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

Year Number of Results
1969 1
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1974 1
1975 4
1976 3
1977 1
1978 3
1979 3
1980 10
1981 5
1982 9
1983 7
1984 3
1985 8
1986 8
1987 8
1988 13
1989 13
1990 15
1991 8
1992 14
1993 15
1994 21
1995 20
1996 18
1997 24
1998 18
1999 28
2000 28
2001 31
2002 26
2003 31
2004 21
2005 29
2006 43
2007 39
2008 36
2009 45
2010 41
2011 57
2012 50
2013 74
2014 58
2015 63
2016 44
2017 47
2018 48
2019 36
2020 44
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2023 28
2024 10

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1,149 results

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Quoted phrase not found in phrase index: "Abnormal long bone morphology"
Page 1
Thalidomide and neurotrophism.
Soper JR, Bonar SF, O'Sullivan DJ, McCredie J, Willert HG. Soper JR, et al. Skeletal Radiol. 2019 Apr;48(4):517-525. doi: 10.1007/s00256-018-3086-2. Epub 2018 Oct 19. Skeletal Radiol. 2019. PMID: 30341712 Free PMC article. Review.
BACKGROUND: Following the thalidomide disaster (1958-62), Henkel and Willert analysed the pattern of dysmelia in the long bones (J Bone Joint Surg Br. 51:399-414, 1969) and the extremities, Willert and Henkel (Z Orthop Ihre Grenzgeb. 107:663-75, 1970). ...RES …
BACKGROUND: Following the thalidomide disaster (1958-62), Henkel and Willert analysed the pattern of dysmelia in the long bones …
Dental impact of anti-fibroblast growth factor 23 therapy in X-linked hypophosphatemia.
Lira Dos Santos EJ, Nakajima K, Po J, Hanai A, Zhukouskaya V, Biosse Duplan M, Linglart A, Shimada T, Chaussain C, Bardet C. Lira Dos Santos EJ, et al. Int J Oral Sci. 2023 Dec 6;15(1):53. doi: 10.1038/s41368-023-00259-8. Int J Oral Sci. 2023. PMID: 38052774 Free PMC article.
Elevated fibroblast growth factor 23 (FGF23) in X-linked hypophosphatemia (XLH) results in rickets and phosphate wasting, manifesting by severe bone and dental abnormalities. Burosumab, a FGF23-neutralizing antibody, an alternative to conventional treatment (phospho …
Elevated fibroblast growth factor 23 (FGF23) in X-linked hypophosphatemia (XLH) results in rickets and phosphate wasting, manifesting by sev …
Adult osteosclerosis.
Evans RA, Hughes WG, Dunstan CR, Lennon WP, Kohan L, Hills E, Wong SY. Evans RA, et al. Metab Bone Dis Relat Res. 1983-1984;5(3):111-7. doi: 10.1016/0221-8747(83)90011-5. Metab Bone Dis Relat Res. 1983. PMID: 6676625
Quantitative bone histology was carried out in five osteosclerotic adults. The bone was extremely hard in all patients, and open biopsy was usually required. ...In this patient some osteoclasts had reduced acid phosphatase activity and long cytoplasmic …
Quantitative bone histology was carried out in five osteosclerotic adults. The bone was extremely hard in all patients, …
Muscle and Bone Impairment in Infantile Nephropathic Cystinosis: New Concepts.
Haffner D, Leifheit-Nestler M, Alioli C, Bacchetta J. Haffner D, et al. Cells. 2022 Jan 5;11(1):170. doi: 10.3390/cells11010170. Cells. 2022. PMID: 35011732 Free PMC article. Review.
Amongst these long-term consequences are renal Fanconi syndrome, hypophosphatemic rickets, malnutrition, hormonal abnormalities, muscular impairment, and intrinsic cellular bone defects in bone cells, due to CTNS mutations. Recent research data in the …
Amongst these long-term consequences are renal Fanconi syndrome, hypophosphatemic rickets, malnutrition, hormonal abnormalities …
Imaging Review of Normal and Abnormal Skeletal Maturation.
Augusto ACL, Goes PCK, Flores DV, Costa MAF, Takahashi MS, Rodrigues ACO, Padula LC, Gasparetto TD, Nogueira-Barbosa MH, Aihara AY. Augusto ACL, et al. Radiographics. 2022 May-Jun;42(3):861-879. doi: 10.1148/rg.210088. Epub 2022 Feb 25. Radiographics. 2022. PMID: 35213260
