Zobrazeno 1 - 10
of 39
pro vyhledávání: '"Georges, Finidori"'
Autor:
Mathilde Gaume, Sarah El Yahiaouni, Marine De Tienda, Genevieve Baujat, Valérie Cormier-Daire, Valérie Dumaine, Stéphanie Pannier, Georges Finidori, Zagorka Pejin
Publikováno v:
International Orthopaedics.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0b5d8917383fddac65d7a2efd68f734f
https://doi.org/10.1007/s00264-023-05818-6
https://doi.org/10.1007/s00264-023-05818-6
Autor:
Tristan Langlais, Ruben Dukan, Stéphanie Pannier, Georges Finidori, Marine De Tienda, Christophe Glorion, Zagorka Pejin
Publikováno v:
Journal of Pediatric Orthopaedics B. 30:257-263
Severe infant osteogenesis imperfecta requires osteosynthesis. Intramedullary tibia's osteosynthesis is a technical challenge given the deformity and the medullar canal's narrowness. We describe an extramedullary technique: 'In-Out-In' K-wires slidin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5c9dbedf12f1cdd684dc646fb93d4fd9
https://doi.org/10.1097/bpb.0000000000000785
https://doi.org/10.1097/bpb.0000000000000785
Autor:
Marine De Tienda, Eloise Duprot, Geneviève Baujat, Stéphanie Pannier, Georges Finidori, Zagorka Pejin, Mathilde Gaume
Publikováno v:
Journal of pediatric orthopedics. 42(1)
BACKGROUND Osteosynthesis of leg fractures and deformities in children with osteogenesis imperfecta should align the skeleton and overcome its fragility during growth with a telescopic effect. A high rate of mechanical complications is associated wit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b511900553f49622139b2366ed9219b2
https://pubmed.ncbi.nlm.nih.gov/34723894
https://pubmed.ncbi.nlm.nih.gov/34723894
Autor:
Federico Di Rocco, Agnès Linglart, Georges Finidori, Zagorka Pejin, Catherine Adamsbaum, Philippe Wicart, Stéphanie Pannier, Justine Bacchetta, Anya Rothenbuhler
Publikováno v:
Archives de pediatrie : organe officiel de la Societe francaise de pediatrie. 28(7)
X-linked hypophosphatemia (XLH) is due to mutations in the PHEX gene leading to unregulated production of FGF23 and uncontrollable hypophosphatemia. XLH is characterized in children by rickets, short stature, waddling gait, and leg bowing of variable
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e21d1a7578f8dc75202542024cf855d9
https://pubmed.ncbi.nlm.nih.gov/34625380
https://pubmed.ncbi.nlm.nih.gov/34625380
Autor:
Zagorka Pejin, Christophe Glorion, Alina Badina, Georges Finidori, Aurélie Andrzejewski, Philippe Wicart
BACKGROUND: Multiple epiphyseal dysplasia (MED) and pseudoachondroplasia (PSACH) are congenital skeletal disorders characterized by irregular epiphyses, mild or severe short stature and early-onset osteoarthritis which frequently affect the hips. The
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ce2da40e02d0cda6acb9f2049ce6c98b
https://doi.org/10.1097/bpo.0000000000001708
https://doi.org/10.1097/bpo.0000000000001708
Publikováno v:
Skeletal Radiology. 47:1015-1019
Multicentric carpotarsal osteolysis (MCTO) is a rare skeletal disorder characterized by progressive carpal and tarsal destruction. The upper and lower limbs may be involved, leading to deformities and joint limitation. These anatomic features may be
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::883ffac27f7eebdcefc1d33c4b06d73d
https://doi.org/10.1007/s00256-018-2874-z
https://doi.org/10.1007/s00256-018-2874-z
Autor:
Stéphanie Pannier, Georges Finidori, Alexandre Debs, Christophe Glorion, De Marine Tienda, Philippe Massard-Combe, Younes Ouchrif, Zagorka Pejin
Publikováno v:
Hand Surgery and Rehabilitation. 40:847
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1dfd915c9941a1ba4ce23111d540ad09
https://doi.org/10.1016/j.hansur.2021.10.078
https://doi.org/10.1016/j.hansur.2021.10.078
Autor:
Edouard Gaillot-Drevon, Marine De Tienda, Georges Finidori, Zagorka Pejin, Stéphanie Pannier, Pierre-Alban Bouche
Publikováno v:
Hand Surgery and Rehabilitation. 40:878
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::de875fa85b17df5181fd32af533d8131
https://doi.org/10.1016/j.hansur.2021.10.164
https://doi.org/10.1016/j.hansur.2021.10.164
Autor:
Agnès Linglart, Philippe Wicart, Christophe Glorion, Aliette Gizard, Georges Finidori, Anya Rothenbuhler, Zaga Pejin, B de Billy
Publikováno v:
Endocrine Connections
Endocrine Connections, Vol 6, Iss 8, Pp 566-573 (2017)
Endocrine Connections, Vol 6, Iss 8, Pp 566-573 (2017)
Background X-linked hypophosphatemic rickets (XLHR) is due to mutations in PHEX leading to unregulated production of FGF23 and hypophosphatemia. XLHR is characterized by leg bowing of variable severity. Phosphate supplements and oral vitamin analogs,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a6ed4e138a44a392052e4d2d63026353
https://doi.org/10.1530/ec-17-0154
https://doi.org/10.1530/ec-17-0154
Autor:
Zagorka, Pejin, Jean-Charles, Auregan, Geneviève, Baujat, Georges, Finidori, Christophe, Glorion
Publikováno v:
La Revue du praticien. 66(2)
When to think of a constitutional bone disease?. Constitutional bone diseases are a heterogenous group of disorders, variably causing: growth anomalies, joint limitation and/or hypermobility, pain, bone frailty and/or dysmorphic elements in the crani
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::2a056389d01c90b5c3015323bb799442
https://pubmed.ncbi.nlm.nih.gov/30512337
https://pubmed.ncbi.nlm.nih.gov/30512337