Antoine Chretien
Overview
Explore the profile of Antoine Chretien including associated specialties, affiliations and a list of published articles.
Author names and details appear as published. Due to indexing inconsistencies, multiple individuals may share a name, and a single author may have variations. MedLuna displays this data as publicly available, without modification or verification
Snapshot
Snapshot
Articles
6
Citations
12
Followers
0
Related Specialties
Related Specialties
Top 10 Co-Authors
Top 10 Co-Authors
Published In
Affiliations
Affiliations
Soon will be listed here.
Recent Articles
1.
Jeannerod G, Chretien A, Andre G, Mabilleau G, Behets C
Biomedicines
. 2025 Jan;
12(12.
PMID: 39767599
Osteogenesis imperfecta (OI) is a rare genetic disorder affecting mainly type I collagen, which leads to bone fragility and deformities. OI patients also present craniofacial abnormalities such as macrocephaly and...
2.
Vettese J, Manon J, Chretien A, Evrard R, Fieve L, Schubert T, et al.
Front Bioeng Biotechnol
. 2024 Apr;
12:1275709.
PMID: 38633664
Large bone defect regeneration remains a major challenge for orthopedic surgeons. Tissue engineering approaches are therefore emerging in order to overcome this limitation. However, these processes can alter some of...
3.
Andre G, Chretien A, Demoulin A, Beersaerts M, Docquier P, Behets C
Int J Mol Sci
. 2023 Dec;
24(23).
PMID: 38069332
Osteogenesis imperfecta (OI) is a rare congenital bone dysplasia generally caused by a mutation of one of the type I collagen genes and characterized by low bone mass, numerous fractures,...
4.
Chretien A, Mabilleau G, Lebacq J, Docquier P, Behets C
Pharmaceuticals (Basel)
. 2023 Jun;
16(6).
PMID: 37375779
Osteogenesis imperfecta (OI) is a genetic disorder of connective tissue characterized by spontaneous fractures, bone deformities, impaired growth and posture, as well as extra-skeletal manifestations. Recent studies have underlined an...
5.
Chretien A, Couchot M, Mabilleau G, Behets C
Int J Mol Sci
. 2022 Sep;
23(17).
PMID: 36077325
Osteogenesis imperfecta (OI) is a genetic disorder of connective tissue characterized by low bone mass and spontaneous fractures, as well as extra-skeletal manifestations, such as dental abnormalities, blue sclera, hearing...
6.
Cardinal M, Chretien A, Roels T, Lafont S, Ominsky M, Devogelaer J, et al.
Front Genet
. 2021 Aug;
12:705505.
PMID: 34447412
Osteogenesis imperfecta (OI), which is most often due to a collagen type 1 gene mutation, is characterized by low bone density and bone fragility. In OI patients, gender-related differences were...