BPG is committed to discovery and dissemination of knowledge
Cited by in F6Publishing
For: Ticho BS, Goldstein AM, Van Praagh R. Extracardiac anomalies in the heterotaxy syndromes with focus on anomalies of midline-associated structures. The American Journal of Cardiology 2000;85:729-34. [DOI: 10.1016/s0002-9149(99)00849-8] [Cited by in Crossref: 78] [Cited by in F6Publishing: 19] [Article Influence: 3.5] [Reference Citation Analysis]
Number Citing Articles
1 Landis BJ, Cooper DS, Hinton RB. CHD associated with syndromic diagnoses: peri-operative risk factors and early outcomes. Cardiol Young 2016;26:30-52. [PMID: 26345374 DOI: 10.1017/S1047951115001389] [Cited by in Crossref: 22] [Cited by in F6Publishing: 7] [Article Influence: 3.1] [Reference Citation Analysis]
2 Bérard A, Levin M, Sadler T, Healy D. Selective Serotonin Reuptake Inhibitor Use During Pregnancy and Major Malformations: The Importance of Serotonin for Embryonic Development and the Effect of Serotonin Inhibition on the Occurrence of Malformations. Bioelectricity 2019;1:18-29. [PMID: 34471805 DOI: 10.1089/bioe.2018.0003] [Cited by in Crossref: 3] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
3 Agarwal R, Varghese R, Jesudian V, Moses J. The heterotaxy syndrome: associated congenital heart defects and management. Indian J Thorac Cardiovasc Surg 2021;37:67-81. [PMID: 33603285 DOI: 10.1007/s12055-020-00935-y] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
4 Lagrotta G, Moises M. Heterotaxy Polysplenia Syndrome in Adulthood: Focused Review and a Case Report. Cureus 2020;12:e6822. [PMID: 32181068 DOI: 10.7759/cureus.6822] [Cited by in Crossref: 1] [Article Influence: 0.5] [Reference Citation Analysis]
5 Ware SM, Aygun MG, Hildebrandt F. Spectrum of clinical diseases caused by disorders of primary cilia. Proc Am Thorac Soc 2011;8:444-50. [PMID: 21926397 DOI: 10.1513/pats.201103-025SD] [Cited by in Crossref: 79] [Cited by in F6Publishing: 50] [Article Influence: 7.9] [Reference Citation Analysis]
6 Kim SJ. Heterotaxy syndrome. Korean Circ J. 2011;41:227-232. [PMID: 21731561 DOI: 10.4070/kcj.2011.41.5.227] [Cited by in Crossref: 43] [Cited by in F6Publishing: 28] [Article Influence: 3.9] [Reference Citation Analysis]
7 Lee MY, Won HS, Shim JY, Lee PR, Lee BS, Kim EA, Kim YH, Park JJ, Yun TJ, Kim A. Prenatal diagnosis of atrial isomerism in the Korean population. Obstet Gynecol Sci 2014;57:193-200. [PMID: 24883290 DOI: 10.5468/ogs.2014.57.3.193] [Cited by in Crossref: 9] [Cited by in F6Publishing: 7] [Article Influence: 1.1] [Reference Citation Analysis]
8 Boos A, Geyer H, Müller U, Peter J, Schmid T, Gerspach C, Previtali M, Rütten M, Sydler T, Schwarzwald CC, Schraner EM, Braun U. Situs ambiguus in a Brown Swiss cow with polysplenia: case report. BMC Vet Res 2013;9:34. [PMID: 23421814 DOI: 10.1186/1746-6148-9-34] [Cited by in Crossref: 3] [Article Influence: 0.3] [Reference Citation Analysis]
9 Lin AE, Krikov S, Riehle-Colarusso T, Frías JL, Belmont J, Anderka M, Geva T, Getz KD, Botto LD; National Birth Defects Prevention Study. Laterality defects in the national birth defects prevention study (1998-2007): birth prevalence and descriptive epidemiology. Am J Med Genet A 2014;164A:2581-91. [PMID: 25099286 DOI: 10.1002/ajmg.a.36695] [Cited by in Crossref: 84] [Cited by in F6Publishing: 71] [Article Influence: 10.5] [Reference Citation Analysis]
10 Anwar A, Jubin J, Raza S, Mirza ZK. A Rare Case of Recurrent Pneumonia in Heterotaxy Syndrome, Polysplenia/Left Isomerism. Cureus 2021;13:e19055. [PMID: 34858743 DOI: 10.7759/cureus.19055] [Reference Citation Analysis]
