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411 results on '"Addor, Marie-Claude"'

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2. Surveillance of multiple congenital anomalies; searching for new associations

3. Risk of congenital malformation after first trimester mRNA COVID-19 vaccine exposure in pregnancy: the COVI-PREG prospective cohort

4. Human-Specific NOTCH2NL Genes Affect Notch Signaling and Cortical Neurogenesis

5. Use of GLP1 receptor agonists in early pregnancy and reproductive safety: a multicentre, observational, prospective cohort study based on the databases of six Teratology Information Services

7. Macrolide and lincosamide antibiotic exposure in the first trimester of pregnancy and risk of congenital anomaly: A European case-control study

8. Signal Detection in EUROmediCAT: Identification and Evaluation of Medication–Congenital Anomaly Associations and Use of VigiBase as a Complementary Source of Reference

9. Surveillance of multiple congenital anomalies; searching for new associations

10. Developmental trajectories of neuroanatomical alterations associated with the 16p11.2 Copy Number Variations

11. Spectrum of congenital anomalies among VACTERL cases: a EUROCAT population-based study

12. Risk of congenital malformation after first trimester mRNA COVID-19 vaccine exposure in pregnancy: the COVI-PREG prospective cohort

14. Epidemiology of septo-optic dysplasia with focus on prevalence and maternal age – A EUROCAT study

15. Quantifying the Effects of 16p11.2 Copy Number Variants on Brain Structure: A Multisite Genetic-First Study

16. The genetics of recurrent hydatidiform moles: new insights and lessons from a comprehensive analysis of 113 patients

17. The role of recessive inheritance in early-onset epileptic encephalopathies: a combined whole-exome sequencing and copy number study

18. Toward the Effective Surveillance of Hypospadias

20. Beta-Blocker Use in Pregnancy and Risk of Specific Congenital Anomalies: A European Case-Malformed Control Study

21. Surveillance of multiple congenital anomalies; searching for new associations

23. Maternal age and the prevalence of congenital heart defects in Europe, 1995–2015: A register‐based study

24. Amniotic band syndrome and limb body wall complex in Europe 1980–2019

25. Risk of congenital malformation following first trimester mRNA COVID-19 vaccine exposure in pregnancy: the COVI-PREG prospective cohort

26. Long term trends in prevalence of neural tube defects in Europe : population based study

27. The Association of H1N1 Pandemic Influenza with Congenital Anomaly Prevalence in Europe : An Ecological Time Series Study

29. Assessment of the Genetic Spectrum of Uncombable Hair Syndrome in a Cohort of 107 Individuals

30. Prevalence of vascular disruption anomalies and association with young maternal age: A EUROCAT study to compare the United Kingdom with other European countries

31. Epidemiology of aplasia cutis congenita: A population‐based study in Europe

32. Prevalence of congenital heart defects in Europe, 2008–2015: A registry‐based study

33. Assessment of the Genetic Spectrum of Uncombable Hair Syndrome in a Cohort of 107 Individuals

35. Estimating Global Burden of Disease due to congenital anomaly: an analysis of European data

36. Epidemiology of hypospadias in Europe: a registry-based study

37. Assessment of the Genetic Spectrum of Uncombable Hair Syndrome in a Cohort of 107 Individuals

38. Gastroschisis in Europe – A Case‐malformed‐Control Study of Medication and Maternal Illness during Pregnancy as Risk Factors

39. Amniotic band syndrome and limb body wall complex in Europe 1980–2019.

40. Epidemiology of aplasia cutis congenita: A population‐based study in Europe.

41. Epidemiology of congenital diaphragmatic hernia in Europe: a register-based study

42. Major Congenital Anomalies in Babies Born With Down Syndrome: A EUROCAT Population-Based Registry Study

43. Prevention of Neural Tube Defects in Europe: A Public Health Failure

44. Epidemiology of Pierre‐Robin sequence in Europe: A population‐based EUROCAT study

46. Mutations in the Human UBR1 Gene and the Associated Phenotypic Spectrum

47. Clinical manifestations in patients with SOS1 mutations range from Noonan syndrome to CFC syndrome

48. Spectrum of congenital anomalies among VACTERL cases: a EUROCAT population-based study

49. Fraser Syndrome: Epidemiological Study in a European Population

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