Detalhe da pesquisa
1.
ALG6-CDG: a recognizable phenotype with epilepsy, proximal muscle weakness, ataxia and behavioral and limb anomalies.
J Inherit Metab Dis;
39(5): 713-723, 2016 09.
Artigo
em Inglês
| MEDLINE
| ID: mdl-27287710
2.
Early postnatal high-dose fat-soluble enteral vitamin A supplementation for moderate or severe bronchopulmonary dysplasia or death in extremely low birthweight infants (NeoVitaA): a multicentre, randomised, parallel-group, double-blind, placebo-controlled, investigator-initiated phase 3 trial.
Lancet Respir Med;
2024 Apr 18.
Artigo
em Inglês
| MEDLINE
| ID: mdl-38643780
3.
Erratum to: ALG6-CDG: a recognizable phenotype with epilepsy, proximal muscle weakness, ataxia and behavioral and limb anomalies.
J Inherit Metab Dis;
39(5): 759, 2016 09.
Artigo
em Inglês
| MEDLINE
| ID: mdl-27498540
4.
Bone Fractures in Children and Young Adults With Type 1 Diabetes: Age Distribution, Fracture Location, and the Role of Glycemic Control.
J Bone Miner Res;
36(12): 2371-2380, 2021 12.
Artigo
em Inglês
| MEDLINE
| ID: mdl-34569646
5.
Severe neurological outcomes after very early bilateral nephrectomies in patients with autosomal recessive polycystic kidney disease (ARPKD).
Sci Rep;
10(1): 16025, 2020 09 29.
Artigo
em Inglês
| MEDLINE
| ID: mdl-32994492
6.
Outbreak report of airborne caterpillar dermatitis in a kindergarten.
Dermatology;
215(1): 5-9, 2007.
Artigo
em Inglês
| MEDLINE
| ID: mdl-17587833
7.
Arginine-vasopressin in catecholamine-refractory septic versus non-septic shock in extremely low birth weight infants with acute renal injury.
Crit Care;
10(3): R71, 2006.
Artigo
em Inglês
| MEDLINE
| ID: mdl-16677425
8.
Early fatal course in siblings with CDG-Ia (caused by two novel mutations in the PMM2 gene): clinical, molecular and autopsy findings.
Eur J Pediatr;
166(4): 377-8, 2007 Apr.
Artigo
em Inglês
| MEDLINE
| ID: mdl-16941129