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MeSH Review

Fibrous Dysplasia, Polyostotic

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Gene context of Fibrous Dysplasia, Polyostotic


Analytical, diagnostic and therapeutic context of Fibrous Dysplasia, Polyostotic


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  2. "Café-au-lait spots" caused by vitiligo in McCune-Albright syndrome. Whyte, M.P., Podgornik, M.N., Zerega, J., Reinus, W.R. J. Bone Miner. Res. (2000) [Pubmed]
  3. Fracture incidence in polyostotic fibrous dysplasia and the McCune-Albright syndrome. Leet, A.I., Chebli, C., Kushner, H., Chen, C.C., Kelly, M.H., Brillante, B.A., Robey, P.G., Bianco, P., Wientroub, S., Collins, M.T. J. Bone Miner. Res. (2004) [Pubmed]
  4. Absence of pubertal gonadotropin secretion in girls with McCune-Albright syndrome. Foster, C.M., Ross, J.L., Shawker, T., Pescovitz, O.H., Loriaux, D.L., Cutler, G.B., Comite, F. J. Clin. Endocrinol. Metab. (1984) [Pubmed]
  5. Male LH-independent sexual precocity in a 3.5-year-old boy caused by a somatic activating mutation of the LH receptor in a Leydig cell tumor. Richter-Unruh, A., Wessels, H.T., Menken, U., Bergmann, M., Schmittmann-Ohters, K., Schaper, J., Tappeser, S., Hauffa, B.P. J. Clin. Endocrinol. Metab. (2002) [Pubmed]
  6. Mutations of the gene encoding the protein kinase A type I-alpha regulatory subunit in patients with the Carney complex. Kirschner, L.S., Carney, J.A., Pack, S.D., Taymans, S.E., Giatzakis, C., Cho, Y.S., Cho-Chung, Y.S., Stratakis, C.A. Nat. Genet. (2000) [Pubmed]
  7. Increased expression of the c-fos proto-oncogene in bone from patients with fibrous dysplasia. Candeliere, G.A., Glorieux, F.H., Prud'homme, J., St-Arnaud, R. N. Engl. J. Med. (1995) [Pubmed]
  8. Activating mutations of the stimulatory G protein in the McCune-Albright syndrome. Weinstein, L.S., Shenker, A., Gejman, P.V., Merino, M.J., Friedman, E., Spiegel, A.M. N. Engl. J. Med. (1991) [Pubmed]
  9. Estrogen receptors in bone in a patient with polyostotic fibrous dysplasia (McCune-Albright syndrome). Kaplan, F.S., Fallon, M.D., Boden, S.D., Schmidt, R., Senior, M., Haddad, J.G. N. Engl. J. Med. (1988) [Pubmed]
  10. Cyclical ovarian function resistant to treatment with an analogue of luteinizing hormone releasing hormone in McCune-Albright syndrome. Comite, F., Shawker, T.H., Pescovitz, O.H., Loriaux, D.L., Cutler, G.B. N. Engl. J. Med. (1984) [Pubmed]
  11. Effect of pamidronate treatment in children with polyostotic fibrous dysplasia of bone. Plotkin, H., Rauch, F., Zeitlin, L., Munns, C., Travers, R., Glorieux, F.H. J. Clin. Endocrinol. Metab. (2003) [Pubmed]
  12. Urinary cyclic adenosine 3',5'-monophosphate response in McCune-Albright syndrome: clinical evidence for altered renal adenylate cyclase activity. Zung, A., Chalew, S.A., Schwindinger, W.F., Levine, M.A., Phillip, M., Jara, A., Counts, D.R., Kowarski, A.A. J. Clin. Endocrinol. Metab. (1995) [Pubmed]
  13. Tamoxifen treatment for precocious puberty in McCune-Albright syndrome: a multicenter trial. Eugster, E.A., Rubin, S.D., Reiter, E.O., Plourde, P., Jou, H.C., Pescovitz, O.H. J. Pediatr. (2003) [Pubmed]
  14. Characterization of gsp-mediated growth hormone excess in the context of McCune-Albright syndrome. Akintoye, S.O., Chebli, C., Booher, S., Feuillan, P., Kushner, H., Leroith, D., Cherman, N., Bianco, P., Wientroub, S., Robey, P.G., Collins, M.T. J. Clin. Endocrinol. Metab. (2002) [Pubmed]
