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Author/Creator van Zwieten, Rob

1. A Homozygous Mutation on the HBA1 Gene Coding for Hb Charlieu (HBA1: c.320T>C) Together with β-Thalassemia Trait Results in Severe Hemolytic Anemia. (4th March 2019)

Authors:
Klei, Thomas R. L.; Kheradmand Kia, Sima; Veldthuis, Martijn; Dehbozorgian, Javad; Karimi, Mehran; Geissler, Judy; Sellink, Erica; Thiel-Valkhof, Marijke; Burger, Patrick; van Alphen, Floris; Meijer, Alexander B.; van Bruggen, Robin; van Zwieten, Rob
Journal:
Hemoglobin
Issue:
Volume 43:Number 2(2019)
Page Start:
77
Record Type:
Journal Article
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2. Analysis of a cohort of 101 CDAII patients: description of 24 new molecular variants and genotype‐phenotype correlations. (29th July 2016)

Authors:
Bianchi, Paola; Schwarz, Klaus; Högel, Josef; Fermo, Elisa; Vercellati, Cristina; Grosse, Regine; van Wijk, Richard; van Zwieten, Rob; Barcellini, Wilma; Zanella, Alberto; Heimpel, Hermann
Journal:
British journal of haematology
Issue:
Volume 175:Number 4(2016)
Page Start:
696
Record Type:
Journal Article
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3. Comparison of Spectrophotometry, Chromate Inhibition, and Cytofluorometry Versus Gene Sequencing for Detection of Heterozygously Glucose-6-Phosphate Dehydrogenase-Deficient Females. (November 2017)

Authors:
Peters, Anna L.; Veldthuis, Martijn; van Leeuwen, Karin; Bossuyt, Patrick M.M.; Vlaar, Alexander P.J.; van Bruggen, Robin; de Korte, Dirk; Van Noorden, Cornelis J.F.; van Zwieten, Rob
Journal:
Journal of histochemistry and cytochemistry
Issue:
Volume 65:Number 11(2017:Nov.)
Page Start:
627
Record Type:
Journal Article
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4. Glucose‐6‐phosphate dehydrogenase deficiency‐associated hemolysis and methemoglobinemia in a COVID‐19 patient treated with chloroquine. Issue 8 (18th June 2020)

Authors:
Kuipers, Maria T.; van Zwieten, Rob; Heijmans, Jarom; Rutten, Caroline E.; de Heer, Koen; Kater, Arnon P.; Nur, Erfan
Journal:
American journal of hematology
Issue:
Volume 95:Issue 8(2020:Aug.)
Page Start:
E194
Record Type:
Journal Article
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6. Partial pyruvate kinase deficiency aggravates the phenotypic expression of band 3 deficiency in a family with hereditary spherocytosis. Issue 3 (24th November 2014)

Authors:
van Zwieten, Rob; van Oirschot, Brigitte A.; Veldthuis, Martijn; Dobbe, Johannes G.; Streekstra, Geert J.; van Solinge, Wouter W.; Schutgens, Roger E.G.; van Wijk, Richard
Journal:
American journal of hematology
Issue:
Volume 90:Issue 3(2015:Mar.)
Page Start:
E35
Record Type:
Journal Article
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7. Rapid diagnosis of hereditary haemolytic anaemias using automated rheoscopy and supervised machine learning. (5th July 2020)

Authors:
Moura, Pedro L.; Dobbe, Johannes G. G.; Streekstra, Geert J.; Rab, Minke A. E.; Veldthuis, Martijn; Fermo, Elisa; van Wijk, Richard; van Zwieten, Rob; Bianchi, Paola; Toye, Ashley M.; Satchwell, Timothy J.
Journal:
British journal of haematology
Issue:
Volume 190:Number 4(2020)
Page Start:
e250
Record Type:
Journal Article
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8. Residual pyruvate kinase activity in PKLR‐deficient erythroid precursors of a patient suffering from severe haemolytic anaemia. (12th April 2017)

Authors:
Klei, Thomas R.L.; Kheradmand Kia, Sima; Veldthuis, Martijn; Beuger, Boukje M.; Geissler, Judy; Dehbozorgian, Javad; Karimi, Mehran; van Bruggen, Robin; van Zwieten, Rob
Journal:
European journal of haematology
Issue:
Volume 98:Number 6(2017:Jun.)
Page Start:
584
Record Type:
Journal Article
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