Anne Morice
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Explore the profile of Anne Morice including associated specialties, affiliations and a list of published articles.
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17
Citations
53
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Recent Articles
1.
Morice A, de La Seigliere A, Kany A, Khonsari R, Bensidhoum M, Puig-Lombardi M, et al.
Bone Res
. 2025 Jan;
13(1):12.
PMID: 39837840
Gain-of-function mutations in fibroblast growth factor receptor (FGFR) genes lead to chondrodysplasia and craniosynostoses. FGFR signaling has a key role in the formation and repair of the craniofacial skeleton. Here,...
2.
Morice A, Panafieu E, de La Seigliere A, Legeai-Mallet L
J Vis Exp
. 2024 Oct;
(211).
PMID: 39400165
Non-stabilized fractures can be made at mandibular sites in mice, thus making it possible to analyze bone repair using an endochondral ossification mode. To most accurately reflect this process in...
3.
Motamedian S, Ahmadi N, Ghaffari S, Niazmand M, Mohaghegh S, Morice A, et al.
J Stomatol Oral Maxillofac Surg
. 2023 Jul;
125(5S1):101553.
PMID: 37422264
Objective: Distraction osteogenesis is one of the treatment options in patients with severe maxillomandibular abnormalities to treat morphological and respiratory problems (obstructive sleep apnea syndrome). The study aimed to evaluate...
4.
Loisay L, Komla-Ebri D, Morice A, Heuze Y, Viaut C, de La Seigliere A, et al.
JCI Insight
. 2023 Jun;
8(12).
PMID: 37345656
Hypochondroplasia (HCH) is a mild dwarfism caused by missense mutations in fibroblast growth factor receptor 3 (FGFR3), with the majority of cases resulting from a heterozygous p.Asn540Lys gain-of-function mutation. Here,...
5.
Morice A, Taverne M, Eche S, Griffon L, Fauroux B, Leboulanger N, et al.
Orphanet J Rare Dis
. 2023 Apr;
18(1):88.
PMID: 37072824
Background: Achondroplasia is the most frequent FGFR3-related chondrodysplasia, leading to rhizomelic dwarfism, craniofacial anomalies, stenosis of the foramen magnum, and sleep apnea. Craniofacial growth and its correlation with obstructive sleep...
6.
Cornille M, Moriceau S, Khonsari R, Heuze Y, Loisay L, Boitez V, et al.
J Exp Med
. 2022 Mar;
219(4).
PMID: 35254402
Crouzon syndrome with acanthosis nigricans (CAN, a rare type of craniosynostosis characterized by premature suture fusion and neurological impairments) has been linked to a gain-of-function mutation (p.Ala391Glu) in fibroblast growth...
7.
Barone S, Morice A, Picard A, Giudice A
J Stomatol Oral Maxillofac Surg
. 2020 Sep;
122(2):162-172.
PMID: 32898673
Surgery-first approach (SFA) has been introduced as an alternative for conventional orthognathic approach (COA) in the treatment of patients with dentoskeletal deformities. This review aimed to evaluate skeletal stability, treatment...
8.
Morice A, Joly A, Ricquebourg M, Maruani G, Durand E, Galmiche L, et al.
BMC Musculoskelet Disord
. 2020 Aug;
21(1):564.
PMID: 32825821
Background: Cherubism is a rare autosomal dominant genetic condition caused by mutations in the SH3BP2 gene. This disease is characterized by osteolysis of the jaws, with the bone replaced by...
9.
Morice A, Neiva C, Fabre M, Spina P, Jouenne F, Galliani E, et al.
Oral Surg Oral Med Oral Pathol Oral Radiol
. 2019 Sep;
129(5):e234-e242.
PMID: 31562035
Unicystic ameloblastoma (UA), a benign odontogenic tumor of the jaw, represents less than a third of all ameloblastomas and seems less aggressive than other types of ameloblastoma. We present here...
10.
ORourke S, Neiva C, Galliani E, Kadlub N, Picard A, Morice A
Facial Plast Surg
. 2019 May;
35(3):286-293.
PMID: 31100767
The use of the Washio retroauricular flap for nasal reconstruction has been infrequently covered in recent literature, particularly concerning the pediatric population. A retrospective study was conducted between 2014 and...