Extractions: Dictionaries: General Computing Medical Legal Encyclopedia Word: Word Starts with Ends with Definition Noun E. A. von Willebrand - Finnish physician who first described vascular hemophilia (1870-1949) Erik Adolf von Willebrand Erik von Willebrand von Willebrand Willebrand ... medico - a licensed medical practitioner; "I felt so bad I went to see my doctor" Legend: Synonyms Related Words Antonyms Some words with "E. A. von Willebrand" in the definition: angiohemophilia
Extractions: Dictionaries: General Computing Medical Legal Encyclopedia Word: Word Starts with Ends with Definition Noun Erik von Willebrand - Finnish physician who first described vascular hemophilia (1870-1949) E. A. von Willebrand Erik Adolf von Willebrand von Willebrand Willebrand ... medico - a licensed medical practitioner; "I felt so bad I went to see my doctor" Legend: Synonyms Related Words Antonyms Some words with "Erik von Willebrand" in the definition: angiohemophilia
Von Willebrand Kampagne Her er du Danmarks Bløderforening Projekter, kampagner, Landsindsamling von willebrand Kampagne. von willebrand oplysningskampagne. http://www.bloderforeningen.dk/neobuilder.2003102212522101000050202.html
Extractions: Her er du : Danmarks Bløderforening Projekter, kampagner, Landsindsamling Von Willebrand Kampagne I Juni 2001 fik Bløderforeningen tilsagn om støtte til at gennemføre en oplysningskampagne om von Willebrands sygdom fra Apotekerfonden af 1991. Kampagnen foregår i samarbejde med de danske hæmofililæger og repræsentanter fra Dansk selskab for almen medicin (DSAM) og Dansk Selskab for Obstetrik og Gynækologi (DSOG). Politikens artikel om von Willebrands sygdom »
Von Willebrand von willebrands sygdom skyldes, at man enten har for lidt eller sletintet - af den størkningsfaktor, som hedder von willebrand-faktor. http://www.bloderforeningen.dk/faktavonwillebrand
Extractions: Her er du : Danmarks Bløderforening Sygdomsfakta Sygdomsbeskrivelser Von Willebrand Von Willebrands sygdom er den mest almindelige blødersygdom i verden og rammer omkring 1% af befolkningen. Både kvinder og mænd kan have von Willebrands sygdom. Men kun få er klar over at de har sygdommen, og kun få kender mulighederne for behandling. Nogle får ofte næseblod men har lært at leve med det. Andre døjer med kraftige menstruationer uden nogensinde at blive behandlet, for "det ligger bare til familien". Men det påvirker ens hverdag, og der skal ikke så meget til for at undgå problemer. Von Willebrands sygdom skyldes, at man enten har for lidt - eller slet intet - af den størkningsfaktor, som hedder von Willebrand-faktor. Det kan også være, at man har faktor nok, men at den er forkert opbygget. Når der er noget galt med von Willebrand-faktoren, tager det længere tid for en blødning at standse. Der findes 3 forskellige hovedtyper af von Willebrands sygdom, hvor type 1 er den mildeste og den mest udbredte. Type 3 er den sværeste, men også den mest sjældne.
Testing Your Knowledge About Von Willebrand Disease Testing Your Knowledge About von willebrand Disease. News Canada. Takethis quiz to test your own knowledge of von willebrand Disease http://www.theallineed.com/ad-health-2/health-039.htm
Extractions: Testing Your Knowledge About Von Willebrand Disease News Canada (NC)-A survey conducted by Leger Marketing in February 2002 showed that Canadians are more likely to identify von Willebrand as a German car, an Austrian coat of arms, or a school of mathematics before it's true definition. Only seven per cent of Canadians chose the correct answer - the most common inherited bleeding disorder.
Hemophilia Of Georgia - Von Willebrand Disease Learn about von willebrand Disease. What is von willebrand Disease? Oneof the most common bleeding disorders is von willebrand Disease. http://www.hog.org/vwd.htm
Extractions: One of the most common bleeding disorders is von Willebrand Disease. It is named for the doctor from Finland who first described it. Von Willebrand Disease is often written and said "vWD." Like hemophilia, vWD is passed on through the genes from parent to child. But unlike hemophilia, men and women have an equal chance of getting vWD. People who have von Willebrand Disease don't have enough of a certain protein in their blood. This protein is called "von Willebrand factor". This factor is needed for platelets in the blood to work right. When a blood vessel is damaged, platelets move to the spot to plug the hole. Von Willebrand factor is what allows the platelets to stick to the blood vessel wall and to each other. In a person with vWD, the platelets can't stick together enough to make a good platelet plug. The bleeding will last longer. Unlike hemophilia, vWD is more likely to cause bleeding under the skin, easy bruising and nosebleeds. People with vWD rarely bleed into their joints. It is possible, though, for a person to have both von Willebrand Disease and hemophilia.
