The Resource 31st Hemophilia Symposium : Hamburg 2000, edited by I. Scharrer, W. Schramm, (electronic resource)

31st Hemophilia Symposium : Hamburg 2000, edited by I. Scharrer, W. Schramm, (electronic resource)

Label
31st Hemophilia Symposium : Hamburg 2000
Title
31st Hemophilia Symposium
Title remainder
Hamburg 2000
Statement of responsibility
edited by I. Scharrer, W. Schramm
Creator
Contributor
Editor
Editor
Subject
Language
  • eng
  • eng
Summary
Some 23. 5% of all members and patients of treatment centers completed the questionnaire. One striking fact is that participation was highest amongst elderly patients with severe hemophilia, whereas only 12. 2% of family members responded. Evaluation of the results revealed that the majority of participants prefer treat­ ment in a hemophilia treatment center with a high reputation, whereas only 2. 7% consider treatment in a specialized practice to be sufficient. The reasons for that are the necessity of the 24-h-availability of a physician, regular qualified examination of joints and muscles, documentation of product batches, laboratory tests and good cooperation with other faculties. As many as 68. 9% of the patients sometimes travel more than 200 km. What certainly plays a role here is trust in the treatment center and its physicians, for it is noticeable that irrespective of the fact that 74. 3% re­ quested standardized treatment regimens for all treatment centers, only about 20% would change to a nearer center. Treatment with factor concentrates is generally considered to be very safe. That is to say, 58. 1 % regard recombinant products to be very safe, whereas only 24. 3% assume this for plasma products. When compared, there were usually no major differences observed regarding outcome (factor consumption, duration of treat­ ment). Increase in maximum storage temperature (47. 2%) and half-life (73%) were the most frequent answers to the question of what features the products should have
http://bibfra.me/vocab/relation/corporateauthor
6MIykIKyNYs
Dewey number
616.15
http://bibfra.me/vocab/relation/httpidlocgovvocabularyrelatorsedt
  • DLq1SHIx1UE
  • c2XTY4aP09E
Image bit depth
0
Language note
English
LC call number
RB45
Literary form
non fiction
http://bibfra.me/vocab/lite/meetingDate
2000
http://bibfra.me/vocab/lite/meetingName
Hemophilia Symposium
Nature of contents
dictionaries
http://bibfra.me/vocab/lite/organizationName
Hämophilie-Symposion
http://library.link/vocab/relatedWorkOrContributorName
  • Scharrer, I.
  • Schramm, W.
http://library.link/vocab/subjectName
  • Hematology
  • Pediatrics
  • Anesthesiology
  • Blood transfusion
  • Critical care medicine
  • Hematology
  • Pediatrics
  • Anesthesiology
  • Blood Transfusion Medicine
  • Intensive / Critical Care Medicine
Label
31st Hemophilia Symposium : Hamburg 2000, edited by I. Scharrer, W. Schramm, (electronic resource)
Instantiates
Publication
Note
Bibliographic Level Mode of Issuance: Monograph
Antecedent source
mixed
Bibliography note
Includes bibliographical references and index
Carrier category
online resource
Carrier category code
  • cr
Color
not applicable
Content category
text
Content type code
  • txt
Contents
Presentation of the Johann-Lukas-Schoenlein-Award -- I. Epidemiology -- HIV Infection and Causes of Death in Patients with Hemophilia in Germany (Year 1999/2000 Survey) -- Hemophilia 2000 — the Annual Survey of the Austrian Hemophilia Centers -- II. Inhibitors in Hemophilia -- Changes in Epitope Specificity and in Distribution of FVIII Antibodies during Immune Tolerance Therapy (ITT) in Hemophilia A Patients with FVIII Antibodies — a Case Report -- Clinical Experience with the Modified Bonn-Malmö Protocol since 1996 -- Course of Inhibitors in mild Hemophilia A with and without Immune Tolerance Treatment -- III. Therapy and Monitoring of Bleeds in Acute- and Intensive Care Medicine -- Management of Bleeding in Surgery and Intensive Care -- IV.. Pediatric Hemostaseology -- Frequency and Profile of viral posttransfusional Infections in Patients from Hemophilia Center Timisoara -- Symptomatic Onset of severe Hemophilia A in Childhood is dependent on the Presence of Prothrombotic Risk Factors -- Differences between Neonates and Adults in Plasmin Inhibitory and Antifibrinolytic Action of Aprotinin -- Shorter PFA-100 Closure Times (CT) in Neonates than in Adults: Role of Red Cells, White Cells, Platelets, and von Willebrand Factor -- V. Free Lectures -- Efficacy and Safety of a High Purity Protein C Concentrate in the Management of Patients