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Hemophilia: more books (101)

Hemophilia and New Hemorrhagic States by K.M. Brinkhous, 1971-01-07
Hemophilia - A Bibliography and Dictionary for Physicians, Patients, and Genome Researchers by Philip M. Parker, 2007-07-17
Beloved warrior: Hemophilia and other battles by Virginia Nyman Arver, 1997
Hemophilia, SCID: Early Gene Therapy Trials Look Promising.(Brief Article): An article from: Family Practice News by Sherry Boschert, 2001-02-15
Avigen granted broad hemophilia A gene therapy patent.: An article from: BIOTECH Patent News
Prothrombin in enzymology, thrombosis, and hemophilia, (American lecture series, publication no. 681. A monograph in the Bannerstone divi-sion of American lectures in hematology) by Walter H Seegers, 1967
Activated Prothrombin Complex Concentrates: Managing Hemophilia with Factor VIII Inhibitor
Recent Advances in Hemophilia by Louis M. Aledort, 1975
HEMOPHILIA: An entry from UXL's <i>UXL Complete Health Resource</i>
Hemofilia: la gran olvidada.(tratamiento y causas)(TT: Hemophilia: the forgotten disease.)(TA: treatment and causes)(Artículo Breve): An article from: Epoca
The hemophilias (Monograph by Dade education) by Andrew E Weiss, 1978
Transfusion and immunology: Plenary session lectures of the XIV Congress of the International Society of Blood Transfusion and the X Congress of the World Federation of Hemophilia, Helsinki ... 1975
Hemophilia Likely to Be First Gene Therapy Cure.: An article from: Internal Medicine News by Timothy F. Kirn, 2001-08-01
Challenges for social work in hemophilia care.(Practice Forum): An article from: Health and Social Work by Gregory Taylor, 2004-05-01

lists with details

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The summary for this Russian page contains characters that cannot be correctly displayed in this language/character set.
http://www.hemophilia.ru/
Friends Of The Iranian Hemophilia Society
Friends of Iranian hemophilia / haemophilia Society. UK charity hemophilia is an inherited, lifelong bleeding disorder. Without appropriate
http://www.fihs.co.uk/
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/

Extractions: 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.
Hemophilia Association Of The Captial Area
The hemophilia Association of the Capital Area (HACA) is a taxexempt, non- profit organization established in 1961 to serve persons with bleeding disorders
http://www.hacacares.org/

Extractions: The Hemophilia Association of the Capital Area (HACA) is a tax-exempt, non- profit organization established in 1961 to serve persons with bleeding disorders and their families in northern Virginia, Washington, DC, and Montgomery and Prince Georges Counties in Maryland. It is a local chapter of the National Hemophilia Foundation. HACA's mission is to improve the quality of life for persons with hemophilia and Von Willebrand's disease and their families; to act as an advocate; to educate; to improve services to its members; to promote research and to raise money to fulfill this purpose.
Hemophilia
hemophilia. Definition hemophilia is a hereditary bleeding disorder in which it takes a long time for the blood to clot and abnormal bleeding occurs.
http://www.healthscout.com/ency/article/000537.htm

Extractions: Channels Home Today Women Men ... Drug Checker Advertisement Disease Injury Nutrition Poison ... Prevention Definition: Hemophilia is a hereditary bleeding disorder in which it takes a long time for the blood to clot and abnormal bleeding occurs. This disease affects mostly males. Diseases in this category include:
Hemophilia Association Of San Diego County
Golf Tournament Event Date(s) Thursday, May 13th, 2004 Location Torrey Pines North Golf Course Click here for more details.
http://www.hasdc.org/

Extractions: preloadRollover("images/intro/donors.gif", "donors"); preloadRollover("images/intro/site_development.gif", "site_development"); preloadRollover("images/intro/hemos_presentation.gif", "hemos_presentation"); preloadRollover("images/scrolling/orange/scroll_up.gif", "scroll_up"); preloadRollover("images/scrolling/orange/scroll_down.gif", "scroll_down"); var n=3; A Chapter of the National Hemophilia Foundation California Coastal Race
Hemophilia Association Of New Jersey - Hemophilia, Bleeding Disorders
The hemophilia Association of New Jersey offers assistance to persons with hemophilia and their families from our office located in East Brunswick.
http://www.hanj.org/