Von Willebrand Disease, Cincinnati Children's Hospital Medical Center Cincinnati Children s Hospital Medical Center discusses von willebrand Disease(vWd) and occurs in both males and females. von willebrand Disease. http://www.cincinnatichildrens.org/health/info/blood/diagnose/von-willebrand.htm
Extractions: The most commonly inherited bleeding disorder is von Willebrand Disease (vWd) and occurs in both males and females. Von Willebrand Factor (vWF) is a clotting protein in the blood. It is produced in the cells that line the blood vessels and then is released into the blood stream. Bleeding occurs when blood vessels are injured. Platelets, a type of blood cell, stick to the injured vessel and form a platelet plug. Von Willebrand factor acts as a glue to help the platelets stick to the injury site. Simultaneously, other coagulation factors work together to form a clot, further sealing the area of damage. Von Willebrand Disease is known as an inherited or genetic disorder meaning it is passed down through families through information in the cells called genes. What are the signs and symptoms of von Willebrand Disease?
Von Willebrand Disease von willebrand Disease. http://omni.ac.uk/browse/mesh/C0042974L0042974.html
Extractions: low graphics broader: Hemorrhagic Disorders other: Hemophilia A Purpura, Thrombocytopenic, Idiopathic Thrombocythemia, Hemorrhagic Thrombocytopenia ... You don't have to be straight to take factor VIII This information booklet is aimed at gay and bisexual men living with a bleeding disorder (specifically haemophilia and von Willebrand's). Produced by the Haemophilia Society, this booklet addresses subjects like safety during sex, sexual health, sexually transmitted infections, and HIV. Links to organisations that can provide advice and support are provided. This 9 page document is in PDF, which requires Adobe Acrobat Reader. von Willebrand Disease Sexual Partners Sex Behavior Patient Education Handout [Publication Type] ... Hemophilia A
Other Bleeding Disorders Including Von Willebrand Disease von willebrand Disease. von willebrand disease (VWD) is a hereditarydisorder characterized by abnormally slow clotting of the blood. http://www.aventisbehring.com/ab/n25243/PFDiseaseCatProd4.htm
Extractions: Plasma Donors ... eNEWS Updates von Willebrand disease (VWD) is a hereditary disorder characterized by abnormally slow clotting of the blood. Patients with von Willebrand disease may have spontaneous and prolonged bleeding from the nose and gums. VWD occurs in about one in 100 persons and affects both males and females. von Willebrand disease occurs when one of the coagulation factors, called von Willebrand factor, does not work properly or when there is not enough in the blood. The lower the level of active von Willebrand factor in a person's blood, the more severe the disease. In many patients with von Willebrand disease, another coagulation factor, factor VIII, is also affected. People with von Willebrand disease need to boost the level of von Willebrand factor and factor VIII in their blood. People with mild or moderate type 1 von Willebrand disease may be infused with the chemical DDAVP (desmopressin acetate) or use a high-concentrate nasal spray containing DDAVP. DDAVP causes the release of von Willebrand factor from storage sites in the body and increases the level in the blood. Patients with type 2 or type 3 von Willebrand disease may need replacement von Willebrand factor and factor VIII.
