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

Year Number of Results
1962 2
1963 92
1964 151
1965 99
1966 116
1967 160
1968 217
1969 177
1970 218
1971 271
1972 293
1973 308
1974 295
1975 256
1976 235
1977 208
1978 275
1979 282
1980 277
1981 376
1982 299
1983 333
1984 350
1985 382
1986 421
1987 598
1988 973
1989 988
1990 1084
1991 1185
1992 1315
1993 1467
1994 1348
1995 1477
1996 1594
1997 1510
1998 1561
1999 1587
2000 1898
2001 2006
2002 1614
2003 1607
2004 1881
2005 1961
2006 2014
2007 1971
2008 1995
2009 1950
2010 2200
2011 2282
2012 2501
2013 2529
2014 2681
2015 2639
2016 2700
2017 2766
2018 2501
2019 2379
2020 2403
2021 2404
2022 2475
2023 2169
2024 606

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71,203 results

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Page 1
Oesophageal atresia.
van Lennep M, Singendonk MMJ, Dall'Oglio L, Gottrand F, Krishnan U, Terheggen-Lagro SWJ, Omari TI, Benninga MA, van Wijk MP. van Lennep M, et al. Nat Rev Dis Primers. 2019 Apr 18;5(1):26. doi: 10.1038/s41572-019-0077-0. Nat Rev Dis Primers. 2019. PMID: 31000707 Review.
Oesophageal atresia (EA) is a congenital abnormality of the oesophagus that is caused by incomplete embryonic compartmentalization of the foregut. ...
Oesophageal atresia (EA) is a congenital abnormality of the oesophagus that is caused by incomplete embryonic compartmentaliza …
Congenital malformations.
Corsello G, Giuffrè M. Corsello G, et al. J Matern Fetal Neonatal Med. 2012 Apr;25 Suppl 1:25-9. doi: 10.3109/14767058.2012.664943. Epub 2012 Mar 14. J Matern Fetal Neonatal Med. 2012. PMID: 22356564 Free article. Review.
Congenital malformations are single or multiple defects of the morphogenesis of organs or body districts identifiable at birth or during the intrauterine life. ...Both genetic and environmental factors, as well as their combination in a multifactorial contest, may induce …
Congenital malformations are single or multiple defects of the morphogenesis of organs or body districts identifiable at birth or dur …
The RASopathies.
Rauen KA. Rauen KA. Annu Rev Genomics Hum Genet. 2013;14:355-69. doi: 10.1146/annurev-genom-091212-153523. Epub 2013 Jul 15. Annu Rev Genomics Hum Genet. 2013. PMID: 23875798 Free PMC article. Review.
Airway Anomalies.
Landry AM, Rutter MJ. Landry AM, et al. Clin Perinatol. 2018 Dec;45(4):597-607. doi: 10.1016/j.clp.2018.07.002. Epub 2018 Sep 11. Clin Perinatol. 2018. PMID: 30396407 Review.
This article reviews congenital anomalies involving the larynx and trachea, including congenital subglottic stenosis, laryngeal webs, laryngeal cleft, and tracheal stenosis. ...
This article reviews congenital anomalies involving the larynx and trachea, including congenital subglottic stenosis, laryngea …
Diversity and dysmorphology.
Kruszka P, Tekendo-Ngongang C, Muenke M. Kruszka P, et al. Curr Opin Pediatr. 2019 Dec;31(6):702-707. doi: 10.1097/MOP.0000000000000816. Curr Opin Pediatr. 2019. PMID: 31693576 Review.
Recognizing patterns of dysmorphic features is a critical step in the diagnosis and management of human congenital anomalies and genetic syndromes. This review presents recent developments in genetic syndromes and their related dysmorphology in diverse populations. ...
Recognizing patterns of dysmorphic features is a critical step in the diagnosis and management of human congenital anomalies and gene …
Pulmonary sequestration.
O'Mara CS, Baker RR, Jeyasingham K. O'Mara CS, et al. Surg Gynecol Obstet. 1978 Oct;147(4):609-16. Surg Gynecol Obstet. 1978. PMID: 360452 Review.
Pulmonary sequestration is an uncommon congenital abnormality in which nonfunctioning lung tissue is supplied by an anomalous systemic artery. ...The sequestration may have a fistulous communication with the upper gastrointestinal tract. Congenital anomalies, …
Pulmonary sequestration is an uncommon congenital abnormality in which nonfunctioning lung tissue is supplied by an anomalous …
Hemihypertrophy.
Leung AK, Fong JH, Leong AG. Leung AK, et al. J R Soc Promot Health. 2002 Mar;122(1):24-7. doi: 10.1177/146642400212200111. J R Soc Promot Health. 2002. PMID: 11989139 Review.
Patent foramen ovale.
Homma S, Messé SR, Rundek T, Sun YP, Franke J, Davidson K, Sievert H, Sacco RL, Di Tullio MR. Homma S, et al. Nat Rev Dis Primers. 2016 Jan 21;2:15086. doi: 10.1038/nrdp.2015.86. Nat Rev Dis Primers. 2016. PMID: 27188965 Review.
Patent foramen ovale (PFO) is the most common congenital heart abnormality of fetal origin and is present in approximately 25% of the worldwide adult population. ...
Patent foramen ovale (PFO) is the most common congenital heart abnormality of fetal origin and is present in approximately 25% …
Prenatally diagnosed congenital portosystemic shunts.
Francois B, Lachaux A, Gottrand F, De Smet S. Francois B, et al. J Matern Fetal Neonatal Med. 2018 May;31(10):1364-1368. doi: 10.1080/14767058.2017.1315093. Epub 2017 Apr 20. J Matern Fetal Neonatal Med. 2018. PMID: 28372492 Review.
The median age at diagnosis was 25 GA (14-38 weeks GA). Eighty patients had 128 associated congenital anomalies. The congenital abnormalities most frequently associated with antenatal diagnosis of CPSS were congenital cardiac disease (30 cases), intrau …
The median age at diagnosis was 25 GA (14-38 weeks GA). Eighty patients had 128 associated congenital anomalies. The congenital …
Classification and Pathology of Congenital and Perinatal Vascular Anomalies of the Head and Neck.
North PE. North PE. Otolaryngol Clin North Am. 2018 Feb;51(1):1-39. doi: 10.1016/j.otc.2017.09.020. Otolaryngol Clin North Am. 2018. PMID: 29217054 Review.
It is important to examine current clinical, histologic, and immunophenotypical features that distinguish the major types of congenital and perinatal vascular anomalies affecting the head and neck. ...This article provides an overview of the features that distinguish the m …
It is important to examine current clinical, histologic, and immunophenotypical features that distinguish the major types of congenital …
71,203 results
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