ABSTRACT Bardet–Biedl syndrome (BBS) is a rare genetic condition with a broad phenotypic spectrum. Knowledge about quality of life, executive functioning, and eating behavior in adults with BBS remains limited. This study aimed to assess health‐related quality of life (HRQoL), everyday executive functioning, and eating behavior in adults with BBS and ...
Cecilie Fremstad Rustad +6 more
wiley +1 more source
Deep cross-modal affective memory networks with adaptive multi-source heterogeneous transfer learning in speech emotion recognition. [PDF]
Zhao X, Liu J, Lin L.
europepmc +1 more source
Stressed Speech Emotion Recognition Using Teager Energy and Spectral Feature Fusion with Feature Optimization. [PDF]
Bandela SR +4 more
europepmc +1 more source
Streamlining Diagnosis of Bardet–Biedl Syndrome: New Diagnostic Algorithm With Updated Criteria
ABSTRACT Considerable advances have been made in our understanding of Bardet–Biedl syndrome (BBS), particularly in its core clinical features and molecular genetics, warranting an update to the existing diagnostic criteria framework. Using a rigorous, evidence‐based, and consensus‐driven process, a multidisciplinary group of international experts and ...
Jeremy J. Pomeroy +16 more
wiley +1 more source
Representation learning with parameterised quantum circuits for advancing speech emotion recognition. [PDF]
Rajapakshe T +4 more
europepmc +1 more source
Speech Emotion Recognition Using Convolution Neural Networks and Multi-Head Convolutional Transformer. [PDF]
Ullah R +9 more
europepmc +1 more source
ABSTRACT Smith–Magenis syndrome (SMS) results from either a recurrent 17p11.2 deletion or pathogenic variants in the retinoic acid induced 1 gene (RAI1). While neurodevelopmental impairment and behavioral dysregulation are well recognized, systematic genotype‐stratified analyses across psychiatric domains remain limited.
Albin Blanc +7 more
wiley +1 more source
Speech analysis and speech emotion recognition in mental disease: a scoping review. [PDF]
Lombardo C +4 more
europepmc +1 more source
ABSTRACT DNM1 encephalopathy is a rare autosomal dominant genetic condition characterized by a range of neurological and developmental manifestations. The typical phenotype is severe, including profound intellectual disability, treatment‐resistant epilepsy, ataxia, and structural brain abnormalities. However, milder presentations have increasingly been
Caroline Crain +6 more
wiley +1 more source
Optimization of speech emotion recognition using hybrid dataset integration and deep learning-based feature fusion with a novel balanced focal entropy loss. [PDF]
Nagro S.
europepmc +1 more source

