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         Hemophilia:     more books (101)
  1. 37th Hemophilia Symposium Hamburg 2006: Epidemiology;Treatment of Inhibitors in Hemophiliacs; Hemophilic Arthropathy and Synovitis; Relevant Hemophilia ... Pediatric Hemostasiology; Free Lectures
  2. Comprehensive Management of Hemophilia by Donna C. Boone, 1976-09
  3. 35th Hemophilia Symposium Hamburg 2004: Epidemiology;Risk of Infections and Inhibitors in Hemophilia; Chronic lic Synovitis and Long-term Results of Orthopedic ... Hemostaseology;Free Lectures
  4. Hemophilia in children (Progress in pediatric hematology/oncology)
  5. Blood Brothers: Ryan, Chris, and Hemophilia by Nancy Shaw, 1990-03
  6. Hemophilia: Medicine & Inventions by iMinds, 2010-05-13
  7. Hemophilia
  8. Hemophilia in the child and adult
  9. 36th Hemophilia Symposium Hamburg 2005: Epidemiology; Hemophilia Therapy - Management of Bleedings and Inhibitors; Orthopedic Treatment in Hemophiliacs; ... Pediatric Hemostaseology; Free Lectures
  10. Hemophilia and Von Willebrand's Disease in the 1990's: A New Decade of Hopes and Challenges : Proceedings of the XIX Congress of the World Federatio (World Federation of Haemophilia//Proceedings) by Jeanne M. Lusher, 1991-07
  11. Blood saga; hemophilia, AIDS, and the survival of a community. by Susan Resnik, 1999
  12. They will probably ask you-- "What is hemophilia?" by Laureen A Kelley, 2001
  13. 32nd Hemophilia Symposium Hamburg 2001: Epidemiology; Genetic Diagnosis of Clotting Disorders; Hemophilia; Hemotherapy in Sepsis; Pediatric Hemostaseology Free Lectures
  14. Surviving the American Medical System in the 21st Century :Stories of American Citizens with Hemophilia: Stories of American Citizens with Hemophilia (Blue Genes) by Ogden M. Forbes, M. Jane Forbes, 2005

21. Îáùåñòâî áîëüíûõ ãåìîôèëèåé/Association For Persons Wit

http://www.blood.ru/hemophilia/

22. Hemophilia Encyclopedia
extensive overviews of key terms and concepts related to hemophilia and itstreatment. Nav Menu Home Patients Families hemophilia Encyclopedia.
http://www.hemophiliagalaxy.com/1_PATIENTS/ENCYCLOPEDIA/
Nav Menu: Home A B C ... Y
A Albumin
Albumin is the most prevalent protein found in blood. It is used as a stabilizer in the manufacturing process of several factor VIII therapies. Albumin is used in the manufacture or formulation of every recombinant factor VIII product currently on the market or under clinical investigation. Antibody
A protein produced by blood plasma cells that binds specifically to substances that the body recognizes as foreign. Once bound, the antibody can lead to the destruction or inactivation of the foreign substance. Inhibitors that occur in response to replacement therapies for hemophilia are antibodies to factor VIII Antihemophilic Factor (AHF)
Another term for factor VIII , which is one of the clotting factors in the blood needed to form fibrin , which in turn helps stop bleeding.
Arthropathy
Chronic joint disease (arthritis) caus ed by repeated and uncontrolled bleeding into joints. This is the leading cause of disability in people living with hemophilia.
B Bleed (hemorrhage)
Bleeding externally or internally. Bruise
A black and blue mark under the skin surface that is caused by bleeding under the skin.

