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         Hemophilia:     more books (100)
  1. Activated Prothrombin Complex Concentrates: Managing Hemophilia with Factor VIII Inhibitor
  2. 36th Hemophilia Symposium Hamburg 2005: Epidemiology; Hemophilia Therapy; Orthopedic Treatment in Hemophiliacs; Hemostaseologic Diagnosis; Pediatric Hemostaseology; Free Lectures
  3. 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
  4. Haemophilia;: Proceedings of the 7th congress of the World Federation of Haemophilia, May 17-20, 1971, Tehran (International congress series) by World Federation of Hemophilia, 1973
  5. USGS-OFR by Laureen A Kelley, 1991
  6. The Hemophilia Handbook.
  7. Raising a Child with Hemophilia - A Practical Guide for Parents (3rd Ed.) by Laureen A.: Kelley, 1999
  8. The hemophilia educational resources list by Rhonda Bisker, 1981
  9. Hemophilia and Related Disorders of Hemostasis
  10. Hemophilia and hemostasis (Progress in clinical and biological research)
  11. Hemophilia: Current medical management by Jonathan C Goldsmith, 1994
  12. Hemophilia: How to be a more responsible, effective parent by Laureen A Kelley, 1994
  13. HIV disease in people with hemophilia: Your questions answered by Glenn F Pierce, 1991
  14. The social and psychological aspects of hemophilia on the hemophiliac and his family (Alternate plan paper / Mankato State University. Vocational Rehabilitation) by Rosemary Braun, 1983

121. 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:

122. 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

123. Introduction: Autoimmune Hemophilia - WrongDiagnosis.com
Introduction to Autoimmune hemophilia as a medical condition including symptoms, diagnosis, misdiagnosis, treatment, prevention, and prognosis.
http://www.wrongdiagnosis.com/a/autoimmune_hemophilia/intro.htm
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Next sections Basic Summary for Autoimmune Hemophilia Glossary for Autoimmune Hemophilia Next chapters: Autoimmune Interstitial Cystitis Autoimmune Diabetes Insipidus Autoimmune Endometriosis Chronic Fatigue Syndrome ... Feedback
Introduction: Autoimmune Hemophilia
Autoimmune Hemophilia: Blood clotting failure caused by autoimmunity. Contents for Autoimmune Hemophilia: Diseases Did we miss something? Please provide feedback or suggestions By using this site you agree to our . Information provided on this site is for informational purposes only; it is not intended as a substitute for advice from your own medical team. The information on this site is not to be used for diagnosing or treating any health concerns you may have - please contact your physician or health care professional for all your medical needs. Please see our IMPORTANT! Use of this site is subject to our

124. Hemophilia A
hemophilia A hemophilia A is a hereditary blood disorder, primarily affecting males Babylonian Jews first described hemophilia more than 1700 years ago;
http://www.ncbi.nlm.nih.gov/books/bv.fcgi?call=bv.View..ShowSection&rid=gnd.sect

125. OMIM - HEMOPHILIA B; HEMB

http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=306900

126. 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

127. Hemophilia Emergency Care

http://www.hemophiliaemergencycare.com/

128. 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.

129. Hemophilia - Health Conditions - Conditions & Treatments - DrugDigest
hemophilia is a bleeding disorder that occurs almost exclusively among boys and men. Currently hemophilia is not curable, but most cases of it can now be
http://www.drugdigest.org/DD/HC/HCIntro/0,4043,550488,00.html
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Hemophilia Introduction In the late 1800s and early 1900s, hemophilia was sometimes called "The Royal Disease", because many members of the English, German, Russian and Spanish royal families either had it or carried it. Until the 1960's, when clotting factors were identified, the only treatment for hemophilia was blood transfusions. Unfortunately, not enough of the needed clotting factors are present in whole blood or blood plasma to stop serious internal bleeding, so most individuals with severe hemophilia died before reaching adulthood. Others suffered painful and disabling joint damage. Today, because hemophilia can be controlled with clotting factor products, most individuals who have it lead nearly normal lives. Excellent resources, including support groups, are available for individuals with hemophilia and their families. Research, especially in the field of gene therapy, offers hope for better treatment and even a cure in the not-too-distant future. What is it?

