Relevant bibliographies by topics / Transfer cask cystem

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  1. Journal articles
  2. Dissertations / Theses
  3. Book chapters

Academic literature on the topic 'Transfer cask cystem'

Author: Grafiati
Published: 4 September 2021
Last updated: 29 July 2025

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Journal articles on the topic "Transfer cask cystem"

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Patel, Pradeep, K. K Pandey, D. Peepra, and U. Katakwar. "Aneurysmal Bone Cyst of the First Metatarsal Reconstructed Using Non Vascular Free Fibular Graft Transfer - A Case Report." International Journal of Science and Research (IJSR) 11, no. 2 (2022): 34–37. http://dx.doi.org/10.21275/sr22129000229.

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Biazotti, Maria Cristina Santoro, Walter Pinto Junior, Maria Cecília Romano Maciel de Albuquerque, et al. "Preimplantation genetic diagnosis for cystic fibrosis: a case report." Einstein (São Paulo) 13, no. 1 (2015): 110–13. http://dx.doi.org/10.1590/s1679-45082015rc2738.

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Cystic fibrosis is an autosomal recessive disorder caused by mutations in the cystic fibrosis transmembrane conductance regulator gene. This disorder produces a variable phenotype including lung disease, pancreatic insufficiency, and meconium ileus plus bilateral agenesis of the vas deferens causing obstructive azoospermia and male infertility. Preimplantation genetic diagnosis is an alternative that allows identification of embryos affected by this or other genetic diseases. We report a case of couple with cystic fibrosis; the woman had the I148 T mutation and the man had the Delta F508 gene
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Ferro, Ashley, Meryl Griffiths, Rona Smith, and Andrew Fry. "Acute kidney injury as the presenting complaint of ceftazidime-induced immune-mediated haemolysis." BMJ Case Reports 12, no. 11 (2019): e232884. http://dx.doi.org/10.1136/bcr-2019-232884.

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We present the case of ceftazidime-induced immune-mediated haemolysis with associated acute kidney injury in a 43-year-old woman. The patient initially presented to the regional cystic fibrosis centre for treatment of an infective exacerbation of cystic fibrosis. After initiation of ceftazidime (a third-generation cephalosporin), renal function rapidly deteriorated and a fall in haemoglobin was noted. On transfer to our care, a haemolysis screen identified immune-mediated haemolysis, and renal biopsy confirmed the finding of acute tubular necrosis secondary to haem pigment. The patient’s renal
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Nisanci, Mustafa, Ismail Sahin, and Serbulent Guzey. "An Extraordinary Case of Axillary Contracture: Trapped Healthy Skin and Its Adnexes Under Contracted Scar." International Surgery 99, no. 4 (2014): 442–46. http://dx.doi.org/10.9738/intsurg-d-13-00127.1.

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Abstract Although striking improvements have been achieved in overall management of burn injury, postburn contractures are still an ongoing challenge to burn surgeons. Axillary adduction contracture is one of the most common types of these disabling postburn complications that usually result from suboptimal treatment after acute burns. An unusual and complicated case of axillary contracture in which the unburned, healthy axillary dome skin was trapped as a cystic mass under the scarred area was reconstructed by transfer of a big (17 × 13-cm) thoracodorsal artery perforator flap after contractu
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Thompson, Christopher St Clair Gaston, Lucy Qian Li, and Alok Sharma. "Coblation of paediatric cystic laryngeal lymphovascular malformations: a safe and effective alternative to tracheostomy." BMJ Case Reports 13, no. 9 (2020): e235596. http://dx.doi.org/10.1136/bcr-2020-235596.

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We describe the case of a 12-hour-old, full-term newborn girl referred to the Ear, Nose and Throat emergency team with increased work of breathing and stridor present at birth. Flexible nasendoscopy revealed a cystic laryngeal lesion obstructing the glottis that prompted securing of the airway with intubation and transfer to a tertiary paediatric centre. On further investigation with MRI and direct visualisation, the lesion was identified as a mixed macro/microcystic laryngeal lymphovascular malformation. The patient successfully underwent a series of microlaryngo–bronchoscopy and coblations o
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Prokic, Aleksandra, Minja Milicic-Lazic, and Igor Djordjevic. "Soft tissue management at delayed implant loading in the aesthetic zone: A case report." Serbian Dental Journal 70, no. 4 (2023): 196–202. http://dx.doi.org/10.2298/sgs2304196p.

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Emergence profile of implant-supported crowns is defined by the characteristics of supracrestal connective tissue (SCT), located between the implant platform and cervical soft tissue margin. This paper reflects the soft tissue contour management of implant-supported screw-retained crowns and the transfer of emergence profile using an indirectly customized impression coping. A 27-year-old male was referred for endosseus implant placement (Straumann BLT 0 4.1 mm ? 12 mm) in a region of a maxillary right central and lateral incisor. Teeth were extracted due to a cystic formation in the mentioned
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7

Pribylov, Sergey A., Tatyana A. Maslova, Vladislav S. Pribylov, Kristina O. Leonidova, Nadezhda N. Pribylova, and Anna P. Kuts. "Long-COVID, severe course, with congenital bronchiectasis, Williams–Campbell syndrome. Case report." Terapevticheskii arkhiv 96, no. 11 (2024): 1089–95. https://doi.org/10.26442/00403660.2024.11.202997.

