Detalhe da pesquisa
1.
Deep phenotyping of the neuroimaging and skeletal features in KBG syndrome: a study of 53 patients and review of the literature.
J Med Genet
; 60(12): 1224-1234, 2023 Nov 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-37586838
2.
Health-related quality of life and metabolic control in immigrant and Italian children and adolescents with type 1 diabetes and in their parents.
Pediatr Diabetes
; 21(6): 1031-1042, 2020 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-32418308
3.
Endocrine Disrupting Chemicals and Type 1 Diabetes.
Int J Mol Sci
; 21(8)2020 Apr 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-32331412
4.
Anthropometric characteristics of newborns with Prader-Willi syndrome.
Am J Med Genet A
; 179(10): 2067-2074, 2019 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-31361394
5.
Endocrine features of Prader-Willi syndrome: a narrative review focusing on genotype-phenotype correlation.
Front Endocrinol (Lausanne)
; 15: 1382583, 2024.
Artigo
em Inglês
| MEDLINE | ID: mdl-38737552
6.
EEG Patterns in Patients with Prader-Willi Syndrome.
Brain Sci
; 11(8)2021 Aug 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-34439664
7.
Glycemic Control Improvement in Italian Children and Adolescents With Type 1 Diabetes Followed Through Telemedicine During Lockdown Due to the COVID-19 Pandemic.
Front Endocrinol (Lausanne)
; 11: 595735, 2020.
Artigo
em Inglês
| MEDLINE | ID: mdl-33424771