Norsk senter for cystisk fibrose Forskningsprosjekter

Publikasjoner

Her finner du en oversikt over publikasjoner som ansatte ved NSCF har utgitt, eller bidratt til i samarbeid med andre fagmiljøer i Norge eller i utlandet.

Du finner også relevante publikasjoner utgitt av fagpersoner ved andre institusjoner i Norge.

Cystisk fibrose

2018:

Transfer of a bla CTX-M-1-carrying plasmid between different Escherichia coli strains within the human gut explored by whole genome sequencing analyses. Knudsen PK, Gammelsrud KW, Alfsnes K, Steinbakk M, Abrahamsen TG, Müller F, Bohlin J. Sci Rep. 2018;8(1):280. doi: 10.1038/s41598-017-18659-2.

Sonographic pancreas echogenicity in cystic fibrosis compared to exocrine pancreatic function and pancreas fat content at Dixon-MRI. Engjom T, Kavaliauskiene G, Tjora E, Erchinger F, Wathle G, Lærum BN, Njølstad PR, Frøkjær JB, Gilja OH, Dimcevski G, Haldorsen IS. PLoS One. 2018;13(7):e0201019. doi: 10.1371/journal.pone.0201019.

Contrast-enhanced ultrasonography of the pancreas shows impaired perfusion in pancreas insufficient cystic fibrosis patients. Engjom T, Nylund K, Erchinger F, Stangeland M, Lærum BN, Mézl M, Jiřík R, Gilja OH, Dimcevski G. BMC Med Imaging. 2018;18(1):14. doi: 10.1186/s12880-018-0259-3.

Kronisk pankreatitt – utredning og behandling. Engjom T, Waage A, Hoem D, Kvamme JM, Hauge T, Dimcevski G. Tidsskr Nor Laegeforen. 2018;138(3). doi: 10.4045/tidsskr.17.0341.

Secretin-stimulated ultrasound estimation of pancreatic secretion in cystic fibrosis validated by magnetic resonance imaging. Engjom T, Tjora E, Wathle G, Erchinger F, Lærum BN, Gilja OH, Haldorsen IS, Dimcevski G. Eur Radiol. 2018;28(4):1495-1503. doi: 10.1007/s00330-017-5115-2.

2017:

Impact of extensive antibiotic treatment on faecal carriage of antibiotic-resistant enterobacteria in children in a low resistance prevalence setting. Knudsen PK, Brandtzaeg P, Høiby EA, Bohlin J, Samuelsen Ø, Steinbakk M, Abrahamsen TG, Müller F, Gammelsrud KW. PLoS One. 2017;12(11):e0187618. doi: 10.1371/journal.pone.0187618.

Evaluation of a novel technique in airway clearance therapy - Specific Cough Technique (SCT) in cystic fibrosis: A pilot study of a series of N-of-1 randomised controlled trials. Gursli S, Sandvik L, Bakkeheim E, Skrede B, Stuge B. SAGE Open Med. 2017;5:2050312117697505. doi: 10.1177/2050312117697505.

Pre-flight evaluation of adult patients with cystic fibrosis: a cross-sectional study. Edvardsen E, Akerø A, Skjønsberg OH, Skrede B. BMC Res Notes. 2017;10(1):84. doi: 10.1186/s13104-017-2386-2.

Secretin-stimulated MRI assessment of exocrine pancreatic function in patients with cystic fibrosis and healthy controls. Madzak A, Engjom T, Wathle GK, Olesen SS, Tjora E, Njølstad PR, Lærum BN, Drewes AM, Dimcevski G, Frøkjær JB, Haldorsen IS. Abdom Radiol (NY). 2017;42(3):890-899. doi: 10.1007/s00261-016-0972-8.

2016:

En syv måneder gammel jente med svette føtter. Gjerstad AC, Storrøsten OT, Bakkeheim E, Handeland K, Bangstad HJ. Tidsskr Nor Laegeforen. 2016;136(19):1609.

