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prednisolone and von Willebrand Diseases

prednisolone has been researched along with von Willebrand Diseases in 5 studies

Prednisolone: A glucocorticoid with the general properties of the corticosteroids. It is the drug of choice for all conditions in which routine systemic corticosteroid therapy is indicated, except adrenal deficiency states.
prednisolone : A glucocorticoid that is prednisone in which the oxo group at position 11 has been reduced to the corresponding beta-hydroxy group. It is a drug metabolite of prednisone.

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.

Research Excerpts

ExcerptRelevanceReference
"Treatment with prednisolone (40 mg/day) started and the bleeding tendency gradually improved."1.31Acquired type 3-like von Willebrand syndrome preceded full-blown systemic lupus erythematosus. ( Hasegawa, H; Hayashi, Y; Kushiro, M; Niiya, K; Niiya, M; Takazawa, Y; Tanimizu, M; Tanimoto, M; Tanio, Y, 2002)

Research

Studies (5)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's2 (40.00)18.2507
2000's2 (40.00)29.6817
2010's1 (20.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Kasatkar, P1
Ghosh, K1
Shetty, S1
Sakai, M1
Shima, M1
Izumi, Y1
Shirahata, A1
Jackson, N1
Hashim, ZA1
Zainal, NA1
Jamaluddin, N1
Niiya, M1
Niiya, K1
Takazawa, Y1
Hayashi, Y1
Tanio, Y1
Kushiro, M1
Tanimizu, M1
Hasegawa, H1
Tanimoto, M1
Ishimaru, F1
Hayashi, H1
Fujita, T1
Tsurumi, N1
Tsuda, T1
Kimura, I1

Other Studies

5 other studies available for prednisolone and von Willebrand Diseases

ArticleYear
An atypical manifestation of acquired von Willebrand syndrome (AVWS) associated with systemic lupus erythematosus (SLE).
    Annals of hematology, 2014, Volume: 93, Issue:1

    Topics: Antibody Specificity; Autoantibodies; Diagnosis, Differential; Factor VIII; Female; Humans; Immunosu

2014
[Acquired von Willebrand syndrome with autoimmune hemolytic anemia].
    [Rinsho ketsueki] The Japanese journal of clinical hematology, 2004, Volume: 45, Issue:3

    Topics: Adolescent; Anemia, Hemolytic, Autoimmune; Antigens; Biomarkers; Coombs Test; Factor VIII; Female; H

2004
Puerperal acquired factor VIII inhibitor causing a von Willebrand-like syndrome in a patient with anti-DNA antibodies.
    Singapore medical journal, 1995, Volume: 36, Issue:2

    Topics: Adult; Antibodies, Antinuclear; Factor VIII; Female; Gingival Hemorrhage; Humans; Lupus Erythematosu

1995
Acquired type 3-like von Willebrand syndrome preceded full-blown systemic lupus erythematosus.
    Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis, 2002, Volume: 13, Issue:4

    Topics: Adolescent; Deamino Arginine Vasopressin; Female; Hemorrhage; Humans; Lupus Erythematosus, Systemic;

2002
[Acquired von Willebrand syndrome with autoimmune hemolytic anemia].
    [Rinsho ketsueki] The Japanese journal of clinical hematology, 1990, Volume: 31, Issue:9

    Topics: Adult; Anemia, Hemolytic, Autoimmune; Female; Humans; Prednisolone; von Willebrand Diseases; von Wil

1990