Recognizing Late Onset Frontotemporal Dementia with the DAPHNE scale: A case report [PDF]
Leonardo Tafarello Martins +3 more
openalex +1 more source
Interpretable differential diagnosis for Alzheimer's disease and Frontotemporal dementia
Huy‐Dung Nguyen +3 more
openalex +1 more source
Social cognition in Korsakoff's syndrome: A meta‐analysis
Abstract Background and aims Korsakoff's syndrome is an alcohol‐related neurocognitive disorder characterized by episodic memory impairments, apathy, confabulations and poor illness‐insight. This meta‐analysis aimed to estimate mean effect sizes of performance in social cognition in people with Korsakoff's syndrome (KS) compared with controls. Method A
Kyra Wijnen +4 more
wiley +1 more source
Dementia assessment and management in primary care settings: a survey of current provider practices in the United States. [PDF]
BACKGROUND:Primary care providers (PCPs) are typically the first to screen and evaluate patients for neurocognitive disorders (NCDs), including mild cognitive impairment and dementia. However, data on PCP attitudes and evaluation and management practices
Bernstein, Alissa +11 more
core +1 more source
Dementia Incidence in Patients With Prurigo Nodularis: An Observational Retrospective Cohort Study
JEADV Clinical Practice, EarlyView.
Madison P. Olexson +3 more
wiley +1 more source
We investigated neuropathological manifestations of hypothermia in 168 cases. Patients aged 65 years or more constituted 80% of the total cohort. Alzheimer's disease was the most common comorbidity, affecting 40% of all patients. Abstract There is a paucity of autopsy‐based studies providing detailed neuropathological characteristics of fatal ...
Shojiro Ichimata +2 more
wiley +1 more source
Pathological progression induced by the frontotemporal dementia-associated R406W tau mutation in patient-derived iPSCs [PDF]
Mutations in the microtubule-associated protein tau (MAPT) gene are known to cause familial frontotemporal dementia (FTD). The R406W tau mutation is a unique missense mutation whose patients have been reported to exhibit Alzheimer\u27s disease (AD)-like ...
et al,, Karch, Celeste M, Nakamura, Mari
core +1 more source
Recall and Recognition in Alzheimer’s Disease and Frontotemporal Dementia
Giulia Caruso +4 more
openalex +2 more sources
Reply: “PGRN Manifesting as Parkinson's Disease: Counseling and Treatment Implications”
Movement Disorders Clinical Practice, EarlyView.
Angelo Antonini +2 more
wiley +1 more source
Increases in sphingomyelin in response to TDP‐43 pathology in the disease‐affected motor cortex of amyotrophic lateral sclerosis (ALS) brain. Abstract Amyotrophic lateral sclerosis (ALS) is a rapidly progressing neurodegenerative disease characterized by the degeneration of motor neurons and the presence of TAR DNA‐binding protein 43 (TDP‐43 ...
Finula I. Isik +4 more
wiley +1 more source