  15. Clinical implications of genetic defects in G proteins. The molecular basis of McCune-Albright syndrome and Albright hereditary osteodystrophy. Ringel, M.D., Schwindinger, W.F., Levine, M.A. Medicine (Baltimore) (1996) [Pubmed]
  16. Activating Gs alpha mutation at the Arg201 codon in liposclerosing myxofibrous tumor. Matsuba, A., Ogose, A., Tokunaga, K., Kawashima, H., Hotta, T., Urakawa, S., Umezu, H., Higuchi, T., Endo, N. Hum. Pathol. (2003) [Pubmed]
  17. Albright hereditary osteodystrophy and del(2) (q37.3) in four unrelated individuals. Phelan, M.C., Rogers, R.C., Clarkson, K.B., Bowyer, F.P., Levine, M.A., Estabrooks, L.L., Severson, M.C., Dobyns, W.B. Am. J. Med. Genet. (1995) [Pubmed]
  18. McCune-Albright syndrome: clinical and molecular evidence of mosaicism in an unusual giant patient. Tinschert, S., Gerl, H., Gewies, A., Jung, H.P., Nürnberg, P. Am. J. Med. Genet. (1999) [Pubmed]
  19. A highly sensitive polymerase chain reaction method detects activating mutations of the GNAS gene in peripheral blood cells in McCune-Albright syndrome or isolated fibrous dysplasia. Lietman, S.A., Ding, C., Levine, M.A. The Journal of bone and joint surgery. American volume. (2005) [Pubmed]
  20. In vitro production of estradiol by ovarian granulosa cells in a case of McCune-Albright syndrome. Manna, C., Epifano, O., Riminucci, M., Baschieri, L., Stefanini, M., Canipari, R. J. Endocrinol. Invest. (1991) [Pubmed]
  21. Osteogenic sarcoma and soft tissue myxoma in a patient with fibrous dysplasia and hemoglobins JBaltimore and S. Witkin, G.B., Guilford, W.B., Siegal, G.P. Clin. Orthop. Relat. Res. (1986) [Pubmed]
  22. Sonography of multinodular thyroid gland in children and adolescents. Garcia, C.J., Daneman, A., Thorner, P., Daneman, D. Am. J. Dis. Child. (1992) [Pubmed]
  23. Skeletal changes in epidermal nevus syndrome: does focal bone disease harbor clues concerning pathogenesis? Heike, C.L., Cunningham, M.L., Steiner, R.D., Wenkert, D., Hornung, R.L., Gruss, J.S., Gannon, F.H., McAlister, W.H., Mumm, S., Whyte, M.P. Am. J. Med. Genet. A (2005) [Pubmed]
  24. Hypersecretion of growth hormone and prolactin in McCune-Albright syndrome. Cuttler, L., Jackson, J.A., Saeed uz-Zafar, M., Levitsky, L.L., Mellinger, R.C., Frohman, L.A. J. Clin. Endocrinol. Metab. (1989) [Pubmed]
  25. A novel GNAS1 mutation, R201G, in McCune-albright syndrome. Riminucci, M., Fisher, L.W., Majolagbe, A., Corsi, A., Lala, R., De Sanctis, C., Robey, P.G., Bianco, P. J. Bone Miner. Res. (1999) [Pubmed]
  26. The role of fibroblast growth factor 23 for hypophosphatemia and abnormal regulation of vitamin D metabolism in patients with McCune-Albright syndrome. Yamamoto, T., Imanishi, Y., Kinoshita, E., Nakagomi, Y., Shimizu, N., Miyauchi, A., Satomura, K., Koshiyama, H., Inaba, M., Nishizawa, Y., Jüppner, H., Ozono, K. J. Bone Miner. Metab. (2005) [Pubmed]
  27. Growth hormone hypersecretion in a girl with McCune-Albright syndrome: comparison with controls and response to a dose of long-acting somatostatin analog. Feuillan, P.P., Jones, J., Ross, J.L. J. Clin. Endocrinol. Metab. (1995) [Pubmed]
  28. A rare case of polyostotic fibrous dysplasia assessed by bone scintigraphy with Tc-99m methylene diphosphonate (MDP). Di Leo, C., Ardemagni, A., Bestetti, A., Tagliabue, L., Del Sole, A., Conte, A., Tarolo, G.L. Nuklearmedizin. (1999) [Pubmed]
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