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Page 1
Frequency of holoprosencephaly in the International Clearinghouse Birth Defects Surveillance Systems: searching for population variations.
Leoncini E, Baranello G, Orioli IM, Annerén G, Bakker M, Bianchi F, Bower C, Canfield MA, Castilla EE, Cocchi G, Correa A, De Vigan C, Doray B, Feldkamp ML, Gatt M, Irgens LM, Lowry RB, Maraschini A, Mc Donnell R, Morgan M, Mutchinick O, Poetzsch S, Riley M, Ritvanen A, Gnansia ER, Scarano G, Sipek A, Tenconi R, Mastroiacovo P. Leoncini E, et al. Among authors: irgens lm. Birth Defects Res A Clin Mol Teratol. 2008 Aug;82(8):585-91. doi: 10.1002/bdra.20479. Birth Defects Res A Clin Mol Teratol. 2008. PMID: 18566978
Sex and congenital malformations: an international perspective.
Lisi A, Botto LD, Rittler M, Castilla E, Bianca S, Bianchi F, Botting B, De Walle H, Erickson JD, Gatt M, De Vigan C, Irgens L, Johnson W, Lancaster P, Merlob P, Mutchinick OM, Ritvanen A, Robert E, Scarano G, Stoll C, Mastroiacovo P. Lisi A, et al. Am J Med Genet A. 2005 Apr 1;134A(1):49-57. doi: 10.1002/ajmg.a.30514. Am J Med Genet A. 2005. PMID: 15704121
International retrospective cohort study of neural tube defects in relation to folic acid recommendations: are the recommendations working?
Botto LD, Lisi A, Robert-Gnansia E, Erickson JD, Vollset SE, Mastroiacovo P, Botting B, Cocchi G, de Vigan C, de Walle H, Feijoo M, Irgens LM, McDonnell B, Merlob P, Ritvanen A, Scarano G, Siffel C, Metneki J, Stoll C, Smithells R, Goujard J. Botto LD, et al. Among authors: irgens lm. BMJ. 2005 Mar 12;330(7491):571. doi: 10.1136/bmj.38336.664352.82. Epub 2005 Feb 18. BMJ. 2005. PMID: 15722368 Free PMC article.
Trends of selected malformations in relation to folic acid recommendations and fortification: an international assessment.
Botto LD, Lisi A, Bower C, Canfield MA, Dattani N, De Vigan C, De Walle H, Erickson DJ, Halliday J, Irgens LM, Lowry RB, McDonnell R, Metneki J, Poetzsch S, Ritvanen A, Robert-Gnansia E, Siffel C, Stoll C, Mastroiacovo P. Botto LD, et al. Among authors: irgens lm. Birth Defects Res A Clin Mol Teratol. 2006 Oct;76(10):693-705. doi: 10.1002/bdra.20307. Birth Defects Res A Clin Mol Teratol. 2006. PMID: 17029289
The spectrum of congenital anomalies of the VATER association: an international study.
Botto LD, Khoury MJ, Mastroiacovo P, Castilla EE, Moore CA, Skjaerven R, Mutchinick OM, Borman B, Cocchi G, Czeizel AE, Goujard J, Irgens LM, Lancaster PA, Martínez-Frías ML, Merlob P, Ruusinen A, Stoll C, Sumiyoshi Y. Botto LD, et al. Among authors: irgens lm. Am J Med Genet. 1997 Jul 11;71(1):8-15. doi: 10.1002/(sici)1096-8628(19970711)71:1<8::aid-ajmg2>3.0.co;2-v. Am J Med Genet. 1997. PMID: 9215761
European recommendations for primary prevention of congenital anomalies: a joined effort of EUROCAT and EUROPLAN projects to facilitate inclusion of this topic in the National Rare Disease Plans.
Taruscio D, Arriola L, Baldi F, Barisic I, Bermejo-Sánchez E, Bianchi F, Calzolari E, Carbone P, Curran R, Garne E, Gatt M, Latos-Bieleńska A, Khoshnood B, Irgens L, Mantovani A, Martínez-Frías ML, Neville A, Rißmann A, Ruggeri S, Wellesley D, Dolk H. Taruscio D, et al. Public Health Genomics. 2014;17(2):115-23. doi: 10.1159/000360602. Epub 2014 Apr 3. Public Health Genomics. 2014. PMID: 24714026
249 results