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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1991 1
1995 2
1996 1
1997 1
2000 1
2001 1
2002 1
2004 2
2007 1
2009 2
2010 2
2011 3
2012 1
2013 1
2014 2
2015 1
2017 2
2018 1
2019 2
2020 2
2021 1
2022 1
2023 0

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29 results

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Page 1
Environmental and individual exposure and the risk of congenital anomalies: a review of recent epidemiological evidence.
Baldacci S, Gorini F, Santoro M, Pierini A, Minichilli F, Bianchi F. Baldacci S, et al. Epidemiol Prev. 2018 May-Aug;42(3-4 Suppl 1):1-34. doi: 10.19191/EP18.3-4.S1.P001.057. Epidemiol Prev. 2018. PMID: 30066535 Free article. Review. English.
According to the Centre for Disease Control and Prevention, approximately 3.3% of live births in the United States have a severe birth defect. ...Cigarette smoking: the literature search identified eight systematic reviews with metanalysis, five multicentre studies, …
According to the Centre for Disease Control and Prevention, approximately 3.3% of live births in the United States have a seve …
Differential diagnosis and diagnostic flow chart of joint hypermobility syndrome/ehlers-danlos syndrome hypermobility type compared to other heritable connective tissue disorders.
Colombi M, Dordoni C, Chiarelli N, Ritelli M. Colombi M, et al. Am J Med Genet C Semin Med Genet. 2015 Mar;169C(1):6-22. doi: 10.1002/ajmg.c.31429. Am J Med Genet C Semin Med Genet. 2015. PMID: 25821090 Review.
In this review, we revise the differential diagnosis of JHS/EDS-HT with those heritable connective tissue disorders which show a significant overlap with the former and mostly include EDS classic, vascular and kyphoscoliotic types, osteogenesis imperfecta, Marfan syndrome, …
In this review, we revise the differential diagnosis of JHS/EDS-HT with those heritable connective tissue disorders which show a significant …
Congenital heart defects in Kabuki syndrome.
Yuan SM. Yuan SM. Cardiol J. 2013;20(2):121-4. doi: 10.5603/CJ.2013.0023. Cardiol J. 2013. PMID: 23558868 Free article. Review.
The most common congenital heart defects were coarctation of the aorta, and atrial and ventricular septal defects. Fifteen (19.7%) patients received surgical repair of congenital heart defects at a mean age of 0.8 1.3 years. …
The most common congenital heart defects were coarctation of the aorta, and atrial and ventricular septal defects …
Congenital heart defects in twin gestations.
Campbell KH, Copel JA, Ozan Bahtiyar M. Campbell KH, et al. Minerva Ginecol. 2009 Jun;61(3):239-44. Minerva Ginecol. 2009. PMID: 19415067 Review.
As ultrasound technology advances, diagnosis of fetal malformations, particularly congenital heart defects (CHD) is becoming standard practice. Currently, a key element of obstetrical care is the use of ultrasound to diagnose chorionicity in multiple g …
As ultrasound technology advances, diagnosis of fetal malformations, particularly congenital heart defects (CHD) is bec …
Clinical Databases and Registries in Congenital and Pediatric Cardiac Surgery, Cardiology, Critical Care, and Anesthesiology Worldwide.
Vener DF, Gaies M, Jacobs JP, Pasquali SK. Vener DF, et al. World J Pediatr Congenit Heart Surg. 2017 Jan;8(1):77-87. doi: 10.1177/2150135116681730. World J Pediatr Congenit Heart Surg. 2017. PMID: 28033081 Review.
The growth in large-scale data management capabilities and the successful care of patients with congenital heart defects have coincidentally paralleled each other for the last three decades, and participation in multicenter congenital heart dise …
The growth in large-scale data management capabilities and the successful care of patients with congenital heart defects …
Clinical and radiologic manifestations of congenital extrahepatic portosystemic shunts: a comprehensive review.
Alonso-Gamarra E, Parrón M, Pérez A, Prieto C, Hierro L, López-Santamaría M. Alonso-Gamarra E, et al. Radiographics. 2011 May-Jun;31(3):707-22. doi: 10.1148/rg.313105070. Radiographics. 2011. PMID: 21571652 Review.
Type 1 usually occurs in girls with associated malformations, such as situs ambiguous with polysplenia and congenital heart defects. Associated anomalies are less frequent in type 2, and symptoms usually develop later without a gender preference. Hepatic ence …
Type 1 usually occurs in girls with associated malformations, such as situs ambiguous with polysplenia and congenital heart …
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 column is the sixth in a series exploring drug-drug interactions (DDIs) with a special emphasis on psychiatric medications. The first 3 columns in this DDI series discussed why patients being treated with psychiatric medications are at increased risk for taking mul …
This column is the sixth in a series exploring drug-drug interactions (DDIs) with a special emphasis on psychiatric medications. The first …
Tissue-tissue interactions during morphogenesis of the outflow tract.
Rentschler S, Jain R, Epstein JA. Rentschler S, et al. Pediatr Cardiol. 2010 Apr;31(3):408-13. doi: 10.1007/s00246-009-9611-2. Epub 2009 Dec 29. Pediatr Cardiol. 2010. PMID: 20039033 Free PMC article. Review.
The heart forms as a linear heart tube that loops and septates to produce a mature four-chambered structure. ...Recent evidence indicates that this process involves the complex interactions of multiple cell types including primary and secondary hear …
The heart forms as a linear heart tube that loops and septates to produce a mature four-chambered structure. ...Recent evidenc …
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 Notch signaling pathway members cause developmental phenotypes that affect the liver, skeleton, heart, eye, face, kidney, and vasculature. Notch associated disorders include the autosomal dominant, multi-system, Alagille syndrome caused by mutations in both a …
Mutations in Notch signaling pathway members cause developmental phenotypes that affect the liver, skeleton, heart, eye, face, kidney …
KMT2C/D COMPASS complex-associated diseases [KCDCOM-ADs]: an emerging class of congenital regulopathies.
Lavery WJ, Barski A, Wiley S, Schorry EK, Lindsley AW. Lavery WJ, et al. Clin Epigenetics. 2020 Jan 10;12(1):10. doi: 10.1186/s13148-019-0802-2. Clin Epigenetics. 2020. PMID: 31924266 Free PMC article. Review.
These evolutionarily conserved proteins regulate DNA promoter and enhancer elements, modulating the activity of diverse cell types critical for embryonic morphogenesis, central nervous system development, and post-natal survival. KMT2C/D COMPASS complexes and their binding …
These evolutionarily conserved proteins regulate DNA promoter and enhancer elements, modulating the activity of diverse cell types cr …
29 results