Zobrazeno 1 - 7
of 7
pro vyhledávání: '"P. H. C. Kremer"'
Autor:
John A. Lees, Bart Ferwerda, Philip H. C. Kremer, Nicole E. Wheeler, Mercedes Valls Serón, Nicholas J. Croucher, Rebecca A. Gladstone, Hester J. Bootsma, Nynke Y. Rots, Alienke J. Wijmega-Monsuur, Elisabeth A. M. Sanders, Krzysztof Trzciński, Anne L. Wyllie, Aeilko H. Zwinderman, Leonard H. van den Berg, Wouter van Rheenen, Jan H. Veldink, Zitta B. Harboe, Lene F. Lundbo, Lisette C. P. G. M. de Groot, Natasja M. van Schoor, Nathalie van der Velde, Lars H. Ängquist, Thorkild I. A. Sørensen, Ellen A. Nohr, Alexander J. Mentzer, Tara C. Mills, Julian C. Knight, Mignon du Plessis, Susan Nzenze, Jeffrey N. Weiser, Julian Parkhill, Shabir Madhi, Thomas Benfield, Anne von Gottberg, Arie van der Ende, Matthijs C. Brouwer, Jeffrey C. Barrett, Stephen D. Bentley, Diederik van de Beek
Publikováno v:
Nature Communications, Vol 10, Iss 1, Pp 1-14 (2019)
Streptococcus pneumoniae is a causative agent of meningitis and bacteremia. In a combined pathogen and host GWAS, Lees et al. find that host genetic variation is associated with both susceptibility and severity of pneumococcal meningitis, and specifi
Externí odkaz:
https://doaj.org/article/676c4fca20864aaa9d086a45a85f61c3
Autor:
Philip H. C. Kremer, John A. Lees, Bart Ferwerda, Arie van de Ende, Matthijs C. Brouwer, Stephen D. Bentley, Diederik van de Beek
Publikováno v:
Frontiers in Medicine, Vol 7 (2020)
Neisseria meningitidis causes sepsis and meningitis in humans. It has been suggested that pathogen genetic variation determines variance in disease severity. Here we report results of a genome-wide association study of 486 N. meningitidis genomes fro
Externí odkaz:
https://doaj.org/article/cc2bc4d694084b1b9e3dd1bda447ea9c
Autor:
Philip H C Kremer, Wilmar M T Jolink, L Jaap Kappelle, Ale Algra, Catharina J M Klijn, SMART and ESPRIT Study Groups
Publikováno v:
PLoS ONE, Vol 10, Iss 11, p e0142338 (2015)
Lobar and non-lobar non-traumatic intracerebral hemorrhage (ICH) are presumably caused by different types of small vessel diseases. The aim of this study was to assess risk factors for ICH according to location.In two large prospective studies, SMART
Externí odkaz:
https://doaj.org/article/f5ebd99f84f140f6bddd9a8cdf9c731e
Autor:
P. H. C. Kremer, G Je Rinkel, Frank P. Diekstra, B. P. C. Koeleman, L.H. van den Berg, Catharina J.M. Klijn, Jan H. Veldink
Publikováno v:
Journal of Neurology, Neurosurgery, and Psychiatry, 87, 693-6
Journal of Neurology, Neurosurgery, and Psychiatry, 87, 7, pp. 693-6
Journal of Neurology, Neurosurgery, and Psychiatry, 87, 7, pp. 693-6
Item does not contain fulltext BACKGROUND: Case-control studies have reported multiple genetic loci to be associated with sporadic brain arteriovenous malformations (AVMs) but most of these have not been replicated in independent populations. The aim
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::79a2530498b74de91b2598109ed8af8b
http://hdl.handle.net/2066/168166
http://hdl.handle.net/2066/168166
Autor:
P. H. C. Kremer, Liam R. Brunham, C. B. Verchere, Michael R. Hayden, L. Dai, Janine K. Kruit, Piers Ruddle, Renmei Tang, W. de Haan
Publikováno v:
Diabetologia. 53:1110-1119
Cellular cholesterol accumulation is an emerging mechanism for beta cell dysfunction in type 2 diabetes. Absence of the cholesterol transporter ATP-binding cassette transporter A1 (ABCA1) results in increased islet cholesterol and impaired insulin se
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e18cdd9d6b7513f8f155865796af3203
https://doi.org/10.1007/s00125-010-1691-2
https://doi.org/10.1007/s00125-010-1691-2
Autor:
G. A. P. de Kort, Jonathan G. Zaroff, Jan H. Veldink, Ludmila Pawlikowska, L.H. van den Berg, Catharina J.M. Klijn, Nasrine Bendjilali, Helen Kim, Stephen Sidney, Shantel Weinsheimer, P. H. C. Kremer, Ynte M. Ruigrok, Bobby P. C. Koeleman, Gabriel J.E. Rinkel
Publikováno v:
Journal of neurology, neurosurgery, and psychiatry, vol 86, iss 5
Journal of Neurology, Neurosurgery and Psychiatry, 86(5), 524. BMJ Publishing Group
Journal of Neurology, Neurosurgery, and Psychiatry, 86, 5, pp. 524-9
Journal of Neurology, Neurosurgery, and Psychiatry, 86, 524-9
Journal of Neurology, Neurosurgery and Psychiatry, 86(5), 524. BMJ Publishing Group
Journal of Neurology, Neurosurgery, and Psychiatry, 86, 5, pp. 524-9
Journal of Neurology, Neurosurgery, and Psychiatry, 86, 524-9
Item does not contain fulltext BACKGROUND: In genome-wide association studies (GWAS) five putative risk loci are associated with intracranial aneurysm. As brain arteriovenous malformations (AVM) and intracranial aneurysms are both intracranial vascul
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5a0cee5ff0b8ac41138fc752510f0d8e
https://dspace.library.uu.nl/handle/1874/331647
https://dspace.library.uu.nl/handle/1874/331647
Autor:
P. H. C. Kremer
Publikováno v:
Clinical Genetics. 73:428-429
Impaired glycosylation and cutis laxa caused by mutations in the vesicular H+-ATPase subunit ATP6V0A2 Kornak et al. (2008) Nature Genetics 40: 32–34
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c6ac54f39dd45a9f48980e61147e97e0
https://doi.org/10.1111/j.1399-0004.2008.00990_3.x
https://doi.org/10.1111/j.1399-0004.2008.00990_3.x