Patient-to-Patient Transmission of Hepatitis C at Iranian Thalassemia Centers Shown by Genetic Characterization of Viral Strains.
Samimi-Rad K, Asgari F, Nasiritoosi M, Esteghamati A, Azarkeyvan A, Eslami SM, Zamani F, Magnius L, Alavian SM, Norder H
Department of Virology, School of Public Health, Tehran University of Medical Sciences, Tehran, IR Iran.
Hepatitis C is prevalent among thalassemia patients in Iran. It is mainly transfusion mediated, in particular among patients treated before 1996 when ...
Haematologica 2013 Apr 12
Sildenafil therapy in thalassemia patients with doppler-defined risk for pulmonary hypertension.
Morris CR, Kim HY, Wood JC, Porter JB, Klings ES, Trachtenberg FL, Sweeters N, Olivieri NF, Kwiatkowski JL, Virzi L, Singer ST, Taher A, Neufeld EJ, Thompson AA, Sachdev V, Larkin S, Suh JH, Kuypers FA, Vichinsky EP
Emory-Childrens Center for Developmental Lung Biology, USA;
Pulmonary hypertension is a common but often overlooked complication associated with thalassemia syndromes. There is limited data on the safety and ef...
Eur. J. Haematol. 2013 Apr 13
Effect of splenectomy on iron balance in patients with ß- Thalassaemia Major: a long term follow up.
Casale M, Cinque P, Ricchi P, Costantini S, Spasiano A, Prossomariti L, Minelli S, Frega V, Filosa A
OBJECTIVE: A retrospective study was performed to explore the effect of splenectomy on iron balance in thalassaemia major (TM). METHODS: 22 TM patient...
Hemoglobin 2013 Apr 12
Evaluation and Comparison of Soluble Transferrin Receptor in Thalassemia Carriers and Iron Deficient Patients.
Khatami S, Dehnabeh SR, Mostafavi E, Kamalzadeh N, Yaghmaei P, Saeedi P, Shariat F, Bagheriyan H, Zeinali S, Akbari MT
Department of Biochemistry, Pasteur Institute of Iran , Tehran , Iran.
Iron is an essential component in the structure of certain molecules such as hemoglobin (Hb), myoglobin, cytochrome C and some enzymes. The iron gatew...
Indian J Med Paediatr Oncol
Stem cell transplant: An experience from eastern India.
Mukhopadhyay A, Gupta P, Basak J, Chakraborty A, Bhattacharyya D, Mukhopadhyay S, Roy UK
Department of Haemato-Oncology, Molecular Biology and Bone Marrow Transplant Unit, Netaji Subhas Chandra Bose Cancer Research Institute, Kolkata, West Bengal, India.
Hematopoietic stem cell transplant using human leukocyte antigen (HLA)-matched sibling or unrelated bone marrow, or related or unrelated cord blood ha...
Hemoglobin 2013 Apr 11
Application of Multiplex Ligation-Dependent Probe Amplification to Screen for ß-Globin Cluster Deletions: Detection of Two Novel Deletions in a Multi Ethnic Population.
Cui J, Azimi M, Baysdorfer C, Vichinsky EP, Hoppe CC
Hemoglobinopathy Reference Laboratory, Children's Hospital & Research Center Oakland , Oakland, California , USA.
Hereditary persistence of fetal hemoglobin (HPFH) and dß-thalassemia (dß-thal) are heterogeneous disorders caused by deletions within the ß-globin gen...
Hemoglobin A2 Lowered by Iron Deficiency and a -Thalassemia: Should Screening Recommendation for ß -Thalassemia Change?
Denic S, Agarwal MM, Al Dabbagh B, El Essa A, Takala M, Showqi S, Yassin J
Department of Medicine, College of Medicine and Health Sciences, United Arab Emirates University, P.O. Box 17666, Al Ain, Abu Dhabi, UAE.
Screening for ß -thalassemia trait (BTT) relies on measuring hemoglobin (Hb) A2. Since multiple factors can affect HbA2 levels, the screening can beco...
The impact of migrations on the health services for rare diseases in europe: the example of haemoglobin disorders.
Angastiniotis M, Vives Corrons JL, Soteriades ES, Eleftheriou A
Thalassaemia International Federation (TIF), 31 Ifigeneias Street, 2007 Strovolos, Nicosia, Cyprus ; European Network for Rare and Congenital Anaemias (ENERCA), 08036 Barcelona, Spain.
Migration from different parts of the world to several European countries leads to the introduction of haemoglobinopathy genes into the population, wh...
Eur. J. Hum. Genet. 2013 Apr 10
Next generation sequencing of SNPs for non-invasive prenatal diagnosis: challenges and feasibility as illustrated by an application to ß-thalassaemia.
Papasavva T, van Ijcken WF, Kockx CE, van den Hout MC, Kountouris P, Kythreotis L, Kalogirou E, Grosveld FG, Kleanthous M
Molecular Genetics Thalassemia Department, The Cyprus Institute of Neurology and Genetics, Nicosia, Cyprus.
ß-Thalassaemia is one of the most common autosomal recessive single-gene disorder worldwide, with a carrier frequency of 12% in Cyprus. Prenatal tests...
Patient Prefer Adherence
Changes in the quality of life of people with thalassemia major between 2001 and 2009.
Gollo G, Savioli G, Balocco M, Venturino C, Boeri E, Costantini M, Forni GL
Regional Palliative Care Network, IRCCS AOU San Martino-IST, Genoa.
The prolonged survival of patients with thalassemia major as a result of the novel therapeutic strategies introduced in the last decade makes patient ...