Detalhe da pesquisa
1.
Novel pathogenic variants in FOXP3 in fetuses with echogenic bowel and skin desquamation identified by ultrasound.
Am J Med Genet A
; 173(5): 1219-1225, 2017 May.
Artigo
Inglês
| MEDLINE | ID: mdl-28317311
2.
PRKAG2 mutations presenting in infancy.
J Inherit Metab Dis
; 40(6): 823-830, 2017 11.
Artigo
Inglês
| MEDLINE | ID: mdl-28801758
3.
Factors associated with neurodevelopment for children with single ventricle lesions.
J Pediatr
; 165(3): 490-496.e8, 2014 Sep.
Artigo
Inglês
| MEDLINE | ID: mdl-24952712
4.
Thoracic endografting in a patient with hereditary hemorrhagic telangiectasia presenting with a descending thoracic aneurysm.
J Vasc Surg
; 51(2): 468-70, 2010 Feb.
Artigo
Inglês
| MEDLINE | ID: mdl-20141966
5.
Frequency of Ventricular Arrhythmias and Other Rhythm Abnormalities in Children and Young Adults With the Marfan Syndrome.
Am J Cardiol
; 122(8): 1429-1436, 2018 10 15.
Artigo
Inglês
| MEDLINE | ID: mdl-30115424
6.
Adrenergic receptor genotypes influence postoperative outcomes in infants in the Single-Ventricle Reconstruction Trial.
J Thorac Cardiovasc Surg
; 154(5): 1703-1710.e3, 2017 11.
Artigo
Inglês
| MEDLINE | ID: mdl-28734628
7.
Pulmonary Arterial Hypertension in Glycogen Storage Disease Type I
J. inborn errors metab. screen
; 5: e160060, 2017. tab
Artigo
Inglês
|
LILACS-Express
| ID: biblio-1090922