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

Year Number of Results
1907 1
1914 3
1916 2
1917 1
1918 1
1919 2
1921 1
1923 1
1925 1
1927 1
1928 2
1930 2
1931 1
1932 2
1944 1
1945 1
1946 5
1947 7
1948 10
1949 6
1950 15
1951 19
1952 27
1953 24
1954 21
1955 24
1956 22
1957 27
1958 24
1959 28
1960 31
1961 30
1962 28
1963 33
1964 46
1965 49
1966 39
1967 53
1968 63
1969 60
1970 52
1971 48
1972 59
1973 53
1974 47
1975 53
1976 48
1977 58
1978 44
1979 60
1980 48
1981 68
1982 65
1983 70
1984 90
1985 77
1986 87
1987 82
1988 109
1989 83
1990 76
1991 69
1992 57
1993 116
1994 86
1995 102
1996 83
1997 72
1998 79
1999 77
2000 98
2001 86
2002 100
2003 97
2004 87
2005 117
2006 115
2007 127
2008 153
2009 123
2010 131
2011 162
2012 177
2013 183
2014 196
2015 223
2016 243
2017 239
2018 242
2019 249
2020 259
2021 283
2022 289
2023 277
2024 298
2025 310
2026 228

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7,358 results

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Page 1
Osteogenesis Imperfecta-Who Needs Rodding Surgery?
Fassier FR. Fassier FR. Curr Osteoporos Rep. 2021 Jun;19(3):264-270. doi: 10.1007/s11914-021-00665-z. Epub 2021 Mar 1. Curr Osteoporos Rep. 2021. PMID: 33646506 Review.
PURPOSE OF REVIEW: The purpose of this review is to precise the indications for intramedullary rodding of long bones in osteogenesis imperfecta, the classic treatment for fractures and deformities in this condition. ...An interdisciplinary approach combining a medic …
PURPOSE OF REVIEW: The purpose of this review is to precise the indications for intramedullary rodding of long bones in osteogenesis …
Osteogenesis imperfecta.
Byers PH, Steiner RD. Byers PH, et al. Annu Rev Med. 1992;43:269-82. doi: 10.1146/annurev.me.43.020192.001413. Annu Rev Med. 1992. PMID: 1580589 Review.
Recent biochemical, linkage, and molecular genetic studies have demonstrated that, in almost every instance, osteogenesis imperfecta results from mutations in the genes that encode the chains of type I collagen. ...Nonetheless, further investigation is needed urgent …
Recent biochemical, linkage, and molecular genetic studies have demonstrated that, in almost every instance, osteogenesis imperfec …
Osteogenesis imperfecta.
Tosi LL. Tosi LL. Curr Opin Pediatr. 1997 Feb;9(1):94-9. doi: 10.1097/00008480-199702000-00019. Curr Opin Pediatr. 1997. PMID: 9088762 Review.
In the past 20 years, tremendous strides have been made in our understanding of the biochemical and genetic abnormalities associated with osteogenesis imperfecta (OI). Prenatal diagnostic techniques have allowed early detection of this disorder, particularly in fami …
In the past 20 years, tremendous strides have been made in our understanding of the biochemical and genetic abnormalities associated with …
Osteogenesis imperfecta.
Cole WG. Cole WG. Baillieres Clin Endocrinol Metab. 1988 Feb;2(1):243-65. doi: 10.1016/s0950-351x(88)80014-4. Baillieres Clin Endocrinol Metab. 1988. PMID: 3044330 Review.
Osteogenesis imperfecta--new perspectives.
Solomons CC, Millar EA. Solomons CC, et al. Clin Orthop Relat Res. 1973 Oct;(96):299-303. Clin Orthop Relat Res. 1973. PMID: 4593330 Review. No abstract available.
Osteogenesis imperfecta--where next?
Smith R. Smith R. J Bone Joint Surg Br. 1997 Mar;79(2):177-8. doi: 10.1302/0301-620x.79b2.7640. J Bone Joint Surg Br. 1997. PMID: 9119836 Review. No abstract available.
[Osteogenesis imperfecta].
Forin V. Forin V. Presse Med. 2007 Dec;36(12 Pt 2):1787-93. doi: 10.1016/j.lpm.2007.01.043. Epub 2007 Jun 8. Presse Med. 2007. PMID: 17560761 Review. French.
Osteogenesis imperfecta is a genetic disorder that causes increased bone fragility and low bone mass. Osteogenesis imperfecta is a rare disease: its estimated prevalence is between 1/10000 and 1/20000 persons. ...
Osteogenesis imperfecta is a genetic disorder that causes increased bone fragility and low bone mass. Osteogenesis i …
Osteogenesis imperfecta: an overview.
Clark C. Clark C. Nurs Stand. 2001 Oct 17-23;16(5):47-52; quiz 53, 55. doi: 10.7748/ns2001.10.16.5.47.c3100. Nurs Stand. 2001. PMID: 11977799 Review.
Osteogenesis imperfecta (brittle bone disease) is a rare hereditary disorder with an increased tendency to fracture. ...
Osteogenesis imperfecta (brittle bone disease) is a rare hereditary disorder with an increased tendency to fracture. ...
Osteogenesis Imperfecta.
Golshani KR, Ludwig MR, Cohn PL, Kruse R. Golshani KR, et al. Del Med J. 2016 Jun;88(6):178-85. Del Med J. 2016. PMID: 27506061 No abstract available.
Osteogenesis imperfecta: questions and answers.
Shapiro JR, Sponsellor PD. Shapiro JR, et al. Curr Opin Pediatr. 2009 Dec;21(6):709-16. doi: 10.1097/MOP.0b013e328332c68f. Curr Opin Pediatr. 2009. PMID: 19907330 Review.
PURPOSE OF REVIEW: Considerable attention has recently been focused on the pathogenesis, diagnosis and treatment of osteogenesis imperfecta. Two new genes have been defined in patients with recessive severe or lethal osteogenesis imperfecta types. ...R …
PURPOSE OF REVIEW: Considerable attention has recently been focused on the pathogenesis, diagnosis and treatment of osteogenesis i …
7,358 results