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Gibson, Hannah Taylor. "Handgrip Strength in Children with Cystic Fibrosis". BYU ScholarsArchive, 2017. https://scholarsarchive.byu.edu/etd/6761.
Pełny tekst źródłaBizzell, Laurie. "Maternal Stress and Cystic Fibrosis". Thesis, University of North Texas, 1996. https://digital.library.unt.edu/ark:/67531/metadc278693/.
Pełny tekst źródłaModi, Avani C. "Adherence in children with cystic fibrosis and asthma". [Gainesville, Fla.] : University of Florida, 2004. http://purl.fcla.edu/fcla/etd/UFE0005641.
Pełny tekst źródłaTypescript. Title from title page of source document. Document formatted into pages; contains 94 pages. Includes Vita. Includes bibliographical references.
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.
Pełny tekst źródłaDavidson, Joanna K. "Nutrition and Bone Density in Children with Cystic Fibrosis". DigitalCommons@USU, 2004. https://digitalcommons.usu.edu/etd/5521.
Pełny tekst źródłaBuntain, 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.
Pełny tekst źródłaDahné, Tova, i 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.
Pełny tekst źródłaAttard, 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.
Pełny tekst źródłaWatson, 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.
Pełny tekst źródłaDakin, Carolyn Women's & 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.
Pełny tekst źródłaOke, 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.
Pełny tekst źródłaBoesch, 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.
Pełny tekst źródłaAdvisor: 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.
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.
Pełny tekst źródłaBogdasarova, 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.
Pełny tekst źródłaJaffe, 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.
Pełny tekst źródłaGathercole, Katie Adele. "The educational experiences of children and young people with cystic fibrosis". Thesis, University of Leeds, 2017. http://etheses.whiterose.ac.uk/18012/.
Pełny tekst źródłaRiddell, 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.
Pełny tekst źródłaKeller, 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.
Pełny tekst źródłaGangell, 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.
Pełny tekst źródłaDrury, 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.
Pełny tekst źródłaOur 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, physical activity and lung function were all consistent predictors.
These results indicate that nutritional status as well as physical activity are key determinants of bone health in CF children and offer a unique opportunity in the prevention of CF-related bone disease. Further vitamin intervention research needs to be done in this population.
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.
Pełny tekst źródłaKwarteng, 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.
Pełny tekst źródłaGayer, 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.
Pełny tekst źródłaSlater, 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.
Pełny tekst źródłaTran, 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.
Pełny tekst źródłaWestwood, 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.
Pełny tekst źródłaCystic 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 shown to be identifiable through the demonstration of elevated electrolyte levels in sweat - the sweat test. After many false starts, the underlying genetic defect was identified in the 1980s, culminating in the identification of the defective gene in 1989. This opened up possibilities of more accurate diagnosis and targeted treatments. Treatment of CF with pancreatic enzyme replacement therapy and antibiotics in the 1950s proved successful in controlling some of the severe and often fatal aspects of the disease. Further refinements to nutritional and antimicrobial therapies in the 1970s and 1980s produced rapid increases in longevity in many patients with CF. In SA, CF' has been identified since the 1950s. Clinical and research activities developed in the 1980s, mainly focused on the epidemiological and genetic aspects. Two clinical studies described features in children in Cape Town and adults in Johannesburg. My own clinical involvement in the RCCH's CF Service in Cape Town since 1992 led to the research activities that make up the bulk of this thesis. The thesis describes a number of aspects of CF as it affects patients in SA. The study population (described in Chapter 2) for most of the projects consists of 181 CF patients born between October 1974 and September 2003 who were identified by a combination of clinical features, positive sweat or genetic tests and/or post-mortem findings. All were resident in the Western Cape Province and received at least part of their health care at the RCCH. One hundred and sixty (88%) were born in the province and 21 settled in the province from elsewhere. Cape Town is unique in SA for its population demographics and the CF patients reflect this. CF has mainly been identified in coloured and white patients. Four black cases have been diagnosed. Compared with the CF population as described in the early 1980s, the CF population in the 21st century is larger (100 versus 64), older and there is a greater proportion of coloured patients. Nearly 3 in every 4 patients live in Cape Town.
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.
Pełny tekst źródłaMcClellan, 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.
Pełny tekst źródłaTitle from document title page. Document formatted into pages; contains v, 111 p. : ill. Includes abstract. Includes bibliographical references (p. 67-76).
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.
Pełny tekst źródłaBabyar, 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.
Pełny tekst źródłaDawson, Kenneth P., i 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.
