Detalhe da pesquisa
1.
WDR81 mutations cause extreme microcephaly and impair mitotic progression in human fibroblasts and Drosophila neural stem cells.
Brain
; 140(10): 2597-2609, 2017 Oct 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-28969387
2.
In Vivo Corneal Confocal Microscopy in Mucolipidosis Type IV.
Ophthalmology
; 128(4): 521, 2021 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-33745525
3.
Neurodevelopmental problems of unaccompanied refugee and migrant children: a new challenge for pediatric neurologists.
Dev Med Child Neurol
; 61(11): 1348, 2019 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-31183863
4.
[Migrant health and ethical requirements]. / Santé des migrants et exigence éthique.
Soins
; 65(843-844): 24-27, 2020.
Artigo
em Francês
| MEDLINE | ID: mdl-32563502
5.
MFN2, a new gene responsible for mitochondrial DNA depletion.
Brain
; 135(Pt 8): e223, 1-4; author reply e224, 1-3, 2012 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-22556188
6.
In utero ultrasound diagnosis of corpus callosum agenesis leading to the identification of orofaciodigital type 1 syndrome in female fetuses.
Birth Defects Res
; 110(4): 382-389, 2018 03 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-29193896