411 results on '"Addor, Marie-Claude"'
Search Results
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
6. Reproductive Safety of Trazodone After Maternal Exposure in Early Pregnancy: A Comparative ENTIS Cohort Study
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
13. Prevalence of valproate syndrome in Europe from 2005 to 2014: A registry based multi-centre study
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
19. Childhood neurodegeneration associated with a specific UBTF variant: a new case report and review of the literature
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
22. Use of asthma medication during pregnancy and risk of specific congenital anomalies: A European case-malformed control study
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
28. Selective serotonin reuptake inhibitor antidepressant use in first trimester pregnancy and risk of specific congenital anomalies: a European register-based 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
34. Metformin Exposure in the First Trimester of Pregnancy and Risk of All or Specific Congenital Anomalies: Exploratory Case-Control Study
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
45. Prenatal diagnosis and epidemiology of multicystic kidney dysplasia in Europe
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
50. Fatal outcome in a female monozygotic twin with X-linked hypohydrotic ectodermal dysplasia (XLHED) due to a de novo t(X;9) translocation with probable disruption of the EDA gene
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