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         Hemophilia:     more books (100)
  1. Hemophilia act of 1973: Hearing, Ninety-third Congress, first session, on S. 1326 by United States. Congress. Senate. Committee on Labor and Public Welfare. Subcommittee on Health., 1974-01-01
  2. Hemophilia and Hemophilioid Diseases
  3. 21st Century Ultimate Medical Guide to Hemophilia - Authoritative Clinical Information for Physicians and Patients (Two CD-ROM Set) by PM Medical Health News, 2009-05-08
  4. Encyclopedia of Family Health; Vol 5: Flotation Therapy - Hemophilia by Jacoby David B, 1998
  5. Molecular diagnosis of hemophilia A and B. Report of five families from Costa Rica.: An article from: Revista de Biología Tropical by Lizbeth Salazar-Sánchez, Guillermo Jiménez-Cruz, et all 2004-09-01
  6. Gene therapy safe, feasible for patients with severe hemophilia A, Phase I study finds.(Brief Article): An article from: Transplant News
  7. Hemophilia - A Bibliography and Dictionary for Physicians, Patients, and Genome Researchers by Philip M. Parker, 2007-07-17
  8. New Aspects of Hemophilia Treatment: 3rd Symposium, September 21-23, 1995 Copenhagen, Denmark (Haemostasis, Vol 26, Suppl 1)
  9. Vox Sanguinis (Viral Safety of Plasma-Derived Replacement Factors for Hemophilia , Vol 67, Suppl 4) by P. M. Mannucci, 1994-12
  10. HEMOPHILIA: An entry from UXL's <i>UXL Complete Health Resource</i>
  11. Gale Encyclopedia of Nursing and Allied Health: Hemophilia by Jr., MD, DrPH L. Fleming Fallon, 2002-01-01
  12. Von Willebrand's Disease and Hemophilia Clinical and Genetic Aspects by Kathelijne Peerlinck, 1994
  13. Gene Therapy Promising for Hemophilia B.(Brief Article): An article from: Family Practice News by Bruce Jancin, 2000-09-15
  14. Hemophilia by Inga Marie Nilsson, 1994

81. Hemophilia
hemophilia. This clotting.). hemophilia was created using the basic design from my last stained glass case, but with a few improvements.
http://www.lucentrigs.com/Hemophilia.htm
HEMOPHILIA HEMOPHILIA was created using the basic design from my last stained glass case, but with a few improvements. By making the entire side of the case removable, the computer was easier to work on. I made the case more durable by reinforcing key points in the case, and using a sturdier mobo tray. In my previous stained glass case, I built the sides from the base upwards. In the new case, the sides were pieced together in flat sections, then the sections were soldered together. This case took 62 hours and 19 minutes to build during the span of three weeks. I received 9 nasty cuts, 5 burns and I consumed 464 oz. of Mountain Dew while creating this case. The Dew also works wonders on soldering-iron burns.
The Hardware inside:
with a Vision Tek GeForce 4 Ti4200
Thank you for checking this out Jer
Please Contact me with any questions or comments. Home

82. Hemophilia - Wikipedia, The Free Encyclopedia
hemophilia. Leopold; Maurice. See also. hemophilia A factor VIII deficiency, classic haemophilia ; hemophilia B - factor IX deficiency, Christmas disease;
http://en.wikipedia.org/wiki/Hemophilia
Hemophilia
From Wikipedia, the free encyclopedia.
Haemophilia or hemophilia is the name of any of several hereditary genetic illnesses that impair the body's ability to heal bleeding wounds. Genetic deficiencies cause lowered plasma clotting factor activity so as to compromise blood-clotting; when a blood vessel is injured, a scab will not form and the vessel can continue to bleed excessively for a very long period of time. The bleeding can be external , if the skin is broken by a scrape, cut or abrasion, or it can be internal Table of contents 1 Treatment
2 Causes

