PedAM
Pediatric Disease Annotations & Medicines
| Disease | motor neuron disease |
| Phenotype | C0338451|frontotemporal dementia |
| Sentences | 6 |
| PubMedID- 24818133 | Using pet-fdg, different patterns of hypometabolism have been observed when the motor neuron disease (mnd) coexists with frontotemporal dementia (ftd). |
| PubMedID- 22300873 | The patients' clinical phenotype at presentation varied: nine patients had frontotemporal dementia with motor neuron disease, 19 had frontotemporal dementia alone, one had mixed semantic dementia with frontal features and three had progressive non-fluent aphasia. |
| PubMedID- 22051030 | Right temporal variant frontotemporal dementia with motor neuron disease. |
| PubMedID- 21624986 | Predicting survival in frontotemporal dementia with motor neuron disease. |
| PubMedID- 21569259 | Our observations further support the concept that tdp-43 proteinopathies represent a spectrum of disorders, where preferential localization of pathogenetic inclusions and neuronal cell loss defines clinical phenotypes ranging from frontotemporal dementia with or without motor neuron disease, to corticobasal syndrome and to a progressive supranuclear palsy-like syndrome. |
| PubMedID- 21616125 | Subventricular zone in motor neuron disease with frontotemporal dementia. |
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