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Rozprawy doktorskie na temat „Cystic fibrosis in children”

Autor: Grafiati

Data publikacji: 4 czerwca 2021

Data aktualizacji: 30 lipca 2024

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1

Gibson, Hannah Taylor. "Handgrip Strength in Children with Cystic Fibrosis." BYU ScholarsArchive, 2017. https://scholarsarchive.byu.edu/etd/6761.

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Background: Body mass index (BMI) is the primary accepted method to determine nutrition status in children with cystic fibrosis (CF); however, lean body mass (LBM) is more strongly associated with pulmonary function. Handgrip strength (HGS) measures muscle function and is reflective of LBM. The aims of this study were to assess if there was a relationship among HGS, nutrition status, and pulmonary function, to assess if HGS changed after hospitalization, and to assess if there was a relationship between HGS and nutrient intake. Methods: Twenty-three children with CF ages 6-18 years participate

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Bizzell, Laurie. "Maternal Stress and Cystic Fibrosis." Thesis, University of North Texas, 1996. https://digital.library.unt.edu/ark:/67531/metadc278693/.

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The purpose of the current study was to examine the relationship between parent and child factors for mothers of children diagnosed with cystic fibrosis to predict mother's psychological distress. Mothers were surveyed to identify measurement models in areas of Child and Parental characteristics and a Full Causal Model of Maternal distress. Factors related to Child Characteristics include general parental stressors and cystic fibrosis specific parental stressors. Factors related to Parental Characteristics include the mother's sense of parental competence and self-esteem. Additional factors re

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Modi, Avani C. "Adherence in children with cystic fibrosis and asthma." [Gainesville, Fla.] : University of Florida, 2004. http://purl.fcla.edu/fcla/etd/UFE0005641.

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Thesis (Ph.D.)--University of Florida, 2004.<br>Typescript. Title from title page of source document. Document formatted into pages; contains 94 pages. Includes Vita. Includes bibliographical references.

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Goodhart, Frances. "What children with cystic fibrosis know about their illness." Thesis, City University London, 2003. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.269436.

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Davidson, Joanna K. "Nutrition and Bone Density in Children with Cystic Fibrosis." DigitalCommons@USU, 2004. https://digitalcommons.usu.edu/etd/5521.

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The purpose of these studies was to further research on bone density in children with cystic fibrosis, particularly as it pertains to nutritional parameters and care. The first paper presented a comparison of a group of 50 children with cystic fibrosis to a group of 32 control children. There were no significant differences between the groups in any of the pertinent bone density measurements. Serum 25(0H) vitamin D was positively correlated with spine density z score in the cystic fibrosis group. The second paper, incorporating all of the information obtained from the first paper, describes an

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6

Buntain, Helen Mary. "Clinical aspects of bone mass accrual in children and adolescents with cystic fibrosis /." [St. Lucia, Qld.], 2005. http://www.library.uq.edu.au/pdfserve.php?image=thesisabs/absthe19505.pdf.

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Dahné, Tova, and Tatyana Filonova. "Cystic Fibrosis and Physical Activity : Total Energy Expenditure and Physical Activity Levels in Children and Adolescents with Cystic Fibrosis." Thesis, Uppsala universitet, Institutionen för folkhälso- och vårdvetenskap, 2012. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-169166.

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Aim: The aim with the current study was to examine the physical activity levels (PAL) in a group of children and adolescents with cystic fibrosis (CF) and compare PAL-values between boys and girls. Further, the aim was to look at the total energy expenditure (TEE) estimated with an activity diary and measured with the accelerometer and compare values between these two measurement methods. Method: The sample consisted of 29 children and adolescents diagnosed with CF where PAL and TEE was measured during a three-day registration with activity diary and the ActiCal© accelerometer. The data was an

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8

Attard, Melanie Jane. "Carriers of responsibility : an existential encounter with parents who know their child is, or could be, a carrier of a mutation in the cystic fibrosis gene." Phd thesis, Faculty of Nursing and Midwifery, 2009. http://hdl.handle.net/2123/7883.

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Watson, Melissa. "Factors affecting the psychological adjustment of children with cystic fibrosis." Thesis, Open University, 2001. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.273318.

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Dakin, Carolyn Women's &amp Children's Health Faculty of Medicine UNSW. "Infection and inflammation in children with cystic fibrosis lung disease." Awarded by:University of New South Wales. Women's & Children's Health, 2009. http://handle.unsw.edu.au/1959.4/44624.

