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Year Number of Results
1991 1
1995 2
1997 1
2000 1
2002 1
2003 1
2004 1
2007 1
2009 1
2012 1
2013 1
2014 3
2017 2
2019 1
2020 1
2021 1
2022 1
2024 0

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19 results

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Page 1
Clinical and molecular effects of CHD7 in the heart.
Corsten-Janssen N, Scambler PJ. Corsten-Janssen N, et al. Am J Med Genet C Semin Med Genet. 2017 Dec;175(4):487-495. doi: 10.1002/ajmg.c.31590. Epub 2017 Oct 31. Am J Med Genet C Semin Med Genet. 2017. PMID: 29088513 Review.
Heart defects caused by loss-of-function mutations in CHD7 are a frequent cause of morbidity and mortality in CHARGE syndrome. Here we review the clinical and molecular aspects of CHD7 that are related to the cardiovascular manifestations of the syndrome. The typ
Heart defects caused by loss-of-function mutations in CHD7 are a frequent cause of morbidity and mortality in CHARGE syndrome.
Drug-Drug Interactions (DDIs) in Psychiatric Practice, Part 6: Pharmacodynamic Considerations.
Preskorn SH. Preskorn SH. J Psychiatr Pract. 2019 Jul;25(4):290-297. doi: 10.1097/PRA.0000000000000399. J Psychiatr Pract. 2019. PMID: 31291209 Review.
This sixth column in the series discusses some key issues related to pharmacodynamic interactions involving commonly used psychiatric medications. The column first discusses 3 types of pharmacological agents that deserve special mention because of the widespread types
This sixth column in the series discusses some key issues related to pharmacodynamic interactions involving commonly used psychiatric medica …
Notch signaling in human development and disease.
Penton AL, Leonard LD, Spinner NB. Penton AL, et al. Semin Cell Dev Biol. 2012 Jun;23(4):450-7. doi: 10.1016/j.semcdb.2012.01.010. Epub 2012 Jan 28. Semin Cell Dev Biol. 2012. PMID: 22306179 Free PMC article. Review.
Mutations in the NOTCH1 receptor are associated with several types of cardiac disease and mutations in NOTCH3 cause the dominant adult onset disorder CADASIL (cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy), a vascular disorder w …
Mutations in the NOTCH1 receptor are associated with several types of cardiac disease and mutations in NOTCH3 cause the dominant adul …
Partial Anomalous Left Pulmonary Artery Anterior Versus Posterior Types: A Systematic Review.
Restrepo CS, Gonzalez TV, Baxi AJ, Saboo SS. Restrepo CS, et al. Tomography. 2022 Jul 27;8(4):1947-1958. doi: 10.3390/tomography8040163. Tomography. 2022. PMID: 36006061 Free PMC article. Review.
PALPAs were more commonly anterior than posterior. Mean age: 5.3 years (SD = 12.4) for anterior and 6.8 years (SD = 18.5) for posterior (p = 0.77). ...In conclusion, respiratory symptoms were the only significant difference between anterior and posterior PALPA types
PALPAs were more commonly anterior than posterior. Mean age: 5.3 years (SD = 12.4) for anterior and 6.8 years (SD = 18.5) for posteri …
Anomalous origin of coronary artery: taxonomy and clinical implication.
Yuan SM. Yuan SM. Rev Bras Cir Cardiovasc. 2014 Oct-Dec;29(4):622-9. doi: 10.5935/1678-9741.20140109. Rev Bras Cir Cardiovasc. 2014. PMID: 25714217 Free PMC article. Review.
METHODS: A comprehensive literature review was made in terms of the taxonomies including "simple", "multiple" and "complex" types of anomalous origin of coronary artery. RESULTS: Anomalous origin of coronary artery can be simply categorized according to the ectopica …
METHODS: A comprehensive literature review was made in terms of the taxonomies including "simple", "multiple" and "complex" types
Cardiac Neural Crest Cells: Their Rhombomeric Specification, Migration, and Association with Heart and Great Vessel Anomalies.
