Disease | lateral sclerosis |
Phenotype | C0497327|dementia |
Sentences | 25 |
PubMedID- 21301036 | [muro disease: amyotrophic lateral sclerosis/parkinsonism-dementia complex in kii peninsula of japan]. |
PubMedID- 26251896 | Similarly, mutations in chchd10 have been originally described in familial amyotrophic lateral sclerosis with fronto-temporal dementia [33]. |
PubMedID- 23421625 | Frontotemporal dementia with amyotrophic lateral sclerosis: a clinical comparison of patients with and without repeat expansions in c9orf72. |
PubMedID- 19405049 | Trpm7 is not associated with amyotrophic lateral sclerosis-parkinsonism dementia complex in the kii peninsula of japan. |
PubMedID- 24807277 | We report an autopsy case of dementia associated with amyotrophic lateral sclerosis (als) in a 73-year-old female. |
PubMedID- 22125525 | The association of dementia with amyotrophic lateral sclerosis (als) is attracting increasing attention, especially after the identification of tdp-43 [1, 2], which may provide a molecular link between dementia and motor involvement. |
PubMedID- 25879588 | Background: because our previous study showed disparate voxel based morphometry (vbm) results between spm and fsl softwares in the brain of amyotrophic lateral sclerosis patients with frontotemporal dementia (als-ftd), we investigated which vbm results may more represent atrophy by comparing with freesurfer's cortical volume and thickness measures. |
PubMedID- 20392940 | Amyotrophic lateral sclerosis-parkinson dementia complex (als-pdc) is a neurodegenerative disease with als, parkinsonism, and alzheimer's symptoms that is prevalent in the guam population. |
PubMedID- 26038313 | Recent studies have shown that expanded d(ggggcc) repeats between exons 1a and 1b in c9orf72 cause amyotrophic lateral sclerosis (als) associated with frontotemporal dementia (30,31). |
PubMedID- 25558820 | Objective: amyotrophic lateral sclerosis/parkinsonism-dementia complex has been described in guam, western papua, and the kii peninsula of japan. |
PubMedID- 25155093 | Screening of chchd10 in a french cohort confirms the involvement of this gene in frontotemporal dementia with amyotrophic lateral sclerosis patients. |
PubMedID- 23626653 | A case of frontotemporal dementia with amyotrophic lateral sclerosis presenting with pathological gambling. |
PubMedID- 25421204 | Amyotrophic lateral sclerosis with frontotemporal dementia presented with prominent psychosis. |
PubMedID- 22124781 | Cycad seed consumption by the native islanders of guam is frequently associated with high rates of amyotrophic lateral sclerosis-parkinsonism dementia complex (als/pdc); furthermore, accompanying pathological examination often exhibits alpha-synuclein inclusions in the neurons of the affected brain. |
PubMedID- 23034079 | Earlier reports of chromosome 9p-linked frontotemporal dementia (ftd) with amyotrophic lateral sclerosis (als) kindreds observed psychosis as a prominent feature in some patients. |
PubMedID- 22179552 | Renton et al.13 demonstrated that this is the causal variant of 9p21-associated amyotrophic lateral sclerosis with frontotemporal dementia (als-ftd). |
PubMedID- 21541771 | The motor neurons were involved in 27 cases (fronto-temporal dementia with amyotrophic lateral sclerosis = ftd-als). |
PubMedID- 25726362 | Mutations in chchd10 have recently been described as a cause of frontotemporal dementia (ftd) comorbid with amyotrophic lateral sclerosis (als). |
PubMedID- 26160823 | The diagnostic criteria for amyotrophic lateral sclerosis/parkinsonism-dementia complex in the kii peninsula of japan (kii als/pdc) have been proposed. |
PubMedID- 21072532 | Familial frontotemporal dementia with amyotrophic lateral sclerosis and a shared haplotype on chromosome 9p. |
PubMedID- 26028194 | Although amyotrophic lateral sclerosis with dementia (als-d) has been characterized by symptoms of fronto-temporal dysfunction, we report two patients with als-d who showed constructive disturbance and low-level perfusion in the parietal areas. |
PubMedID- 21987561 | Clinical and pathological correlations have been well established between sd and ftld-tdp-43 type 3, similar to those observed between yuasa-mitsuyama-type amyotrophic lateral sclerosis with dementia (alsd) and tdp-43 proteinopathy type 2. |
PubMedID- 25869998 | Defining the genetic connection linking amyotrophic lateral sclerosis (als) with frontotemporal dementia (ftd). |
PubMedID- 20625088 | Neurobehavioral features in frontotemporal dementia with amyotrophic lateral sclerosis. |
PubMedID- 23836460 | Objective: amyotrophic lateral sclerosis (als) is associated with frontotemporal dementia (ftd) in 14% of cases. |
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