Zobrazeno 1 - 10
of 33
pro vyhledávání: '"Zagorka Pejin"'
Autor:
David Dawei Yang, Geneviève Baujat, Antoine Neuraz, Nicolas Garcelon, Claude Messiaen, Arnaud Sandrin, Gérard Cheron, Anita Burgun, Zagorka Pejin, Valérie Cormier-Daire, François Angoulvant
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 15, Iss 1, Pp 1-9 (2020)
Abstract Background Children with rare bone diseases (RBDs), whether medically complex or not, raise multiple issues in emergency situations. The healthcare burden of children with RBD in emergency structures remains unknown. The objective of this st
Externí odkaz:
https://doaj.org/article/440bf011fb0a44a7b4c9789b8319b39f
Autor:
Stéphanie Pannier, Zagorka Pejin, Pascal Jehanno, Marine de Tienda, Alina Badina, Christophe Glorion
Publikováno v:
Revue de Chirurgie Orthopédique et Traumatologique. 108:S106-S114
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b35e2a40d3a87407e908c5c1cb4ef92e
https://doi.org/10.1016/j.rcot.2022.06.028
https://doi.org/10.1016/j.rcot.2022.06.028
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:
Sophie Rondeau, Lucie Griffon, Geneviève Baujat, Duy Bo Nguyen, Valérie Cormier-Daire, Pauline Marzin, Michel Zerah, Sonia Khirani, Romain Luscan, Vincent Couloigner, Caroline Michot, Brigitte Fauroux, Zagorka Pejin
Publikováno v:
American Journal of Medical Genetics Part A. 185:2108-2118
Sleep-disordered breathing (SDB) is common in patients with skeletal dysplasias. The aim of our study was to analyze SDB and respiratory management in children with rare skeletal dysplasias. We performed a retrospective analysis of patients with spon
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a748ca8d6c0c3dc4a3f34bf286016fde
https://doi.org/10.1002/ajmg.a.62236
https://doi.org/10.1002/ajmg.a.62236
Autor:
Damien Bonnet, Valérie Cormier-Daire, Briac Thierry, Zagorka Pejin, Caroline Michot, Christophe Delacourt, Maryse Bonnière, Muriel Le Bourgeois, Pauline Marzin, Gilles Phan, Sophie Rondeau, Andrea Dancasius, Diala Khraiche, Geneviève Baujat, Anne Cavau
Publikováno v:
Genetics in Medicine. 23:331-340
Purpose Geleophysic dysplasia (GD) and acromicric dysplasia (AD) are characterized by short stature, short extremities, and progressive joint limitation. In GD, cardiorespiratory involvement can result in poor prognosis. Dominant variants in the FBN1
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::51a485cab1dafb58e678e4e35de3049d
https://doi.org/10.1038/s41436-020-00994-x
https://doi.org/10.1038/s41436-020-00994-x
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
Autor:
Pauline, Marzin, Briac, Thierry, Andrea, Dancasius, Anne, Cavau, Caroline, Michot, Sophie, Rondeau, Geneviève, Baujat, Gilles, Phan, Maryse, Bonnière, Muriel, Le Bourgeois, Diala, Khraiche, Zagorka, Pejin, Damien, Bonnet, Christophe, Delacourt, Valérie, Cormier-Daire
Publikováno v:
Genetics in medicine : official journal of the American College of Medical Genetics. 23(2)
Geleophysic dysplasia (GD) and acromicric dysplasia (AD) are characterized by short stature, short extremities, and progressive joint limitation. In GD, cardiorespiratory involvement can result in poor prognosis. Dominant variants in the FBN1 and LTB
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::66cf118b5e3e1ac580710856b1ce99da
https://pubmed.ncbi.nlm.nih.gov/33082559
https://pubmed.ncbi.nlm.nih.gov/33082559