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The purpose of this study was to examine the relationships between inflammation, infection and lung function in cystic fibrosis during the evolution of lung disease in childhood and early adolescence. The developmental stages of childhood and the progression of lung disease together affected the methods and techniques used in the study, with the consequence that the work for this thesis fell naturally into two parts. The first part concerned the study of early lung disease in infants and young children who were unable to expectorate or to cooperate with lung function testing. In the second par

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Oke, Carolyn Louise. "Social skills of children with cystic fibrosis and their siblings." Thesis, National Library of Canada = Bibliothèque nationale du Canada, 1997. http://www.collectionscanada.ca/obj/s4/f2/dsk3/ftp05/mq20894.pdf.

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12

Boesch, Richard Paul. "Outcomes and complications of fundoplication in children with cystic fibrosis." Cincinnati, Ohio : University of Cincinnati, 2008. http://www.ohiolink.edu/etd/view.cgi?acc_num=ucin1204839634.

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Thesis (M.S. of Epidemiology)--University of Cincinnati, 2008.<br>Advisor: Dr. James E Heubi. Title from electronic thesis title page (viewed May 12, 2008). Includes abstract. Keywords: fundoplication; cystic fibrosis; pulmonary function; nutrition. Includes bibliographical references.

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13

BOESCH, RICHARD PAUL. "Outcomes and complications of fundoplication in children with cystic fibrosis." University of Cincinnati / OhioLINK, 2008. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1204839634.

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14

Bogdasarova, Karina. "Oral Microbial Community Composition in Young Children with Cystic Fibrosis." The Ohio State University, 2014. http://rave.ohiolink.edu/etdc/view?acc_num=osu1404331049.

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Jaffe, Adam. "Assessment and feasibility of gene therapy for cystic fibrosis in children." Thesis, Imperial College London, 2000. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.589769.

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16

Gathercole, Katie Adele. "The educational experiences of children and young people with cystic fibrosis." Thesis, University of Leeds, 2017. http://etheses.whiterose.ac.uk/18012/.

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Children with medical conditions may experience significant challenges in education, of which there is often low awareness within schools. Yet, there is a dearth of research into cystic fibrosis (CF) and education. Research about CF commonly takes a medicalised or psychological standpoint and therefore the educational experiences of children and young people with condition are largely unknown. Educational research has focused on children with varying medical conditions, although most studies regard them as a homogenous group. CF remains distinctive from other conditions because it is invisible

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Riddell, Amy. "The muscle-bone in children and adolescents with and without cystic fibrosis." Thesis, University of Cambridge, 2016. https://www.repository.cam.ac.uk/handle/1810/268034.

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Introduction: Puberty is a crucial period for rapid changes in bone mineral, size, geometry, and microarchitecture. The mechanostat theory postulates that increased mechanical loading will affect bone phenotype and strength during development and in later life. Individuals with cystic fibrosis (CF) have an increased risk of developing osteoporosis and fragility fractures in young adulthood, which may be caused by poor growth. The aim was to investigate whether sex and disease status modified the relationship between: 1) puberty and bone, and 2) muscle and bone. This would contribute to the und

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18

Keller, Bigna Magdalena. "Growth in prepubertal children with cystic fibrosis, homozygous for the \223DF508 mutation /." [S.l.] : [s.n.], 2001. http://www.ub.unibe.ch/content/bibliotheken_sammlungen/sondersammlungen/dissen_bestellformular/index_ger.html.

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Gangell, Catherine Louise. "Evaluation of the forced oscillation technique for clinical assessment of young children with cystic fibrosis." University of Western Australia. School of Paediatrics and Child Health, 2008. http://theses.library.uwa.edu.au/adt-WU2008.0213.

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Background: Measurements of lung function are routinely used in patients with cystic fibrosis (CF) to provide information that may be clinically relevant. Spirometry is the conventional lung function measurement used, however young children find spirometry difficult to perform and often cannot achieve the strict acceptability criteria for the test. The forced oscillation technique (FOT) is a lung function measurement that only requires tidal breathing and is easy for young children to perform. However, there is limited information about the utility of this technique in the clinical assessment

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20

Drury, Donna. "Vitamin D and K status and bone health in pediatric cystic fibrosis patients." Thesis, McGill University, 2006. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=101116.

