Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Anne Werner Hauge"'
Publikováno v:
Hald, J, Plesner, A, Hauge, A W & Bruunsgaard, H 2022, ' Detection of the novel HLA allele, HLA-DQA1*01:65, identified in a Danish donor ', HLA, vol. 99, no. 1, pp. 66-67 . https://doi.org/10.1111/tan.14438
HLA-DQA1*01:65 differs from HLA-DQA1*01:03 in exon 1 at amino acid -7 a valine to methionine substitution.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::faa002dfe633cd18f0d72e1dee33c83d
https://curis.ku.dk/ws/files/305535206/LINI_tan.14438.pdf
https://curis.ku.dk/ws/files/305535206/LINI_tan.14438.pdf
Publikováno v:
HLAREFERENCES. 98(1)
HLA-DPA1*01:46 differs from HLA-DPA1*01:03 in exon 2 at amino acid 85; Aspartate to Asparagine substitution.
Autor:
Helle, Bruunsgaard, Anne Werner, Hauge
Publikováno v:
Ugeskrift for laeger. 182(49)
Allogeneic haematopoietic stem cell transplantation is a clinical example of precision medicine, as one individual donor is selected for one individual patient based on genetic findings in the human leukocyte antigen (HLA) system. Unrelated donor sea
Autor:
Helena Mora-Jensen, Anne Werner Hauge, Kit P. Lund, Søren Schwartz Sørensen, Frank Eriksson, Helle Bruunsgaard
Publikováno v:
Web of Science
The importance of the human leukocyte antigen (HLA) system in kidney transplantation is well-known, but it remains unexplored if patient HLA antigens constitute independent risk factors in complications after transplantation. We hypothesized that spe
Autor:
A-L Esserlind, Han Le, Navid Mohamadpour Toyserkani, Jes Olesen, Anne Werner Hauge, Stacy Steinberg, Niels Grarup, M. Kirchmann, F Bettella, Hreinn Stefansson, Thomas Werge, Torben Hansen, Anne Francke Christensen
Publikováno v:
Esserlind, A-L, Christensen, A F, Le, H, Kirchmann, M, Hauge, A W, Toyserkani, N, Hansen, T, Grarup, N, Werge, T, Steinberg, S, Bettella, F, Stefansson, H & Olesen, J 2013, ' Replication and meta-analysis of common variants identifies a genome-wide significant locus in migraine ', European Journal of Neurology, vol. 20, no. 5, pp. 765-772 . https://doi.org/10.1111/ene.12055
BACKGROUND AND PURPOSE: Genetic factors contribute to the aetiology of the prevalent form of migraine without aura (MO) and migraine with typical aura (MTA). Due to the complex inheritance of MO and MTA, the genetic background is still not fully esta
Publikováno v:
Scandinavian Journal of Pain. 4:48-52
Background and aims NXN-188 is a combined neuronal nitric oxide synthase (nNOS) inhibitor and 5HT-1B/1D receptor agonist which has previously shown efficacy in the acute treatment of migraine. Nitric oxide (NO) is involved in the pathogenesis of migr
Publikováno v:
European Journal of Neurology. 19:603-609
Background and purpose: Although the genetics of familial hemiplegic migraine are being unraveled, this is not the case for the prevalent types of migraine. However, a recent genome wide association study (GWAS) reported an association of the single
Publikováno v:
Cephalalgia. 31:416-438
Objective The aim of the present study was to characterize perceived consistent triggers of migraine with aura (MA). Method Questionnaires specifically designed to characterize various trigger factors were sent to 181 participants identified in an ea
Autor:
Anne Werner Hauge, Mohammed S Asghar, Henrik Winther Schytz, Karl Bang Christensen, Jes Olesen
Publikováno v:
The Lancet Neurology. 8:718-723
Summary Background Migraine with aura is thought likely to be caused by cortical spreading depression (CSD). Tonabersat inhibits CSD, and we therefore investigated whether tonabersat has a preventive effect in migraine with aura. Methods In this rand
Publikováno v:
Cephalalgia. 30:346-353
The aim of the present study was to identify trigger factors in migraine with aura (MA). A total of 629 MA patients representative of the Danish population were sent a questionnaire listing 16 trigger factors thought to be relevant as well as space f