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Journal of the Neurological Sciences, ISSN 0022-510X, 2015, Volume 351, Issue 1, pp. 179 - 183
Journal Article
Journal Article
Muscle & Nerve, ISSN 0148-639X, 01/2016, Volume 53, Issue 1, pp. 49 - 57
Journal Article
Journal Article
Neuromuscular Disorders, ISSN 0960-8966, 2015, Volume 25, Issue 11, pp. 843 - 851
Journal Article
Journal Article
European Journal of Neurology, ISSN 1351-5101, 02/2013, Volume 20, Issue 2, pp. 251 - 258
Background and purpose: The phenotype of IBMPFD [inclusion body myopathy with Paget's disease of the bone and frontotemporal dementia (FTD)] associated with... 
motor neuron disease | arkinson's disease | neuropsychology | frontotemporal dementia | genetic and inherited disorders | neurodegenerative disorders (other than dementia) | myopathies | neuropathology | Genetic and inherited disorders | Parkinson's disease | Neuropathology | Motor neuron disease | Neurodegenerative disorders (other than dementia) | Myopathies | Neuropsychology | Frontotemporal dementia | CRITERIA | DIAGNOSIS | VCP | DEMENTIA | PATHOLOGY | FRONTOTEMPORAL LOBAR DEGENERATION | NEUROSCIENCES | PAGET-DISEASE | CLINICAL NEUROLOGY | INCLUSION-BODY MYOPATHY | DISORDER | BONE | Central Nervous System - metabolism | Humans | Middle Aged | Valosin Containing Protein | Muscular Dystrophies, Limb-Girdle - complications | Central Nervous System - pathology | Osteitis Deformans - metabolism | Male | Osteitis Deformans - diagnosis | Osteitis Deformans - genetics | DNA-Binding Proteins - metabolism | Frontotemporal Dementia - metabolism | Frontotemporal Dementia - complications | Myositis, Inclusion Body - diagnosis | Muscular Dystrophies, Limb-Girdle - genetics | Cell Cycle Proteins - genetics | Myositis, Inclusion Body - pathology | Female | Parkinson Disease - metabolism | Muscular Dystrophies, Limb-Girdle - pathology | Frontotemporal Dementia - pathology | Frontotemporal Dementia - genetics | Parkinson Disease - complications | Genetic Predisposition to Disease - genetics | Muscular Dystrophies, Limb-Girdle - diagnosis | Parkinson Disease - pathology | Parkinson Disease - genetics | Frontotemporal Dementia - diagnosis | Myositis, Inclusion Body - genetics | Osteitis Deformans - complications | Osteitis Deformans - pathology | Phenotype | Muscular Dystrophies, Limb-Girdle - metabolism | Pedigree | Myositis, Inclusion Body - complications | Polymorphism, Single Nucleotide - genetics | Myositis, Inclusion Body - metabolism | Adenosine Triphosphatases - genetics | Aged | Aphasia | Nervous system diseases | Genetic aspects | Genetic disorders | Mutation | Index Medicus | Parkinson’s disease
Journal Article