Extractions: All information that appears on the Hemophilia Association of New Jersey website, including links to other websites, is for your general information only. The Hemophilia Association of New Jersey makes no endorsements for or against medical treatments and/or therapies. Please consult your physician, or local treatment center before pursuing any course of treatment.
Blood Clotting
Loss of the genes for tissue factor or; factor 7. in knockout mice is lethal. hemophilia A and B. Treating hemophilia A and B. What can be done?
http://users.rcn.com/jkimball.ma.ultranet/BiologyPages/C/Clotting.html

Extractions: Index to this page Blood Clotting When blood vessels are cut or damaged, the loss of blood from the system must be stopped before shock and possible death occur. This is accomplished by solidification of the blood, a process called coagulation or clotting. A blood clot consists of Platelet aggregation and fibrin formation both require the proteolytic enzyme thrombin . Clotting also requires: Damaged cells display a surface protein called tissue factor TF Tissue factor binds to activated Factor The TF-7 heterodimer is a protease with two substrates: Factor and Factor Let's follow Factor first.
The DRM WebWatcher: Hemophilia
This section of The DRM WebWatcher describes the best online resources about hemophilia.
http://www.disabilityresources.org/HEMOPHILIA.html

Extractions: Home Subjects States Librarians ... Contact Us The DRM WebWatcher Hemophilia Updated 7/17/2000 A B C D ... About/Hint/Link Hemophilia is a sex-linked hereditary bleeding disorder where one of the plasma proteins needed to form a clot is missing or reduced. Here are some good places to find out more. Centers for Disease Control and Prevention - Hematologic Diseases Branch (HDB) The HDB is mandated by Congress to reduce the complications of hemophilia and other bleeding and clotting disorders. This site provides information about the branch; the archive includes statistical documents and related material. Hemophilia Home Page This is an extensive personal home page compiled by an individual with hemophilia and AIDS. Topics range from general information to HIV compensation/litigation, research, gene therapy, AIDS-related information, Spanish resources and much more. There's also a chat server and listserv information. National Hemophilia Foundation Information about bleeding disorders, news, research, programs, documents, and much more. Check out the new online education program. World Federation of Hemophilia The federation is an international nonprofit volunteer-based organization "dedicated to introducing, improving and maintaining care for persons with hemophilia and related disorders." Its web site includes an extensive online library, a Treatment Centre Directory, product recalls and info, events, "Ask the Doc," and an extensive, well-organized list of links and mailing lists. Visitors should note that the site is sponsored by several medical companies.
Department Of Medicine - Hemophilia Treatment Center
The hemophilia Treatment Center provides comprehensive services to children, adults and their families with hemophilia, Von Willebrand Disease and related
http://www.lij.edu/lijh/hemophilia.html

Extractions: Jahan Roofeh, MD, Orthopedist About the Hemophilia Treatment Center The Long Island Jewish Hemophilia Treatment Center serves as the Federally designated regional hemophilia program for Long Island. The center provides comprehensive services to children, adults and their families with hemophilia, von Willebrand Disease and related disorders. The Treatment Center is located in the Hematology/Oncology Building in Room 350. Telephone: hemophilia@lij.edu Mission/Purpose "We are committed to providing lifelong, accessible, state of the art, family centered hemophilia treatment. Our mission is to foster a high level of autonomy in the management of hemophilia through continuous family and patient education. We believe this goal is facilitated through community advocacy that promotes optimum treatment for all affected families." The Team Approach The Regional Comprehensive Hemophilia Treatment Center offers the skills of experienced hemophilia specialists and provides the following services:
Hemophilia Foundation Of Oregon | Welcome
Welcome. Welcome to the hemophilia Foundation of Oregon s website! This site is dedicated to providing information to Oregon and
http://www.hfo.info/

