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The Journal of Clinical Endocrinology & Metabolism, ISSN 0021-972X, 12/2014, Volume 99, Issue 12, pp. 4408 - 4422
Journal Article
British Journal of Cancer, ISSN 0007-0920, 08/2012, Volume 107, Issue 4, pp. 646 - 651
BACKGROUND: Patients with prostate cancer tend to die from bone metastases. Until now, no evidence has shown that Paget's disease of bone (PDB) affects the... 
Paget's disease | bone metastasis | prostate cancer | SURVIVAL | ONCOLOGY | TUMOR | DICKKOPF-1 | EPIDEMIOLOGY | Osteitis Deformans - complications | Prostatic Neoplasms - pathology | Time Factors | Humans | Middle Aged | Bone Neoplasms - secondary | Male | Aged | Prostatic Neoplasms - complications | Case-Control Studies | Prostatic Neoplasms - mortality | Index Medicus | Clinical Study
Journal Article
Journal of Bone and Mineral Research, ISSN 0884-0431, 02/2015, Volume 30, Issue 2, pp. 264 - 273
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
Journal of Neuroscience, ISSN 0270-6474, 06/2010, Volume 30, Issue 22, pp. 7729 - 7739
Journal Article
Otology & Neurotology, ISSN 1531-7129, 07/2017, Volume 38, Issue 6, pp. 907 - 915
Journal Article
Journal of Bone and Mineral Research, ISSN 0884-0431, 06/2008, Volume 23, Issue 6, pp. 819 - 825
Journal Article
Clinical Nuclear Medicine, ISSN 0363-9762, 11/2016, Volume 41, Issue 11, pp. 877 - 878
Journal Article
Bone, ISSN 8756-3282, 2010, Volume 48, Issue 2, pp. 281 - 285
Abstract Context Paget's disease of bone (PDB) is a focal disorder of bone metabolism with overgrowth of affected bone resulting in the skeletal complications... 
Orthopedics | Aging | Paget's disease of bone | Quality of life | MACULAR DEGENERATION | ENDOCRINOLOGY & METABOLISM | Osteitis Deformans - complications | Osteitis Deformans - pathology | Humans | Middle Aged | Osteitis Deformans - physiopathology | Aged, 80 and over | Quality of Life | Adult | Surveys and Questionnaires | Aged | Index Medicus
Journal Article
Genes to Cells, ISSN 1356-9597, 08/2010, Volume 15, Issue 8, pp. 911 - 922
Valosin-containing protein (VCP) has been shown to colocalize with abnormal protein aggregates, such as nuclear inclusions of Huntington disease and... 
CLEARANCE | GENE | P97/VALOSIN-CONTAINING PROTEIN | AGGRESOME FORMATION | P97/VCP | VCP MUTATIONS | GENETICS & HEREDITY | VCP/P97 | NEURODEGENERATION | ENDOPLASMIC-RETICULUM | FAMILY | CELL BIOLOGY | Humans | Valosin Containing Protein | Osteitis Deformans - metabolism | Osteitis Deformans - genetics | Frontotemporal Dementia - metabolism | Frontotemporal Dementia - complications | Cell Cycle Proteins - genetics | Inclusion Bodies - metabolism | Frontotemporal Dementia - pathology | Frontotemporal Dementia - genetics | Cell Line | Muscular Diseases - metabolism | Drosophila | Cell Cycle Proteins - metabolism | Adenosine Triphosphatases - metabolism | Muscular Diseases - pathology | Osteitis Deformans - complications | Inclusion Bodies - genetics | Osteitis Deformans - pathology | Animals | Inclusion Bodies - pathology | Muscular Diseases - complications | Adenosine Triphosphatases - genetics | Muscular Diseases - genetics | Mutation | Proteins | Parkinson's disease | Huntington's chorea | Adenosine triphosphatase | Index Medicus | valosin-containing protein | Polyglutamine | Neurodegenerative diseases | Adenosinetriphosphatase | proteasome inhibitors | Bone diseases | Huntington's disease | Lewy bodies | Eye | Machado-Joseph disease | Inclusion bodies | Aging | Degeneration | Frontotemporal dementia | Movement disorders | Myopathy
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 | GENE-MUTATIONS | VALOSIN-CONTAINING-PROTEIN | IBMPFD | LOBAR DEGENERATION | ALS | genotype-phenotype | FAMILY | FEATURES | HETEROGENEITY | TDP-43 | GENETICS & HEREDITY | DISORDER | 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 | Index Medicus | Paget’s disease of bone
Journal Article