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617 results

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The Complexity of Genotype-Phenotype Correlations in Hereditary Spherocytosis: A Cohort of 95 Patients: Genotype-Phenotype Correlation in Hereditary Spherocytosis.
van Vuren A, van der Zwaag B, Huisjes R, Lak N, Bierings M, Gerritsen E, van Beers E, Bartels M, van Wijk R. van Vuren A, et al. Among authors: van beers e, van wijk r, van der zwaag b. Hemasphere. 2019 Aug 7;3(4):e276. doi: 10.1097/HS9.0000000000000276. eCollection 2019 Aug. Hemasphere. 2019. PMID: 31723846 Free PMC article.
Erythrocytosis associated with a novel missense mutation in the HIF2A gene.
van Wijk R, Sutherland S, Van Wesel AC, Huizinga EG, Percy MJ, Bierings M, Lee FS. van Wijk R, et al. Among authors: van wesel ac. Haematologica. 2010 May;95(5):829-32. doi: 10.3324/haematol.2009.017582. Epub 2009 Dec 8. Haematologica. 2010. PMID: 20007141 Free PMC article.
Ribosomal protein mutations induce autophagy through S6 kinase inhibition of the insulin pathway.
Heijnen HF, van Wijk R, Pereboom TC, Goos YJ, Seinen CW, van Oirschot BA, van Dooren R, Gastou M, Giles RH, van Solinge W, Kuijpers TW, Gazda HT, Bierings MB, Da Costa L, MacInnes AW. Heijnen HF, et al. Among authors: van oirschot ba, van wijk r, van dooren r, van solinge w. PLoS Genet. 2014 May 29;10(5):e1004371. doi: 10.1371/journal.pgen.1004371. eCollection 2014. PLoS Genet. 2014. PMID: 24875531 Free PMC article.
Solving a cold case of haemolysis: back to the basics.
Bijleveld R, de Kok J, van der Zwaag B, van Wijk R, Diekman T. Bijleveld R, et al. Among authors: van wijk r, van der zwaag b. Neth J Med. 2015 Feb;73(2):86-9. Neth J Med. 2015. PMID: 25753074 Free article.
Novel Homozygous Mutation of the Internal Translation Initiation Start Site of VHL is Exclusively Associated with Erythrocytosis: Indications for Distinct Functional Roles of von Hippel-Lindau Tumor Suppressor Isoforms.
Bartels M, van der Zalm MM, van Oirschot BA, Lee FS, Giles RH, Kruip MJ, Gitz-Francois JJ, Van Solinge WW, Bierings M, van Wijk R. Bartels M, et al. Among authors: van der zalm mm, van oirschot ba, van wijk r, van solinge ww. Hum Mutat. 2015 Nov;36(11):1039-42. doi: 10.1002/humu.22846. Epub 2015 Aug 17. Hum Mutat. 2015. PMID: 26224408
Severe Ankyrin-R deficiency results in impaired surface retention and lysosomal degradation of RhAG in human erythroblasts.
Satchwell TJ, Bell AJ, Hawley BR, Pellegrin S, Mordue KE, van Deursen CT, Braak NH, Huls G, Leers MP, Overwater E, Tamminga RY, van der Zwaag B, Fermo E, Bianchi P, van Wijk R, Toye AM. Satchwell TJ, et al. Among authors: van wijk r, van der zwaag b, van deursen ct. Haematologica. 2016 Sep;101(9):1018-27. doi: 10.3324/haematol.2016.146209. Epub 2016 May 31. Haematologica. 2016. PMID: 27247322 Free PMC article.
Red Cell Properties after Different Modes of Blood Transportation.
Makhro A, Huisjes R, Verhagen LP, Mañú-Pereira Mdel M, Llaudet-Planas E, Petkova-Kirova P, Wang J, Eichler H, Bogdanova A, van Wijk R, Vives-Corrons JL, Kaestner L. Makhro A, et al. Among authors: van wijk r. Front Physiol. 2016 Jul 15;7:288. doi: 10.3389/fphys.2016.00288. eCollection 2016. Front Physiol. 2016. PMID: 27471472 Free PMC article.
Profound spherocytosis in adulthood: Acquired, hereditary or both?
Langeveld TJC, van Rossum AP, van der Zwaag B, van Wijk R, Vlasveld LT. Langeveld TJC, et al. Among authors: van wijk r, van der zwaag b, van rossum ap. Int J Lab Hematol. 2017 Oct;39(5):e117-e120. doi: 10.1111/ijlh.12685. Epub 2017 May 10. Int J Lab Hematol. 2017. PMID: 28488802 No abstract available.
Is Increased Intracellular Calcium in Red Blood Cells a Common Component in the Molecular Mechanism Causing Anemia?
Hertz L, Huisjes R, Llaudet-Planas E, Petkova-Kirova P, Makhro A, Danielczok JG, Egee S, Del Mar Mañú-Pereira M, van Wijk R, Vives Corrons JL, Bogdanova A, Kaestner L. Hertz L, et al. Among authors: van wijk r. Front Physiol. 2017 Sep 6;8:673. doi: 10.3389/fphys.2017.00673. eCollection 2017. Front Physiol. 2017. PMID: 28932200 Free PMC article.
617 results