Zobrazeno 1 - 10
of 180
pro vyhledávání: '"E. Endreffy"'
Autor:
I Ferreiro-Neira, M Calaza, E Alonso-Perez, M Marchini, R Scorza, G D Sebastiani, F J Blanco, I Rego, R Pullmann, C G Kallenberg, M Bijl, F N Skopouli, M Mavromati, S Migliaresi, N Barizzone, S Ruzickova, C Dostal, R E Schmidt, T Witte, C Papasteriades, I Kappou-Rigatou, E Endreffy, A Kovacs, J Ordi-Ros, E Balada, P Carreira, J J Gomez-Reino, A Gonzalez
Publikováno v:
GENES AND IMMUNITY, 8(5), 429-438. Nature Publishing Group
Genetic variation in the interferon regulatory factor 5 (IRF5) gene affects systemic lupus erythematosus (SLE) susceptibility. However, association is complex and incompletely defined. We obtained fourteen European sample collections with a total of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::65c62b9a1cb5143393de67d945ecb26a
https://research.rug.nl/en/publications/c17d758a-60f7-43a7-af46-9400e3d9e1e7
https://research.rug.nl/en/publications/c17d758a-60f7-43a7-af46-9400e3d9e1e7
Publikováno v:
Journal of medical virology. 65(3)
On the basis of the sequence variation of the glycoprotein B (gB) gene, human cytomegalovirus (HCMV) can be classified into four gB genotypes. Genotyping of HCMV from congenital infections was carried out on the assumption that the envelope gB may in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::31a69931d859c9e7f850d0c775ade256
https://pubmed.ncbi.nlm.nih.gov/11596091
https://pubmed.ncbi.nlm.nih.gov/11596091
Autor:
A, Kovács, E, Szekeres, L, Berek, E, Endreffy, L, Kovács, E, Makula, J, Eller, G, Pokorny, I B, Petri
Publikováno v:
Acta microbiologica et immunologica Hungarica. 47(4)
Though at present there is no evidence-based algorithm for the treatment of primary Sjögren's syndrome, it is generally accepted that glucocorticosteroid (GS) therapy must be introduced in cases with severe systemic manifestations. As the side-effec
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::a51ead95840e524c5446fde6a1b5b4af
https://pubmed.ncbi.nlm.nih.gov/11056762
https://pubmed.ncbi.nlm.nih.gov/11056762
Deletion patterns of dystrophin gene in Hungarian patients with Duchenne/Becker muscular dystrophies
Autor:
Aranka László, Béla Melegh, István Raskó, F Fodor, Eva Morava, E Endreffy, F Mechler, P Gyurus, A Herczegfalvi, Gábor Tóth
Publikováno v:
Neuromuscular disorders : NMD. 9(8)
Deletion pattern analysis of the dystrophin gene was performed in 159 Hungarian patients with Duchenne/Becker muscular dystrophy. In 116 cases (73% of total patients), exon deletions were detected by PCR amplification. In 37 patients (31.9% of patien
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ac71e882e4cfc1e818994d8d038be6f0
https://pubmed.ncbi.nlm.nih.gov/10619712
https://pubmed.ncbi.nlm.nih.gov/10619712
Publikováno v:
Experimental and clinical immunogenetics. 13(3-4)
We describe here the genetic variability of HLA-DRB1, -DQA, and -DQB in 140 healthy individuals from Hungary, including 95 randomly selected adults and 45 newborns. Allele and haplotype frequencies as well as linkage disequilibria were calculated. It
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::9866aa6647d959b7c27c3f5156635961
https://pubmed.ncbi.nlm.nih.gov/9165274
https://pubmed.ncbi.nlm.nih.gov/9165274
Publikováno v:
Orvosi hetilap. 135(8)
Deletion analysis of the dystrophin gene (Xp21) was carried out by examinations of the most frequently deleted 18 exons (3., 4., 6., 8., 12., 13., 17., 19., 43., 44., 45., 47., 48., 49., 50., 51., 52. and 60. exon) and the muscle specific promoter in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::8a974d4402f65d5a372c36877475b4de
https://pubmed.ncbi.nlm.nih.gov/8139842
https://pubmed.ncbi.nlm.nih.gov/8139842
Publikováno v:
Acta microbiologica et immunologica Hungarica. 41(1)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::9d9d8949f0e35dc54e8432de4f4daa5c
https://pubmed.ncbi.nlm.nih.gov/7921847
https://pubmed.ncbi.nlm.nih.gov/7921847
Publikováno v:
Haematologia. 25(2)
HLA-DR beta-RFLP analysis of serologically 1 or 2 DR-antigen compatible renal allograft donors and recipients (D/R), selected for DRw6 antigen (study group), or for other DR antigens (control group) and its correlation with the graft outcome revealed
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::c4c76a4e13d13c7e6c208f045a2c277d
https://pubmed.ncbi.nlm.nih.gov/7902315
https://pubmed.ncbi.nlm.nih.gov/7902315
Publikováno v:
Acta paediatrica Hungarica. 32(2)
A retrospective analysis of the HLA-DR antigens was performed at the DR beta DNA locus by the means of restriction fragment length polymorphism (RFLP) in the case of a two-times kidney transplanted paediatric patient and in 16 adult kidney donor reci
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::15496ec636aa38e73bf1daafbc4ea0f3
https://pubmed.ncbi.nlm.nih.gov/1356380
https://pubmed.ncbi.nlm.nih.gov/1356380
Publikováno v:
Acta paediatrica Hungarica. 32(2)
Linked marker haplotype analysis of 16 cystic fibrosis (CF)-affected children, 3 fetuses, 1 healthy child and their parents was performed by restriction fragment length polymorphism (RFLP) for J3.11, Met H, Met D, XV-2c, KM.19 markers. Polymerase cha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::fc6945645b5ec9a7a2f3abadac824498
https://pubmed.ncbi.nlm.nih.gov/1356379
https://pubmed.ncbi.nlm.nih.gov/1356379