Andrea De Giacomo
Biographic Data
| ID | 6537896 |
|---|---|
| NAME | Andrea De Giacomo |
| GIVEN NAMES | Andrea |
| FAMILY NAME | De Giacomo |
| SIGNATURE | DE GIACOMO A |
| AFFILIATIONS | University of Bari Aldo Moro |
| ORCID | 0000-0002-3454-1679 |
| VERIFIED | Yes |
| TOTAL WORKS | 8 |
| TOTAL CITATIONS | 0 |
| AUTHOR COUNT | 8 |
| EDITOR COUNT | 0 |
| FIRST PUBLICATION YEAR | 2000 |
| LATEST PUBLICATION YEAR | 2026 |
| H-INDEX | 0 |
Q11.2 Deletion Syndrome, Oral-Maxillo-Facial Manifestations and Cognitive Functioning
Background: 22q11.2 deletion syndrome (22q11.2 DS) is a rare genetic syndrome characterized by high phenotypic variability, with an incidence of approximately 1:4000 live births. Most of the existing literature consists of case reports or case series, making it challenging to obtain large cohorts for data comparison and drawing generalizable conclusions. Aim: The aim of this article is to share the clinical experience of patients with 22q11.2 DS …
Machine learning and deep learning applied to EEG and fNirs for early autism spectrum disorder diagnosis
The results demonstrated the potential of DL and ML algorithms applied to EEG and fNIRS signals for early ASD assessment, supporting the development of personalized intervention strategies grounded in robust neurophysiological evidence
Associations Between Social Functioning and Indicators of University Student Engagement
Less socially adaptive behaviors have often been underestimated in university students, with limited research addressing their impact on academic functioning. This study aimed to identify distinct profiles of social functioning difficulties in university students and to examine their associations with academic engagement, learning difficulties, and psychological distress. A cross-sectional, web-based survey was conducted with 540 undergraduate un…
New Trigger for Stroke-like Episode in Sturge–Weber Syndrome
Background . Sturge-Weber syndrome (SWS) is a rare non-hereditary neurovascular disorder characterized by capillary-venous malformations on the face, ocular vascular anomalies, and leptomeningeal capillary-venous malformations. Patients with SWS often experience cerebral perfusion impairment, increasing their risk for stroke-like episodes, seizures, and motor and cognitive impairments. Methods . We report the case of a 2-year-old boy diagnosed wi…
Dysregulation Profile in Preschoolers with Autism Spectrum Disorder
Background/Objectives : Autism Spectrum Disorder (ASD) is a lifelong neurodevelopmental condition characterized by social communication impairments and repetitive behaviors. Recent reports show that one in thirty-six 8-year-old children are autistic, signifying a considerable public health concern. According to previous studies, emotional dysregulation (ED) affects 50-60% of individuals with ASD and includes symptoms such as poor emotional contro…
Peripheral Iron Levels in Autism Spectrum Disorders vs. Other Neurodevelopmental Disorders
Autism Spectrum Disorder (ASD) is characterized by deficits in social skills and specific behaviors and interests. Among other environmental factors, iron may play a role in the development of ASD. The aim of this study is to compare the iron status of children with ASD with that of children affected by neurodevelopmental disorders other than ASD (OND). A total of 167 patients were enrolled, including 93 children with ASD and 74 children with OND…
Psychological Effects and Quality of Life in Parents and Children with Jia-Associated Uveitis
Juvenile idiopathic arthritis (JIA) is a chronic inflammatory disease common in children and young adults. Uveitis is the most frequent serious extra-articular JIA manifestation and can lead to severe ocular complications, vision loss, and permanent blindness. This study aims to evaluate the psychological condition and the quality of life of children affected by JIA associated with uveitis (JIA-U) and the repercussion of this condition on parents…
Evaluating Three Models of Intimate Relationships
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Evaluating Three Models of Intimate Relationships
Peripheral Iron Levels in Autism Spectrum Disorders vs. Other Neurodevelopmental Disorders
Autism Spectrum Disorder (ASD) is characterized by deficits in social skills and specific behaviors and interests. Among other environmental factors, iron may play a role in the development of ASD. The aim of this study is to compare the iron status of children with ASD with that of children affected by neurodevelopmental disorders other than ASD (OND). A total of 167 patients were enrolled, including 93 children with ASD and 74 children with OND…
Psychological Effects and Quality of Life in Parents and Children with Jia-Associated Uveitis
Juvenile idiopathic arthritis (JIA) is a chronic inflammatory disease common in children and young adults. Uveitis is the most frequent serious extra-articular JIA manifestation and can lead to severe ocular complications, vision loss, and permanent blindness. This study aims to evaluate the psychological condition and the quality of life of children affected by JIA associated with uveitis (JIA-U) and the repercussion of this condition on parents…
Dysregulation Profile in Preschoolers with Autism Spectrum Disorder
Background/Objectives : Autism Spectrum Disorder (ASD) is a lifelong neurodevelopmental condition characterized by social communication impairments and repetitive behaviors. Recent reports show that one in thirty-six 8-year-old children are autistic, signifying a considerable public health concern. According to previous studies, emotional dysregulation (ED) affects 50-60% of individuals with ASD and includes symptoms such as poor emotional contro…
Associations Between Social Functioning and Indicators of University Student Engagement
Less socially adaptive behaviors have often been underestimated in university students, with limited research addressing their impact on academic functioning. This study aimed to identify distinct profiles of social functioning difficulties in university students and to examine their associations with academic engagement, learning difficulties, and psychological distress. A cross-sectional, web-based survey was conducted with 540 undergraduate un…
New Trigger for Stroke-like Episode in Sturge–Weber Syndrome
Background . Sturge-Weber syndrome (SWS) is a rare non-hereditary neurovascular disorder characterized by capillary-venous malformations on the face, ocular vascular anomalies, and leptomeningeal capillary-venous malformations. Patients with SWS often experience cerebral perfusion impairment, increasing their risk for stroke-like episodes, seizures, and motor and cognitive impairments. Methods . We report the case of a 2-year-old boy diagnosed wi…
Q11.2 Deletion Syndrome, Oral-Maxillo-Facial Manifestations and Cognitive Functioning
Background: 22q11.2 deletion syndrome (22q11.2 DS) is a rare genetic syndrome characterized by high phenotypic variability, with an incidence of approximately 1:4000 live births. Most of the existing literature consists of case reports or case series, making it challenging to obtain large cohorts for data comparison and drawing generalizable conclusions. Aim: The aim of this article is to share the clinical experience of patients with 22q11.2 DS …
Machine learning and deep learning applied to EEG and fNirs for early autism spectrum disorder diagnosis
The results demonstrated the potential of DL and ML algorithms applied to EEG and fNIRS signals for early ASD assessment, supporting the development of personalized intervention strategies grounded in robust neurophysiological evidence
Psychology (5 works) · Autism Spectrum Disorder Research (4 works) · Clinical Psychology (4 works) · Medicine (4 works) · Autism (3 works) · Autism spectrum disorder (3 works) · Clinical Psychology (3 works) · Pediatrics (3 works) · CBCL (2 works) · Checklist (2 works)