Page last updated: 2024-10-28

hydroxyurea and Orphan Diseases

hydroxyurea has been researched along with Orphan Diseases in 4 studies

Orphan Diseases: Rare diseases that have not been well studied.

Research

Studies (4)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's4 (100.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Platto, J1
Alexander, CE1
Kurtzman, DJB1
Vencato, E1
Manfredi, R1
Zamò, A1
Chilosi, M1
Beccari, S1
De Franceschi, L1
Bandyopadhyay, D1
Manna, S1
Hajra, A1
Bhattacharya, TD1
Inoue, S1
Okiyama, N1
Okune, M1
Shiraki, N1
Kessoku, R1
Fujimoto, M1

Reviews

1 review available for hydroxyurea and Orphan Diseases

ArticleYear
Clinical and histological characteristics of livedo racemosa in essential thrombocythemia: A report of two cases and review of the published works.
    The Journal of dermatology, 2017, Volume: 44, Issue:1

    Topics: Aged; Aspirin; Calreticulin; Humans; Hydroxyurea; Janus Kinase 2; Livedo Reticularis; Male; Middle A

2017

Other Studies

3 other studies available for hydroxyurea and Orphan Diseases

ArticleYear
A Violaceous, Photodistributed Cutaneous Eruption and Leg Ulcer in a Woman With Essential Thrombocytosis.
    JAMA dermatology, 2018, 01-01, Volume: 154, Issue:1

    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.
    American journal of hematology, 2014, Volume: 89, Issue:12

    Topics: Anemia, Sickle Cell; Cytapheresis; Female; Histiocytic Necrotizing Lymphadenitis; Humans; Hydroxyure

2014
Atypical CML with massive splenic infarct: an extremely rare presentation.
    BMJ case reports, 2015, Nov-12, Volume: 2015

    Topics: Abdominal Pain; Anemia; Anti-Inflammatory Agents, Non-Steroidal; Antineoplastic Agents; Fatal Outcom

2015