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  • Von Recklinghausens disease(neurofibromatosis)
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  • von willebrand s disease
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  • von Willebrands disease
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  • von willebrands factor
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  • hyperostosis corticalis generalisata ; Von Buchem s disease
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  • lindau-von hippel diseaes
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  • phenomenon, von Magnus
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  • von economo disease
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  • von gierkes disease
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  • von hippel-lindau disease
    ÆùÈüÆç ¸°µµ¿ìº´(¡­Ü»)
  • von recklinghausens disease
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  • von-myenberg complexes
    Æù¸ÞÀÌ¿£¹ö±×º¹ÇÕü
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  • von Willebrand's disease
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vWD von Willebrand Disease
vWF von Willebrand Factor
MW Mallory-Weiss [syndrome]; mean weight; megawatt; microwave; Minot-von Willebrand [syndrome]; molecul...
VIIIvwf von Willebrand factor
VW vascular wall; vessel wall; von Willebrand's [disease]
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AVWS Acquired von Willebrand syndrome
vWF Anti-von Willebrand factor
VIII-VWF VIII-von Willebrand factor
vWF FVIII)/von Willebrand factor
FVIII-vWF Factor VIII-von Willebrand Factor
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    von Willebrand Áúȯ
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CancerWEB ¿µ¿µ ÀÇÇлçÀü ¸ÂÃã °Ë»ö °á°ú : 5 ÆäÀÌÁö: 1
Von Willebrand disease <disease, haematology> A hereditary platelet disorder caused by defective or deficient Von Willebrand factor, a protein involved in normal blood clotting, that reduces adhesion to collagen but not aggregation. Both bleeding time and coagulation are increased. Factor VIII levels are secondarily reduced.
Symptoms include nosebleeds, bleeding gums, heavy menstrual bleeding, bruising and skin rashes.
Inheritance: autosomal dominant.
(30 Sep 1997)
Von Willebrand factor Plasma factor involved in platelet adhesion through an interaction with Factor VIII.
See: Von Willebrand disease.
(18 Nov 1997)
von Willebrand factor-degrading protease <enzyme> A large protease from normal human plasma that degrades vwf at the 842tyr-843met peptide bond
Registry number: EC 3.4.24.-
Synonym: vwf-cleaving protease
(26 Jun 1999)
Von Willebrand's disease <disease> This congenital disease, which is caused a deficiency of a blood factor that promotes platelet adhesion, is characterised by prolonged bleeding and poor blood coagulation.
(09 Oct 1997)
von Willebrand, E <person> Finnish physician, 1870-1949.
See: von Willebrand's disease.
(05 Mar 2000)
CancerWEB ¿µ¿µ ÀÇÇлçÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 1
Alder, Albert von <person>
See: Alder's anomaly, Alder bodies.
(05 Mar 2000)
Ammon, Friedrich von <person> German ophthalmologist and pathologist, 1799-1861.
See: Ammon's fissure, Ammon's prominence.
(05 Mar 2000)
Andernach, Johann von <person> German physician, 1505-1574.
See: Andernach's ossicles.
(05 Mar 2000)
Baer, Karl von <person> German-Russian embryologist, 1792-1876.
See: Baer's law, Baer's vesicle.
(05 Mar 2000)
Baeyer, Johann von <person> German chemist and Nobel laureate, 1835-1917.
See: Baeyer's theory.
(05 Mar 2000)
Bamberger, Heinrich von <person> Austrian physician, 1822-1888.
See: Bamberger's albuminuria, Bamberger's disease, Bamberger's sign.
(05 Mar 2000)
Basedow, Karl von <person> German physician, 1799-1854.
See: Basedow's disease, Basedow's pseudoparaplegia, Jod-Basedow phenomenon, Basedow's goiter.
(05 Mar 2000)
Baumgarten, P Clemons von <person> German pathologist, 1848-1928.
See: Baumgarten's veins, Cruveilhier-Baumgarten disease, Cruveilhier-Baumgarten murmur, Cruveilhier-Baumgarten sign, Cruveilhier-Baumgarten syndrome.
(05 Mar 2000)
Bechterew, Vladimir von <person> Russian neurologist, 1857-1927.
See: Bechterew's band, Bechterew's disease, layer of Bechterew, Bechterew's nucleus, Bechterew's sign, line of Bechterew, band of Kaes-Bechterew, Bechterew-Mendel reflex, Mendel-Bechterew reflex.