23. Www.web-depot.com/hemophilia
Similar pages hemophilia of Georgia Home Page This site is dedicated to providing information on the opportunities availablethrough hemophilia of Georgia for Georgia families who have hemophilia, von
http://www.web-depot.com/hemophilia

24. Cell Genesys, Inc.
Focused on the development and commercialization of cancer vaccines and gene therapies to treat various cancers including leukemia, hemophilia A and B, restenosis after angioplasty and Parkinson's disease.
http://www.cellgenesys.com

25. Description
of hemophilia. This page is intended for the general public, providinggeneralized information about coagulation. hemophilia Awareness Pages.......
http://www.hemophilia.net/descript.htm

26. World Federation Of Hemophilia FAQ
Information and safety issues about blood collection, hemophilia, and blood products.
http://www.wfh.org/ShowDoc.asp?Rubrique=28&Document=42

27. VersaPharm
Pharmaceutical developer and marketer of specialty prescription products to the United States, working to develop and deliver pharmaceuticals primarily for treatment areas of Tuberculosis, hemophilia, and other blood disorders.
http://www.versapharm.com/
VersaPharm Incorporated develops and markets specialty prescription products to the United States: Pharmaceuticals for Tuberculosis, Hemophilia, Anthrax, STD, blood disorders and other diseases. By using this website, you agree to be bound by the Terms of Service and Purchase currently in effect. Click here to enter website
Terms of Service
Mailing Address
VersaPharm Incorporated
P. O. Box 7509
Marietta, GA 30065-1509 Phone
or 770 499-8100
Fax
E-mail

Info@VersaPharm.com
© 2001-3 VersaPharm Incorporated - Website design and maintenance by Photel International If you have problems with this Website,
please contact the Webmaster 043 020 011 M Date Last Updated: April 03, 2003

28. Hemophilia: What Is It?
hemophilia link, DNA Learning Center Link, Concept 1 Children resembletheir parents. Learn how Mendel worked out inheritance in pea plants.
http://www.yourgenesyourhealth.org/ygyh/mason/ygyh.html?syndrome=hemo

29. Your Genes, Your Health
Offers a DNA Learning Center's multimedia guide to genetic, inherited disorders Fragile X syndrome, Marfan syndrome, cystic fibrosis and hemophilia are discussed in detail.
http://www.yourgenesyourhealth.org
The information within this web site is for educational purposes only, and should not be used as medical advice. A physician should be consulted for any diagnosis and treatment options.
Visit the companion site! No list menu at left? Get QuickTime Player (TM) is also required.

30. Tunnel
For information in English, please go to this site Swedish hemophilia Society.
http://www.xpress.se/fbis/english.html
For information in English, please go to this site: Swedish Hemophilia Society
Nepal - our twinning partner This site works best with Internet Explorer.
Download Explorer here

31. MEDLINEplus Medical Encyclopedia: Factor V Deficiency
Provides brief information about this inherited bleeding disorder, which is similar to hemophilia. Includes causes, symptoms, and prognosis.
http://www.nlm.nih.gov/medlineplus/ency/article/000550.htm
Skip navigation
Medical Encyclopedia
Other encyclopedia topics: A-Ag Ah-Ap Aq-Az B-Bk ... Z
Factor V deficiency
Contents of this page:
Illustrations
Blood clot formation Blood clots Alternative names Return to top Parahemophilia; Owren's disease   Definition Return to top Factor V deficiency is an inherited abnormal blood coagulation disorder caused by a deficiency of the plasma protein Factor V.   Causes, incidence, and risk factors Return to top Normal blood coagulation is a complex process involving as many as 20 different plasma proteins , which are known as blood coagulation factors. A series of complex chemical reactions using these factors takes place very rapidly to form an insoluble protein called fibrin that stops bleeding When certain coagulation factors are deficient or missing, the chain reaction does not take place normally. Factor V deficiency is caused by inheriting a defective Factor V gene. In this disorder, bleeding ranges from mild to severe. The disease is similar to hemophilia , except bleeding into joints is less common. Bleeding can occur almost anywhere in the body, and death from hemorrhage has occurred with this disorder.

