121. DermAtlas: Online Dermatology Image Library Dermatology Image,vascular Malformat hemophiliahemophilia is a genetic (inherited) bleeding disorder caused by a shortage of substances called clotting http://dermatlas.med.jhmi.edu/derm/result.cfm?Diagnosis=-97811613

122. Hemophilia Society Of Colorado The hemophilia Society of Colorado advocates for persons living with The society also strives to increase public awareness about hemophilia and related http://www.cohemo.org/

Mission Statement The Hemophilia Society of Colorado advocates for persons living with hemophilia and other coagulation disorders and their related complications by providing assistance, support, and education. The society also strives to increase public awareness about Hemophilia and related disorders. 655 Broadway, Suite # 575 Denver CO 80203 (888) 687-CLOT FAX: (303) 629-7035 Email: hsc@cohemo.org Mountain States Regional Hemophilia and Thrombosis Center Website design and website hosting by EduCyber

123. Cancer And Blood Diseases | Hemophilia hemophilia is a disorder in which one of the 11 bloodclotting factors is missing At UCSF Children s Hospital, the pediatric hemophilia Treatment Center http://www.ucsfhealth.org/childrens/medical_services/cancer/hemophilia/

University of California, San Francisco About UCSF Search Welcome Hospitals and Clinics Appointments Billing ... 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. For more information, please call:

124. Hemophilia hemophilia is an inherited bleeding, or coagulation, disorder. Children with hemophilia lack the ability to stop bleeding because of the low levels, http://ymghealthinfo.org/content.asp?page=P00093

125. Disease Category Listing (379): Hemophilia CenterWatch Listing of Clinical Research Trials for hemophilia. http://www.centerwatch.com/patient/studies/cat379.html

Clinical Trials: Hemophilia California Duarte; City of Hope National Medical Center An International, Randomized, Controlled Trial of Immune-Tolerance Induction Duarte; City of Hope National Medical Center Epidemiology and Treatment of Circulating Anticoagulants in Patients with Hemophilia and von Willibrand's Disease. - The Hemophilia Research Society Duarte; City of Hope National Medical Center Hemophilia Inhibitor Genetics Study Los Angeles; UCLA Los Angeles; Children's Hospital of Los Angeles Colorado Aurora; University of Colorado Health and Science Center Aurora; University of Colorado Health and Science Center Michigan Detroit; Children's Hospital of Michigan Detroit; Children's Hospital of Michigan New Jersey New Brunswick; Robert Wood Johnson Medical School New Brunswick; Robert Wood Johnson University North Carolina Chapel Hill; University of North Carolina at Chapel Hill Chapel Hill; Comprehensive Hemophilia Center Ohio Cincinnati; Cincinnati Children's Hospital Dayton; Children's Medical Center Dayton; Children's Medical Center Pennsylvania Hershey; Milton S. Hershey Med Ctr.

126. Hemophilia A Genes and disease provides short descriptions of inherited disorders. It is hosted by the National Center for Biotechnology Information (NCBI), http://www.ncbi.nlm.nih.gov/disease/hemoA.html

This Genes and Disease page has been moved to: Please update your bookmarks. If you are not automatically transported to the new page after 15 seconds, click on this link Genome View HEMA on chromosome X Databases PubMed the literature LocusLink collection of gene-related information OMIM catalog of human genes and disorders Information National Hemophilia Foundation a nonprofit organization dedicated to finding cures for inherited bleeding disorders HEMOPHILIA A Treatment of Hemophilia A has progressed rapidly since the middle of the last century when patients were infused with plasma or processed plasma products to replace Factor VIII. HIV contamination of human blood supplies and the consequent HIV infection of most hemophiliacs in the mid-1980s forced the development of alternate Factor VIII sources for replacement therapy, including monoclonal antibody purified Factor VIII and recombinant Factor VIII, both of which are used in replacement therapies today. Development of a gene replacement therapy for Hemophilia A has reached the clinical trial stage, and results so far have been encouraging. Investigators are still evaluating the long-term safety of these therapies, and it is hoped that a genetic cure for hemophilia will be generally available in the future.

127. OMIM - HEMOPHILIA B; HEMB http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=306900

128. The Hemophilia Alliance The Alliance is a notfor-profit organization that comprises hemophilia The hemophilia Alliance s Vision To ensure high quality, accessible and http://www.hemoalliance.org/

@import url(hemo.css); THE HEMOPHILIA ALLIANCE Integrating Pharmacy with Comprehensive Care Homepage About The Alliance Information Joining The Alliance ... Tell Us Your Story Welcome Who is the Hemophilia Alliance? The Alliance is a not-for-profit organization that comprises Hemophilia Treatment Centers (HTC's that either have, or are seeking to have, factor delivery programs under Section 340B of the PHS Act. The purpose of the Alliance is to promote the common interests of these HTC's. The Hemophilia Alliance's Vision To ensure high quality, accessible and affordable patient care, the Hemophilia Alliance, Inc. will be the resource of choice for HTC's utilizing factor distribution programs. Contact Information E-mail: info@hemoalliance.org Phone: 202.466.6550

129. Hemophilia Emergency Care http://www.hemophiliaemergencycare.com/

130. Virtual Children's Hospital: CQQA: Hemophilia Common Questions, Quick Answers on hemophilia. If a parent has hemophilia, their child is more likely to have hemophilia. http://www.vh.org/pediatric/patient/pediatrics/cqqa/hemophilia.html