3 History

4 See also
...
edit
Treatment
Haemophilia can be controlled quite successfully today by regular injections of a given clotting factor such as Factor VIII edit
Causes
Haemophilia is generally caused by a mutation affecting the genes encoding one of the clotting factors . These genes are located on the so-called X chromosome , so haemophilia is a sex-linked trait. Women have two X-chromosomes whereas men have one X and one Y-Chromosome. Since the mutations causing the disease are recessive , a woman carrying the defect on one of her X-chromosomes will not be affected by it, as the equivalent allele on her other chromosome would express itself to produce the necessary clotting factors. However the Y-chromosome in men has no

83. HIV & Hemophilia Menu
HIV You. HIV hemophilia. Introduction to hemophilia. Important Questions Answers About HIV and hemophilia. New Recombinant Product for hemophilia B.
http://www.hivpositive.com/f-HIVyou/f-Hemophilia/3-HemoSubMenu.html

Introduction to Hemophilia

HIV and Hemophilia
Report from The Institute of Medicine New Recombinant Product for Hemophilia B

Introduction to Hemophilia

HIV and Hemophilia
Report from The Institute of Medicine New Recombinant Product for Hemophilia B ...
Go to the HIVpositive.com Main Menu

84. HIV & Hemophilia: Introduction
HIV You. Introduction to hemophilia. What Is hemophilia? hemophilia is a disorder in which one of the plasma proteins needed to
http://www.hivpositive.com/f-HIVyou/f-Hemophilia/3-intro.html
Introduction to Hemophilia
What Is Hemophilia?
How Common Is Hemophilia? How Does Someone Get Hemophilia? Symptoms and Treatment of Bleeding Episodes ...
Return to the Hemophilia Menu
What Is Hemophilia?
Hemophilia is a disorder in which one of the plasma proteins needed to form a clot is missing or reduced. The most common type of hemophilia is factor VIII deficiency, or hemophilia A. The second most common type is factor IX deficiency or hemophilia B. When a person with hemophilia is injured, he does not bleed harder or faster than normal, but will have prolonged bleeding because he cannot make a firm clot. Small cuts on the skin are usually not a problem, but bleeding in any deeper area can be prolonged. Some bleeding episodes occur as a result of injury, but many occur seemingly without cause.
Go to the HIVpositive.com Main Menu
Return to the Hemophilia Menu
How Common Is Hemophilia?
Estimates indicate that approximately one in 10,000 males born in the US has hemophilia. All races and socio-economic groups are affected equally.
Go to the HIVpositive.com Main Menu

85. Welcome To The Home Page For The Louisiana Hemophilia Foundation
Welcome to the home of the Louisiana hemophilia Foundation. Copyright © 2004 Louisiana hemophilia Foundation Last modified 04/22/04.
http://www.louisianahemophilia.org/
Laissez Les Bons Temps Rouler! (Let the good times roll!) The Club
No one over 18 allowed!
We are a
Capital Area
United Way Agency. Many thanks
to the
Capital Area United Way Welcome to the home of the Louisiana Hemophilia Foundation. We are a 501 (3)(C) not-for-profit organization. Serving the bleeding disorder community since 1976.
Our mission is to improve the quality of life and assist persons affected by inherited bleeding disorders by providing education, advocacy, support services and by promoting research. Register Now for Annual Meeting
June 25-27 - Baton Rouge, LA
Call LHF at 800-749-1680 or 225-291-1675 in the Baton Rouge area, for more information or to register your attendance.
Click here for the brochure.
Click here for the Annual Meeting registration form. Summer Camp Apply Now! Summer cam p is males and females between the ages of 6-14 with a bleeding disorder (not for their siblings without a bleeding disorder). There is no charge for camp. Get a Camp Application! For teens 15 and over with a bleeding disorder, we have a (CIT) Counselor in Training program. Come join us as Camp Counselor! For more information contact LHF.