with severe Congenital Protein C Deficiency -- Respective Roles of Factors II, VII, IX, and X in the Procoagulant Activity of FEIBA -- Capillary Microscopic and Rheological Dimensions for the Diagnosis of von-Willebrand-Disease in Comparison with other Hemorrhagic Diatheses -- Evaluation of Denaturing High Performance Liquid Chromatography (DHPLC) in the Analysis of Hemophilia A -- Vla. Poster: Clinic and Casuistic -- Rheumatoid Arthritis in a Patient with Hemophilia Arthropathy — a Case Report -- Recurrent Fatal Intracranial Hemorrhage (ICH) in Two Non-Identical Twins suffering from Hemophilia B (Factor IX Activity < 1%) -- Progression of Thrombosis under Low Molecular Weight Heparin without Heparin-Induced Thrombocytopenia in a young Man: a Case Report -- Cardiac Tamponade in a Patient with acquired Factor VIII Inhibitor and Chronic Renal Failure -- Endoscopic Cholecystectomy in a 55-year-old Patient with Heparin-Induced Thrombocytopenia Type II and Replacement of Mitral and Aortic Valve and Tricuspidal Valve Anular Plasty -- Vlb. Poster: Hemophilia -- Successful Orthopedic Operations in Hemophilic Adults with Inhibitors against Factor VIII -- Evaluation of Clinical Efficacy of rFVIIa in Pediatrics -- Risk Factors for Thrombosis in Hemophilia — an Analysis -- Status of Pain in Patients with severe Haemophilic Arthropathies -- Results of a 5-year Clinical Study with a B-domain Deleted FVIII Concentrate (rFVIII-SQ) -- Outpatient Treatment with Radiosynoviorthesis in Hemophilic Arthropathy -- Requirements for Future Hemophilia Treatment from the Patients’ Point of View -- Vic. Poster: Hemorrhagic Diathesis -- Molecular Basis of von Willebrand Disease Type IIC Miami -- Hemorrhagic Diathesis through acquired Factor XIII Inhibitor -- Liver Transplantation in a Patient with severe von Willebrand Disease Type 3: Levels of von Willebrand Factor Following Transplantation -- Clincal Course and Laboratory Findings in a Patient with a New Mutation Causing Wiskott-Aldrich Syndrome -- Role of acquired and inherited Prothrombotic Risk Factors in Pediatric Cerebral Venous Thrombosis — Preliminary Results of a Multicenter Case-Control Study -- Analysis of the Fibrinogen Genes of 40 Patients with Suspicion of Dys-, Hypo- or Afibrinogenemia -- Vld. Poster: Thrombophilic Diathesis -- Hereditary Antithrombin Deficiency — Results of a Family Study -- Elevated Factor IX and Factor XI as Risk Factors for Venous Thrombosis and Stroke -- Thrombophilic Risk Parameters in Juvenile »Idiopathic« Stroke Patients -- Inquiry into the Significance of Constantly Raised FVIII Values as a Factor in Thrombophilia -- Do Statins Increase the Homocysteine Level? -- Alpha 2-Macroglobulin Level regulates the Anticoagulant Cofactor Activity of Protein S in Cord and Adult Plasma -- Combined Prothrombotic Defects and Contraceptives — Risk Factor for Deep Venous Thrombosis in Adolescence -- Role of 23 bp Insertion in Exon 3 of the Endothelial Cell Protein C Receptor Gene in Venous Thrombophilia
Dimensions
unknown
Edition
1st ed. 2002.
Extent
1 online resource (XXX, 287 p.)
File format
multiple file formats
Form of item
online
Isbn
9783642593833
Level of compression
uncompressed
Media category
computer
Media type code
  • c
Other control number
10.1007/978-3-642-59383-3
Quality assurance targets
absent
Reformatting quality
access
Specific material designation
remote
System control number
  • (CKB)3400000000104689
  • (SSID)ssj0000809190
  • (PQKBManifestationID)11439107
  • (PQKBTitleCode)TC0000809190
  • (PQKBWorkID)10793350
  • (PQKB)11372961
  • (DE-He213)978-3-642-59383-3
  • (MiAaPQ)EBC3094367
  • (EXLCZ)993400000000104689
Label
31st Hemophilia Symposium : Hamburg 2000, edited by I. Scharrer, W. Schramm, (electronic resource)
Publication
Note
Bibliographic Level Mode of Issuance: Monograph
Antecedent source
mixed
Bibliography note
Includes bibliographical references and index
Carrier category
online resource
Carrier category code
  • cr
Color
not applicable
Content category
text
Content type code
  • txt
Contents
