340 related articles for article (PubMed ID: 32145937)
1. 22q11.2 deletion syndrome is associated with increased mortality in adults with tetralogy of Fallot and pulmonary atresia with ventricular septal defect.
Kauw D; Woudstra OI; van Engelen K; Meijboom FJ; Mulder BJM; Schuuring MJ; Bouma BJ
Int J Cardiol; 2020 May; 306():56-60. PubMed ID: 32145937
[TBL] [Abstract][Full Text] [Related]
2. 22q11.2 Deletion Syndrome is under-recognised in adult patients with tetralogy of Fallot and pulmonary atresia.
van Engelen K; Topf A; Keavney BD; Goodship JA; van der Velde ET; Baars MJ; Snijder S; Moorman AF; Postma AV; Mulder BJ
Heart; 2010 Apr; 96(8):621-4. PubMed ID: 20357389
[TBL] [Abstract][Full Text] [Related]
3. Relation of genotype 22q11 deletion to phenotype of pulmonary vessels in tetralogy of Fallot and pulmonary atresia-ventricular septal defect.
Chessa M; Butera G; Bonhoeffer P; Iserin L; Kachaner J; Lyonnet S; Munnich A; Sidi D; Bonnet D
Heart; 1998 Feb; 79(2):186-90. PubMed ID: 9538314
[TBL] [Abstract][Full Text] [Related]
4. 22q11.2 Deletion syndrome is associated with perioperative outcome in tetralogy of Fallot.
Mercer-Rosa L; Pinto N; Yang W; Tanel R; Goldmuntz E
J Thorac Cardiovasc Surg; 2013 Oct; 146(4):868-73. PubMed ID: 23312975
[TBL] [Abstract][Full Text] [Related]
5. 22q11.2 Deletion Status and Perioperative Outcomes for Tetralogy of Fallot with Pulmonary Atresia and Multiple Aortopulmonary Collateral Vessels.
Mercer-Rosa L; Elci OU; Pinto NM; Tanel RE; Goldmuntz E
Pediatr Cardiol; 2018 Jun; 39(5):906-910. PubMed ID: 29520463
[TBL] [Abstract][Full Text] [Related]
6. Pulmonary atresia with ventricular septal defect: prevalence of deletion 22q11 in the different anatomic patterns.
Anaclerio S; Marino B; Carotti A; Digilio MC; Toscano A; Gitto P; Giannotti A; Di Donato R; Dallapiccola B
Ital Heart J; 2001 May; 2(5):384-7. PubMed ID: 11392644
[TBL] [Abstract][Full Text] [Related]
7. Impact of a 22q11.2 Microdeletion on Adult All-Cause Mortality in Tetralogy of Fallot Patients.
van Mil S; Heung T; Malecki S; Van L; Chang J; Breetvelt E; Wald R; Oechslin E; Silversides C; Bassett AS
Can J Cardiol; 2020 Jul; 36(7):1091-1097. PubMed ID: 32348848
[TBL] [Abstract][Full Text] [Related]
8. Prevalence and clinical manifestations of 22q11.2 microdeletion in adults with selected conotruncal anomalies.
Beauchesne LM; Warnes CA; Connolly HM; Ammash NM; Grogan M; Jalal SM; Michels VV
J Am Coll Cardiol; 2005 Feb; 45(4):595-8. PubMed ID: 15708709
[TBL] [Abstract][Full Text] [Related]
9. Chromosome 22q11.2 microdeletion in children with conotruncal heart defects: frequency, associated cardiovascular anomalies, and outcome following cardiac surgery.
Ziolkowska L; Kawalec W; Turska-Kmiec A; Krajewska-Walasek M; Brzezinska-Rajszys G; Daszkowska J; Maruszewski B; Burczynski P
Eur J Pediatr; 2008 Oct; 167(10):1135-40. PubMed ID: 18172682
[TBL] [Abstract][Full Text] [Related]
10. Anterograde blood flow associated with modified Blalock-Taussig shunt does not modify pulmonary artery growth compared with modified Blalock-Taussig shunt alone.
Lenoir M; Desnous B; Rahmani B; El Gueddari N; Aries É; El Louali F; Aldebert P; Ovaert C; Metras D; Macé L; Fouilloux V
Arch Cardiovasc Dis; 2021 Apr; 114(4):268-276. PubMed ID: 33509744
[TBL] [Abstract][Full Text] [Related]
11. A loss-of-function mutation p.T256M in NDRG4 is implicated in the pathogenesis of pulmonary atresia with ventricular septal defect (PA/VSD) and tetralogy of Fallot (TOF).
