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         Anemia:     more books (100)
  1. Super Cell Anemia by duncan b. barlow, 2008-01-09
  2. Nutritional Anemias (Modern Nutrition (Boca Raton, Fla.).)
  3. Let's Talk About Sickle Cell Anemia (Let's Talk Library) by Melanie Apel Gordon, 1999-12
  4. What You can do About Anemia (The Dell Medical Library) by Marilyn Larkin, 1993-03-01
  5. Anemia: A Guide to Causes, Treatment and Prevention (Women's Health) by Jill Davies, 1994-05
  6. Anemia by B. A. Floyd, 2002-12-10
  7. Cooley's Anemia: Eighth Symposium (Annals of the New York Academy of Sciences) by Fla.) Cooley's Anemia Symposium (2005 Lake Buena Vista, Elliott P. Vichinsky, 2006-01
  8. Iron Deficiency Anemia: Recommended Guidelines for the Prevention, Detection, and Management Among U.S. Children and Women of Childbearing Age by Detection, and Management of Iron Deficiency Anemia Among U.S. Children and Women of Childbearing Age Committee on the Prevention, Institute of Medicine, 1994-01-01
  9. Everything You Need to Know About Anemia (Need to Know Library) by Allison J. Ross, 2000-08
  10. Renal Anemia: Conflicts and Controversies
  11. Aplastc Anemia and Other Autoimmune Diseases (Help Your Body Heal Itself)
  12. Aplastic Anemia: Acquired and Inherited by Neal S. Young, Blanche P. Alter, 1994-01-15
  13. Aplastic Anemia and Other Bone Marrow Failure Syndromes
  14. Anemia in the Elderly

21. Aplastic Anemia & MDS International Foundation, Inc. - Serving Patients With Apl
Aplastic anemia MDS (Myelodysplastic Syndromes) International Foundation,Inc. It wasn t until 1904 that this disorder was termed aplastic anemia.
http://www.aplastic.org/diseases.shtml
The is the only organization in the world maintaining a voluntary Patient Registry to keep track of aplastic anemia, MDS and PNH patients for statistical analysis. Because these are not reportable diseases, statistics are not available to assist research and medical studies. Patients or family members may complete the Patient Registry Questionnaire online or download a print version and postal mail the form to us. Learn more about aplastic anemia, MDS and PNH. Read recent news items. Find out about clinical studies for aplastic anemia, MDS or PNH patients. In the United States, thousands of men, women and children are stricken with these non-contagious bone marrow diseases every year. They occur when the bone marrow stops making enough healthy blood cells. Although all of the causes are still unknown, they have been linked to toxins and viruses that we are in contact with every day. APLASTIC ANEMIA MDS PNH Aplastic anemia can be traced as far back as 1888 when a famous German pathologist, Dr. Paul Ehrlich, studied the case of a pregnant woman who died of bone marrow failure. It wasn't until 1904 that this disorder was termed aplastic anemia. Aplastic anemia occurs when the bone marrow stops making enough blood cells. The bone marrow is almost empty of blood forming cells and is described as

22. Cooley's Anemia Foundation
Profile Senator Arlen Specter. Welcome to the home of the Cooley s anemia Foundation. TheEighth Cooley s anemia Symposium will take place in March, 2005.
http://www.thalassemia.org/
CAF Home About Thalassemia Medical Information Local Chapters ...
Profile: Senator Arlen Specter
Welcome to the home of the Cooley's Anemia Foundation. This information is for patients and their families, medical personnel, donors, Foundation volunteers, and anyone interested in learning about Cooley's Anemia and other forms of the genetic blood disorder, thalassemia.
What is Thalassemia?
To Live News Sunday, June 6th 2004 Singer, Designer Support CAF Craig Butler 05.18.04 Anna Vissi, who occupies a unique place in Greek music, and award-winning jewelry designer Doris Panos are lending their talents to support CAF. FULL STORY
CAF Patients Address Congress Craig Butler 05.08.04 Two individuals with thalassemia urged an important Congressional committee to continue funding of programs that impact the thalassemia community. FULL STORY
NYAS and CAF Schedule Symposium Craig Butler 04.14.04 The Eighth Cooley's Anemia Symposium will take place in March, 2005. FULL STORY
Patient Profile: Jesal Kapasi Craig Butler 04.07.04 "I never learned to see thalassemia as a limiting factor."

