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Neuropathology, ISSN 0919-6544, 12/2014, Volume 34, Issue 6, pp. 589 - 595
Journal Article
Lancet, The, ISSN 0140-6736, 2014, Volume 384, Issue 9950, pp. 1273 - 1281
Journal Article
Journal Article
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 | Index Medicus
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 9/2008, Volume 105, Issue 39, pp. 15208 - 15213
Journal Article
Nihon rinsho. Japanese journal of clinical medicine, ISSN 0047-1852, 01/2017, Volume 75, Issue 1, p. 56
Parkinson's disease (PD) is a common neurodegenerative disorder. In 2015, The Movement Disorder Society Clinical Diagnostic Criteria for PD was published. In... 
Diagnosis, Differential | Humans | Neurodegenerative Diseases - diagnosis | Parkinson Disease - diagnosis
Journal Article
Acta Neuropathologica, ISSN 0001-6322, 3/2012, Volume 123, Issue 3, pp. 381 - 394
Journal Article
Journal of the Wakayama Medical Society, ISSN 0043-0013, 12/2013, Volume 64, Issue 4, pp. 108 - 112
Journal Article
Nature Communications, ISSN 2041-1723, 08/2016, Volume 7, Issue 1, pp. 12547 - 12547
Optineurin (OPTN) mutations cause neurodegenerative diseases, including amyotrophic lateral sclerosis (ALS) and glaucoma. Although the ALS-associated E478G... 
AUTOPHAGY RECEPTOR | ACTIVATION | IMMUNE-SYSTEM | POLYUBIQUITIN | RECOGNITION | MULTIDISCIPLINARY SCIENCES | CHAIN ASSEMBLY COMPLEX | MITOPHAGY | NF-KAPPA-B | NEMO | CELL-DEATH | Index Medicus
Journal Article
Lancet, The, ISSN 0140-6736, 2015, Volume 385, Issue 9964, pp. 226 - 227
  Mandy Keijzer-Veen and colleagues reported no difference in relapse rates between the two treatment groups of rituximab and conventional immunosuppressive... 
Internal Medicine | Glucocorticoids - therapeutic use | Humans | Immunosuppressive Agents - therapeutic use | Female | Male | Nephrotic Syndrome - drug therapy | Antibodies, Monoclonal, Murine-Derived - therapeutic use | Care and treatment | Kidney diseases | Drug therapy | Rodents | Pharmaceuticals | Index Medicus | Abridged Index Medicus
Journal Article