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دسته بندی: درمان ویرایش: 1 نویسندگان: Inge Scharrer, Wolfgang Schramm, G. Auerswald, A. Kurth, J. Oldenburg, W. Schramm, B. Zieger سری: ISBN (شابک) : 3540367144, 9783540367154 ناشر: سال نشر: 2006 تعداد صفحات: 333 زبان: English فرمت فایل : PDF (درصورت درخواست کاربر به PDF، EPUB یا AZW3 تبدیل می شود) حجم فایل: 7 مگابایت
در صورت تبدیل فایل کتاب 36th Hemophilia Symposium Hamburg 2005: Epidemiology; Hemophilia Therapy - Management of Bleedings and Inhibitors; Orthopedic Treatment in Hemophiliacs; ... Pediatric Hemostaseology; Free Lectures 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 سی و ششمین سمپوزیوم هموفیلی هامبورگ 2005: اپیدمیولوژی; درمان هموفیلی - مدیریت خونریزی ها و مهارکننده ها. درمان ارتوپدی در بیماران هموفیلی; ... هموستازولوژی کودکان; سخنرانی های رایگان 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 مشارکت در سی و ششمین سمپوزیوم هموفیلی، هامبورگ 2005 است. موضوعات اصلی اپیدمیولوژی، درمان هموفیلی، درمان ارتوپدی در بیماران هموفیلی، تشخیص هموستازولوژیک و هموستازولوژی کودکان است. این حجم با مقالات و پوسترهای رایگان متعددی در مورد هموفیلی، مهارکنندههای هموفیلی و تشخیصی کامل شده است.
This book contains the contribution to the 36th Hemophilia Symposium, Hamburg 2005. The main topics are epidemiolgy, hemophilia therapy, orthopedic treatment in hemophiliacs, hemostaseologic diagnosis and pediatric hemostaseology. The volume is rounded off by numerous free papers and posters on hemophilia, inhibitors in hemophilia and diagnostics.
Front Matter....Pages I-XXXIV
Front Matter....Pages 1-1
HIV Infection and Causes of Death in Patients with Hemophilia in Germany (Year 2004/2005 Survey)....Pages 3-14
Development of the German Hemophilia Register....Pages 15-15
National Hemophilia Registry - Source of Information about the Quality of Hemophilia Medical Care in a Developing Country....Pages 16-20
Front Matter....Pages 21-21
Regulation of Factor VIII Life-Cycle by Receptors from LDL Receptor Superfamily....Pages 23-33
Update of the Inhibitor-Immunology-Study....Pages 34-39
Therapy of Acquired Hemophilia - Immunoadsorption and Rituximab Treatment for Immunosuppression and Substitution of Coagulation Factors....Pages 40-47
Front Matter....Pages 49-49
Osteoporosis and Hemophilia - Is there a Correlation and Is there a Problem?....Pages 51-53
Orthopedic Evaluation of the Lower Extremity in 249 Children: A Multicenter Trial....Pages 54-56
Simultaneous Bilateral Total Knee Arthroplasty in Hemophilic Arthopathy....Pages 57-62
Alternative Therapy such as the Acupuncture of the Skull for Hemophilic Arthropathy....Pages 63-66
Endoprosthetics of Large Joints in Patients Infected with HIV....Pages 67-67
Front Matter....Pages 69-69
Factor VIII Methods: Which Assay Principle for which Indication?....Pages 71-74
Global ECAT Survey on Factor VIII Inhibitor Testing: Results of an Inter-Laboratory Pilot Study....Pages 75-77
A Practical Concept for Pre-Operative Identification and Improved Management of Patients at Risk for Bleeding....Pages 78-89
Front Matter....Pages 91-91
Intravascular Tissue Factor in Cord vs Adult Whole Blood....Pages 93-95
Perioperative Coagulation Screening in Children - Reasons and Results....Pages 96-100
Thrombin Generation in Children....Pages 101-107
Front Matter....Pages 109-109
Working-Group of the German Hemophilia Assistants - History, Purpose and Goals....Pages 111-113
The Endogenous Thrombin Potential as a New Parameter for the Peri-Operative Monitoring in Conjunction with Endo-Prosthetic Supply due to Hemophilic Arthropathy....Pages 114-117
Identification of Inhibitor Epitopes in Acquired Hemophilia by Phage Display....Pages 118-128
Front Matter....Pages 109-109
Spectrum of Molecular Defects and Mutation Detection Rate in Patients with Mild and Moderate Hemophilia A....Pages 129-132
Recombinant Factor VIIa for Major Surgery in Severe Factor XI Deficiency: Pharmacodynamic Monitoring Using Thromboelastometry....Pages 133-136
Front Matter....Pages 137-137
Establishment of a Web-Based Documentation System for Quality Assurance of Hemophilia Treatment in Mecklenburg/Western Pomeranian: a Pilot Study....Pages 139-139
Successful Angiographic Embolization of Recurrent Elbow Joint Bleeds in one Patient with Severe Hemophilia A....Pages 140-143