86. Hemophilia -- Topic Overview
hemophilia Topic Overview What is hemophilia? hemophilia is a rare genetic bleeding disorder caused by a shortage of certain clotting factors.
http://my.webmd.com/hw/health_guide_atoz/hw191400.asp
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You are in Medical Library Choose a Topic Our Content Sources Ask A Question Clinical Trials Health Guide A-Z Health Topics Symptoms Medical Tests Medications ... Credits Hemophilia Topic Overview What is hemophilia? Hemophilia is a rare genetic bleeding disorder caused by a shortage of certain clotting factors . Blood-clotting factors are needed to help stop bleeding after a cut or injury and to prevent spontaneous bleeding. The hemophilia gene can contain many different errors, leading to different degrees of abnormality in the amount of clotting factor produced. There are two major types of hemophilia:
  • Hemophilia A is caused by a deficiency of active clotting factor VIII (8). Approximately 80% of all people with hemophilia have type A, and most of these cases are severe. Approximately 1 out of every 5,000 male babies is born with hemophilia A.

87. AHF - What Is Hemophilia?
Disclaimer Privacy Policy. WHAT IS hemophilia? hemophilia is a disorder caused by an error in a person’s genetic code. hemophilia is a lifelong disorder.
http://www.ahfinfo.com/ahfinfo/whatishemophilia.html
AHF, Inc.
E-MAIL: info@ahfinfo.com AHF® Inc.
Privacy Policy

WHAT IS HEMOPHILIA? This special genetic code, passed to an unborn child, is supposed to signal a series of steps that help control bleeding by clotting. The steps needed to form a clot depend upon a series of proteins called factors. This error in genetic code means that some of the factors are missing or that they are not working correctly in a person with hemophilia. This causes people with hemophilia to bleed longer but not faster. Surface bleeds, on the outside of the body, are fairly easy to stop, even for people with hemophilia. Internal bleeding, such as bleeding into joints or muscles, can mean that it is only possible for a clot to form after the person has taken medication called clotting factor. More than 15,000 people have hemophilia A or hemophilia B in the United States. There are other bleeding disorders where one or more of the clotting factors is missing. People with hemophilia A are missing factor VIII and those with hemophilia B are missing factor IX, others may be missing factors I, II, VII, etc. There are also other bleeding disorders. The most common of which is von Willebrand disease, and many more people have von Willebrand disease than have hemophilia. Individuals with bleeding disorders can be missing a little, a lot, or almost all of that particular factor needed to form clots and stop bleeding. These are called mild, moderate, and severe levels of disorder. The level of severity will predict how often a person will develop a bleed, how difficult it will be for them to form a clot, and how much clotting medication they will need in order to form a clot.

88. Hemophilia, HIV, Hepatitis C HCV Lawsuit
Lieff Cabraser is representing persons with hemophilia A Global Tragedy Tens of Thousands of People With hemophilia Worldwide Exposed To HIV.
http://www.hemophilia-litigation.com/
SUMMARY
Persons with hemophilia in the United States, Latin America, Europe, Asia, the Middle East and Africa were infected with contaminated blood products. Lieff Cabraser is representing clients from around the world in lawsuits filed in U.S. courts against American blood companies that sold in the U.S. and exported contaminated blood worldwide.
E-mail Us

Media Center
Resources for Reporters and Articles for Clients

We are investigating the blood factor products and conduct of the American blood companies around the world, including in the following nations:
Argentina Austria Brazil Chile Colombia Costa Rica Denmark Ecuador Germany Hong Kong India Indonesia Iran Israel Italy Jordan Korea Malaysia New Zealand Panama Paraguay Peru Phillipines Portugal Puerto Rico Singapore Sri Lanka South Africa Sweden Taiwan Thailand United Kingdom Uruguay Venezuela
Introduction: Lawsuits by Persons with Hemophilia Printer-friendly version Lieff Cabraser Heimann & Bernstein, LLP, represents persons with hemophilia worldwide, or their survivors and estates, who received blood products manufactured by American companies in the early to mid-1980's. The blood products were known as factor concentrate, Factor VIII ("antihemophilic factor" or "AHF") and Factor IX, and were manufactured and sold in the U.S., and exported worldwide. The blood products were known as anti-hemophilic factor or "Factor VIII" and "Factor IX."

