Detalhe da pesquisa
1.
Fate of melatonin orally administered in preterm newborns: Antioxidant performance and basis for neuroprotection.
J Pineal Res
; 76(1): e12932, 2024 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-38111174
2.
Severe Streptococcus equi Subspecies zooepidemicus Outbreak from Unpasteurized Dairy Product Consumption, Italy.
Emerg Infect Dis
; 29(5): 1020-1024, 2023 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-37081588
3.
A PUS7 gene pathogenic variant causing self-injurious behavior, sleep disturbances, and developmental delay: A case report.
Am J Med Genet A
; 191(7): 1953-1958, 2023 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-37067188
4.
Genotype-phenotype correlations in SCN8A-related disorders reveal prognostic and therapeutic implications.
Brain
; 145(9): 2991-3009, 2022 09 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-34431999
5.
Long-Term Visual and Neurodevelopmental Outcomes in Two Children with Congenital Nystagmus Secondary to Methadone Exposure In utero.
Neuropediatrics
; 54(6): 412-416, 2023 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-37579766
6.
Cerebral folate transporter deficiency syndrome in three siblings: Why genetic testing for developmental and epileptic encephalopathies should be performed early and include the FOLR1 gene.
Am J Med Genet A
; 185(8): 2526-2531, 2021 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-34008900
7.
Further delineation and long-term evolution of electroclinical phenotype in Mowat Wilson Syndrome. A longitudinal study in 40 individuals.
Epilepsy Behav
; 124: 108315, 2021 Oct 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-34619538
8.
Impact of Covid-19 epidemic on the activities of a blood centre, transfusion support for infected patients and clinical outcomes.
Transfus Med
; 31(3): 160-166, 2021 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-33269544
9.
Clinical-Grade Expanded Regulatory T Cells Are Enriched with Highly Suppressive Cells Producing IL-10, Granzyme B, and IL-35.
Biol Blood Marrow Transplant
; 26(12): 2204-2210, 2020 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-32961369
10.
Cognitive improvement after cochlear implantation in deaf children with associated disabilities.
Dev Med Child Neurol
; 62(12): 1429-1436, 2020 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-32914885
11.
Position paper on the preparation of immune plasma to be used in the treatment of patients with COVID-19.
Transfus Apher Sci
; 59(4): 102817, 2020 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-32532691
12.
The spectrum of intermediate SCN8A-related epilepsy.
Epilepsia
; 60(5): 830-844, 2019 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-30968951
13.
Homocysteine and education but not lipoprotein (a) predict estimated 10-year risk of cardiovascular disease in blood donors: a community based cross-sectional study.
BMC Cardiovasc Disord
; 19(1): 177, 2019 07 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-31349819
14.
Phenotype and genotype of 87 patients with Mowat-Wilson syndrome and recommendations for care.
Genet Med
; 20(9): 965-975, 2018 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-29300384
15.
Higher cyclophosphamide dose grants optimal stem cell collection after daratumumab-based induction in multiple myeloma.
Haematologica
; 108(12): 3502-3505, 2023 Dec 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-37439346
16.
Defining the electroclinical phenotype and outcome of PCDH19-related epilepsy: A multicenter study.
Epilepsia
; 59(12): 2260-2271, 2018 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-30451291
17.
A report from the SIdEM: Italy.
Transfus Apher Sci
; 62(4): 103761, 2023 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-37495449
18.
Etiology and Prognosis of Severe Ventriculomegaly Diagnosed at Late Gestation.
Ultraschall Med
; 39(6): 675-689, 2018 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-29975968
19.
Expanding the phenotype of MED 17 mutations: Description of two new cases and review of the literature.
Am J Med Genet B Neuropsychiatr Genet
; 177(8): 687-690, 2018 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-30345598
20.
Neuroimaging findings in Mowat-Wilson syndrome: a study of 54 patients.
Genet Med
; 19(6): 691-700, 2017 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-27831545