Schussler O, Gharibeh L, Mootoosamy P, Murith N, Tien V, Rougemont AL, Sologashvili T, Suuronen E, Lecarpentier Y, Ruel M. Schussler O, et al. Cell Mol Neurobiol. 2021 Apr;41(3):403-429. doi: 10.1007/s10571-020-00863-w. Epub 2020 May 13. Cell Mol Neurobiol. 2021. PMID: 32405705 Review.
Outflow tract abnormalities are the most frequent congenital heart defects. These are due to the absence or dysfunction of the two main cell types, i.e., neural crest cells and secondary heart field cells that migrate in opposite directions at t …
Outflow tract abnormalities are the most frequent congenital heart defects. These are due to the absence or dysfunction …
SWI/SNF chromatin-remodeling complexes in cardiovascular development and disease.
Bevilacqua A, Willis MS, Bultman SJ. Bevilacqua A, et al. Cardiovasc Pathol. 2014 Mar-Apr;23(2):85-91. doi: 10.1016/j.carpath.2013.09.003. Epub 2013 Oct 4. Cardiovasc Pathol. 2014. PMID: 24183004 Free PMC article. Review.
Our understanding of congenital heart defects has been recently advanced by whole exome sequencing projects, which have identified de novo mutations in many genes encoding epigenetic regulators. ...While these studies indicate a critical role of SWI/SNF compl …
Our understanding of congenital heart defects has been recently advanced by whole exome sequencing projects, which have …
Anomalies of visceroatrial situs.
Ghosh S, Yarmish G, Godelman A, Haramati LB, Spindola-Franco H. Ghosh S, et al. AJR Am J Roentgenol. 2009 Oct;193(4):1107-17. doi: 10.2214/AJR.09.2411. AJR Am J Roentgenol. 2009. PMID: 19770335 Review.
Accurate determination of situs is essential because anomalies of situs are associated with an increased incidence of complex congenital heart disease. CONCLUSION: We propose a methodical diagnostic approach to determining the visceroatrial situs and cardiac configu …
Accurate determination of situs is essential because anomalies of situs are associated with an increased incidence of complex congenital
The World Database for Pediatric and Congenital Heart Surgery: The Dawn of a New Era of Global Communication and Quality Improvement in Congenital Heart Disease.
St Louis JD, Kurosawa H, Jonas RA, Sandoval N, Cervantes J, Tchervenkov CI, Jacobs JP, Sakamoto K, Stellin G, Kirklin JK. St Louis JD, et al. World J Pediatr Congenit Heart Surg. 2017 Sep;8(5):597-599. doi: 10.1177/2150135117725458. World J Pediatr Congenit Heart Surg. 2017. PMID: 28901228 Review.
The World Society for Pediatric and Congenital Heart Surgery was founded with the mission to "promote the highest quality comprehensive cardiac care to all patients with congenital heart disease, from the fetus to the adult, regardless of the patient's …
The World Society for Pediatric and Congenital Heart Surgery was founded with the mission to "promote the highest quality comp …
A systematic review on the efficacy and safety of transcatheter device closure of ventricular septal defects (VSD).
Yang L, Tai BC, Khin LW, Quek SC. Yang L, et al. J Interv Cardiol. 2014 Jun;27(3):260-72. doi: 10.1111/joic.12121. Epub 2014 Apr 29. J Interv Cardiol. 2014. PMID: 24773223 Free article. Review.
The random effects model was used to obtain pooled estimates of success and complications. RESULTS: A total of 37 publications comprising 4,406 patients with VSD (perimembranous = 3,758, muscular = 419, intracristal = 47, doubly committed subarterial = 36, multiple
The random effects model was used to obtain pooled estimates of success and complications. RESULTS: A total of 37 publications comprising …
19 results