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Tree Code Decoding Methods
Zamazal, Zdeněk ; Lambertová, Petra (referee) ; Němec, Karel (advisor)
This thesis deals with applying knowledge of data channel coding and concerns about possibilities of tree codes decoding. It describes several decoding methods and inquires their ins and outs. Basic knowledge of theory of information is necessary, it is presumed that reader is familiar with convolutional codes and coder definitions. Criterions for choosing decoding method are introduced and lightely described. A decoder is designed using method choosed by denoted criterions. Implementation of the decoder, using Matlab Simulink enviroment, has taken part in the thesis. Function of the decoder is verified in simulation.
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Burnout syndrome in swimmers of age-group categories
Slámová, Jana ; Zenáhlík, Aleš (advisor) ; Hubená, Kristýna (referee)
Title: Burnout syndrome in swimmers of age-group categories Objectives: The aim of this work was to systematically map and analyze empirical knowledge about burnout syndrome in competitive swimmers under 18 years of age. Methods: This work was created in the form of a review study. Specifically, the purpose was to get as close as possible to the design of the scoping review. The search for relevant sources was carried out on the basis of predetermined criteria in the Scopus and Web of Science databases, and the Google Scholar search engine was also used as a complement. Results: There were found 7 relevant articles where 5 of them dealt with factors related to the development of burnout in young swimmers, one included a comparison of burnout scores between swimmers and volleyball players, and one article examined the psychometric properties of the Athlete Burnout Questionnaire adapted for children under 13 years of age. The results that stem from the analysis of these articles in most cases confirmed the hypotheses regarding the burnout syndrome in athletes, however, despite the assumption, a positive relationship between early specialization and the development of burnout was not proven. Keywords: syndrome, burnout, maladaptive, swimming, youth, dropout
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Person with Teacher Collins syndrom in context with coordinated care and quality of life, case study
KOUBOVÁ, Michaela
Bachelor thesis deals with the issue of Treacher Collins syndrome. Treacher Collins Syndrome is a rare genetic disease that is distinctly manifested by deformities in the face. Due to the different appearance and ignorance of the syndrome, it is difficult, for the public, to integrate individuals into society. These factors impede the mental well-being of both the individual and his family. This work is divided into theoretical and research part. In the theoretical part, the subject of this syndrome is elaborated based on relevant sources, so that the reader be well versed in this issue. It deals with the definition of Treacher Collins syndrome, its history, description of symptoms, and causes. The thesis also mentions methods of prenatal diagnosis and the development of such an individual. The next part focuses on comprehensive care of individuals. It includes special pedagogical care, health and social care. It deals primarily with the education of individuals, surgical interventions, compensatory aids, and the integration of individuals with Treacher Collins syndrome into society. The research part consists of a case study of a specific individual with Treacher Collins syndrome and his family. This part has been aimed to obtain and process information concerning the state of health, personal and family case history, available medical care, education, interests and life quality of the individual and his family. An in-depth interview and analysis of specific documents were used to obtain data. The research revealed a lot of interesting information. It turned out that the quality of life is influenced by levels of parental competencies, quality of health care, and the functionality of integration into the education system.
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Case study of physiotherapy treatment of a patient with Guillain Barre Syndrome
Císař, Tomáš ; Kučerová, Ilona (advisor) ; Novotná, Irena (referee)
Title: Case study of physiotherapy care for patients with Guillain-Barre syndrome. Objective: Summary of theoretical knowledge and the processing of study reports of patients diagnosed with Guillain-Barré syndrome. Abstract: The thesis consists of two parts. The general section includes anatomical and neurophysiological aspects of GBS characterized by its brief history, treatment, diagnosis, and precipitating factors. A special section is devoted to a case study and rehabilitation plan for the patient. Therapy was directed primarily to improve quality of life. The case study was prepared at the time of practice from 17. 2. to 29. 2. 2011 at the neurology department at the district hospital in Kladno a.s. Keywords: Guillain-Barré, syndrome, kazuistics, neurology, peripreral polyradikuloneuritis.
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Genetics of Craniosynostosis.
Valterová, Simona ; Křepelová, Anna (advisor) ; Baxová, Alice (referee)
Craniosynostoses are premature fusions of one or more cranial sutures. They affect all cranial sutures and are the main symptom of many genetic syndromes. Syndromes connected with craniosynostosis are serious disorders associated with skeleton abnormalities, limb malformations or mental disability. These syndroms are caused by different mutations in FGFR1, FGFR2, FGFR3, TWIST1, EFNB1, RECQL4, and RAB23 genes. The aim of this review was to summarize contemporary knowledge of phenotype and genetic basis of these diseases.
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Genetics of Craniosynostosis.
Valterová, Simona ; Křepelová, Anna (advisor) ; Baxová, Alice (referee)
Craniosynostoses are premature fusions of one or more cranial sutures. They affect all cranial sutures and are the main symptom of many genetic syndromes. Syndromes connected with craniosynostosis are serious disorders associated with skeleton abnormalities, limb malformations or mental disability. These syndroms are caused by different mutations in FGFR1, FGFR2, FGFR3, TWIST1, EFNB1, RECQL4, and RAB23 genes. The aim of this review was to summarize contemporary knowledge of phenotype and genetic basis of these diseases.
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The issue of care for children with MCAP syndrome.
PŘÍPLATOVÁ, Iveta
For most of the people MCAP syndrome is an unknown term. It is actually an illness, where the gene is changed for unknown reasons, leading to macrocephaly and capillary malformations. The syndrome entails its own symptoms and complications, which are the focus of this paper and which are described below. The goal of the thesis was to find out the specifics of care for children with MCAP syndrome. Interviews and observations were conducted with two families of children with this syndrome. The interviews were made with the mothers of the children. The results of the interviews and observations are outlined in the text, which is divided into two parts. The life of the child, from birth to present day, is described in the first part of the text. All symptoms, signs and complications are also included in this part. The second part of the text deals with collection of data according to the model of Virginia Henderson. The result shows that even though some of the children's symptoms are mutual for both of them, every child is born also with different symptoms. Therefore every child is unique. The interviews showed that no one in the Czech Republic has ever had the experience with this syndrome and the level of awareness of the syndrome among the health care stuff is very small or none at all. There is also no Czech literature published on this topic in the Czech Republic. There can only be found foreign articles written in English language that are not intelligible for a big part of the population. This thesis can be a helpful manual for some other families that give birth to a child with this syndrome and it can further help to spread information of the illness also to all readers, who are interested in this topic. That is also the reason, why the article on the topic of MCAP syndrome is going to be published in a professional journal.
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