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         Sickle Cell Anemia:     more books (19)
  1. In the Blood: Sickle Cell Anemia and the Politics of Race (Critical Histories) by Melbourne Tapper, 1998-01
  2. Sickle Cell Anemia (Diseases and People) by Alvin Silverstein, Virginia B. Silverstein, et all 1997-01
  3. Hope and Destiny: A Patient's and Parent's Guide to Sickle Cell Anemia by Allan Platt, Alan Sacerdote, 2006-04-01
  4. The Sickle Cell Anemia Update (Disease Update) by Alvin Silverstein, Virginia B. Silverstein, et all 2006-08
  5. Menace In My Blood: My Affliction With Sickle-Cell Anemia by Ola Tamedu, 2006-01-24
  6. Let's Talk About Sickle Cell Anemia (Let's Talk Library) by Melanie Apel Gordon, 1999-12
  7. Sickle Cell Anemia (What Does It Mean to Have?)
  8. Sickle Cell Anemia by David Gerrick, 1978-06
  9. Sickle Cell Anemia - A Bibliography and Dictionary for Physicians, Patients, and Genome Researchers by Philip M. Parker, 2007-07-18
  10. Back to Our Roots: Cooking for the Control of Sickle Cell Anemia And Disease Prevention by Dawud Ujamaa, 2005-11-03
  11. The Official Patient's Sourcebook on Sickle Cell Anemia: Directory for the Internet Age by Icon Health Publications, 2005-01-31
  12. Crystals in My Bones: One Sickle Cell Anemia Journey by Bern Brewer, 2005-11-30
  13. Dying in the City of the Blues: Sickle Cell Anemia and the Politics of Race and Health.(Book Review): An article from: Journal of Southern History by Gregory Michael Dorr, 2002-11-01
  14. Sickle cell anemia: A selected annotated bibliography by Lenwood G Davis, 1978

101. InteliHealth:
anemia, Reviewed by the Faculty of Harvard Medical School sicklecell anemia Expected Duration. sickle-cell anemia is a lifelong problem. Prevention.
http://www.intelihealth.com/IH/ihtIH/WSIHW000/14294/29411/195959.html?d=dmtHealt

102. FamilyFun: Health Encyclopedia: Sickle-Cell Anemia
An excerpt on sicklecell anemia from the Disney Encyclopedia of Baby and Child Care. WHEN SHOULD I SUSPECT THAT MY CHILD HAS sickle-cell anemia?
http://familyfun.go.com/parenting/child/health/childhealth/dony79enc_ansickcel/
Search FamilyFun Tools
Parent Problem Solver

Field Guide to Parenting

Pregnancy Calendar
... Solutions A to Z Anemia: Sickle-Cell
This disease is an inherited blood disorder that occurs almost exclusively in blacks. It is caused by an abnormality in the pigment hemoglobin hemoglobin S WHEN SHOULD I SUSPECT THAT MY CHILD HAS SICKLE-CELL ANEMIA?
All black infants should be screened for sickle-cell anemia at birth. This is particularly important if there is any history of the disease in the family. A definitive diagnosis can be made with simple blood tests.
WHAT CAUSES SICKLE-CELL ANEMIA?
Sickle-cell disorders are passed genetically from parent to child. If both parents have a gene for hemoglobin S., their child has a 25 percent chance of inheriting both genes and getting sickle-cell anemia. If only one gene is inherited, half of the child's hemoglobin will be normal and will prevent the disease from developing. These children have sickle-cell trait and are usually healthy; however, they can pass on the abnormal gene to their children. One in 12 blacks are healthy carriers of the sickle-cell gene. HOW DOES SICKLE-CELL ANEMIA DEVELOP?

103. Sickle Cell Society
sickle cell Society UK based charity which provides care and information on sickle cell anaemia (anemia) and other sickle cell disorders to sufferers, health
http://www.sicklecellsociety.org/
Sickle Cell Society
54 Station Road
London, NW10 4UA
UK Tel 020 8961 7795
Fax 020 8961 8346
info@sicklecellsociety.org

Latest Sickle News Exciting Job Opportunities
Jeff Johnson Memorial London Bike Ride 2003

For the 17th year, the Sickle Cell Society's supporters took to the roads... Latest Events
The Latest Events organised by SCS. What is Sickle Cell Anaemia? How can I volunteer my help? Questions and Answers Planet Sickle
A special site for young people with Sickle Cell document.write(text); //> For more information contact the Sickle Cell Society on 020 8961 7795. Information, Counselling and caring for those with Sickle Cell Disorders and their families marks our 25th anniversary.

