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ویرایش: نویسندگان: Dr. H. Krebs, Prof. Dr. W. Schramm (auth.), Professor Dr. med. I. Scharrer, Professor Dr. med. W. Schramm (eds.) سری: ISBN (شابک) : 9783540228868, 9783540270225 ناشر: Springer Berlin Heidelberg سال نشر: 2005 تعداد صفحات: 413 زبان: English فرمت فایل : PDF (درصورت درخواست کاربر به PDF، EPUB یا AZW3 تبدیل می شود) حجم فایل: 5 مگابایت
کلمات کلیدی مربوط به کتاب سیزدهمین سمپوزیوم هموفیلی: هامبورگ 2003: هماتولوژی، بیهوشی، پزشکی انتقال خون، ارتوپدی جراحی، اطفال، اپیدمیولوژی
در صورت تبدیل فایل کتاب 34th Hemophilia Symposium: Hamburg 2003 به فرمت های PDF، EPUB، AZW3، MOBI و یا DJVU می توانید به پشتیبان اطلاع دهید تا فایل مورد نظر را تبدیل نمایند.
توجه داشته باشید کتاب سیزدهمین سمپوزیوم هموفیلی: هامبورگ 2003 نسخه زبان اصلی می باشد و کتاب ترجمه شده به فارسی نمی باشد. وبسایت اینترنشنال لایبرری ارائه دهنده کتاب های زبان اصلی می باشد و هیچ گونه کتاب ترجمه شده یا نوشته شده به فارسی را ارائه نمی دهد.
این کتاب شامل مشارکتهای سی و چهارمین سمپوزیوم هموفیلی،
هامبورگ 2003 است. موضوعات اصلی عفونت و اپیدمیولوژی HIV، مدیریت
خونریزی در بیماران هموفیلی با مهارکنندهها، مشکلات ارتوپدی و
درمان در بیماران هموفیلی، درمان با پروتئین C و هموستازولوژی
کودکان است. این حجم با مقالات و پوسترهای رایگان متعددی در مورد
هموفیلی، بیماران هموفیلی با مهارکنندهها، ترومبوفیلی و تشخیص
مولکولی تکمیل شده است.
This book contains the contributions to the 34th Hemophilia
Symposium, Hamburg 2003. The main topics are HIV infection and
epidemiology, management of bleedings in hemophiliacs with
inhibitors, orthopedic problems and therapy in hemophiliacs,
therapy with protein C and pediatric hemostaseology. The volume
is rounded off by numerous free papers and posters on
hemophilia, hemophiliacs with inhibitors, thrombophilia and
molecular diagnostics.
HIV Infection and Causes of Death in Patients with Hemophilia in Germany (Year 2002/2003 Survey)....Pages 3-13
Hemophilia in Austria — The Annual Survey of the Austrian Hemophilia Centers....Pages 14-18
Lithuanian Hemophilia Register: Update 2003....Pages 19-21
Guidelines for Treatment of Patients with Hemophilia and Inhibitors....Pages 25-32
Bolus Injection of Recombinant Factor VIIa (NovoSeven) can be More Effective than Continuous Infusion in Inhibitor Patients with Severe Hemophilia A....Pages 33-37
The Role of Therapy Regimen and Age at First Exposure on Inhibitor Development in Patients with Severe Hemophilia A....Pages 38-41
Presentation of the Inhibitor-Immunology-Study....Pages 42-47
Current Clinical Investigations Involving FEIBA....Pages 48-51
Major Orthopedic Reconstructions in an Inhibitor Patient — A Case Report....Pages 55-58
Total Hip Replacement in Patients with Severe Bleeding Disorders A 30 Years Single Center Experience....Pages 59-63
MRI Staging of Hemophilic Joints in Comparison with the Radiological Score and the Clinical Dates of Children and Young Adults....Pages 64-70
Orthopedic Knee Replacement in Hemophilic Patients....Pages 71-76
Treatment of Adults with Sepsis-Induced Coagulopathy and Purpura Fulminans with a Plasma-Derived Protein C Concentrate (Ceprotin)....Pages 79-88
Comparison of the Anticoagulant Action of Recombinant Human Activated Protein C in Cord with that in Adult Plasma....Pages 89-93
The Relationship between Protein C Activity and the Endogenous Thrombin Potential in Controls and Septic Patients....Pages 94-100