89. Http://www.theceonetwork.com/cgi-bin/team.cgi?id=An202834&action=show
Florida Chapter National hemophilia Foundation. Links. Poster Kids Coloring Book Contest (click here for more Information). March is hemophilia Awareness Month!
http://www.floridahemophilia.com/
Florida Chapter
National Hemophilia Foundation Links For Your Information
Florida Chapter Newsletter
Florida Chapter Program Services

Camp Application

Calendar of Events
...
Pebble Beach Drawing
Anyone not receiving our award winning newsletter can e-mail us your name and address at hemoph5011@aol.com . This newsletter has important and updated information plus activities going on around the state. The newsletter and this website are for you, so any input or links you feel should be on our list, please e-mail them to us including any of your personal webpages. If there is a picture or article you would like to include in our newsletter please e-mail it and it will get to our editor. We can always use your help. Don't forget to see who our sponsors are and visit their sites including Amazon.com and CD Now. Florida Chapter
Home Office Numbers:

Toll Free - 1-888-880-8330
Fax: 1-727-856-2257 Links to Donations: Everytime you make a purchase through our Amazon link or CD NOW located below, a percentage of your purchase is donated to our Chapter. Thank you in advance! If you have comments or sugguestions, please feel free to e-mail us at

90. Hemophilia Clinical Trials And New Treatments
Explains the importance of participating in hemophilia clinical trials and how even participants who take placebos contribute and benefit from volunteering.
http://www.hemophilia-clinical-trials.com/
Hemophilia Clinical Trials and New Treatments
Hemophilia is a blood disorder that interferes with the blood clotting process. People with hemophilia either lack the clotting factors needed to stop bleeding, or possess abnormal clotting factors. The disease is usually inherited, and affects men far more often than women.
Hemophiliacs bleed for longer when injured than people with normal levels of clotting factors. Internal bleeding is a serious problem, and people with severe hemophilia may bleed into muscles and joints several times a week. Despite popular belief, hemophilia does not make people bleed faster, rather the blood takes longer to clot.
Clinical Trial Research and Hemophilia
Treatments for hemophilia focus on replacing the missing clotting factors. Such treatments require intravenous doses of clotting factors, and in severe cases are required several times a week. Clinical trials are investigating gene therapy treatments for hemophilia, in the hopes of discovering longer-lasting and more effective treatments.
While gene therapy research continues, other clinical trials investigate new methods of producing clotting factors. One of the most recent hemophilia treatments, ADVATE Antihemophilic Factor (Recombinant) was approved by the FDA in 2003 after successful clinical trials. ADVATE is used to prevent bleeding, and to prepare people with hemophilia for surgery. ADVATE research led to the use of genetically altered ovaries from Chinese hamsters, which produce a clotting agent called Factor VIII. Clinical research trials proved the new treatment and its production safe for human use.

91. Discovery Health Hemophilia A
hemophilia A is an inherited condition. It results from a lack of an important blood clotting protein. search, hemophilia A. By Thomas Fisher, MD.
http://health.discovery.com/diseasesandcond/encyclopedia/675.html

92. Discovery Health Hemophilia B
hemophilia B is an inherited bleeding disorder affecting mostly men. This disease search, hemophilia B. By Thomas Fisher, MD. hemophilia B
http://health.discovery.com/diseasesandcond/encyclopedia/676.html

