10 results on '"Zymak-Zakutnia, Natalya"'
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2. Prevalence of valproate syndrome in Europe from 2005 to 2014: A registry based multi-centre study
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Morris, Joan K., Garne, Ester, Loane, Maria, Addor, Marie-Claude, Barisic, Ingeborg, Bianchi, Fabrizio, Gatt, Miriam, Lanzoni, Monica, Lynch, Catherine, Mokoroa, Olatz, Nelen, Vera, Neville, Amanda, O'Mahony, Mary T., Randrianaivo-Ranjatoelina, Hanitra, Rissmann, Anke, Tucker, David, de Walle, H.E.K., Zymak-Zakutnia, Natalya, and Rankin, Judith
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- 2018
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3. Maternal age and the prevalence of congenital heart defects in Europe, 1995–2015: A register‐based study
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Mamasoula, Chrysovalanto, primary, Bigirumurame, Theophile, additional, Chadwick, Thomas, additional, Addor, Marie‐Claude, additional, Cavero‐Carbonell, Clara, additional, Dias, Carlos M., additional, Echevarría‐González‐de‐Garibay, Luis‐Javier, additional, Gatt, Miriam, additional, Khoshnood, Babak, additional, Klungsoyr, Kari, additional, Randall, Kay, additional, Stoianova, Sylvia, additional, Haeusler, Martin, additional, Nelen, Vera, additional, Neville, Amanda J., additional, Perthus, Isabelle, additional, Pierini, Anna, additional, Bertaut‐Nativel, Bénédicte, additional, Rissmann, Anke, additional, Rouget, Florence, additional, Schaub, Bruno, additional, Tucker, David, additional, Wellesley, Diana, additional, Zymak‐Zakutnia, Natalya, additional, Barisic, Ingeborg, additional, de Walle, Hermien E.K., additional, Lanzoni, Monica, additional, Sayers, Gerardine, additional, Mullaney, Carmel, additional, Pennington, Lindsay, additional, and Rankin, Judith, additional
- Published
- 2023
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4. Prevalence of congenital heart defects in Europe, 2008–2015: A registry‐based study
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Mamasoula, Chrysovalanto, primary, Addor, Marie‐Claude, additional, Carbonell, Clara Cavero, additional, Dias, Carlos M., additional, Echevarría‐González‐de‐Garibay, Luis‐Javier, additional, Gatt, Miriam, additional, Khoshnood, Babak, additional, Klungsoyr, Kari, additional, Randall, Kay, additional, Stoianova, Sylvia, additional, Haeusler, Martin, additional, Nelen, Vera, additional, Neville, Amanda J., additional, Perthus, Isabelle, additional, Pierini, Anna, additional, Bertaut‐Nativel, Bénédicte, additional, Rissmann, Anke, additional, Rouget, Florence, additional, Schaub, Bruno, additional, Tucker, David, additional, Wellesley, Diana, additional, Zymak‐Zakutnia, Natalya, additional, Barisic, Ingeborg, additional, de Walle, Hermien E. K., additional, Lanzoni, Monica, additional, Mullaney, Carmel, additional, Pennington, Lindsay, additional, and Rankin, Judith, additional
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- 2022
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5. Epidemiology of hypospadias in Europe: a registry-based study
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Bergman, Jorieke E. H., Loane, Maria, Vrijheid, Martine, Pierini, Anna, Nijman, Rien J. M., Addor, Marie-Claude, Barisic, Ingeborg, Béres, Judit, Braz, Paula, Budd, Judith, Delaney, Virginia, Gatt, Miriam, Khoshnood, Babak, Klungsøyr, Kari, Martos, Carmen, Mullaney, Carmel, Nelen, Vera, Neville, Amanda J., O’Mahony, Mary, Queisser-Luft, Annette, Randrianaivo, Hanitra, Rissmann, Anke, Rounding, Catherine, Tucker, David, Wellesley, Diana, Zymak-Zakutnia, Natalya, Bakker, Marian K., and de Walle, Hermien E. K.
