Sökning: "Heart Rate physiology"
Visar resultat 1 - 5 av 43 avhandlingar innehållade orden Heart Rate physiology.
1. Aspects of central integrative and efferent mechanisms in cardiovascular reflex control
Sammanfattning : .... LÄS MER
2. Heart and lung function - in health and disease : methodological studies in clinical physiology
Sammanfattning : The human heart and lungs constitute an intricate and dynamic system. Various clinical physiological examinations can be used to evaluate cardio-pulmonary function and identify abnormalities. Thus, it is important to understand how normal physiology presents, to be able to identify pathological findings. LÄS MER
3. Physiology of Adventure Racing : with emphasis on circulatory response and cardiac fatigue
Sammanfattning : The overall aims of this thesis were to elucidate the circulatory responses to ultra-endurance exercise (Adventure Racing), and furthermore, to contribute to the clarification of the so called “exercise-induced cardiac fatigue” in relation to said exercise. An Adventure race (AR) varies in duration from six hours to over six days, in which the participants have to navigate through a number of check-points over a pre-set course, using a combination of three or more endurance/outdoor sports, e. LÄS MER
4. Autonomic cardiac control in long QT syndrome : clinical studies of arrhythmogenic triggers
Sammanfattning : Background: Long QT syndrome (LQTS) is an inherited cardiac disease characterized by prolonged cardiac repolarization and an increased risk for life-threatening arrhythmias. These arrhythmias are typically triggered by adrenergic stimuli, such as physical activity and intense emotions, implicating that the sympathetic part of the autonomic nervous system (ANS) is involved in arrhythmogenesis. LÄS MER
5. Cardiac arrhythmias and heart rate variability in familial amyloidotic polyneuropathy : A clinical study before and after liver transplantation
Sammanfattning : Familial amyloidotic polyneuropathy (FAP), found in the northernmost counties in Sweden, is a rare, lethal and inherited amyloidosis. The disease is caused by mutated transthyretin (TTR). The mutation is characterized by an exchange of valine for methionine at position 30 (ATTRVal30Met). LÄS MER