prednisone has been researched along with Camurati-Engelmann Disease in 8 studies
Prednisone: A synthetic anti-inflammatory glucocorticoid derived from CORTISONE. It is biologically inert and converted to PREDNISOLONE in the liver.
prednisone : A synthetic glucocorticoid drug that is particularly effective as an immunosuppressant, and affects virtually all of the immune system. Prednisone is a prodrug that is converted by the liver into prednisolone (a beta-hydroxy group instead of the oxo group at position 11), which is the active drug and also a steroid.
Excerpt | Relevance | Reference |
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"Camurati-Engelmann disease (CED) is a rare form of progressive bone dysplasia due to mutations in the transforming factor gene TGFB1 on chromosome 19q13." | 1.39 | A family with Camurati-Engelman disease. The role of the missense p.R218C mutation in TGFB1 in bones and endocrine glands. ( Allgrove, J; Anastasiadou, V; Neocleous, V; Phylactou, LA; Shammas, C; Skordis, N; Toumba, M, 2013) |
"We suggest that the progressive diaphyseal dysplasia gene has a function in endochondral bone formation and that its mutation is a dynamic one with repeat expansion enhanced in father-to-son transmission." | 1.30 | Progressive diaphyseal dysplasia: a three-generation family with markedly variable expressivity. ( Saraiva, JM, 1997) |
"The authors have studied two cases of progressive diaphyseal dysplasia (Camurati Engelmann's disease)." | 1.27 | Progressive diaphyseal dysplasia: Camurati-Engelmann's disease. ( Calorio, D; Cartesegna, M; Crova, M; Lazzarone, C, 1983) |
"Progressive diaphyseal dysplasia is characterized clinically by crippling leg pain, fatigue, headache, poor appetite, muscle weakness, and waddling gait." | 1.27 | Progressive diaphyseal dysplasia: evaluation of corticosteroid therapy. ( Alon, U; Berant, M; Kaftori, JK; Naveh, Y, 1985) |
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 3 (37.50) | 18.7374 |
1990's | 1 (12.50) | 18.2507 |
2000's | 0 (0.00) | 29.6817 |
2010's | 4 (50.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Pijls, BG | 1 |
Steentjes, K | 1 |
Schoones, JW | 1 |
Dijkstra, SP | 1 |
Combier, A | 1 |
Palazzo, E | 1 |
Forien, M | 1 |
Gardette, A | 1 |
Dieudé, P | 1 |
Ottaviani, S | 1 |
Toumba, M | 1 |
Neocleous, V | 1 |
Shammas, C | 1 |
Anastasiadou, V | 1 |
Allgrove, J | 1 |
Phylactou, LA | 1 |
Skordis, N | 1 |
Mazaheri, P | 1 |
Nadkarni, G | 1 |
Lowe, E | 1 |
Hines, P | 1 |
Vuica, M | 1 |
Griffin, M | 1 |
Resar, LM | 1 |
Lazzarone, C | 1 |
Cartesegna, M | 1 |
Crova, M | 1 |
Calorio, D | 1 |
Saraiva, JM | 1 |
Naveh, Y | 1 |
Alon, U | 1 |
Kaftori, JK | 1 |
Berant, M | 1 |
Lindstrom, JA | 1 |
2 reviews available for prednisone and Camurati-Engelmann Disease
Article | Year |
---|---|
Ribbing disease: a systematic review.
Topics: Adult; Anti-Inflammatory Agents, Non-Steroidal; Camurati-Engelmann Syndrome; Female; Glucocorticoids | 2018 |
Failure of conventional treatment and losartan in Camurati-Engelmann disease: A case report.
Topics: Adult; Analgesics; Anti-Inflammatory Agents, Non-Steroidal; Camurati-Engelmann Syndrome; Drug Therap | 2018 |
6 other studies available for prednisone and Camurati-Engelmann Disease
Article | Year |
---|---|
A family with Camurati-Engelman disease. The role of the missense p.R218C mutation in TGFB1 in bones and endocrine glands.
Topics: Amino Acid Substitution; Anti-Inflammatory Agents; Bone and Bones; Calcium, Dietary; Camurati-Engelm | 2013 |
Ghosal hematodiaphyseal dysplasia: a rare cause of a myelophthisic anemia.
Topics: Adult; Anemia, Myelophthisic; Anti-Inflammatory Agents; Camurati-Engelmann Syndrome; Female; Humans; | 2010 |
Progressive diaphyseal dysplasia: Camurati-Engelmann's disease.
Topics: Bone Diseases, Developmental; Camurati-Engelmann Syndrome; Humans; Male; Middle Aged; Prednisone; Ti | 1983 |
Progressive diaphyseal dysplasia: a three-generation family with markedly variable expressivity.
Topics: Adolescent; Adult; Camurati-Engelmann Syndrome; Child; Female; Genomic Imprinting; Humans; Male; Mic | 1997 |
Progressive diaphyseal dysplasia: evaluation of corticosteroid therapy.
Topics: Adolescent; Adult; Camurati-Engelmann Syndrome; Child; Child, Preschool; Drug Administration Schedul | 1985 |
Diaphyseal dysplasia (Engelmann) treated with corticosteroids.
Topics: Adolescent; Bone Diseases, Developmental; Camurati-Engelmann Syndrome; Child; Child, Preschool; Huma | 1974 |