23. What Is Fanconi Anemia And How Is It Diagnosed?
Information about Fanconi anemia for patients, families, physicians, andresearch scientists. What Is Fanconi anemia And How Is It Diagnosed?
http://www.fanconi.org/WhatisFA.html
What Is Fanconi Anemia And How Is It Diagnosed? Fanconi anemia (FA), named for Swiss pediatrician, Guido Fanconi, is one of the inherited anemias that leads to bone marrow failure (aplastic anemia). It is a recessive disorder: if both parents carry a defect (mutation) in the same FA gene, each of their children has a 25% chance of inheriting the defective gene from both parents. When this happens, the child will have FA.
There are at least seven FA genes: A, C, D2, E, F, G and BRCA2 (as announced in the article entitled Biallelic Inactivation of BRCA2 in Fanconi Anemia in the July 26, 2002 edition of Science ). Six of these genes have been cloned. These six account for more than 85% of the cases of Fanconi anemia. Mutations in FA-A and FA-C account for FA in 76% of patients worldwide. FA occurs equally in males and females. It is found in all ethnic groups. Though considered primarily a blood disease, it may affect all systems of the body. Many patients eventually develop acute myelogenous leukemia (AML). Older patients are extremely likely to develop head and neck, esophogeal, gastrointestinal, vulvar and anal cancers. Patients who have had a successful bone marrow transplant and, thus, are cured of the blood problem associated with FA still must have regular examinations to watch for signs of cancer. Many patients do not reach adulthood.

24. Aplastic Anemia & Myelodysplastic Syndromes International Foundation, Inc. - Ser
AAMDS's mission is to serve as a resource directory for patient assistance and emotional support; provide educational materials and updated medical information; and financially support research to find effective treatments for aplastic anemia and myelodysplastic syndromes.
http://www.aamds.org
In The News - Updates on diseases and treatments. Frequently Asked Questions Want to Talk? - Network with other patients and families.
Enroll in our Patient Registry to help researchers compile data on these diseases Merchandise
Purchases help Fight AA and MDS
Collaborative Clinical Trials Study Group

You are Visitor No:
P.O. Box 613 Annapolis, Maryland 21404-0613 USA
Tel: 800.747.2820 Fax 410.867.0240 E-Mail help@aamds.org
We subscribe to the
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of the Health On the Net Foundation This site was selected for inclusion in Current Web Contents , published by ISI (Institute for Scientific Information); and MedlinePlus Health Information , published by NLM (National Library of Medicine).
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25. Familydoctor.org/009.xml
familydoctor.org/639.xml More results from familydoctor.org Welcome to The American Sickle Cell anemia AssociationA United Way Agency.
http://familydoctor.org/009.xml

Advanced Search
familydoctor.org Home Women Anemia What is anemia? What can cause low iron levels? How is anemia diagnosed? Can anemia be prevented? ... Can iron pills cause problems?
Anemia: When Low Iron Is the Cause
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What is anemia?
Anemia occurs when your blood doesn't have enough hemoglobin. Hemoglobin is a protein in your red blood cells that carries oxygen from your lungs to the rest of your body. A common cause of anemia is not having enough iron. (Your body needs iron to make hemoglobin.) Return to top
Symptoms of anemia
  • Often, no symptoms
  • Paleness
  • Feeling tired
  • Unusual shortness of breath during exercise
  • Fast heartbeat
Return to top
What can cause low iron levels?
A number of things can cause you to be low in iron: Lack of iron in the diet . This is mostly a problem for children and young women. Children who drink a lot of milk and don't eat iron-rich foods and young women who follow "fad" diets may be at risk for iron deficiency. Growth spurts . Children under age 3 are growing so fast that their bodies may have a hard time keeping up with the amount of iron they need. Pregnancy Blood loss . This is a common reason for iron deficiency anemia in adults. Heavy periods may cause anemia. Blood loss can also be caused by internal bleeding, usually in the digestive tract. A stomach ulcer, ulcerative colitis, cancer, or taking aspirin or similar medicine for a long time can cause bleeding in your stomach or intestines. That's why it's important to find the reason for a low iron level.

