Tetralogy of Fallot
"Tetralogy of Fallot" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
A combination of congenital heart defects consisting of four key features including VENTRICULAR SEPTAL DEFECTS; PULMONARY STENOSIS; RIGHT VENTRICULAR HYPERTROPHY; and a dextro-positioned AORTA. In this condition, blood from both ventricles (oxygen-rich and oxygen-poor) is pumped into the body often causing CYANOSIS.
| Descriptor ID |
D013771
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| MeSH Number(s) |
C14.240.400.849 C14.280.400.849 C16.131.240.400.849
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| Concept/Terms |
Tetralogy of Fallot- Tetralogy of Fallot
- Tetralogy, Fallot's
- Tetralogy, Fallot
- Tetralogy, Fallots
- Fallot's Tetralogy
- Fallot Tetralogy
- Fallots Tetralogy
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Below are MeSH descriptors whose meaning is more general than "Tetralogy of Fallot".
Below are MeSH descriptors whose meaning is more specific than "Tetralogy of Fallot".
This graph shows the total number of publications written about "Tetralogy of Fallot" by people in this website by year, and whether "Tetralogy of Fallot" was a major or minor topic of these publications.
To see the data from this visualization as text, click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 2014 | 0 | 1 | 1 | | 2015 | 1 | 0 | 1 | | 2020 | 1 | 0 | 1 | | 2021 | 1 | 0 | 1 | | 2024 | 1 | 0 | 1 | | 2025 | 2 | 0 | 2 |
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Below are the most recent publications written about "Tetralogy of Fallot" by people in Profiles.
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Moore JP, Ghantous E, Waldmann V, Bessière F, Babouri N, Cohen MI, O'Leary ET, Patel NS, Nazer B, Tan W, Fish FA, Dalal AS, Mariucci E, Tan RB, Lloyd MS, McLeod CJ, Anderson CC, Kanter RJ, Johnson BV, Wang B, Chang PM, Khairy P. Clinical and Electrophysiological Characteristics of Inducible Polymorphic Ventricular Tachycardia in Repaired Tetralogy of Fallot. JACC Clin Electrophysiol. 2025 Aug; 11(8):1807-1816.
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Moore JP, Waldmann V, Bessi?re F, Babouri N, Cohen MI, O'Leary ET, Patel NS, Nazer B, Tan W, Fish FA, Dalal AS, Mariucci E, Tan RB, Lloyd MS, McLeod CJ, Anderson CC, Kanter RJ, Johnson BV, Wang B, Chang PM, Newlon CA, Su J, Shannon KM, Bradfield JS, Shivkumar K, Aboulhosn JA, Khairy P. Age-Related Ventricular Tachycardia Substrate Characteristics for Repaired Tetralogy of Fallot Before Transcatheter Pulmonary Valve Placement. JACC Clin Electrophysiol. 2025 Mar; 11(3):551-562.
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Ramdat Misier NL, Moore JP, Nguyen HH, Lloyd MS, Dubin AM, Mah DY, Czosek RJ, Khairy P, Chang PM, Nielsen JC, Aydin A, Pilcher TA, O'Leary ET, Shivkumar K, de Groot NMS. Long-Term Outcomes of Cardiac Resynchronization Therapy in Patients With Repaired Tetralogy of Fallot: A Multicenter Study. Circ Arrhythm Electrophysiol. 2024 03; 17(3):e012363.
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?koric-Milosavljevic D, Lahrouchi N, Bosada FM, Dombrowsky G, Williams SG, Lesurf R, Tjong FVY, Walsh R, El Bouchikhi I, Breckpot J, Audain E, Ilgun A, Beekman L, Ratbi I, Strong A, Muenke M, Heide S, Muir AM, Hababa M, Cross L, Zhou D, Pastinen T, Zackai E, Atmani S, Ouldim K, Adadi N, Steindl K, Rauch A, Brook D, Wilsdon A, Kuipers I, Blom NA, Mulder BJ, Mefford HC, Keren B, Joset P, Kruszka P, Thiffault I, Sheppard SE, Roberts A, Lodder EM, Keavney BD, Clur SB, Mital S, Hitz MP, Christoffels VM, Postma AV, Bezzina CR. Rare variants in KDR, encoding VEGF Receptor 2, are associated with tetralogy of Fallot. Genet Med. 2021 10; 23(10):1952-1960.
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Grunert M, Appelt S, Sch?nhals S, Mika K, Cui H, Cooper A, Cyganek L, Guan K, Sperling SR. Induced pluripotent stem cells of patients with Tetralogy of Fallot reveal transcriptional alterations in cardiomyocyte differentiation. Sci Rep. 2020 07 02; 10(1):10921.
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Chan SS, Whitehead KK, Kim TS, Fu GL, Keller MS, Fogel MA, Harris MA. Repaired tetralogy of Fallot with coexisting unrepaired partial anomalous pulmonary venous connection is associated with diminished right ventricular ejection fraction and more severe right ventricular dilation. Pediatr Radiol. 2015 Sep; 45(10):1465-71.
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Evans W, Castillo W, Rollins R, Luna C, Kip K, Ludwick J, Madan N, Ciccolo M, Galindo A, Rothman A, Mayman G, Cass K, Thomas V, Restrepo H, Acherman R. Moving towards universal prenatal detection of critical congenital heart disease in southern Nevada: a community-wide program. Pediatr Cardiol. 2015 Feb; 36(2):281-8.
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Rodemoyer A, Kibiryeva N, Bair A, Marshall J, O'Brien JE, Bittel DC. A tissue-specific gene expression template portrays heart development and pathology. Hum Genomics. 2014 Mar 11; 8:6.
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Bittel DC, Zhou XG, Kibiryeva N, Fiedler S, O'Brien JE, Marshall J, Yu S, Liu HY. Ultra high-resolution gene centric genomic structural analysis of a non-syndromic congenital heart defect, Tetralogy of Fallot. PLoS One. 2014; 9(1):e87472.
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O'Brien JE, Kibiryeva N, Zhou XG, Marshall JA, Lofland GK, Artman M, Chen J, Bittel DC. Noncoding RNA expression in myocardium from infants with tetralogy of Fallot. Circ Cardiovasc Genet. 2012 Jun; 5(3):279-86.
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