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Items: 1 to 20 of 108

1.

Epidemiology of congenital cerebral anomalies in Europe: a multicentre, population-based EUROCAT study.

Morris JK, Wellesley DG, Barisic I, Addor MC, Bergman JEH, Braz P, Cavero-Carbonell C, Draper ES, Gatt M, Haeusler M, Klungsoyr K, Kurinczuk JJ, Lelong N, Luyt K, Lynch C, O'Mahony MT, Mokoroa O, Nelen V, Neville AJ, Pierini A, Randrianaivo H, Rankin J, Rissmann A, Rouget F, Schaub B, Tucker DF, Verellen-Dumoulin C, Wiesel A, Zymak-Zakutnia N, Lanzoni M, Garne E.

Arch Dis Child. 2019 Jun 26. pii: archdischild-2018-316733. doi: 10.1136/archdischild-2018-316733. [Epub ahead of print]

PMID:
31243007
2.

Paper 2: EUROCAT public health indicators for congenital anomalies in Europe.

Khoshnood B, Greenlees R, Loane M, Dolk H; EUROCAT Project Management Committee; EUROCAT Working Group.

Birth Defects Res A Clin Mol Teratol. 2011 Mar;91 Suppl 1:S16-22. doi: 10.1002/bdra.20776. Epub 2011 Mar 4. Review.

3.

Epidemiology of Dandy-Walker Malformation in Europe: A EUROCAT Population-Based Registry Study.

Santoro M, Coi A, Barišić I, Garne E, Addor MC, Bergman JEH, Bianchi F, Boban L, Braz P, Cavero-Carbonell C, Gatt M, Haeusler M, Kinsner-Ovaskainen A, Klungsøyr K, Kurinczuk JJ, Lelong N, Luyt K, Materna-Kiryluk A, Mokoroa O, Mullaney C, Nelen V, Neville AJ, O'Mahony MT, Perthus I, Randrianaivo H, Rankin J, Rissmann A, Rouget F, Schaub B, Tucker D, Wellesley D, Yevtushok L, Pierini A.

Neuroepidemiology. 2019 Jul 12:1-11. doi: 10.1159/000501238. [Epub ahead of print]

PMID:
31302658
4.

The prevalence of congenital anomalies in Europe.

Dolk H, Loane M, Garne E.

Adv Exp Med Biol. 2010;686:349-64. doi: 10.1007/978-90-481-9485-8_20. Review.

PMID:
20824455
5.

Termination of pregnancy for fetal anomaly after 23 weeks of gestation: a European register-based study.

Garne E, Khoshnood B, Loane M, Boyd P, Dolk H; EUROCAT Working Group.

BJOG. 2010 May;117(6):660-6. doi: 10.1111/j.1471-0528.2010.02531.x.

6.

Trends in the prevalence, risk and pregnancy outcome of multiple births with congenital anomaly: a registry-based study in 14 European countries 1984-2007.

Boyle B, McConkey R, Garne E, Loane M, Addor MC, Bakker MK, Boyd PA, Gatt M, Greenlees R, Haeusler M, Klungsøyr K, Latos-Bielenska A, Lelong N, McDonnell R, Métneki J, Mullaney C, Nelen V, O'Mahony M, Pierini A, Rankin J, Rissmann A, Tucker D, Wellesley D, Dolk H.

BJOG. 2013 May;120(6):707-16. doi: 10.1111/1471-0528.12146. Epub 2013 Feb 6.

7.

Congenital hydrocephalus--prevalence, prenatal diagnosis and outcome of pregnancy in four European regions.

Garne E, Loane M, Addor MC, Boyd PA, Barisic I, Dolk H.

Eur J Paediatr Neurol. 2010 Mar;14(2):150-5. doi: 10.1016/j.ejpn.2009.03.005. Epub 2009 May 2.

PMID:
19410489
8.

Estimating Global Burden of Disease due to congenital anomaly: an analysis of European data.

Boyle B, Addor MC, Arriola L, Barisic I, Bianchi F, Csáky-Szunyogh M, de Walle HEK, Dias CM, Draper E, Gatt M, Garne E, Haeusler M, Källén K, Latos-Bielenska A, McDonnell B, Mullaney C, Nelen V, Neville AJ, O'Mahony M, Queisser-Wahrendorf A, Randrianaivo H, Rankin J, Rissmann A, Ritvanen A, Rounding C, Tucker D, Verellen-Dumoulin C, Wellesley D, Wreyford B, Zymak-Zakutnia N, Dolk H.

Arch Dis Child Fetal Neonatal Ed. 2018 Jan;103(1):F22-F28. doi: 10.1136/archdischild-2016-311845. Epub 2017 Jun 30.

9.

Epidemiology of multiple congenital anomalies in Europe: a EUROCAT population-based registry study.

Calzolari E, Barisic I, Loane M, Morris J, Wellesley D, Dolk H, Addor MC, Arriola L, Bianchi F, Neville AJ, Budd JL, Klungsoyr K, Khoshnood B, McDonnell B, Nelen V, Queisser-Luft A, Rankin J, Rissmann A, Rounding C, Tucker D, Verellen-Dumoulin C, de Walle H, Garne E.

