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Trénink sprinterky ve specializované etapě přípravy. Autoanalýza vlastního tréninku / Sprinter's training in the specialized phase of the conditioning - Selfanalysis of one's own trainingStrnadová, Lenka January 2015 (has links)
Title: Sprinter's training in the specialized phase of the conditioning Selfanalysis of one's own training Goals: The main goal of this dissertation is to review the development of my own performance and to evaluate the training in the specialized phase of the conditioning. Next goal is to evaluate the individual development and the results of chosen STU, that are important for short smooth sprint, and afterthat to compare those indicators. Methods: Data for the explorative part were gained by the method of content-selfanalysis of training documents, and we I evaluated chosen special training indicators of those documents. We mainly focused on development of acceleration maximum speed, followed by the development of speed endurance and running with load (total volume in km). Results: The results of chosen training indicators are processed to the table and graphic form. The form of comments is used for analysis of sport preparation, setting up the compensative exercises, health condition and evaluation of performance' development during four years period with two different coaches. The load was increasing in all chosen STU. The individual approach of the coach and communication with the client was very important aspect, that also contributed to the conclusion, that the best results were reached with...
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Avaliação da carga viral plasmática do HTLV-1 em indivíduos assintomáticos e desenvolvendo a mielopatia associada ao HTLV-1/paraparesia espástica tropical (HAM/TSP). / Evaluation of HTLV-1 plasmatic viral load in asymptomatic and HTLV-1-associated myelopathy/Tropical spastic paraparesis (HAM/TSP) individuals.Cabral, Fábio Aparecido Barbosa 05 July 2010 (has links)
O vírus linfotrópico das células T humanas tipo 1 (HTLV-1), é responsável por patologias como a mielopatia associada ao HTLV-1 ou paraparesia espástica tropical (HAM/TSP) e a leucemia/linfoma das células T do adulto (ATL) dentre outras. As vias de replicação até hoje demonstradas, não suportam a hipótese de um estado virêmico. Neste estudo, a detecção de partículas virais plasmáticas foi executada, por PCR em Tempo Real e Nested PCR em 190 amostras de pacientes infectados pelo HTLV-1(assintomáticos ou com HAM/TSP), em acompanhamento, no Instituto de Infectologia Emílio Ribas. 12 indivíduos (8%) testados por PCR em tempo real (n=150) e 6 indivíduos (18%) testados por Nested PCR (n=33, dado que sete amostras foram excluídas da análise) apresentaram RNA do HTLV-1 detectável no plasma. Em conclusão, foi possível identificar RNA plasmático do HTLV-1, tanto em pessoas assintomáticas quanto com HAM/TSP. Esta detecção abre novas possibilidades de discussão sobre a replicação do HTLV-1 e das vias de transmissão, sugerindo maiores investigações para elucidar o assunto. / The human T-cell lymphotropic virus type1 (HTLV-1) is responsible for some pathologies such as HTLV-1-associated myelopathy/tropical spastic paraparesis (HAM/TSP) and Adult T-cell Leukemia/ Lymphoma (ATL) among others. Its ways of replication so far presented do not support the hypothesis of a viremic stage. In this study, the detection of the plasmatic viral load was performed by real time PCR and Nested PCR in 190 samples from HTLV-1 infected individuals (Either Asymptomatic or HAM/TSP cases) following up at Instituto de Infectologia Emílio Ribas. 12 individuals (8%) tested by Real time PCR (n= 150) and 6 individuals (18%) tested by Nested PCR (n= 33, given that 7 samples were excluded from the analysis) presented detectable HTLV-1 RNA in the plasma. In conclusion, it was possible to indentify HTLV-1 plasmatic RNA in asymptomatic carriers as well as in HAM/TSP cases. This detection opens new possibilities of discussion about HTLV-1 replication and transmission pathways, suggesting further investigation for clarifying this matter.
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Avaliação da carga viral plasmática do HTLV-1 em indivíduos assintomáticos e desenvolvendo a mielopatia associada ao HTLV-1/paraparesia espástica tropical (HAM/TSP). / Evaluation of HTLV-1 plasmatic viral load in asymptomatic and HTLV-1-associated myelopathy/Tropical spastic paraparesis (HAM/TSP) individuals.Fábio Aparecido Barbosa Cabral 05 July 2010 (has links)
O vírus linfotrópico das células T humanas tipo 1 (HTLV-1), é responsável por patologias como a mielopatia associada ao HTLV-1 ou paraparesia espástica tropical (HAM/TSP) e a leucemia/linfoma das células T do adulto (ATL) dentre outras. As vias de replicação até hoje demonstradas, não suportam a hipótese de um estado virêmico. Neste estudo, a detecção de partículas virais plasmáticas foi executada, por PCR em Tempo Real e Nested PCR em 190 amostras de pacientes infectados pelo HTLV-1(assintomáticos ou com HAM/TSP), em acompanhamento, no Instituto de Infectologia Emílio Ribas. 12 indivíduos (8%) testados por PCR em tempo real (n=150) e 6 indivíduos (18%) testados por Nested PCR (n=33, dado que sete amostras foram excluídas da análise) apresentaram RNA do HTLV-1 detectável no plasma. Em conclusão, foi possível identificar RNA plasmático do HTLV-1, tanto em pessoas assintomáticas quanto com HAM/TSP. Esta detecção abre novas possibilidades de discussão sobre a replicação do HTLV-1 e das vias de transmissão, sugerindo maiores investigações para elucidar o assunto. / The human T-cell lymphotropic virus type1 (HTLV-1) is responsible for some pathologies such as HTLV-1-associated myelopathy/tropical spastic paraparesis (HAM/TSP) and Adult T-cell Leukemia/ Lymphoma (ATL) among others. Its ways of replication so far presented do not support the hypothesis of a viremic stage. In this study, the detection of the plasmatic viral load was performed by real time PCR and Nested PCR in 190 samples from HTLV-1 infected individuals (Either Asymptomatic or HAM/TSP cases) following up at Instituto de Infectologia Emílio Ribas. 12 individuals (8%) tested by Real time PCR (n= 150) and 6 individuals (18%) tested by Nested PCR (n= 33, given that 7 samples were excluded from the analysis) presented detectable HTLV-1 RNA in the plasma. In conclusion, it was possible to indentify HTLV-1 plasmatic RNA in asymptomatic carriers as well as in HAM/TSP cases. This detection opens new possibilities of discussion about HTLV-1 replication and transmission pathways, suggesting further investigation for clarifying this matter.
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