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.
Complete agenesis of corpus callosum and unilateral cortical formation anomalies detected on fetal MR imaging: a phenotype strongly associated with the male fetuses.
Eur Radiol
; 33(3): 2258-2265, 2023 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-36264312
3.
Onset of Chiari type 1 malformation: insights from a small series of intrauterine MR imaging cases.
Neuroradiology
; 65(9): 1387-1394, 2023 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-37329352
4.
Get Your Molar Tooth Right: Joubert Syndrome Misdiagnosis Unmasked by Whole-Exome Sequencing.
Cerebellum
; 21(6): 1144-1150, 2022 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-34846692
5.
Changes in appearance of cortical formation abnormalities in the foetus detected on sequential in utero MR imaging.
Eur Radiol
; 31(3): 1367-1377, 2021 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-32885300
6.
Cortical formation abnormalities on foetal MR imaging: a proposed classification system trialled on 356 cases from Italian and UK centres.
Eur Radiol
; 30(10): 5250-5260, 2020 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-32405748
7.
Prenatal magnetic resonance imaging within the 26th week of gestation may predict the fate of isolated upward rotation of the cerebellar vermis: insights from a multicentre study.
Eur Radiol
; 30(4): 2161-2170, 2020 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-31900695
8.
Impact of a posttraumatic cerebral infarction on outcome in patients with TBI: the Italian multicenter cohort INCEPT study.
Crit Care
; 24(1): 33, 2020 02 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-32014041
9.
Intracranial calcifications in childhood: Part 2.
Pediatr Radiol
; 50(10): 1448-1475, 2020 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-32642802
10.
Intracranial calcifications in childhood: Part 1.
Pediatr Radiol
; 50(10): 1424-1447, 2020 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-32734340
11.
Imaging of temporal bone inflammations in children: a pictorial review.
Neuroradiology
; 61(9): 959-970, 2019 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-31321462
12.
Hypothalamic malformations in patients with X-linked deafness and incomplete partition type 3.
Neuroradiology
; 61(8): 949-952, 2019 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-31177298
13.
Brain-injured Survivors of Monochorionic Twin Pregnancies Complicated by Single Intrauterine Death: MR Findings in a Multicenter Study.
Radiology
; 288(2): 582-590, 2018 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-29688161
14.
Neurovisual Assessment in Children with Ataxia Telangiectasia.
Neuropediatrics
; 49(1): 26-34, 2018 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-28992644
15.
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
16.
Loss-of-function mutations in TBC1D20 cause cataracts and male infertility in blind sterile mice and Warburg micro syndrome in humans.
Am J Hum Genet
; 93(6): 1001-14, 2013 Dec 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-24239381
17.
Spinal lipoma as a dysembryogenetic anomaly: Four unusual cases of ectopic iliac rib within the spinal lipoma.
Birth Defects Res A Clin Mol Teratol
; 106(7): 530-5, 2016 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-27087621
18.
The hyperkinetic movement disorder of FOXG1-related epileptic-dyskinetic encephalopathy.
Dev Med Child Neurol
; 58(1): 93-7, 2016 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-26344814
19.
Oral-facial-digital syndrome type VI: is C5orf42 really the major gene?
Hum Genet
; 134(1): 123-6, 2015 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-25407461
20.
Prenatal findings in oral-facial-digital syndrome type VI: Report of three cases and literature review.
Prenat Diagn
; 39(8): 652-655, 2019 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-31158925