Výsledky vyhledávání - "Anna, Zambrano"

Akademický článek

Ocular Motility Abnormalities in Ehlers-Danlos Syndrome: An Observational Study

Autor: Anna Maria Comberiati, Ludovico Iannetti, Raffaele Migliorini, Marta Armentano, Marika Graziani, Luca Celli, Anna Zambrano, Mauro Celli, Magda Gharbiya, Alessandro Lambiase

Publikováno v: Applied Sciences, Vol 13, Iss 9, p 5240 (2023)

Purpose: To evaluate ocular motility (OM) abnormalities associated with Ehlers-Danlos Syndrome (EDS). Materials and methods: In this cross-sectional observational study, patients with EDS underwent a complete orthoptic examination. The following orth

Externí odkaz: https://doaj.org/article/f47b5aaf433d4ae684fc62d2f21fd9bc

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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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Polyostotic Fibrous Dysplasia Mimicking Bone Involvement in Hodgkin Lymphoma: A Pediatric Case and Literature Review

Autor: Anna Maria Testi, Fiorina Giona, Alessandro Corsi, A. Turchetti, Maria Luisa Moleti, L. Celli, Miriam D'Avanzo, Anna Zambrano, Mauro Celli, Gianfranco Lapietra

Bone involvement in Hodgkin lymphoma (HL) is rare. The differential diagnosis between HL bone localization and other malignant or benign skeletal diseases is challenging. We report the case of a girl affected by classic HL, initially staged IVA becau

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4464209f8033ec181d60c24e4f1e1207
http://hdl.handle.net/11573/1444586

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New 3D Cone Beam CT Imaging Parameters to Assist the Dentist in Treating Patients with Osteogenesis Imperfecta

Autor: Francesca Pepe, Mauro Celli, Valeria Luzzi, Daniela Messineo, Gaetano Ierardo, Anna Zambrano, L. Celli, Antonella Polimeni, A. Turchetti

Publikováno v: Healthcare
Volume 8
Issue 4
Healthcare, Vol 8, Iss 546, p 546 (2020)

(1) Background: The aim of the work is to identify some imaging parameters in osteogenesis imperfecta to assist the dentist in the diagnosis, planning, and orthodontic treatment of Osteogenesis Imperfecta (OI) using 3D cone beam Computed Tomography (

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0d9900cbdbfb1a90366d4e8a95dda8f5
https://pubmed.ncbi.nlm.nih.gov/33321783

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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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