Zobrazeno 1 - 10
of 255
pro vyhledávání: '"H. Kollberg"'
Publikováno v:
Tissue Antigens. 10:287-290
Thirty-three patients with Cystic Fibrosis were HLA typed. Relative risk values and phenotype frequencies were calculated. No statistically significant differences in the HLA antigen distribution were found among the patients with Cystic Fibrosis.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c4add6977c9d1cd9c3bcc9ec07f8e707
https://doi.org/10.1111/j.1399-0039.1977.tb00759.x
https://doi.org/10.1111/j.1399-0039.1977.tb00759.x
Autor:
H Kollberg, Ragnhild Kornfält, Lars Holmberg, Charlotta Schaedel, Lena Hjelte, Marie Johannesson, I de Monestrol
Publikováno v:
Clinical Genetics. 56:318-322
Children with cystic fibrosis (CF) diagnosed by neonatal screening have a better nutritional development and other advantages compared with those in a nonscreened group. The two-tier immunoreactive trypsinogen (IRT)/DNA screening protocol has been fo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d18338a4e589092be13bc25c023f735d
https://doi.org/10.1034/j.1399-0004.1999.560410.x
https://doi.org/10.1034/j.1399-0004.1999.560410.x
Autor:
S. Dumcius, Niels Høiby, V. Vavrova, H. Kollberg, C. Bohmova, Lena Hjelte, Tacjana Pressler, Burkhard Tümmler, Steven P. Conway
Publikováno v:
Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society. 10
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 of increased morbidity and mortality in CF. Chronic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8f7b1af5ed379892266b9aeb8c3a7dc7
https://pubmed.ncbi.nlm.nih.gov/21658646
https://pubmed.ncbi.nlm.nih.gov/21658646
Publikováno v:
Journal of Cystic Fibrosis. 8
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e01050a3d73033eccd6522a9933fbf90
Autor:
H. Kollberg
Publikováno v:
Journal of Cystic Fibrosis. 14:S88
Objectives Clinical studies with CF-patients on Anti-psIgY (Anti-Pseudomonas IgY) to prevent infections with PA (Pseudomonas aeruginosa) in order to find out efficacy and adverse events have been running in Sweden for 20 years. Anti-psIgY has got Orp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a82f512e1d45a56267642519cabb345e
https://doi.org/10.1016/s1569-1993(15)30300-3
https://doi.org/10.1016/s1569-1993(15)30300-3
Autor:
H, Kollberg, R, Lidman
Publikováno v:
Lakartidningen. 98(8)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::ce0b1d2ebe4d2732fae60ed2ff6ffb8b
https://pubmed.ncbi.nlm.nih.gov/11265570
https://pubmed.ncbi.nlm.nih.gov/11265570
Publikováno v:
Lakartidningen. 97(20)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::bb61535a6534eac537bba041fc82c516
https://pubmed.ncbi.nlm.nih.gov/10909227
https://pubmed.ncbi.nlm.nih.gov/10909227
Autor:
C, Schaedel, L, Hjelte, I, de Monestrol, M, Johannesson, H, Kollberg, R, Kornfält, L, Holmberg
Publikováno v:
Clinical genetics. 56(4)
Children with cystic fibrosis (CF) diagnosed by neonatal screening have a better nutritional development and other advantages compared with those in a nonscreened group. The two-tier immunoreactive trypsinogen (IRT)/DNA screening protocol has been fo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::97b66219192ecaa37606582fb196c477
https://pubmed.ncbi.nlm.nih.gov/10636451
https://pubmed.ncbi.nlm.nih.gov/10636451
Autor:
H, Kollberg
Publikováno v:
Lakartidningen. 96(32-33)
First rate collaboration between clinicians and research scientists in a multiplicity of fields have brought new hope to patients with cystic fibrosis (CF). The gene, mutations of which give rise to the disease, has been exhaustively mapped, and the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::42e466522493ba52926d1fadd688a888
https://pubmed.ncbi.nlm.nih.gov/10479796
https://pubmed.ncbi.nlm.nih.gov/10479796
Autor:
H, Kollberg
Publikováno v:
Lakartidningen. 96(30-31)
Cystic fibrosis (CF) is a general exocrinopathy chiefly characterised by airway and nutritional symptoms, though several other organ systems may also be affected. Intensive collaboration between clinicians and research scientists has enabled great ad
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::9c74b465a1460c5d4369c77c47efec54
https://pubmed.ncbi.nlm.nih.gov/10459238
https://pubmed.ncbi.nlm.nih.gov/10459238