Relevant bibliographies by topics / Ollier disease

Contents

  1. Journal articles
  2. Dissertations / Theses
  3. Book chapters
  4. Conference papers

Academic literature on the topic 'Ollier disease'

Author: Grafiati
Published: 9 March 2023
Last updated: 10 March 2023

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Journal articles on the topic "Ollier disease"

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D’Angelo, Luca, Luca Massimi, Alessandro Narducci, and Concezio Di Rocco. "Ollier disease." Child's Nervous System 25, no. 6 (March 27, 2009): 647–53. http://dx.doi.org/10.1007/s00381-009-0873-z.

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Ali, Mohammed Iftekar. "Ollier disease." Apollo Medicine 14, no. 1 (March 2017): 72–74. http://dx.doi.org/10.1016/j.apme.2017.01.006.

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Cerny, Milena, Hannes A. Rudiger, Berengere Aubry-Rozier, Eric Dugert, and Fabio Becce. "Enchondromatosis (Ollier disease)." Arthritis & Rheumatism 65, no. 11 (October 28, 2013): 2886. http://dx.doi.org/10.1002/art.38115.

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Choh, Suhil A., and Naseer A. Choh. "Multiple enchondromatosis (Ollier disease)." Annals of Saudi Medicine 29, no. 1 (January 2009): 65–67. http://dx.doi.org/10.5144/0256-4947.2009.65.

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P, Correa Bellido, and Wadhwani WJ. "Ollier´s disease: Multiple enchondromatosis." International Journal of Orthopaedics Sciences 7, no. 4 (October 1, 2021): 409–11. http://dx.doi.org/10.22271/ortho.2021.v7.i4f.2910.

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Koc, Filiz, and Zafer Koc. "Ollier Disease Anaplastic Mixed Oligoastrocytoma." Neurosurgery Quarterly 16, no. 4 (December 2006): 195–97. http://dx.doi.org/10.1097/01.wnq.0000214039.38720.b4.

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Le, Bryan B., and Ba D. Nguyen. "Ollier Disease With Digital Enchondromatosis." Clinical Nuclear Medicine 39, no. 8 (August 2014): e375-e378. http://dx.doi.org/10.1097/rlu.0000000000000284.

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Laios, Konstantinos, Konstantinos Markatos, and George Androutsos. "Louis-Léopold-Xavier-Édouard Ollier (1830-1900): An Innovative Orthopedic Surgeon." Surgical Innovation 24, no. 4 (April 9, 2017): 402–4. http://dx.doi.org/10.1177/1553350617702310.

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Louis-Léopold-Xavier-Édouard Ollier (1830-1900) was a pioneer in orthopedics considered as the founder of modern orthopedic surgery. He was a skillful and experimenter surgeon. He invented many new surgical techniques in orthopedic surgery and many new surgical instruments. His most known discovery is Ollier’s disease.
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Kumar, Avinash, Vijay Kumar Jain, Minakshi Bharadwaj, and Rajendra Kumar Arya. "Ollier Disease: Pathogenesis, Diagnosis, and Management." Orthopedics 38, no. 6 (June 1, 2015): e497-e506. http://dx.doi.org/10.3928/01477447-20150603-58.

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Saleh, M., J. A. Fernandes, M. J. Bell, S. S. Madan, K. Robinson, and P. D. Kasliwal. "Limb reconstruction in Ollier\'s disease." Strategies in Trauma and Limb Reconstruction 10, no. 1 (April 10, 2015): 49–54. http://dx.doi.org/10.1007/s11751-015-0223-5.

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Dissertations / Theses on the topic "Ollier disease"

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PIAI, ANNA. "Diagnostic performance and organ dose evaluation in radiological diagnosis and follow-up of Ollier enchondromatosis pediatric patients: a phantom study." Doctoral thesis, Università degli Studi di Milano, 2021. http://hdl.handle.net/2434/883102.

