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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1903 2
1907 1
1908 1
1910 2
1911 2
1912 1
1913 2
1915 1
1918 2
1920 1
1922 2
1923 1
1924 11
1925 2
1926 1
1928 1
1932 3
1933 2
1934 2
1935 3
1936 5
1945 1
1946 4
1947 9
1948 9
1949 3
1950 7
1951 20
1952 13
1953 13
1954 17
1955 17
1956 8
1957 18
1958 19
1959 14
1960 11
1961 14
1962 11
1963 25
1964 20
1965 19
1966 22
1967 38
1968 27
1969 27
1970 20
1971 32
1972 27
1973 27
1974 21
1975 33
1976 38
1977 29
1978 30
1979 31
1980 23
1981 25
1982 29
1983 33
1984 33
1985 31
1986 33
1987 34
1988 27
1989 31
1990 36
1991 21
1992 39
1993 34
1994 37
1995 44
1996 36
1997 29
1998 58
1999 39
2000 36
2001 35
2002 27
2003 37
2004 35
2005 40
2006 48
2007 44
2008 52
2009 56
2010 78
2011 79
2012 87
2013 65
2014 82
2015 92
2016 88
2017 100
2018 112
2019 97
2020 91
2021 39
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Search Results

2,646 results
Results by year
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Page 1
Fibrodysplasia ossificans progressiva: diagnosis, management, and therapeutic horizons.
Pignolo RJ, Shore EM, Kaplan FS. Pignolo RJ, et al. Pediatr Endocrinol Rev. 2013 Jun;10 Suppl 2(0 2):437-48. Pediatr Endocrinol Rev. 2013. PMID: 23858627 Free PMC article. Review.
Fibrodysplasia ossificans progressiva (FOP), a rare and disabling genetic condition characterized by congenital malformations of the great toes and progressive heterotopic endochondral ossification (HEO) which is the most catastrophic of HEO disorders in huma
Fibrodysplasia ossificans progressiva (FOP), a rare and disabling genetic condition characterized by congenital malform
Therapeutic advances for blocking heterotopic ossification in fibrodysplasia ossificans progressiva.
Wentworth KL, Masharani U, Hsiao EC. Wentworth KL, et al. Br J Clin Pharmacol. 2019 Jun;85(6):1180-1187. doi: 10.1111/bcp.13823. Epub 2019 Jan 6. Br J Clin Pharmacol. 2019. PMID: 30501012 Free PMC article. Review.
Fibrodysplasia ossificans progressiva (FOP) is a rare genetic disease in which heterotopic bone forms in muscle and soft tissue, leading to joint dysfunction and significant disability. ...
Fibrodysplasia ossificans progressiva (FOP) is a rare genetic disease in which heterotopic bone forms in muscle and sof
Fibrodysplasia ossificans progressiva: lessons learned from a rare disease.
Akyuz G, Gencer-Atalay K, Ata P. Akyuz G, et al. Curr Opin Pediatr. 2019 Dec;31(6):716-722. doi: 10.1097/MOP.0000000000000802. Curr Opin Pediatr. 2019. PMID: 31693578 Review.
PURPOSE OF REVIEW: Fibrodysplasia ossificans progressiva (FOP) is an extremely rare and severely disabling autosomal dominant disease that is yet to be clearly understood. ...
PURPOSE OF REVIEW: Fibrodysplasia ossificans progressiva (FOP) is an extremely rare and severely disabling autosomal do …
Fibrodysplasia ossificans progressiva in China.
She D, Zhang K. She D, et al. Bone. 2018 Apr;109:101-103. doi: 10.1016/j.bone.2017.11.016. Epub 2017 Nov 22. Bone. 2018. PMID: 29175272 Review.
Fibrodysplasia ossificans progressiva (FOP) is an ultra-rare and devastating disorder characterized by cumulative episodes of progressive heterotopic ossification. ...