32. HEMOPHILIA A
hemophilia A. DEFINITION 4. hemophilia with Factor VIIIc Inhibitors. massive dosesof Factor VIIIc concentrate; plasmapheresis with replacement of Factor VIIIc;
http://www.icondata.com/health/pedbase/files/HEMOPHIL.HTM
  • Pediatric Database (PEDBASE)
  • Last Updated: 4/23/94
    HEMOPHILIA A
    DEFINITION:
    A coagulation disorder characterized by a deficiency in Factor VIIIc resulting in a bleeding diathesis.
    EPIDEMIOLOGY:
    • incidence: 1/10,000 (80-85% of Hemophilias)
    • age of onset:
    • risk factors:
      • familial - x-linked recessive
        • chrom.#: Xq28
        • gene: coagulation factor VIIIc
        PATHOGENESIS:
        1. Background
        • Factor VIII is a complex of two components each with different genetic control and biochemical functions:
        • 1. Factor VIIIc - coagulation protein
        • 2. Factor VIIIvW - platelet adhesion protein
        • Factor VIIIc is the final component of the Intrinsic Pathway and in the presence of activated Factor IX, activates Factor
        • X within the Common Pathway
        • Factor VIIIc is complexed with Factor VIIIvW, the latter acting as a carrier protein
        • in Hemophilia A, the plasma levels of Factor VIIIvW are normal
          • female carriers and male fetuses in utero have a Factor VIIIc/Factor VIIIvW ratio less than 1 (normally this ratio is equal to 1)
          2. Genetic Defect
          • 1. Severe
            • onset of bleeding in the newborn period
              • Factor VIIIc does not cross the placenta
              • hematomas after injections or circumcision
              • hemarthroses and deep tissue hemorrhages
            • bleeding may be spontaneous
            • clinical evidence of increased bleeding in 90% of these patients by 1 yr of age
          • 2. Moderate
  • 33. Alphanate Online Alphanate Description Antihemophilic Factor - RxList Monographs
    with links to full prescribing for this Factor VIII replacement used to prevent and control bleeding in patients with hemophilia A.......
    http://www.rxlist.com/cgi/generic2/hemofilm.htm
    Antihemophilic Factor RxPulse Industry Update: Claritin OTC Switch HEADLINES Please, take our 1 second survey! MEN'S HEALTH ... WEIGHT LOSS
    DESCRIPTION
    Antihemophilic Factor (Human) (AHF), Hemofil M, Method M, Monoclonal Purified, is a sterile, nonpyrogenic, dried preparation of antihemophilic factor (Factor VIII, Factor VIII:C, AHF) in concentrated form with a specific activity range of 2 to 15 AHF International Units/mg of total protein. When reconstituted with the appropriate volume of diluent, it contains approximately 12.5 mg/mL Albumin (Human), 1.5 mg/mL polyethylene glycol (3350), 0.055 M histidine and 0.030 M glycine as stabilizing agents. In the absence of the added Albumin (Human), the specific activity is approximately 2,000 AHF International Units/mg of protein. It also contains, per AHF International Unit, not more than 0.1 ng mouse protein, 18 ng organic solvent (tri-n-butyl phosphate) and 50 ng detergent (octoxynol 9). See Clinical PHARMACOLOGY Hemofil M AHF is prepared by the Method M process from pooled human plasma by immunoaffinity chromatography utilizing a murine monoclonal antibody to Factor VIII:C, followed by an

    34. HEMOPHILIA C
    Pediatric Database (PEDBASE); Discipline H O; Last Updated 8/28/93hemophilia C. DEFINITION A coagulation disorder characterized
    http://www.icondata.com/health/pedbase/files/HEMOPHI3.HTM
  • Pediatric Database (PEDBASE)
  • Last Updated: 8/28/93
    HEMOPHILIA C
    DEFINITION:
    A coagulation disorder characterized by a deficiency in Factor XI resulting in a bleeding diathesis.
    EPIDEMIOLOGY:
    • incidence: rare (2-3% of Hemophilias)
    • age of onset:
      • childhood
    • risk factors:
      • familial - autosomal recessive
        • chrom.#: 4q35
        • gene: coagulation factor XI
      • Ashkenazi Jews
      PATHOGENESIS:
      1. Background
      • Factor XI is a component of the Intrinsic Pathway and in its activated form (XIa) activates Factor IX
      2. Genetic Defect
      • only homozygotes have a bleeding problem
      • no spontaneous bleeding
      CLINICAL FEATURES:
      1. Hematological Manifestations
      • epistaxis
      • hematuria
      • menorrhagia
      • postoperative and post trauma
      INVESTIGATIONS:
      1. Serum
      • prolonged PTT
      • decreased Factor XI
        • homozygotes: 1-10% of normal
        • heterozygotes: 30-65% of normal
      • normal PT, bleeding time, thrombin time, platelet count
      MANAGEMENT:
      1. Supportive
      • avoid trauma and anticoagulants (i.e., ASA)
      • pressure and cold compresses to bleeding sites
      2. Replacement Therapy
      • Fresh Frozen Plasma
        • 10-15cc/kg q24h
  • 35. Hemophilia Federation Of America - Index
    Please Enter Here, © 2001 hemophilia Federation of America All Rights Reserved
    http://www.hemophiliafed.org/
    Please Enter Here