A novel Direct MIC-gradient Strip Method to screen for antibiotic-resistant faecal Enterobacteriaceae. Gammelsrud KW, Knudsen PK, Høiby EA.J Microbiol Methods. 2016;129:94-97. doi: 10.1016/j.mimet.2016.08.007.

Implementation of newborn screening for cystic fibrosis in Norway. Results from the first three years. Lundman E, Gaup HJ, Bakkeheim E, Olafsdottir EJ, Rootwelt T, Storrøsten OT, Pettersen RD. J Cyst Fibros. 2016;15(3):318-24. doi: 10.1016/j.jcf.2015.12.017.

2015

Epidemiology of nontuberculous mycobacteria among patients with cystic fibrosis in Scandinavia. Qvist T, Gilljam M, Jönsson B, Taylor-Robinson D, Jensen-Fangel S, Wang M, Svahn A, Kötz K, Hansson L, Hollsing A, Hansen CR, Finstad PL, Pressler T, Høiby N, Katzenstein TL; Scandinavian Cystic Fibrosis Study Consortium (SCFSC). J Cyst Fibros. 2015;14(1):46-52. doi: 10.1016/j.jcf.2014.08.002.

Diagnostic Accuracy of a Short Endoscopic Secretin Test in Patients With Cystic Fibrosis. Engjom T, Erchinger F, Lærum BN, Tjora E, Aksnes L, Gilja OH, Dimcevski G. Pancreas. 2015;44(8):1266-72. doi: 10.1097/MPA.0000000000000425.

Ultrasound echo-intensity predicts severe pancreatic affection in cystic fibrosis patients. Engjom T, Erchinger F, Lærum BN, Tjora E, Gilja OH, Dimcevski G. PLoS One. 2015;10(3):e0121121. doi: 10.1371/journal.pone.0121121

Diagnostic accuracy of secretin-stimulated ultrasonography of the pancreas assessing exocrine pancreatic failure in cystic fibrosis and chronic pancreatitis. Engjom T, Erchinger F, Tjora E, Lærum BN, Georg D, Gilja OH. Scand J Gastroenterol. 2015;50(5):601-10. doi: 10.3109/00365521.2015.1004363

2012

Cystic fibrosis research in allied health and nursing professions. Bradley JM, Madge S, Morton AM, Quittner AL, Elborn JS; Allied Health and Nursing Professions Working Group, European Cystic Fibrosis Society. J Cyst Fibros. 2012;11(5):387-92. doi: 10.1016/j.jcf.2012.03.004.

2011

Dietary intake and nutritional status in a Scandinavian adult cystic fibrosis-population compared with recommendations. Moen IE, Nilsson K, Andersson A, Fagerland MW, Fluge G, Hollsing A, Gilljam M, Mared L, Pressler T, Santi H, Storrøsten OT, Hjelte L. Food Nutr Res. 2011;55. doi: 10.3402/fnr.v55i0.7561.

2010

Inverse relation between vitamin D and serum total immunoglobulin G in the Scandinavian Cystic Fibrosis Nutritional Study. Pincikova T, Nilsson K, Moen IE, Karpati F, Fluge G, Hollsing A, Knudsen PK, Lindblad A, Mared L, Pressler T, Hjelte L; Scandinavian Cystic Fibrosis Study Consortium. Eur J Clin Nutr. 2011;65(1):102-9. doi: 10.1038/ejcn.2010.194.

Gender differences in the Scandinavian cystic fibrosis population. Olesen HV, Pressler T, Hjelte L, Mared L, Lindblad A, Knudsen PK, Laerum BN, Johannesson M; Scandinavian Cystic Fibrosis Study Consortium. Pediatr Pulmonol. 2010;45(10):959-65. doi: 10.1002/ppul.21265.

