Academic literature on the topic 'Surgical anomalies'

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Journal articles on the topic "Surgical anomalies"

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Jan, AG, S. Biscette, D. Ginn, R. Pasic, and K. Isaacson. "Surgical Management of Mullerian Anomalies." Journal of Minimally Invasive Gynecology 23, no. 7 (2016): S154. http://dx.doi.org/10.1016/j.jmig.2016.08.520.

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MILLER, RACHEL J., and LESLEY L. BREECH. "Surgical Correction of Vaginal Anomalies." Clinical Obstetrics and Gynecology 51, no. 2 (2008): 223–36. http://dx.doi.org/10.1097/grf.0b013e31816d2181.

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Krstic, Z. D., M. Lukac, R. Lukac, Z. Smoljanic, V. Vukadinovic, and D. Varinac. "Surgical treatment of cloacal anomalies." Pediatric Surgery International 17, no. 4 (2001): 329–33. http://dx.doi.org/10.1007/s003830000522.

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Dasgupta, Roshni. "Surgical Management of Vascular anomalies." Current Otorhinolaryngology Reports 2, no. 4 (2014): 285–91. http://dx.doi.org/10.1007/s40136-014-0066-5.

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Imoto, Yutaka. "Surgical Treatment of Coronary Artery Anomalies." Pediatric Cardiology and Cardiac Surgery 32, no. 2 (2016): 122–28. http://dx.doi.org/10.9794/jspccs.32.122.

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Lukac, Marija, Sanja Sindjic, Zoran Krstic, et al. "Surgical management of congenital lung anomalies." Srpski arhiv za celokupno lekarstvo 132, suppl. 1 (2004): 77–81. http://dx.doi.org/10.2298/sarh04s1077l.

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Prenatal diagnosis allows for insight into the evaluation of fetal lung anomalies. Serial ultrasonographic studies of fetuses helped in evaluation and definition of the natural course of these lesions as well as necessity for fetal therapy. It has been found that the overall prognosis depends on the size of the lung mass and the secondary derangement of normal lung tissue and cardiovascular system. Although much is known about the prenatal course of these anomalies, little is known about the postnatal course of asymptomatic patients. Infants who are symptomatic at birth require early surgical
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Sharma, Sanjeev, Jeri L. Dobbs, and Adnan Cobanoglu. "Surgical Correction of Vascular Ring Anomalies." Asian Cardiovascular and Thoracic Annals 8, no. 4 (2000): 344–46. http://dx.doi.org/10.1177/021849230000800411.

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Yacoub, Magdi, and John Pepper. "Surgical treatment of coronary artery anomalies." Current Opinion in Cardiology 6, no. 6 (1991): 929–34. http://dx.doi.org/10.1097/00001573-199112000-00011.

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Hubbell, Richard N., and Peter S. Ihm. "Current surgical management of vascular anomalies." Current Opinion in Otolaryngology & Head and Neck Surgery 8, no. 6 (2000): 441–47. http://dx.doi.org/10.1097/00020840-200012000-00001.

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Kayalar, Nihan, Harold M. Burkhart, Joseph A. Dearani, Frank Cetta, and Hartzell V. Schaff. "Congenital Coronary Anomalies and Surgical Treatment." Congenital Heart Disease 4, no. 4 (2009): 239–51. http://dx.doi.org/10.1111/j.1747-0803.2009.00301.x.

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Dissertations / Theses on the topic "Surgical anomalies"

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Lauck, Leisa C. "Speech outcomes following surgical management of velopharyngeal dysfunction a survey of craniofacial anomalies teams /." Cincinnati, Ohio : University of Cincinnati, 2005. http://www.ohiolink.edu/etd/view.cgi?acc%5Fnum=ucin1116254418.

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LAUCK, LEISA C. "SPEECH OUTCOMES FOLLOWING SURGICAL MANAGEMENT OF VELOPHARYNGEAL DYSFUNCTION: A SURVEY OF CRANEOFACIAL ANOMALIES TEAMS." University of Cincinnati / OhioLINK, 2005. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1116254418.

