Treatment with hydroxyurea in a patient compound heterozygote for a high oxygen affinity hemoglobin and β‐thalassemia minor
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Veröffentlicht in: | American journal of hematology 2009-11, Vol.84 (11), p.766-768 |
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container_title | American journal of hematology |
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creator | Gaudreau, Pierre‐Olivier Weng, Xiaoduan Cournoyer, Ghislain Robin, Louise Gagnon, Carmen Soulières, Denis |
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doi_str_mv | 10.1002/ajh.21526 |
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Hemoglobinopathies</subject><subject>beta-Thalassemia - blood</subject><subject>beta-Thalassemia - genetics</subject><subject>Biological and medical sciences</subject><subject>Diseases of red blood cells</subject><subject>Follow-Up Studies</subject><subject>Hematologic and hematopoietic diseases</subject><subject>Hemoglobins, Abnormal - metabolism</subject><subject>Heterozygote</subject><subject>Humans</subject><subject>Hydroxyurea - therapeutic use</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Oxygen - metabolism</subject><issn>0361-8609</issn><issn>1096-8652</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp10DFOwzAUBmALgWgpDFwAeWFgaGs7sZOMVQUUVIkF5siJ7cRVEkd2qhIGxBE4CwfhEJwEl1YwMdmyv_896QfgHKMJRohM-aqcEEwJOwBDjBI2jhklh2CIAob9HSUDcOLcCiGMwxgdgwFOojiKkmgIXh-t5F0tmw5udFfCshfWPPdr_wp1Azlseae3v7mpW7NuBCxlJ6156QvTSaiM9abURQl9qpA-oZRudNd7V5uiMtl2io99fny9vXclr7hzstYc1rox9hQcKV45ebY_R-Dp5vpxvhgvH27v5rPlOA9oxMY4U5zGCWUKCUEyLChVcUbCBGMSsoDyKKQkVjyOGcskoSHFTGUhEzQQSmIRjMDVbm5ujXNWqrS1uua2TzFKtx2mvsP0p0NvL3a2XWe1FH9yX5oHl3vAXc4rZXmTa_frCEEhY2zrpju30ZXs_9-Yzu4Xu9XfJVCMTg</recordid><startdate>200911</startdate><enddate>200911</enddate><creator>Gaudreau, Pierre‐Olivier</creator><creator>Weng, Xiaoduan</creator><creator>Cournoyer, Ghislain</creator><creator>Robin, Louise</creator><creator>Gagnon, Carmen</creator><creator>Soulières, Denis</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><general>Wiley-Liss</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>200911</creationdate><title>Treatment with hydroxyurea in a patient compound heterozygote for a high oxygen affinity hemoglobin and β‐thalassemia minor</title><author>Gaudreau, Pierre‐Olivier ; Weng, Xiaoduan ; Cournoyer, Ghislain ; Robin, Louise ; Gagnon, Carmen ; Soulières, Denis</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3576-1bfa58956f0dd2b1d55f8b2491124635a74528fa8866be254516fb46d53dfe1d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Adult</topic><topic>Anemias. 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source | Wiley Online Library - AutoHoldings Journals; MEDLINE; Wiley Online Library Free Content; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals |
subjects | Adult Anemias. Hemoglobinopathies beta-Thalassemia - blood beta-Thalassemia - genetics Biological and medical sciences Diseases of red blood cells Follow-Up Studies Hematologic and hematopoietic diseases Hemoglobins, Abnormal - metabolism Heterozygote Humans Hydroxyurea - therapeutic use Male Medical sciences Oxygen - metabolism |
title | Treatment with hydroxyurea in a patient compound heterozygote for a high oxygen affinity hemoglobin and β‐thalassemia minor |
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