Detalhe da pesquisa
1.
Clinical and molecular characterizations of 11 new patients with type 1 Feingold syndrome: Proposal for selecting diagnostic criteria and further genetic testing in patients with severe phenotype.
Am J Med Genet A
; 185(4): 1204-1210, 2021 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-33442900
2.
Human breast milk as source of sphingolipids for newborns: comparison with infant formulas and commercial cow's milk.
J Transl Med
; 18(1): 481, 2020 12 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-33317546
3.
A patient with novel MBOAT7 variant: The cerebellar atrophy is progressive and displays a peculiar neurometabolic profile.
Am J Med Genet A
; 182(10): 2377-2383, 2020 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-32744787
4.
Relationship between Fatty Acids Composition/Antioxidant Potential of Breast Milk and Maternal Diet: Comparison with Infant Formulas.
Molecules
; 25(12)2020 Jun 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-32599866
5.
Efficacy and safety of pharmacological treatments for patent ductus arteriosus closure: A systematic review and network meta-analysis of clinical trials and observational studies.
Pharmacol Res
; 148: 104418, 2019 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-31479749
6.
Minipuberty assessment in newborns with hypoxic ischemic encephalopathy treated with therapeutic hypothermia: a single-center case-control study.
Front Pediatr
; 11: 1201668, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-37416822
7.
Functional echocardiographic assessment of myocardial performance in anemic premature infants: a pilot study.
Pediatr Cardiol
; 33(4): 554-61, 2012 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-22274640
8.
Impact of blood sampling technique on reproducibility of viscoelastic coagulation monitor (VCM™) system test results in the neonate.
J Matern Fetal Neonatal Med
; 35(25): 6998-7004, 2022 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-34304670
9.
Sphingomyelin in Human Breast Milk might be Essential for the Hippocampus Maturation.
Front Biosci (Landmark Ed)
; 27(8): 247, 2022 08 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-36042186
10.
A Rare Case of Brachyolmia with Amelogenesis Imperfecta Caused by a New Pathogenic Splicing Variant in LTBP3.
Genes (Basel)
; 12(9)2021 09 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-34573388
11.
Porencephaly in an Italian neonate with foetal alcohol spectrum disorder: A case report.
Medicine (Baltimore)
; 99(31): e21384, 2020 Jul 31.
Artigo
em Inglês
| MEDLINE | ID: mdl-32756128
12.
Congenital Self-Healing Langerhans Cell Histiocytosis: A Rare Presentation of Blueberry Muffin Baby "Spectrum".
Dermatopathology (Basel)
; 6(2): 37-40, 2019.
Artigo
em Inglês
| MEDLINE | ID: mdl-31192198
13.
Soy-Based Infant Formula: Are Phyto-Oestrogens Still in Doubt?
Front Nutr
; 5: 110, 2018.
Artigo
em Inglês
| MEDLINE | ID: mdl-30533415
14.
Evidence of impaired microvascular dilatation in preterms with acute respiratory distress syndrome.
Int J Cardiol
; 241: 83-86, 2017 Aug 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-28410842
15.
Delivery in Asymptomatic Italian Woman with SARS-CoV-2 Infection.
Mediterr J Hematol Infect Dis
; 12(1): e2020033, 2020.
Artigo
em Inglês
| MEDLINE | ID: mdl-32395222