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Pyruvate kinase deficiency and severe congenital hemolytic anemia in a double heterozygous patient with paternal transmission of an early germ-line de novo mutation.
Mañú-Pereira Mdel M, Gonzalez-Roca E, van Solinge WW, Llaudet-Planas E, Sevilla J, Montllor L, Mensa-Vilaro A, Ploos van Amstel HK, van Wijk R, Vives-Corrons J. Mañú-Pereira Mdel M, et al. Among authors: van wijk r, van solinge ww. Am J Hematol. 2015 Dec;90(12):E217-9. doi: 10.1002/ajh.24178. Epub 2015 Nov 17. Am J Hematol. 2015. PMID: 26315463 Free article. No abstract available.
Hematological Parameters Improve Prediction of Mortality and Secondary Adverse Events in Coronary Angiography Patients: A Longitudinal Cohort Study.
Gijsberts CM, den Ruijter HM, de Kleijn DPV, Huisman A, Ten Berg MJ, van Wijk RHA, Asselbergs FW, Voskuil M, Pasterkamp G, van Solinge WW, Hoefer IE. Gijsberts CM, et al. Medicine (Baltimore). 2015 Nov;94(45):e1992. doi: 10.1097/MD.0000000000001992. Medicine (Baltimore). 2015. PMID: 26559287 Free PMC article.
Molecular basis of pyruvate kinase deficiency among Tunisians: description of new mutations affecting coding and noncoding regions in the PKLR gene.
Jaouani M, Manco L, Kalai M, Chaouch L, Douzi K, Silva A, Macedo S, Darragi I, Boudriga I, Chaouachi D, Fitouri Z, Van Wijk R, Ribeiro ML, Abbes S. Jaouani M, et al. Among authors: van wijk r. Int J Lab Hematol. 2017 Apr;39(2):223-231. doi: 10.1111/ijlh.12610. Epub 2017 Jan 30. Int J Lab Hematol. 2017. PMID: 28133914
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.
617 results