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Printer friendly dictionary, encyclopedia and thesaurus - the free dictionary 4,294,805,063 visitors served. Forum join the word of the day mailing list for webmasters thefreedictionary google bing? viagra pill appearance Word / article starts with ends with text dictionary/thesaurus medicaldictionary legaldictionary financialdictionary acronyms  idioms encyclopedia wikipediaencyclopedia? Hemophilia c    also found in: dictionary/thesaurus, encyclopedia, wikipedia 0. 01 sec. Hemophilia /heâ·moâ·philâ·ia/ (he″mo-filâ´e-ah) a hereditary hemorrhagic diathesis due to deficiency of a blood coagulation factor. cheap viagra no prescription Hemophilia aâ  classical h. Viagra sales online ; an x-linked recessive form due to deficiency of coagulation factor viii. Hemophilia bâ  christmas disease; an x-linked recessive form due to deficiency of coagulation factor ix. buy viagra online without rx Hemophilia câ  an autosomal disorder due to lack of coagulation factor xi; seen predominantly in persons of jewish ancestry and characterized by minor bleeding, mild bruising, severe prolonged postsurgical bleeding, and abnormal clotting test times. Classical hemophiliaâ  h. A. Vascular hemophiliaâ  von willebrand's disease. Hemophilia c, a hereditary blood disorder, transmitted as an x-linked recessive trait and caused by a deficiency of factor xi, the plasma thromboplastin antecedent. The condition is clinically similar to but may be less severe than hemophilia a. Also called rosenthal's syndrome. See also coagulation factor , hemophilia. cheap viagra no prescription Hemophilia [he′mo-fil´e-ah] a hereditary disorder characterized by a strong tendency to bleed. The most common types are carried as sex-linked genes with females carrying the trait and disease manifestations almost always in males. (occasionally, women carrying the trait for hemophilia a or b have bleeding manifestations themselves, probably as a result of nonrandom inactivation of their x chromosomes and overexpression of the x chromosome coding for hemophilia; these women are referred to as symptomatic carriers. ) all daughters of affected men will be carriers for the gene of hemophilia. The two most common types are hemophilia a and hemophilia b. Over 80 per cent of patients have hemophilia a (classical hemophilia), which is characterized by a deficiency of coagulation factor viii. Hemophilia b (called also christmas disease) affects about 15 per cent of hemophiliacs and is characterized by a deficiency of coagulation factor ix. Other coagulation factor deficiencies are less common, with patients suffering either milder bleeding or thrombotic episodes. Symptoms. Bleeding in hemophilic patients is variable, depending on the level of deficiency of the clotting factor. Approximately 60 per cent of persons with hemoph 2000 ilia a or b are severely affected and may have spontaneous bleeding without any recognized trauma. Soft tissue bleeding from the neck, lower face, and tongue may cause grave consequences if not treated. Hematuria and gastrointestinal bleeding are likely, and hemarthrosis (bleeding into joints) can lead to painful stiffening and permanent disability. buy viagra paypal uk The leading cause of death, however, is intracranial bleeding. Hemorrhagic complications can be avoided or minimized with early and adequate factor replacement therapy. Hemophilia a is characterized by a factor viii level of from 0 to 30 per cent of normal. The partial thromboplastin time (ptt) is usually prolonged. The platelet count, bleeding time, and prothrombin time (pt) are normal. cheap viagra no prescription In hemophilia b there is a low factor ix level and the prothrombin time is usually prolonged. Treatment. The treatment of persons with hemophilia depends on the severity of their disease and the nature of a given bleeding episode. order viagra online from canada Several therapeutic materials are available for correction of the clotting defect in hemophilia a. Factor viii is present in commercial lyophilized factor viii concentrates, cryoprecipitate , fresh whole blood, and fresh frozen plasma. Purified factor viii concentrate, however, is the treatment of choice. Successful treatment of those with mild hemophilia a can often be done with desmopressin (ddavp). While factor ix is present in fresh frozen plasma, it is not concentrated in cryoprecipitate, so that the latter is not useful for treatment of hemophilia b. Factor ix is present in two commercially prepared concentrates, known as factor ix complex concentrates and coagulation factor ix concentrates. All persons with hemophilia should be immunized with hepatitis b vaccine. Suspected bleeding into the central nervous system must be promptly treated; when this happens, consultation with or transfer to a hemophilia treatment center is mandatory. Early treatment of hemarthroses is essential for maintenance of joint health; infusions administered within 4 to 6 hours of onset of symptoms are sufficient to stop bleeding and restore joint function. buy viagra for men Medically supervised home infusion therapy has become an integral part of the comprehensive care of patients with bleeding disorders and has facilitated the treatment of bleeding episodes outside the hospital setting. Cheap viagra Patient care. Advances in therapy have greatly improved the prognosis and management of hemophilia, but new issues have emerged, including the.

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