104. Sickle Cell Information Center Home Page
The Mission of the sickle cell Information Center www.SCInfo.org. SponsorshipThis sickle cell Information Web Site is Sponsored by the following partners
http://www.emory.edu/PEDS/SICKLE/
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105. Sickle Cell Disease
Overview. Brief History of sickle cell Disease Hemoglobin Basics Hemoglobin Synthesis How Does sickle Cause Disease? Why is sickle cell Disease so Variable?
http://sickle.bwh.harvard.edu/menu_sickle.html
Overview
Brief History of Sickle Cell Disease
Hemoglobin Basics

Hemoglobin Synthesis

How Does Sickle Cause Disease?
...
Sickle Cell Trait
Management Considerations
Development of a Comprehensive Care Program for Patients with Sickle Cell Disease
Management Overview

Outpatient Management Issues

Newborn Screening
...
Bone Marrow Transplantation

Children's Hospital Oakland Cord Blood Program
Transition of Patients with Sickle Cell Disease from Pediatric to Adult Care
Research
Red Cell Hydration and Sickle Cell Disease

106. Information Center For Sickle Cell And Thalassemic Disorders
Enter. Kenneth R. Bridges, MD. Welcomesickle cell DiseaseThalassemia InformationInformation Center OverviewLinks. StudyWeb
http://sickle.bwh.harvard.edu/

Kenneth R. Bridges, M.D.
[Welcome] [Sickle Cell Disease] [Thalassemia Information]
Kenneth R. Bridges, M.D.
[Welcome] [Sickle Cell Disease] [Thalassemia Information] ... [Links]

107. FAQs Frequently Asked Questions
Ask a question contact the sickle cell Center staff at aplatt@emory.edu. Copyright © 1997 sickle cell Information Center Last modified June 11, 2002.
http://www.scinfo.org/faq.htm
Frequently Asked Questions (FAQs) - Questions submitted to the Web site by patients, clinicians, and others Click on a Topic Category: Sickle Cell Disease Bone Marrow and Stem Cell Transplant Sickle Cell Trait and G6PD Students and Teachers ... Sickle Cell Newborn Screening Ask a question - contact the Sickle Cell Center staff at aplatt@emory.edu Send mail to aplatt@emory.edu with questions or comments about this web site.
Sickle Cell Information Center
Last modified: June 11, 2002

108. Red Blood Cell Physiology
Peripheral blood 1 day. Red Blood cell survival Normal RBC 120 days; Abnormal RBC Resources MMWR Iron Deficiency anemia Prevention http//www.cdc.gov/mmwr/pdf/rr
http://www.fpnotebook.com/HEM39.htm
Home About Links Index ... Editor's Choice document.write(code); Advertisement Hematology and Oncology Examination Anemia Red Blood Cell Physiology Cardiovascular Medicine Deep Vein Thrombosis Probability Red Blood Cell Physiology Hemoglobin Production Iron Reticulocyte 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 Examination Index Anemia CV DVT Probability
  • Physiology: Erythropoietin Primary hormone regulator of RBC production Erythropoietin sources Fetus: Monocyte and Macrophage system in liver Postnatal: Peritubular cells in kidney Physiology: Iron Total Body Iron Men: 50 mg/kg (or 3.8 grams for 75 kg man)
  • 109. Hematopathology
    Here is another example of sickled erythrocytes in a patient with Hgb SS who presented with severe abdominal pain in sickle crisis. The sickled cells are prone
    http://medlib.med.utah.edu/WebPath/HEMEHTML/HEME062.html
    Here is another example of sickled erythrocytes in a patient with Hgb SS who presented with severe abdominal pain in sickle crisis. The sickled cells are prone to stick together, plugging smaller vessels and leading to decreased blood flow with ischemia.

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