    36. Comprehensive Hemophilia Treatment Center
    Specialty section of larger website provides detailed information on hemophilia conditions, describing available treatment programs for children and adults, procedures for contact.
    http://www.mcg.edu/centers/Hemo/index.html

    37. Gene Therapy Website
    The Gene Therapy Program is located in the Department of Medicine and affiliated with the Stanley S. Scott Cancer Center and the Center for Human and Molecular Genetics at Louisiana State University Health Sciences Center at New Orleans. The major aim of the LSUHSC Gene Therapy Program is to develop new therapies for a series of genetic and acquired diseases including Cystic Fibrosis, hemophilia, Krabbes Disease and infectious diseases such as AIDS, TB, and pneumonia.
    http://www.medschool.lsumc.edu/GeneTherapy/Default.htm
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    38. Hemophilia Reports
    hemophilia Links. MRI Findings in Hemophilic Joints Treated With Radiosynoviorthesis.Anaerobic Power and Muscle Strength in Young Patients With hemophilia A.
    http://www.mmhc.com/hemo/
    mmhc home
    Hemophilia Links
    The following are articles in this month's journal.Use our archive to search for previous articles.
    Volume 7, Number 4
    Intraosseous Hematoma in a Newborn as a Presenting Sign of Factor VIII Deficiency

    MRI Findings in Hemophilic Joints Treated With Radiosynoviorthesis

    Anaerobic Power and Muscle Strength in Young Patients With Hemophilia A

    MultiMedia Health Care/Freedom LLC

    For more information, email info@mmhc.com

    39. Care For Life
    hemophilia home care, full service pharmacy that provides all products and therapies (including alternative therapies such as herbal remedies, vitamins and weight gain supplements) needed to treat hemophilia, other bleeding disorders and their complications including HIV, AIDS, hepatitis, liver disease, joint disease and arthritis.
    http://www.careforlife.com/

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    Learn what Care for Life can offer you and your patients!
    Factor Mat

    These effective learning tools were developed for you by Care for Life's experienced clinical staff.
    Ask the Pharmacist

    Bleeding Disorders

    Infectious Disease States
    MentalHealth ... Respiratory

    40. Hemophiliaofiowa.org
    FEDERACION ESPANOLA DE HEMOFILIA. You are visitor FastCounter by LinkExchangeSince 1 April, 1999. Please bookmark this page for counting purposes.
    http://www.hemophiliaofiowa.org/
    This page last revised: Welcome!!!!!
    What Is Hemophilia?... Chapter Profile...
    (Also here; Membership, Donation and Scholarship Information)
    "THE BLOOD LINK "...
    (The electronic version of our quarterly newsletter, "The Bloodline", which is produced to keep members informed of educational information, activities, meetings and to help provide support.)
    Social Events and Activities
    Contact Information... Other Important Links... "TEEN CONNECTION", Keep your eyes on this page! This is for you! (TEEN CONNECTION is an APEX sponsored program that the Hemophilia of Iowa, Inc. is in the process of incorporating into its operations.) For more information, please contact Pam Doell (with APEX) here. This page is hosted by LIGHTHOUSE COMMUNICATIONS, INC If you are in need of registering your domain name, click here for www.nameme.net .......THANK YOU !!!!!!!!!!!!!! Your input is appreciated. Please e-mail your questions or comments to the Web Page Administrator.

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