Primary and secondary ossification centers (SOCs), which form the diaphysis and the epiphysis of long bones, respectively, are formed by endochondral and intramembranous ossification processes. ...These can be related to residual red marrow (especially in the metaph …
Primary and secondary ossification centers (SOCs), which form the diaphysis and the epiphysis of long bones, respectively, are …
Hydrocephalus and Chiari type I malformation.
Di Rocco C, Frassanito P, Massimi L, Peraio S. Di Rocco C, et al. Childs Nerv Syst. 2011 Oct;27(10):1653-64. doi: 10.1007/s00381-011-1545-3. Epub 2011 Sep 17. Childs Nerv Syst. 2011. PMID: 21928030 Review.
INTRODUCTION: [corrected] Hydrocephalus has been related to Chiari type I malformation (CIM) for a long time. The pathogenesis of this association is complex and still debated. ...Another pathogenetic hypothesis is based on the clinical and radiological data from patients …
INTRODUCTION: [corrected] Hydrocephalus has been related to Chiari type I malformation (CIM) for a long time. The pathogenesis of thi …
Mechanical determinants of bone modeling.
Frost HM. Frost HM. Metab Bone Dis Relat Res. 1982;4(4):217-29. doi: 10.1016/0221-8747(82)90031-5. Metab Bone Dis Relat Res. 1982. PMID: 6763662 Review.
In angulated long bone malunions in children, bone architectural changes arise which act consistently in kind, location, and direction, while the associated bone strain-stress patterns become definable as qualitative differences from the norm. ...The a …
In angulated long bone malunions in children, bone architectural changes arise which act consistently in kind, location …
Bruck Syndrome: Beyond the Obvious.
Tran CT, Smet ME, Forsey J, Zankl A, Nayyar R. Tran CT, et al. Fetal Diagn Ther. 2022;49(11-12):479-485. doi: 10.1159/000527594. Epub 2022 Dec 7. Fetal Diagn Ther. 2022. PMID: 36476632
CASE PRESENTATION: We present a prenatally diagnosed case of Bruck syndrome in a young multiparous woman, with no notable personal, family or obstetric history. A 12-week ultrasound raised the suspicion of short long bones, subsequently confirmed at 16 weeks. In add …
CASE PRESENTATION: We present a prenatally diagnosed case of Bruck syndrome in a young multiparous woman, with no notable personal, family o …
Osteoarthritis, entheses, and long bone cross-sectional geometry in the Andes: Usage, history, and future directions.
Becker SK. Becker SK. Int J Paleopathol. 2020 Jun;29:45-53. doi: 10.1016/j.ijpp.2019.08.005. Epub 2019 Aug 28. Int J Paleopathol. 2020. PMID: 31473173 Review.
Akin to approaches encouraged by Verano (1997) in the Andes, and Ortner (2011, 2012) for general paleopathological studies, this article focuses on accurate descriptions and definitions of osteoarthritis, entheses, and long bone cross-sectional geometry. By evaluati …
Akin to approaches encouraged by Verano (1997) in the Andes, and Ortner (2011, 2012) for general paleopathological studies, this article foc …
Bone disease in pediatric chronic kidney disease.
Wesseling-Perry K. Wesseling-Perry K. Pediatr Nephrol. 2013 Apr;28(4):569-76. doi: 10.1007/s00467-012-2324-4. Epub 2012 Oct 14. Pediatr Nephrol. 2013. PMID: 23064662 Free PMC article. Review.
Children with long-standing chronic kidney disease (CKD) display clinical symptoms of bone disease, including bony deformities and fractures, which contribute to long-standing disability. ...Although bone biopsy is the only available method for assessi …
Children with long-standing chronic kidney disease (CKD) display clinical symptoms of bone disease, including bony deformities …
1,149 results