11 Ugas Charcape CF, Alpaca Rodriguez LR, Matos Rojas IA, Lazarte Rantes CI, Valdez Quintana M, Katekaru Tokeshi DA, Epelman M. Characterisation of computed tomography angiography findings in paediatric patients with heterotaxy. Pediatr Radiol 2019;49:1142-51. [PMID: 31165901 DOI: 10.1007/s00247-019-04434-0] [Cited by in Crossref: 3] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
12 Sadler TW. Establishing the Embryonic Axes: Prime Time for Teratogenic Insults. J Cardiovasc Dev Dis 2017;4:E15. [PMID: 29367544 DOI: 10.3390/jcdd4030015] [Cited by in Crossref: 4] [Cited by in F6Publishing: 3] [Article Influence: 0.8] [Reference Citation Analysis]
13 Kothari SS. Non-cardiac issues in patients with heterotaxy syndrome. Ann Pediatr Cardiol 2014;7:187-92. [PMID: 25298693 DOI: 10.4103/0974-2069.140834] [Cited by in Crossref: 32] [Cited by in F6Publishing: 24] [Article Influence: 4.0] [Reference Citation Analysis]
14 Pharoah PO. Prevalence and pathogenesis of congenital anomalies in cerebral palsy. Arch Dis Child Fetal Neonatal Ed 2007;92:F489-93. [PMID: 17428819 DOI: 10.1136/adc.2006.107375] [Cited by in Crossref: 34] [Cited by in F6Publishing: 25] [Article Influence: 2.3] [Reference Citation Analysis]
15 Huseynova R, Bin Mahmoud LA, AlJohani E, Huseynov O, Abdelrahim A, AlOmran KA. Rare Extracardiac Anomalies Presented with Right Heterotaxy Syndrome in a Newborn Baby: A Case Report. Am J Case Rep 2020;21:e923341. [PMID: 32491997 DOI: 10.12659/AJCR.923341] [Reference Citation Analysis]
16 Kiran VS, Choudhary S, Shaik A, Gadabanahalli K, Raj V, Bhat V. The Spectrum of Cardiac Anomalies Associated with Heterotaxy: A Single-Center Study of a Large Series Based on Computed Tomography. Pediatr Cardiol 2020;41:1414-24. [PMID: 32556488 DOI: 10.1007/s00246-020-02402-2] [Reference Citation Analysis]
17 Grzymkowski J, Wyatt B, Nascone-Yoder N. The twists and turns of left-right asymmetric gut morphogenesis. Development 2020;147:dev187583. [PMID: 33046455 DOI: 10.1242/dev.187583] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
18 Escobar-Diaz MC, Friedman K, Salem Y, Marx GR, Kalish BT, Lafranchi T, Rathod RH, Emani S, Geva T, Tworetzky W. Perinatal and infant outcomes of prenatal diagnosis of heterotaxy syndrome (asplenia and polysplenia). Am J Cardiol 2014;114:612-7. [PMID: 24996551 DOI: 10.1016/j.amjcard.2014.05.042] [Cited by in Crossref: 29] [Cited by in F6Publishing: 20] [Article Influence: 3.6] [Reference Citation Analysis]
19 Ortega-Zhindón DB, Flores-Sarria IP, Minakata-Quiróga MA, Angulo-Cruzado ST, Romero-Montalvo LA, Cervantes-Salazar JL. [Isomorfismo cardiaco: Una perspectiva multidisciplinaria]. Arch Cardiol Mex 2021;91:470-9. [PMID: 34491249 DOI: 10.24875/ACM.20000567] [Reference Citation Analysis]
20 Loomba R, Shah PH, Anderson RH. Fetal Magnetic Resonance Imaging of Malformations Associated with Heterotaxy. Cureus 2015;7:e269. [PMID: 26180693 DOI: 10.7759/cureus.269] [Cited by in Crossref: 2] [Cited by in F6Publishing: 9] [Article Influence: 0.3] [Reference Citation Analysis]
21 Ware SM, Peng J, Zhu L, Fernbach S, Colicos S, Casey B, Towbin J, Belmont JW. Identification and functional analysis of ZIC3 mutations in heterotaxy and related congenital heart defects. Am J Hum Genet 2004;74:93-105. [PMID: 14681828 DOI: 10.1086/380998] [Cited by in Crossref: 190] [Cited by in F6Publishing: 163] [Article Influence: 10.0] [Reference Citation Analysis]
22 Weiand G, Mangold G. [Accessory spleen in the pancreatic tail -- a neglected entity? A contribution to embryology, topography and pathology of ectopic splenic tissue]. Chirurg 2003;74:1170-7. [PMID: 14673541 DOI: 10.1007/s00104-003-0714-7] [Cited by in Crossref: 7] [Cited by in F6Publishing: 5] [Article Influence: 0.4] [Reference Citation Analysis]