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Type 3 von Willebrand Disease

A subtype of von Willebrand disease that results from a total or near total deficiency of VON WILLEBRAND FACTOR.
Also Known As:
von Willebrand Disease, Type 3; Type 3 VWD; Type 3 Von Willebrand's Disease; Von Willebrand Disease, Severe Form
Networked: 149 relevant articles (5 outcomes, 15 trials/studies)

Relationship Network

Disease Context: Research Results

Related Diseases

1. Hemorrhage
2. Hemophilia A (Haemophilia)
3. Duchenne Muscular Dystrophy (Muscular Dystrophy, Becker)
4. Palmoplantar Keratoderma (Keratosis Palmaris et Plantaris)
5. Familial Exudative Vitreoretinopathies

Experts

1. Federici, Augusto B: 8 articles (01/2022 - 05/2003)
2. Budde, Ulrich: 7 articles (01/2022 - 11/2005)
3. Baronciani, Luciano: 6 articles (01/2022 - 05/2003)
4. Federici, A B: 6 articles (10/2008 - 10/2000)
5. Oldenburg, Johannes: 5 articles (03/2022 - 11/2019)
6. Lassila, Riitta: 5 articles (01/2022 - 07/2019)
7. Leebeek, Frank W G: 5 articles (01/2022 - 07/2011)
8. Mannucci, Pier Mannuccio: 5 articles (01/2022 - 05/2003)
9. Peyvandi, Flora: 5 articles (01/2022 - 05/2003)
10. Yadegari, Hamideh: 4 articles (03/2022 - 11/2019)

Drugs and Biologics

Drugs and Important Biological Agents (IBA) related to Type 3 von Willebrand Disease:
1. IsoantibodiesIBA
2. Factor VIII (Coagulation Factor VIII)IBA
3. emicizumabIBA
4. von Willebrand FactorIBA
5. human F8 proteinFDA Link
6. Deamino Arginine Vasopressin (Desmopressin)FDA LinkGeneric
7. RNA (Ribonucleic Acid)IBA
8. AntigensIBA
9. Cysteine (L-Cysteine)FDA Link
10. Messenger RNA (mRNA)IBA

Therapies and Procedures

1. Therapeutics
2. Operative Surgical Procedures
3. Cesarean Section (Caesarean Section)
4. Contraindications
5. Abdominoplasty