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Hemophilia:     more books (100)

Orthopedic Surgery in Patients with Hemophilia by P.M. Mannucci, 2008-07-01 Haemophilia: Proceedings of the IX Congress of the World Federation of Haemophilia, Istanbul, 20-22 August, 1974 (International congress series) by World Federation of Hemophilia, 1975 Raising a Child with Hemophilia: A Practical Buide for Parents by by Laureen a Kelley, 1999-01-01 LEGACY THE HEMOPHILIA OF YESTERDAY INSIGHTS ON THE LIFE WITH HEMOPHILIA FROM THE JOURNALS OF RALPH DEAN RYTTING THE WAR YEARS 1942-1944 by MATTHEW DEAN BARKDULL, 2006 Handbook on hemophilia and other bleeding disorders by dr syed numan, 2010-01-08 Cell Genesys obtains results from preclinical hemophilia gene therapy studies.(Brief Article): An article from: BIOTECH Patent News "The Gift Of Experience": Excerpts from conversations with 21 Men With hemophilia and their caregivers (Volume 1) by Laura Gray, Christine Chamberlain, 2010-04-24 Pooling Blood: A journey of two girls with hemophilia and their parents' struggle to keep them alive by Cheryl Nineff D'Ambrosio, 2010-02-22 Joshua The Knight of the Red Snake (What is Hemophilia?) by Laureen A. Kelley, 2001 Living With Hemophilia by Peter Jones, 1974-06 The Gift of Experience: Conversations About Hemophilia by Laura Gray, Christine Chamberlain, 2008-04-16 Curtis & Jerry on Mount Omega (Adventures with Hemophilia) by Celynd Scaglione, 2006 Minutes of the patients. Hemophilia. / Protokol vedeniya bolnykh. Gemofiliya. by unknown, 2006 Gale Encyclopedia of Medicine: Hemophilia by Jennifer F. Wilson MS, 2002-01-01

lists with details

61. Welcome To Hemophilia Health Services
    Home About Us FactorCare Why HHS Bleeding Disorders Bloodstone Magazine Just For Kids Terms ©Copyright 2002 hemophilia Health Services, Inc.  
    http://www.accredohealth.net/hhs/

62. MSN Learning & Research - Hemophilia
    hemophilia, hereditary blood disease involving the inability of blood to clot, or coagulate, leading to hemorrhage, or bleeding.  
    http://encarta.msn.com/encnet/refpages/RefArticle.aspx?refid=761570021

63. Hemophilia - Bayer Pharmaceutical
    Home What is hemophilia? Berkeley, CA Clayton, NC Resources Feedback Products. LatestNews Product Literature. Journal of hemophilia Reports. The Parents Resource  
    http://www.hemophiliabayer.com/

64. Choice Source Therapeutics
    Provide hemophilia care for patients.  
    http://www.choicesource.com

65. Hemophilia - Bayer Pharmaceutical - What Is Hemophilia?
    Clinical Questions? Call our Clinical Communications Dept. 1800-288-8371 (selectoption 1). What is hemophilia? hemophilia CARE IN THE UNITED STATES.  
    http://www.hemophiliabayer.com/What_is_Hemophilia_/what_is_hemophilia_.html
    
    Extractions: Hemophilia is a genetic disorder characterized by the deficiency or absence of one of the proteins (or factors) in blood plasma that is responsible for clotting. Low levels of one of these plasma proteins result in bleeding and difficulty clotting in the affected individual. There are more than a dozen clotting factors in our bodies. The most common deficiency of a clotting protein is factor VIII although any one of these can be deficient or absent. The second most common deficiency is Factor IX deficiency. There are factor VIII and IX concentrates that are manufactured to treat these two types of hemophilia. Treatment for hemophilia Manufacturers, like Bayer, have developed concentrates containing Factor VIII and IX clotting factors that are used for treatment of persons with hemophilia. These clotting factor concentrates are packaged in a freeze-dried form that requires reconstitution with sterile water before being infused into the vein of a person with hemophilia. Click here for information on Bayer Pharmaceutical's line of hemophilia products.