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The European Council Directive 2013/59/Euratom included pediatric exposure in the special practices for which appropriate medical radiological equipment and practical techniques have to be ensured. Children are generally more sensitive to X-rays than adults, mainly due to rapid cell growth and replication, and a longer lifespan after exposure. Hence, the optimization of protection is a priority factor and it shall involve all the practical aspects of medical radiological procedures, from the selection of equipment to quality assurance and the assessment of patient doses. These concepts are strongly endorsed by health care organizations dedicated to providing safe and high-quality pediatric imaging, particularly in modalities involving higher radiation doses, such as computed tomography and fluoroscopy. IRCCS Istituto Ortopedico Galeazzi is a reference center for the diagnosis and treatment of pediatric orthopedic and traumatological diseases, including orthopedic tumors. Ollier disease is a rare skeletal disorder characterized by the presence of multiple enchondromas, which are intraosseous, usually benign, cartilage tumors. Although the enchondromas start out as benign, they may become malignant, so children affected by the disease undergo multiple radiographs over time. Special effort is thus required to reduce the risk of radiation-induced cancers, and the benefit provided by radiological procedures has to be properly balanced with the health risk associated with ionizing radiation. The principal aim of this study was to evaluate the applicability of a relatively novel low-dose technique based on a slot scanning technology (EOS imaging system), for the diagnosis and follow-up of Ollier disease. For this purpose, a 5-year-old anthropomorphic phantom was specifically purchased to evaluate the diagnostic and dosimetric performances of the system. Digital radiography (DR) and computed tomography (CT), the current gold standards for diagnosis and monitoring, were evaluated for comparison. Ollier enchondromas were simulated with homemade bone structures stuck on the phantom, which was then imaged with DR, CT, and the EOS system at three different scanning speeds. To assess the diagnostic power of the imaging system, non-expert observers and experienced radiologists measured the inserts dimensions and compared them with those derived from CT and DR. Interobserver and intermodality reproducibilities were evaluated through Bland-Altman analysis. Furthermore, the accuracy in the size estimation was investigated by comparing the measured dimensions with the real ones. Dosimetric evaluations were performed for each imaging technique through Monte Carlo (MC) simulations and in-phantom measurements with thermoluminescent dosimeters (TLDs). The validation of MC simulations with TL dosimetry was necessary for the EOS system as no reference was found in the literature. Three speed levels of the EOS X-ray tube, and two DR acquisition protocols, respectively suited for diagnosis and follow-up, were investigated. The measured organ doses were used to calculate effective dose according to the ICRP 103 recommendations. Risks of radiation-induced cancers were estimated in the form of Lifetime Attributable Risk (LAR). The EOS system performed similarly to DR and CT in both detection and measurement of enchondromas-like inserts. Excellent intermodality reliability and interobserver reproducibility were obtained for each imaging technique. EOS fast protocol provided a reduction of effective and organ doses with respect to DR acquisitions performed with the diagnostic protocol. When the DR protocol optimized for follow-up was considered, instead, no significant dose sparing was observed, neither in organ doses nor in effective dose. CT doses were considerably higher than doses of EOS and DR, regardless of the acquisition protocol or speed level. Comparable LARs were observed for EOS acquisitions performed with the fast protocol and DR examinations with the follow-up protocol. DR diagnosis protocol was found to be equivalent, in terms of radiological risk, to the EOS intermediate speed level. The risk associated with CT examinations was two orders of magnitude higher than of the other techniques. This work showed that the EOS system has the same diagnostic capability as DR and CT to detect and measure enchondromas-like inserts in a pediatric phantom, but delivering lower doses. Although no dose reduction was found with respect to DR follow-up protocol, EOS fast protocol still provides low doses, and the two techniques were found to be equivalent in terms of LAR. Thus, it may be considered a valid solution for both the diagnosis and followup of patients with Ollier disease or other bone pathologies, allowing easier and faster exams, which is a crucial aspect in pediatric applications.
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Javaheri, Anahita [Verfasser], de Angelis Martin [Akademischer Betreuer] Hrabé, and Markus W. [Akademischer Betreuer] Ollert. "Phenotyping of mice with genetic defects relevant to allergic diseases: Proteinase 3/neutrophil elastase double-knockout mice / Anahita Javaheri. Gutachter: Martin Hrabé de Angelis ; Markus W. Ollert. Betreuer: Martin Hrabé de Angelis." München : Universitätsbibliothek der TU München, 2011. http://d-nb.info/1014330068/34.