Evaluation of Thrombotic Events in Hemophiliacs Undergoing Major Orthopedic Surgery Without Thrombosis Prophylaxis....Pages 144-146
Motivating Patients and Parents to Document Treatment Correctly....Pages 147-149
Fit for Life Competition: Everyone’s a Winner....Pages 150-152
Blood Borne Infections in Hemophiliacs in a Developing Country. A Single Center Experience....Pages 153-158
Hemophilia Center Frankfurt - Twinning Center for Nairobi/Kenya....Pages 159-160
Economic Evaluation of Orthopedic and Surgical Interventions in Hemophiliacs - Not Only Direct Medical Costs Matter....Pages 161-167
The Occurrence of Factor VIII Inhibitor in a Patient with Mild Hemophilia A - During Treatment with Interferon for Chronic Hepatitis C....Pages 171-172
Severe Hemophilia A Patient with High-Titer Inhibitor, use of TGA in the Monitoring of Bypassing Therapy....Pages 173-174
EUREKA - an European Registry for Orthopedic Surgery in Hemophiliacs with Inhibitors....Pages 175-175
Double Balloon Enteroscopy (DBE) with Argon Plasma Laser Coagulation (APC) for a Patient with Heyde’s Syndrome....Pages 179-183
Successful Liver Transplantation in a Patient with Anti-Thrombocyte Antibodies and Severe Hemophilia A....Pages 184-186
Peri- and Postoperative Course of 95 Patients with von-Willebrand’s Disease....Pages 187-189
Pregnancy in a Patient with Congenital Antithrombin Deficiency....Pages 190-194
Successful Inhibitor-Elimination with Rituximab in Acquired Hemophilia A and a Patient with a Carrier Status for Hemophilia A: Two Case Reports....Pages 195-199
An Interesting Family Case of von-Willebrand-Syndrome....Pages 200-200
Clinical Manifestations of Dysfibrinogenemia in Relation to the Fibrinogen Gene Mutation....Pages 201-202
Front Matter....Pages 137-137
Thrombin Generation in a Hemophilic Newborn....Pages 203-209
Rapid and Sensitive Detection of Heterozygous Deletions of one or more Exons in Hemophilia A Females by Multiplex PCR and DHPLC Technique....Pages 213-216
Molecular Genetic Analysis in Patients with Inherited Factor V Deficiency....Pages 217-219
Expression Analysis of C1-Inhibitor Mutants Confirms Causality of Missense Mutations for Hereditary Angioedema....Pages 220-223
Expression of the γ-Glutamyl Carboxylase (GGCX) Containing the Arg485Pro Mutation Found in two Unrelated VKCFD1 Patients....Pages 224-228
Concentration of Soluble Endothelial Protein C Receptor (EPCR) in Plasma in Relation to Age, Sex, BMI and Hemostasis Parameters....Pages 229-234
Thrombin Generation is Age-Dependent in Children as well as in Adults....Pages 235-239
Effects of PFA-100 in Preoperative Screening for von Willebrand Disease in 310 Patients....Pages 240-242
Control of Aspirin Effect in Chronic Cardiovascular Patients Using two Whole Blood Platelet Function Assays: PFA-100 and Multiple Electrode Aggregometry....Pages 243-251
Difficulties in the Interpretation of the Term »Patient-Related« in the Scope of the Introduction of a Remuneration of Additional Payments According to the OPS....Pages 255-256
Factor VIII as Positive Regulator of Activated Platelets....Pages 257-262
Characterization of Three Novel Mutations in the Sodium Binding Site of Coagulation Factor X....Pages 263-271
Characterization of a Mutation in the 5′ Flanking Region and a Novel IVS7 Splice site Mutation in a Patient with Severe FVII Deficiency....Pages 272-278
On the Molecular Basis of Warfarin Resistance in Rats....Pages 279-283
Influence of Factor V HR2 on Endogenous Thrombin Potential and Clinical Phenotype in Factor VII Deficiency....Pages 284-290
Splice Site Mutations Effect on the F8 mRNA Splicing....Pages 291-294
Species-Specific Variation of VKORC1-Activity and Resistance to Warfarin....Pages 295-297
Various Missense Mutations in the Vitamin K Epoxide Reductase Complex Subunit 1 (VKORC1) Cause Hereditary Coumarin Resistance....Pages 298-301
Establishment of an International Registry of Patients with Congenital FXIII Deficiency....Pages 302-304
The Impact of Freezing of Plasma Samples, AB0 Blood Group and Acute-Phase Reaction on Detecting Mild Factor VIII Deficiency and Increased Factor VIII Levels as a Risk Factor for Venous Thromboembolism....Pages 305-309
Front Matter....Pages 137-137
Thrombin Generation in Severely Obese Children....Pages 310-314
Back Matter....Pages 315-320