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The objective of this study was to investigate the extent to which vitamin D and K are associated with bone health in pediatric cystic fibrosis (CF) patients. We hypothesized that: (1) the prevalence of vitamin D and K deficiencies would be high despite routine vitamin therapy, (2) bone health would be reduced and (3) vitamin K and D status would be associated with bone health.<br>Our results showed poor bone mineral mass in these CF children despite mild disease and good nutritional status. Neither vitamin K nor D was a predictor of bone health but weight and height Z-scores, fat-free mass, p

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21

Cotter, Breda. "The journey through school for children with cystic fibrosis : an interpretive phenomenological analysis." Thesis, University of Newcastle upon Tyne, 2016. http://hdl.handle.net/10443/3302.

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This study set out to explore the experiences of children making their way through school with a diagnosis of Cystic Fibrosis. Cystic Fibrosis is a chronic illness which requires a rigorous treatment regimen and for which there is no cure. It is a recessively inherited disorder which affects multiple organ systems and involves a life expectancy of approximately 40 years. It is the most common life-threatening disorder in the Caucasian race (Wennstrom et al., 2011) and the incidence in Ireland is the world’s highest (Farrell, 2008). The aim of the study was to explore identity construction amon

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22

Kwarteng, Owusu Sandra. "Cystic fibrosis in black African children in South Africa: a case control study." Master's thesis, Faculty of Health Sciences, 2020. http://hdl.handle.net/11427/32272.

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Background Cystic fibrosis (CF) is described more commonly in Caucasian populations in whom p.Phe508del is the most common mutation. There is a paucity of data of CF in black African children. The aim of this study was to describe and compare the presentation and outcomes of black African children with CF to those with p.Phe508del genotype. Methods A retrospective case-controlled study was conducted from January 2000 – March 2018 of children with CF attending two CF centres in South Africa. Presentation, genotype, nutrition and pulmonary function outcomes of black African children were compare

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23

Gayer, Debra A. "Family functioning, marital status, and coparental cooperation as predictors of mother's adherence to prescribed CF treatments /." free to MU campus, to others for purchase, 1997. http://wwwlib.umi.com/cr/mo/fullcit?p9841288.

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Slater, Shalonda K. "The relationship between stress and depression in primary caregivers of children with cystic fibrosis." [Gainesville, Fla.]: University of Florida, 2003. http://purl.fcla.edu/fcla/etd/UFE0000792.

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Tran, Therese Marie Pascale Thi My Dung. "Steatorrhea and nutritional condition in cystic fibrosis children effects of a proton-pump inhibitor /." [Maastricht : Maastricht : Unigraphic, Rijksuniversiteit Limburg] ; University Library, Maastricht University [Host], 1996. http://arno.unimaas.nl/show.cgi?fid=6273.

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Westwood, Anthony Thomas Read. "Cystic fibrosis in children and adolescents in the Western Cape : epidemiological and clinical aspects." Master's thesis, University of Cape Town, 2005. http://hdl.handle.net/11427/10745.

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Includes bibliographical references (leaves 284-314).<br>Cystic fibrosis (CF) is an autosomal recessive genetic disease caused by mutations on chromosome 7 in the gene for the CFTR protein. This gene encodes for a chloride channel on the apical surface of certain epithelial cells. The clinical manifestations of CF largely arise out of the resultant defect in water and electrolyte secretions in exocrine glands and epithelia such as are found in the pancreas, respiratory, gastrointestinal and genital tracts and sweat glands. First delineated as a clinical entity in the mid-20th century, CF was s

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Hourigan, Shannon Estelle. "Improving Nutrition in Toddlers and Preschool Children with Cystic Fibrosis: Behavioral Parent Training Intervention." VCU Scholars Compass, 2012. http://scholarscompass.vcu.edu/etd/2818.

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The purpose of this single-case study was to pilot a developmentally sensitive adaptation of an evidence-based intervention aimed at improving nutrition in children with cystic fibrosis (CF). Children with CF must adhere to a high-calorie diet to prevent malnutrition and maintain health. Toddler and preschool age children present a unique feeding challenge to parents as they begin to exert independence and exhibit a variety of challenging behaviors. Parents trying to adhere to CF nutrition guidelines often use ineffective strategies that inadvertently encourage children not to eat. This six-w

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McClellan, Catherine B. "Evaluation of time out based discipline strategy to manage children's noncompliance with cystic fibrosis treatment." Morgantown, W. Va. : [West Virginia University Libraries], 2004. https://etd.wvu.edu/etd/controller.jsp?moduleName=documentdata&jsp%5FetdId=3518.

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Thesis (Ph. D.)--West Virginia University, 2004.<br>Title from document title page. Document formatted into pages; contains v, 111 p. : ill. Includes abstract. Includes bibliographical references (p. 67-76).