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- 2015
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6. Maternal risk factors for the VACTERL association: A EUROCAT case–control study
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van de Putte, Romy, primary, van Rooij, Iris A.L.M., additional, Haanappel, Cynthia P., additional, Marcelis, Carlo L.M., additional, Brunner, Han G., additional, Addor, Marie‐Claude, additional, Cavero‐Carbonell, Clara, additional, Dias, Carlos M., additional, Draper, Elizabeth S., additional, Etxebarriarteun, Larraitz, additional, Gatt, Miriam, additional, Khoshnood, Babak, additional, Kinsner‐Ovaskainen, Agnieszka, additional, Klungsoyr, Kari, additional, Kurinczuk, Jenny J., additional, Latos‐Bielenska, Anna, additional, Luyt, Karen, additional, O'Mahony, Mary T., additional, Miller, Nicola, additional, Mullaney, Carmel, additional, Nelen, Vera, additional, Neville, Amanda J., additional, Perthus, Isabelle, additional, Pierini, Anna, additional, Randrianaivo, Hanitra, additional, Rankin, Judith, additional, Rissmann, Anke, additional, Rouget, Florence, additional, Schaub, Bruno, additional, Tucker, David, additional, Wellesley, Diana, additional, Wiesel, Awi, additional, Zymak‐Zakutnia, Natalya, additional, Loane, Maria, additional, Barisic, Ingeborg, additional, de Walle, Hermien E.K., additional, Bergman, Jorieke E.H., additional, and Roeleveld, Nel, additional
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- 2020
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7. Spectrum of congenital anomalies among VACTERL cases: a EUROCAT population-based study
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van de Putte, Romy, primary, van Rooij, Iris A. L. M., additional, Marcelis, Carlo L. M., additional, Guo, Michel, additional, Brunner, Han G., additional, Addor, Marie-Claude, additional, Cavero-Carbonell, Clara, additional, Dias, Carlos M., additional, Draper, Elizabeth S., additional, Etxebarriarteun, Larraitz, additional, Gatt, Miriam, additional, Haeusler, Martin, additional, Khoshnood, Babak, additional, Klungsoyr, Kari, additional, Kurinczuk, Jenny J., additional, Lanzoni, Monica, additional, Latos-Bielenska, Anna, additional, Luyt, Karen, additional, O’Mahony, Mary T., additional, Miller, Nicola, additional, Mullaney, Carmel, additional, Nelen, Vera, additional, Neville, Amanda J., additional, Perthus, Isabelle, additional, Pierini, Anna, additional, Randrianaivo, Hanitra, additional, Rankin, Judith, additional, Rissmann, Anke, additional, Rouget, Florence, additional, Schaub, Bruno, additional, Tucker, David, additional, Wellesley, Diana, additional, Wiesel, Awi, additional, Zymak-Zakutnia, Natalya, additional, Loane, Maria, additional, Barisic, Ingeborg, additional, de Walle, Hermien E. K., additional, Roeleveld, Nel, additional, and Bergman, Jorieke E. H., additional
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- 2019
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8. Congenital Anomalies Associated with Trisomy 18 or Trisomy 13: A Registry-Based Study in 16 European Countries, 2000-2011
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Springett, Anna, Wellesley, Diana, Greenlees, Ruth, Loane, Maria, Addor, Marie-Claude, Arriola, Larraitz, Bergman, Jorieke, Cavero-Carbonell, Clara, Csaky-Szunyogh, Melinda, Draper, Elizabeth S., Garne, Ester, Gatt, Miriam, Haeusler, Martin, Khoshnood, Babak, Klungsoyr, Kari, Lynch, Catherine, Dias, Carlos Matias, McDonnell, Robert, Nelen, Vera, O'Mahony, Mary, Pierini, Anna, Queisser-Luft, Annette, Rankin, Judith, Rissmann, Anke, Rounding, Catherine, Stoianova, Sylvia, Tuckerz, David, Zymak-Zakutnia, Natalya, Morris, Joan K., and Reproductive Origins of Adult Health and Disease (ROAHD)
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Adult ,Heart Defects, Congenital ,Male ,SEX-DIFFERENCES ,Time Factors ,Adolescent ,TRISOMIES ,Pregnancy Complications/diagnosis ,Gestational Age ,Trisomy ,Nervous System Malformations ,Europe/epidemiology ,Congenital Abnormalities ,Nervous System Malformations/diagnosis ,Young Adult ,Pregnancy ,Prenatal Diagnosis ,Prevalence ,Humans ,trisomy 18 ,MALFORMATIONS ,DOWN-SYNDROME ,Registries ,Fetal Death ,trisomy 13 ,Chromosomes, Human, Pair 18/genetics ,Chromosomes, Human, Pair 13 ,MORTALITY ,cardiac anomalies ,Registries/statistics & numerical data ,Infant, Newborn ,NATURAL-HISTORY ,DEFECTS ,Prognosis ,Trisomy/genetics ,Congenital Abnormalities/diagnosis ,Europe ,Pregnancy Complications ,Patau syndrome ,SURVIVAL ,Heart Defects, Congenital/diagnosis ,MATERNAL AGE ,Chromosomes, Human, Pair 13/genetics ,Female ,Chromosomes, Human, Pair 18 ,Trisomy 18 Syndrome ,Edwards syndrome - Abstract
The aim of this study was to examine the prevalence of trisomies 18 and 13 in Europe and the prevalence of associated anomalies. Twenty-five population-based registries in 16 European countries provided data from 2000-2011. Cases included live births, fetal deaths (20+ weeks' gestation), and terminations of pregnancy for fetal anomaly (TOPFAs). The prevalence of associated anomalies was reported in live births. The prevalence of trisomy 18 and trisomy 13 were 4.8 (95%CI: 4.7-5.0) and 1.9 (95%CI: 1.8-2.0) per 10,000 total births. Seventy three percent of cases with trisomy 18 or trisomy 13 resulted in a TOPFA. Amongst 468 live born babies with trisomy 18, 80% (76-83%) had a cardiac anomaly, 21% (17-25%) had a nervous system anomaly, 8% (6-11%) had esophageal atresia and 10% (8-13%) had an orofacial cleft. Amongst 240 Live born babies with trisomy 13, 57% (51-64%) had a cardiac anomaly, 39% (33-46%) had a nervous system anomaly, 30% (24-36%) had an eye anomaly, 44% (37-50%) had polydactyly and 45% (39-52%) had an orofacial cleft. For babies with trisomy 18 boys were less likely to have a cardiac anomaly compared with girls (OR = 0.48 (0.30-0.77) and with trisomy 13 were less likely to have a nervous system anomaly [OR = 0.46 (0.27-0.77)]. Babies with trisomy 18 or trisomy 13 do have a high proportion of associated anomalies with the distribution of anomalies being different in boys and girls. © 2015 Wiley Periodicals, Inc.
