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Author/Creator Dehbozorgian, Javad

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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4. Effectiveness of β‐thalassemia prenatal diagnosis in Southern Iran: a cohort study. (15th October 2015)

Authors:
Moghadam, Mohamad; Karimi, Mehran; Dehghani, Seyed Javad; Dehbozorgian, Javad; Montazeri, Somaye; Javanmardi, Elham; Asadzade, Rahimeh; Amiri, Azizollah; Saghatoleslam, Zahra; Sotodegan, Fatemosadat; Morshedi, Nazila; Imanifard, Jaber; Afrasiabi, Abdolreza
Journal:
Prenatal diagnosis
Issue:
Volume 35:Number 12(2015:Dec.)
Page Start:
1238
Record Type:
Journal Article
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6. 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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