| Titolo |
Pubblicato in |
Anno |
| Real-Life Functioning in 22q11.2 Deletion Syndrome in Relation to Neurocognitive Abilities and Psychotic Symptoms: A Comparison With Idiopathic Schizophrenia |
JOURNAL OF INTELLECTUAL DISABILITY RESEARCH |
2024 |
| Recognition of facial emotion expressions and perceptual processes in 22q11.2 deletion syndrome |
EARLY INTERVENTION IN PSYCHIATRY |
2023 |
| Transpositions of the great arteries versus aortic dextropositions. A review of some embryogenetic and morphological aspects |
THE ANATOMICAL RECORD |
2023 |
| Clinical variability in DYNC2H1-related skeletal ciliopathies includes Ellis-van Creveld syndrome |
EUROPEAN JOURNAL OF HUMAN GENETICS |
2023 |
| Prenatal screening and diagnostic considerations for 22q11.2 microdeletions |
GENES |
2023 |
| The relationship between motor symptoms, signs, and parkinsonism with facial emotion recognition deficits in individuals with 22q11.2 deletion syndrome at high genetic risk for psychosis |
ACTA NEUROLOGICA SCANDINAVICA |
2023 |
| Updated clinical practice recommendations for managing children with 22q11.2 deletion syndrome |
GENETICS IN MEDICINE |
2023 |
| Cardiac function in adolescents and young adults with 22q11.2 deletion syndrome without congenital heart disease |
EUROPEAN JOURNAL OF MEDICAL GENETICS |
2023 |
| Social cognition and real‐life functioning in patient samples with 22q11.2 deletion syndrome with or without psychosis, compared to a large sample of patients with schizophrenia only and healthy controls |
JOURNAL OF NEUROPSYCHOLOGY |
2023 |
| Hypertrophic Cardiomyopathy in RASopathies: Diagnosis, Clinical Characteristics, Prognostic Implications, and Management |
HEART FAILURE CLINICS |
2022 |
| Clinical Manifestations of 22q11.2 Deletion Syndrome |
HEART FAILURE CLINICS |
2022 |
| Social Cognition Impairments in 22q11.2DS Individuals With and Without Psychosis: A Comparison Study With a Large Population of Patients With Schizophrenia |
SCHIZOPHRENIA BULLETIN OPEN |
2022 |
| COVID-19 Severity, Cardiological Outcome, and Immunogenicity of mRNA Vaccine on Adult Patients With 22q11.2 DS |
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY. IN PRACTICE |
2022 |
| 22q11.2 Deletion Syndrome: Impact of Genetics in the Treatment of Conotruncal Heart Defects |
CHILDREN |
2022 |
| Clinical Risk Factors for Aortic Root Dilation in Patients with 22q11.2 Deletion Syndrome: A Longitudinal Single-Center Study |
GENES |
2022 |
| Crossed pulmonary arteries: An underestimated cardiovascular variant with a strong association with genetic syndromes{\textemdash}A report of 74 cases with systematic review of the literature |
AMERICAN JOURNAL OF MEDICAL GENETICS. PART A |
2022 |
| Social cognition impairments in 22q11.2DS individuals with and without psychosis: a comparison study with a large population of patients with schizophrenia |
SCHIZOPHRENIA BULLETIN OPEN |
2022 |
| Anatomically corrected malposition of the great arteries (S,L,D) with mutation of Nodal gene |
CARDIOLOGY IN THE YOUNG |
2022 |
| The secrets of the frogs heart |
PEDIATRIC CARDIOLOGY |
2022 |
| Single ventricle: amphibians and human beings |
WORLD JOURNAL OF PEDIATRICS |
2022 |