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Radoje, Simić. "Kliničke i patohistološke karakteristike urođenog rascepa vrata u prednjoj srednjoj liniji i njihov značaj za diferencijalnu dijagnozu i hirurško lečenje." Phd thesis, Univerzitet u Novom Sadu, Medicinski fakultet u Novom Sadu, 2015. https://www.cris.uns.ac.rs/record.jsf?recordId=94511&source=NDLTD&language=en.

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Urođeni rascep sa naborom u prednjoj srednjoj liniji vrata (UR-N PSLV) je retka anomalija sa oko 100-150 bolesnika opisanih u literaturi. Tipičan rascep se sastoji od atrofične, ružičaste kože u obliku žleba, kožne prominencije na gornjem kraju i potkožnog sinusa na donjem kraju tzv. rascepa. Ispod ovih elemenata nalazi se potkožna vezivno-mišićna traka koja izaziva nabor na vratu. Izolovani nabor vrata, kao jedan od tipova rascepa, ima samo potkožnu traku i podbradnu kožnu izraslinu. U radu analiziramo seriju od 11 bolesnika sa UR-N PSLV operisanih u periodu od 12 godina (jul 1998. - j
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Books on the topic "Surgical anomalies"

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Narayan, Deepak, Shanta E. Kapadia, Gopal Kodumudi, and Nalini Vadivelu, eds. Surgical and Perioperative Management of Patients with Anatomic Anomalies. Springer International Publishing, 2021. http://dx.doi.org/10.1007/978-3-030-55660-0.

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Embryology and anomalies of the facial nerve and their surgical implications. Raven Press, 1991.

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Grosvenor, Theodore P. Primary care optometry: Anomalies of refraction and binocular vision. 3rd ed. Butterworth-Heinemann, 1996.

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Goodrich, James Tait. Craniofacial Anomalies: Growth and Development From A Surgical Perspective. Thieme Medical Publishers, 1995.

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T, Goodrich James, and Hall Craig D, eds. Craniofacial anomalies: Growth and development from a surgical perspective. Thieme Medical Publishers, 1995.

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Orthodontic-Surgical Treatment of Dentofacial Anomalies: An Integrated Esthetic-functional Approach. Quintessence Publishing (IL), 2005.

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Sataloff, Johnathan. Embryology and Anomalies of the Facial Nerve and Their Surgical Implications. Jaypee Brothers Medical Publishers (P) Ltd., 2014. http://dx.doi.org/10.5005/jp/books/12224.

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Karmody, Collin S. Atlas of the Congenital Anomalies of the Neck: Tips on Surgical Management. Singular Publishing Group Inc, 2001.

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Contributions to the Reference handbook of the medical sciences, on anatomical anomalies, surgery, and surgical anatomy. [s.n.], 1995.

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1920-, Skandalakis John Elias, and Gray Stephen Wood 1915-, eds. Embryology for surgeons: The embryological basis for the treatment of congenital anomalies. 2nd ed. Williams & Wilkins, 1994.

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Book chapters on the topic "Surgical anomalies"

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Jose, R., Mary O’Brien, and Frank Burke. "Congenital Hand Anomalies." In European Surgical Orthopaedics and Traumatology. Springer Berlin Heidelberg, 2014. http://dx.doi.org/10.1007/978-3-642-34746-7_87.

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Karpelowsky, J., and L. Tebogo Hlabangana. "Branchial Cleft Anomalies." In ABC of Pediatric Surgical Imaging. Springer Berlin Heidelberg, 2010. http://dx.doi.org/10.1007/978-3-540-89385-1_9.

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Fayez, Jamil A. "Surgical Correction of Uterine Anomalies." In Comprehensive Manuals of Surgical Specialties. Springer New York, 1986. http://dx.doi.org/10.1007/978-1-4612-4860-6_18.

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Su, Jeannie Jiwon, José Murillo B. Netto, and Adam B. Hittelman. "Urologic Anomalies and Surgical Implications." In Surgical and Perioperative Management of Patients with Anatomic Anomalies. Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-030-55660-0_13.

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Zhu, Xiaodong. "Congenital Anomalies of the Tricuspid Valve." In Surgical Atlas of Cardiac Anatomy. Springer Netherlands, 2014. http://dx.doi.org/10.1007/978-94-017-9409-1_16.

