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A multi-country study of prevalence and early childhood mortality among children with omphalocele.
Nembhard WN, Bergman JEH, Politis MD, Arteaga-Vázquez J, Bermejo-Sánchez E, Canfield MA, Cragan JD, Dastgiri S, de Walle HEK, Feldkamp ML, Nance A, Gatt M, Groisman B, Hurtado-Villa P, Kallén K, Landau D, Lelong N, Lopez-Camelo J, Martinez L, Morgan M, Pierini A, Rissmann A, Šípek A, Szabova E, Tagliabue G, Wertelecki W, Zarante I, Bakker MK, Kancherla V, Mastroiacovo P. Nembhard WN, et al. Among authors: gatt m. Birth Defects Res. 2020 Dec;112(20):1787-1801. doi: 10.1002/bdr2.1822. Epub 2020 Oct 17. Birth Defects Res. 2020. PMID: 33067932 Free PMC article.
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. Among authors: gatt m. 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
Gastroschisis and associated defects: an international study.
Mastroiacovo P, Lisi A, Castilla EE, Martínez-Frías ML, Bermejo E, Marengo L, Kucik J, Siffel C, Halliday J, Gatt M, Annerèn G, Bianchi F, Canessa MA, Danderfer R, de Walle H, Harris J, Li Z, Lowry RB, McDonell R, Merlob P, Metneki J, Mutchinick O, Robert-Gnansia E, Scarano G, Sipek A, Pötzsch S, Szabova E, Yevtushok L. Mastroiacovo P, et al. Among authors: gatt m. Am J Med Genet A. 2007 Apr 1;143A(7):660-71. doi: 10.1002/ajmg.a.31607. Am J Med Genet A. 2007. PMID: 17357116
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: gatt m. 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
Maternal age-specific risk of non-chromosomal anomalies.
Loane M, Dolk H, Morris JK; EUROCAT Working Group. Loane M, et al. BJOG. 2009 Jul;116(8):1111-9. doi: 10.1111/j.1471-0528.2009.02227.x. Epub 2009 May 29. BJOG. 2009. PMID: 19485989 Free article.
Valproic acid monotherapy in pregnancy and major congenital malformations.
Jentink J, Loane MA, Dolk H, Barisic I, Garne E, Morris JK, de Jong-van den Berg LT; EUROCAT Antiepileptic Study Working Group. Jentink J, et al. N Engl J Med. 2010 Jun 10;362(23):2185-93. doi: 10.1056/NEJMoa0907328. N Engl J Med. 2010. PMID: 20558369 Free article. Review.
How valid are the rates of Down syndrome internationally? Findings from the International Clearinghouse for Birth Defects Surveillance and Research.
Leoncini E, Botto LD, Cocchi G, Annerén G, Bower C, Halliday J, Amar E, Bakker MK, Bianca S, Canessa Tapia MA, Castilla EE, Csáky-Szunyogh M, Dastgiri S, Feldkamp ML, Gatt M, Hirahara F, Landau D, Lowry RB, Marengo L, McDonnell R, Mathew TM, Morgan M, Mutchinick OM, Pierini A, Poetzsch S, Ritvanen A, Scarano G, Siffel C, Sípek A, Szabova E, Tagliabue G, Vollset SE, Wertelecki W, Zhuchenko L, Mastroiacovo P. Leoncini E, et al. Among authors: gatt m. Am J Med Genet A. 2010 Jul;152A(7):1670-80. doi: 10.1002/ajmg.a.33493. Am J Med Genet A. 2010. PMID: 20578135 Free article.
303 results