No description available.

The thesis focuces on the causes of muscle injuries in sport ninepin bowling. The theoretical part defines the muscle groups of the body, but also various muscle injuries that may occur during sports. It also describes the characteristics ninepin bowling, its trainning process and lifestyle players. The practical part of the thesis through research focuses the causes of muscle injuries and lifestyle players. The research is based on a survey, which was attended by people who ninepin bowling in the past operated or still operate it.

The main workload of the diploma thesis is to find the level of physical activity among adolescents between the ages of 16 and 18 years. Research is part of the nationwide detection of fitness and healthy lifestyle of youth. The theoretical part deals with the main characteristics of probands in the developmental stage of adolescence and the action of movement activity on their organism. The research section includes data, that was monitored using the Yamax Digiwalker SW-700 pedometer. A standardized IPEN questionnaire on the Indares.com website was also helped by the level of physical activity. The survey was started in December 2017 and the second part in March 2018. The research was attended by 37 students at the Medical School in Český Krumlov, of which 7 boys and 30 girls. The survey show, that boys are more active than girls. The average number of steps is 11,773 / day for boys and the highest measured value is 16,799 steps / day. A total of girls' steps are on average 10,781 steps. Both sexes meet the recommended daily number of steps. Nowadays, any physical activity has many beneficial effects on the body. Influence to technology and media, many students stay home after school and have not energy expenditure.

Title: Compensatory exercise for women artistic gymnasts Objectives: Aim of the thesis was to discover deviations from correct posture and to verify efficiency of suggested compensatory exercise for women artistic gymnasts. Used methods: Study involved 9 girls (average age: 12 ± 0,7 years) who have been training gymnastics for 6,22 years in average. Individual subjects were tested for correct posture, tight muscles and hypermobility. Afterwards, an exercise plan stretched into five months was applied (21 lessons common for all the subjects, 14 lessons under a trainer's supervision for each subject individually and 59 at-home lessons). After completing the exercise plan, second testing was run. Results: Majority of the tested group was detected with hypermobility. At the beginning of the study, all the subjects had mild muscle tightness at least on one of the tested muscles (most often hip flexors). Having applying the exercise plan, status of three subjects (33,33 % of the group) has been compensated. Five subjects (55,55 %) have improved the status of at least one tight muscle. Key words: Diagnosis, gymnastics, compensatory exercise, muscular system, posture, hypermobility, tight muscles.

No description available.

Les déformations rachidiennes se réfèrent aux patients avec une courbure anormal de la colonne vertébrale qui ont terminé leur croissance. Par leur prévalence, leur impact clinique, et le taux relativement élevé d'échecs chirurgicaux, elles représentent un défi thérapeutique. La recherche a permis de démontrer que la préservation ou la restauration de l'alignement, sont des éléments clé du traitement chirurgical. L'objectif de cette thèse était d'analyser le traitement des patients avec DR, avec un intérêt particulier pour la restauration de l'alignement sagittal et l'évaluation musculaire. Fondé sur une analyse rétrospective d'une base de données multicentriques, les deux premiers articles présentent une évaluation du traitement chirurgical en termes d'efficacité clinique et de réalignement radiographique. Les écarts entre la planification préopératoire et l'exécution opérationnelle ont aussi été étudiés avec une collecte de données prospectives, et ont mis en évidence la nécessité de mieux comprendre le rôle des muscles dans le maintien de la posture. Par conséquent, deux protocoles pour la caractérisation des principaux muscles impliqués dans l'alignement sagittal ont été validés. Les deux méthodes sont basées sur la segmentation manuelle d'acquisition IRM spécifique (méthode de Dixon) afin d'obtenir l'infiltration graisseuse en plus du volume musculaire. Une des méthodes permet d'obtenir la reconstruction 3D des muscles et donc de générer des modèles musculo-squelettiques personnalisés. L'autre ouvre la voie à une pratique clinique car nécessite seulement la segmentation de quatre coupes pour obtenir une évaluation des principaux groupes musculaires. Enfin, à partir de la première méthode, le système musculaire de patients avec DR a été décrit. / Adult spinal deformity(ASD) refers to abnormal curvatures of the spine in patients who have completed their growth. Due to its prevalence, clinical impact, and the relatively high rate of surgical failures, they represent a therapeutic challenge. Research has been able to demonstrate that the preservation or the restoration of the sagittal alignment, are key objectives of surgical treatment. The objective of this thesis is to analyze the treatment of ASD patients, with particular interest in restoration of sagittal alignment and to develop tools to assess the spino-pelvic musculature of ASD patients. Based on an analysis of a multicenter database, the first two articles present an evaluation of the surgical treatment in term of clinical effectiveness and radiographic realignment. In addition, the discrepancies between surgical preoperative planning and operative execution have been studied with a prospective data collection, and have highlighted the necessity to understand better the role of the muscles in the maintaining of the posture. Therefore two methods for the characterization of the muscles involved in the sagittal alignment have been validated. Both methods are based on manual segmentation of specific MRI acquisition (Dixon methods) in order to obtain precise fat infiltration quantification in addition to muscular volume. One method permits to obtain 3D reconstruction able to generate patient–specific musculoskeletal model. The other one open the path to a clinical purpose, because necessitate only segmentation of four slices to obtain an relevant evaluation of the muscular system. Finally, thanks to the first protocol the muscular system of ASD patients have been described.

