Detalhe da pesquisa
1.
Discovery of specific mutations in spinal muscular atrophy patients by next-generation sequencing.
Neurol Sci;
42(5): 1827-1833, 2021 May.
Artigo
em Inglês
| MEDLINE
| ID: mdl-32895776
2.
Ginsenoside Rg3 inhibits pulmonary fibrosis by preventing HIF-1α nuclear localisation.
BMC Pulm Med;
21(1): 70, 2021 Feb 27.
Artigo
em Inglês
| MEDLINE
| ID: mdl-33639908
3.
Loss of RAD9B impairs early neural development and contributes to the risk for human spina bifida.
Hum Mutat;
41(4): 786-799, 2020 04.
Artigo
em Inglês
| MEDLINE
| ID: mdl-31898828
4.
Choroid Plexus Papilloma of Bilateral Lateral Ventricle in an Infant Conceived by in vitro Fertilization.
Pediatr Neurosurg;
53(6): 401-406, 2018.
Artigo
em Inglês
| MEDLINE
| ID: mdl-30391955
5.
A unique methylation pattern co-segregates with neural tube defect statuses in Han Chinese pedigrees.
Neurol Sci;
38(12): 2153-2164, 2017 Dec.
Artigo
em Inglês
| MEDLINE
| ID: mdl-28980068
6.
Polymorphisms in FZD3 and FZD6 genes and risk of neural tube defects in a northern Han Chinese population.
Neurol Sci;
35(11): 1701-6, 2014 Nov.
Artigo
em Inglês
| MEDLINE
| ID: mdl-24816679
7.
Identification of novel rare mutations of DACT1 in human neural tube defects.
Hum Mutat;
33(10): 1450-5, 2012 Oct.
Artigo
em Inglês
| MEDLINE
| ID: mdl-22610794
8.
Immune characteristics of children with autoimmune encephalitis and the correlation with a short-term prognosis.
Ital J Pediatr;
48(1): 94, 2022 Jun 13.
Artigo
em Inglês
| MEDLINE
| ID: mdl-35698204
9.
The Clinical and Imaging Characteristics Associated With Neurological Sequelae of Pediatric Patients With Acute Necrotizing Encephalopathy.
Front Pediatr;
9: 655074, 2021.
Artigo
em Inglês
| MEDLINE
| ID: mdl-34046375
10.
Intracranial Medulloepithelioma in a Child: A Case Report.
Turk Neurosurg;
29(6): 957-960, 2019.
Artigo
em Inglês
| MEDLINE
| ID: mdl-29757453
11.
Immature teratoma of the posterior fossa in an infant: case report.
Turk Pediatri Ars;
54(2): 125-128, 2019.
Artigo
em Inglês
| MEDLINE
| ID: mdl-31384148
12.
A novel mutation in a common pathogenic gene (SETD5) associated with intellectual disability: A case report.
Exp Ther Med;
18(5): 3737-3740, 2019 Nov.
Artigo
em Inglês
| MEDLINE
| ID: mdl-31656537
13.
Association of neural tube defects with maternal alterations and genetic polymorphisms in one-carbon metabolic pathway.
Ital J Pediatr;
45(1): 37, 2019 Mar 14.
Artigo
em Inglês
| MEDLINE
| ID: mdl-30867013
14.
Retraction Note: Immune characteristics of children with autoimmune encephalitis and the correlation with a short-term prognosis.
Ital J Pediatr;
49(1): 163, 2023 Dec 05.
Artigo
em Inglês
| MEDLINE
| ID: mdl-38053189
15.
Authors' Response.
Turk Pediatri Ars;
55(3): 334, 2020.
Artigo
em Inglês
| MEDLINE
| ID: mdl-33061768
16.
A Novel Two-Nucleotide Deletion of MMADHC Gene Causing cblD Disease in a Chinese Family.
Chin Med J (Engl);
131(20): 2477-2479, 2018 Oct 20.
Artigo
em Inglês
| MEDLINE
| ID: mdl-30334532
17.
Dermoid cyst of the posterior fossa associated with congenital dermal sinus in a child.
World J Pediatr;
4(1): 66-9, 2008 Feb.
Artigo
em Inglês
| MEDLINE
| ID: mdl-18402257
18.
Neuroimages of persistent falcine sinus in children.
World J Pediatr;
5(1): 63-4, 2009 Feb.
Artigo
em Inglês
| MEDLINE
| ID: mdl-19172336