Results 81 to 90 of about 3,877 (214)
American Journal of Biological Anthropology, Volume 185, Issue 4, December 2024.Abstract Objectives Between the Irish late medieval (AD 1150–c.1550) (LMP) and post‐medieval (AD c.1550–1800) (PMP) periods, colonial practices changed land ownership. Contextualizing these periods within a biocultural political economy framework supports increasing social inequality in the PMP, which we expect to be reflected in different skeletal ...
Melissa A. Clark +3 more
wiley +1 more source
Case Reports in Orthopedics, 2013 Spondylolysis is reported as a stress fracture of the pars interarticularis with a strong hereditary basis. Three cases of lumbar spondylolysis in juveniles from the same family are reported, and the genetics of the condition are reviewed. The first boy,
Atsuhisa Yamada +5 more
doaj +1 more source
Spina Bifida Occulta in Medieval and Postmedieval Times in Eastern Romania [PDF]
Memoirs of the Scientific Sections of the Romanian Academy, 2016 This paper provides bioarchaeological evidence of Spina Bifida Occulta (SBO) in human skeletons discovered in medieval and post-medieval sites of Eastern Romania and evaluates its prevalence and patterns by examining its relationship to age, sex, type of
Vasilica-Monica Groza +3 more
doaj
Neural tube defects-disorders of neurulation and related embryonic processes [PDF]
, 2013 Neural tube defects (NTDs) are severe congenital malformations affecting 1 in every 1000 pregnancies. ‘Open’ NTDs result from failure of primary neurulation as seen in anencephaly, myelomeningocele (open spina bifida), and craniorachischisis ...
Copp, AJ, Greene, NDE
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New perspectives on evolutionary medicine: the relevance of microevolution for human health and disease [PDF]
, 2013 Evolutionary medicine (EM) is a growing field focusing on the evolutionary basis of human diseases and their changes through time. To date, the majority of EM studies have used pure theories of hominin macroevolution to explain the present-day state of ...
A Saniotis +72 more
core +2 more sources
Lumbosacral hypertrichosis as a cutaneous manifestation of dysraphism
JEADV Clinical Practice, Volume 4, Issue 1, Page 331-332, March 2025.
Sarah Preis +2 more
wiley +1 more source
Sacral agenesis: a pilot whole exome sequencing and copy number study [PDF]
, 2016 Background: Caudal regression syndrome (CRS) or sacral agenesis is a rare congenital disorder characterized by a constellation of congenital caudal anomalies affecting the caudal spine and spinal cord, the hindgut, the urogenital system, and the lower ...
Campbell, Desmond D. +11 more
core +1 more source
Anal canal duplication in an 11-year-old-child [PDF]
, 2013 Anal canal duplication (ACD) is the least frequent digestive duplication. Symptoms are often absent but tend to increase with age. Recognition is, however, important as almost half of the patients with ACD have concomitant malformations.
De Bruyne, Ruth +8 more
core +3 more sources
European Journal of Pediatric Surgery Reports, 2014 Retroperitoneum is a relatively uncommon site for pediatric teratomas. Rarely, such tumors can have an intraspinal extension and few cases of retroperitoneal teratomas associated with spinal dysraphism have been reported.
Anand Sinha +4 more
doaj +1 more source
Neural tube defects in Australia: An epidemiological report [PDF]
This report describes the prevalence and trends of neural tube defects (NTD) in Australia during the past decade to provide baseline prevalence of NTD, prior to the implementation of mandatory folic acid fortification of bread flour in September 2009 ...
Australian Institute of Health and Welfare +3 more
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