No description available.

Sphaerodoridae is a group of benthic marine worms (Annelida) characterized by the presence of spherical tubercles covering their whole surface. They are commonly considered as belonging to Phyllodocida although sistergroup relationships are still far from being understood. Primary homology assessments of their morphological features are lacking, hindering the appraisal of evolutionary relationships between taxa. Therefore, our detailed morphological investigation focuses on different Sphaerodoridae as well as on other members of Phyllodocida using an integrative approach combining scanning electron microscopy (SEM) as well as immunohistochemistry with standard neuronal (anti-5-HT) and muscular (phalloidin-rhodamine) markers and subsequent CLSM analysis of whole mounts and sections. Furthermore, we provide histological (HES) and light microscopical data to shed light on the structures and hypothetical function of sphaerodorid key morphological features. We provide fundamental details into the sphaerodorid morphology supporting a Phyllodocida ancestry of these enigmatic worms. However, the muscular arrangement and the presence of an axial muscular pharynx is similar to conditions observed in other members of the Errantia too. Furthermore, nervous system and muscle staining as well as SEM and histological observations of different types of tubercles indicate a homology of the so called microtubercles, present in the long-bodied sphaerodorids, to the dorsal cirri of other Errantia. The macrotubercles seem to represent a sphaerodorid autapomorphy based on our investigations. Therefore, our results allow comparisons concerning morphological patterns between Sphaerodoridae and other Phyllodocida and constitute a starting point for further comparative investigations to reveal the evolution of the remarkable Sphaerodoridae.

