Results 51 to 60 of about 444,058 (336)
ABSTRACT Background Apolipoprotein ε4 (APOE ε4) is a potent genetic risk factor for Alzheimer's disease (AD). However, its role in cerebral small vessel disease (CSVD) remains unclear. Given the clinical and pathological similarities between CSVD and AD, this study aimed to investigate the associations of APOE ε4 gene dosage with cognitive function and
Tingru Jin +6 more
wiley +1 more source
Opioid Drugs and Sensorineural Hearing Loss [PDF]
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Mahbobeh Oroei +2 more
doaj
Neural Processing of Cognitive Control in an Emotionally Neutral Context in Anxiety Patients
Impaired cognitive control plays a crucial role in anxiety disorders and is associated with deficient neural mechanisms in the fronto-parietal network. Usually, these deficits were found in tasks with an emotional context.
Nicola König +4 more
doaj +1 more source
Mixture Density Networks, Human Articulatory Data and Acoustic-to-Articulatory Inversion of Continuous Speech [PDF]
Researchers have been investigating methods for retrieving the articulation underlying an acoustic speech signal for more than three decades. A successful method would find many applications, for example: low bit-rate speech coding, helping individuals ...
Richmond, K.
core
Autosomal Recessive Spastic Ataxia of Charlevoix‐Saguenay in Two Half‐Siblings
ABSTRACT Autosomal recessive spastic ataxia of Charlevoix‐Saguenay (ARSACS) is caused by biallelic pathogenic variants in the SACS gene. We report the clinical, radiologic and neurophysiologic features of a pair of half‐siblings who presented with progressive cerebellar ataxia, peripheral neuropathy and upper motor neuron signs.
Dennis Yeow +6 more
wiley +1 more source
Background: With the advancement of knowledge, increasing science production and competition, evaluation of scientific products becomes one of the challenging and undeniable necessary subjects.
Navid Ahmady Roozbahany, Omid Shafagh
doaj +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
Evaluation of the Efficacy of Surgery for Treatment of Septal Perforation
Background: The majority of septal perforations are caused by trauma either with or without infection. In most of the cases trauma is related to the surgery.
Bigan Naghibzadeh +2 more
doaj +1 more source
Difficulties in diagnostics of non-organic hearing loss as a manifestation of a conversion disorder- a case report. [PDF]
Dorota Kapustka +2 more
openalex +1 more source
A European perspective on auditory processing disorder-current knowledge and future research focus [PDF]
Current notions of \u201chearing impairment,\u201d as reflected in clinical audiological practice, do not acknowledge the needs of individuals who have normal hearing pure tone sensitivity but who experience auditory processing difficulties in everyday ...
Bamiou, Doris-Eva +22 more
core +7 more sources

