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Vikita Mehta, Abirami Kirubarajan, Amir Sabouhanian, Sanasi M. Jayawardena, Priya Chandrakumaran, Nila Thangavelu, Refai Cader, Sachith Mettananda, Dayananda Bandara, Shawn Khan, David J. Weatherall, Angela Allen, Anuja P. Premawardhena, Nancy F. Olivieri
Acta Haematol (2022) 145 (3): 334–343.
Published Online: 09 November 2021
... complication in patients with the inherited hemoglobin disorders. In thalassemia, the literature is limited, and factors associated with the development of leg ulcers in hemoglobin E (HbE) beta thalassemia, the most common form of severe beta-thalassemia worldwide, have not previously been reported. Methods...
Acta Haematol (1991) 85 (3): 156–159.
Published Online: 20 February 2009
.... Niscea Division of *Radiation Oncology, bHematology-Oncology, and c Pediatric Hematology-Oncology, The New York Hospital-Cornell Medical Center, and Cornell University Medical College, New York, N.Y., USA Key Words. Beta-thalassemia Extramedullary hematopoiesis Radiotherapy Spinal cord compression...
Acta Haematol (1993) 89 (2): 80–81.
Published Online: 18 February 2009
... to in the content or advertisements. Beta-thalassemia Genetic counseling Polymerase chain reaction Prenatal diagnosis Original Paper Acta Haematol 1993;89:80-81 Tsang-Ming Ko3 b Li-Hui Tsengb Fon-Jou Hsiehab Sou-Ming Chuangh Tzu-Yao Lee3 b Departments of Obstetrics and Gynecology, and Medical Genetics...
Acta Haematol (2001) 104 (4): 181–184.
Published Online: 22 March 2001
...S. Güleşken; H. Ören; C. Vergin; N. Şanlı; H. Gülen; C. Uçar; G. İrken The aim of the present study was to evaluate the point mutations of beta-thalassemia patients from the Aegean region of Turkey by using an allele-specific oligonucleotide hybridization technique. DNA isolated from peripheral...