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We present a clinical observation of an 18-year-old female patient with congenital bronchiectasis combined with congenital cystic degeneration of the upper lobes of both lungs, Williams–Campbell syndrome, long-COVID, severe course. The patient was treated in infectious disease department (three times), with subsequent transfer to pulmonology department of Kursk Regional Multi-Purpose Clinical Hospital from 31.01.2023 to 02.05.2023. The patient was going to have lung transplantation, registered in Shumakov Federal Research Center of Transplantology and Artificial Organs earlier. The patient was
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8

Ng, Irene Ai Ting, Hiang Jin Tan, Adrian Kah Heng Chiow, and Thiruchelvam Nita. "Surgical management of rare hepatobiliary sarcomas in a regional teaching hospital: a collaborative model for optimal care with case studies." BMJ Case Reports 17, no. 9 (2024): e260975. http://dx.doi.org/10.1136/bcr-2024-260975.

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Sarcomas are challenging and conventionally referred to sarcoma specialist centres. In select cases with required surgical expertise, collaboration with a quaternary sarcoma centre rather than an upfront transfer of care may reduce logistic challenges without compromising patient care.We present a case series of three rare tumours of hepatobiliary origin—two cases of undifferentiated embryonal liver sarcoma in adults and one case of follicular dendritic sarcoma of the cystic lymph node.All three patients underwent surgery in a non-sarcoma specialist centre by hepatobiliary specialist surgeons
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Botticelli, Gianluca, Marco Severino, Gianmaria Fabrizio Ferrazzano, et al. "Excision of Lower Lip Mucocele Using Injection of Hydrocolloid Dental Impression Material in a Pediatric Patient: A Case Report." Applied Sciences 11, no. 13 (2021): 5819. http://dx.doi.org/10.3390/app11135819.

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Oral mucocele is a benign cystic exophytic lesion affecting the minor salivary gland and is especially present in pediatric patients (3% under 14 years). It is characterized by an extravasation or retention of fluid or mucus in the submucosal tissue of the minor salivary glands. Several surgical techniques have been proposed over the years, including the excision of the mucocele by using the injection of a hydrocolloid impression material in the light of the cyst to prevent the collapse of the cystic wall and solidify the lesion, resulting in a better cleavage plan. The combined clinical appro
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Wilson, A. M., H. L. Slack, S. A. Soosay, et al. "Lymphangioleiomyomatosis A Series of Three Case Reports Illustrating the Link with High Oestrogen States." Scottish Medical Journal 46, no. 5 (2001): 150–52. http://dx.doi.org/10.1177/003693300104600509.

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Lymphangioleiornyomatosis is a rare lung disorder characterised by cystic air spaces and smooth muscle proliferation. The condition, which most commonly presents with dyspnoea, pneumothoraces or cough, is only described in fernales and is most commonly diagnosed during childbearing years. Three cases are presented which illustrate typical features of the disease and the association with high oestrogen levels. The first had recurrent pneumothoraces during her first pregnancy. The second lady was post menopausal at diagnosis but her symptoms predated her menopause. The third, presented with dysp
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Dissertations / Theses on the topic "Transfer cask cystem"

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Corujeira, José Gouveia Pereira. "A situation awareness interface for a bi-wheeled industrial hovercraft: design, development and evaluation." Master's thesis, 2010. http://hdl.handle.net/10400.13/332.

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The intention of this thesis is to develop a prototype interface that enables an operator to control a bi-wheeled industrial hovercraft that will work within a fusion power plant if the automation system fails. This fusion power plant is part of the ITER project a conjoint effort of various industrialized countries to develop cleaner sources of energy. The development of the interface prototype will be based on situation awareness concepts, which provide a means to understand how human operators perceive the world around, then process that information and make decisions based on the knowledge
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Book chapters on the topic "Transfer cask cystem"

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Meulemans, J., C. Van Lierde, P. Delaere, J. J. Vranckx, and V. Vander Poorten. "New Developments in Surgery for Malignant Salivary Gland Tumors." In Critical Issues in Head and Neck Oncology. Springer International Publishing, 2023. http://dx.doi.org/10.1007/978-3-031-23175-9_19.

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AbstractMalignant salivary gland tumors (MSGTs) are of key interest for head and neck surgeons since surgery with adjuvant radiotherapy is considered the treatment of choice in most patients. In this respect, recently, interesting developments in ablative and reconstructive procedures have been proposed. Regarding the ablative part, transoral surgery, both with laser (transoral laser microsurgery or TLM) and robot (transoral robotic surgery or TORS) is increasingly used as a less invasive surgical treatment of malignant minor salivary gland tumors (MiSGMT) of the oropharynx, larynx and hypopha
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Parrington, John. "New Gene Therapy." In Redesigning Life. Oxford University Press, 2020. http://dx.doi.org/10.1093/oso/9780198766834.003.0008.

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Modern medicine has advanced tremendously in the 20<sup>th</sup> century, yet many people still die each year from conditions like heart attacks, cancer, and infectious diseases. Genome editing looks set to transform clinical medicine over the next few decades, because it now makes it possible to alter genes either in a living person, or in an infectious agent like a virus. One particular type of disease where genome editing is likely to have a big impact is single gene disorders such as cystic fibrosis, Huntington’s disorder, and muscular dystrophy. Because these disorders are due to a mutati
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