La mutagenèse chimique aléatoire par l’Ethyl-Nitroso-Urée (ENU), dont la puissance a été largement démontrée au cours de ces dernières décennies dans la création de modèles murins constitue un outil remarquable et essentiel en génomique fonctionnelle. Cette approche est en effet d’un apport considérable pour la compréhension de la fonction des gènes et de leur régulation et constitue un accélérateur pour identifier des éléments clés dans une voie de signalisation. Cette approche systématique, basée sur le criblage simultané d’un grand nombre de souris ne nécessite aucune connaissance préalable sur l’identité et la fonction des gènes étudiés. Les mutants sont identifiés au travers de cribles phénotypiques spécifiques, hiérarchisés et non-invasifs. L’identification du gène et de la mutation causale responsable du phénotype sont réalisés par un travail de cartographie génique en utilisant une série de marqueurs polymorphes ou par séquençage nouvelle génération. L’objectif de ma thèse a été de caractériser au niveau phénotypique et moléculaire, 3 lignées murines indépendantes issues de deux cribles ENU, un crible récessif et un crible dominant sensibilisé. Le premier crible visait à développer des modèles de pathologies humaines, à partir duquel a été isolée la lignée vdb, qui présente des défauts du système vestibulaire dus à une mutation dans le gène otog codant pour l’otogeline, et constitue un modèle de surdité chez l’homme. Le deuxième crible avait été mis en place dans le but d’approfondir nos connaissances fondamentales sur le développement du système squeletto-musculaire chez les mammifères, plus particulièrement chez l’homme et le bovin. Les analyses de deux lignées issues de ce crible, GMA24 et GMA06, ont permis d’identifier la mutation dans le gène Phex pour les souris GMA24 qui présentent un retard de croissance et constituent un modèle pour la maladie XLH (X-Linked Hypophosphatemic Rickets) chez l’homme. Pour les souris GMA06 présentant une hypermusculature, la mutation a été localisée sur le chromosome 2 et son identification est en cours. Ces trois modèles murins constituent des outils intéressants qui peuvent s’ajouter aux modèles déjà existants pour la surdité, la maladie XLH et les maladies type myopathies pour mieux appréhender les mécanismes moléculaires impliqués dans ces pathologies et les interactions génétiques mises en jeu dans l’objectif de tester de nouvelles thérapies. / The random chemical mutagenesis with the Ethyl-Nitroso-Urea (ENU), whose power has been widely demonstrated during these last decades in the murine models creation, is a remarkable and essential tool in functional genomics. This approach is indeed a significant contribution to the understanding of the genes’ function and regulation; it also establishes an accelerator to identify the key elements in a signaling pathway. This systematic approach, based on the simultaneous screening of a large number of mice, requires no prior knowledge on the identity and the function of the studied genes. The mutants are identified through specific, hierarchical and non-invasive phenotypic screens. The identification of the gene and the causal mutation responsible for the mutant phenotype are achieved by gene mapping by using a series of polymorphic markers or by new generation sequencing. The objective of my thesis has been to characterize at the phenotypic and molecular level 3 independent murine lines from two ENU screens, a recessive and a sensitized dominant one. The first screen aimed to develop models for human diseases, from which has been isolated the vbd murine line, presenting vestibular system defects due to a mutation in the Otog gene coding for the otogelin. This mouse line presents a model for human deafness. The second screen had been established in order to deepen our fundamental knowledge on the skeletto-muscular system development in mammals, more particularly in humans and cattle. Analyzes of two lines from this screen, GMA24 and GMA06, have allowed to identify the mutation in Phex gene for GMA24 mice showing a growth retardation and modeling XLH (X-linked Hypophosphatemic rickets) disease in humans. For the GMA06 mice presenting an increase muscle mass, the mutation has been localized on chromosome 2 and its identification is in progress. These three murine models are interesting added tools to the existing models for deafness, XLH and myopathies diseases for a better understanding of the molecular mechanisms and genetic interactions involved in these pathologies and so testing new therapies.

Sphaerodoridae is a group of benthic marine worms (Annelida) characterized by the presence of spherical tubercles covering their whole surface. They are commonly considered as belonging to Phyllodocida although sistergroup relationships are still far from being understood. Primary homology assessments of their morphological features are lacking, hindering the appraisal of evolutionary relationships between taxa. Therefore, our detailed morphological investigation focuses on different Sphaerodoridae as well as on other members of Phyllodocida using an integrative approach combining scanning electron microscopy (SEM) as well as immunohistochemistry with standard neuronal (anti-5-HT) and muscular (phalloidin-rhodamine) markers and subsequent CLSM analysis of whole mounts and sections. Furthermore, we provide histological (HES) and light microscopical data to shed light on the structures and hypothetical function of sphaerodorid key morphological features. We provide fundamental details into the sphaerodorid morphology supporting a Phyllodocida ancestry of these enigmatic worms. However, the muscular arrangement and the presence of an axial muscular pharynx is similar to conditions observed in other members of the Errantia too. Furthermore, nervous system and muscle staining as well as SEM and histological observations of different types of tubercles indicate a homology of the so called microtubercles, present in the long-bodied sphaerodorids, to the dorsal cirri of other Errantia. The macrotubercles seem to represent a sphaerodorid autapomorphy based on our investigations. Therefore, our results allow comparisons concerning morphological patterns between Sphaerodoridae and other Phyllodocida and constitute a starting point for further comparative investigations to reveal the evolution of the remarkable Sphaerodoridae.