Results 41 to 50 of about 10,729 (247)
An Out‐of‐Place Etiology: Recognizing FMR1 Premutation in the Memory Clinic
ABSTRACT The FMR1 gene premutation (55–200 CGG repeats) is usually associated with a wide range of symptoms and phenotypes within the Fragile X‐tremor/ataxia syndrome (FXTAS), but may also manifest as predominant or isolated cognitive decline. We describe three male patients referred for progressive cognitive impairment and behavioral changes. Standard
Guido Greco +7 more
wiley +1 more source
Epigenetic Modifications lead towards Neurodegeneration
Background: The foremost factor involved in Neurodegeneration is the impact of epigenetic modifications; through its nature to epigenetically mark the neuron-associated genes, also, by affecting cognitive functions and damaging neurons that promote ...
Anna Askari +4 more
doaj +1 more source
Neuropsychiatric Symptoms Mimicking Dementia in a Patient Treated With Imatinib
ABSTRACT Tyrosine kinase inhibitors are the cornerstone of chronic myeloid leukemia treatment. Newer agents have more potency and a broader spectrum of action, but also a higher potential for neuropsychiatric side effects. We present a case of a patient on imatinib who developed progressive cognitive, mood, and behavioral alterations.
Ashley Jones +3 more
wiley +1 more source
Preliminary study of neuroimaging and psychophysiology in adults with ADHD
Attention Deficit Hyperactivity Disorder (ADHD) affects in both children and adults leading to poor executive functioning and quality of life. However, very little study focuses on neuroimaging and psychophysiology in the adults with ADHD.
Ni Chun Hung +6 more
doaj
Adult‐Onset Subacute Sclerosing Panencephalitis Presenting With Subacute Cognitive Deficits
ABSTRACT We describe the case of a 41‐year‐old man diagnosed with adult‐onset subacute sclerosing panencephalitis (SSPE). The patient presented with subacute progressive cognitive deficits and a neuropsychological profile indicating predominant frontoparietal dysfunction. MRI showed only mild parietal‐predominant cerebral atrophy.
Dennis Yeow +4 more
wiley +1 more source
Clinically Relevant Outcome Measures in Women With Adrenoleukodystrophy
ABSTRACT Adrenoleukodystrophy is a rare inherited peroxisomal disease caused by pathogenic variants in the ABCD1 gene located on the X chromosome. Although the most severe central nervous system and adrenal complications typically affect only men with adrenoleukodystrophy, the majority of women develop myeloneuropathy symptoms in adulthood.
Chenwei Yan +3 more
wiley +1 more source
Iván Pávlov research grant: open science for learning and research in cardiovascular ...
Frank Hernández-García +3 more
doaj
Clustering Algorithm Reveals Dopamine‐Motor Mismatch in Cognitively Preserved Parkinson's Disease
ABSTRACT Objective To explore the relationship between dopaminergic denervation and motor impairment in two de novo Parkinson's disease (PD) cohorts. Methods n = 249 PD patients from Parkinson's Progression Markers Initiative (PPMI) and n = 84 from an external clinical cohort.
Rachele Malito +14 more
wiley +1 more source
Iván Pavlov Cardiovascular Psychophysiology Research Grant: a commitment to the development of ...
Yoander Nápoles-Zaldívar +1 more
doaj
Sea-Wave: Speech Envelope Reconstruction From Auditory EEG With an Adapted WaveNet
Speech envelope reconstruction from EEG is shown to bear clinical potential to assess speech intelligibility. Linear models are commonly used to this end, but they have recently been outperformed in reconstruction scores by non-linear deep neural ...
Liuyin Yang +2 more
doaj +1 more source

