M.C. Addor

Discipline

Anthropologie biologique (4)

Type de document

Articles (35) Recensions (1)

Co-auteur

Date

Source

Mot-clé

Human beings (27) Pregnancy (20) Abnormalities, Human (20) Pregnancy (20) Cases (19) Cases (19) risque (13) Europe (13) Europe (13) Risk (13) Europe (13) Population (12) Childbirth (12) Population (12) Abnormalities (11) Plants--Abnormalities (11) Animals--Abnormalities (11) nourisson (10) surveillance (10) taux (10) nourrisson (10) Birth (9) Parturition (9) Labor (Obstetrics) (9) Birth (9) naissance (9) temps (durée) (8) exposition (8) adulte (8) Methods (8)

Documents écrit par M.C. Addor (35) | parle de M.C. Addor (0)

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.
K. Dao et al. (24 avr. 2024)
Surveillance of multiple congenital anomalies; searching for new associations.
J.K. Morris et al.
Risk of congenital malformation after first trimester mRNA COVID-19 vaccine exposure in pregnancy: the COVI-PREG prospective cohort.
G. Favre et al.
Amniotic band syndrome and limb body wall complex in Europe 1980-2019.
JEH Bergman et al.
Reproductive Safety of Trazodone After Maternal Exposure in Early Pregnancy: A Comparative ENTIS Cohort Study.
K. Dao et al. (2023)
Prevalence of vascular disruption anomalies and association with young maternal age: A EUROCAT study to compare the United Kingdom with other European countries.
J.K. Morris et al. (1 déc. 2022)
Prevalence of congenital heart defects in Europe, 2008-2015: A registry-based study.
C. Mamasoula et al. (1 déc. 2022)
Prevention of Neural Tube Defects in Europe: A Public Health Failure.
J.K. Morris et al. (2021)
Maternal risk factors for the VACTERL association: A EUROCAT case-control study.
R. van de Putte et al. (15 mai 2020)
Childhood neurodegeneration associated with a specific UBTF variant: a new case report and review of the literature.
F. Bastos et al. (13 janv. 2020)
The role of recessive inheritance in early-onset epileptic encephalopathies: a combined whole-exome sequencing and copy number study.
S.M. Papuc et al.
Metformin exposure in first trimester of pregnancy and risk of all or specific congenital anomalies: exploratory case-control study.
J.E. Given et al. (25 juin 2018)
Beta-Blocker Use in Pregnancy and Risk of Specific Congenital Anomalies: A European Case-Malformed Control Study.
JEH Bergman et al.
Trends in congenital anomalies in Europe from 1980 to 2012.
J.K. Morris et al. (2018)
Estimating Global Burden of Disease due to congenital anomaly: an analysis of European data.
B. Boyle et al.
Novel promoters and coding first exons in DLG2 linked to developmental disorders and intellectual disability.
C. Reggiani et al. (19 juil. 2017)
EUROmediCAT signal detection: an evaluation of selected congenital anomaly-medication associations.
J.E. Given et al.
Prevalence of microcephaly in Europe: population based study.
J.K. Morris et al. (13 sept. 2016)
Mutations in MAP3K7 that Alter the Activity of the TAK1 Signaling Complex Cause Frontometaphyseal Dysplasia.
E.M. Wade et al. (4 août 2016)
PIK3CA-associated developmental disorders exhibit distinct classes of mutations with variable expression and tissue distribution.
G. Mirzaa et al. (16 juin 2016)
Lamotrigine use in pregnancy and risk of orofacial cleft and other congenital anomalies.
H. Dolk et al. (3 mai 2016)
Long term trends in prevalence of neural tube defects in Europe: population based study.
B. Khoshnood et al. (24 nov. 2015)
Epidemiology of hypospadias in Europe: a registry-based study.
J.E. Bergman et al. (2015)
Mutations in tubulin genes are frequent causes of various foetal malformations of cortical development including microlissencephaly.
A. Laquerrière et al. (2014)
Prevalence and risk of Down syndrome in monozygotic and dizygotic multiple pregnancies in Europe: implications for prenatal screening.
B. Boyle et al. (2014)

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