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Hemophilia:     more books (101)

31st Hemophilia Symposium Hamburg 2000 The 2002 Official Patient's Sourcebook on Hemophilia 34th Hemophilia Symposium Hamburg 2003: HIV Infection and Epidemiology; Management of Bleedings in Hemophiliacs with Inhibitors;Orthopedic Problems and ... C;Pediatric Hemostaseology;Free Lectures Diagnosis and treatment of hemophilia;: A practical guide by Herbert S Strauss, 1972 Hemophilia Care in the New Millennium (Advances in Experimental Medicine and Biology) Textbook of Hemophilia Hemophilia: Webster's Timeline History, 1820 - 2007 by Icon Group International, 2009-02-20 33rd Hemophilia Symposium Hamburg 2002: Epidemiology; New Findings and Possibilities in the Therapy of Antibodies; Hemophilia: Therapeutic Exercise and ... Pediatric Hemostasiology; Free Lectures Hemophilia - A Medical Dictionary, Bibliography, and Annotated Research Guide to Internet References by Health Publica Icon Health Publications, 2004-01-09 30th Hemophilia Symposium Hamburg 1999: HIV Infection and Epidemiology in Hemophilia; Gene Therapy in Hemophilia A and B; Therapy of Hepatitis C; Inhibitors ... Pediatric Hemostasiology; Case Reports Handbook of Hematology Research: Hemorheology, Hemophilia and Blood Coagulation (Recent Advances in Hematology Research) Hemophilia: A Study in Hope and Reality by Alfred Hyman Katz, 1970-06 Treatment of Hemophilia and Von Willebrand's Disease: New Developments by Robert G. Westphal, 1990-05 Orthopedic Surgery in Patients with Hemophilia

lists with details

41. 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
    
    Extractions: @import url(/medlineplus/images/advanced.css); Skip navigation Other encyclopedia topics: A-Ag Ah-Ap Aq-Az B-Bk ... Z Contents of this page: 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. In this disorder, bleeding ranges from mild to severe. When certain coagulation factors are deficient or missing, the chain reaction does not take place normally. Factor V is rare, and can be caused by inheriting a defective Factor V gene or by acquiring an antibody that interferes with normal Factor V function. An inhibitor of Factor V can be acquired after giving birth, after surgery, with automimmune diseases and certain cancers, in patients being treated wtih a certain type of fibrin glue, and from unknown sources.

42. Octagen Corporation | Developing New Therapies For Hemophilia
    Privately held company developing therapies for hemophilia and other genetic disorders, using recombinant Factor VIII and gene therapy. Includes clinical trial status, licensing, corporate profile and contacts in Bala Cynwyd, Pennsylvania.  
    http://www.octagen.com/

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

44. A Little Web Page About Me...
    Personal information, photos, growing up with hemophilia and favourite links.  
    http://hometown.aol.com/jscott420/JScott420.html
    
    Extractions: htmlAdWH('93212823', '728', '90'); Main Other Disabilities CNN, MSNBC, ... FOX NEWS Growing up and living with Hemophilia... I am 26 years old, living with severe Hemophilia A. As a kid, dealing with hemophilia and/or other types of bleeding disorders is a little bit more difficult than when you get older. When I was a young kid, I had to learn what my body could handle without causing internal bleeding. I wanted to play football, I wanted to wrestle, I wanted to jump on our trampoline with my older sister and cousins.. :) just had to learn the hard way in some of those cases.. well, this is me.. just chillin gettin ready to head out for a bit.. I'm a very romantic guy, always out to please my lady.. ;) My main interests are camping, rafting, hiking, rock climbing, boating, playing the lastest video games, fixin up my car, checkin out the stars at night when its clear. I am a counselor for a youth camp for kids with bleeding disorders, helping kids have a chance to experience activities that they otherwise would not have the opportunity to fully participate in. E-mail me for additional information about camp.

45. Hemophilia
    hemophilia resources, support groups, clinics with genetic counselors and geneticists.  
    http://www.kumc.edu/gec/support/hemophil.html

46. FAMOHIO Hemophilia Home Page
    Promotes the sharing of knowledge, experiences and concerns among those individuals with hemophilia and related bleeding disorders.  
    http://www.famohio.org/
    
    Extractions: Welcome To FAMOHIO ! FAMOHIO promotes the sharing of knowledge, experiences and concerns among those individuals with hemophilia and related bleeding disorders. FAMOHIO is a registered 501(c)(3) charity. Click on the FAMOHIO logo to enter the main site or select one of the shortcuts below. Visitors To FAMOHIO Portions of the FAMOHIO web site were last updated on August 30, 2005 FAMOHIO 2006 will be August 4 - 6 in Columbus, Ohio. FAMOHIO, Inc

47. Care For Life
    Provides products and therapies designed to treat hemophilia and other bleeding disorders.  
    http://www.careforlife.com/

48. Hemophilia - Medical Information On Treatment Options, And Links To Other Sites.
    Information on hemophilia, diagnosis, symptoms, treatment issues, and patient information.  
    http://www.mdsa.bc.ca/hemophilia.html
    
