eRAM
encyclopedia of Rare Disease Annotation for Precision Medicine
| Disease | amyotrophic lateral sclerosis |
| Symptom | C0497327|dementia |
| Sentences | 28 |
| PubMedID- 23836460 | Objective: amyotrophic lateral sclerosis (als) is associated with frontotemporal dementia (ftd) in 14% of cases. |
| PubMedID- 25155093 | Screening of chchd10 in a french cohort confirms the involvement of this gene in frontotemporal dementia with amyotrophic lateral sclerosis patients. |
| PubMedID- 26515622 | Frontotemporal dysfunction and dementia in amyotrophic lateral sclerosis. |
| 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- 23626653 | A case of frontotemporal dementia with amyotrophic lateral sclerosis presenting with pathological gambling. |
| PubMedID- 25879588 | 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- 19405049 | amyotrophic lateral sclerosis-parkinsonism dementia complex (als/pdc) is a distinct neurodegenerative disorder characterized by als pathology with neurofibrillary tangles (nfts) in the spinal cord and brain. |
| PubMedID- 26519438 | The evolution of caregiver burden in frontotemporal dementia with and without amyotrophic lateral sclerosis. |
| PubMedID- 21072532 | Familial frontotemporal dementia with amyotrophic lateral sclerosis and a shared haplotype on chromosome 9p. |
| PubMedID- 25558820 | Objective: amyotrophic lateral sclerosis/parkinsonism-dementia complex has been described in guam, western papua, and the kii peninsula of japan. |
| 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- 26160823 | Diagnostic criteria for amyotrophic lateral sclerosis/parkinsonism-dementia complex in the kii peninsula, japan. |
| PubMedID- 20625088 | Neurobehavioral features in frontotemporal dementia with amyotrophic lateral sclerosis. |
| 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- 22179552 | Renton et al.13 demonstrated that this is the causal variant of 9p21-associated amyotrophic lateral sclerosis with frontotemporal dementia (als-ftd). |
| PubMedID- 23421625 | Frontotemporal dementia with amyotrophic lateral sclerosis: a clinical comparison of patients with and without repeat expansions in c9orf72. |
| PubMedID- 25726362 | Mutations in chchd10 have recently been described as a cause of frontotemporal dementia (ftd) comorbid with amyotrophic lateral sclerosis (als). |
| 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- 22125525 | Amnesia in frontotemporal dementia with amyotrophic lateral sclerosis, masquerading alzheimer's disease. |
| PubMedID- 21301036 | Muro disease: amyotrophic lateral sclerosis/parkinsonism-dementia complex in kii peninsula of japan. |
| PubMedID- 22300876 | The hexanucleotide repeat expansion in c9orf72 is an important cause of frontotemporal dementia with and without amyotrophic lateral sclerosis, and is sometimes associated with primary progressive aphasia. |
| PubMedID- 20697052 | Background: tar dna-binding protein 43, encoded by the tardbp gene, has been identified as the major pathological protein of frontotemporal lobar dementia (ftld) with or without amyotrophic lateral sclerosis (als) and sporadic als. |
| PubMedID- 21541771 | The motor neurons were involved in 27 cases (fronto-temporal dementia with amyotrophic lateral sclerosis = ftd-als). |
| PubMedID- 25421204 | amyotrophic lateral sclerosis with frontotemporal dementia presented with prominent psychosis. |
| PubMedID- 25869998 | Defining the genetic connection linking amyotrophic lateral sclerosis (als) with frontotemporal dementia (ftd). |
| PubMedID- 22246868 | Recent findings highlight a pathologic and functional convergence in amyotrophic lateral sclerosis (als) and amyotrophic lateral sclerosis with frontotemporal dementia (als-ftd) at the level of protein recycling and disposal. |
| 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- 24807277 | We report an autopsy case of dementia associated with amyotrophic lateral sclerosis (als) in a 73-year-old female. |
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