Detalhe da pesquisa
1.
Dexmedetomidine versus fentanyl for sedation in extremely preterm infants.
Pediatr Int
; 65(1): e15581, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-37428855
2.
Rotavirus Vaccination Can Be Performed Without Viral Dissemination in the Neonatal Intensive Care Unit.
J Infect Dis
; 217(4): 589-596, 2018 01 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-29165657
3.
Maturation of the QT Variability Index is Impaired in Preterm Infants.
Pediatr Cardiol
; 39(5): 902-905, 2018 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-29532107
4.
A Family with Craniofrontonasal Syndrome: The First Report of Familial Cases of Craniofrontonasal Syndrome with Bilateral Cleft Lip and Palate.
Cleft Palate Craniofac J
; 55(7): 1026-1029, 2018 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-28140668
5.
Relationship between QT and JT peak interval variability in prepubertal children.
Ann Noninvasive Electrocardiol
; 22(4)2017 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-28211121
6.
Electrocardiographic RR and QT Interval Variability in Patients with Atrial Septal Defect and Healthy Children.
Pediatr Cardiol
; 38(3): 582-587, 2017 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-28058479
7.
A PDE3A mutation in familial hypertension and brachydactyly syndrome.
J Hum Genet
; 61(8): 701-3, 2016 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-27053290
8.
Intragenic duplication in the PKHD1 gene in autosomal recessive polycystic kidney disease.
BMC Med Genet
; 16: 98, 2015 Oct 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-26502924
9.
Inflammation aggravates heterogeneity of ventricular repolarization in children with Kawasaki disease.
Pediatr Cardiol
; 35(7): 1268-72, 2014 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-24823886
10.
A case of 46,XY disorders of sex development with congenital heart disease caused by a GATA4 variant.
Congenit Anom (Kyoto)
; 62(5): 203-207, 2022 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-35751412
11.
Elimination of Mutant mtDNA by an Optimized mpTALEN Restores Differentiation Capacities of Heteroplasmic MELAS-iPSCs.
Mol Ther Methods Clin Dev
; 20: 54-68, 2021 Mar 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-33376755
12.
FOXA2 gene mutation in a patient with congenital complex pituitary hormone deficiency.
Eur J Med Genet
; 62(11): 103570, 2019 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-30414530