L Hjelte
Overview
Explore the profile of L Hjelte including associated specialties, affiliations and a list of published articles.
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Articles
48
Citations
559
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Recent Articles
1.
Pincikova T, Paquin-Proulx D, Sandberg J, Flodstrom-Tullberg M, Hjelte L
Clin Exp Immunol
. 2017 May;
189(3):359-371.
PMID: 28470739
Persistent inflammatory response in cystic fibrosis (CF) airways is believed to play a central role in the progression of lung damage. Anti-inflammatory treatment may slow lung disease progression, but adverse...
2.
Pincikova T, Paquin-Proulx D, Sandberg J, Flodstrom-Tullberg M, Hjelte L
Eur J Clin Nutr
. 2016 Dec;
71(2):203-205.
PMID: 27966575
Background/objectives: Vitamin D insufficiency in cystic fibrosis is common. Vitamin D3 is currently preferred over D2. We aimed to study the efficacy of vitamin D2 and D3 at increasing serum...
3.
Pincikova T, Nilsson K, Moen I, Fluge G, Hollsing A, Knudsen P, et al.
Diabetologia
. 2011 Sep;
54(12):3007-15.
PMID: 21901282
Aims/hypothesis: Many cystic fibrosis patients are vitamin D-insufficient. Cystic fibrosis-related diabetes is a major complication of cystic fibrosis. The literature suggests that vitamin D might possess certain glucose-lowering properties. We...
4.
Bilton D, Canny G, Conway S, Dumcius S, Hjelte L, Proesmans M, et al.
J Cyst Fibros
. 2011 Jun;
10 Suppl 2:S79-81.
PMID: 21658647
Pulmonary exacerbations represent a key outcome variable in clinical trials of cystic fibrosis (CF). As there is variation in the trigger for use of intravenous antibiotics compared to the use...
5.
Pressler T, Bohmova C, Conway S, Dumcius S, Hjelte L, Hoiby N, et al.
J Cyst Fibros
. 2011 Jun;
10 Suppl 2:S75-8.
PMID: 21658646
Chronic pulmonary infection with P. aeruginosa develops in most patients with cystic fibrosis (CF); by adulthood 80% of patients are infected and chronic P. aeruginosa infection is the primary cause...
6.
Geborek A, Hjelte L
J Cyst Fibros
. 2011 Mar;
10(3):187-92.
PMID: 21354377
Background: Despite numerous studies a clear relationship between genotype and pulmonary phenotype has not been established within the group pancreatic insufficient cystic fibrosis (CF) patients. We studied the relationship between...
7.
Pincikova T, Nilsson K, Moen I, Karpati F, Fluge G, Hollsing A, et al.
Eur J Clin Nutr
. 2010 Sep;
65(1):102-9.
PMID: 20859300
Background/objectives: The hallmark of cystic fibrosis (CF) is chronic lung inflammation. The severity of lung disease is closely correlated with immunoglobulin G (IgG) levels. Beyond its contribution to the bone...
8.
Goubau C, Wilschanski M, Skalicka V, Lebecque P, Southern K, Sermet I, et al.
Thorax
. 2009 Mar;
64(8):683-91.
PMID: 19318346
Background: In patients with symptoms suggestive of cystic fibrosis (CF) and intermediate sweat chloride values (30-60 mmol/l), extensive CFTR gene mutation analysis and nasal potential difference (NPD) measurement are used...
9.
Fluge G, Olesen H, Gilljam M, Meyer P, Pressler T, Storrosten O, et al.
J Cyst Fibros
. 2009 Mar;
8(3):198-202.
PMID: 19303374
Background: The co-morbidity of cystic fibrosis (CF) and celiac disease (CD) has been reported sporadically since the 1960s. To our knowledge, this is the first time a systematic screening is...
10.
Lindstrom M, Camner P, Falk R, Hjelte L, Philipson K, Svartengren M
Eur Respir J
. 2005 Feb;
25(2):317-23.
PMID: 15684297
Impaired mucociliary clearance is a hallmark of cystic fibrosis (CF). Early morphological changes first appear in the small airways. Lung clearance was investigated in 11 young CF adults with mild-to-moderate...