Peng J; Wang Q; Meng Z; Wang J; Zhou Y; Zhou S; Song W; Chen S; Chen AF; Sun K
FEBS Open Bio; 2021 Feb; 11(2):375-385. PubMed ID: 33211401
[TBL] [Abstract][Full Text] [Related]
12. The role of 22q11.2 deletion syndrome in the relationship between congenital heart disease and scoliosis.
Homans JF; de Reuver S; Heung T; Silversides CK; Oechslin EN; Houben ML; McDonald-McGinn DM; Kruyt MC; Castelein RM; Bassett AS
Spine J; 2020 Jun; 20(6):956-963. PubMed ID: 31958577
[TBL] [Abstract][Full Text] [Related]
13. A rare mosaic 22q11.2 microdeletion identified in a Chinese family with recurrent fetal conotruncal defects.
Chen W; Li X; Sun L; Sheng W; Huang G
Mol Genet Genomic Med; 2019 Aug; 7(8):e847. PubMed ID: 31297990
[TBL] [Abstract][Full Text] [Related]
14. Genome-Wide Association Study to Find Modifiers for Tetralogy of Fallot in the 22q11.2 Deletion Syndrome Identifies Variants in the
Guo T; Repetto GM; McDonald McGinn DM; Chung JH; Nomaru H; Campbell CL; Blonska A; Bassett AS; Chow EWC; Mlynarski EE; Swillen A; Vermeesch J; Devriendt K; Gothelf D; Carmel M; Michaelovsky E; Schneider M; Eliez S; Antonarakis SE; Coleman K; Tomita-Mitchell A; Mitchell ME; Digilio MC; Dallapiccola B; Marino B; Philip N; Busa T; Kushan-Wells L; Bearden CE; Piotrowicz M; Hawuła W; Roberts AE; Tassone F; Simon TJ; van Duin EDA; van Amelsvoort TA; Kates WR; Zackai E; Johnston HR; Cutler DJ; Agopian AJ; Goldmuntz E; Mitchell LE; Wang T; Emanuel BS; Morrow BE;
Circ Cardiovasc Genet; 2017 Oct; 10(5):e001690. PubMed ID: 29025761
[TBL] [Abstract][Full Text] [Related]
15. Frequent association of 22q11.2 deletion with tetralogy of Fallot.
Maeda J; Yamagishi H; Matsuoka R; Ishihara J; Tokumura M; Fukushima H; Ueda H; Takahashi E; Yoshiba S; Kojima Y
Am J Med Genet; 2000 Jun; 92(4):269-72. PubMed ID: 10842294
[TBL] [Abstract][Full Text] [Related]
16. Determinants of outcome after surgical treatment of pulmonary atresia with ventricular septal defect and major aortopulmonary collateral arteries.
Carotti A; Albanese SB; Filippelli S; Ravà L; Guccione P; Pongiglione G; Di Donato RM
J Thorac Cardiovasc Surg; 2010 Nov; 140(5):1092-103. PubMed ID: 20850144
[TBL] [Abstract][Full Text] [Related]
17. Molecular screening for 22Q11.2 deletion syndrome in patients with congenital heart disease.
Huber J; Peres VC; de Castro AL; dos Santos TJ; da Fontoura Beltrão L; de Baumont AC; Cossio SL; Dalberto TP; Riegel M; Cañedo AD; Schaan BD; Pellanda LC
Pediatr Cardiol; 2014 Dec; 35(8):1356-62. PubMed ID: 24880467
[TBL] [Abstract][Full Text] [Related]
18. Late risk of outcomes for adults with repaired tetralogy of Fallot from an inception cohort spanning four decades.
Hickey EJ; Veldtman G; Bradley TJ; Gengsakul A; Manlhiot C; Williams WG; Webb GD; McCrindle BW
Eur J Cardiothorac Surg; 2009 Jan; 35(1):156-64; discussion 164. PubMed ID: 18848456
[TBL] [Abstract][Full Text] [Related]
19. Preoperative total pulmonary blood flow predicts right ventricular pressure in patients early after complete repair of tetralogy of Fallot and pulmonary atresia with major aortopulmonary collateral arteries.
Grosse-Wortmann L; Yoo SJ; van Arsdell G; Chetan D; Macdonald C; Benson L; Honjo O
J Thorac Cardiovasc Surg; 2013 Nov; 146(5):1185-90. PubMed ID: 23414777
[TBL] [Abstract][Full Text] [Related]
20. 22q11.2 deletion detected by
Ramírez-Velazco A; Rivera H; Vásquez-Velázquez AI; Aguayo-Orozco TA; Delgadillo-Pérez S; Domínguez MG
Colomb Med (Cali); 2018 Sep; 49(3):219-222. PubMed ID: 30410196
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]