PLATELET AGGREGATION IN BETA-THALASSEMIA PATIENTS

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Hammad Tufail Chaudhary
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PLATELET AGGREGATION IN BETA-THALASSEMIA PATIENTS

Cure of beta-thalassemia is quite expensive and available to minority of patients. In this regard, data about decreased platelet aggregation in majority of subjects is helpful for development in the field of prevention of complications of beta thalassemia, especially when beta-thalassemia is not uncommon in Pakistan.

The article was published by
El artículo fue publicado por

Saudi Journal for Health Sciences
Volume / Volumen: 1
Number / Número: 2
First and last pages / Páginas inicial-final: 92-98
Year / Año: 2012
Month / Mes: may

This journal, which is covered by SIIC Data Bases,
is part of the bibliographic collections of the Biblioteca Biomédica (BB) SIIC.
Esta revista, clasificada por SIIC Data Bases,
integra el acervo bibliográfico de la Biblioteca Biomédica (BB) SIIC.

Principal institution where the research took place
Institución principal de la investigación
Department of Haematology and Transfusion Medicine, Children's Hospital and The Institute of Child Health, Lahore, Pakistan, Lahore, Punjab, Pakistan

Authors' Report
Crónica del Autor
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Bibliographic references
Referencias bibliográficas

Anjum S, Tayyab M, Shah SH, Chaudry N. Detection of beta-thalassaemia trait: A study of fifty families. J Ayub Med Coll Abbottabad 13:11-13, 2001.
Eldor A, Lellouche F, Goldfarb A, Rachmilewitz EA, Maclouf J. In vivo platelet activation in beta-thalassemia major reflected by increased platelet-thromboxane urinary metabolites. Blood 77:1749-1753, 1991.
Eldor A, Maclouf J, Lellouche F, Ben-Yashar V, Barenholz Y, Durst R, et al. A chronic hypercoagulable state and life-long platelet activation in beta thalassemia major. Southeast Asian J Trop Med Public Health 24:92-95, 1993.
Eldor A, Maclouf J, Lellouche F, Ben-Yashar V, Barenholz Y, Durst R, et al. A chronic hypercoagulable state and life-long platelet activation in beta thalassemia major. Southeast Asian J Trop Med Public Health 24:92-95, 1993.
Eldor A, Rachmilewitz EA. The hypercoagulable state in thalassemia. Blood 99:36-43, 2002.
Eldor A. Hemorrhagic tendency in beta-thalassemia major. Isr J Med Sci 14:1132-1134, 1978.
Ghani R, Manji MA, Ahmed N. Hemoglobinopathies among five major ethnic groups in Karachi, Pakistan. Southeast Asian J Trop Med Public Health 33:855-861, 2002.
Hussain MA, Hutton RA, Pavlidou O, Hoffbrand AV. Platelet function in beta-thalassemia major. J Clin Pathol 32:429-433, 1979.
Ruf A, Pick M, Deutsch V, Patscheke H, Goldfarb A, Rachmilewitz EA, et al. In-vivo platelet activation correlates with red cell anionic phospholipid exposure in patients with beta-thalassemia major. Br J Haematol 98:51-56, 1997.
Unchern S, Laoharuangpanya N, Phumala N, Sipankapracha P, Pootrakul P, Fucharoen S, et al. The effects of vitamin E on platelet activity in beta-thalassaemia patients. Br J Haematol 123:738-744, 2003.

Other articles written by the author Hammad Tufail Chaudhary
Otros artículos de Hammad Tufail Chaudhary

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The authors' report was accepted on La crónica del autor fue aprobada el 2021, march 9	Published in siicsalud Publicado en siicsalud 2021, june 7

The article is strictly related to the following sections of siicsalud
El artículo se relaciona estrictamente con las siguientes secciones de siicsalud

Haematology
/ Hematología

and secondarily related to the following sections
y secundariamente con las siguientes secciones

Hematological Biochemistry
Bioquímica Hematológica

Biochemistry
Bioquímica

Clinical Chemistry
Diagnóstico por Laboratorio

Paediatrics
Pediatría

Information about the full text
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Frequency of Platelet Aggregation Defecs in Children Suffering From B-Thalassemia

Author / Autor
Hammad Tufail Chaudhary¹

1 Dr, Medical College, Taif University, Taif, Saudi Arabia, Taif, Arabia Saudí, Assistant Professor

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Saudi Journal for Health Sciences

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