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Whyte, Dorothy A. "The experience of families caring for a child with cystic fibrosis : a nursing response." Thesis, University of Edinburgh, 1989. http://hdl.handle.net/1842/8370.

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This thesis is concerned with families and chronic illness in childhood. The specific focus of the study is the nursing contribution to support of the family. A longitudinal study of the experience of four families caring for a child with cystic fibrosis was carried out using the ethnographic approach. Analysis of the four case studies provides insight to the effect of cystic fibrosis on each family member and on family interaction. The psychosocial transition by which the families moved from seeing themselves as healthy families to accepting the reality of a long-term health problem is descri

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Babyar, Heather Michelle. "The Role of Social Media in the Relationship Between Social Support and Adherence in Children with Cystic Fibrosis." Kent State University / OhioLINK, 2016. http://rave.ohiolink.edu/etdc/view?acc_num=kent1469545679.

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Dawson, Kenneth P., and mikewood@deakin edu au. "Cystic fibrosis in children of the Eastern Arabian Peninsula : A clinical, spatial and genetic study." Deakin University. School of biological and chemical sciences, 2003. http://tux.lib.deakin.edu.au./adt-VDU/public/adt-VDU20050728.091141.

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Aim: The aim of this thesis is to describe the process by which the inherited disease, cystic fibrosis, (CF) was recognised as an important clinical entity in the United Arab Emirates (UAE) and the Sultanate of Oman (Oman). It examines the clinical presentation of the first patients and assesses their degree of severity. Further, it describes the first studies carried out to determine the underlying CF mutations associated with the disease in the UAE and Oman. An estimate is offered of the birth frequency of the condition. Overall, the cultural, geographical and historical aspect of the societ

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Stapleton, Denise R. "Development, implementation and evaluation of a nutrition education and behaviour program for children with cystc fibrosis." Thesis, Curtin University, 2001. http://hdl.handle.net/20.500.11937/784.

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Background: Cystic fibrosis (CF) is a genetically inherited disease which adversely affects the respiratory and gastrointestinal systems. Malnutrition is a major clinical problem in individuals with the disease. Nutritional interventions are warranted as improvements in nutritional status could improve the rates of morbidity and mortality associated with the disease. The review of the literature indicated the need to develop a behavioural-based nutrition prevention program in order for children to achieve CF dietary requirements and appropriate pancreatic enzyme replacement therapy.Methods: Th

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Saynor, Zoe Louise. "Assessment and interpretation of aerobic exercise (dys)function in paediatric patients with cystic fibrosis." Thesis, University of Exeter, 2016. http://hdl.handle.net/10871/21875.

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The purpose of this thesis was to extend our understanding of the assessment and interpretation of aerobic exercise function of paediatric patients with cystic fibrosis (CF). The first investigation sought to establish (1) the validity of traditional criteria to verify maximal oxygen (V ̇O2max) during a maximal cardiopulmonary exercise test (CPET); and (2) the utility of supramaximal verification (Smax) to confirm V ̇O2max. Traditional criteria significantly underreported V ̇O2max, whilst Smax was shown to provide a valid measurement in this patient group. The reproducibility of this CPET prot

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Luna, Ruth Ann. "The Clinical Utility of Molecular Typing of Multiply-resistant Pseudomonas aeruginosa in Children with Cystic Fibrosis." VCU Scholars Compass, 2010. http://scholarscompass.vcu.edu/etd/2060.

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Chronic infection with P. aeruginosa is expected in patients with cystic fibrosis (CF), but the ability to delay, prevent, or better manage infection with multiply-resistant P. aeruginosa (MRPA) can potentially increase quality of life and extend survival. The Texas Children’s Hospital CF Care Center has identified an endemic MRPA strain (dominant clone), and this study aimed to identify risk factors for acquisition of the clone as well as determine differences in patient outcome associated with subsequent infection with the clone. The study included 71 patients with CF with documented MRPA i

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Jenkins, Bradlee A. "Effect of Asthma and Cystic Fibrosis on Health Utilization and Education Progress in Children and Adolescents." Digital Commons @ East Tennessee State University, 2013. https://dc.etsu.edu/honors/108.

