Articles
Volume 7 Supplement 1
International Meeting on Fibrous Dysplasia/McCune-Albright Syndrome and Cherubism
Proceedings
International Meeting on Fibrous Dysplasia/McCune-Albright Syndrome and Cherubism: Best Clinical Practice and Future Research
Bethesda, MD, USA
3-5 October 2010
Edited by Michael T Collins
The International Meeting on Fibrous Dysplasia/McCune-Albright Syndrome and Cherubism: Best Clinical Practice and Future Research was funded by the Fibrous Dysplasia Foundation, and the National Institutes of Health (Division of Intramural Research National Institute of Dental and Craniofacial Research and Office of Rare Diseases). Publication of the proceedings was funded by the Fibrous Dysplasia Foundation and an unrestricted grant from Zimmer.
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The surgical management of fibrous dysplasia of bone Robert P Stanton, Ernesto Ippolito, Dempsey Springfield, Lynn Lindaman, Shlomo Wientroub, Arabella Leet Orphanet Journal of Rare Diseases 2012, 7(Suppl 1):S1 (24 May 2012) |
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Clinical guidelines for the management of craniofacial fibrous dysplasia JS Lee, EJ FitzGibbon, YR Chen, HJ Kim, LR Lustig, SO Akintoye, MT Collins, LB Kaban Orphanet Journal of Rare Diseases 2012, 7(Suppl 1):S2 (24 May 2012) |
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Pathophysiology and medical treatment of pain in fibrous dysplasia of bone Roland D Chapurlat, Deborah Gensburger, Juan M Jimenez-Andrade, Joseph R Ghilardi, Marilyn Kelly, Patrick Mantyh Orphanet Journal of Rare Diseases 2012, 7(Suppl 1):S3 (24 May 2012) |
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McCune-Albright syndrome and the extraskeletal manifestations of fibrous dysplasia Michael T Collins, Frederick R Singer, Erica Eugster Orphanet Journal of Rare Diseases 2012, 7(Suppl 1):S4 (24 May 2012) |
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The role of SH3BP2 in the pathophysiology of cherubism Ernst J Reichenberger, Michael A Levine, Bjorn R Olsen, Maria E Papadaki, Steven A Lietman Orphanet Journal of Rare Diseases 2012, 7(Suppl 1):S5 (24 May 2012) |
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Cherubism: best clinical practice Maria E Papadaki, Steven A Lietman, Michael A Levine, Bjorn R Olsen, Leonard B Kaban, Ernst J Reichenberger Orphanet Journal of Rare Diseases 2012, 7(Suppl 1):S6 (24 May 2012) |