26. Hemolytic Anemia
Looks at the course, management and complications of this disease.
http://www.fpnotebook.com/HEM49.htm
Home About Links Index ... Editor's Choice document.write(code); Advertisement Hematology and Oncology Hemolysis Anemia Hemolytic Anemia Hemolytic Anemia Causes G6PD Deficiency Assorted Pages Paroxysmal Cold Hemoglobinuria Blackwater fever March Hemoglobinuria Paroxysmal Nocturnal Hemoglobinuria ... Ham Test Hemolytic Anemia Microangiopathic Anemia Hemolysis Book Home Page Cardiovascular Medicine Dentistry Dermatology Emergency Medicine Endocrinology Gastroenterology General Medicine Geriatric Medicine Gynecology Hematology and Oncology HIV Infectious Disease Jokes Laboratory Neonatology Nephrology Neurology Obstetrics Ophthalmology Orthopedics Otolaryngology Pediatrics Pharmacology Prevention Psychiatry Pulmonology Radiology Rheumatology Sports Medicine Surgery Urology Chapter Hematology and Oncology Index Anemia Cancer Coagulopathy Cardiovascular Medicine Dermatology Endocrinology Otolaryngology Examination Gastroenterology Hemoglobin Hemolysis Histiocytosis HIV Infectious Disease Laboratory Leukemia General Pulmonology Lymph Marrow Neurology Obstetrics Orthopedics Pediatrics Pharmacology Platelet Prevention Procedure Psychiatry Rheumatology Sarcoma Surgery Symptom Evaluation Vascular Page Hemolysis Index Anemia Anemia Causes Anemia G6PD Hemoglobinuria Cold Hemoglobinuria Malaria Hemoglobinuria March Hemoglobinuria Nocturnal Methemoglobinemia
  • See Also Anemia Anemia with Reticulocytosis Causes See Hemolytic Anemia Causes Common Causes Lymphoproliferative Disorders Chronic Lymphocytic Leukemia Non-Hodgkin's Lymphoma Iatrogenic Hemolytic Anemia Medications (Most common cause)
  • 27. The American Sickle Cell Anemia Association - FAQ'S
    Search The Site. What is Sickle Cell anemia. What causes Sickle Cell anemia.How common is Sickle Cell anemia. What are signs of Sickle Cell anemia.
    http://www.ascaa.org/faq.asp
    A United Way Agency Categories Who We Are
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    28. A.R.E. Clinic -- Cayce Links Ear Infection With Anemia
    Is there a connection between anemia and chronic ear infection?
    http://areclinic.org/articles.asp?ArticleID=6&src=m

    29. National Anemia Action Council NAAC - Anemia Symptoms Diagnosis
    Provides complete guide to anemia for professionals. Also offers researchinformation anemia, Ask a NAAC Expert Question What other tests
    http://www.anemia.org/index.jsp

    30. The Body: Fatigue
    Information resources on HIV/AIDS related fatigue from TheBody.com.
    http://www.thebody.com/treat/fatigue.html
    Fatigue
    Got questions about fatigue and anemia? Ask The Body's expert Dr. Robert J. Frascino
    The Basics
    Research and News See also: Anemia Depression
    Sponsored in part by:
    The Basics

    31. Anemia
    Provides anemia research and studies on diseases associated with anemia such asCRI chronic renal insufficiency, ESRD end stage renal disease, CKD chronic
    http://www.anemia.org/about_anemia/anemia_overview.jsp