    Extractions: Haemophilia or hemophilia is the name of any of several hereditary genetic illnesses that impair the body's ability to control bleeding. Genetic deficiencies (or, very rarely, an autoimmune disorder) cause lowered plasma clotting factor activity so as to compromise blood-clotting; when a blood vessel is injured, a scab will not form and the vessel can continue to bleed excessively for a very long period of time. The bleeding can be external, if the skin is broken by a scrape, cut or abrasion, or it can be internal, into muscles, joints or hollow organs. Causes Haemophilia is generally caused by a mutation affecting the genes encoding one of the clotting factors. The genes for the most common form, Haemophilia A , are located on the X chromosome, so haemophilia is usually a sex-linked trait. Women have two X-chromosomes, whereas men have one X and one Y chromosome. Since the mutations causing the disease are recessive, a woman carrying the defect on one of her X-chromosomes will not be affected by it, as the equivalent allele on her other chromosome would express itself to produce the necessary clotting factors. However the Y-chromosome in men has no gene for factors VIII or IX. If the gene responsible for blood clotting on a man's X-chromosome is deficient there is no equivalent on the Y-chromosome, so the deficient gene is not masked by the dominant allele and he will develop the illness. Since a man receives his single X-chromosome from his mother, the son of a healthy woman silently carrying the deficient gene will have a 50% chance of inheriting that gene from her and with it the disease. In contrast, for a woman to inherit the disease, she must receive two deficient X-chromosomes, one from her mother and the other from her father (who must therefore be a haemophiliac himself). Hence haemophilia is far more common among men than women. However, haemophiliac daughters are more common than they once were, as improved treatment for haemophilia means that more men survive to adulthood and become parents. Adult women with haemophilia menstruate periodically, so they must take clotting factor to survive.

49. NHF | MASAC Recommendation #130 | Use Of Therapeutic Ultrasound To Aid In Blood
    Recommendations approved by the Medical and Scientific Advisory Council (MASAC) of the National hemophilia Foundation regarding the use of therapeutic ultrasound to aid in blood resorption  
    http://www.hemophilia.org/research/masac/masac130.htm
    
    Extractions: MASAC Document #130 MASAC Recommendation Regarding the Use of Therapeutic Ultrasound to Aid in Blood Resorption The following recommendation was approved by the Medical and Scientific Advisory Council (MASAC) of the National Hemophilia Foundation on March 24, 2002, and adopted by the NHF Board of Directors on April 15, 2002. Background Therapeutic ultrasound is a physical modality in which nonionizing radiation, in the form of sound, is transferred to the body's tissues and absorbed as heat. It is applied at frequencies of 1.0 MHz and 3.0 MHz and is the most commonly used deep-heating modality, capable of reaching depths of five centimeters and more below body surface. Ultrasound, like short-wave diathermy, may be applied in the continuous format or in pulsed waves to apply therapeutic heat and nonthermal effects. One intended use of ultrasound is to achieve the benefits of deep heating. As with other methods of therapeutic heat, the use of ultrasound in this capacity is thought to increase collagen extensibility, circulation, pain threshold, enzymatic activity, cell membrane permeability, and nerve conduction velocity. Conversely, use of ultrasound in the pulsed mode has been proposed to have the nonthermal effects of acoustic streaming, cavitation, and micromassage caused by the mechanical vibration of the sound waves. Nonthermal benefits are reported to increase cellular activity and protein synthesis and to decrease edema. Until recently, ultrasound was applied clinically in hopes of gaining the above benefits, based on a limited theoretical basis. However, in a recent review published by Baker et al. in

50. Royal Hemophilia Pedigree
    A Pedigree of hemophilia in the Royal Families of Europe World Federation of hemophilia National hemophilia Foundation hemophilia Home Page  
    http://www.people.virginia.edu/~rjh9u/roylhema.html

51. FACTOR FOUNDATION HOME
    Locating financial support for those dealing with hemophilia and related bleeding disorders. Membership.  
    http://www.factorfoundation.org/

52. Hemophilia Of Iowa, Inc
    What is hemophilia? Chapter Profile Social Events and Activities The BloodLink Contact Information Other Important Links  
    http://www.hemophiliaofiowa.org/

53. Welcome To The Nevada Childhood Cancer Foundation
    Organization provides social, emotional, psychological and educational support for families of children with critical illnesses including HIV/AIDS, hemophilia, sickle cell anemia, cancer, and immunological and renal diseases.  
    http://nvccf.org
    
    Extractions: The Nevada Childhood Cancer Foundation, working side-by-side with the medical team, provides social, emotional, educational and psychological support services to families of all children who are diagnosed with life threatening or critical illnesses such as cancer, HIV/AIDS, sickle cell anemia and other immunological diseases. 12th Annual

54. How To Deal With Hemophilia
    If a person has hemophilia, his blood doesn t clot as it should. What does that mean? Find out in this article for kids.  
    http://kidshealth.org/kid/health_problems/blood/hemophilia.html
    
