1
|
Marie PJ, de Pollak C, Chanson P and Lomri
A: Increased proliferation of osteoblastic cells expressing the
activating Gs alpha mutation in monostotic and polyostotic fibrous
dysplasia. Am J Pathol. 150:1059–1069. 1997.
|
2
|
Riminucci M, Kuznetsov SA, Cherman N,
Corsi A, Bianco P and Gehron Robey P: Osteoclastogenesis in fibrous
dysplasia of bone: In situ and in vitro analysis of IL-6
expression. Bone. 33:434–442. 2003. View Article : Google Scholar : PubMed/NCBI
|
3
|
Lane JM, Khan SN, O'Connor WJ, et al:
Bisphosphonate therapy in fibrous dysplasia. Clin Orthop. 382:6–12.
2001. View Article : Google Scholar : PubMed/NCBI
|
4
|
Isaia GC, Lala R, Defilippi C, et al: Bone
turnover in children and adolescents with McCune-Albright syndrome
treated with pamidronate for bone fibrous dysplasia. Calcif Tissue
Int. 71:121–128. 2002. View Article : Google Scholar : PubMed/NCBI
|
5
|
Chapurlat RD, Hugueny P, Delmas PD and
Meunier PJ: Treatment of fibrous dysplasia of bone with intravenous
pamidronate: long-term effectiveness and evaluation of predictors
of response to treatment. Bone. 35:235–242. 2004. View Article : Google Scholar : PubMed/NCBI
|
6
|
Chapurlat RD: Medical therapy in adults
with fibrous dysplasia of bone. J Bone Miner Res. 21(Suppl 2):
114–119. 2006. View Article : Google Scholar : PubMed/NCBI
|
7
|
Yamomoto T, Ozono K, Shima M, Yoshikawa H
and Okada S: Alendronate and pharmacological doses of 1 alpha OHD3
therapy in a patient with McCune-Albright syndrome and accompanying
hypophosphatemia. J Bone Miner Metab. 20:170–173. 2002. View Article : Google Scholar : PubMed/NCBI
|
8
|
Khadilkar VV, Khadilkar AV and Maskati GB:
Oral bisphosphonates in polyostotic fibrous dysplasia. Indian
Pediatr. 40:894–896. 2003.PubMed/NCBI
|
9
|
Kitagawa Y, Tamai K and Ito H: Oral
alendronate treatment for polyostotic fibrous dysplasia: a case
report. J Orthop Sci. 9:521–525. 2004. View Article : Google Scholar : PubMed/NCBI
|
10
|
Aragão AL and Silva IN: Oral Alendronate
Treatment for Severe Polyostotic Fibrous Dysplasia due to
McCune-Albright Syndrome in a Child: A Case Report. Int J Pediatr
Endocrinol. Oct 4–2010.(E-pub ahead of print).
|
11
|
Harris WH, Dudley HR Jr and Barry RJ: The
natural history of fibrous dysplasia. An orthopaedic, pathological,
and roentgenographic study. J Bone Joint Surg Am. 44:A207–A233.
1962.PubMed/NCBI
|
12
|
Sissons HA and Malcolm AJ: Fibrous
dysplasia of bone: case report with autopsy study 80 years after
the original clinical recognition of the bone lesions. Skeletal
Radiol. 26:177–183. 1997.PubMed/NCBI
|
13
|
Szendrói M, Rahóty P, Antal I and Kiss J:
Fibrous dysplasia associated with intramuscular myxoma (Mazabraud's
syndrome): a long-term follow-up of three cases. J Cancer Res Clin
Oncol. 124:401–406. 1998.
|
14
|
Plotkin H, Rauch F, Zeitlin L, Munns C,
Travers R and Glorieux FH: Effect of pamidronate treatment in
children with polyostotic fibrous dysplasia of bone. J Clin
Endocrinol Metab. 88:4569–4575. 2003. View Article : Google Scholar : PubMed/NCBI
|
15
|
Collins MT, Kushner H, Reynolds JC, et al:
An instrument to measure skeletal burden and predict functional
outcome in fibrous dysplasia of bone. J Bone Miner Res. 20:219–226.
2005. View Article : Google Scholar : PubMed/NCBI
|