93. The Coalition For Hemophilia B, Inc.
The Coalition for hemophilia B, Inc. newsletters From the Coalition for hemophilia B John Taylor is the Chairman of the Coalition
http://www.boygenius.com/cfb/
The Coalition for Hemophilia B, Inc.
newsletters From the Coalition for HEMOPHILIA B John Taylor is the Chairman of the Coalition for Hemophilia B. He and his wife, Joyce, are the parents of a young child who has moderate/severe Hemophilia B. They started the Coalition when they began to encounter the many problems that Hemophilia B families must face on a day to day basis. They were encouraged to act by many scientists and research doctors who felt the same frustration that they did about the snail's pace of the progress with the disease. The Coalition is guided by a Board that includes researchers, doctors, lawyers, parents, and patients. There are nine in total but the reach among the medical research communicty is exteneded by a Scientific Advisory Board. The Coalition is funded by a large gift from John Taylor and his wife as well as by a fund raising effort that targets foundations interested in research and in developing cures for diseases. The Coalition tries to work closely with anyone who is interested in improving the therapies and general well-being of those who suffer from Hemophilia B; however, the Coalition's focus is on improving the future through research, development of products, advocacy, and therapeutic advances. Many of the day to day operations of the Coalition are handled by Kim Phelan. For more information please contact Kim.

94. HFNC Online Website
Between ages 15 to 20? Click Here for JC/AC Forms! Age 21 and up? Click Here for Adult Staff Applications. hemophilia Foundation of Northern California.
http://www.hfnconline.org/
HFNC "Camp Hemotion" 2003
The Hemophilia Foundation of Northern California is a volunteer, non-profit organization serving the needs of persons with hemophilia and related bleeding disorders. It is dedicated to the treatment and cure of hemophilia, related disorders and their complications, including HIV infection. It strives to support research, encourage and promote treatment, provide education, promote outreach and advocate for the families of those affected by bleeding disorders and their complications. Click Here to see who recieved our chapter Volunteer of the Year Award at the NHF Annual Meeting in Salt Lake City*

HFNC Annual Berkeley Repertory Theatre Fundraiser
Saturday, April 24, 2004
8:00 PM Curtain Click Here for Info on tickets!

95. Puget Sound Blood Center Online

http://www.psbc.org/medical/patient/_frm/frm_hemophilia_care.htm

96. Kentucky Hemophilia Foundation
The KHF provides services,advocacy, support and information for people with hemophilia and their families. What, exactly, is hemophilia?
http://www.kyhemo.org/
Most people recognize hemophilia as the “bleeder’s disease.” But few understand the intense physical, financial, and emotional strain it puts on a family. These challenges are the reasons the Kentucky Hemophilia Foundation was created. What, exactly, is hemophilia?
Hemophilia is a bleeding disorder that affects 1 of every 7,500 males form birth. A similar disorder, von Willebrand disease, affects both males and females equally. Bleeding disorders result in spontaneous and prolonged bleeding due to the lack of clotting factors in the blood. They are chronic disorders, for which there is no cure Kentucky Hemophilia
Foundation, Inc.
982 Eastern Parkway
Louisville, KY 40217
(502) 634-9995 (FAX)
1 (800) 582-CURE (2873) info@kyhemo.org Home About Us Programs/Services ... E-mail
Site Design by Rawlings Creative Group

97. Cancer And Blood Diseases | Hemophilia
hemophilia. Print Format. hemophilia is a disorder in which one of the 11 bloodclotting factors is missing or reduced, resulting in bruising and bleeding.
http://www.ucsfhealth.org/childrens/medical_services/cancer/hemophilia/
University of California, San Francisco About UCSF Quick Links... Admissions Appointments Billing Calendar Clinical Trials Clinics Conditions and Treatments Contact a Patient Contact Us Directions and Maps For Health Professionals Jobs Make A Donation Medical Dictionary Medical Tests News Patient Profiles Specialized Services UCSF Medical Center Volunteer Services Search
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Cancer and Blood Diseases Topics Hemophilia To Visit Us ... Other Resources Hemophilia Print Format Hemophilia is a disorder in which one of the 11 blood-clotting factors is missing or reduced, resulting in bruising and bleeding. Caused by a sex-linked defective gene, it affects about one in 5,000 boys born in the United States. Although hemophilia typically is inherited, a third of the cases may result from a new genetic mutation. The most common type of hemophilia, caused by a lack of clotting factor VIII, is called hemophilia A or classic hemophilia. The second most common type is caused by a lack of clotting factor IX and is called hemophilia B or Christmas disease, named for Stephen Christmas, the first person diagnosed with the factor IX deficiency. Hemophilia A and B occur almost always in boys. A third, very rare type of hemophilia, called Hemophilia C, is caused by a lack of clotting factor XI and can occur in both girls and boys. At UCSF Children's Hospital, the pediatric Hemophilia Treatment Center offers the most comprehensive care for children with hemophilia throughout Northern California. Through our research, we also provide the latest advances in treating complications of the disease.

