Publications (922)
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Prevalance and patterns of antidepressant use among women of reproductive age in Northern Ireland (NI)
Prevalance and patterns of antidepressant use among women of reproductive age in Northern Ireland (NI)
Wemakor, A, Dolk H, Casson K, de Jong-van den Berg L
Pharmacoepidemiology and Drug Safety, 2012 , 21: (3) 426
Subjects: Medication During Pregnancy, Prevalence & Perinatal Mortality, Prevention & Risk Factors, Survival & Neuro Development Outcomes -
Prevalence of esophageal atresia among 18 International Birth Defects Surveillance Programs
Prevalence of esophageal atresia among 18 International Birth Defects Surveillance Programs
Nassar N, Leoncini E, Amar E, Arteaga-Vazquez J, Bakker M, Bower C, Canfield M, Castilla E, Cocchi G, Correa A, Csaky-Szunyogh M, Feldkamp M, Khoshnood B, Landau D, Lelong N, Lopez-Camelo J, Lowry B, McDonnell R, Merlob P, Metneki J, Morgan M, Mutchinick O, Palmer NM, Rissmann A, Siffel C, Sipek A, Szabova E, Tucker D, Mastroiacovo P
Birth Defects Research (Part A), 2012 , 94: 893 - 899
Subjects: Prenatal Screening & Diagnosis, Prevalence & Perinatal Mortality
Anomalies: Digestive System Anomalies -
Prevalence, timing of diagnosis and mortality of newborns with congenital heart defects: a population-based study
Prevalence, timing of diagnosis and mortality of newborns with congenital heart defects: a population-based study
Khoshnood B, Lelong N, Houyel L, Thieulin A-C, Jouannic J-M, Magnier S, Delezoide A-L, Magny J-F, Rambaud C, Bonnet D, Goffinet F, EPICARD Study Group,
Heart, 2012 , 98: (22) 1667 - 1673
Subjects: Prenatal Screening & Diagnosis, Prevalence & Perinatal Mortality
Anomalies: Congenital Heart Anomalies -
Rare chromosome abnormalities, prevalence and prenatal diagnosis rates from population based congenital anomaly registers in Europe
Rare chromosome abnormalities, prevalence and prenatal diagnosis rates from population based congenital anomaly registers in Europe
Wellesley D, Dolk H, Boyd P, Greenlees R, Haeusler M, Nelen V, Garne E, Khoshnood B, Doray B, Rissmann A, Mullaney C, Calzolari E, Bakker M, Salvador J, Addor M-C, Draper E, Rankin J, Tucker D
European Journal of Human Genetics, 2012 , 20: (5) 521 - 526
Subjects: Prenatal Screening & Diagnosis, Prevalence & Perinatal Mortality -
Rate of preterm birth in pregnant women with vitamin E treatment: a population-based study
Rate of preterm birth in pregnant women with vitamin E treatment: a population-based study
Bartfai Z, Bartfai L, Nedeczky I, Puho EH, Banhidy F, Czeizel AE
Journal of Maternal-Fetal and Neonatal Medicine, 2012 , 25: (6) 575 - 580
Subjects: Medication During Pregnancy, Prevention & Risk Factors -
Schizencephaly prevalence, prenatal diagnosis and clues to etiology: a register-based study
Schizencephaly prevalence, prenatal diagnosis and clues to etiology: a register-based study
Howe DT, Rankin J, Draper E
Ultrasound in Obstetrics and Gynecology, 2012 , 39: (1) 75 - 82
Subjects: Prenatal Screening & Diagnosis, Prevalence & Perinatal Mortality
Anomalies: Nervous System (other than NTD) -
Seasonality of Congenital Anomalies in Europe, from '4th Congress of European Academy of Paediatric Societies', 5-9 October 2012, Istanbul
Seasonality of Congenital Anomalies in Europe, from '4th Congress of European Academy of Paediatric Societies', 5-9 October 2012, Istanbul
Luteijn M, Dolk H and EUROCAT Working Group
Archives of Disease in Childhood, 2012 , 97: (S2) A72 - A73
Subjects: Clusters and Trends, Other, Prevalence & Perinatal Mortality, Surveillance Methodology -
Spectrum of congenital anomalies in pregnancies with pregestational diabetes
Spectrum of congenital anomalies in pregnancies with pregestational diabetes
Garne E, Loane M, Dolk H, Barisic I, Addor M-C, Arriola L, Bakker M, Calzolari E, Dias C M, Doray B, Gatt M, Klungsoyr K, Nelen V, O'Mahony M, Pierini A, Randrianaivo-Ranjatoelina H, Rankin J, Rissmann A, Tucker D, Verellen-Dumoulin C, Wiesel A
Birth Defects Research (Part A), 2012 , 94: 134 - 140
Subjects: Prevention & Risk Factors -
Subtelomeric deletion of chromosome 10p15.3: clinical findings and molecular cytogenic characterization
Subtelomeric deletion of chromosome 10p15.3: clinical findings and molecular cytogenic characterization
DeScipio C, Conlin L, Rosenfeld J, Tepperberg J, Pasion R, Patel A, McDonald MT, Aradhya S, Ho D, Goldstein J, McGuire M, Mulchandani S, Medne L, Rupps R, Serrano AH, Thorland EC, Tsai A, Hilhorst-Hofstee Y, Ruivenkamp C, van Esch H, Addor M-C, et al
American Journal of Medical Genetics Part A, 2012 , 158A: 2152 - 2161
Anomalies: Chromosomal (other than Down Syndrome) -
The evolution of prenatal screening and diagnosis and its impact on an unselected population over an 18-year period.
The evolution of prenatal screening and diagnosis and its impact on an unselected population over an 18-year period.
Boyd P, Rounding C, Chamberlain P, Wellesley D, Kurinczuk J
British Journal of Obstetrics and Gynaecology, 2012 , 119: (9) 1131 - 1140
Subjects: Prenatal Screening & Diagnosis, Prevention & Risk Factors, Survival & Neuro Development Outcomes