Antibodies Against Annexin V, Cardiolipin and β 2 -Glycoprotein 1 or APC-Resistance in Patients with Recurrent Miscarriage or In-Vitro-Fertilization-Failures....Pages 103-106
Diagnostics of Platelet Function Disorders by Lumi-Aggregometry — Results and Comparison of Methods....Pages 107-115
Management of a Premature Infant below 1500 g with Hemophilia A....Pages 116-118
Elevated Factor VIIIC: Ag in Children with Venous Thrombosis and Stroke — Preliminary Results of a Case-Control Study....Pages 119-124
Functional Disorders and Treatment Modalities in Hemophilic Children....Pages 125-134
HLA Profile in Acquired Hemophilia....Pages 137-141
Characterization of Polyclonal Factor VIII-Inhibitory Antibodies....Pages 142-152
Frequency and Inhibitor Risk of the Intron-1-Inversion Mutation in the German Hemophilia Population....Pages 153-155
Effect of FVIII on Clotting Time and Thrombin Potential in Tissue Factor-Activated Hemophilia A Plasma....Pages 156-161
Bleeding Tendency in Factor XI Deficiency: Report on two Families and the Detection of a Novel Mutation within the Factor XI Gene....Pages 165-169
Multiple Distal Pseudotumours in a Patient with Severe Hemophilia A and High Titer Inhibitors....Pages 170-177
HIV Resistance to Antiretroviral Therapy in Romania....Pages 178-181
Ileopsoas Hemophilic Pseudotumour with Externalized Bowel Fistulation....Pages 182-187
Reduction of Proteoglycan Synthesis in Chondrocytes Depending on Concentration and Duration of Iron Overload....Pages 188-190
Bleeding Tendency of Carriers of Hemophilia A — Dependent on the Age of the Carriers?....Pages 191-195
Clinical Investigation of Orthopedic Outcome in Patients with Severe Hemophilia Under Prophylactic Treatment. Disadvantage of a late Prophylactic Treatment?....Pages 196-198
Operative Treatment of Ankle Equinus Deformity in Hemophiliacs....Pages 199-204
Spontaneous Empyema of Joints and Staphylococcal Sepsis in a Patient with Severe Hemophilia A....Pages 205-206
The Role of VWF:Ag II in Patients with Acquired von Willebrand Disease....Pages 207-211
Contamination of Coagulation Factor Concentrates with Human Parvovirus Genotype 2 DNA is Less Frequent than Contamination with Genotype 1 (B19) DNA....Pages 212-224
The Hemophilia Assistant in Germany....Pages 225-227
“Need” in Hemophilia A — a Qualitative Study....Pages 228-231
Fit for Life — Fitness Levels of Young Hemophiliacs Today....Pages 232-237
The Austrian “Haemofit-Program” - a two Years work-out Experience of People with Hemophilia (PwH)....Pages 238-241
Methods for Testing Pharmacodynamic Variables of Hemophilia and Inhibitor Therapy: Thrombin Generation Assay and Other Tests....Pages 245-252
Immune Tolerance in an Inhibitor Patient with Severe Hemophilia A — Comparison of two Different Treatment Schedules Including Rituximab....Pages 253-256
The Endogenous Thrombin Potential as a Monitoring Parameter in a Patient with an Acquired Hemophilia A....Pages 257-260
Case report: 58-Year-Old Hemophilia A Patient with High-Titer Inhibitor Development and Introduction of a Multicenter PTP-Inhibitor Study....Pages 261-263
First Data of a Prospective Study About Incidence of Inhibitors During and After Continuous Infusion of Different Factor Concentrates Given During and After Surgical Procedures in Hemophilia A or B and von Willebrand Disease....Pages 264-266