98. EMedicine - Hemophilia, Type B : Article By Brendan R Furlong, MD
hemophilia, Type B hemophilia B is an inherited, X-linked, recessive disorder resulting in deficiency of functional plasma coagulation factor IX.
http://www.emedicine.com/emerg/topic240.htm
(advertisement) Home Specialties CME PDA ... Patient Education Articles Images CME Patient Education Advanced Search Link to this site Back to: eMedicine Specialties Emergency Medicine Hematology And Oncology
Hemophilia, Type B
Last Updated: June 15, 2001 Rate this Article Email to a Colleague AUTHOR INFORMATION Section 1 of 10 Author Information Introduction Clinical Differentials ... Bibliography
Author: Brendan R Furlong, MD , Associate Medical Director, MedSTAR Transport, Department of Emergency Medicine, Washington Hospital Center Coauthor(s): Mary A Furlong, MD , Fellow, Soft Tissue Pathology, Armed Forces Institute of Pathology Brendan R Furlong, MD, is a member of the following medical societies: American College of Emergency Physicians Editor(s): William Gossman, MD , Assistant Professor, Department of Emergency Medicine, Chicago Medical School; Project Medical Director, Department of Emergency Medicine, Mount Sinai Hospital; Francisco Talavera, PharmD, PhD , Senior Pharmacy Editor, Pharmacy, eMedicine; Jeffrey L Arnold, MD, FACEP, FAAEM

99. EMedicine - Hemophilia, Type A : Article By Brendan R Furlong, MD
hemophilia, Type A hemophilia A is an inherited, X-linked, recessive disorder resulting in deficiency of functional plasma coagulation factor VIII.
http://www.emedicine.com/emerg/topic239.htm
(advertisement) Home Specialties CME PDA ... Patient Education Articles Images CME Patient Education Advanced Search Link to this site Back to: eMedicine Specialties Emergency Medicine Hematology And Oncology
Hemophilia, Type A
Last Updated: June 15, 2001 Rate this Article Email to a Colleague AUTHOR INFORMATION Section 1 of 10 Author Information Introduction Clinical Differentials ... Bibliography
Author: Brendan R Furlong, MD , Associate Medical Director, MedSTAR Transport, Department of Emergency Medicine, Washington Hospital Center Coauthor(s): Mary A Furlong, MD , Fellow, Soft Tissue Pathology, Armed Forces Institute of Pathology Brendan R Furlong, MD, is a member of the following medical societies: American College of Emergency Physicians Editor(s): William Gossman, MD , Assistant Professor, Department of Emergency Medicine, Chicago Medical School; Project Medical Director, Department of Emergency Medicine, Mount Sinai Hospital; Francisco Talavera, PharmD, PhD , Senior Pharmacy Editor, Pharmacy, eMedicine; Jeffrey L Arnold, MD, FACEP, FAAEM

100. Hardin MD : Hemophilia
From the University of Iowa, the *best* lists of Internet sources in hemophilia. hemophilia. We list the best sites that list the sites . hemophilia Foundation;
http://www.lib.uiowa.edu/hardin/md/hemophilia.html
Hemophilia
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The URL for this page is http://www.lib.uiowa.edu/hardin/md/hemophilia.html Last updated Tuesday, Feb 24, 2004 [hemophelia, hemophila] [17417

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