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Acta Neuropathologica, ISSN 0001-6322, 2014, Volume 127, Issue 3, pp. 407 - 418
Journal Article
Journal of Neurology, Neurosurgery and Psychiatry, ISSN 0022-3050, 2013, Volume 84, Issue 2, pp. 163 - 169
Background Significant heterogeneity in clinical features of frontotemporal lobar degeneration (FTLD) and amyotrophic lateral sclerosis (ALS) cases with the... 
HEXANUCLEOTIDE REPEAT EXPANSION | SURGERY | DEMENTIA | LOBAR DEGENERATION | PSYCHIATRY | ALZHEIMERS-DISEASE | CLINICAL CHARACTERISTICS | CLINICAL NEUROLOGY | CHROMOSOME 9P | BEHAVIORAL VARIANT | MUTATIONS | SPECTRUM | PATHOLOGICAL FEATURES | Frontotemporal Lobar Degeneration - pathology | Magnetic Resonance Imaging - psychology | DNA Repeat Expansion - genetics | Humans | Middle Aged | Atrophy - pathology | Magnetic Resonance Imaging - methods | Male | Case-Control Studies | Neuroimaging - psychology | Neuropsychological Tests - statistics & numerical data | Frontotemporal Lobar Degeneration - mortality | Female | C9orf72 Protein | Neuroimaging - methods | Frontotemporal Lobar Degeneration - psychology | Amyotrophic Lateral Sclerosis - genetics | Cognition Disorders - pathology | Amyotrophic Lateral Sclerosis - psychology | Cognition Disorders - genetics | DNA-Binding Proteins - genetics | Disease Progression | Amyotrophic Lateral Sclerosis - mortality | Cognition Disorders - mortality | Proteins - genetics | Amyotrophic Lateral Sclerosis - pathology | Cognition Disorders - complications | Age of Onset | Survival Analysis | Brain - pathology | Frontotemporal Lobar Degeneration - genetics | Psychological aspects | Usage | Medical examination | Mentally disabled persons | Neuropsychological tests | Amyotrophic lateral sclerosis | Diagnosis | Frontotemporal dementia | Risk factors | neuropsychological tests | C9orf72 | neuroimaging
Journal Article
Journal Article
Acta Neuropathologica, ISSN 0001-6322, 6/2012, Volume 123, Issue 6, pp. 825 - 839
C9ORF72-hexanucleotide repeat expansions and ubiquilin-2 (UBQLN2) mutations are recently identified genetic markers in amyotrophic lateral sclerosis (ALS) and... 
Pathology | Neurosciences | Medicine & Public Health | UBQLN1 | Amyotrophic lateral sclerosis | Frontotemporal lobar degeneration | C9ORF72 | UBQLN2 | DNA-BINDING | REPEAT EXPANSION | PROTEIN | ALZHEIMERS-DISEASE | AMYOTROPHIC-LATERAL-SCLEROSIS | PATHOLOGY | NEUROSCIENCES | CLINICAL NEUROLOGY | TDP-43 PROTEINOPATHIES | MUTATIONS | DIAGNOSTIC-CRITERIA | SUPEROXIDE-DISMUTASE | Frontotemporal Lobar Degeneration - pathology | Ubiquitins - genetics | Humans | Middle Aged | Male | DNA-Binding Proteins - metabolism | DNA Repeat Expansion | Frontotemporal Lobar Degeneration - mortality | Aged, 80 and over | Cell Cycle Proteins - genetics | Female | C9orf72 Protein | Ubiquitins - metabolism | Amyotrophic Lateral Sclerosis - genetics | Cell Cycle Proteins - metabolism | DNA-Binding Proteins - genetics | Mutation - genetics | Amyotrophic Lateral Sclerosis - mortality | Proteins - genetics | Amyotrophic Lateral Sclerosis - pathology | Proteins - metabolism | Age of Onset | Amyotrophic Lateral Sclerosis - metabolism | Inclusion Bodies - pathology | Aged | Frontotemporal Lobar Degeneration - genetics | Cerebellum | Immunohistochemistry | Spinal cord | Prognosis | Neurodegenerative diseases | Neuropathology | Antibodies | Data processing | Axons | Genetic markers | Inclusion bodies | Genetic analysis | Mutation | Frontotemporal dementia | Hippocampus
Journal Article
Acta Neuropathologica, ISSN 0001-6322, 2/2014, Volume 127, Issue 2, pp. 283 - 295
Journal Article
Alzheimer Disease and Associated Disorders, ISSN 0893-0341, 04/2012, Volume 26, Issue 2, pp. 166 - 170
Journal Article
Neuroepidemiology, ISSN 0251-5350, 12/2011, Volume 37, Issue 3-4, pp. 166 - 167
Journal Article
Archives of Neurology, ISSN 0003-9942, 11/2009, Volume 66, Issue 11, pp. 1359 - 1364
BACKGROUND Frontotemporal dementia and amyotrophic lateral sclerosis are neurodegenerative diseases associated with TAR DNA-binding protein 43– and... 
LOBAR DEGENERATION | TDP-43 | ALS | COGNITIVE IMPAIRMENT | DISORDERS | AMYOTROPHIC-LATERAL-SCLEROSIS | PATHOLOGY | DIAGNOSTIC-CRITERIA | CLINICAL NEUROLOGY | Motor Neuron Disease - complications | Humans | Middle Aged |