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Hraška, Viktor, and Peter Murín. "Left Ventricular Outflow Tract Anomalies." In Surgical Management of Congenital Heart Disease I. Springer Berlin Heidelberg, 2012. http://dx.doi.org/10.1007/978-3-642-24169-7_3.

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Rubinstein, Jill C., James S. Farrelly, David Stitelman, and Emily Christison-Lagay. "Anomalies of the Gastrointestinal Tract." In Surgical and Perioperative Management of Patients with Anatomic Anomalies. Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-030-55660-0_9.

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Cha, Charles, and Whitney S. Brandt. "Surgical Anatomy of the Hepatobiliary System." In Surgical and Perioperative Management of Patients with Anatomic Anomalies. Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-030-55660-0_10.

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Beretta, Federica, Giuseppe Talamonti, Giuseppe D’Aliberti, Gabriele Canzi, Fabio Mazzoleni, and Alberto Bozzetti. "Surgical Indications and Treatment for Cranial Occipital Anomalies." In Positional Plagiocephaly. Springer International Publishing, 2014. http://dx.doi.org/10.1007/978-3-319-06118-4_8.

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Li, Xiaochuan, Lan Zhu, Qing Dai, and Jingjing Lu. "The Diagnosis of Female Reproductive Tract Anomalies." In Atlas of Surgical Correction of Female Genital Malformation. Springer Netherlands, 2015. http://dx.doi.org/10.1007/978-94-017-7246-4_2.

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Conference papers on the topic "Surgical anomalies"

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Cesnjevar, R., F. Harig, A. Purbujo, et al. "Tracheobronchial Compression by Congenital Vascular Anomalies – Surgical Procedures and Results." In 49th Annual Meeting of the German Society for Thoracic and Cardiovascular Surgery. Georg Thieme Verlag KG, 2020. http://dx.doi.org/10.1055/s-0040-1705307.

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Iaquinto, Joseph M., and Jennifer S. Wayne. "Flatfoot and Its Surgical Treatments: a Computational Model of Common Procedures." In ASME 2010 Summer Bioengineering Conference. American Society of Mechanical Engineers, 2010. http://dx.doi.org/10.1115/sbc2010-19592.

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Adult Acquired Flatfoot Deformity (AAFD) is a multi-stage degenerative joint disease. Common indicators are distinct morphological anomalies of the affected foot and the presence of pain and/or weakness along the posterior tibial tendon path. Early treatment (Stage I) can effect favorable results with nonoperative techniques including shoe orthotics. Surgical treatment begins at Stage II, which is characterized by more profound deep tissue damage to ligaments and tendons of the arch. The level of severity increases in Stages III and IV with significant joint damage including to the ankle [1].
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Dur, Onur, Ergin Kocyildirim, Curt G. Degroff, et al. "Pulsatile Efficiency and Pediatric Venous Assist Options in Failing Fontan Patients." In ASME 2010 Summer Bioengineering Conference. American Society of Mechanical Engineers, 2010. http://dx.doi.org/10.1115/sbc2010-19644.

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Single ventricle (SV) anomalies are the fifth most common heart defect (2000 patients per year) and the leading cause of death from all structural birth defects. Total cavopulmonary connection (TCPC) is the last stage of the palliative surgical reconstruction i.e. Fontan procedure for the infants with SV. A large number of children continue to benefit from the Fontan operation. However, despite many refinements of the surgical procedure in the past 20 years, a relatively high proportion of patients demonstrate a gradual decline in functional capacity and premature death. Most of these failing
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Sen-Hild, B., U. Yörüker, A. Sprengel, et al. "Outcomes of Biventricular Surgical Treatment for Interrupted Aortic Arch with/without Associated Complex Cardiac Anomalies: A Single-Center Experience in 16 Years." In 48th Annual Meeting German Society for Thoracic, Cardiac, and Vascular Surgery. Georg Thieme Verlag KG, 2019. http://dx.doi.org/10.1055/s-0039-1678759.