Acquired Thrombophilia in Patients on Hemodialysis with Recurrent Vascular Access Thrombosis....Pages 269-271
Is Travelling a Risk Factor for Venous Thrombosis in Individuals with Factor V Leiden in Heterozygous Form?....Pages 272-274
Popliteal Artery Embolism in Abdominal Aortal Thrombus with Liver Abscesses Caused by Heterozygous Prothrombin Mutation with Protein S Deficiency and Factor VIII Elevation....Pages 275-276
Effect of the new Direct Thrombin Inhibitor Melagatran in Cord and Adult Plasma: an in-vitro Examination....Pages 277-287
Higher Concentrations of Heparin and Hirudin are Required to Inhibit Thrombin Generation in Tissue Factor-Activated Cord Compared to Adult Plasma....Pages 288-297
Molecular Genetic Analysis in Patients with Inherited Thrombophilia and Antithrombin, Protein C or Protein S Deficiency....Pages 298-301
Analysis of Thrombophilic Risk Factors in Patients Suffering from Ocular Thrombotic Complications....Pages 302-303
Protein C Concentrate for the Treatment of Veno Occlusive Disease in a boy with Nephroblastoma....Pages 304-306
Homozygous Factor X Gene Mutation Gly380Arg is Associated to Perinatal Intracranial Hemorrhage....Pages 309-313
Mutation Analysis of the C1 Inhibitor Gene....Pages 314-316
Novel and Recurrent Mutations in the Gamma-Glutamyl Carboxylase (GGCX) Gene....Pages 317-320
First Case of Compound Heterozygous Mutations in the Kininogen Gene Causing Severe High Molecular Weight Kininogen Deficiency....Pages 321-326
Sequence of the rat Factor VIII cDNA....Pages 327-330
Mutation Profiling in Congenital FXIIIA Deficiency: Detection of 6 Novel Mutations....Pages 331-333
Functional Analysis of the Factor VIII B Domain....Pages 334-337
Expressing Recombinant Coagulation Factors in Yeast and Insect Cells....Pages 338-340
Long Term Optimisation of F8 Gene Mutation Screening by DHPLC....Pages 341-343
Expression Studies of Recombinant FVIII Proteins Exhibiting Mutations in the B-Domain....Pages 344-347
Genetic Variability of the Factor VIII Gene in the Normal Population....Pages 348-350
Three Novel Microdeletions and the First Insertion / Deletion in Patients with Factor X Deficiency....Pages 351-354
SNP Map of the Protein C Gene....Pages 355-357
Characterization of Factor VIII-Von Willebrand Factor (FVIII-VWF)-Complex Concentrates Under Shear Stress....Pages 361-367
Procedural Rules of a National Hemophilia Register in Germany....Pages 368-368
Quality Management of Clotting Factor Replacement Therapy in Medical Institutions — Advantage or Obligation....Pages 369-372
Proteus Syndrome: Successful Therapy of Severe Migraine Symptoms with low Molecular Weight Heparin....Pages 373-377
Administration of Recombinant Factor FVIIa (NovoSeven, NovoNordisk) in a Patient with Glanzmann Thrombasthenia....Pages 378-379
Combined Heterozygous Factor XIII-Deficiency in a Family Case Report....Pages 380-382
Resistance to Coumarin in a 55-year-old Patient with Chronic Arrhythmia....Pages 383-384
Investigation of the Tendency to Bleeding in Patients with low Activity of Plasminogen Activator Inhibitor-1 (PAI-1)....Pages 385-388
The Importance of Pre-Analytic Conditions on the Determination of VWF Parameters....Pages 389-393
Recombinant FVIIa in Chemotherapy Related Thrombocytopenic Bleedings....Pages 394-395