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582 related items for PubMed ID: 22133093

  • 1. Fibrodysplasia ossificans progressiva: clinical and genetic aspects.
    Pignolo RJ, Shore EM, Kaplan FS.
    Orphanet J Rare Dis; 2011 Dec 01; 6():80. PubMed ID: 22133093
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  • 4. Fibrodysplasia ossificans progressiva (FOP): watch the great toes!
    Kartal-Kaess M, Shore EM, Xu M, Schwering L, Uhl M, Korinthenberg R, Niemeyer C, Kaplan FS, Lauten M.
    Eur J Pediatr; 2010 Nov 01; 169(11):1417-21. PubMed ID: 20577760
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  • 5. Fibrodysplasia ossificans progressiva.
    Kaplan FS, Le Merrer M, Glaser DL, Pignolo RJ, Goldsby RE, Kitterman JA, Groppe J, Shore EM.
    Best Pract Res Clin Rheumatol; 2008 Mar 01; 22(1):191-205. PubMed ID: 18328989
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  • 6. Fibrodysplasia Ossificans Progressiva: A Challenging Diagnosis.
    De Brasi D, Orlando F, Gaeta V, De Liso M, Acquaviva F, Martemucci L, Mastrominico A, Di Rocco M.
    Genes (Basel); 2021 Jul 30; 12(8):. PubMed ID: 34440363
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  • 8. The ACVR1 R206H mutation found in fibrodysplasia ossificans progressiva increases human induced pluripotent stem cell-derived endothelial cell formation and collagen production through BMP-mediated SMAD1/5/8 signaling.
    Barruet E, Morales BM, Lwin W, White MP, Theodoris CV, Kim H, Urrutia A, Wong SA, Srivastava D, Hsiao EC.
    Stem Cell Res Ther; 2016 Aug 17; 7(1):115. PubMed ID: 27530160
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  • 10. Depletion of Mast Cells and Macrophages Impairs Heterotopic Ossification in an Acvr1R206H Mouse Model of Fibrodysplasia Ossificans Progressiva.
    Convente MR, Chakkalakal SA, Yang E, Caron RJ, Zhang D, Kambayashi T, Kaplan FS, Shore EM.
    J Bone Miner Res; 2018 Feb 17; 33(2):269-282. PubMed ID: 28986986
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  • 12. The obligatory role of Activin A in the formation of heterotopic bone in Fibrodysplasia Ossificans Progressiva.
    Alessi Wolken DM, Idone V, Hatsell SJ, Yu PB, Economides AN.
    Bone; 2018 Apr 17; 109():210-217. PubMed ID: 28629737
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  • 13. Fibrodysplasia ossificans progressiva: middle-age onset of heterotopic ossification from a unique missense mutation (c.974G>C, p.G325A) in ACVR1.
    Whyte MP, Wenkert D, Demertzis JL, DiCarlo EF, Westenberg E, Mumm S.
    J Bone Miner Res; 2012 Mar 17; 27(3):729-37. PubMed ID: 22131272
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  • 14. BMP signaling and skeletal development in fibrodysplasia ossificans progressiva (FOP).
    Towler OW, Shore EM.
    Dev Dyn; 2022 Jan 17; 251(1):164-177. PubMed ID: 34133058
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  • 15. Role of altered signal transduction in heterotopic ossification and fibrodysplasia ossificans progressiva.
    Shore EM, Kaplan FS.
    Curr Osteoporos Rep; 2011 Jun 17; 9(2):83-8. PubMed ID: 21340697
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  • 16. Overexpression of Wild-Type ACVR1 in Fibrodysplasia Ossificans Progressiva Mice Rescues Perinatal Lethality and Inhibits Heterotopic Ossification.
    Yamamoto M, Stoessel SJ, Yamamoto S, Goldhamer DJ.
    J Bone Miner Res; 2022 Nov 17; 37(11):2077-2093. PubMed ID: 35637634
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  • 17. Fibrodysplasia ossificans progressiva: diagnosis, management, and therapeutic horizons.
    Pignolo RJ, Shore EM, Kaplan FS.
    Pediatr Endocrinol Rev; 2013 Jun 17; 10 Suppl 2(0 2):437-48. PubMed ID: 23858627
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  • 18. The congenital great toe malformation of fibrodysplasia ossificans progressiva? - A close call.
    Towler OW, Shore EM, Xu M, Bamford A, Anderson I, Pignolo RJ, Kaplan FS.
    Eur J Med Genet; 2017 Jul 17; 60(7):399-402. PubMed ID: 28473268
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  • 19. A case of Fibrodysplasia Ossificans Progressiva associated with a novel variant of the ACVR1 gene.
    Cappato S, Traberg R, Gintautiene J, Zara F, Bocciardi R.
    Mol Genet Genomic Med; 2021 Oct 17; 9(10):e1774. PubMed ID: 34347384
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  • 20. Classical and atypical Fibrodysplasia Ossificans Progressiva in India.
    Madhuri V, Santhanam M, Sugumar LK, Rajagopal K, Chilbule SK.
    Ann Hum Genet; 2015 Jul 17; 79(4):245-52. PubMed ID: 26058333
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