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308 results

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Page 1
Prenatal diagnosis and prevalence of critical congenital heart defects: an international retrospective cohort study.
Bakker MK, Bergman JEH, Krikov S, Amar E, Cocchi G, Cragan J, de Walle HEK, Gatt M, Groisman B, Liu S, Nembhard WN, Pierini A, Rissmann A, Chidambarathanu S, Sipek A Jr, Szabova E, Tagliabue G, Tucker D, Mastroiacovo P, Botto LD. Bakker MK, et al. Among authors: gatt m. BMJ Open. 2019 Jul 2;9(7):e028139. doi: 10.1136/bmjopen-2018-028139. BMJ Open. 2019. PMID: 31270117 Free PMC article.
Prenatal diagnosis of severe structural congenital malformations in Europe.
Garne E, Loane M, Dolk H, De Vigan C, Scarano G, Tucker D, Stoll C, Gener B, Pierini A, Nelen V, Rösch C, Gillerot Y, Feijoo M, Tincheva R, Queisser-Luft A, Addor MC, Mosquera C, Gatt M, Barisic I. Garne E, et al. Among authors: gatt m. Ultrasound Obstet Gynecol. 2005 Jan;25(1):6-11. doi: 10.1002/uog.1784. Ultrasound Obstet Gynecol. 2005. PMID: 15619321 Free 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
Preventing neural tube defects in Europe: a missed opportunity.
Busby A, Abramsky L, Dolk H, Armstrong B, Addor MC, Anneren G, Armstrong N, Baguette A, Barisic I, Berghold A, Bianca S, Braz P, Calzolari E, Christiansen M, Cocchi G, Daltveit AK, De Walle H, Edwards G, Gatt M, Gener B, Gillerot Y, Gjergja R, Goujard J, Haeusler M, Latos-Bielenska A, McDonnell R, Neville A, Olars B, Portillo I, Ritvanen A, Robert-Gnansia E, Rösch C, Scarano G, Steinbicker V. Busby A, et al. Among authors: gatt m. Reprod Toxicol. 2005 Sep-Oct;20(3):393-402. doi: 10.1016/j.reprotox.2005.03.009. Reprod Toxicol. 2005. PMID: 15927445
Survey of informed consent for registration of congenital anomalies in Europe.
Busby A, Ritvanen A, Dolk H, Armstrong N, De Walle H, Riaño-Galán I, Gatt M, McDonnell R, Nelen V, Stone D. Busby A, et al. Among authors: gatt m. BMJ. 2005 Jul 16;331(7509):140-1. doi: 10.1136/bmj.331.7509.140. BMJ. 2005. PMID: 16020855 Free PMC article. No abstract available.
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
308 results