130 related articles for article (PubMed ID: 38277413)
61. Anatomophysiologic basis of tetralogy of Fallot and its clinical implications.
Duro RP; Moura C; Leite-Moreira A
Rev Port Cardiol; 2010 Apr; 29(4):591-630. PubMed ID: 20734579
[TBL] [Abstract][Full Text] [Related]
62. Gene expression in cardiac tissues from infants with idiopathic conotruncal defects.
Bittel DC; Butler MG; Kibiryeva N; Marshall JA; Chen J; Lofland GK; O'Brien JE
BMC Med Genomics; 2011 Jan; 4():1. PubMed ID: 21208432
[TBL] [Abstract][Full Text] [Related]
63. The aortic arch in tetralogy of Fallot: types of branching and clinical implications.
Prabhu S; Kasturi S; Mehra S; Tiwari R; Joshi A; John C; Karl TR
Cardiol Young; 2020 Aug; 30(8):1144-1150. PubMed ID: 32638692
[TBL] [Abstract][Full Text] [Related]
64. Oxygen and lack of oxygen in fetal and placental development, feto-placental coupling, and congenital heart defects.
Llurba Olive E; Xiao E; Natale DR; Fisher SA
Birth Defects Res; 2018 Dec; 110(20):1517-1530. PubMed ID: 30576091
[TBL] [Abstract][Full Text] [Related]
65. San Luis Valley recombinant chromosome 8 and tetralogy of Fallot: a review of chromosome 8 anomalies and congenital heart disease.
Gelb BD; Towbin JA; McCabe ER; Sujansky E
Am J Med Genet; 1991 Sep; 40(4):471-6. PubMed ID: 1746613
[TBL] [Abstract][Full Text] [Related]
66. Uncorrected pink tetralogy of Fallot in an adult patient: incidental CT findings.
Siriapisith T; Wasinrat J; Tresukosol D
J Cardiovasc Comput Tomogr; 2010; 4(1):58-61. PubMed ID: 19717356
[TBL] [Abstract][Full Text] [Related]
67. JAG1 mutation in a patient with deletion 22q11.2 syndrome and tetralogy of Fallot.
Digilio MC; Luca AD; Lepri F; Guida V; Ferese R; Dentici ML; Angioni A; Marino B; Dallapiccola B
Am J Med Genet A; 2013 Dec; 161A(12):3133-6. PubMed ID: 23956173
[TBL] [Abstract][Full Text] [Related]
68. Construction and investigation of a circRNA-associated ceRNA regulatory network in Tetralogy of Fallot.
Yu H; Wang X; Cao H
BMC Cardiovasc Disord; 2021 Sep; 21(1):437. PubMed ID: 34521346
[TBL] [Abstract][Full Text] [Related]
69. Hypoxia-inducible factor-1 alpha regulates the role of vascular endothelial growth factor on pulmonary arteries of rats with hypoxia-induced pulmonary hypertension.
Li QF; Dai AG
Chin Med J (Engl); 2004 Jul; 117(7):1023-8. PubMed ID: 15265376
[TBL] [Abstract][Full Text] [Related]
70. Tetralogy of Fallot in the fetus in the current era.
Poon LC; Huggon IC; Zidere V; Allan LD
Ultrasound Obstet Gynecol; 2007 Jun; 29(6):625-7. PubMed ID: 17405110
[TBL] [Abstract][Full Text] [Related]
71. Methylation status of CpG sites in the NOTCH4 promoter region regulates NOTCH4 expression in patients with tetralogy of Fallot.
Zhu Y; Ye M; Xu H; Gu R; Ma X; Chen M; Li X; Sheng W; Huang G
Mol Med Rep; 2020 Nov; 22(5):4412-4422. PubMed ID: 33000281
[TBL] [Abstract][Full Text] [Related]
72. Unrepaired tetralogy of Fallot in a 71 years old woman: A case report and review of the literature.
Ghaderi F; Kazemi T; Jafari-Nozad AM
Echocardiography; 2023 Nov; 40(11):1269-1275. PubMed ID: 37632152
[TBL] [Abstract][Full Text] [Related]
73. Tetralogy of Fallot associated with chromosome 22q11.2 deletion in adolescents and young adults.
Momma K; Takao A; Matsuoka R; Imai Y; Muto A; Osawa M; Takayama M
Genet Med; 2001; 3(1):56-60. PubMed ID: 11339379
[TBL] [Abstract][Full Text] [Related]
74. Treatment of tetralogy of Fallot hypoxic spell with intranasal fentanyl.
Tsze DS; Vitberg YM; Berezow J; Starc TJ; Dayan PS
Pediatrics; 2014 Jul; 134(1):e266-9. PubMed ID: 24936003
[TBL] [Abstract][Full Text] [Related]
75. Application of the comet assay for assessment of oxidative DNA damage in circulating lymphocytes of Tetralogy of Fallot patients.
Srujana K; Begum SS; Rao KN; Devi GS; Jyothy A; Prasad MH
Mutat Res; 2010 Jun; 688(1-2):62-5. PubMed ID: 20227426
[TBL] [Abstract][Full Text] [Related]
76. Deletion of HIF-1α partially rescues the abnormal hyaloid vascular system in Cited2 conditional knockout mouse eyes.
Huang TQ; Wang Y; Ebrahem Q; Chen Y; Cheng C; Doughman YQ; Watanabe M; Dunwoodie SL; Yang YC
Mol Vis; 2012; 18():1260-70. PubMed ID: 22665973
[TBL] [Abstract][Full Text] [Related]
77. [Study on the relationship between 22q11 microdeletion and congenital heart disease].
Du YR; Yang HJ; Tan Z; Huang Y; Li SL; Tian JW; Zhang GY; Li P; Fu SB
Yi Chuan; 2005 Nov; 27(6):873-6. PubMed ID: 16378931
[TBL] [Abstract][Full Text] [Related]
78. Association of tetralogy of Fallot with a distinct region of del22q11.2.
Kessler-Icekson G; Birk E; Weintraub AY; Barhum Y; Kotlyar V; Schlesinger H; Rockah R; Vidne BA; Frisch A
Am J Med Genet; 2002 Feb; 107(4):294-8. PubMed ID: 11840485
[TBL] [Abstract][Full Text] [Related]
79. Hypoxia-inducible factor-1α, vascular endothelial growth factor, inducible nitric oxide synthase, and endothelin-1 expression correlates with angiogenesis in congenital heart disease.
Yin HL; Luo CW; Dai ZK; Shaw KP; Chai CY; Wu CC
Kaohsiung J Med Sci; 2016 Jul; 32(7):348-55. PubMed ID: 27450023
[TBL] [Abstract][Full Text] [Related]
80. The risk for four specific congenital heart defects associated with assisted reproductive techniques: a population-based evaluation.
Tararbit K; Lelong N; Thieulin AC; Houyel L; Bonnet D; Goffinet F; Khoshnood B;
Hum Reprod; 2013 Feb; 28(2):367-74. PubMed ID: 23178272
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
