Kolexia
Rigonnot Luc
Gynécologie
Centre Hospitalier Sud Francilien
Corbeil-Essonnes, France
19 Activités
1 Followers

Scientifique
Digital
Production scientifique
Activités par an
Expertise
Sujets de recherche
{{person.topmesh1.name}} Arthrogrypose Malformations du système nerveux Complications infectieuses de la grossesse Zoonoses Cardiopathies congénitales COVID-19 Anomalies morphologiques congénitales de la main Chondrodysplasie ponctuée Traumatismes néonatals

Industries

Merck-Serono
1 collaboration(s)
Dernière en 2022
EXELTIS SANTE
1 collaboration(s)
Dernière en 2023
AstraZeneca
1 collaboration(s)
Dernière en 2023
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Dernières activités

Phenotypic spectrum and genomics of undiagnosed arthrogryposis multiplex congenita.
Journal of medical genetics   05 avril 2021
Frequency of differential placental transfer to twins of maternal antiretroviral medications.
European journal of obstetrics, gynecology, and reproductive biology   10 novembre 2020
Retrospective Description of Pregnant Women Infected with Severe Acute Respiratory Syndrome Coronavirus 2, France.
Emerging infectious diseases   06 juillet 2020
Neonatal morbidity associated with vaginal delivery of noncephalic second twins.
American journal of obstetrics and gynecology   05 février 2018
98: Neonatal outcomes according to second twin presentation after vaginal delivery of the first twin
Society for Maternal-Fetal Medicine 38th Annual Meeting   01 janvier 2018
Loss-of-Function Mutations in LGI4, a Secreted Ligand Involved in Schwann Cell Myelination, Are Responsible for Arthrogryposis Multiplex Congenita.
American journal of human genetics   16 mars 2017
Severe X-linked chondrodysplasia punctata in nine new female fetuses.
Prenatal diagnosis   30 mars 2015
Mutations in CNTNAP1 and ADCY6 are responsible for severe arthrogryposis multiplex congenita with axoglial defects.
Human molecular genetics   06 décembre 2013
KIF7 mutations cause fetal hydrolethalus and acrocallosal syndromes.
Nature genetics   08 mai 2011
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