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1. A Case Series of α-Thalassemia Intermedia Due to Compound Heterozygosity for Hb Adana [HBA2: c179G>A (or HBA1); p.Gly60Asp] With Other α-Thalassemias in Malay Families. (August 2014)

2. A Unique Interaction of IVS-I-1 (G>A) (HBA2: c.95+1G>A) with Hb Adana (HBA2: c.179G>A) Presenting as Transfusion-Dependent α-Thalassemia. (4th July 2018)

3. Application of Molecular Diagnostics in Detection of β-Thalassemia and Hemoglobin Variants at Hospital Canselor Tuanku Muhriz UKM, Kuala Lumpur, Malaysia. (2nd November 2019)

5. Increased basal oxidation of peroxiredoxin 2 and limited peroxiredoxin recycling in glucose‐6‐phosphate dehydrogenase‐deficient erythrocytes from newborn infants. Issue 7 (17th March 2014)

7. Updates on Laboratory Tests for Diagnosis of Glucose-6-Phosphate Dehydrogenase Deficiency in Malaysia. (2nd November 2019)