIA - analysis | Protein Transport | Amyotrophic Lateral Sclerosis - pathology | Asian Continental Ancestry Group | Pedigree | Mutant Proteins - chemistry | Adolescent | Amyotrophic Lateral Sclerosis - metabolism | Polymorphism, Single Nucleotide - genetics | Aged | Consanguinity | Superoxide Dismutase-1 | Mutant Proteins - analysis | Codon, Nonsense - genetics | Sequence Deletion - genetics | Cellular proteins | Gene mutations | Physiological aspects | Amyotrophic lateral sclerosis | Genetic aspects | Research | Health aspects | Risk factors | Haplotypes | Studies | Genes | Genetics | Amino acids | Mutation | Family medical history | Chromosomes | Apoptosis
Journal Article
Lancet Neurology, The, ISSN 1474-4422, 2017, Volume 16, Issue 7, pp. 505 - 512
Journal Article
Journal Article
Internal medicine (Tokyo, 1992), ISSN 0918-2918, 2017, Volume 56, Issue 2, pp. 211 - 214
We herein report the case of a 57-year-old woman presenting with a biopsy-proven tumefactive demyelinating lesion as her first clinical event. Subsequently,... 
relapsing-remitting | recurrent | tumefactive demyelinating lesions | multiple sclerosis | natalizumab | Relapsing-remitting | Multiple sclerosis | Recurrent | Natalizumab | Tumefactive demyelinating lesions | Biopsy | Demyelination | Medical treatment | Monoclonal antibodies | Interferon | Lesions
Journal Article
Internal medicine (Tokyo, 1992), ISSN 0918-2918, 2017, Volume 56, Issue 13, pp. 1733 - 1737
Journal Article
Journal Article
Acta Neuropathologica, ISSN 0001-6322, 2/2011, Volume 121, Issue 2, pp. 207 - 218
Journal Article
Brain, ISSN 0006-8950, 9/2011, Volume 134, Issue 9, pp. 2595 - 2609
Journal Article