pamidronate has been researched along with Chondrodystrophic Myotonia in 2 studies
| Excerpt | Relevance | Reference |
|---|---|---|
| "Cammurati-Engelmann's Disease or Progressive Diaphyseal Dysplasia (PDD), is a rare autosomal dominant disorder, sometimes non hereditable, which begins in childhood, and is characterized by symmetrical excess of osseous apposition in diaphysis and metaphysis of long bones." | 1.30 | [Clinical, humoral and scintigraphic assessment of a bisphosphonate as potential treatment of diaphyseal dysplasia: Ribbing and Cammurati-Engelmann diseases]. ( de Rubin, ZS; Ghiringhelli, G; Mansur, JL, 1997) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 1 (50.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 1 (50.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Munns, CF | 1 |
| Fahiminiya, S | 1 |
| Poudel, N | 1 |
| Munteanu, MC | 1 |
| Majewski, J | 1 |
| Sillence, DO | 1 |
| Metcalf, JP | 1 |
| Biggin, A | 1 |
| Glorieux, F | 1 |
| Fassier, F | 1 |
| Rauch, F | 1 |
| Hinsdale, ME | 1 |
| de Rubin, ZS | 1 |
| Ghiringhelli, G | 1 |
| Mansur, JL | 1 |
2 other studies available for pamidronate and Chondrodystrophic Myotonia
| Article | Year |
|---|---|
Homozygosity for frameshift mutations in XYLT2 result in a spondylo-ocular syndrome with bone fragility, cataracts, and hearing defects.
Topics: Base Sequence; Cataract; Craniofacial Abnormalities; Diphosphonates; Exome; Eye Diseases, Hereditary | 2015 |
[Clinical, humoral and scintigraphic assessment of a bisphosphonate as potential treatment of diaphyseal dysplasia: Ribbing and Cammurati-Engelmann diseases].
Topics: Adolescent; Aged; Camurati-Engelmann Syndrome; Diphosphonates; Female; Humans; Osteochondrodysplasia | 1997 |