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Shih, Tzu-Ching, Tzyy-Leng Horng, and Fong-Lin Chen. "Computational Fluid Dynamics Simulation of Airflow Alteration in the Trachea Before and After Vascular Ring Surgery." In ASME 2013 Summer Bioengineering Conference. American Society of Mechanical Engineers, 2013. http://dx.doi.org/10.1115/sbc2013-14360.

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Vascular rings, congenital intracardic anomalies of the aortic arch and the vessels emerging from the heart, completely encircle the trachea and esophagus [1]. The vascular ring results in narrowing and obstruction of the trachea and the esophagus. Due to the existence of a complete or partial vascular ring compressing either the trachea or esophagus, symptoms of a vascular ring in children include cough, stridor, chronic cough, dysphagia, persistent wheeze, and noisy breathing [2]. Some studies reported that the vascular ring surgery provides an excellent chance to improve the patient respira
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Rákóczi, I., Gy Geró, J. Demeter, and I. Gáti. "INFLUENCE OF GLUCOSE AND INSULIN OF PROSTACYCLIN SYNTHESIS IN CULTURED TR0PH0BLAST CELLS." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1643373.

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It is known that placental cells can produce prostacyclin /PGI2/. At present, the physiological role of trophoblast PGI2 production can only be speculative. PGI2 produced by trophoblast may help to prevent the platelet aggregation and thrombosis in spiral arteries and it can also explain the maintance of, and blood flow through, the spiral arteries during endovascular trophoblast invasion in early pregnancy. It has been previously shown that increased glucose concentrations in the incubation fluid can inhibit the formation of PGI2 by rat aortic rings. The aim of present investigation was to st
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Medelli´n Castillo, Hugo I., and Manuel A. Ochoa Alfaro. "Development of a Tridimensional Visualization and Model Reconstruction System Based on Computed Tomographic Data." In ASME 2011 International Mechanical Engineering Congress and Exposition. ASMEDC, 2011. http://dx.doi.org/10.1115/imece2011-62822.

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Medical image processing constitutes an important research area of the biomedical engineering since it provides accurate human body information for 3D visualization and analysis, diagnostic, surgical treatment planning, surgical training, prosthesis and implant design, wafer and surgical guides design. Computed tomography (CT) and magnetic resonance imaging (MRI) have had a great impact in the medicine since they can represent complex three dimensional (3D) anomalities or deformities. In this paper, the development of a system for tridimensional visualization and model reconstruction based on
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Zhang, Shenwei, Jason Yan, Shahani Kariyawasam, Terry Huang, and Mohammad Al-Amin. "A More Accurate and Precise Method for Large Metal Loss Corrosion Assessment." In 2018 12th International Pipeline Conference. American Society of Mechanical Engineers, 2018. http://dx.doi.org/10.1115/ipc2018-78233.

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Pipeline integrity decisions are highly sensitive to the assessment model. A less accurate and less precise model can conservatively trigger many unnecessary actions such as excavations without providing additional safety. Therefore, a more accurate and precise model will reduce excavations and provide higher assurance of safety. This is akin to using a more precise surgical tool such as a laser for cutting out a brain tumor where you can cut closer to the edge and be assured of cutting out more of the tumor (safer) and yet cut less of the surrounding brain tissue (less conservative). This pap
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Silva, Jefferson, Eduardo Alchieri, Jacir Bordim, and João Gondim. "Um Plano de Controle Seguro e Distribuído para Redes Definidas por Software." In XX Workshop de Testes e Tolerância a Falhas. Sociedade Brasileira de Computação - SBC, 2019. http://dx.doi.org/10.5753/wtf.2019.7712.

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Redes Definidas por Software (SDN) surgiram como um novo paradigma para gerenciamento de redes, definindo uma arquitetura que separa os planos de dados e de controle. Uma arquitetura SDN baseada em um controlador centralizado não escala e nem tolera falhas, pois apresenta um ponto único de falhas. Controladores distribuídos baseados em um modelo de consistência após um tempo para gerenciamento do estado da rede também apresentam sérios problemas: um modelo de programação complexo para as aplicações de rede; e pode gerar anomalias na rede. Consequentemente, soluções considerando um modelo de da
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