66. Canadian Hemophila Society: BC Chapter
    Information about the organization and its mission, news archive, links and contact details. Also an in depth look at the disease itself including management.  
    http://www.hemophiliabc.ca
    
    Extractions: BC Hemophilia Charity Golf Classic We tee off at Swan-E-Set Bay Resort and Country Club with a 12:30 shotgun start. After a round of golf and lunch, the day wraps up in style with a banquet dinner, speeches and charity auction. Come out as an individual golfer or really get into the game and enter your team of four to support the BC Chapter of the Canadian Hemophilia Society.

67. HSC- Hemophilia Society Of Colorado
    HSC Home Page click here.  
    http://www.cohemo.org/

68. Tonya's Page
    This page is dedicated to my son, who has hemophilia.  
    http://members.tripod.com/~TKCDAC/index-2.html

69. HEMOPHILIA
    hemophilia. Background hemophilia is the oldest known hereditary bleedingdisorder. There are two types of hemophilia, A and B (Christmas Disease).  
    http://www.nhlbi.nih.gov/health/public/blood/other/hemophel.htm
    
    Extractions: Background Challenges : The most important challenges facing the hemophilia patient, health care provider, and research community today are: Safety of products used for treatment; Management of the disease including inhibitor formation, irreversible joint damage, and life-threatening hemorrhage; and Progress toward a cure. Safety of Products Used for Treatment : In the past 10 to 15 years, advances in screening of blood donors, laboratory testing of donated blood, and techniques to inactivate viruses in blood and blood products have remarkably increased the safety of blood products used to treat hemophilia. Although treatment-related infection with the AIDS virus or most of the hepatitis viruses is a thing of the past, these measures do not completely avoid viruses such as hepatitis A and parvo virus. These infections are rare; nevertheless, they can pose a threat. Researchers are working to improve procedures to destroy these viruses. To ensure absolute safety from transfusion-transmitted viruses and other agents, hemophiliacs may now be treated with factor VIII which has been produced through biotechnology. This product, recombinant factor VIII, is manufactured by a process entirely free of blood products. It, thus, contains only the factor VIII necessary to treat the disease and none of the other components of blood or attendant unwanted agents. Although the cost of this product exceeds that of the blood-derived product, it is clearly the treatment of choice for those, such as newborns, who have not yet been exposed to blood products. A factor IX product has also been produced by such a process and is currently in clinical trials. Once this product is shown to be safe and effective, all hemophiliacs will have available a treatment for bleeding which is totally free of any contaminating agents.

70. Gentiva Health Services - Page Not Found
    Designed to help you understand hemophilia, von Willebrand's disease and other bleeding disorders and provide valuable information.  
    http://www.gentiva.com/consumer/hemophilia/
    
    Extractions: We are sorry, but the URL you requested could not be found. The page you are looking for may have been renamed, moved, or deleted. If you feel you have reached this page in error, please use the Back button of your browser or check the address you entered and try again. If you reached this page from another part of gentiva.com, please let us know so we can fix the problem. Please check the URL for spelling, capitalization, and punctuation errors, and click the "reload" button on your browser. To view a current site map of gentiva.com click here , or to return to the gentiva.com home page click here Company Information Services Investor Relations ... Legal Statement

71. Hemophilia Update: 1997
    hemophilia UPDATE 1997. Background effective. Antibody inhibitorsare more likely to occur in individuals with severe hemophilia.  
    http://www.nhlbi.nih.gov/health/public/blood/other/hemo_97.htm
    
