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Page 1
Epidemiology of Pierre-Robin sequence in Europe: A population-based EUROCAT study.
Santoro M, Coi A, Barišić I, Pierini A, Addor MC, Baldacci S, Ballardini E, Boban L, Braz P, Cavero-Carbonell C, de Walle HEK, Draper ES, Gatt M, Haeusler M, Klungsøyr K, Kurinczuk JJ, Materna-Kiryluk A, Lanzoni M, Lelong N, Luyt K, Mokoroa O, Mullaney C, Nelen V, O'Mahony MT, Perthus I, Randrianaivo H, Rankin J, Rissmann A, Rouget F, Schaub B, Tucker D, Wellesley D, Zymak-Zakutnia N, Garne E. Santoro M, et al. Among authors: lanzoni m. Paediatr Perinat Epidemiol. 2021 Sep;35(5):530-539. doi: 10.1111/ppe.12776. Epub 2021 Jun 16. Paediatr Perinat Epidemiol. 2021. PMID: 34132407
Epidemiology of septo-optic dysplasia with focus on prevalence and maternal age - A EUROCAT study.
Garne E, Rissmann A, Addor MC, Barisic I, Bergman J, 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, Rouget F, Schaub B, Tucker D, Verellen-Dumoulin C, Wellesley D, Wiesel A, Zymak-Zakutnia N, Lanzoni M, Morris JK. Garne E, et al. Among authors: lanzoni m. Eur J Med Genet. 2018 Sep;61(9):483-488. doi: 10.1016/j.ejmg.2018.05.010. Epub 2018 May 10. Eur J Med Genet. 2018. PMID: 29753093
Prevalence of valproate syndrome in Europe from 2005 to 2014: A registry based multi-centre study.
Morris JK, Garne E, Loane M, Addor MC, Barisic I, Bianchi F, Gatt M, Lanzoni M, Lynch C, Mokoroa O, Nelen V, Neville A, O'Mahony MT, Randrianaivo-Ranjatoelina H, Rissmann A, Tucker D, de Walle HEK, Zymak-Zakutnia N, Rankin J. Morris JK, et al. Among authors: lanzoni m. Eur J Med Genet. 2018 Sep;61(9):479-482. doi: 10.1016/j.ejmg.2018.05.008. Epub 2018 May 18. Eur J Med Genet. 2018. PMID: 29753923
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. Morris JK, et al. Among authors: lanzoni m. Arch Dis Child. 2019 Dec;104(12):1181-1187. doi: 10.1136/archdischild-2018-316733. Epub 2019 Jun 26. Arch Dis Child. 2019. PMID: 31243007
Epidemiology of achondroplasia: A population-based study in Europe.
Coi A, Santoro M, Garne E, Pierini A, Addor MC, Alessandri JL, Bergman JEH, Bianchi F, Boban L, Braz P, Cavero-Carbonell C, Gatt M, Haeusler M, Klungsøyr K, Kurinczuk JJ, Lanzoni M, Lelong N, Luyt K, Mokoroa O, Mullaney C, Nelen V, Neville AJ, O'Mahony MT, Perthus I, Rankin J, Rissmann A, Rouget F, Schaub B, Tucker D, Wellesley D, Wisniewska K, Zymak-Zakutnia N, Barišić I. Coi A, et al. Among authors: lanzoni m. Am J Med Genet A. 2019 Sep;179(9):1791-1798. doi: 10.1002/ajmg.a.61289. Epub 2019 Jul 11. Am J Med Genet A. 2019. PMID: 31294928
Spectrum of congenital anomalies among VACTERL cases: a EUROCAT population-based study.
van de Putte R, van Rooij IALM, Marcelis CLM, Guo M, Brunner HG, Addor MC, Cavero-Carbonell C, Dias CM, Draper ES, Etxebarriarteun L, Gatt M, Haeusler M, Khoshnood B, Klungsoyr K, Kurinczuk JJ, Lanzoni M, Latos-Bielenska A, Luyt K, O'Mahony MT, Miller N, Mullaney C, Nelen V, Neville AJ, Perthus I, Pierini A, Randrianaivo H, Rankin J, Rissmann A, Rouget F, Schaub B, Tucker D, Wellesley D, Wiesel A, Zymak-Zakutnia N, Loane M, Barisic I, de Walle HEK, Roeleveld N, Bergman JEH. van de Putte R, et al. Among authors: lanzoni m. Pediatr Res. 2020 Feb;87(3):541-549. doi: 10.1038/s41390-019-0561-y. Epub 2019 Sep 9. Pediatr Res. 2020. PMID: 31499513
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. Kinsner-Ovaskainen A, et al. Among authors: lanzoni m. Eur J Med Genet. 2018 Sep;61(9):513-517. doi: 10.1016/j.ejmg.2018.03.008. Epub 2018 Mar 27. Eur J Med Genet. 2018. PMID: 29597096 Free article. Review.
Beckwith Wiedemann syndrome: A population-based study on prevalence, prenatal diagnosis, associated anomalies and survival in Europe.
Barisic I, Boban L, Akhmedzhanova D, Bergman JEH, Cavero-Carbonell C, Grinfelde I, Materna-Kiryluk A, Latos-Bieleńska A, Randrianaivo H, Zymak-Zakutnya N, Sansovic I, Lanzoni M, Morris JK. Barisic I, et al. Among authors: lanzoni m. Eur J Med Genet. 2018 Sep;61(9):499-507. doi: 10.1016/j.ejmg.2018.05.014. Epub 2018 May 31. Eur J Med Genet. 2018. PMID: 29753922
EUROCAT: an update on its functions and activities.
Tucker FD, Morris JK; JRC Management Committee; Neville A, Garne E, Kinsner-Ovaskainen A, Lanzoni M, Loane MA, Martin S, Nicholl C, Rankin J, Rissmann AK. Tucker FD, et al. Among authors: lanzoni m. J Community Genet. 2018 Oct;9(4):407-410. doi: 10.1007/s12687-018-0367-3. Epub 2018 May 7. J Community Genet. 2018. PMID: 29736796 Free PMC article.
Correction to: EUROCAT: an update on its functions and activities.
Tucker FD, Morris JK; JRC-EUROCAT Management Committee; Neville A, Garne E, Kinsner-Ovaskainen A, Lanzoni M, Loane MA, Martin S, Nicholl C, Rankin J, Rissmann AK. Tucker FD, et al. Among authors: lanzoni m. J Community Genet. 2019 Apr;10(2):323. doi: 10.1007/s12687-018-0392-2. J Community Genet. 2019. PMID: 30361973 Free PMC article.
71 results