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Book chapters on the topic "Ollier disease"

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Rozbruch, S. Robert. "Humeral Lengthening and Deformity Correction in Ollier Disease: Distraction Osteogenesis with a Multiaxial Correction Frame." In Limb Lengthening and Reconstruction Surgery Case Atlas, 1–7. Cham: Springer International Publishing, 2015. http://dx.doi.org/10.1007/978-3-319-02767-8_256-1.

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Ruggles, Daniel, Pablo Wagner, and John E. Herzenberg. "Humeral Deformity Secondary to Ollier Disease: Angular Correction and Lengthening with a Taylor Spatial Frame." In Limb Lengthening and Reconstruction Surgery Case Atlas, 1–9. Cham: Springer International Publishing, 2015. http://dx.doi.org/10.1007/978-3-319-02767-8_323-1.

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Ruggles, Daniel, Pablo Wagner, and John E. Herzenberg. "Case 80: Humeral Deformity Secondary to Ollier Disease – Angular Correction and Lengthening with a Taylor Spatial Frame." In Limb Lengthening and Reconstruction Surgery Case Atlas, 557–62. Cham: Springer International Publishing, 2015. http://dx.doi.org/10.1007/978-3-319-18020-5_323.

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Slawik, Marc, Felix Beuschlein, Katrina Light, Roger Mulder, Gordon Dent, Mark G. Buckley, Stephen T. Holgate, et al. "Ollier's Disease." In Encyclopedia of Molecular Mechanisms of Disease, 1520–21. Berlin, Heidelberg: Springer Berlin Heidelberg, 2009. http://dx.doi.org/10.1007/978-3-540-29676-8_1317.

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Park, Yong-Koo. "Multiple Enchondromatosis (Ollier’s Disease)." In Tumors and Tumor-Like Lesions of Bone, 253–58. London: Springer London, 2015. http://dx.doi.org/10.1007/978-1-4471-6578-1_17.

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Na, Kiyong, and Yong-Koo Park. "Multiple Enchondromatosis (Ollier’s Disease)." In Tumors and Tumor-Like Lesions of Bone, 257–65. Cham: Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-030-28315-5_19.

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Fabbri, Nicola, and Davide Donati. "Multiple Chondromas (Chondromatosis, Ollier’s Disease) Associated Condition: Maffucci’s Syndrome." In Atlas of Musculoskeletal Tumors and Tumorlike Lesions, 61–64. Cham: Springer International Publishing, 2013. http://dx.doi.org/10.1007/978-3-319-01748-8_14.

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Eralp, Levent, and Ilker Eren. "Case 62: Correction of Long Bone Deformities due to Ollier’s Disease with Ilizarov Method." In Limb Lengthening and Reconstruction Surgery Case Atlas, 415–19. Cham: Springer International Publishing, 2015. http://dx.doi.org/10.1007/978-3-319-18020-5_244.

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Rozbruch, S. Robert. "Case 81: Humeral Lengthening and Deformity Correction in Ollier’s Disease: Distraction Osteogenesis with a Multiaxial Correction Frame." In Limb Lengthening and Reconstruction Surgery Case Atlas, 563–68. Cham: Springer International Publishing, 2015. http://dx.doi.org/10.1007/978-3-319-18020-5_256.

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Richards, B. Stephens, Alexander Cherkashin, and Mikhail Samchukov. "Varus Deformity of the Distal Femur and LLD Secondary to Ollier’s Disease Corrected by Gradual Deformity Correction and Lengthening." In Limb Lengthening and Reconstruction Surgery Case Atlas, 1–9. Cham: Springer International Publishing, 2014. http://dx.doi.org/10.1007/978-3-319-02767-8_84-1.

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Conference papers on the topic "Ollier disease"

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Venteicher, Andrew, Michael Mcdowell, Ezequiel Goldschmidt, Eric Wang, Carl Snyderman, and Paul Gardner. "Propensity for Hemorrhagic Presentation of Skull Base Chondrosarcoma in Patients with Ollier Disease and Maffucci Syndrome." In 29th Annual Meeting North American Skull Base Society. Georg Thieme Verlag KG, 2019. http://dx.doi.org/10.1055/s-0039-1679691.

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You might also be interested in the extended bibliographies on the topic 'Ollier disease' for particular source types:
Journal articles
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