Pełny tekst źródłaStapleton, 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.
Pełny tekst źródłaSaynor, 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.
Pełny tekst źródłaLuna, 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.
Pełny tekst źródłaJenkins, 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.
Pełny tekst źródłaRussell, 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.
Pełny tekst źródłaStapleton, 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.
Pełny tekst źródławith a child who has CF. The 'objective assessment of knowledge indicated a significant m improvement in' children's knowledge in the short-term. There were no statistically significant improvements in any of the other parameters assessed. The lack of significant improvements in self-management, behaviour, dietary intake and anthropometry may have been because the program had no effect, the parameters assessed or the instruments used (particularly the questionnaires) were not sufficiently sensitive, the sample size (which was determined by the CF population available) was too small or the duration of the intervention and follow-up was too short.Conclusion: Carers' unanimous recommendation of Go and Grow with CF, together with high levels of perceived learning, reported increase in confidence and improvement in children's knowledge in the short-term, indicate the benefits of the program.Although there was no statistically significant improvement in the anthropometric measurements after the intervention, 'the extensive data obtained during this study suggest that measurements of height and weight may underestimate the presence of poor nutritional status. It is likely that comprehensive assessments of body composition of children with CF would be useful in detecting mild degrees of malnutrition and in providing information about the effects of nutritional status on morbidity and mortality associated with the disease.Fat-based pancreatic enzyme replacement therapy dosing warrants further investigation given that parents had a strong preference for this method and that fat absorption remains abnormal in the majority of individuals who have pancreatic insufficiency. Evaluation of all pancreatic enzyme replacement therapy dosing methods are needed and this research suggests that dose should be assessed on a meal and snack basis, rather than just on daily intake, in order ++
for levels of adherence to be examined.The apparent absence of a long-term effect of a single exposure to the program on knowledge suggests that regular, ongoing education and counselling is required by families to reinforce aspects related to the child's current stage of development and disease status.
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.
Pełny tekst źródłaAurora, 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/.
Pełny tekst źródłaVandenbroucke, 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.
Pełny tekst źródłaCox, 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.
Pełny tekst źródłaPassweg, 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.
Pełny tekst źródłaBooth, 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.
Pełny tekst źródłaSantos, 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.
Pełny tekst źródłaObjetivo: 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 Database scoring scale (PEDro) Resultados: Foram incluídos 7 artigos com um total de 317 participantes com score total de 7 pontos de acordo com a PEDro. Dos estudos incluídos nesta revisão, todos avaliaram os efeitos do exercício terapêutico em crianças e jovens. Dois avaliaram os efeitos de um programa de exercícios num suporte digital comparando com um treino tradicional, 2 avaliaram a combinação de um programa de exercícios com um treino dos músculos inspiratórios, 1 avaliou os efeitos do exercício nas alterações posturais e barapométricas, 1 verificou os efeitos do treino aeróbio na função pulmonar e outro avaliou os efeitos da associação entre o treino aeróbio e o treino de força na função pulmonar. Conclusão: A fisioterapia tem um papel indispensável no tratamento de crianças e jovens com FQ.
Objetive: To determine a physiotherapy intervention in children and young cystic fibrosis (CF). Methodology: Computerized research was carried out in the Scopus, Web of Science and Pubmed databases with the objective of obtaining randomized articles controlled by assessing the effects of the physiotherapy intervention in children and young people with CF. Research was carried out between July and August 2019. Methodological quality was assessed using the Physiotherapy Evidence Database scoring scale (PEDro). Results: Were included 7 articles, with a total of 317 participants with a total score of 7 on the PEDro. The studies in this review, all of them evaluated the effects of therapeutic exercise on children and young. Two assessed the effects of an exercise program on a digital medium compared to a traditional workout, 2 the combination of an exercise program with inspiratory muscle training, 1 assessed the effects of exercise on postural and barapometric changes, 1 verified the effects of aerobic training on lung function and another evaluated the effects of the association between aerobic training and strength training have on lung function. Conclusion: Physiotherapy has an indispensable role in the treatment of CF in children and young people.
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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.
Pełny tekst źródłaUrquhart, 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/.
Pełny tekst źródłaDeeley, 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.
Pełny tekst źródłaSantos, 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.
Pełny tekst źródłaTese (doutorado) - Universidade Estadual de Campinas, Faculdade de Ciencias Medicas
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Doutorado
Saude da Criança e do Adolescente
Doutor em Saude da Criança e do Adolescente
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.
Pełny tekst źródłaMinasian, 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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