    32. GRUPO ANEMIA DE MELILLA
    Comunidad de librepensadores, charla de car¡cter descontra­do.
    http://communities.msn.com.mx/GRUPOANEMIADEMELILLA/home.htm
    var nEditorialCatId = 167; Principal Hotmail Grupos y Gente Grupos ... Ayuda GRUPO ANEMIA DE MELILLA GRUPOANEMIADEMELILLA@groups.msn.com Novedades Únete ahora Panel de mensajes Imágenes ... Recomienda este grupo a un amigo Nuevos mensajes Ver todos pongamos q hablo de madrizzzzz
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    33. Information On Anemia Produced By Medical Doctors
    What is anemia? anemia is having less than the normal number of red blood cellsor less hemoglobin than normal in the blood. How is anemia detected?
    http://www.medicinenet.com/Anemia/article.htm
    document.write(''); MedicineNet Home Cancer Home > Anemia Advanced Search
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    Anemia
    What is anemia? Anemia is having less than the normal number of red blood cells or less hemoglobin than normal in the blood. How is anemia detected? Anemia is usually detected or at least confirmed by a complete blood cell (CBC) count. What is a complete blood cell (CBC) count? In a CBC test, the different types of cells in the blood are counted and examined. Today, much of this work is often automated and done by machine. Six tests make up a CBC:
    • Red blood cell (RBC) count Hematocrit Hemoglobin White blood cell (WBC) count Differential blood count (the "diff") Platelet count
    Only the first three of these tests: the red blood cell (RBC) count, the hematocrit, and the hemoglobin, are relevant to the diagnosis of anemia. What is the red blood cell (RBC) count?

    34. Anemia :: Health-Science.Com ::
    anemia. One of the most common disorders caused by nutritional deficiencyis anemia due to an insufficiency of B12. This including. anemia.
    http://www.health-science.com/anemia_frame.html
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    Anemia
    One of the most common disorders caused by nutritional deficiency is anemia due to an insufficiency of B-12. This nutrient has the largest molecular structure of any single vitamin and consequently presents a serious absorption problem.
    The typical approaches to treating anemia are to administer large dosages of ferrous sulfate (iron sulfate) which may cause gastrointestinal bleeding, or a 1 c.c. (1000 mcg.) intramuscular injection of vitamin B-12, which is difficult to maintain over a long period of time.
    Absorption of B-12 in the diet is reduced by an erosion of the mucous lining of the intestines and decreased hydrochloric acid production in the stomach. Stress has also been implicated in reducing the amount of blood flow to the stomach wall (eschemia), and thus inhibiting the absorption of B-12.
    Further, many people are lacking a protein called "Intrinsic Factor" that may also be necessary for absorption. Vegetarians are often at risk of deficiency because B-12 is only found in animal products.
    Recently, a number of researchers have found that the Schilling Test, the standard for measuring B-12 in the blood, does not accurately account for utilization of B-12.

    35. Pernicious Anemia - Cancer: Health And Medical Information About Cancer Detectio
    Pernicious anemia. Pernicious anemia is a blood disorder caused by a lackof vitamin B12. Nowadays, pernicious anemia is not so pernicious.
    http://www.medicinenet.com/Pernicious_Anemia/article.htm
    document.write(''); MedicineNet Home Cancer Home > Pernicious Anemia Advanced Search
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    Pernicious Anemia
    Pernicious anemia is a blood disorder caused by a lack of vitamin B12. Patients who have this disorder do not produce a protein (intrinsic factor) in the stomach that allows the body to absorb vitamin B12. Pernicious anemia is characterized by the presence in the blood of large, immature, nucleated cells (megaloblasts) that are forerunners of red blood cells. (Red blood cells, when mature, have no nucleus). Pernicious anemia is therefore one of the types of megaloblastic anemia. Doctors diagnose pernicious anemia when a patient with a low red blood cell count has large red blood cells and white blood cells with large, multi-lobed nuclei. The patient often has antibodies in the blood called intrinsic factor and parietal cell antibodies. A test that measures that lack of absorption of B12 (Schillings test) can be used to support the diagnosis. Nowadays, pernicious anemia is not so pernicious. Pernicious anemia is simply treated with vitamin B12. The vitamin B12 has to be administered by injection because people with pernicious anemia do not have adequate protein intrinsic factor (or an effective form of intrinsic factor) and so cannot absorb vitamin B12 taken by mouth.

    36. Katelyn Rose Hubbell Beats Aplastic Anemia
    Personal page of this young resident that won her battle against Severe Aplastic anemia.
    http://www.katyhubbell.com/
    Click a flag above to translate this page into the language of your choice! To Katelyn Rose Hubbell's
    Aplastic Anemia Website!
    Katelyn in May, 2004...looking all grown up! Happy 5th "re-birthday" Katy!!!
    Taking a cell call from her agent! :o) If you're looking for NEW pictures (added 12/08/03).. CLICK HERE! Katy's Story Katelyn Rose Hubbell turned four years old on June 26th 1997, and had a big party at her home in Fisher, Illinois. She was a happy, healthy little girl, until July 11, 1997 when she was diagnosed with a life threatening bone marrow failure disease called Severe Aplastic Anemia. In case you didn't know, bone marrow is the soft spongy material inside your bones that is home to stem cells. Stem Cells are the little factories that produce the three types of blood cells, that along with a liquid called plasma, makes up your blood. In people with Aplastic Anemia, the workers in the "factory" go on strike. They do not produce enough blood cells to keep the patient alive. There are three main types of blood cells.