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Aims. To determining the effect of asthma, cystic fibrosis (CF), and both on healthcare utilization, absences from school, and rate of progress in school. Background. Previous studies on academic progression and health care utilization in children with the respiratory diseases of asthma and CF have been limited or conflicting. Design. Non experimental, cross-sectional, secondary data analysis using a multilevel probability sample. Methods. The response of all persons under 18 years of age in the U.S. 1997-2012 National Health Interview Survey to interviewer questions on demographic, educationa

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Russell, Jeremy. "Innovative psychological strategies for the management of distress amongst young people with cystic fibrosis." Thesis, Queensland University of Technology, 2021. https://eprints.qut.edu.au/207787/2/Jeremy_Russell_Thesis.pdf.

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Cystic Fibrosis (CF) and its treatment pose challenges to young people and their families. This research identified the psychological needs of young people with CF, assessed the feasibility of a brief treatment, and examined whether aspects could be delivered by a social robot. Thoughts young people had about their distress were an important target. The new treatment helped the young people develop a positive story of life they shared with their family, and resulted in reduced distress. Use of a social robot was feasible, and aided engagement. The research provides a foundation for further wor

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Stapleton, Denise R. "Development, implementation and evaluation of a nutrition education and behaviour program for children with cystc fibrosis." Curtin University of Technology, School of Public Health, 2001. http://espace.library.curtin.edu.au:80/R/?func=dbin-jump-full&object_id=13047.

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Background: Cystic fibrosis (CF) is a genetically inherited disease which adversely affects the respiratory and gastrointestinal systems. Malnutrition is a major clinical problem in individuals with the disease. Nutritional interventions are warranted as improvements in nutritional status could improve the rates of morbidity and mortality associated with the disease. The review of the literature indicated the need to develop a behavioural-based nutrition prevention program in order for children to achieve CF dietary requirements and appropriate pancreatic enzyme replacement therapy.Methods: Th

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Schurer, Geertruida Wilhelmina. "Changes in body composition, anaerobic muscle power, and pulmonary function with age in children with cystic fibrosis." Thesis, National Library of Canada = Bibliothèque nationale du Canada, 1997. http://www.collectionscanada.ca/obj/s4/f2/dsk2/ftp04/mq24505.pdf.

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Aurora, Paul. "Multiple-breath inert gas washout to detect inhomogeneity of ventilation distribution in preschool children with cystic fibrosis." Thesis, University College London (University of London), 2005. http://discovery.ucl.ac.uk/1445299/.

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Measurement of lung function in preschool children (those aged two to five years) is notoriously difficult. The aims of this thesis were to determine whether multiple- breath inert gas washout (MBW) could be performed successfully in preschool children, and whether MBW indices were more sensitive for detecting cystic fibrosis (CF) lung disease in preschool children than spirometry indices. First, quality control criteria for data collection and interpretation in children with and without CF were examined. 75% of preschool children successfully performed spirometry at first attempt, but adult c

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Vandenbroucke, Natalie Joëlle. "Lung function determinants and mortality of children and adolescents with cystic fibrosis in South Africa 2007-2016." Master's thesis, Faculty of Health Sciences, 2019. https://hdl.handle.net/11427/31782.

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Objectives: Cystic fibrosis (CF) is one of the commonest inherited disorders in South Africa, affecting all population groups. Progressive pulmonary disease with declining forced expiratory volume in one second (FEV1) is the main predictor of morbidity and mortality in individuals with CF. This study aimed to describe the change in lung function, nutritional status and mortality of children and adolescents with CF, attending the Red Cross War Memorial Children’s Hospital (RCWMCH) CF Clinic and to identify factors associated with poor pulmonary function outcomes and mortality. Methods: A retros

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Cox, Madison Allen. "Self-Reports of Hearing and Tinnitus Related to Audiometry in Children and Young Adults with Cystic Fibrosis." Walsh University Honors Theses / OhioLINK, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=walshhonors1588691309804014.

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Passweg, Jakob. "Salivary caffeine clearance for measurement of liver function in children with liver disease, cystic fibrosis and epilepsy /." [S.l : s.n.], 1987. http://www.ub.unibe.ch/content/bibliotheken_sammlungen/sondersammlungen/dissen_bestellformular/index_ger.html.

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Booth, Erin B. "Influence of Contextual Factors and Self Efficacy on Self- Management in Parents of Children with Cystic Fibrosis." VCU Scholars Compass, 2017. https://scholarscompass.vcu.edu/etd/5152.

