hydroxyurea has been researched along with von Willebrand Diseases in 7 studies
von Willebrand Diseases: Group of hemorrhagic disorders in which the VON WILLEBRAND FACTOR is either quantitatively or qualitatively abnormal. They are usually inherited as an autosomal dominant trait though rare kindreds are autosomal recessive. Symptoms vary depending on severity and disease type but may include prolonged bleeding time, deficiency of factor VIII, and impaired platelet adhesion.
| Excerpt | Relevance | Reference |
|---|---|---|
| " In the past 5 years from May 1986, 14 operations were conducted in our clinic on 13 patients, consisting of 4 with von Willebrand disease (vWd), 1 with hemophilia B, 4 who had warfarin administration, 3 with essential thrombocythemia and 2 with spherocytosis." | 3.68 | [Clinical experience of urological surgery of the patients with hemostatic disorder or hemolytic disease]. ( Kinoshita, S; Matsubuchi, T; Matsumiya, K; Nishimura, K; Oka, T; Takaha, M; Tsujimura, A; Yasui, M; Yasunaga, Y, 1992) |
| "Hydroxyurea treatment was initiated, leading to a gradual decrease in platelet count." | 1.62 | Differential diagnostic and treatment difficulties in a patient with acquired von Willebrand syndrome. ( Bedekovics, J; Bereczky, Z; Illés, Á; Kracskó, B; Magyari, F; Schlammadinger, Á, 2021) |
| "Non-melanoma skin cancers were reported in 51 patients (27%)." | 1.40 | Cyclical thrombocytosis, acquired von Willebrand syndrome and aggressive non-melanoma skin cancers are common in patients with Philadelphia-negative myeloproliferative neoplasms treated with hydroxyurea. ( Forsyth, C; Grigg, A; Verner, E, 2014) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 3 (42.86) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 3 (42.86) | 24.3611 |
| 2020's | 1 (14.29) | 2.80 |
| Authors | Studies |
|---|---|
| Magyari, F | 1 |
| Kracskó, B | 1 |
| Bedekovics, J | 1 |
| Bereczky, Z | 1 |
| Illés, Á | 1 |
| Schlammadinger, Á | 1 |
| Verner, E | 1 |
| Forsyth, C | 1 |
| Grigg, A | 1 |
| Kreher, S | 1 |
| Ochsenreither, S | 1 |
| Trappe, RU | 1 |
| Pabinger, I | 1 |
| Bergmann, F | 1 |
| Petrides, PE | 1 |
| Koschmieder, S | 1 |
| Matzdorff, A | 1 |
| Tiede, A | 1 |
| Griesshammer, M | 1 |
| Riess, H | 1 |
| Rolf, N | 1 |
| Suttorp, M | 1 |
| Budde, U | 1 |
| Siegert, G | 1 |
| Knoefler, R | 1 |
| van Genderen, PJ | 2 |
| Michiels, JJ | 2 |
| van der Poel-van de Luytgaarde, SC | 1 |
| van Vliet, HH | 1 |
| Leenknegt, H | 1 |
| Matsumiya, K | 1 |
| Nishimura, K | 1 |
| Tsujimura, A | 1 |
| Yasunaga, Y | 1 |
| Oka, T | 1 |
| Takaha, M | 1 |
| Yasui, M | 1 |
| Kinoshita, S | 1 |
| Matsubuchi, T | 1 |
7 other studies available for hydroxyurea and von Willebrand Diseases
| Article | Year |
|---|---|
Differential diagnostic and treatment difficulties in a patient with acquired von Willebrand syndrome.
Topics: Aged, 80 and over; Blood Transfusion; Enzyme Inhibitors; Hemorrhage; Humans; Hydroxyurea; Male; Thro | 2021 |
Cyclical thrombocytosis, acquired von Willebrand syndrome and aggressive non-melanoma skin cancers are common in patients with Philadelphia-negative myeloproliferative neoplasms treated with hydroxyurea.
Topics: Adult; Aged; Aged, 80 and over; Female; Humans; Hydroxyurea; Janus Kinase 2; Leukemia, Myeloid, Chro | 2014 |
Prophylaxis and management of venous thromboembolism in patients with myeloproliferative neoplasms: consensus statement of the Haemostasis Working Party of the German Society of Hematology and Oncology (DGHO), the Austrian Society of Hematology and Oncolo
Topics: Anticoagulants; Disease Susceptibility; Drug Interactions; Female; Hemorrhage; Heparin, Low-Molecula | 2014 |
Essential thrombocythaemia in a teenage girl resulting in acquired von Willebrand syndrome with joint haemorrhage and menorrhagia.
Topics: Adolescent; Antigens, CD34; Blood Cell Count; Blood Platelets; Female; Hemorrhage; Humans; Hydroxyur | 2010 |
Acquired von Willebrand disease as a cause of recurrent mucocutaneous bleeding in primary thrombocythemia: relationship with platelet count.
Topics: Adult; Bleeding Time; Female; Hemorrhage; Humans; Hydroxyurea; Mucous Membrane; Platelet Count; Skin | 1994 |
The paradox of bleeding and thrombosis in thrombocythemia: is von Willebrand factor the link?
Topics: Aged; Alkylating Agents; Aspirin; Erythromelalgia; Female; Fibrinolytic Agents; Hemorrhage; Hemorrha | 1997 |
[Clinical experience of urological surgery of the patients with hemostatic disorder or hemolytic disease].
Topics: Adult; Aged; Blood Coagulation Factors; Blood Transfusion, Autologous; Child; Child, Preschool; Fact | 1992 |