Presentation of the Johann-Lukas-Schoenlein-Award -- I. Epidemiology -- HIV Infection and Causes of Death in Patients with Hemophilia in Germany (Year 1999/2000 Survey) -- Hemophilia 2000 — the Annual Survey of the Austrian Hemophilia Centers -- II. Inhibitors in Hemophilia -- Changes in Epitope Specificity and in Distribution of FVIII Antibodies during Immune Tolerance Therapy (ITT) in Hemophilia A Patients with FVIII Antibodies — a Case Report -- Clinical Experience with the Modified Bonn-Malmö Protocol since 1996 -- Course of Inhibitors in mild Hemophilia A with and without Immune Tolerance Treatment -- III. Therapy and Monitoring of Bleeds in Acute- and Intensive Care Medicine -- Management of Bleeding in Surgery and Intensive Care -- IV.. Pediatric Hemostaseology -- Frequency and Profile of viral posttransfusional Infections in Patients from Hemophilia Center Timisoara -- Symptomatic Onset of severe Hemophilia A in Childhood is dependent on the Presence of Prothrombotic Risk Factors -- Differences between Neonates and Adults in Plasmin Inhibitory and Antifibrinolytic Action of Aprotinin -- Shorter PFA-100 Closure Times (CT) in Neonates than in Adults: Role of Red Cells, White Cells, Platelets, and von Willebrand Factor -- V. Free Lectures -- Efficacy and Safety of a High Purity Protein C Concentrate in the Management of Patients with severe Congenital Protein C Deficiency -- Respective Roles of Factors II, VII, IX, and X in the Procoagulant Activity of FEIBA -- Capillary Microscopic and Rheological Dimensions for the Diagnosis of von-Willebrand-Disease in Comparison with other Hemorrhagic Diatheses -- Evaluation of Denaturing High Performance Liquid Chromatography (DHPLC) in the Analysis of Hemophilia A -- Vla. Poster: Clinic and Casuistic -- Rheumatoid Arthritis in a Patient with Hemophilia Arthropathy — a Case Report -- Recurrent Fatal Intracranial Hemorrhage (ICH) in Two Non-Identical Twins suffering from Hemophilia B (Factor IX Activity < 1%) -- Progression of Thrombosis under Low Molecular Weight Heparin without Heparin-Induced Thrombocytopenia in a young Man: a Case Report -- Cardiac Tamponade in a Patient with acquired Factor VIII Inhibitor and Chronic Renal Failure -- Endoscopic Cholecystectomy in a 55-year-old Patient with Heparin-Induced Thrombocytopenia Type II and Replacement of Mitral and Aortic Valve and Tricuspidal Valve Anular Plasty -- Vlb. Poster: Hemophilia -- Successful Orthopedic Operations in Hemophilic Adults with Inhibitors against Factor VIII -- Evaluation of Clinical Efficacy of rFVIIa in Pediatrics -- Risk Factors for Thrombosis in Hemophilia — an Analysis -- Status of Pain in Patients with severe Haemophilic Arthropathies -- Results of a 5-year Clinical Study with a B-domain Deleted FVIII Concentrate (rFVIII-SQ) -- Outpatient Treatment with Radiosynoviorthesis in Hemophilic Arthropathy -- Requirements for Future Hemophilia Treatment from the Patients’ Point of View -- Vic. Poster: Hemorrhagic Diathesis -- Molecular Basis of von Willebrand Disease Type IIC Miami -- Hemorrhagic Diathesis through acquired Factor XIII Inhibitor -- Liver Transplantation in a Patient with severe von Willebrand Disease Type 3: Levels of von Willebrand Factor Following Transplantation -- Clincal Course and Laboratory Findings in a Patient with a New Mutation Causing Wiskott-Aldrich Syndrome -- Role of acquired and inherited Prothrombotic Risk Factors in Pediatric Cerebral Venous Thrombosis — Preliminary Results of a Multicenter Case-Control Study -- Analysis of the Fibrinogen Genes of 40 Patients with Suspicion of Dys-, Hypo- or Afibrinogenemia -- Vld. Poster: Thrombophilic Diathesis -- Hereditary Antithrombin Deficiency — Results of a Family Study -- Elevated Factor IX and Factor XI as Risk Factors for Venous Thrombosis and Stroke -- Thrombophilic Risk Parameters in Juvenile »Idiopathic« Stroke Patients -- Inquiry into the Significance of Constantly Raised FVIII Values as a Factor in Thrombophilia -- Do Statins Increase the Homocysteine Level? -- Alpha 2-Macroglobulin Level regulates the Anticoagulant Cofactor Activity of Protein S in Cord and Adult Plasma -- Combined Prothrombotic Defects and Contraceptives — Risk Factor for Deep Venous Thrombosis in Adolescence -- Role of 23 bp Insertion in Exon 3 of the Endothelial Cell Protein C Receptor Gene in Venous Thrombophilia
Dimensions
unknown
Edition
1st ed. 2002.
Extent
1 online resource (XXX, 287 p.)
File format
multiple file formats
Form of item
online
Isbn
9783642593833
Level of compression
uncompressed
Media category
computer
Media type code
  • c
Other control number
10.1007/978-3-642-59383-3
Quality assurance targets
absent
Reformatting quality
access
Specific material designation
remote
System control number
  • (CKB)3400000000104689
  • (SSID)ssj0000809190
  • (PQKBManifestationID)11439107
  • (PQKBTitleCode)TC0000809190
  • (PQKBWorkID)10793350
  • (PQKB)11372961
  • (DE-He213)978-3-642-59383-3
  • (MiAaPQ)EBC3094367
  • (EXLCZ)993400000000104689

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