Zobrazeno 1 - 10
of 33
pro vyhledávání: '"H. E. Heier"'
Autor:
H. E. Heier, S. Jeansson
Publikováno v:
Vox Sanguinis. 82:87-111
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1edb3c5f5046b78a51bfacc7c906f0cb
https://doi.org/10.1046/j.0042-9007.2001.00147_18.x
https://doi.org/10.1046/j.0042-9007.2001.00147_18.x
Autor:
C P, Engelfriet, H W, Reesink, G, Garratty, R, Knight, M, de Silva, M, Contreras, M A, Overbeeke, L, Porcelijn, M, Lin, C C, So, A C, Schmidt-Melbye, H E, Heier, R J, Sokol, D J, Booker, R, Stamps, L, Barbolla, C, Zamora, M, Hernández-Jodra, ZupańskaB, M, Goldman, A, Long, F, Décary
Publikováno v:
Vox Sanguinis. 78:200-207
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bdacccafab870f1cdde6acc2a25387e4
https://doi.org/10.1159/000031181
https://doi.org/10.1159/000031181
Publikováno v:
Transfusion Medicine. 2:7-15
Binding patterns of mouse monoclonal antibodies (mAb) to P1, Pk, N, I, H, Y or A antigens were visualized in the backscatter electron imaging mode of a scanning electron microscope by indirect immunogold labelling. Experiments were performed at room
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b69cb333defdc89208ded5ed5245e595
https://doi.org/10.1111/j.1365-3148.1992.tb00129.x
https://doi.org/10.1111/j.1365-3148.1992.tb00129.x
Publikováno v:
Vox sanguinis. 94(2)
Reasons for predonation deferral of young potential donors and prospects of recruiting and retaining young people (age 18-29) as voluntary blood donors were studied.Three different sources of data were analysed: (i) the subsequent donation history of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::e7525cd2b5c06cd3af64151c35c3b614
https://pubmed.ncbi.nlm.nih.gov/18067488
https://pubmed.ncbi.nlm.nih.gov/18067488
Autor:
J, Coste, H W, Reesink, C P, Engelfriet, S, Laperche, S, Brown, M P, Busch, H T, Cuijpers, R, Elgin, B, Ekermo, J S, Epstein, O, Flesland, H E, Heier, G, Henn, J M, Hernandez, I K, Hewlett, C, Hyland, A J, Keller, T, Krusius, S, Levicnik-Stezina, G, Levy, C K, Lin, A R, Margaritis, L, Muylle, C, Niederhauser, C, Neiderhauser, S, Pastila, J, Pillonel, J, Pineau, C L, van der Poel, C, Politis, W K, Roth, S, Sauleda, C R, Seed, D, Sondag-Thull, S L, Stramer, M, Strong, E C, Vamvakas, C, Velati, M A, Vesga, A, Zanetti
Publikováno v:
Vox sanguinis. 88(4)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::19f3aec17ac7e466699940a1bd2108b6
https://pubmed.ncbi.nlm.nih.gov/16262764
https://pubmed.ncbi.nlm.nih.gov/16262764
Autor:
H E, Heier
Publikováno v:
Tidsskrift for den Norske laegeforening : tidsskrift for praktisk medicin, ny raekke. 121(26)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::95df021492041aa3574fa0cee0824278
https://pubmed.ncbi.nlm.nih.gov/11757433
https://pubmed.ncbi.nlm.nih.gov/11757433
Autor:
H E, Heier
Publikováno v:
Tidsskrift for den Norske laegeforening : tidsskrift for praktisk medicin, ny raekke. 120(18)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::fdfb0340d5790187991fa4b5855ed6b3
https://pubmed.ncbi.nlm.nih.gov/11006745
https://pubmed.ncbi.nlm.nih.gov/11006745
Autor:
H E, Heier
Publikováno v:
Tidsskrift for den Norske laegeforening : tidsskrift for praktisk medicin, ny raekke. 119(5)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::2b901f1a16e188927e22061c76d83fe4
https://pubmed.ncbi.nlm.nih.gov/10081361
https://pubmed.ncbi.nlm.nih.gov/10081361
Publikováno v:
Vox sanguinis. 75(1)
The published sequence of the weak. A subgroup Ael gene from Swedish individuals showed a G insertion in exon VII, causing a frameshift at codon 268 (the A1 gene has 353 codons). We wished to sequence exons VI and VII of two Norwegian Ael individuals
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::8681089b76dcdd71495deed4f0574ef6
https://pubmed.ncbi.nlm.nih.gov/9745153
https://pubmed.ncbi.nlm.nih.gov/9745153
Publikováno v:
Tidsskrift for den Norske laegeforening : tidsskrift for praktisk medicin, ny raekke. 118(2)
Haemochromatosis is an inherited, recessive trait and is among the most common genetic diseases in Norway. It is caused by a pathological increase in the absorption of iron from the intestine. This in turn leads to excessive deposits of iron in the o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::00d1c89d3c35dcb2e91fbe2f686f37b5
https://pubmed.ncbi.nlm.nih.gov/9638063
https://pubmed.ncbi.nlm.nih.gov/9638063