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CN1699 Our Business - Guide for Agents
分类
Hematology
5740
Global Medical University
5648
Allergy
1833
Anatomy & Morphology
1616
Andrology
414
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1353
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5924
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335
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104
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7515
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31825
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338
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9125
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9572
Biotechnology & Applied Microbiology
8992
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33375
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1546
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716
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11561
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4452
Chemistry, Applied
12010
Chemistry, Medicinal
9067
Chemistry, Multidisciplinary
19774
Clinical Immunology & Infectious Disease
473
Clinical Medicine
9207
Clinical Neurology
17448
Clinical Psychology & Psychiatry
1529
Critical Care Medicine
3481
Dentistry, Oral Surgery & Medicine
14232
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7813
Developmental Biology
7331
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645
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2036
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4424
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26097
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3888
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451
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5065
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275
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12869
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7554
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16184
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5322
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349
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17062
Health Policy & Services
623
Immunology
27265
Infectious Diseases
14831
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3015
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1212
Medical Informatics
2436
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433
Medicine, General & Internal
47573
Medicine, Legal
548
Medicine, Research & Experimental
19438
Microbiology
25197
Mycology
0
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5585
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1410
Neurology
4870
Neurosciences
42984
Nursing
9996
Nutrition & Dietetics
8236
Obstetrics & Gynecology
8764
Oncology
56108
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10559
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4678
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12293
Orthopedics, Rehabilitation & Sports Medicine
1900
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1603
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5205
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1095
Pathology
5258
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22942
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4938
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37816
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13274
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9435
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620
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863
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21376
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5404
Psychology, Applied
97
Psychology, Biological
365
Psychology, Clinical
843
Psychology, Developmental
225
Psychology, Educational
149
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136
Psychology, Mathematical
0
Psychology, Multidisciplinary
1628
Psychology, Psychoanalysis
41
Psychology, Social
116
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2327
Public, Environmental & Occupational Health
29122
Quantum Science & Technology
0
Radiology, Nuclear Medicine & Imaging
13243
Radiology, Nuclear Medicine & Medical Imaging
8204
Rehabilitation
3124
Remote Sensing
0
Reproductive Biology
3076
Reproductive Medicine
1265
Research/Laboratory Medicine & Medical Technology
4231
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7715
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6348
Social Sciences, Biomedical
1265
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2853
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36288
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4472
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938
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314
Urology & Nephrology
13959
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35
Virology
2524
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0
渠道
HAEMOPHILIA
143
Hematology\Oncology
3
Medrxiv - Hematology
186
AMERICAN JOURNAL OF HEMATOLOGY
248
BIOLOGY OF BLOOD AND MARROW TRANSPLANTATION
20
BLOOD CANCER JOURNAL
521
BRITISH JOURNAL OF HAEMATOLOGY
460
CIRCULATION RESEARCH
383
CRITICAL REVIEWS IN ONCOLOGY HEMATOLOGY
612
JOURNAL OF CLINICAL APHERESIS
57
JOURNAL OF THROMBOSIS AND HAEMOSTASIS
258
LANCET HAEMATOLOGY
29
THERAPEUTIC ADVANCES IN HEMATOLOGY
35
ACTA HAEMATOLOGICA
159
BEST PRACTICE & RESEARCH CLINICAL HAEMATOLOGY
144
BLOOD COAGULATION & FIBRINOLYSIS
69
BLOOD PURIFICATION
188
CURRENT OPINION IN HEMATOLOGY
42
EUROPEAN JOURNAL OF HAEMATOLOGY
95
EXPERIMENTAL HEMATOLOGY & ONCOLOGY
261
INTERNATIONAL JOURNAL OF LABORATORY HEMATOLOGY
231
HAMOSTASEOLOGIE
190
ASIAN JOURNAL OF TRANSFUSION SCIENCE
20
EGYPTIAN JOURNAL OF HAEMATOLOGY
35
HEMASPHERE
404
HEMATOLOGY REPORTS
17
IRAQI JOURNAL OF HEMATOLOGY
88
CURRENT HEMATOLOGIC MALIGNANCY REPORTS
109
INTERNATIONAL JOURNAL OF HEMATOLOGY
605
JOURNAL OF HEMATOPATHOLOGY
128
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Acquired haemophilia A: Insight into treatment and outcomes from an Australian tertiary referral centre
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Social participation is reduced in type 3 Von Willebrand disease patients and in patients with a severe bleeding phenotype
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Pain memories: A new concept to consider in the management of chronic pain in people with haemophilia
Corresponding Author Anna J. Wells Haemophilia, Haemostasi...
