TITLE

Thalassaemia in the British

AUTHOR(S)
Vella, F
PUB. DATE
September 1973
SOURCE
British Medical Journal;9/15/1973, Vol. 3 Issue 5880, p594
SOURCE TYPE
Academic Journal
DOC. TYPE
Article
ABSTRACT
No abstract available.
ACCESSION #
64108267

 

Related Articles

  • Antenatal screening for sickle cell in primary care.  // Primary Health Care;Nov2010, Vol. 20 Issue 9, p13 

    The article reports on a study which reveals that British targets of offering antenatal screening for thalassaemia and sickle cell disease are not being met, published in the "British Medical Journal."

  • SICKLE CELL and THALASSAEMIA screening. Dyson, Simon // Practice Nurse;5/27/2005, Vol. 29 Issue 10, p17 

    Presents information on inherited blood disorders sickle cell and thalassaemia. Forms of screening which is potentially relevant to practice nurses undertaken by the British National Health Service sickle cell/thalassaemia screening programme; Medical background on the diseases; Preventive...

  • Prevalence and molecular basis of α thalassaemia in British South Asians. Hassall, O. W.; Tillyer, M. L.; Old, J. M. // Journal of Medical Screening;Mar1998, Vol. 5 Issue 1, p31 

    Objectives To determine the prevalence and molecular basis of α thalassaemia in the British South Asian population, and the implications for genetic screening for haemoglobin disorders. Methods 397 South Asian subjects were screened for haemoglobinopathy with measurement of full blood count,...

  • Haemoglobinopathies. Hill, Barry // Independent Nurse;12/5/2011, p25 

    The article discusses haemoglobinopathies or the production of abnormal forms of haemoglobin as of December 2011. It explores inherited haemolytic anaemia, the most common causes of which are sickle cell anaemia, thalassaemia and hereditary spherocytosis. It notes that sickle cell disease and...

  • Thalassaemia: The Biography. MacIntyre, Ross // Journal of Heredity;Sep2011, Vol. 102 Issue 5, p640 

    The article reviews the book "Thalassaemia: The Biography," by David Weatherall.

  • A national screening policy for sickle cell disease and thalassaemia major for the United Kingdom. Streetly, Allison // BMJ: British Medical Journal (International Edition);05/20/2000, Vol. 320 Issue 7246, p1353 

    Editorial. Criticizes the screening programs for sickle cell disease and thalassaemia major among the inner city populations in Great Britain. Systematic reviews of the British National Health Service Health Technology Assessment Program on the screening tests; Problems with selective...

  • Poster presentations: 3. Molecular Genetics.  // Journal of Medical Genetics;Sep2002 Supplement, Vol. 39, pS83 

    Discusses the abstract of the research paper entitled 'Two novel mutations found in a study of beta thalassaemia in the Scottish population,' by Patricia Bignelli, A. Jani et al and presented during the British Human Genetics Conference at the University of York in England in September 2002.

  • Penang bands jam for thalassaemia benefit. SANGEETHA, A. // Malay Mail;7/12/2012, p8 

    The article features the Penang Thalassaemia Society in Malaysia which helps thalassaemia patient through discounts in medicine, emotional support and workshops.

  • MedEconomics: Websites on haemoglobinopathies. Barnard, Keith // GP: General Practitioner;1/20/2006, p68 

    The article provides information on several Web sites related to haemoglobinopathies. The Web page www.emedicine.com/med/topic2260.htm provides information on beta-thalassaemia. These pages give the user an expansive account of the disease, and explains that, in some parts of the world, it might...

  • Co-inheritance of α-thalassaemia and β-thalassaemia in a prenatal screening population in mainland China. Li, Jian; Xie, Xing-Mei; Liao, Can; Li, Dong-Zhi // Journal of Medical Screening;Dec2014, Vol. 21 Issue 4, p167 

    The article presents a study to determine the prevalence of α-thalassaemia in β-thalassaemia individuals in a Chinese population. Topics discussed under study include hospital-based programme for prenatal screening of thalassaemias, use of standard diagnostic marker for β-thalassaemia...

Share

Read the Article

Courtesy of THE LIBRARY OF VIRGINIA

Sorry, but this item is not currently available from your library.

Try another library?
Sign out of this library

Other Topics