Fibrodysplasia ossificans progressiva (FOP) is an ultra-rare and devastating disorder characterized by cumulative episo
Fibrodysplasia ossificans progressiva: The patient voice.
Cali IL, Rossano L. Cali IL, et al. Bone. 2018 Apr;109:291-294. doi: 10.1016/j.bone.2017.05.017. Epub 2017 May 23. Bone. 2018. PMID: 28549688 Review.
The following essays are the personal statements of two remarkable young individuals, Ian Cali and Laura Rossano, who candidly share their perspectives on living life with fibrodysplasia ossificans progressiva (FOP). These essays are excerpts from the opening …
The following essays are the personal statements of two remarkable young individuals, Ian Cali and Laura Rossano, who candidly share their p …
Fibrodysplasia ossificans progressiva: clinical and genetic aspects.
Pignolo RJ, Shore EM, Kaplan FS. Pignolo RJ, et al. Orphanet J Rare Dis. 2011 Dec 1;6:80. doi: 10.1186/1750-1172-6-80. Orphanet J Rare Dis. 2011. PMID: 22133093 Free PMC article. Review.
Fibrodysplasia ossificans progressiva (FOP) is a severely disabling heritable disorder of connective tissue characterized by congenital malformations of the great toes and progressive heterotopic ossification that forms qualitatively normal bone in characteri
Fibrodysplasia ossificans progressiva (FOP) is a severely disabling heritable disorder of connective tissue characteriz
Fibrodysplasia ossificans progressiva: a current review of imaging findings.
Bauer AH, Bonham J, Gutierrez L, Hsiao EC, Motamedi D. Bauer AH, et al. Skeletal Radiol. 2018 Aug;47(8):1043-1050. doi: 10.1007/s00256-018-2889-5. Epub 2018 Feb 14. Skeletal Radiol. 2018. PMID: 29445932 Review.
OBJECTIVE: Fibrodysplasia ossificans progressiva is a rare genetic disorder characterized by congenital skeletal deformities and soft tissue masses that progress to heterotopic ossification. ...CONCLUSIONS: Recognition of the imaging manifestations of fibr
OBJECTIVE: Fibrodysplasia ossificans progressiva is a rare genetic disorder characterized by congenital skeletal deform …
Fibrodysplasia ossificans progressiva (stone man syndrome): a case report.
Shah ZA, Rausch S, Arif U, El Yafawi B. Shah ZA, et al. J Med Case Rep. 2019 Dec 1;13(1):364. doi: 10.1186/s13256-019-2297-z. J Med Case Rep. 2019. PMID: 31785620 Free PMC article.
Fibrodysplasia ossificans progressiva has worldwide prevalence of about 1 in 2 million births. Nearly 90% of patients with fibrodysplasia ossificans progressiva are misdiagnosed and mismanaged and thus undergo unnecessarily interventions.
Fibrodysplasia ossificans progressiva has worldwide prevalence of about 1 in 2 million births. Nearly 90% of patients w
Fibrodysplasia ossificans progressiva: Review and research activities in Japan.
Haga N, Nakashima Y, Kitoh H, Kamizono J, Katagiri T, Saijo H, Tsukamoto S, Shinoda Y, Sawada R, Nakahara Y. Haga N, et al. Pediatr Int. 2020 Jan;62(1):3-13. doi: 10.1111/ped.14065. Pediatr Int. 2020. PMID: 31774601 Review.
Fibrodysplasia ossificans progressiva (FOP) is a rare genetic skeletal disorder manifesting progressive heterotopic ossification (HO) and congenital malformation of the great toes. ...
Fibrodysplasia ossificans progressiva (FOP) is a rare genetic skeletal disorder manifesting progressive heterotopic oss
Fibrodysplasia ossificans progressiva.
Kumar RR, Dasgupta S, Suman SK, Kumar U. Kumar RR, et al. Rheumatology (Oxford). 2020 Jul 1;59(7):1789. doi: 10.1093/rheumatology/kez479. Rheumatology (Oxford). 2020. PMID: 31624833 No abstract available.
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