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Year Number of Results
1945 1
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1947 7
1948 4
1949 8
1950 1
1951 5
1952 18
1953 17
1954 24
1955 11
1956 14
1957 29
1958 26
1959 22
1960 26
1961 34
1962 26
1963 16
1964 40
1965 82
1966 140
1967 153
1968 230
1969 293
1970 344
1971 448
1972 370
1973 400
1974 602
1975 617
1976 558
1977 636
1978 638
1979 704
1980 716
1981 740
1982 815
1983 861
1984 974
1985 983
1986 1017
1987 1021
1988 979
1989 1130
1990 1238
1991 1292
1992 1480
1993 1624
1994 1560
1995 1783
1996 1839
1997 1987
1998 2133
1999 2325
2000 2526
2001 2562
2002 2577
2003 2782
2004 3040
2005 3364
2006 3556
2007 3866
2008 4336
2009 4345
2010 4579
2011 5037
2012 5489
2013 6098
2014 6448
2015 6327
2016 6307
2017 6400
2018 6546
2019 6961
2020 7245
2021 6990
2022 6435
2023 5562
2024 2692

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138,338 results

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Quoted phrase not found in phrase index: "Abnormality of prenatal development or birth"
Page 1
The ESHRE/ESGE consensus on the classification of female genital tract congenital anomalies.
Grimbizis GF, Gordts S, Di Spiezio Sardo A, Brucker S, De Angelis C, Gergolet M, Li TC, Tanos V, Brölmann H, Gianaroli L, Campo R. Grimbizis GF, et al. Hum Reprod. 2013 Aug;28(8):2032-44. doi: 10.1093/humrep/det098. Epub 2013 Jun 14. Hum Reprod. 2013. PMID: 23771171 Free PMC article.
STUDY DESIGN, SIZE AND DURATION: The European Society of Human Reproduction and Embryology (ESHRE) and the European Society for Gynaecological Endoscopy (ESGE) have established a common Working Group, under the name CONUTA (CONgenital UTerine Anomalies), with the go …
STUDY DESIGN, SIZE AND DURATION: The European Society of Human Reproduction and Embryology (ESHRE) and the European Society for Gynae …
Prenatal exome sequencing analysis in fetal structural anomalies detected by ultrasonography (PAGE): a cohort study.
Lord J, McMullan DJ, Eberhardt RY, Rinck G, Hamilton SJ, Quinlan-Jones E, Prigmore E, Keelagher R, Best SK, Carey GK, Mellis R, Robart S, Berry IR, Chandler KE, Cilliers D, Cresswell L, Edwards SL, Gardiner C, Henderson A, Holden ST, Homfray T, Lester T, Lewis RA, Newbury-Ecob R, Prescott K, Quarrell OW, Ramsden SC, Roberts E, Tapon D, Tooley MJ, Vasudevan PC, Weber AP, Wellesley DG, Westwood P, White H, Parker M, Williams D, Jenkins L, Scott RH, Kilby MD, Chitty LS, Hurles ME, Maher ER; Prenatal Assessment of Genomes and Exomes Consortium. Lord J, et al. Lancet. 2019 Feb 23;393(10173):747-757. doi: 10.1016/S0140-6736(18)31940-8. Epub 2019 Jan 31. Lancet. 2019. PMID: 30712880 Free PMC article.
Testing for aneuploidy and CNVs is routine during the investigation of fetal structural anomalies, but there is little information on the clinical usefulness of genome-wide next-generation sequencing in the prenatal setting. We therefore aimed to evaluate the proportion of …
Testing for aneuploidy and CNVs is routine during the investigation of fetal structural anomalies, but there is little information on the cl …
Laryngo-tracheo-oesophageal clefts.
Leboulanger N, Garabédian EN. Leboulanger N, et al. Orphanet J Rare Dis. 2011 Dec 7;6:81. doi: 10.1186/1750-1172-6-81. Orphanet J Rare Dis. 2011. PMID: 22151899 Free PMC article. Review.
A laryngo-tracheo-esophageal cleft (LC) is a congenital malformation characterized by an abnormal, posterior, sagittal communication between the larynx and the pharynx, possibly extending downward between the trachea and the esophagus. The estimated annual incidence …
A laryngo-tracheo-esophageal cleft (LC) is a congenital malformation characterized by an abnormal, posterior, sagittal communi …
Congenital portosystemic venous shunt.
Papamichail M, Pizanias M, Heaton N. Papamichail M, et al. Eur J Pediatr. 2018 Mar;177(3):285-294. doi: 10.1007/s00431-017-3058-x. Epub 2017 Dec 14. Eur J Pediatr. 2018. PMID: 29243189 Free PMC article. Review.
They occur during liver and systemic venous vascular embryogenesis and are associated with other congenital abnormalities. They carry a higher risk of benign and malignant liver tumors and, if left untreated, can result in significant medical complications including …
They occur during liver and systemic venous vascular embryogenesis and are associated with other congenital abnormalities. The …
Fetal akinesia.
Hammond E, Donnenfeld AE. Hammond E, et al. Obstet Gynecol Surv. 1995 Mar;50(3):240-9. doi: 10.1097/00006254-199503000-00028. Obstet Gynecol Surv. 1995. PMID: 7739837 Review.
Normal fetal growth and development during pregnancy is highly dependent upon adequate fetal movement. Limitation of movement, regardless of the underlying cause, can result in a particular pattern of abnormal fetal morphogenesis. This phenotype is termed the fetal …
Normal fetal growth and development during pregnancy is highly dependent upon adequate fetal movement. Limitation of movement, regard …
Rare Upper Airway Anomalies.
Windsor A, Clemmens C, Jacobs IN. Windsor A, et al. Paediatr Respir Rev. 2016 Jan;17:24-8. doi: 10.1016/j.prrv.2015.07.001. Epub 2015 Jul 10. Paediatr Respir Rev. 2016. PMID: 26277452 Review.
A broad spectrum of congenital upper airway anomalies can occur as a result of errors during embryologic development. In this review, we will describe the clinical presentation, diagnosis, and management strategies for a few select, rare congenital malformati …
A broad spectrum of congenital upper airway anomalies can occur as a result of errors during embryologic development. In this …
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 …
Mayer-Rokitansky-Küster-Hauser syndrome as an interdisciplinary problem.
Liszewska-Kapłon M, Strózik M, Kotarski Ł, Bagłaj M, Hirnle L. Liszewska-Kapłon M, et al. Adv Clin Exp Med. 2020 Apr;29(4):505-511. doi: 10.17219/acem/118850. Adv Clin Exp Med. 2020. PMID: 32348039 Free article. Review.
The Mayer-Rokitansky-Kuster-Hauser (MRKH) syndrome, also known as Mullerian agenesis or aplasia, is a congenital disease manifested by the aplasia of the uterus and the upper 2/3 of the vagina; its incidence is 1 in 4,000-5,000 female live births. ...
The Mayer-Rokitansky-Kuster-Hauser (MRKH) syndrome, also known as Mullerian agenesis or aplasia, is a congenital disease manifested b …
Human laterality disorders.
Peeters H, Devriendt K. Peeters H, et al. Eur J Med Genet. 2006 Sep-Oct;49(5):349-62. doi: 10.1016/j.ejmg.2005.12.003. Epub 2006 Jan 3. Eur J Med Genet. 2006. PMID: 16461029 Review.
Heterotaxia is a group of congenital disorders characterized by a misplacement of one or more organs according to the left-right axis. ...
Heterotaxia is a group of congenital disorders characterized by a misplacement of one or more organs according to the left-right axis …
138,338 results
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