Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Results by year

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

Year Number of Results
1945 5
1946 27
1947 17
1948 21
1949 21
1950 52
1951 56
1952 43
1953 33
1954 33
1955 40
1956 36
1957 36
1958 30
1959 29
1960 37
1961 39
1962 39
1963 56
1964 54
1965 64
1966 72
1967 95
1968 100
1969 83
1970 105
1971 104
1972 116
1973 99
1974 96
1975 102
1976 98
1977 118
1978 100
1979 97
1980 95
1981 128
1982 133
1983 137
1984 162
1985 146
1986 170
1987 215
1988 210
1989 247
1990 173
1991 196
1992 159
1993 156
1994 168
1995 171
1996 170
1997 162
1998 159
1999 173
2000 201
2001 216
2002 208
2003 201
2004 199
2005 230
2006 255
2007 282
2008 243
2009 263
2010 326
2011 314
2012 384
2013 379
2014 345
2015 342
2016 335
2017 342
2018 350
2019 339
2020 394
2021 425
2022 407
2023 352
2024 119

Text availability

Article attribute

Article type

Publication date

Search Results

12,013 results

Results by year

Filters applied: . Clear all
Page 1
Neurofibromatosis 1.
Friedman JM. Friedman JM. 1998 Oct 2 [updated 2022 Apr 21]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. 1998 Oct 2 [updated 2022 Apr 21]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. PMID: 20301288 Free Books & Documents. Review.
CLINICAL CHARACTERISTICS: Neurofibromatosis 1 (NF1) is a multisystem disorder characterized by multiple cafe au lait macules, intertriginous freckling, multiple cutaneous neurofibromas, and learning disability or behavior problems. ...Less common but potentially mor …
CLINICAL CHARACTERISTICS: Neurofibromatosis 1 (NF1) is a multisystem disorder characterized by multiple cafe au lait macules, …
Orthopedic Manifestations of Abuse.
Milner JD, Hartnett DA, DeFroda SF, Blackburn AZ, Cruz AI Jr, Daniels AH. Milner JD, et al. Am J Med. 2021 Mar;134(3):306-309. doi: 10.1016/j.amjmed.2020.09.031. Epub 2020 Oct 26. Am J Med. 2021. PMID: 33121957 Review.
Therefore, this review evaluates current literature regarding the orthopedic manifestations of abuse in hopes of increasing physician awareness....
Therefore, this review evaluates current literature regarding the orthopedic manifestations of abuse in hopes of increasing ph …
Orthopedic manifestations of child abuse.
Milner JD, Hartnett DA, DeFroda SF, Slingsby BA, Silber ZS, Blackburn AZ, Daniels AH, Cruz AI Jr. Milner JD, et al. Pediatr Res. 2022 Sep;92(3):647-652. doi: 10.1038/s41390-021-01850-7. Epub 2021 Nov 24. Pediatr Res. 2022. PMID: 34819655 Review.
By increasing awareness, through medical provider education and increased screening, earlier detection of abuse may prevent more serious injuries and consequences. This review evaluates current literature regarding the orthopedic manifestations of child abuse in hop …
By increasing awareness, through medical provider education and increased screening, earlier detection of abuse may prevent more serious inj …
Neurofibromatosis update.
Crawford AH, Schorry EK. Crawford AH, et al. J Pediatr Orthop. 2006 May-Jun;26(3):413-23. doi: 10.1097/01.bpo.0000217719.10728.39. J Pediatr Orthop. 2006. PMID: 16670560 Review.
For those with musculoskeletal involvement, the most important issue is early recognition. Spinal deformity, congenital tibial dysplasia (congenital bowing and pseudarthrosis), and disorders of excessive bone and soft-tissue growth are the three types of musculoskel …
For those with musculoskeletal involvement, the most important issue is early recognition. Spinal deformity, congenital tibial dys
Quantitative Ultrasound and Tibial Dysplasia in Neurofibromatosis Type 1.
Stevenson DA, Hanson H, Stevens A, Carey J, Viskochil D, Sheng X, Wheeler K, Slater H. Stevenson DA, et al. J Clin Densitom. 2018 Apr-Jun;21(2):179-184. doi: 10.1016/j.jocd.2017.03.004. Epub 2017 Apr 21. J Clin Densitom. 2018. PMID: 28438404
In infancy, physiologic bowing of the lower leg can be confused with pathologic tibial dysplasia in NF1. Little is known about the bone physiology of the tibiae prior to fracture or predictors of fracture. ...Radiographs of all individuals with a clinical diagnosis …
In infancy, physiologic bowing of the lower leg can be confused with pathologic tibial dysplasia in NF1. Little is known about …
Genetic and Metabolic Conditions.
Stankovits LM, Lopyan AH. Stankovits LM, et al. Pediatr Clin North Am. 2020 Feb;67(1):23-43. doi: 10.1016/j.pcl.2019.09.005. Pediatr Clin North Am. 2020. PMID: 31779835 Review.
A wide of array of patients with genetic and metabolic conditions present with orthopedic manifestations. This article discusses the most common conditions seen in a typical pediatric orthopedic practice. ...
A wide of array of patients with genetic and metabolic conditions present with orthopedic manifestations. This article discuss …
Neurofibromatosis 1.
Ferner RE. Ferner RE. Eur J Hum Genet. 2007 Feb;15(2):131-8. doi: 10.1038/sj.ejhg.5201676. Epub 2006 Sep 6. Eur J Hum Genet. 2007. PMID: 16957683 Review.
Neurofibromatosis 1 predisposes affected individuals to the development of benign and malignant tumours that are frequently disfiguring and difficult to manage. ...
Neurofibromatosis 1 predisposes affected individuals to the development of benign and malignant tumours that are frequently di
Neurofibromatosis.
Frank-Stromborg M. Frank-Stromborg M. Semin Oncol Nurs. 1992 Nov;8(4):265-71. doi: 10.1016/0749-2081(92)90039-6. Semin Oncol Nurs. 1992. PMID: 1480857 Review.
Pediatric Neuromuscular Disorders.
Michel C, Collins C. Michel C, et al. Pediatr Clin North Am. 2020 Feb;67(1):45-57. doi: 10.1016/j.pcl.2019.09.002. Pediatr Clin North Am. 2020. PMID: 31779836 Review.
The most common disorders include cerebral palsy and myelodysplasia. The orthopedic manifestations of these disorders can be treated operatively or nonoperatively. ...
The most common disorders include cerebral palsy and myelodysplasia. The orthopedic manifestations of these disorders can be t …
Orthopedic Manifestations of Lead Toxicity.
Meyers AL, Woodbury MP, Nelson RA. Meyers AL, et al. Orthopedics. 2020 Jul 1;43(4):e202-e207. doi: 10.3928/01477447-20200415-06. Epub 2020 Apr 23. Orthopedics. 2020. PMID: 32324246 Review.
Because lead has a significant effect on mineralized tissue such as bone, the purpose of this review was to identify and analyze the orthopedic manifestations of lead poisoning. The effects of lead at the cellular level, on the hematopoietic system, in osteoporosis, …
Because lead has a significant effect on mineralized tissue such as bone, the purpose of this review was to identify and analyze the orth
12,013 results
You have reached the last available page of results. Please see the User Guide for more information.