(05 Mar 2000)
Bezold, Albert von <person> German physiologist, 1836-1868.
See: Bezold's ganglion, Bezold-Jarisch reflex.
(05 Mar 2000)
Biesiadecki, Alfred von <person> Polish physician, 1839-1888.
See: Biesiadecki's fossa.
(05 Mar 2000)
Brucke, Ernst von <person> Austrian physiologist, 1819-1892.
See: Brucke's muscle, Brucke's tunic, Brucke-Bartley phenomenon.
(05 Mar 2000)
Brudzinski, Josef von <person> Polish physician, 1874-1917.
See: Brudzinski's sign.
(05 Mar 2000)
Brunn, Albert von <person> German anatomist, 1849-1895.
See: Brunn's membrane, Brunn's nests.
(05 Mar 2000)
Bruns, Ludwig von <person> German neurologist, 1858-1916.
See: Bruns ataxia, Bruns' nystagmus.
(05 Mar 2000)
MeSH(Medical Subject Headings) ¸ÂÃã °Ë»ö (http://www.nlm.nih.gov) °á°ú : 2 ÆäÀÌÁö: 1
  • von Willebrand Disease - »õâ Group of hemorrhagic disorders in which the von Willebrand factor (Factor VIII-related antigen) is either quantitatively or qualitatively abnormal. They are usually inherited as an autosomal dominant trait though rare kindreds are autosomal recessive. Symptoms vary depending on severity and disease type but may include prolonged bleeding time, deficiency of factor VIII, and impaired platelet adhesion.
    Synonyms : von Willebrand's Disease, Angiohemophilias, Disease, von Willebrand, Disease, von Willebrand's, Hemophilias, Vascular, Vascular Hemophilia, Vascular Hemophilias, von Willebrands Disease
  • von Willebrand Factor - »õâ A high-molecular-weight plasma protein, produced by endothelial cells and megakaryocytes, that is part of the factor VIII/von Willebrand factor complex. The von Willebrand factor has receptors for collagen, platelets, and ristocetin activity as well as the immunologically distinct antigenic determinants. It functions in adhesion of platelets to collagen and hemostatic plug formation. The prolonged bleeding time in von Willebrand's disease is due to the deficiency of this factor.
    Synonyms : F VIII-vWf, Factor VIIIR-Ag, Factor VIIIR-RCo, Plasma Factor VIII Complex, Ristocetin Cofactor, Ristocetin-Willebrand Factor, vWF Ag, von Willebrand Factor Type IIB, von Willebrand Protein, Ag, vWF, Antigen, Factor VIII-Related, Cofactor, Ristocetin, F VIII vWf
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von Willebrand's disease a form of hemophilia discovered by Erik von Willebrand; a genetic disorder that is inherited as an autosomal recessive trait; characterized by a deficiency of the coagulation factor and by mucosal bleeding
Ãâó: wordnet.princeton.edu/perl/webwn
von Willebrand's d. a congenital bleeding disorder, usually of autosomal dominant inheritance, characterized by deficiency of von Willebrand's factor, with prolonged bleeding time and often impairment of adhesion of platelets on glass beads, associated with epistaxis and increased bleeding after trauma or surgery, menorrhagia, and postpartum bleeding. Several different types have been distinguished, ranging from mild to severe. Called also angiohemophilia, pseudohemophilia, vascular hemophilia, Minot-von Willebrand syndrome, and Willebrand's syndrome.
Ãâó: www.mercksource.com/pp/us/cns/cns_health_library.j...
von Willebrand's disease, factor see under disease and factor.
Ãâó: www.mercksource.com/pp/us/cns/cns_health_library.j...
von Willebrand's f. a glycoprotein synthesized in endothelial cells and megakaryocytes that circulates complexed to factor VIII (see under coagulation f's); it mediates adhesion of platelets to damaged epithelial surfaces and may participate in platelet aggregation. Deficiency results in the prolonged bleeding time seen in von Willebrand's disease. NOTE: this factor was originally considered to be part of factor VIII, so that in older terminology the term factor VIII generally refers to the complex of the two factors.
Ãâó: www.mercksource.com/pp/us/cns/cns_health_library.j...
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von Willebrand Finnish physician who first described vascular hemophilia (1870-1949)
von Willebrand a form of hemophilia discovered by Erik von Willebrand
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