    37. Welcome To Schein Pharmaceutical, Inc.
    The Company's brand products group has developed an expertise in the management of anemia in nephrology, and is looking to expand this expertise to iron management. In addition, the Company develops, manufactures and markets a broad generic product line including both solid and sterile dosage products.
    http://www.schein-rx.com/

    38. Anemia
    Band from Rochester, NY whose site features pictures and MP3s.
    http://www.angelfire.com/band/anemia
    var cm_role = "live" var cm_host = "angelfire.lycos.com" var cm_taxid = "/memberembedded"
    Click to come in.

    well there is a flash thing there but... if u have an older browser it wont show up, u should upgrade it to the newest ver. (for free) and then it will work.

    39. ADAP Drugs: Erythropoeitin
    Used to treat anemia associated with HIV infection or AZT therapy.(EPO, Epogen, Eprex, Procrit, epoetin alfa)
    http://www.atdn.org/access/drugs/eryt.html
    erythropoeitin
    (EPO, Epogen, Eprex, Procrit, epoetin alfa) Drug description
    Erythropoetin is used to treat anemia associated with HIV infection or AZT therapy. Anemia is a condition due to a low number of red blood cells. Erythropoetin is a natural hormone secreted by the kidneys that acts on the bone marrow to stimulate production of red blood cells. Recombinant EPO is a synthetic version of this hormone. EPO is approved for treatment of anemia in both AZT-treated HIV+ people, and people with chronic kidney failure. Ortho Biotech, who makes Procrit, has a Patient Assistance Program wich can be reached at (800) 553-3851). Side effects
    EPO is generally well tolerated. Side effects can include chest pain, swelling due to retention of fluid, fast heart beat, headache, high blood pressure, increase in number and concentration of circulating red blood cells, seizures, shortness of breath, skin rash, pain in joints, diarrhea, nausea, fatigue, or flu-like syndrome after each dose. Dosage
    EPO must be injected. Initial dosage in studies was 100 units/kg IV 3 times weekly for 8-12 weeks. If the response to treatment is not satisfactory in terms of reducing transfusion requirement after 8 weeks, the dose may be increased by 50-100 units/kg. How long it may take to work
    In studies, many individuals who received transfusions did not require them after 2-3 months of treatment with EPO.

    40. Sickle Cell Anemia
    Sickle cell anemia occurs when a person inherits two abnormal genes that causetheir red blood cells to change shape. What Is Sickle Cell anemia?
    http://kidshealth.org/teen/diseases_conditions/blood/sickle_cell_anemia.html

    KidsHealth
    Teens Blood Disorders
    Sickle cell anemia is a hereditary disorder that mostly affects people of African ancestry, but also occurs in other ethnic groups, including people who are of Mediterranean and Middle Eastern descent. More than 70,000 Americans have sickle cell anemia. And about 2 million Americans - and one in 12 African Americans - have sickle cell trait (this means they carry one gene for the disease, but do not have the disease itself). Sickle cell anemia occurs when a person inherits two abnormal genes (one from each parent) that cause their red blood cells to change shape. Instead of being flexible and round, these cells are more rigid and curved in the shape of the farm tool known as a sickle - that's where the disease gets its name. The shape is similar to a crescent moon. What Is Sickle Cell Anemia?
    Sickle cell anemia is a blood disorder that affects hemoglobin (pronounced: hee -muh-glow-bin), a protein found in red blood cells that helps carry oxygen throughout the body. Red blood cells with normal hemoglobin ( HbA ) move easily through the bloodstream, delivering oxygen to all of the cells of the body. Normal red blood cells are shaped like doughnuts with the centers partially scooped out and are soft and flexible.

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