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Cystic Fibrosis, a life threatening autosomal recessive genetic disease, is characterized by a defective gene resulting in the production of thick mucus that obstructs the lungs and pancreas. CF requires intensive management performed at the home. An initial pilot study was performed to describe knowledge of CF related diabetes (CFRD) in adults with CF. The findings of this study, which demonstrated that adults with CF lacked sufficient knowledge about CFRD confirmed the need to explore additional factors of self-management guided by a theoretical framework. The second study presented in this

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Santos, José Manuel Mendes Pereira dos. "Intervenção da fisioterapia em crianças e jovens com fibrose quística: uma revisão sistemática." Bachelor's thesis, [s.n.], 2020. http://hdl.handle.net/10284/9183.

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Projeto de Graduação apresentado à Universidade Fernando Pessoa como parte dos requisitos para obtenção do grau de Licenciado em Fisioterapia<br>Objetivo: Determinar a intervenção da fisioterapia em crianças e jovens com Fibrose Quística (FQ). Metodologia: Pesquisa computorizada nas bases de dados Scopus, Web of Science e Pubmed com o objetivo de obter artigos randomizados controlados que avaliassem os efeitos da intervenção da fisioterapia em crianças e jovens com FQ. A pesquisa foi realizada entre Julho e Agosto 2019. A qualidade metodológica foi avaliada através da Physiotherapy Evidence Da

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O'Haver, Judith. "Parental Perceptions of Risk and Protective Factors Associated with the Adaptation of Siblings of Children with Cystic Fibrosis." Diss., The University of Arizona, 2007. http://hdl.handle.net/10150/194222.

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When a child is diagnosed with a chronic life threatening illness there is a significant impact on the entire family. Siblings are at risk for psychological adaptation problems because of their unique relationship with the ill child and the effect of that illness on family functioning. Few studies have been reported which examine the impact of chronic life-threatening illnesses in children on healthy siblings.The purpose of this study was to investigate the predisposing risk and protective factors that affect the psychological adaptation of healthy siblings of a child with Cystic Fibrosis (C

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Urquhart, D. S. "Exploration of the relationship between hypoxia and measures of clinical status and inflammation in children with cystic fibrosis." Thesis, University College London (University of London), 2010. http://discovery.ucl.ac.uk/19232/.

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Hypoxia in cystic fibrosis (CF) may occur during sleep, and also during exercise, chest exacerbations and air travel. No standardised definition of nocturnal hypoxia in CF exists. Theoretical evidence suggests hypoxia may have a deleterious impact on clinical status in CF, due to effects on upregulation of pro-inflammatory cytokines, changes in Pseudomonas aeruginosa growth patterns, and causation of pulmonary hypertension. It was hypothesised that hypoxia, and resultant inflammation would adversely affect clinical phenotype in CF. Forty-one children with CF were studied, each undergoing home

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Deeley, Linda G. "Children with siblings with cystic fibrosis : impact of the illness and strategies used to cope, from the child's perspective." Thesis, University of Southampton, 1996. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.243145.

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Santos, Camila Isabel da Silva. "Efeito da antibioticoterapia e da fisioterapia respiratoria na função pulmonar de pacientes com fibrose cistica em exacerbação pulmonar aguda." [s.n.], 2008. http://repositorio.unicamp.br/jspui/handle/REPOSIP/309972.

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Orientador: Jose Dirceu Ribeiro<br>Tese (doutorado) - Universidade Estadual de Campinas, Faculdade de Ciencias Medicas<br>Made available in DSpace on 2018-08-11T19:35:15Z (GMT). No. of bitstreams: 1 Santos_CamilaIsabeldaSilva_D.pdf: 2500777 bytes, checksum: c518d6dc61d6fc76e5b9ba79c05ca5e4 (MD5) Previous issue date: 2008<br>Doutorado<br>Saude da Criança e do Adolescente<br>Doutor em Saude da Criança e do Adolescente

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Sheridan, Helen Sarah. "The practical use of the Multiple Breath Washout test in children : biological variability in health and disease." Thesis, University of Edinburgh, 2017. http://hdl.handle.net/1842/29543.

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The Multiple Breath Washout (MBW) test is increasingly being recognised as a sensitive method of detecting early small airways lung disease. Indices of MBW include lung clearance index (LCI), Scond and Sacin. Factors that affect MBW variability have not been fully established. This thesis presents five studies which examine MBW repeatability in children with and without cystic fibrosis (CF) or asthma. MBW was performed using 0.2% sulphur hexafluoride and the modified Innocor (Innovision). Testing was performed at the Clinical Research Facility of the Royal Hospital for Sick Children in Edinbur

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Minasian, Caro. "A randomised, cross-over, comparative study of inhaled mannitol, daily rhDNase and a combination of both in children with cystic fibrosis." Thesis, Imperial College London, 2010. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.528305.

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