 

Publikasjoner utgitt før 2010

Co-morbidity of cystic fibrosis and celiac disease in Scandinavian cystic fibrosis patients. Fluge G, Olesen HV, Gilljam M, Meyer P, Pressler T, Storrösten OT, Karpati F, Hjelte L. J Cyst Fibros. 2009;8(3):198-202. doi: 10.1016/j.jcf.2009.02.002.

Differences in prevalence and treatment of Pseudomonas aeruginosa in cystic fibrosis centres in Denmark, Norway and Sweden. Knudsen PK, Olesen HV, Høiby N, Johannesson M, Karpati F, Laerum BN, Meyer P, Pressler T, Lindblad A; Scandinavian CF Study Consortium (SCFSC). J Cyst Fibros. 2009;8(2):135-42. doi: 10.1016/j.jcf.2008.11.001.

Diagnostic significance of measurements of specific IgG antibodies to Pseudomonas aeruginosa by three different serological methods. Pressler T, Karpati F, Granström M, Knudsen PK, Lindblad A, Hjelte L, Olesen HV, Meyer P, Høiby N; Scandinavian CF Study Consortium. J Cyst Fibros. 2009;8(1):37-42. doi: 10.1016/j.jcf.2008.08.002.

Chronic Illness as a Challenge to the Attachment Process. Ødegård W. Clinical Child Psychology and Psychiatry 2005;10(1):13-22. doi: 10.1177/1359104505048787.

Anti-neutrophil cytoplasmatic antibodies and lung disease in cystic fibrosis. Dorlöchter L, Carlsson M, Olafsdottir EJ, Røksund OD, Rosendahl K, Fluge G. J Cyst Fibros. 2004;3(3):179-83.

Shwachman-Kulczycki score and resting energy expenditure in cystic fibrosis. Dorlöchter L, Helgheim V, Røksund OD, Rosendahl K, Fluge G. J Cyst Fibros. 2003;2(3):148-51.

Resting energy expenditure and lung disease in cystic fibrosis. Dorlöchter L, Røksund O, Helgheim V, Rosendahl K, Fluge G. J Cyst Fibros. 2002;1(3):131-6.

High resolution CT in cystic fibrosis--the contribution of expiratory scans. Dorlöchter L, Nes H, Fluge G, Rosendahl K. Eur J Radiol. 2003;47(3):193-8.

Faecal elastase-1 and fat-soluble vitamin profiles in patients with cystic fibrosis in Western Norway. Dorlöchter L, Aksnes L, Fluge G. Eur J Nutr. 2002;41(4):148-52.

Høyoppløsningscomputertomografi av lungene ved cystisk fibrose. Dorlöchter L, Røksund OD, Fluge G, Rosendahl K. Tidsskr Nor Laegeforen. 2002;122(16):1549-51.

Proposal of a CT scoring system of the paranasal sinuses in diagnosing cystic fibrosis. Eggesbø HB, Søvik S, Dølvik S, Eiklid K, Kolmannskog F. Eur Radiol. 2003;13(6):1451-60.

Infeksjoner med atypiske mycobakterier hos barn. Heier I, Knudsen PK ,  Wathne KO. Tidsskr Nor Legeforen 2003;123:800-2.
Hyperlink: https://tidsskriftet.no/2003/03/aktuelt/infeksjoner-med-atypiske-mykobakterier-hos-barn

Cystisk fibrose i et pasientperspektiv. Wahl AK, Rustøen T, Gjengedal E, Homme J, Hanestad BR. Tidsskr Nor Legeforen 2003;123: 2580-2.

Maternal and fetal morbidity in pregnancies of Norwegian and Swedish women with cystic fibrosis. Ødegaard I, Stray-Pedersen B, Hallberg K, Haanaes OC, Storrøsten OT, Johannesson M. Acta Obstet Gynecol Scand. 2002;81(8):698-705.

