Zobrazeno 1 - 10
of 509
pro vyhledávání: '"Peter Beighton"'
Publikováno v:
BDJ Open, Vol 7, Iss 1, Pp 1-6 (2021)
Abstract Taurodontism is a dental anomaly defined by enlargement of the pulp chamber of multirooted teeth with apical displacement of the pulp floor and bifurcation of the roots. Taurodontism can be an isolated trait or part of a syndrome. A study wa
Externí odkaz:
https://doaj.org/article/ac4ff498874a432c813df7e2e014b776
Autor:
Peter Beighton, Filip M. Vanhoenacker
Publikováno v:
Seminars in musculoskeletal radiology
This history page in the series “Leaders in MSK Radiology” is dedicated to the achievements of the Polish radiologist Kazimierz Kozlowski, whose name is associated with the Kozlowski type of spondylometaphyseal dysplasia.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0baee307bd7521b6ef5f632c0b1c2f16
https://hdl.handle.net/10067/1956290151162165141
https://hdl.handle.net/10067/1956290151162165141
Autor:
Peter Beighton, Filip M. Vanhoenacker
Publikováno v:
Seminars in musculoskeletal radiology
This history page in the series “Leaders in MSK Radiology” is dedicated to the achievements of Dr. John Caffey, whose name is associated with infantile cortical hyperostosis, also known as Caffey's disease.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cc0f1e4510da1d99d6e0c8f34ee17557
https://hdl.handle.net/10067/1945100151162165141
https://hdl.handle.net/10067/1945100151162165141
Autor:
Filip M. Vanhoenacker, Peter Beighton
Publikováno v:
Seminars in musculoskeletal radiology
This history page in the series “Leaders in MSK Radiology” is dedicated to the memory and achievements of the French physician Jacques Calvé, whose name is partially associated with the medical eponym Legg-Calvé-Perthes disease.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7701707455d865e9041cb4f7463261aa
https://doi.org/10.1055/s-0042-1757602
https://doi.org/10.1055/s-0042-1757602
Autor:
Kebashni Thandrayen, Alvera Vorster, Gameda Benefeld, Safiye Yildiz, Raj Ramesar, Jorge da Rocha, George Rebello, Alina I. Esterhuizen, Stephanie Julius, Peter Beighton, Lisa Roberts, John M. Pettifor, S. L. Sellars, Shrinav Dawlat, Komala Pillay, Surita Meldau
Publikováno v:
Human Mutation. 41:1871-1876
More than two decades ago, a recessive syndromic phenotype affecting kidneys, eyes, and ears, was first described in the endogamous Afrikaner population of South Africa. Using whole-exome sequencing of DNA from two affected siblings (and their carrie
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b61bc758576c1c1c2f18ebf8371572f3
https://doi.org/10.1002/humu.24094
https://doi.org/10.1002/humu.24094
Publikováno v:
BDJ Open
BDJ Open, Vol 7, Iss 1, Pp 1-6 (2021)
BDJ Open, Vol 7, Iss 1, Pp 1-6 (2021)
Taurodontism is a dental anomaly defined by enlargement of the pulp chamber of multirooted teeth with apical displacement of the pulp floor and bifurcation of the roots. Taurodontism can be an isolated trait or part of a syndrome. A study was conduct
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::03dc8b11e5aa8f7f2fbd1a3a41634eb0
https://pubmed.ncbi.nlm.nih.gov/34244468
https://pubmed.ncbi.nlm.nih.gov/34244468
Publikováno v:
SAMJ: South African Medical Journal, Volume: 111, Issue: 1, Pages: 57-60, Published: JAN 2021
Background. Namaqualand hip dysplasia (NHD) is a mild form of spondyloepiphyseal dysplasia in which progressive arthropathy of the hip joint is a major manifestation. The disorder was documented in a multigenerational South African (SA) family with a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::78420f81fb72139893a0af1d7a7e50d4
http://www.scielo.org.za/scielo.php?script=sci_arttext&pid=S0256-95742021000100016&lng=en&tlng=en
http://www.scielo.org.za/scielo.php?script=sci_arttext&pid=S0256-95742021000100016&lng=en&tlng=en
Autor:
Neuseli Lamari, Peter Beighton
This book provides a clear and concise guide to hypermobility in medicine and physiotherapy. Each chapter is written with a uniform style, including illustrations highlighting the clinical characteristics of manifestations related to hypermobili
Publikováno v:
Clinical geneticsREFERENCES. 99(1)
Osteogenesis imperfecta (OI) is a relatively common genetic skeletal disorder with an estimated frequency of 1 in 20 000 worldwide. The manifestations are diverse and although individually rare, the several different forms contribute to the productio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c1186388da1f9ddc59fbd27612bd877f
https://pubmed.ncbi.nlm.nih.gov/32901963
https://pubmed.ncbi.nlm.nih.gov/32901963
Publikováno v:
British Dental Journal. 221:727-730
Hereditary dentine dysplasias (HDD) such as dentinogenesis imperfecta (DI) and dentine dysplasia (DD) are a group of genetic conditions characterised by an abnormal dentine structure due to disturbances in the formation, composition, or organisation
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b2e016231c7f80c465654bc98ae713b2
https://doi.org/10.1038/sj.bdj.2016.915
https://doi.org/10.1038/sj.bdj.2016.915