Cinzia Galasso
ScholarGPS® ID: 98593063857406
Affiliation History
Field
Medicine
Discipline
Psychiatry
Top Specialties
Intellectual Disability | Growth Hormone | Hormone | Medical Genetics | Autism | Epilepsy | Chromosome
Metrics Summary
Publication Count
68
Predicted Citations
1,266
Predicted h-index
18
Ranking
Publications and Citation History
Publications based on Top Specialties
Types of Publication
- Publications
- Books
- Patents
- NIH/NSF
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A longitudinal characterization of the adaptive and behavioral profile in Sotos syndrome (journal article) American Journal of Medical Genetics Part A, volume 194, issue 6 (2024). |
Sleep disturbances and behavioral symptoms in pediatric Sotos syndrome (journal article) Frontiers in Neurology, volume 15 (2024). |
Short report: Autistic symptoms in Sotos syndrome, preliminary results from a case-control study (journal article) Research in Developmental Disabilities, volume 145 (2024). |
Clinical, Sociodemographic, and Psychological Factors Associated with Transition Readiness in Patients with Epilepsy (journal article) Brain Sciences, volume 14, issue 1, pages 21- (2023). |
Cognitive, adaptive and behavioral profile in Sotos syndrome children with 5q35 microdeletion or intragenic variants (journal article) American Journal of Medical Genetics Part A, volume 191, issue 7, pages 1836-1848 (2023). |
Deletion of a Single Lysine Residue at Position 292 of CAMK2A Disrupts Protein Function, Causing Severe Epileptic Encephalopathy and Intellectual Disability (journal article) Genes, volume 14, issue 7, pages 1353- (2023). |
Presence of neurologic signs in children with neurofibromatosis type 1 (journal article) Minerva Pediatrics, volume 75, issue 1 (2023). |
Parental Stress and Disability in Offspring: A Snapshot during the COVID-19 Pandemic (journal article) Brain Sciences, volume 11, issue 8, pages 1040- (2021). |
COVID-19 and social responsiveness: A comparison between children with Sotos syndrome and autism (journal article) Psychiatry Research, volume 299 (2021). |
Tremor is a major feature of 9p13 deletion syndrome (journal article) American Journal of Medical Genetics Part A, volume 182, issue 11, pages 2694-2698 (2020). |
Defective proteasome biogenesis into skin fibroblasts isolated from Rett syndrome subjects with MeCP2 non-sense mutations (journal article) Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease, volume 1866, issue 7, pages 165793- (2020). |
Molecular and Cellular Biochemistry, volume 463, issue 1-2, pages 101-113 (2020). |
Cognitive phenotype and language skills in children with achondroplasia (journal article) Minerva Pediatrica, volume 71, issue 4 (2019). |
Wearable-based electronics to objectively support diagnosis of motor impairments in school-aged children (journal article) Journal of Biomechanics, volume 83 (2019). |
Retention of Mitochondria in Mature Human Red Blood Cells as the Result of Autophagy Impairment in Rett Syndrome (journal article) Scientific Reports, volume 7, issue 1 (2017). |
Brain and Development, volume 39, issue 6, pages 464-469 (2017). |
Oxygen exchange and energy metabolism in erythrocytes of Rett syndrome and their relationships with respiratory alterations (journal article) Molecular and Cellular Biochemistry, volume 426, issue 1-2, pages 205-213 (2017). |
Is it confirmed the presence of neurological soft signs in children with Neurofibromatosis type 1? (journal article) Minerva pediatrica (2016). |
Cognitive phenotype and language skills in children with achondroplasia. (journal article) Minerva pediatrica (2016). |
Planning Deficit in Children With Neurofibromatosis Type 1 (journal article) Journal of Child Neurology, volume 29, issue 10, pages 1320-1326 (2014). |