hydroxyurea has been researched along with Orphan Diseases in 4 studies
Orphan Diseases: Rare diseases that have not been well studied.
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 0 (0.00) | 29.6817 |
2010's | 4 (100.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Platto, J | 1 |
Alexander, CE | 1 |
Kurtzman, DJB | 1 |
Vencato, E | 1 |
Manfredi, R | 1 |
Zamò, A | 1 |
Chilosi, M | 1 |
Beccari, S | 1 |
De Franceschi, L | 1 |
Bandyopadhyay, D | 1 |
Manna, S | 1 |
Hajra, A | 1 |
Bhattacharya, TD | 1 |
Inoue, S | 1 |
Okiyama, N | 1 |
Okune, M | 1 |
Shiraki, N | 1 |
Kessoku, R | 1 |
Fujimoto, M | 1 |
1 review available for hydroxyurea and Orphan Diseases
Article | Year |
---|---|
Clinical and histological characteristics of livedo racemosa in essential thrombocythemia: A report of two cases and review of the published works.
Topics: Aged; Aspirin; Calreticulin; Humans; Hydroxyurea; Janus Kinase 2; Livedo Reticularis; Male; Middle A | 2017 |
3 other studies available for hydroxyurea and Orphan Diseases
Article | Year |
---|---|
A Violaceous, Photodistributed Cutaneous Eruption and Leg Ulcer in a Woman With Essential Thrombocytosis.
Topics: Aged; Biopsy, Needle; Dermatomyositis; Exanthema; Female; Follow-Up Studies; Humans; Hydroxyurea; Im | 2018 |
A rare disorder in an orphan disease: Kikuchi-Fujimoto disease in a young-adult patient with sickle cell anemia.
Topics: Anemia, Sickle Cell; Cytapheresis; Female; Histiocytic Necrotizing Lymphadenitis; Humans; Hydroxyure | 2014 |
Atypical CML with massive splenic infarct: an extremely rare presentation.
Topics: Abdominal Pain; Anemia; Anti-Inflammatory Agents, Non-Steroidal; Antineoplastic Agents; Fatal Outcom | 2015 |