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Cutaneous Manifestations of Cystic Fibrosis

REFERENCES 1. Bernstein ML, McCusker MM, Grant-Kels JM. Cutaneous manifestations of cystic fibrosis. Pediatr Dermatol . 2008;25:150-157. 2. Strandvik B. Relation between essential fatty acid metabolism and gastrointestinal symptoms in cystic fibrosis. Acta Paediatr Scand Suppl . 1989;363:58-63. 3. Darmstadt GL, McGuire J, Ziboh VA. Malnutrition-associated rash of cystic fibrosis. Pediatr Dermatol . 2000;7:337-347. 4. Phillips RJ, Crock CM, Dillon MJ, et al. Cystic fibrosis presenting as kwashiorkor with florid skin rash. Arch Dis Child

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Cystic fibrosis related diabetes

References 1. Southern KW, Munck A, Pollitt R, Travert G, Zanolla L, Dankert-Roelse J, et al. A survey of newborn screening for cystic fibrosis in Europe. J Cyst Fibros. 2007;6:57–65. 2. Popa I, Pop L, Popa Z, Schwarz MJ, Hambleton G, Malone GM, et al. Cystic fibrosis mutations in Romania. Eur J Pediatr. 1997;156:212–213. 3. O’Sullivan BP, Freedman SD. Cystic fibrosis. Lancet. 2009 May;373(9678):1891–904. 4. Ciuca IM, Pop L, Ranetti A., Popescu I.M, et all, Ursodeoxicholic acid effects on cystic fibrosis liver disease, Farmacia, 63: 543

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Celiac Disease and Cystic Fibrosis: Challenges to Differential Diagnosis

References 1. Pohl JF, Judkins J, Meihls S, et al. Cystic Fibrosis and Celiac Disease: Both Can Occur Together. Clinical Pediatrics 2011;50(12)1153-5. 2. Davis, PB. Cystic Fibrosis Since 1938. Centennial Review. Am J RespirCrit Care Med 2006;173:475-82. 3. Walkowiak J, Blask-Osipa A, Lisowska A, et al. Cystic fibrosis is a risk factor for celiac disease. Acta ABP Bioch Pol 2010;57(1):115-8. 4. Genkova ND, Yankov IV, Bosheva MN, et al. Cystic fibrosis and celiac disease - multifaceted and similar

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HAIR DEPIGMENTATION AND DERMATITIS – AN UNEXPECTED PRESENTATION OF CYSTIC FIBROSIS

References 1. Salvatore D, Buzzetti R, Baldo E, Forneris M, Lucidi V, Manunza D, et al. An overview of international literature from cystic fibrosis registries. Part 3. Disease incidence, genotype/phenotype correlation, microbiology, pregnancy, clinical complications, lung transplantation, and miscellanea. J Cyst Fibros. 2011; 10(2): 71-85. 2. Nielsen OH, Larsen BF. The incidence of anemia, hypoproteinemia, and edema in infants as presenting symptoms of cystic fibrosis: A retrospective survey of the frequency of this symptom

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Neonatal Cystic Fibrosis Screening in Latvia: A Pilot Project

References Anonymous (2009). Cystic fibrosis transmembrane conductance regulator. [PUBMED] Bobadilla, J., L., Farrell, M.H., Farrell, P.M. (2002). Applying CFTR molecular genetics to facilitate the diagnosis of cystic fibrosis through screening. Adv. Pediatr. , 49 , 131-190. Corbetta, C., Seia, M., Bassotti, A., Ambrosioni, A., Giunta, A., Padoan, R. (2002). Screening for cystic fibrosis in newborn infants: Results of a pilot programme based on a two tier protocol (IRT

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Cystic fibrosis - general review on sinonasal complications and case report

REFERENCES 1. Rowe S.M., Miller S., Sorscher E.J. - Cystic fibrosis. N Engl J Med., 2005;352(19):1992-2001. 2. Cystic Fibrosis Foundation Patient Registry 2011 Annual Data Report. Bethesda, MD: Cystic Fibrosis Foundation, 2012. 3. Oomen K.P., April M.M. - Sinonasal manifestations in Cystic fibrosis. Int J Otolaryngol., 2012;2012:789572. doi: 10.1155/2012/789572. Epub 2012 Aug 5. 4. Brihaye P., Jorissen M., Clement P.A. - Chronic rinosinusistis in cystic fibrosis (mucoviscidosis). Acta Otorhinolaryngol Belg., 1997;51(4):323-337. 5

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Cystic fibrosis and celiac disease - multifaceted and similar

References 1. Davis PB. Cystic Fibrosis Since 1938. Am J Respir Crit Care Med 2006;173:475-82. 2. Kostovski A, Zdraveska N. Coagulopathy as initial manifestation of concomitant celiac disease and cystic fi brosis: a case report. Journal of Medical Case Reports 2011;5:116-9. 3. Walkowiak J, Blask-Osipa A, Lisowska A, et al. Cystic fi brosis is a risk factor for celiac disease. Acta Biochim Pol 2010;57(1):115-8. 4. Pletcher BA. Pulmonary manifestations of genetic diseases. In: Turcios I, Nelson L

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Emotional health in children and adolescents with cystic fibrosis

’Alfonco P. Le langage du dessin, Delachaux et Nestle AS, 1955. 5. Blair C, Cull A, Freeman CP. Psychosocial functioning of young adults with cystic fibrosis and their families. Thorax, 1994; 49: 798–802. 6. Canning EH, Kelleher K. Performance of screening tools for mental health problems in chronically ill children. Arch Pediatr Adolesc Med, 1994; 148: 272–278. 7. Canning EH, Hanser SB, Shade KA, Boyce WT. Mental disorders in chronically ill children:parent-child discrepancy and physician identification, Pediatrics, 1992; 90: 692–696. 8. Canning EH

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Analysis of Bone Metabolism in Children with Cystic Fibrosis

REFERENCES 1. Buzzetti R, Salvatore D, Baldo E, et al. An overview of international literature from cystic fibrosis registries: 1. Mortality and survival studies in cystic fibrosis. J Cyst Fibros 2009; 8: 229–37 2. Kanis JA. Osteoporosis, revised edition, 1997, Blackwell Healthcare 3. Cashman KD, Seamans K. Bone health, genetics, and personalized nutrition. Genes Nutr. 2007; 2: 47-51 4. Davies JH, Evans AJ, Gregory JW. Bone mass acquisition in healthy children. Arch Dis Child 2005; 90: 373-378. 5. Sermet-Gaudelus I, Souberbielle JC

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Pulmonary exacerbation due to colistin-resistant Stenotrophomonas maltophilia in a Bulgarian cystic fibrosis patient

References 1. Ratjen F, Döring G. Cystic Fibrosis. Lancet 2003; 361:681-9. 2. Ciofu O, Hansen CR, Høiby N. Respiratory bacterial infections in cystic fibrosis. Curr Opin Pulm Med 2013;19(3):251-258. 3. O’Sullivan BP, Freedman SD. Cystic fibrosis. Lancet 2009;373:1891-1904. 4. Döring G, Flume P, Heijerman H, Elborn JS, for the Consensus Study Group. Treatment of lung infection in patients with cystic fibrosis: current and future strategies. J Cyst Fibros 2012;11:461-479. 5. Høiby N

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