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Low and fixed dose of hydroxyurea is effective and safe in patients with HbSß(+) thalassemia with IVS1-5(G→C) mutation.
Dehury, Snehadhini; Purohit, Prasanta; Patel, Siris; Meher, Satyabrata; Kullu, Bipin Kishore; Sahoo, Lulup Kumar; Patel, Nayan Kumar; Mohapatra, Alok Kumar; Das, Kishalaya; Patel, Dilip Kumar.
Affiliation
  • Dehury S; Sickle Cell Clinic and Molecular Biology Laboratory, Veer Surendra Sai Medical College, Burla, Sambalpur, Odisha, India.
Pediatr Blood Cancer ; 62(6): 1017-23, 2015 Jun.
Article in En | MEDLINE | ID: mdl-25546091

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Thalassemia / Hemoglobin, Sickle / Hydroxyurea / Mutation Type of study: Observational_studies Limits: Adolescent / Adult / Child / Child, preschool / Female / Humans / Male Language: En Journal: Pediatr Blood Cancer Journal subject: HEMATOLOGIA / NEOPLASIAS / PEDIATRIA Year: 2015 Document type: Article Affiliation country: India Country of publication: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Thalassemia / Hemoglobin, Sickle / Hydroxyurea / Mutation Type of study: Observational_studies Limits: Adolescent / Adult / Child / Child, preschool / Female / Humans / Male Language: En Journal: Pediatr Blood Cancer Journal subject: HEMATOLOGIA / NEOPLASIAS / PEDIATRIA Year: 2015 Document type: Article Affiliation country: India Country of publication: United States