Birth Defects Res A Clin Mol Teratol. 2014 Apr;100(4):270-6. doi: 10.1002/bdra.23240. Epub 2014 Apr 11.

PMID:
24723551
10.

Sex chromosome trisomies in Europe: prevalence, prenatal detection and outcome of pregnancy.

Boyd PA, Loane M, Garne E, Khoshnood B, Dolk H; EUROCAT working group.

Eur J Hum Genet. 2011 Feb;19(2):231-4. doi: 10.1038/ejhg.2010.148. Epub 2010 Aug 25.

11.

Major congenital anomalies in a Danish region.

Garne E, Hansen AV, Birkelund AS, Andersen AM.

Dan Med J. 2014 Jun;61(6):A4825.

PMID:
24947618
12.

Congenital clubfoot in Europe: A population-based study.

Wang H, Barisic I, Loane M, Addor MC, Bailey LM, Gatt M, Klungsoyr K, Mokoroa O, Nelen V, Neville AJ, O'Mahony M, Pierini A, Rissmann A, Verellen-Dumoulin C, de Walle HEK, Wiesel A, Wisniewska K, de Jong-van den Berg LTW, Dolk H, Khoshnood B, Garne E.

Am J Med Genet A. 2019 Apr;179(4):595-601. doi: 10.1002/ajmg.a.61067. Epub 2019 Feb 10.

PMID:
30740879
13.

[Prevalence of selected congenital anomalies in the Czech Republic: renal and cardiac anomalies and congenital chromosomal aberrations].

Šípek A, Gregor V, Horáček J, Šípek A Jr, Langhammer P.

Epidemiol Mikrobiol Imunol. 2013 Sep;62(3):112-28. Czech.

PMID:
24116699
14.

Prevalence of microcephaly in Europe: population based study.

Morris JK, Rankin J, Garne E, Loane M, Greenlees R, Addor MC, Arriola L, Barisic I, Bergman JE, Csaky-Szunyogh M, Dias C, Draper ES, Gatt M, Khoshnood B, Klungsoyr K, Kurinczuk JJ, Lynch C, McDonnell R, Nelen V, Neville AJ, O'Mahony MT, Pierini A, Randrianaivo H, Rissmann A, Tucker D, Verellen-Dumoulin C, de Walle HE, Wellesley D, Wiesel A, Dolk H.

BMJ. 2016 Sep 13;354:i4721. doi: 10.1136/bmj.i4721.

15.

Oesophageal atresia: prevalence, prenatal diagnosis and associated anomalies in 23 European regions.

Pedersen RN, Calzolari E, Husby S, Garne E; EUROCAT Working group.

Arch Dis Child. 2012 Mar;97(3):227-32. doi: 10.1136/archdischild-2011-300597. Epub 2012 Jan 13.

PMID:
22247246
16.

Congenital heart defects in La Réunion Island: a 6-year survey within a EUROCAT-affiliated congenital anomalies registry.

Bourdial H, Jamal-Bey K, Edmar A, Caillet D, Wuillai F, Bernede-Bauduin C, Boumahni B, Robillard PY, Kauffmann E, Laffitte A, Touret Y, Cuillier F, Fourmaintraux A, Alessandri JL, Gérardin P, Randrianaivo H.

Cardiol Young. 2012 Oct;22(5):547-57. doi: 10.1017/S1047951112000054. Epub 2012 Feb 13.

PMID:
22325463
17.

Prevalence and associated factors for agenesis of corpus callosum in Emilia Romagna (1981-2015).

Ballardini E, Marino P, Maietti E, Astolfi G, Neville AJ.

Eur J Med Genet. 2018 Sep;61(9):524-530. doi: 10.1016/j.ejmg.2018.06.004. Epub 2018 Jun 12.

PMID:
29902589
18.

Arthrogryposis multiplexa congenita: an epidemiologic study of nearly 9 million births in 24 EUROCAT registers.

Hoff JM, Loane M, Gilhus NE, Rasmussen S, Daltveit AK.

Eur J Obstet Gynecol Reprod Biol. 2011 Dec;159(2):347-50. doi: 10.1016/j.ejogrb.2011.09.027. Epub 2011 Oct 17.

PMID:
22005589
19.

A sustainable solution for the activities of the European network for surveillance of congenital anomalies: EUROCAT as part of the EU Platform on Rare Diseases Registration.

Kinsner-Ovaskainen A, Lanzoni M, Garne E, Loane M, Morris J, Neville A, Nicholl C, Rankin J, Rissmann A, Tucker D, Martin S.

Eur J Med Genet. 2018 Sep;61(9):513-517. doi: 10.1016/j.ejmg.2018.03.008. Epub 2018 Mar 27. Review.

20.

Improved prenatal detection of chromosomal anomalies.

Frøslev-Friis C, Hjort-Pedersen K, Henriques CU, Krogh LN, Garne E.

Dan Med Bull. 2011 Aug;58(8):A4293.

PMID:
21827720

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