Anemia Research - Symptoms, Diagnosis, Diet, Treatment, Causes

Anemia Research Today is a free monthly online journal that collates and summarizes the latest research about Anemia, including details on symptoms, diagnosis, diet, treatment, causes.


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Volume 2 (2005), Issue 12 (December)

  1. Changes in the epidemiology of thalassemia in North America: a new minority disease.
    Pediatrics, 116(6): e818-25. [Abstract] [Full-text]
  2. Prenatal exclusion/confirmation of Fanconi anemia via flow cytometry: a pilot study.
    Fetal Diagn Ther, 21(1): 118-24. [Abstract] [Full-text]
  3. Manifestation of mirror syndrome after fetoscopic laser photocoagulation in severe twin-twin transfusion syndrome.
    Fetal Diagn Ther, 21(1): 51-4. [Abstract] [Full-text]
  4. Optimal interval between middle cerebral artery velocity measurements when monitoring pregnancies complicated by red cell alloimmunization.
    Fetal Diagn Ther, 21(1): 22-5. [Abstract] [Full-text]
  5. Massive feto-maternal hemorrhage: diagnosis by cardiotocography, Doppler ultrasonography and ST waveform analysis of fetal electrocardiography.
    Fetal Diagn Ther, 21(1): 8-12. [Abstract] [Full-text]
  6. Long term cardiac follow up of severe twin to twin transfusion syndrome after intrauterine laser coagulation.
    Heart, 92(1): 95-100. [Abstract] [Full-text]
  7. Red blood cells, platelets and polymorphonuclear neutrophils of patients with sickle cell disease exhibit oxidative stress that can be ameliorated by antioxidants.
    Br J Haematol, 132(1): 108-13. [Abstract] [Full-text]
  8. An exploratory study of physiological correlates of neurodevelopmental delay in infants with sickle cell anaemia.
    Br J Haematol, 132(1): 99-107. [Abstract] [Full-text]
  9. Seasonal variation of pretransfusion hemoglobin levels in patients with thalassemia major.
    Blood, 107(1): 355-7. [Abstract] [Full-text]
  10. Microcytic anemia and hepatic iron overload in a child with compound heterozygous mutations in DMT1 (SCL11A2).
    Blood, 107(1): 349-54. [Abstract] [Full-text]
  11. Congenital dyserythropoietic anemia type I (CDA I): molecular genetics, clinical appearance, and prognosis based on long-term observation.
    Blood, 107(1): 334-40. [Abstract] [Full-text]
  12. Discontinuing prophylactic transfusions used to prevent stroke in sickle cell disease.
    N Engl J Med, 353(26): 2769-78. [Abstract] [Full-text]
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Anemia Research Today Archive:

Volume 1 (2004)
  Issue 1 (September)
  Issue 2 (October)
  Issue 3 (November)
  Issue 4 (December)

Volume 2 (2005)
  Issue 1 (January)
  Issue 2 (February)
  Issue 3 (March)
  Issue 4 (April)
  Issue 5 (May)
  Issue 6 (June)
  Issue 7 (July)
  Issue 8 (August)
  Issue 9 (September)
  Issue 10 (October)
  Issue 11 (November)
  Issue 12 (December)

Volume 3 (2006)
  Issue 1 (January)
  Issue 2 (February)
  Issue 3 (March)
  Issue 4 (April)
  Issue 5 (May)
  Issue 6 (June)
  Issue 7 (July)
  Issue 8 (August)
  Issue 9 (September)
  Issue 10 (October)
  Issue 11 (November)
  Issue 12 (December)

Volume 4 (2007)
  Issue 1 (January)
  Issue 2 (February)
  Issue 3 (March)
  Issue 4 (April)
  Issue 5 (May)
  Issue 6 (June)
  Issue 7 (July)
  Issue 8 (August)
  Issue 9 (September)
  Issue 10 (October)
  Issue 11 (November)
  Issue 12 (December)

Volume 5 (2008)
  Issue 1 (January)
  Issue 2 (February)
  Issue 3 (March)
  Issue 4 (April)
  Issue 5 (May)
  Issue 6 (June)
  Issue 7 (July)



Anemia Books

Hope and Destiny: A Patient's and Parent's Guide to Sickle Cell Disease and Sickle Cell Trait

Hope and Destiny: A Patient's and Parent's Guide to Sickle Cell Disease and Sickle Cell Trait