130. 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.
Hurricane Katrina
Updates! Information and Services If you are a Hemophilia Chapter and receive a call for assistance from Louisiana Families that are in your area, please contact us so that we may work together in providing services. Thank you so much for making our families part of your family! Contact LHF at 225-291-1675 or 1-800-749-1680.
LHF Updates To contact the Tulane Hemophilia Treatment Center staff, call Sue duTreil at 800-230-9797 or 337-261-9787. The direct number for Gulf States Hemophilia Center is 713-500-8360. They will be assisting patients with their factor/Medical needs. If you normally receive your product from a home health representative, but are having trouble reaching your representative please call the LHF office. If you are dislocated from Hurricane Katrina and are willing to relocate we are getting some offers from people across the country who would like to provide housing for people. Please contact us and we will assist you in getting more information.

131. 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

132. Andrews, Tom A Language Of Hemophilia
Finally, the poet finds words for the endless rhythm of hemophilia, The Language of hemophilia is an exploration of sounds and words and phrases that
http://endeavor.med.nyu.edu/lit-med/lit-med-db/webdocs/webdescrips/andrews12148-
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Andrews, Tom A Language of Hemophilia
Genre Poem (17 pp.) Keywords Anatomy Arthritis Body Self-Image Disability ... Trauma Summary This long poem in 20 sections seeks to explore, dissect, and create a language for the experience of hemophilia. "Blood pools in a joint / The limb locks . . . " The poet first dissects words like "trans / fusion" and "hema / toma," and showers the reader with images (like splatters of blood?). In section 5 he states his purpose in the familiar jargon of educational objectives and later, in section 10, he utilizes spacing and line breaks to convert standard admonitions into poetry; for example, "These child- / ren should / not / be / punished, and / their / play with / other / children / should / be super- / vised . . . " Isolated phrases and sentences appearsome from the hospital and some from the "outside" world. In some phrases the worlds of outside and inside mix, as in "Arterial sunrise, capillary dusk." Section 13 consists of laboratory reports. The poem breathes in and out, between syllables and long lines, between prosaic statements and poetic images. Finally, the poet finds words for the endless rhythm of hemophilia, "Gratitude and / fearYour relentless / rhythmI move to / it still . . . "

133. HFNC Online Website
WANT TO VOLUNTEER FOR The hemophilia Foundation of Northern California? It is dedicated to the treatment and cure of hemophilia, related disorders and
http://www.hfnconline.org/
We are a proud member of the Agency # 925240
Click here to read about our HFNC 2004 Scholarship Winners!
Click here to read about and apply for the HFNC 2005 Memorial Scholarships!
WANT TO VOLUNTEER FOR The Hemophilia Foundation of Northern California?
Click on the icon above to download and complete our Volunteer Information Form! Tell us what you are interested in volunteering for and fax the completed form to our offices at 510-568-6111. We thank you in advance for volunteering your time and effort to support HFNC!
4:00 p.m to 8:00 p.m. Fairmont Sonoma Mission
100 Boyes Boulevard
Sonoma, CA 95476
CLICK HERE for all of the details!

Click Here for directions to the Fairmont Sonoma Mission Inn!
Hemophilia Foundation of
Northern California
Wine Country Classic

Golf Tournament

Monday, August 15, 2005
12:00 Noon Shotgun Start!
Sonoma Golf Club
17700 Arnold Drive Sonoma, CA 95476
Click Here for the 2005 Registration Form! Click Here for the schedule of the day, accomodation information, and other stuff!
WE'VE MOVED TO A NEW LOCATION!! "Camp Hemotion"

134. 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

135. Mendelian Laws Apply To Human Beings.

http://www.dnaftb.org/dnaftb/13/concept/

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