Výsledky vyhledávání - "Patrizia, D'Eufemia"

Akademický článek

Brain-Type Creatine Kinase Release from Cultured Osteoclasts Exposed to Neridronate in Children Affected by Osteogenesis Imperfecta Type 1

Autor: Maria Felicia Faienza, Albina Tummolo, Mauro Celli, Roberto Finocchiaro, Laura Piacente, Francesca Di Serio, Grazia Paola Nicchia, Giacomina Brunetti, Patrizia D’Eufemia

Publikováno v: Biomedicines, Vol 11, Iss 2, p 458 (2023)

Brain-type creatine kinase (CK-BB) increases during osteoclastogenesis, with high circulating amounts in type I osteogenesis imperfecta (OI) following treatment with neridronate, a bisphosphonate able to inhibit osteoclast activity and survival. The

Externí odkaz: https://doaj.org/article/fd02d20e5e604d13a6defe785450ed65

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Treatment of tibial deformities with the Fassier–Duval telescopic nail and minimally invasive percutaneous osteotomies in patients with osteogenesis imperfecta type III

Autor: Mauro Celli, Filippo Maria Ranaldi, Lorena Martini, Anna Zambrano, Pietro Persiani, Ciro Villani, Patrizia D'Eufemia

Publikováno v: Journal of Pediatric Orthopaedics B. 28:179-185

Osteogenesis imperfecta (OI) is a rare congenital osteodystrophy. Patients with OI present with osteoporosis, extreme bone fragility and severe deformities of the lower limbs, which predispose them to frequent fractures. The aim of our study is to de

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::324af87b7a70de713251d720155c998c
https://doi.org/10.1097/bpb.0000000000000536

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Elastic intramedullary nailing of the femur fracture in patients affected by osteogenesis imperfecta type 3: Indications, limits and pitfalls

Autor: Mauro Celli, Lorena Martini, Filippo Maria Ranaldi, L. Celli, Patrizia D'Eufemia, Pietro Persiani, Ciro Villani, Anna Zambrano

Publikováno v: Injury. 50

Introduction Patients with Osteogenesis Imperfecta (OI) Type 3 may exhibit both primitive deformities and secondary fracture malunions on a femoral level. The orthopaedic surgeon’s objective is to cure the deformities in order to prevent fractures

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::100f9635076d90a4547355cf831d23c7
https://pubmed.ncbi.nlm.nih.gov/30827706

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Genotype-phenotype correlation study in 364 osteogenesis imperfecta Italian patients

Autor: Luca Sangiorgi, Mauro Celli, Manila Boarini, Morena Tremosini, Maria Gnoli, Margherita Maioli, Patrizia D'Eufemia, Paolo Versacci, Serena Corsini, Anna Zambrano, Elena Pedrini, Marina Mordenti

Publikováno v: European Journal of Human Genetics

Osteogenesis imperfecta (OI) is a rare genetic disorder of the connective tissue and 90% of cases are due to dominant mutations in COL1A1 and COL1A2 genes. To increase OI disease knowledge and contribute to patient follow-up management, a homogeneous

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c039dce8a6c2e18cff56185f341626b7
http://hdl.handle.net/11573/1260654

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Clinical and biochemical response to neridronate treatment in a patient with osteoporosis-pseudoglioma syndrome (OPPG)

Autor: Y. D’Alfonso, A. Febbo, Patrizia D'Eufemia, A. Turchetti, L. Celli, Anna Zambrano, Pietro Persiani, Mauro Celli

Osteoporosis-pseudoglioma syndrome (OPPG) is a rare autosomal recessive syndrome characterized by juvenile-onset osteoporosis and ocular abnormalities due to a low-density lipoprotein receptor-related protein 5 (LRP5) gene mutation. Treatment with bi

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::daf23337ff4ccad38bfeba4e4239b27e
http://hdl.handle.net/11573/1002021

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Isolated olecranon fractures in children affected by osteogenesis imperfecta type I treated with single screw or tension band wiring system: outcomes and pitfalls in relation to bone mineral density

Autor: Pietro Persiani, Filippo Maria Ranaldi, Claudia de Cristo, Lorena Martini, Jole Graci, Patrizia D'Eufemia, Anna Zambrano, Ciro Villani

Publikováno v: Medicine

The purpose of this study is to compare the results of 2 techniques, tension band wiring (TBW) and fixation with screws, in olecranon fractures in children affected with osteogenesis imperfecta (OI) type I. Between 2010 and 2014, 21 olecranon fractur

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ef0e3609d3e78404845c1927697af7a0
http://hdl.handle.net/11573/961853

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Erratum to: Serum creatine kinase isoenzymes in children with osteogenesis imperfecta

Autor: A. Turchetti, Patrizia D'Eufemia, Anna Zambrano, Mauro Celli, R. Finocchiaro, L. Celli, Pietro Persiani, Valentina Lodato, S. Finocchiaro

Publikováno v: Osteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA. 28(1)

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2500bca6d3d6e2634d982e8ce53e2d50
https://pubmed.ncbi.nlm.nih.gov/27562566

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Osteogenesis imperfecta and clubfoot-a rare combination: Case report and review of the literature

Autor: Ciro Villani, Lorena Martini, Mauro Celli, Filippo Maria Ranaldi, Patrizia D'Eufemia, Anna Zambrano, Pietro Persiani

Publikováno v: Medicine

Background: Osteogenesis imperfecta (OI) is a rare congenital genetic osteodystrophy, which has a prevalence of 1:20,000. OI is caused by the mutation of the COL1A1/COL1A2 genes, leading to a deficit of quality and/or quantity in the synthesis of pro

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9f924e8780822fbc12388f6bd797d25b
https://pubmed.ncbi.nlm.nih.gov/27495102

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