hydroxyurea has been researched along with Angiohemophilia in 7 studies
| 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 Angiohemophilia
| 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 |