    Extractions: Advances in treatment over the last three decades have permitted a near-normal lifestyle and life-span for many individuals with hemophilia. The introduction of factor VIII concentrate products in the 1970s allowed treatment at home and largely replaced the need for transfusion of whole blood or plasma in the hospital. An unfortunate result of increased freedom from bleeding as a cause of disability and death was infection with hepatitis from products made from pooled plasma. This culminated in the early 1980s with the unexpected and devastating infection of about 70 % of severe hemophiliac patients with HIV, the cause of AIDS. Since then, the development and improvement of methods for inactivating viruses with lipid envelopes in plasma, including factor VIII and IX concentrates, has improved the safety of transfused products to the point where the threat of infection with HIV, hepatitis B(HBV) or hepatitis C (HCV) viruses has been essentially eliminated. Safety of Products Used in Treatment Over the last few years, improved procedures have led to high purity plasma-derived factor VIII and factor IX products which appear to be safer when subjected to viral inactivation procedures than were the previous lower potency materials. "First generation" recombinant factor VIII, produced without human plasma, became available in 1992. This added a measure of safety especially from non-enveloped viruses, although the need for human albumen to stabilize the factor left a tiny and currently hypothetical risk of human infectious agent transmission. The first recombinant factor IX preparation is now in clinical trials. It is a "second generation" product which is manufactured and packaged without any human or animal plasma proteins. A similarly produced factor VIII concentrate is under development.

72. Hemophilia
    hemophilia. incidence knees elbows ankles hips shoulders wrists.results in secondary OA (DDx acromegaly, ochronosis, spondyloepiphyseal  
    http://chorus.rad.mcw.edu/doc/01019.html

73. Haemostasis Forum
    Dedicated to supplying information on haemophilia to medical and health care professionals, providing an excellent opportunity to interact with worldwide specialists in the field of haematology.  
    http://www.hemophilia-forum.org/
    
    Extractions: This is a web site dedicated to supplying information on haemophilia to medical and health care professionals, providing an excellent opportunity to interact with worldwide specialists in the field of haematology. Each month the contents of these pages are updated and reviewed by a panel of independent haemophilia specialists. Please click on Faculty Info. This forum is supported by an educational grant from Novo Nordisk A/S. If you would like to access this site, please click on 'Register Now' and submit your details. If you have already registered, please enter your username and password and click on 'accept'. Enter your details here please

74. AHF - What Is Hemophilia?
    Disclaimer Privacy Policy. WHAT IS hemophilia? hemophilia is a disorder causedby an error in a person’s genetic code. hemophilia is a lifelong disorder.  
    http://www.ahfinfo.com/ahfinfo/whatishemophilia.html
    
    Extractions: 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.

75. Hemophilia, Clotting Factor, Infusion, Hemophilia Care, Von Willebrand Disease,
    Providing next-day hospital and home delivery of several blood products.Category Business Healthcare Products and Services Blood Products Care, von Willebrand disease. The hemophilia Disease Management Company31 Moody Road PO Box 985 Enfield, CT 06083 1-800-243-4621.  
    http://www.ahfinfo.com/

76. Index
    Florida Chapter Of The National hemophilia Foundation, Inc. This pageis designed to pass information on to our community and to  
    http://www.geocities.com/HotSprings/1809/
    
    Extractions: Foundation Links For Your Information 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 Newsletter Annual Membership Meeting Calendar Of Events Chapter's Officers and Board Members ... Photo Gallery Florida Chapter

77. HAVEN
    HAVEN is an independent organization in Northwestern PA. W Provides patients and their families with information about their condition, treatment options and patient rights.  
    http://members.tripod.com/haven8361/

78. Welcome To The Utah Hemophilia Foundation
    http://www.hemophiliautah.org/

79. Bayer
    at Bayer Biological Products have been dedicated to developing and producing noveltreatments that extend and enhance the lives of people with hemophilia.  
    http://www.bayer-hemophilia-awards.com/
    
    Extractions: For more than 30 years, scientists and researchers at Bayer Biological Products have been dedicated to developing and producing novel treatments that extend and enhance the lives of people with hemophilia. Bayer believes the Hemophilia Awards Program can improve the lives of patients with hemophilia by supporting research and education worldwide. The next steps for the next generation…

80. GeneReviews: Hemophilia A
    Your browser does not support HTML frames so you must view hemophilia Ain a slightly less readable form. Please follow this link to do so.  
    http://www.geneclinics.org/profiles/hemo-a/

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