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Neurology, ISSN 0028-3878, 07/2014, Volume 83, Issue 1, pp. 98 - 99
Sporadic inclusion body myositis (IBM) is distinguished from other inflammatory myopathies based on clinical and histopathologic features, including slowly... 
AUTOIMMUNITY | CLINICAL NEUROLOGY | Humans | Middle Aged | Myositis, Inclusion Body - complications | Female | Male | Aged | Leukemia, Lymphocytic, Chronic, B-Cell - complications | 132 | Clinical | Scientific Notes | 185
Journal Article
Journal Article
Journal of Neurology, Neurosurgery & Psychiatry, ISSN 0022-3050, 04/2016, Volume 87, Issue 4, pp. 373 - 378
Journal Article
Clinical Genetics, ISSN 0009-9163, 05/2013, Volume 83, Issue 5, pp. 422 - 431
Valosin containing protein (VCP) disease associated with inclusion body myopathy, Paget disease of the bone and frontotemporal dementia is a progressive... 
genotype–phenotype | valosin containing protein | frontotemporal dementia | amyotrophic lateral sclerosis | inclusion body myopathy | Paget's disease of bone | Amyotrophic lateral sclerosis | Inclusion body myopathy | Valosin containing protein | Frontotemporal dementia | Genotype-phenotype | VALOSIN-CONTAINING-PROTEIN | LOBAR DEGENERATION | genotype-phenotype | FAMILY | HETEROGENEITY | GENE | TDP-43 | MUTATION | GENETICS & HEREDITY | Exons | Humans | Middle Aged | Valosin Containing Protein | Male | Frontotemporal Dementia - mortality | Osteitis Deformans - diagnosis | Young Adult | Frontotemporal Dementia - complications | Myositis, Inclusion Body - diagnosis | Myositis, Inclusion Body - mortality | Cell Cycle Proteins - genetics | Adult | Female | Electromyography | Genetic Association Studies | Osteitis Deformans - mortality | Cell Cycle Proteins - metabolism | Adenosine Triphosphatases - metabolism | Genotype | Neural Conduction | Frontotemporal Dementia - diagnosis | Myositis, Inclusion Body - genetics | Osteitis Deformans - complications | Biopsy | Myositis, Inclusion Body - complications | Adenosine Triphosphatases - genetics | Aged | Muscle, Skeletal - pathology | Mutation | Medical research | Analysis | Genes | Medical genetics | Medicine, Experimental | Genetic aspects | Dementia | Proteins | Genotype & phenotype | Pathology | Bone diseases | Genomics | Paget’s disease of bone
Journal Article
Journal Article
Ophthalmic Plastic and Reconstructive Surgery, ISSN 0740-9303, 01/2016, Volume 33, Issue 3S Suppl 1, pp. S161 - S162
Sporadic inclusion body myositis is the most commonly acquired type of idiopathic inflammatory myopathy in people aged 50 and above. There is early weakness... 
Blepharoptosis - etiology | Diagnosis, Differential | Myositis, Inclusion Body - diagnosis | Biopsy | Humans | Myositis, Inclusion Body - complications | Ophthalmoplegia - diagnosis | Female | Aged | Blepharoptosis - diagnosis | Muscle, Skeletal - pathology | Ophthalmoplegia - etiology
Journal Article