Malattia Di Von Willebrand Su Scovato! Translate this page Malattia Di von willebrand - Vedi i Siti inerenti Malattia Di von willebrandsu Scovato.it! Abbiamo scovato Malattia Di von willebrand! http://www.scovato.it/bellezza_benessere/salute/malattia di von willebrand.html
HemophiliaVillage.com Also includes information on von willebrand disease. von willebranddisease. Discusses von willebrand disease and treatment options. http://www.hemophilia-village.net/von-willebrand-disease.htm
Extractions: helpful? yes no The conditions covered in this entry are haemophilia A, haemophilia B (Christmas disease), von Willebrand disease and some other coagulation defects. The haemophilias (hemophilias - US) are a group of inheritable blood disorders characterised by various defects in the blood clotting system. The clotting factors present in blood were initially known by Roman numerals, numbered from I to XIII. More recently described factors have been given names and some deficiencies are associated with excessive, rather than reduced, blood coagulation. Factor VIII is deficient in classical haemophilia, also known as haemophilia A. Factor IX is deficient in haemophilia B (also known as Christmas disease). Von Willebrand factor is deficient in von Willebrand disease and this results in a failure of platelet and vessel wall function with an associated reduction in factor VIII. In haemophilia A and B it is almost always males who are affected, with haemophilia A being five times as frequent as haemophilia B. Thus there are currently about 5,000 people with haemophilia A and 1,000 people with haemophilia B in the UK. Von Willebrand disease occurs equally in males and females and about 5,000 patients are registered in the UK but the real number of affected people is almost certainly much greater. These conditions affect all racial groups and occur worldwide.
Malattia Di Von Willebrand - Salute Translate this page Malattia Di von willebrand - Vedi i Siti inerenti Malattia Di von willebrandsu TuttoRicerche.it! .- Cercato Malattia Di von willebrand -.-. http://www.tuttoricerche.it/k46297_malattia-di-von-willebrand/
Extractions: Answer: The condition you have, von Willebrand's disease, is an inherited disorder that alters the blood's ability to clot. It's usually inherited as an autosomal dominant condition so that your daughter has, statistically, about a 50/50 chance of also having this disorder. Fortunately, the bleeding tendency in this condition is usually very mild, so mild that it is believed to be an underidentified, quite common disorder. It seems to occur in about 1 in 100 people, although the exact incidence is unknown. It occurs equally in men and women and in all racial groups. We have the technology available at major medical centers to identify the platelet and serum abnormalities on a small blood sample. In the newborn period it's difficult to be sure of the results, but after that, it's a matter of when you want to draw the blood sample. Clinically there is rarely a problem in infancy. When a toddler starts getting around and is likely to get a bump or two, this condition shows up, often as a bloody nose or a mouth cut that is slow to stop bleeding.
Extractions: Indication for Use: For use in adult patients for treatment and prevention of bleeding in hemophilia A (classic hemophilia) and in adult and pediatric patients for treatment of spontaneous and trauma-induced bleeding episodes in severe von Willebrand disease and in mild and moderate von Willebrand disease where use of desmopressin is known or suspected to be inadequate
Verenigingen Hemofilie En Ziekte Van Von Willebrand Verenigingen Hemofilie en Ziekte van von willebrand. Vereniging vanHemofilielijders en von willebrandzieken vzw (AHVH) Dekenijstraat http://www.health.fgov.be/AGP/nl/praktische-informatie/verenigingen/verenigingen
Comparative Coagulation Lab - Canine Von Willebrand Disease NYS Animal Health Diagnostic Lab, Coag Section Home. Canine von willebrandDisease. Background. Clinical Signs. Treatment. Laboratory Diagnosis. http://web.vet.cornell.edu/public/coaglab/clinical_topics/vWD.htm
Hemophilia Is The Most Common Bleeding Disorder Lists bleeding disorders, including hemophilia and von willebrand s disease. Treatmentof von willebrand s disease may not be necessary for daily life. http://www.coagulation-factors.com/html/bleeding-disorders.php3
Extractions: Bleeding disorders are the opposite of thrombophilia, and include hemophilia, von Willebrand's disease, and thrombocytopenia. Rather than causing a deep vein thrombosis or embolism, bleeding disorders make clot formation difficult. People with bleeding disorders bleed easily, and may lose excessive amounts of blood from injuries, surgery, or dental work. Severe bleeding disorders may even cause spontaneous bleeding. Hemophilia is perhaps the best known of the bleeding disorders. Hemophilia is a genetic disorder caused by mutations of genes on the X chromosome. Because the mutated gene is recessive, the majority of hemophiliacs are male. A more detailed explanation of the role genetics play in hemophilia can be found on the Causes of Hemophilia web site. Von Willebrand's factor is a protein that allows platelets to form temporary plugs at sites of blood vessel injury: an event that is essential if a solid blood clot is to form. Von Willebrand's disease causes defects in von Willebrand's factor, impairing the ability of platelet cells to 'cling' to an injury and form a plug.
