WorldCat Identities

Lusher, Jeanne M. 1935-

Overview
Works: 22 works in 71 publications in 2 languages and 840 library holdings
Genres: Conference papers and proceedings 
Roles: Editor, Other
Publication Timeline
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Most widely held works by Jeanne M Lusher
Factor VIII/vWF and platelet formation and function in health and disease : a tribute to Marion I. Barnhart by Marion I Barnhart( Book )

18 editions published in 1987 in English and held by 269 WorldCat member libraries worldwide

Sickle cell; a scope publication [by] Marion I. Barnhart, Raymond L. Henry [and] Jeanne M. Lusher by Marion I Barnhart( Book )

10 editions published between 1974 and 1976 in English and held by 255 WorldCat member libraries worldwide

Sickle cell by Marion I Barnhart( Book )

9 editions published between 1974 and 1979 in English and held by 87 WorldCat member libraries worldwide

Hemophilia and von Willebrand's disease in the 1990s : a new decade of hopes and challenges : proceedings of the XIX Congress of the World Federation of Hemophilia, Washington, D.C., 14-19 August 1990 by World Federation of Hemophilia( Book )

7 editions published in 1991 in English and held by 78 WorldCat member libraries worldwide

Acquired bleeding disorders in children( Book )

6 editions published in 1981 in English and Undetermined and held by 74 WorldCat member libraries worldwide

Inhibitors to Coagulation Factors by Louis M Aledort( )

1 edition published in 1996 in English and held by 43 WorldCat member libraries worldwide

Inhibitors to coagulation factors by Louis M Aledort( )

1 edition published in 1996 in English and held by 9 WorldCat member libraries worldwide

The proceeding papers investigate the integration of modern concepts of immunology and hematology toward the design of potential new therapies for the prevention or elimination of antibodies to F. VIII and F. IX. The current research anticipates gene therapy for hemophilias and the implications of inhibitors in such a course of treatment. Papers include discussions on: the molecular and antigenic structure of factors VIII and IX and von Willebrand factor, the human immune response molecular basis, genetic variation and the immune response, inhibitor treatment, coagulation tolerance, and panel discussions
Acquired bleeding disorders in children( Book )

4 editions published in 1981 in English and held by 6 WorldCat member libraries worldwide

Acquired hemophilia : continuing medical education monograph by David Green( Book )

1 edition published in 1990 in English and held by 4 WorldCat member libraries worldwide

Factor eight VIII vWF and function in health and disease : a tribute to Marion F. Barnhart( Book )

1 edition published in 1987 in English and held by 2 WorldCat member libraries worldwide

Sickle cell( Visual )

1 edition published in 1975 in English and held by 2 WorldCat member libraries worldwide

Self-instructional unit presents scanning electron microscope comparisons of normal and sickled red blood cells. Presents photographs and radiographs of sickle cell anemia manifestations (dactylitis, bone changes, leg ulcers)
Acquired bleeding disorders in children( Book )

1 edition published in 1981 in English and held by 1 WorldCat member library worldwide

Hemophilia and von Willebrand's disease in the 1990s a new decade of hopes and challenges ; Washington, D.C., 14-19 August 1990( Book )

1 edition published in 1991 in German and held by 1 WorldCat member library worldwide

The Detection of Sickle Cell Disease in Large Human Populations by an Automated Technique by Robert M Nalbandian( Book )

2 editions published in 1971 in English and held by 1 WorldCat member library worldwide

A total of 2,939 specimens was tested in this mixed population of both military and civilian individuals. Complete agreement among the results of all tests was obtained. An automated test for the determination of S hemoglobin can be performed at the rate of 60 per hour per AutoAnalyzer unit on 0.5 ml of whole blood with accuracy and reliability on large human populations. The successful field trials we have conducted may be regarded as a prototype model for the survey of metropolitan and military populations leading to case-finding of sickle cell disease. These cases may then be directed to medical genetic counseling and for possible treatment with urea. This is the first large-scale human population survey by specific automated techniques diagnostic for the molecular lesion of S hemoglobin. The automated mass survey technique is proven and awaits immediate application to appropriate segments of our national population. This diagnostic technique appropriately fielded can yield substantial contributions to the development of accurate statistics and to the control and eventual elimination of this lethal genetic affliction, sickle cell disease. The impediment to the widespread use of this proven technique is the high cost per test due to the use of the proprietary Sickledex solution. (Author)
Sickledex test for S hemoglobin : a critique by Robert M Nalbandian( Book )

1 edition published in 1971 in English and held by 1 WorldCat member library worldwide

When the reagents, reactions, and principles of the Sickledex test are understood in terms of modern molecular biology, it is believed that the Sickledex test can be an invaluable and productive tool in the discovery not only of hemoglobin S but other hemoglobinopathies as well, provided: (1) certain pitfalls of false positive and false negative reactions are recognized; (2) urea is used to modify the test; and (3) all positive Sickledex specimens are subsequently studied by hemoglobin electrophoresis technique. (Author)
Automated Dithionite Test for the Rapid, Inexpensive Detection of Hemoglobin S and Non-S Sickling Hemoglobinopathies by Robert M Nalbandian( Book )

1 edition published in 1971 in English and held by 1 WorldCat member library worldwide

The adaptation to an automated version of the dithionite tube test and the urea-dithionite tube test as discussed in USAMRL Report No. 942 is presented. The automated dithionite test makes it possible to screen 120 hemoglobin specimens per hour at a reagent cost of approximately 2 cents to 4 cents each. Increased specificity of the results may be obtained but at the expense of half the rate of the automated dithionite test. Thus, about 60 determinations per hour can be performed at about 4 cents to 8 cents per set. Both automated methods have proven to be highly reliable in extended field trials in military and civilian populations. (Author)
Dithionite Tube Test - A Rapid, Inexpensive Technique for the Detection of Hemoglobin S and Non-S Sickling Hemoglobin by Robert M Nalbandian( Book )

1 edition published in 1971 in English and held by 1 WorldCat member library worldwide

An extensive field trial of the dithionite and the urea-dithionite tube tests indicates that the molecular theories of this method are supported by actual clinical tests. It is demonstrated that blood specimens appropriately collected at one site can be mailed at ambient temperatures for subsequent processing at a geographically remote laboratory without adverse effect on the accuracy or reliability of the test. The test, performed in 5 minutes, has a reagent cost of about 2 cents per determination. It is of considerable interest that these testing techniques will detect not only hemoglobins S and C (Harlem), a structural variant of S, but other non-S sickling hemoglobins such as Bart's, C (Georgetown), and perhaps Alexandra and rare hemoglobinopathies of low solubility such as Kings County and Stanleyville II. The dithionite and urea-dithionite tests, however, will provide rapid, accurate, reliable, and inexpensive screening for hemoglobin S. (Author)
Acquired bleeding disorders( Book )

in English and held by 1 WorldCat member library worldwide

 
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Audience Level
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Audience level: 0.55 (from 0.38 for Acquired b ... to 0.99 for Dithionite ...)

Languages
English (65)

German (2)