    Extractions: Hemophilia (say: hee-muh- fih -lee-uh) is a genetic disorder in which a person's blood does not clot properly. "Hemo" means blood and "philia" means a tendency toward. A person who has hemophilia has a tendency to bleed excessively. Think of the last time you had a cut or scrape. When the bleeding stops on its own, you're seeing clotting in action. A Bit About Blood If your blood is clotting normally, your body naturally protects itself. Platelets , which are "sticky cells," go to where the bleeding occurs and cover the hole, plugging it up. This is the first step in the clotting process. When the platelets plug the hole, they release chemicals that attract more sticky platelets and also activate various clotting factors, which are proteins in the blood. These proteins mix with the platelets to form fibers, which make the clot stronger and stop the bleeding. Our bodies have 12 clotting factors that work together to make fibrinogen (say: fy- brih -nuh-jun), the substance that makes the fibers. Trouble begins if the body is missing one of these factors.

55. TSE - Transmissible Spongiform Encephalopathies
    List of all transmissible spongiform encephalopathies affecting humans.  
    http://www.hemophilia.ca/en/4.2.php

56. Hemophilia
    For guys with a rare bleeding disorder called hemophilia, minor cuts and bruises can be a big deal. The good news is that it s a lot easier to control now  
    http://kidshealth.org/teen/diseases_conditions/blood/hemophilia.html
    
    Extractions: Hemophilia is a disease that prevents a person's blood from clotting properly, which means that the person bleeds more than a person without hemophilia does. It's a genetic disorder, which means it's the result of a change in genes that's either inherited (passed on from parent to child) or that happens during development in the womb. "Hemo" means blood and "philia" means a tendency toward. A person who has hemophilia has a tendency to bleed excessively. Hemophilia affects mostly boys, although it's very rare: Only about one in every 8,000 boys is born with hemophilia. The disease can affect people of any race or nationality. For most people, when they get a cut, the body naturally protects itself. Sticky cells in the blood called platelets go to where the bleeding is and plug up the hole. This is the first step in the clotting process. When the platelets plug the hole, they release chemicals that attract more sticky platelets and also activate various proteins in the blood known as

57. Îáùåñòâî áîëüíûõ ãåìîôèëèåé/Association For Persons Wit
    Top/World/Russian/Здоровье/Заболевания/Гемофилия  
    http://www.blood.ru/hemophilia/

58. Welcome To HFA
    The hemophilia Federation of America is a national nonprofit organization HFA provides HAWC (hemophilia Adult Weekend Camp) information and registration  
    http://www.hemophiliafed.org/
    
    Extractions: /*********************************************** * AnyLink CSS Menu script- © Dynamic Drive DHTML code library (www.dynamicdrive.com) * This notice MUST stay intact for legal use * Visit Dynamic Drive at http://www.dynamicdrive.com/ for full source code ***********************************************/ Home FAQ Annual Report Patient Notification ... Contact Us URGENT MESSAGE TO ALL! In times of crisis, "Family comes first"! The Hemophilia Federation of America announces the creation of the Hemophilia Disaster Relief Fund to assist families with blood clotting disorders that have been affected by natural disasters. To donate to this fund, click below: DONATE TO THE HFA DISASTER RELIEF FUND Thanks to our donors (opens in a new window) OUR MISSION T he Hemophilia Federation of America is a national nonprofit organization that assists and advocates for the blood clotting disorders community. OUR VISION T he vision of the Hemophilia Federation of America is that the blood clotting disorders community has removed all barriers to both choice of treatment and quality of life. SYMPOSIUM 2006 Our 2006 Annual Meeting and Symposium will be held March 30 through April 2, 2006 in St. Louis, Missouri. Click the link below for more information.

59. Medical And Hemophilia References
    Personal page from Rick and Linda Thomas.  
    http://www.geocities.com/HotSprings/3160/medpage.html

60. EMedicine - Hemophilia, Type B : Article By Brendan R Furlong, MD
    hemophilia, Type B hemophilia B is an inherited, X-linked, recessive disorder resulting in deficiency of functional plasma coagulation factor IX.  
    http://www.emedicine.com/emerg/topic240.htm
    
    Extractions: (advertisement) Home Specialties Resource Centers CME ... Patient Education Articles Images CME Patient Education Advanced Search Consumer Health Link to this site Back to: eMedicine Specialties Emergency Medicine Hematology And Oncology Last Updated: June 23, 2004 Rate this Article Email to a Colleague AUTHOR INFORMATION Section 1 of 10 Author Information Introduction Clinical Differentials ... Bibliography Author: Brendan R Furlong, MD , Clinical Chief, Department of Emergency Medicine, Georgetown University Hospital Coauthor(s): Mary A Furlong, MD , Assistant Professor, Department of Pathology, Georgetown University School of Medicine Brendan R Furlong, MD, is a member of the following medical societies: American College of Emergency Physicians Editor(s): William Gossman, MD , Assistant Professor, Department of Emergency Medicine, Rosalind Franklin University of Medicine and Science, Project Medical Director, Department of Emergency Medicine, Mount Sinai Hospital; Francisco Talavera, PharmD, PhD

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