Prevalence and outcome of pregnancies in Norwegian and Swedish women with cystic fibrosis. Ødegaard I, Stray-Pedersen B, Hallberg K, Haanaes OC, Storrøsten OT, Johannesson M. Acta Obstet Gynecol Scand. 2002;81(8):693-7.

CT characterization of inflammatory paranasal sinus disease in cystic fibrosis. Eggesbø HB, Søvik S, Dølvik S, Kolmannskog F. Acta Radiol. 2002;43(1):21-8.

CT characterization of developmental variations of the paranasal sinuses in cystic fibrosis. Eggesbø HB, Søvik S, Dølvik S, Eiklid K, Kolmannskog F. Acta Radiol. 2001;42(5):482-93.

Complementary role of MR imaging of ethmomaxillary sinus disease depicted at CT in cystic fibrosis. Eggesbø HB, Dølvik S, Stiris M, Søvik S, Storrøsten OT, Kolmannskog F. Acta Radiol. 2001;42(2):144-50.

Hypoplasia of the sphenoid sinuses as a diagnostic tool in cystic fibrosis. Eggesbø HB, Eken T, Eiklid K, Kolmannskog F. Acta Radiol. 1999;40(5):479-85.

Cystisk fibrose i Helseregion Vest. Fluge G. Tidsskr Nor Laegeforen. 2000;120(5):568-71.

Typing of Pseudomonas aeruginosa strains in Norwegian cystic fibrosis patients. Fluge G, Ojeniyi B, Høiby N, Digranes A, Ciofu O, Hunstad E, Haanaes OC, Storrøsten OT. Clin Microbiol Infect. 2001;7(5):238-43.

Primær ciliedyskinesi

2018:

Variation in treatment strategies for the eradication of Pseudomonas aeruginosa in primary ciliary dyskinesia across European centers. Crowley S, Holgersen MG, Nielsen KG. Chron Respir Dis. 2018:1479972318787919. doi: 10.1177/1479972318787919.

2017:

Growth and nutritional status, and their association with lung function: a study from the international Primary Ciliary Dyskinesia Cohort. Goutaki M, Halbeisen FS, Spycher BD, Maurer E, Belle F, Amirav I, Behan L, Boon M, Carr S, Casaulta C, Clement A, Crowley S, Dell S, Ferkol T, Haarman EG, Karadag B, Knowles M, Koerner-Rettberg C, Leigh MW, Loebinger MR, Mazurek H, Morgan L, Nielsen KG, Phillipsen M, Sagel SD, Santamaria F, Schwerk N, Yiallouros P, Lucas JS, Kuehni CE; PCD Israeli Consortium; Swiss PCD Group; French Reference Centre for Rare Lung Diseases. Eur Respir J. 2017;50(6). pii: 1701659. doi: 10.1183/13993003.01659-2017.

Protracted bacterial bronchitis in children. Øymar K, Mikalsen IB, Crowley S. Tidsskr Nor Laegeforen. 2017;137(14-15). doi: 10.4045/tidsskr.16.0843.

2016:

The international primary ciliary dyskinesia cohort (iPCD Cohort): methods and first results. Goutaki M, Maurer E, Halbeisen FS, Amirav I, Barbato A, Behan L, Boon M, Casaulta C, Clement A, Crowley S, Haarman E, Hogg C, Karadag B, Koerner-Rettberg C, Leigh MW, Loebinger MR, Mazurek H, Morgan L, Nielsen KG, Omran H, Schwerk N, Scigliano S, Werner C, Yiallouros P, Zivkovic Z, Lucas JS, Kuehni CE; PCD Italian Consortium; Swiss PCD Group; French Reference Centre for Rare Lung Diseases; Genetic Disorders of Mucociliary Clearance Consortium. Eur Respir J. 2017;49(1). pii: 1601181. doi: 10.1183/13993003.01181-2016.

Primær ciliedyskinesi. Crowley S. Tidsskr Nor Laegeforen. 2016;136(2):128-30. doi: 10.4045/tidsskr.15.0390.


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