Pediatrics Common Questions, Quick Answers Hemophilia Donna D'Alessandro, M.D. Lindsay Huth, B.A. Peer Review Status: Internally Reviewed Creation Date: April 2002 Last Revision Date: April 2002 Common Questions, Quick Answers What is hemophilia What causes it? Who can get it? ... When should I call the doctor? What is hemophilia? Hemophilia is a blood disorder. The blood is not able to clot (stop bleeding) as well as it should. There are three common types; Type A, Type B, and Type C. Type A is the most common. Type B is also known as the "Christmas disease." What causes it? It can be caused by congenital defects, or birth defects (problems in a baby's growth and development before birth). It often results because important things (such as proteins) are missing from the blood to help it clot. It can be inherited (passed from parent to child through genes). Who can get it? Type A and B are most common in men. If a parent has hemophilia, their child is more likely to have hemophilia. What are the signs and symptoms? Patients may bleed anywhere.

131. Welcome To The Home Page For The Louisiana Hemophilia Foundation Louisiana hemophilia Foundation. Laissez Les Bons Temps Rouler! (Let the good times roll!) Welcome to the home of the Louisiana hemophilia Foundation. 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 (C) (3) 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. Here is a list of our upcoming events. Please save these dates on your calendar. To register your attendance or for more information please contact us at If you don't have Adobe Acrobat Reader you can go to their site and get it now. August 27, 2005 - Update! For those of you who reserved a spot for the Zephyr's game in July and received your confirmation letter, please join us on our new date Saturday, August 27, 2005. We will be on the "Home Run Deck." Check in time is 10:30 AM. The game starts at noon. Hamburgers, hotdogs, cold drinks and a cash bar will be available. This event is sponsored by Factor Health Management. So come out and have fun with us! We are not taking new reservations for this event . For more information call Let's play ball! It's this Saturday Morning. See you there!

132. Hemophilia hemophilia A and hemophilia B are clinically indistinguishable, The changing prognosis of classic hemophilia (factor VIII deficiency ). http://www.5mcc.com/Assets/SUMMARY/TP0406.html

Hemophilia DESCRIPTION: Hemophilia A and hemophilia B are clinically indistinguishable, inherited bleeding disorders due to a deficiency of coagulant factor VIII (hemophilia A) or factor IX (hemophilia B) Disease severity is determined by percent of coagulant factor present Moderate; 2-5% System(s) affected: Hemic/Lymphatic/Immunologic Genetics: Both hemophilia A and hemophilia B are X-linked, recessive Incidence/Prevalence in USA: Hemophilia A - 10 in 100,000 males Hemophilia B - 2 in 100,000 males Predominant age: Both are congenital conditions Severe disease generally noted at birth or in first year Mild disease may not be diagnosed until young adulthood Predominant sex: CAUSES: Congenital Synonyms: Hemophilia A Factor VIII deficiency Classic hemophilia Hemophilia B Factor IX deficiency Christmas disease ICD-9-CM: 286.0 Hemophilia A 286.1 Hemophilia B REFERENCES: Jones PK, Ratnoff OD. The changing prognosis of classic hemophilia (factor VIII 'deficiency'). Ann Int Med 1991;114(8):641-8 Schwartz RS, et al. Human Recombinant DNA-Derived Antihemophilic Factor (Factor VIII) in the Treatment of Hemophilia A. N Engl J Med 1990;323(26):1800-5 Author(s): W. Paul Bowman, MD

133. BHPR - Ricky Ray Trust: Blood-Clotting Disorders & HIV - Home The Ricky Ray hemophilia Relief Fund was established by the US Congress in 1998 to make compassionate payments of $100000 to certain individuals with blood http://bhpr.hrsa.gov/rickyray/

The javascript used on this site for creative design effects is not supported by your browser. Please note that this will not affect access to the content on this web site. Setup Instructions Ricky Ray Hemophilia Relief Fund Frequently Asked Questions Forms Update : More than $555 million in compassionate payments to more than 7,100 eligible individuals and survivors has been committed. All petitions postmarked no later than November 13, 2001 have been processed for payment. No petitions postmarked after November 13, 2001 will be accepted. (5-2-2003) Information about survivors who received less than $100,000 on behalf of an eligible individual (Federal Register, 10-2-2002) History The Ricky Ray Hemophilia Relief Fund was established by the U.S. Congress in 1998 to make compassionate payments of $100,000 to certain individuals with blood clotting disorders, such as hemophilia, who were treated with anti-hemophilc factor between July 1, 1982 and December 31, 1987, and who contracted HIV. Certain spouses and children who contracted HIV from these individuals and specified survivors were also eligible to receive payment. By regulation, petitions filed for payment under the Ricky Ray Hemophilia Relief Fund were required to be postmarked between July 31, 2000 through November 13, 2001.

134. Haemostasis Forum This is a web site dedicated to supplying information on haemophilia to medical and health care professionals, providing an excellent opportunity to http://www.haemophilia-forum.org/

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 User name: Password: Cancel Accept Preview this site Register ... Forgot Password

135. Index Of /~hfm . DIR Parent Directory 08Jan-2002 1149 -. Apache/1.3.29 Server at ic.net Port 80.......Index of /~hfm. Name Last modified Size http://ic.net/~hfm/

Index of /~hfm Name Last modified Size Description ... Parent Directory 08-Jan-2002 11:49 - Apache/1.3.29 Server at ic.net Port 80

136. Mendelian Laws Apply To Human Beings. http://www.dnaftb.org/dnaftb/13/concept/

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