Detalhe da pesquisa
1.
Cerebral Oximetry Monitoring in Extremely Preterm Infants.
N Engl J Med
; 388(16): 1501-1511, 2023 Apr 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-37075142
2.
NON-pharmacological Approach Less Invasive Surfactant Administration (NONA-LISA) trial: protocol for a randomised controlled trial.
Pediatr Res
; 2024 Jan 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-38200325
3.
Congenital Heart Defects and Indices of Fetal Cerebral Growth in a Nationwide Cohort of 924 422 Liveborn Infants.
Circulation
; 133(6): 566-75, 2016 Feb 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-26769743
4.
Congenital Heart Defects and Indices of Placental and Fetal Growth in a Nationwide Study of 924 422 Liveborn Infants.
Circulation
; 134(20): 1546-1556, 2016 Nov 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-27742737
5.
Congenital Heart Defects and Measures of Fetal Growth in Newborns with Down Syndrome or 22q11.2 Deletion Syndrome.
J Pediatr
; 175: 116-122.e4, 2016 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-27245297
6.
Chromosome 22q11.2 duplication is rare in a population-based cohort of Danish children with cardiovascular malformations.
Am J Med Genet A
; 158A(3): 509-13, 2012 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-22302736
7.
The prevalence of chromosome 22q11.2 deletions in 2,478 children with cardiovascular malformations. A population-based study.
Am J Med Genet A
; 158A(3): 498-508, 2012 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-22190294
8.
Can clinical assessment detect 22q11.2 deletions in patients with cardiac malformations? A review.
Eur J Med Genet
; 54(1): 3-8, 2011.
Artigo
em Inglês
| MEDLINE | ID: mdl-20965293
9.
Children diagnosed with congenital cardiac malformations at the national university departments of pediatric cardiology: positive predictive values of data in the Danish National Patient Registry.
Clin Epidemiol
; 3: 61-6, 2011 Feb 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-21386975
10.
[22q11 deletion syndrome: considerable phenotype variability]. / 22q11-deletionssyndrom: faenotypisk meget variabelt.
Ugeskr Laeger
; 172(13): 1047-8, 2010 Mar 29.
Artigo
em Dinamarquês
| MEDLINE | ID: mdl-20350480
11.
Detecting 22q11.2 deletions by use of multiplex ligation-dependent probe amplification on DNA from neonatal dried blood spot samples.
J Mol Diagn
; 12(2): 147-51, 2010 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-20075206
12.
[22q11 deletion syndrome]. / 22q11-deletionssyndrom.
Ugeskr Laeger
; 172(13): 1038-46, 2010 Mar 29.
Artigo
em Dinamarquês
| MEDLINE | ID: mdl-20350479