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Haemophilia
Protein C and S Deficiency in Deep Vein Thrombosis Patients Referred to Iranian Blood Transfusion Organization, Kermanshah
Understanding Haemophilia
Understanding Haemophilia CHAPTER 2
Terminology Resource File
Delivery of Treatment for Haemophilia
Guidelines for the Management of Haemophilia in Australia
PDFS/ED517971.Pdf
Inheritance of Factor VII and Protein S Deficiency Together with Factor V
Pregnancy in Women with Inherited Bleeding Disorders
Complications in Clotting Find out How Haemophilia Can
Bleeding Disorders in Congenital Syndromes Susmita N
Pathway for Adult Patients with Inherited Bleeding Disorders: Emergency Surgery Please Contact Haemophilia Team for All Patients with Bleeding Disorders
Uses and Abuses of Fresh Frozen Plasma for the Treatment of Bleeding
Factor XI Deficiency
FRACP Lecture Series AGENDA Investigations Haemophilia
Current Practices in Haemophilic Patients Undergoing Orthopedic Surgery ‑ a Systematic Review
Bleeding Thrombotic and Platelet Disorder TIER1 Genes (V.ISTH 2019.1)
Information About Pregnancy for Haemophilia Carriers
Top View
Guidelines for the Management of Hemophilia
Glanzmann's Thrombasthenia and Bernard-Soulier Syndrome
Lymphocyte Subset Ratios and Factor VIII Usage in Haemophilia
Gynaecological and Obstetric Management of Women with Inherited Bleeding Disorders
Understanding Haemophilia
Report on Haemophilia Registries Workshop 8 June 2018 Patient Registries Initiative
Acquired Haemophilia Mimicking Dermatitis Artefacta
In Hemophilia a with Or Without Factor Viii Inhibitors
Joint Replacement Surgery in Hemophilia
Download PDF 1.8MB
Guidelines for the Emergency Treatment and Management of Patients with Haemophilia & Bleeding Disorders
Carriers of Haemophilia
Factor XI Deficiency
Atypical Bleeding Due to Idiopathic Thrombocytopenia in Association with Low Factor VIII Levels M F Riordan,Fghhill
Standards for Clinical Care of Adults with Sickle Cell Disease in the UK
INHERITED COAGULATION DISORDERS in PREGNANCY David Lagrew, MD, Saddleback Memorial Medical Center
Severe Haemophilia a and Sickle Cell Disease
Spinal Epidural Haematoma in a Patient with Haemophilia-B
How to Manage a Patient with Haemophilia and ACS Requiring PCI: a Battle Between Bleeding and Thrombosis
June 2018 Monitoring International Trends
ACQUIRED HEMOPHILIA Revised Edition
Mild Or Moderate Haemophilia - How Will It Affect My Life? Information for Patients
The Obstetric Experience of Carriers of Haemophilia
A Rare Seen Hemorrhage Disorder: Factor XI Deficiency Hemophilia C
Inherited Thrombocytopenia Panel Thrombocytopenia Will Be Identified with This Panel, Including Aug; 43(8): 732–734
Clinical Guidelines Postgrad Med J: First Published As 10.1136/Pgmj.72.844.87 on 1 February 1996
Factor XI Deficiency
NCBDDD 2018 Annual Report
Jebmh.Com Review Article
Reproductive Health in Women with Bleeding Disorders
Rare Bleeding Disorders
Immunological Aspects of Inhibitor Development in Haemophilia
Haemophilia A
MASAC Document #206 (Replaces #174)
What Are the Goals of Gene Therapy Research?
Wellcome Witnesses to Twentieth Century Medicine
Bernard-Soulier Syndrome
Cell Disease and Severe Haemophilia A: Thromboelastography Profiles
Molecular Genetics of Hemophilia A: Clinical Perspectives
Case Report “Sickle Cell Trait and Haemophilia: a Rare Association”
Bernard‐Soulier Syndrome
General Surgery in Haemophiliac Patients Postgrad Med J: First Published As 10.1136/Pmj.76.898.494 on 1 August 2000
S41598-021-95066-8.Pdf
Do Prothrombotic Factors Influence Clinical Phenotype of Severe Haemophilia? a Review of the Literature Karin Van Dijk1,2, Johanna G
Package Insert
Occurrence of Protein S Deficiency
Types of Bleeding Disorders
Mild Haemophilia
Management of COVID‐19‐Associated Coagulopathy in Persons with Haemophilia
Gene Therapy for Haemophilia
Derived Factor VIII (FVIII) Concentrate Is Rare and Not Necessarily Triggered by FVIII
Autosomal Dominant Thrombocytopenia Panel: Gene, Clinical Phenotype, OMIM Number and Inheritance Pattern
Sickle Cell Health Policy: Regional Rare Blood Disorder Synergies
Impaired Cell Mediated Immunity in Haemophilia in the Absence of Infection with Human Immunodeficiency Virus
Bleeding Disorders
Mild Haemophilia B
What Causes Genetic Conditions?
Haemophilia Postgrad Med J: First Published As 10.1136/Pgmj.73.858.201 on 1 April 1997
Surgery and Coagulopathy: Pre-Op Assessment and Optimisation Dr Catherine Roughley Haemostasis Consultant Kent Haemophilia Centre, EKHUFT Intro…
Surgery and Bleeding Disorders
The Obstetric and Gynaecological Management of Women with Inherited Bleeding Disorders
Guideline on Recombinant and Plasma-Derived FVIII Products