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Nephrotic syndrome in two haemophilia B children with inhibitor under low‐dose immune tolerance induction combined with rituximab‐based immunosuppressant protocol
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Immune tolerance induction in the era of emicizumab – still the first choice for patients with haemophilia A and inhibitors?
Abstract Introduction The development of inhibitory antibodies is a severe complication of clotting factor replacement the...
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Impact of obesity on factor VIII and von Willebrand factor levels in patients with Type 1 von Willebrand disease and low von Willebrand factor: An analysis of the ATHNdataset
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Successful perioperative prophylaxis with susoctocog alfa in a patient with acquired haemophilia A: A case study
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The relationship between chronic pain and psychosocial aspects in patients with haemophilic arthropathy. A cross‐sectional study
Abstract Background Pain is a major characteristic in haemophilic arthropathy. Identifying the psychosocial variables affe...
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Determining causes of death among individuals with haemophilia in Afghanistan
Abstract Introduction Haemophilia is a well-known bleeding disorder that affects people worldwide. The main therapeutic st...
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Off‐label use of emicizumab in persons with acquired haemophilia A and von Willebrand disease: A scoping review of the literature
Abstract Introduction Since the approval of emicizumab, a bispecific, factor VIII-mimetic antibody, for use in person...
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Patients on emicizumab prophylaxis with previously tolerized inhibitors: Is there a risk of inhibitors recurrence?
Early View LETTER TO THE EDITOR Eman Hassan, Corresponding Author Depa...
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Is immune tolerance induction conceivable in haemophilia with inhibitors in a low‐middle income country? Real‐world data from Tunisia
Corresponding Author emnahammami1993@gmail.com orcid.org/0...
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Clinical outcomes after joint surgery in patients on turoctocog alfa pegol (N8‐GP) prophylaxis: A post hoc analysis
Abstract Introduction Joint damage in haemophilia often requires surgical correction. However, the surgery effect on bleed...
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Dental habits and oral health in children and adolescents with bleeding disorders: A single‐institution cross‐sectional study
Abstract Introduction Oral health is an important component of care at haemophilia treatment centres (HTCs). Correlations ...
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Low‐dose immune tolerance induction therapy in children of Arab descent with severe haemophilia A, high inhibitor titres and poor prognostic factors for immune tolerance induction treatment success
Abstract Introduction Immune Tolerance Induction (ITI) is the first-choice therapy to eradicate Factor VIII (FVIII) neutra...
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Vaccination in children with inherited bleeding disorders: Does the use of plasma an d factor affect the response to the vaccine: An institutional registry
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Zero incidence of factor VIII inhibitors and successful haemostatic response in previously factor VIII‐treated patients with haemophilia A switching to turoctocog alfa in a noninterventional study
Abstract Introduction Turoctocog alfa (NovoEight®) is a B-domain-truncated recombinant factor VIII (FVIII) approved f...
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Sexual issues in people with haemophilia: Awareness and strategies for overcoming communication barriers
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Port removal in patients receiving emicizumab prophylaxis: A single centre experience and review of the literature
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A distinct common p.Gln317* mutation among causative LMAN1 genetic mutations of combined factor V and factor VIII deficiency in five Taiwanese families
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Evaluation of anti‐factor VIII antibodies in haemophilia A subjects switching products following a provincial tender
Molecular Diagnostic Laboratory, Centre Hospitalier Universitaire Sainte-Justine, Montréal, Canada ...
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rFIXFc prophylaxis improves pain and levels of physical activity in haemophilia B: Post hoc analysis of B‐LONG using haemophilia‐specific quality of life questionnaires
Abstract Introduction Recurrent bleeding in severe haemophilia B causes painful hemarthroses and reduces capacity for phys...
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Bleeding patterns in patients before and after diagnosis of von Willebrand disease: Analysis of a US medical claims database
Abstract Introduction Von Willebrand disease (VWD) is the most common inherited bleeding disorder. The bleeding phenotype ...
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Excess weight gain in the paediatric bleeding disorders population: Impact of the COVID‐19 Pandemic
Abstract Introduction The COVID-19 pandemic has resulted in lifestyle changes for children. The aim of this study was to e...
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Trends of outcomes and healthcare utilization following orthopaedic procedures in adults with haemophilia: A 3‐decade retrospective review
Abstract Introduction Haemophilic arthropathy is a serious complication of haemophilia often requiring surgical interventi...
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Efficacy and safety evaluation of Fanhdi®, a plasma‐derived factor VIII/ von Willebrand factor concentrate, in Von Willebrand's disease patients undergoing surgery or invasive procedures: A prospective clinical study
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In vitro effects of emicizumab on activated clotting time in blood samples from cardiac surgical patients
Abstract Background Heparin management in hemophilia A (HA) patients with a factor VIII (FVIII) inhibitor can be challengi...
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