Extractions: The Hemophilia Foundation of Oregon (HFO) was founded in Portland in 1963 by a small group of parents of children with hemophilia. Its goal has always been to improve the quality of life of those living with bleeding disorders and related diseases, and those who care for them. It serves individuals, their families and friends living in Oregon and Clark County, Washington. HFO is a volunteer organization dedicated to providing education and support to families affected by hemophilia and other bleeding disorders. Nationally, there are approximately 20,000 individuals with hemophilia; 400 with bleeding disorders in the Foundation's service area alone. Including family, friends and caregivers, many thousands of people are touched by hemophilia.
Center For Cancer And Blood Disorders At Children's Medical Center Dallas
hemophilia The hemophilia condition. Program Highlights Membership on various committees of the National hemophilia Foundation. Nurse
http://www.childrens.com/ccbd/hematology/hemophilia_index.cfm
Midwest Hemophilia Association - Home
Improving the quality of life for those affected by hemophilia and other bleeding disorders. The Midwest hemophilia Association
http://www.midwest-hemophilia.org/

Extractions: The Midwest Hemophilia Association is a non-profit organization formed to promote awareness, provide group support, educate, and facilitate communication for the bleeding disorders community of Kansas and Missouri. We provide information on available treatments, insurance and reimbursement issues, and related legislative efforts. We also sponsor educational seminars and conferences, publish a quarterly newsletter, and hold special social events for the benefit of our members. In an effort to ease the adjustment to living wtih a chronic bleeding disorder, MHA's First Steps program provides an avenue of support and education for families of newly diagnosed hemophiliacs. In addition, the MHA collaborates with Children's Mercy Hospital to have a one-week camp every August in Lawson, Missouri specifically for kids with bleeding disorders. This is free of charge to the camper and his family.
Hemophilia Of Indiana - Home
HomePage . Welcome! hemophilia of Indiana, Inc. has a 40year history of serving persons with bleeding disorders throughout Indiana
http://www.hemophiliaofindiana.org/
HealingWell.com Library - News And Articles
HealthPortal Diseases and Conditions Genetic Congenital hemophilia. Gene Therapy for hemophilia Passes Test Altered cells may correct genetic flaw.
http://healingwellhemonco.subportal.com/health/Diseases_and_Conditions/Genetic_C
NovoSevenÂ® US Patient Information
En Español. Introduction hemophilia and inhibitors. More than 15,000 people in the United States have hemophilia. Of those, as many
http://www.us.novoseven.com/content/us_vers/us_patient_information.asp

Extractions: Home Hemostasis ... Visit novonordisk-us.com Patient information Print What is hemophilia? How do you get hemophilia? What are the signs and symptoms of hemophilia? ... En Espa±ol Introduction: Hemophilia and inhibitors More than 15,000 people in the United States have hemophilia. Of those, as many as 20% can expect to develop inhibitors (antibodies) to their coagulation therapy. The following questions were prepared to explain what inhibitors are, how they affect choice of therapy, and how they can be "outsmarted" so that people with hemophilia are able to receive effective treatments. A glossary is also provided in this web site to help define terms that are related to hemophilia. This information is supplied to help patients and their families gain a better understanding of hemophilia and its treatment so that they can more easily discuss their questions and concerns with healthcare providers. Normally, when bleeding occurs, the blood launches into a 2-phase response to stop it. First, platelets become sticky and clump together at the site of the injury forming a platelet plug. Next, blood coagulation rapidly replaces this unstable platelet plug with a chemically stable fibrin clot. This takes place through a series of chemical reactions in the blood that involve substances called clotting factors. When there is a deficiency or absence of either blood factor VIII (factor 8) or factor IX (factor 9), it short-circuits the coagulation process resulting in uncontrolled bleeding that is called hemophilia. People lacking sufficient factor VIII have hemophilia A and people lacking sufficient factor IX have hemophilia B.
HemophiliaSupport.org : National Hemophilia Foundation, Delaware Valley Chapter
http://www.hemophiliasupport.org/
InteliHealth: Hemophilia
surgeries that is listed and crossreferenced in an AZ format. hemophilia. Reviewed by the Faculty of Harvard Medical School hemophilia
http://www.intelihealth.com/IH/ihtIH?t=10115&p=~br,IHW|~st,408|~r,WSIHW000|~b,*
Disease Category Listing (379): Hemophilia
Clinical Trials hemophilia. Arizona. Phoenix; Phoenix Children s Hospital and von Willibrand s Disease. The hemophilia Research Society.
http://www.centerwatch.com/patient/studies/cat379.html
Haemostasis Forum
This is a web site dedicated to supplying information on haemophilia to medical and health care professionals, providing an excellent opportunity to interact
http://www.haemophilia-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

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