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B P C Koeleman

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Articles 40
Citations 852
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Recent Articles
1.
Dirkx N, Weuring W, De Vriendt E, Smal N, van de Vondervoort J, van t Slot R, et al.
BMC Biol . 2023 Jul; 21(1):156. PMID: 37443005
Background: Prime editing (PE) is the most recent gene editing technology able to introduce targeted alterations to the genome, including single base pair changes, small insertions, and deletions. Several improvements...
2.
Stevelink R, Koeleman B, Sander J, Jansen F, Braun K
Eur J Neurol . 2018 Sep; 26(6):856-864. PMID: 30223294
Background And Purpose: Juvenile myoclonic epilepsy (JME) is a common epilepsy syndrome for which treatment response is generally assumed to be good. We aimed to determine the prevalence and prognostic...
3.
de Lange I, Rump P, Neuteboom R, Augustijn P, Hodges K, Kistemaker A, et al.
Neurogenetics . 2017 Jul; 18(3):147-153. PMID: 28669061
Pathogenic variants in the PCDH19 gene are associated with epilepsy, intellectual disability (ID) and behavioural disturbances. Only heterozygous females and mosaic males are affected, likely due to a disease mechanism...
4.
de Jong V, van der Slik A, Laban S, van t Slot R, Koeleman B, Zaldumbide A, et al.
Genes Immun . 2016 Jul; 17(6):342-8. PMID: 27467285
Autoreactive CD8(+) T cells recognizing autoantigens expressed by pancreatic islets lead to the destruction of insulin-producing beta cells in type 1 diabetes (T1D), but these T cells also occur in...
5.
Berghuis B, de Haan G, van den Broek M, Sander J, Lindhout D, Koeleman B
Eur J Neurol . 2016 Jun; 23(9):1393-9. PMID: 27333872
The use of carbamazepine (CBZ) and oxcarbazepine (OXC) as first-line antiepileptic drugs in the treatment of focal epilepsy is limited by hyponatremia, a known adverse effect. Hyponatremia occurs in up...
6.
de Jong V, Zaldumbide A, van der Slik A, Laban S, Koeleman B, Roep B
Genes Immun . 2015 Dec; 17(1):75-8. PMID: 26656450
Cytotoxic T-lymphocyte-associated protein 4 (CTLA4) is a protein receptor that downregulates the immune system. CTLA4 gene variants associate with various autoimmune diseases, including type 1 diabetes. Fine mapping of the...
7.
Kremer P, Koeleman B, Rinkel G, Diekstra F, van den Berg L, Veldink J, et al.
J Neurol Neurosurg Psychiatry . 2015 Aug; 87(7):693-6. PMID: 26272027
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...
8.
Kremer P, Koeleman B, Pawlikowska L, Weinsheimer S, Bendjilali N, Sidney S, et al.
J Neurol Neurosurg Psychiatry . 2014 Jul; 86(5):524-9. PMID: 25053769
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 vascular diseases and AVMs...
9.
Bossini-Castillo L, de Kovel C, Kallberg H, van t Slot R, Italiaander A, Coenen M, et al.
Ann Rheum Dis . 2014 Feb; 74(3):e15. PMID: 24532677
Introduction: Rheumatoid arthritis (RA) patients can be classified based on presence or absence of anticitrullinated peptide antibodies (ACPA) in their serum. This heterogeneity among patients may reflect important biological differences...
10.
Boraska V, Franklin C, Floyd J, Thornton L, Huckins L, Southam L, et al.
Mol Psychiatry . 2014 Feb; 19(10):1085-94. PMID: 24514567
Anorexia nervosa (AN) is a complex and heritable eating disorder characterized by dangerously low body weight. Neither candidate gene studies nor an initial genome-wide association study (GWAS) have yielded significant...