- Published
- 2015
9. Hirschsprung's disease prevalence in Europe: A register based study
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Best, Kate E., primary, Addor, Marie-Claude, additional, Arriola, Larraitz, additional, Balku, Eszter, additional, Barisic, Ingeborg, additional, Bianchi, Fabrizio, additional, Calzolari, Elisa, additional, Curran, Rhonda, additional, Doray, Berenice, additional, Draper, Elizabeth, additional, Garne, Ester, additional, Gatt, Miriam, additional, Haeusler, Martin, additional, Bergman, Jorieke, additional, Khoshnood, Babak, additional, Klungsoyr, Kari, additional, Martos, Carmen, additional, Materna-Kiryluk, Anna, additional, Matias Dias, Carlos, additional, McDonnell, Bob, additional, Mullaney, Carmel, additional, Nelen, Vera, additional, O'Mahony, Mary, additional, Queisser-Luft, Annette, additional, Randrianaivo, Hanitra, additional, Rissmann, Anke, additional, Rounding, Catherine, additional, Sipek, Antonin, additional, Thompson, Rosie, additional, Tucker, David, additional, Wellesley, Diana, additional, Zymak-Zakutnia, Natalya, additional, and Rankin, Judith, additional
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- 2014
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10. Congenital anomalies associated with trisomy 18 or trisomy 13: A registry-based study in 16 European countries, 2000-2011.
- Author
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Springett A, Wellesley D, Greenlees R, Loane M, Addor MC, Arriola L, Bergman J, Cavero-Carbonell C, Csaky-Szunyogh M, Draper ES, Garne E, Gatt M, Haeusler M, Khoshnood B, Klungsoyr K, Lynch C, Dias CM, McDonnell R, Nelen V, O'Mahony M, Pierini A, Queisser-Luft A, Rankin J, Rissmann A, Rounding C, Stoianova S, Tuckerz D, Zymak-Zakutnia N, and Morris JK
- Subjects
- Adolescent, Adult, Chromosomes, Human, Pair 18 genetics, Congenital Abnormalities diagnosis, Europe epidemiology, Female, Fetal Death, Gestational Age, Heart Defects, Congenital diagnosis, Heart Defects, Congenital epidemiology, Heart Defects, Congenital genetics, Humans, Infant, Newborn, Male, Nervous System Malformations diagnosis, Nervous System Malformations epidemiology, Nervous System Malformations genetics, Pregnancy, Pregnancy Complications diagnosis, Prenatal Diagnosis, Prevalence, Prognosis, Time Factors, Trisomy 18 Syndrome, Young Adult, Chromosomes, Human, Pair 13 genetics, Congenital Abnormalities epidemiology, Congenital Abnormalities genetics, Pregnancy Complications epidemiology, Pregnancy Complications genetics, Registries statistics & numerical data, Trisomy genetics
- Abstract
The aim of this study was to examine the prevalence of trisomies 18 and 13 in Europe and the prevalence of associated anomalies. Twenty-five population-based registries in 16 European countries provided data from 2000-2011. Cases included live births, fetal deaths (20+ weeks' gestation), and terminations of pregnancy for fetal anomaly (TOPFAs). The prevalence of associated anomalies was reported in live births. The prevalence of trisomy 18 and trisomy 13 were 4.8 (95%CI: 4.7-5.0) and 1.9 (95%CI: 1.8-2.0) per 10,000 total births. Seventy three percent of cases with trisomy 18 or trisomy 13 resulted in a TOPFA. Amongst 468 live born babies with trisomy 18, 80% (76-83%) had a cardiac anomaly, 21% (17-25%) had a nervous system anomaly, 8% (6-11%) had esophageal atresia and 10% (8-13%) had an orofacial cleft. Amongst 240 Live born babies with trisomy 13, 57% (51-64%) had a cardiac anomaly, 39% (33-46%) had a nervous system anomaly, 30% (24-36%) had an eye anomaly, 44% (37-50%) had polydactyly and 45% (39-52%) had an orofacial cleft. For babies with trisomy 18 boys were less likely to have a cardiac anomaly compared with girls (OR = 0.48 (0.30-0.77) and with trisomy 13 were less likely to have a nervous system anomaly [OR = 0.46 (0.27-0.77)]. Babies with trisomy 18 or trisomy 13 do have a high proportion of associated anomalies with the distribution of anomalies being different in boys and girls., (© 2015 Wiley Periodicals, Inc.)
- Published
- 2015
- Full Text
- View/download PDF
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